Literature DB >> 33842694

Grandchild's IQ is associated with grandparental environments prior to the birth of the parents.

Jean Golding1, Gerard van den Berg2, Kate Northstone1, Matthew Suderman1, Genette Ellis1, Yasmin Iles-Caven1, Steve Gregory1, Marcus Pembrey1.   

Abstract

Background. Despite convincing animal experiments demonstrating the potential for environmental exposures in one generation to have demonstrable effects generations later, there have been few relevant human studies. Those that have been undertaken have demonstrated associations, for example, between exposures such as nutrition and cigarette smoking in the grandparental generation and outcomes in grandchildren. We hypothesised that such transgenerational associations might be associated with the IQ of the grandchild, and that it would be likely that there would be differences in results between the sexes of the grandparents, parents, and children. Method. We used three-generational data from the Avon Longitudinal Study of Parents and Children (ALSPAC).  We incorporated environmental factors concerning grandparents (F0) and focussed on three exposures that we hypothesised may have independent transgenerational associations with the IQ of the grandchildren (F2): (i) UK Gross Domestic Product (GDP) at grandparental birth year; (ii) whether grandfather smoked; and (iii) whether the grandmother smoked in the relevant pregnancy. Potential confounders were ages of grandparents when the relevant parent was born, ethnic background, education level and social class of each grandparent. Results. After adjustment, all three target exposures had specific associations with measures of IQ in the grandchild. Paternal grandfather smoking was associated with reduced total IQ at 15 years; maternal grandfather smoking with reduced performance IQ at 8 years and reduced total IQ at 15.  Paternal grandmother smoking in pregnancy was associated with reduced performance IQ at 8, especially in grandsons. GDP at grandparents' birth produced independent associations of reduced IQ with higher GDP; this was particularly true of paternal grandmothers. Conclusions. These results are complex and need to be tested in other datasets. They highlight the need to consider possible transgenerational associations in studying developmental variation in populations. Copyright:
© 2021 Golding J et al.

Entities:  

Keywords:  ALSPAC; Cognition; GDP; Grandfather; Grandmaternal smoking; IQ; Transgenerational effects

Year:  2021        PMID: 33842694      PMCID: PMC8008356          DOI: 10.12688/wellcomeopenres.16205.2

Source DB:  PubMed          Journal:  Wellcome Open Res        ISSN: 2398-502X


Introduction

Studies of IQ variation in populations have revealed several unexplained phenomena. Twin studies of IQ show greater correlation in monozygotic than same-sex dizygotic twins resulting in heritability estimates ranging from 0.5 to 0.8 ( Plomin & Deary, 2015), with estimates rising throughout early development, reaching around 0.8 at 18–20 years and continuing at that level well into adulthood. ( Bouchard, 2013). This heritability is generally assumed to be genetic – large numbers of genetic variants each with tiny effects – but to date genome wide association studies (GWAS) explain only a relatively small proportion of the variance in IQ. A recent, large-scale GWAS meta-analyses, that combined IQ and educational attainment data, found that common SNPs were only able to account for roughly half of the overall heritability of the phenotype ( Lam ). As with the heritability of height and other complex traits ( Boyle ; Yang ) there is a tendency to assume that any missing heritability in IQ is due to many, as yet undiscovered, DNA sequence variants. Whilst this is plausible, the possible contribution of environmental exposures both directly and indirectly through non-genetic (or epigenetic) biological inheritance should not be ignored. There is consistent evidence in several industrialised countries that the IQ of the population has risen over the decades, known as the Flynn effect ( Dickens & Flynn, 2001; Pietschnig & Voracek, 2015; Trahan ). A meta-analysis of studies published by 1997 also found evidence supporting the hypothesis that there was a strong intrauterine effect that accounted for some of the heritability estimates ( Devlin ). There is evidence that aspects of diet, such as prenatal diet of the mother and whether the infant was breast fed, also have strong associations with IQ in the child ( Hibbeln ; Kramer ). Furthermore, exposures need not be direct to have an influence. There is increasing evidence that intrauterine environments may affect not only the developing fetus but also the subsequent generation. Using grandmaternal smoking in pregnancy as the exposure, we have demonstrated this for grandchild’s growth, particularly in adolescence ( Golding ). As part of these initial intergenerational anthropometric studies using data from the Avon Longitudinal Study of Parents and Children (ALSPAC), we showed that boys with both mothers and paternal grandmothers who had smoked in pregnancy had significantly smaller heads at birth than their peers whose mothers had smoked but whose paternal grandmothers had not smoked. This intriguing finding was robust to the effects of confounding by current lifestyle and socio-economic background ( Pembrey ). Knowing the evidence that a small head circumference at birth is associated with a lower IQ later in childhood ( Gale ), we demonstrated that these particular boys had lower IQ scores on average, and that this was particularly due to the verbal component ( Pembrey ). We should emphasise, however, that this was part of a study focused on anthropometric outcomes, and we have recently begun to investigate this question in terms of a range of neurological and behavioural outcomes. We have so far uncovered associations between maternal grandmother smoking prenatally and autistic traits in the grandchild ( Golding ), and between paternal grandmother smoking and early onset myopia in the grandchild ( Williams ). The present study is focused on the grandparental environment prior to the birth of the parents and cognition in the grandchildren in childhood and late adolescence. The currently available data on grandparental exposures include grandfathers’ smoking, the GDP of the year of birth of each grandparent (both the trend and the business cycle), in addition to grandmaternal smoking during the pregnancy resulting in the birth of the parent, where tentative transgenerational associations with the grandchild’s IQ have already been observed. We hypothesise that grandfathers’ smoking may show transgenerational IQ associations, since smoking by fathers in mid-childhood is associated with altered growth and development of their offspring into adulthood ( Golding ; Northstone ). The GDP of the year of the birth of the grandparents is a potential candidate for transgenerational associations, given recent population findings of associations between this factor and both newborn health ( van den Berg ) and cardiovascular health in adulthood ( Alessie ). Most inter/transgenerational associations can be expected to have contributions from social patterning, genetic (DNA sequence) inheritance and non-genetic gametic inheritance, such as transmission of epigenetic information to the next generation(s). Understanding the contribution of each to the variation in cognitive ability will be an immense challenge, needing comprehensive, multigenerational, prospective cohort studies. The current study represents a start. For the purposes of this paper, which does not include molecular/epigenetic analyses, we will just use ‘transgenerational’ as a general term for the observed associations between grandparental exposures and grandchild’s outcomes, irrespective of whether direct exposure of the germline destined for the grandchild may have occurred.

Methods

The study sample

ALSPAC is a pre-birth cohort designed to determine the environmental and genetic factors that are associated with health and development of the study offspring ( Boyd ; Fraser ; Golding ). It recruited pregnant women who were resident in Avon, UK with expected dates of delivery between 1st April 1991 and 31st December 1992 (an estimated 80% of the eligible population). The initial number of pregnancies enrolled was 14,541 (for these at least one questionnaire had been returned or a “Children in Focus” clinic had been attended by 19/07/99). Of these initial pregnancies, there was a total of 14,676 fetuses, resulting in 14,062 live births and 13,988 children who were alive at 1 year of age. Data were collected at various time-points using self-completion questionnaires, biological samples, hands-on measurements, and linkage to other data sets. Full details of all the data collected are available on the study website: www.bristol.ac.uk/alspac/researchers/data-access/data-dictionary/. As part of the study design, there was a concerted effort before the child’s birth to obtain from each of the parents (F1) details of their own parents (F0). The pregnant women were sent four questionnaires during pregnancy, one of which requested details of their parents; in parallel they were sent two questionnaires for their partners to complete, one of which included similar questions on the partner’s own parents.

Ethical approval

Ethical approval for the study was obtained from the ALSPAC Ethics and Law Committee (ALEC) (ALEC IRB00003312) (registered on the Office of Human Research Protections database as UBristol IRB#1) and the three NHS Local Research Ethics Committees (LRECs) that covered the study area (Southmead, Bristol & Weston and Frenchay). ALEC agreed that consent was implied if questionnaires were returned ( Birmingham, 2018). Further detailed information on the ways in which confidentiality of the cohort is maintained and a full list of ethical approvals may be found on the study website: http://www.bristol.ac.uk/alspac/researchers/research-ethics/

The outcome measures: IQ tested at ages 8 and 15

The study children (F2) were invited to attend for a half day of tests when they were aged 8. The tests included the WISC-III UK ( Wechsler ) to assess cognitive function. At the time it was the most up to date version of the Weschler Intelligence Scale for Children, the most widely used individual ability test worldwide. We used a short form of the measure with alternate items (always starting with item number 1 in the standard form) for all subtests, except for the coding subtest which was administered in its full form. This resulted in a reduction in the length of the session and the children were less likely to tire; such reduced formats of the WISC have been used successfully in several studies (e.g. Finch & Childress, 1975; Stricker ). The tests were administered by members of the ALSPAC psychology team and the WISC IQ scores (verbal, performance and total IQ) were calculated from the total scaled scores using the look-up tables provided in the WISC manual. When the study children were aged 15, the Wechsler Abbreviated Scale of Intelligence, Second Edition (WASI-II) ( McCrimmon & Smith, 2013; Wechsler, 2011) was administered. This is an updated abbreviated measure of cognitive intelligence designed for individuals 6 to 90 years of age. It was developed to quickly and accurately estimate cognitive intelligence when administration of a full battery was not feasible or necessary. The full WASI-II consists of four subtests, selected as those with the highest factor loadings on g, the estimate of general intelligence. Because of time and cost restraints just two subtests were administered in ALSPAC: the vocabulary and matrix reasoning subtests, which were combined to form the Full-Scale IQ-2 subtest.

The exposures

The questionnaires sent to the parents (F1) during pregnancy elicited information on the following items of relevance to this project: The smoking histories of each of their own parents (i.e. the study grandparents (F0)). Parents were asked: ‘Did your mother ever smoke?’ If the response was ‘yes’, they were asked: ‘Did she smoke when she was expecting you?’ and given the option responses ‘yes / no/ don’t know’. Thus, the parents who replied ’don’t know’, had a mother (F0) who smoked but the parent (F1) was unsure whether she had smoked during her pregnancy. As with our other studies, we have analysed these data assuming that these women did smoke during pregnancy ( Golding ; Miller ; Miller ; Pembrey ). This assumption was shown to have face validity by demonstrating that the mean birthweight of this group of study mothers was reduced when compared with those who reported that their mother had definitely not smoked in pregnancy ( Pembrey ). The ages of each grandparent (F0) when the study parent (F1) was born. For each of the four study grandparents (F0) their years of birth were estimated from details of their ages at the time of birth of the relevant parent and the age of the parent when the study child was born. Two variables are based on the annual real Gross Domestic Product per capita (GDP) at the time of the birth of each grandparent. This is based on the total amount produced in the UK in a year, per inhabitant, and corrected for inflation. “Corrected for inflation” here means that everything is expressed in terms of 1990 US dollars. The annual real GDP per capita comes from Maddison (2003); Maddison, 2013 (updated) who provided internationally comparable historical macro-economic time series of such variables. Somewhat loosely, the annual real GDP per capita indicates the average economic activity per inhabitant in each year. We have used both the annual real GDP decomposed into a trend and a business cycle. The trend captures long-run trends in economic activity. The cycle is the business cycle fluctuating along the trend. The decomposition is the Hodrick-Prescott filter with smoothing parameter 100, over the years 1835–2001. The sum of trend and cycle equals the original variable. The social class of each grandparent (based on their occupations as reported by their offspring, the study parents (F1). The educational qualifications of each grandparent (grouped into the equivalent of O-level or higher, and lower than this). Ethnic group (grouped as white and all other). Parity (for grandmothers only) – i.e. whether the study parent was the first or later birth to that grandmother. These variables were considered as possible inter/trans-generational candidates and/or possible confounders ( Table 1).
Table 1.

Characteristics of the study grandparents (F0) according to their likely categorisation.

Measure of grandparentsMGMMGFPGMPGF
Year of birthSSSS
GDP at year of birthITTT
Business cycle at year of birthITTT
Age at birth of parentS+IS+TS+TS+T
Ethnic groupS+GS+GS+GS+G
Education levelS+GS+GS+GS+G
Social classSSSS
Parity of grandmother at birth of parentS+I-S+T-
Grandmother smoked in pregnancy resulting in parentI-T-
Ever smokedITTT

Exposures are categorised according to whether the associations with grandchild’s (F2) IQ are likely to be transgenerational (T), intergenerational (I), genetic (G) or socially transmitted (S).

MGM = maternal grandmother; MGF = maternal grandfather; PGM = paternal grandmother; PGF = paternal grandfather.

Exposures are categorised according to whether the associations with grandchild’s (F2) IQ are likely to be transgenerational (T), intergenerational (I), genetic (G) or socially transmitted (S). MGM = maternal grandmother; MGF = maternal grandfather; PGM = paternal grandmother; PGF = paternal grandfather. MGM = maternal grandmother; MGF = maternal grandfather; PGM = paternal grandmother; PGF = paternal grandfather. N denotes the number of the original population of parents who completed questions on their own parents. the proportions whose study child had a valid IQ measure are shown in columns 4 and 5.

Statistical approach

The analyses are designed to determine the relationships between different aspects of the environment of the grandparents (F0) of the study children (F2), particularly those that might indicate an inter- or trans-generational association (see Table 1). Among those that might indicate such a mechanism, we highlight: (a) the grandmother who smoked cigarettes during the pregnancy that resulted in the birth of the study parent (F1); (b) the study grandfather who smoked (we have assumed that all such smokers will have started smoking before the study parent was conceived); (c) the trend level in the GDP of the year of birth of each grandparent; and (d) the business cycle at the year of birth of each grandparent (independent of the trend). The variables that are more likely to be confounders were the education levels, ethnic group, social class and year of birth of each grandparent. We were agnostic about assignment of grandparental ages and parity of the grandmother at the birth of the parent to just one of these two categories of variables as they could be considered to be in either category. We analysed the data in a hypothesis free structure, taking care to ensure that we avoided Type I errors as much as possible; consequently, we did not allow for multiple testing. However, based on previous results from the animal and human literature, we hypothesised that if there were effects of an inter/trans-generational nature, we anticipated that the associations would differ between the sexes. We therefore analysed the grandsons and granddaughters separately for each of the maternal and paternal inheritance lines. The IQ score of the child was analysed as a continuous variable (using multiple regression). The initial analyses were unadjusted. In order to take account of the collinearity between many of the factors considered we employed a backwards step-wise approach using all grandparental variables that were associated with the unadjusted outcome at P<0.05 to determine the factors independently associated with the grandchild’s IQ level. The analyses were undertaken for each parent (F1), and for each sex of the F2 generation. Because this was a hypothesis-generating study we did not apply any correction for multiple testing. Nor did we use features of the parents as confounders. Instead, the social and educational features of the grandparents were used in the stepwise regression as confounders (which is essentially controlling for the socio-economic features of the parents’ childhoods). To then take into account other aspects of the parents and/or of the children as confounders would likely identify mechanisms by which the associations between exposures to the grandparents and the child’s IQ may have taken place, and could nullify the transgenerational effects themselves. Determining the possible mechanisms by which any transgenerational effects occur will be an important exercise for the future. In order to clarify the methodology, we first describe in detail the results for the Total IQ at age 8, so that the reader may understand the logical sequence of analyses. Thereafter we summarise the results in the text for other outcomes and illustrate the results in Extended data, Tables S1–S28b ( Iles Caven ).

Results

Total IQ at age 8

The numbers of parents who originally answered the questions on their own parents is shown in Table 2. These were answered in self-completion questionnaires when the mother was pregnant – by definition, she was resident in the study area at the time. In general, the study fathers were less likely to have answered these questions than the study mothers.
Table 2.

The data available for analysis.

Measure AvailableGrandparentN% (n) IQ at 8% (n) IQ at 15
Year of birth
MGM1092557.4 (6268)41.4 (4523)
MGF874567.3 (5889)49.0 (4282)
PGM808458.1 (4696)42.9 (3468)
PGF769358.8 (4523)43.3 (3334)
Ethnic origin
MGM1206655.7 (6717)40.0 (4824)
MGF1201855.7 (6694)40.0 (4803)
PGM967956.1 (5427)40.9 (3958)
PGF964656.1 (5412)41.0 (3952)
Education level
MGM925255.4 (5129)40.7 (3763)
MGF881055.0 (4844)40.2 (3542)
PGM750556.0 (4200)40.7 (3054)
PGF754455.9 (4214)40.7 (3069)
Smoked – ever
MGM1267752.1 (6605)37.3 (4728)
MGF1244952.4 (6526)37.5 (4674)
PGM964656.2 (5417)40.9 (3945)
PGF892156.3 (5024)41.2 (3671)
Parity
MGM1243254.7 (6798)39.2 (4879)
PGM368856.1 (2070)43.0 (1587)
Smoked in pregnancy
MGM1262052.1 (6576)37.3 (4705)
PGM960256.2 (5393)40.9 (3930)

MGM = maternal grandmother; MGF = maternal grandfather; PGM = paternal grandmother; PGF = paternal grandfather. N denotes the number of the original population of parents who completed questions on their own parents. the proportions whose study child had a valid IQ measure are shown in columns 4 and 5.

The first 8 years of the study resulted in many household moves of the study families, including within Avon, within the United Kingdom and to the rest of the world. The study children (F2) who did not attend to have their IQ measured included: those who were living outside the study area, those whose parents decided that the visit would not be appropriate for their child (e.g. children with autism), those who were lost to follow up or who had died. For children (F2) whose parents (F1) had answered the questions on their own parents (F0) the proportion who had IQ scores measured was approximately 55% at age 8, and 40% at age 15. IQ measures were less likely to have been obtained when the parents (F1) were younger and/or had lower levels of education or were resident in public housing (data not shown). The ways in which the mean IQ of the grandchildren varied with characteristics of their four grandparents is shown in Table 3. These unadjusted data show that the maternal grandparents were more likely (at P<0.01) to have grandchildren with significantly higher mean IQ if they: (a) were born before the Second World War (1940), and especially if before 1930; (b) were born when the GDP level was low; (c) had an educational qualification of at least O-level standard; (d) gave birth to the study parent at age 25 or older; (e) were of a relatively high social standing; (f) were non-smokers; and if (g) the maternal grandmother had not smoked when expecting the study parent (F1). There was a marginal decrease in grandchild’s IQ if the maternal grandmother (but no other grandparents) was non-white. Information on the grandmother’s parity at the birth of the study mother was available in a reduced sample; there was an association if the study father was the paternal grandmother’s first-born child.
Table 3.

Mean IQ of grandchildren at age 8 for information on the grandparents.

When more than 2 categories are given P-values are given for trend; associations when P<0.05 are highlighted in bold; and potential transgenerational associations are printed in red).

MGMMGFPGMPGF
Year of birth
    <1920 108.8 108.7 107.7 108.3
    1920-4 107.7 107.3
    1925-9 107.4 107.2 107.9 108.3
    1930-4 106.3 105.9 108.2 107.8
    1935-9 104.9 104.0 106.2 104.6
    1940-4 103.0 101.9 102.7 103.0
    1945+ 99.0 98.8 99.7 98.9
Total N 6268 [a] 5889 [a] 3732 [a] 3595 [a]
Year of birth [w] -3.04 [a] -2.57 [a] -2.05 [a] -1.80 [a]
Business cycle at birth [x] -2.81 [a] -2.68 [a] -2.23 [a] -2.15 [a]
GDP at birth [y] -0.10 -0.08 -0.29 0.00
Ethnic group
    White 104.5 104.5105.3105.4
    Non-white 101.2 102.9103.8104.4
Total N 6717 [d] 669454275412
Education level
    ≥O-level 108.9 109.3 110.3 109.5
    <O-level 103.4 102.6 104.0 104.0
Total N 5129 [a] 4844 [a] 4200 [a] 4214 [a]
Ever smoked
    Yes 103.6 103.7 104.3 105.0
    No 105.3 106.3 106.7 107.2
Total N 6605 [a] 6526 [a] 5417 [a] 5024 [b]
Age at birth of parent (F1)
    <25 102.5 102.5 103.9 103.5
    25–34 106.1 105.4 107.1 106.8
    35–39 106.4 107.1 106.9 107.1
    40+ 106.0 107.1
Total N 6268 [a] 5889 [a] 4696 [a] 4518 [a]
Trend with age [z] +1.81 [a] +1.30 [a] +1.32 [a] +1.11 [a]
Social class
I 107.7 111.2 114.4 111.4
II 108.7 108.4 108.3 108.5
IIINm 105.2 106.4 106.0 107.8
IIIM 101.4 101.8 103.5 103.0
IV 102.3 102.9 103.8 103.2
V 100.0 98.4 100.7 102.5
Total N 3791 [az] 5597 [az] 2865 [az] 5033 [az]
Parity at birth of parent
0102.9 108.2
1+105.1 105.5
Total N6798 2070 [b]
Grandmother smoked in pregnancy
    Yes 102.9 - 103.9 -
    No 105.1 - 106.4 -
Total N 6576 [a] - 5393 [a] -

MGM = maternal grandmother; MGF = maternal grandfather; PGM = paternal grandmother; PGF = paternal grandfather. aP<0.0001; bP<0.001; dP<0.05. wtrend per 5-year grouping; xtrend standardised GDP per year; [y]Trend per year of birth; ztrend per category above.

Mean IQ of grandchildren at age 8 for information on the grandparents.

When more than 2 categories are given P-values are given for trend; associations when P<0.05 are highlighted in bold; and potential transgenerational associations are printed in red). MGM = maternal grandmother; MGF = maternal grandfather; PGM = paternal grandmother; PGF = paternal grandfather. aP<0.0001; bP<0.001; dP<0.05. wtrend per 5-year grouping; xtrend standardised GDP per year; [y]Trend per year of birth; ztrend per category above. These associations are put in context when the R 2 values (contribution to the variance) from each variable are considered ( Table 4). This shows that, when using the unadjusted comparisons, the major contributor to the variance of the grandchild’s IQ level are the grandparents’ years of birth, the GDP trend level at the time of their birth, their education levels and their social classes.
Table 4.

Summary of unadjusted associations (R 2%) between grandparental background features and their grandchild’s 8-year-old total IQ.

Potential transgenerational associations are printed in red.

Measure concerning Grandparent (F0)MGMMGFPGMPGF
nR 2%nR 2%nR 2%NR 2%
Year of birth62683.14 [a] 58892.26 [a] 37321.45 [a] 35951.13 [a]
GDP at birth 6268 2.83 [a] 5889 2.45 [a] 3732 1.70 [a] 3595 1.54 [a]
Business cycle 6268 0.00 5889 0.00 3732 0.03 3595 0.00
Ethnic origin67170.06 [d] 66940.0254270.0254120.01
Education level51292.57 [a] 48443.88 [a] 42003.24 [a] 42142.64 [a]
Smoked 6605 0.26 [b] 6526 0.47 [b] 5417 0.53 [a] 5024 0.30 [a]
Age at birth of parent (F1)62681.19 [a] 58890.61 [a] 46960.64 [a] 45180.44 [a]
Social class37912.83 [a] 55974.27 [a] 28632.21 [a] 50333.03 [a]
Parity 67980.00--20700.60 [b] --
Smoked when expecting parent 6576 0.39 [a] - - 5393 0.55 [a] - -

MGM = maternal grandmother; MGF = maternal grandfather; PGM = paternal grandmother; PGF = paternal grandfather.

aP<0.0001; bP<0.001; dP<0.05.

Summary of unadjusted associations (R 2%) between grandparental background features and their grandchild’s 8-year-old total IQ.

Potential transgenerational associations are printed in red. MGM = maternal grandmother; MGF = maternal grandfather; PGM = paternal grandmother; PGF = paternal grandfather. aP<0.0001; bP<0.001; dP<0.05. Contribution to the variance is not equivalent to effect sizes and does not necessarily indicate which factors are independent of one another. We therefore first carried out backwards step-wise multiple regression using the variables in the maternal line. Dropped from the final model were the following potential transgenerational associations: the GDP trend level associated with the maternal grandmother’s year of birth, whether the maternal grandfather was a smoker, whether the grandmother smoked in the pregnancy resulting in the birth of the study mother. The independent factors associated with the grandchild’s IQ were all features where the transgenerational associations were likely to be learnt rather than inherited ( Table 5).
Table 5.

Results of stepwise analysis of grandchild’s total IQ at 8 involving the maternal line.

β is the standardised regression coefficient with 95% confidence interval; potential transgenerational associations are printed in red.

Unadjusted analysesAdjusted analysis
Maternal lineNβ [95% CI]Pb [95% CI]P
Maternal grandmother’s year of birth [x] 6267-0.36 [-0.41. -0.31] 1.3 x 10 -45 -0.53 [-0.64, -0.41] 6.4 x 10 -19
GDP in MGM’s birth year [ y ] 6267 -2.89 [-3.30, -2.47] 1.5 x 10 -42
Mother’s ethnicity: white v non-white 67163.30 [0.15, 6.46] 0.040
Maternal grandmother’s education level 51282.59 [2.25, 2.94] 1.1 x 10 -48 1.33 [0.84, 1.81] 8.3 x 10 -8
Maternal grandfather’s education level 48432.70 [2.38, 3.01] 1.4 x 10 -60 1.07 [0.60, 1.54] 8.1 x 10 -6
Maternal grandfather ever smoked 6525 -2.59 [-3.50, -1.68] 2.8 x 10 -8
Grandmother’s age at birth of mother 62670.30 [0.24, 0.38] 4.7 x 10 -18 -0.33 [-0.49, -0.16] 1.3 x 10 -4
Grandfather’s age at birth of mother 58880.19 [0.13, 0.26] 2.2 x 10 -9
MGM parity at birth of mother 6797-0.13 [-0.96, 0.71]0.763
Maternal grandfather’s social class 5596-2.76 [-3.11, -2.42] 4.5 x 10 -55 -1.33 [-1.82, -0.85] 6.1 x 10 -8
MGM smoked when pregnant with mother 6576 -2.15 [-2.99, -1.32] < 0.0001

xTrend in IQ per year of grandparent’s birth; ytrend in IQ per standardised GDP per year; MGM = maternal grandmother. N = 3670; R 2 = 9.85%

Results of stepwise analysis of grandchild’s total IQ at 8 involving the maternal line.

β is the standardised regression coefficient with 95% confidence interval; potential transgenerational associations are printed in red. xTrend in IQ per year of grandparent’s birth; ytrend in IQ per standardised GDP per year; MGM = maternal grandmother. N = 3670; R 2 = 9.85% The pattern of association between the characteristics of the paternal grandparents and the grandchild’s IQ was similar to that shown for the maternal grandparents, with positive associations if the grandparents were born prior to the Second World War; were more educated; were non-smokers; aged 25 at least at the birth of the study father; belonged to a non-manual social class based on their occupations. In addition, there was a negative association when the paternal grandmother smoked in the pregnancy resulting in the birth of the study father ( Table 3). We used a similar analysis for the paternal line as was carried out for the maternal line. Of the highly significant unadjusted associations, only one of the presumed transgenerational associations remained in the adjusted analysis: the GDP trend level in the paternal grandmothers’ year of birth ( Table 6). The adjusted result: β = -1.86; 95% CI -2.50, -1.22; P = 1.2 × 10 -8 suggests that the lower the GDP trend level at the paternal grandmothers’ birth, the higher the IQ level of her grandchild.
Table 6.

Results of stepwise analysis of grandchild’s total IQ at 8 involving the paternal line.

β is the standardised regression coefficient with 95% confidence interval; potential transgenerational associations are printed in red.

Unadjusted analysesAdjusted analysis
PATERNAL LINENβ [95% CI]Pβ [95% CI]P
Paternal grandmother’s year of birth [x] 3736-0.23 [-0.29, -0.17] 1.7 x 10 -13
Paternal grandfather’s year of birth [x] 3599-0.19 [-0.25, -0.13] 1.3 x 10 -10
GDP in PGM’s birth year [ y ] 3736 -2.31 [-2.86, -1.76] 1.5 x 10 -16 -1.86 [-2.50, -1.22] 1.2 x 10 -8
Paternal grandmother’s education level 42002.54 [2.18, 2.91] 5.1 x 10 -41 2.18 [1.69, 2.66] 2.8 x 10 -18
Paternal grandfather’s education level 42142.07 [1.73, 2.40] 1.4 x 10 -32
Grandmother’s age at birth of father 46960.22 [0.14, 0.30] 4.1 x 10 -8
Grandfather’s age at birth of father 45180.16 [0.09, 0.23] 7.4 x 10 -6
Paternal grandfather’s social class 5033-2.37 [-2.74, -2.00] 1.4 x 10 -35 -1.05 [-1.59, -0.52] 1.3 x 10 -4
PGM smoked when pregnant with father 5393 -2.47 [-3.36, -1.58] <0.0001

xTrend in IQ per year of grandparent’s birth; ytrend in IQ per standardised GDP per year; PGM = paternal grandmother. N=2708; R 2=6.10%

Results of stepwise analysis of grandchild’s total IQ at 8 involving the paternal line.

β is the standardised regression coefficient with 95% confidence interval; potential transgenerational associations are printed in red. xTrend in IQ per year of grandparent’s birth; ytrend in IQ per standardised GDP per year; PGM = paternal grandmother. N=2708; R 2=6.10% Comparison of the separate analyses of the maternal grandparents according to the sex of the grandchild showed that no potential transgenerational association was retained in either model ( Extended data, Tables S1 and S2) ( Iles Caven ). However, for the paternal line, as with the sexes combined, there were associations with the trend in GDP with the year of birth of the paternal grandmother for both the grandsons and granddaughters. There were major differences in effect sizes between the sexes in the adjusted trend in GDP of the paternal grandmother’s birth year. For both the grandsons and granddaughters, the adjusted regression coefficient had a P value < 4×10 -4, but the association relating to the granddaughters was significantly more negative than that for the grandsons (P for interaction < 0.05) ( Table 7 and Extended data, Tables S3 and S4) ( Iles Caven ).
Table 7.

Summary of all adjusted results with potential transgenerational associations associated with 8-year-old grandchild’s total IQ.

See Extended data, Tables S1–S27 ( Iles Caven ) for details of analyses.

Exposure to GrandparentF0OutcomeSex of Grandchildβ [95% CI]
GDP of birth year y PGMTotal IQ at 8All-1.86 [-2.50, -1.22] a
Boys-1.74 [-2.70, -0.78] a
Girls-3.08 [-4.34, -1.82] a
PGFTotal IQ at 15All-2.99 [-3.82, -2.15] a
Girls-2.28 [-3.12, -1.44] a
PGMVerbal IQ at 8All-2.81 [-3.77, -1.85] a
Boys-2.04 [-2.98, -1.09] a
Girls-3.10 [-4.41, -1.80] a
PGMPerformance IQGirls-2.74 [-4.05, -1.43] a
MGMTotal IQ at 15All-2.01 [-3.68, -0.33] d
Boys-4.73 [-5.90, -3.55] a
MGFPerformance IQAll-2.00 [-2.61, -1.38] a
MGMBoys-1.80 [-2.64, -0.97] a
GDP business cycle z PGMVerbal IQ at 8Girls+0.90 [+0.04, +1.75] d
Grandfather smokedPGFTotal IQ at 15All-2.75 [-4.40, -1.09] c
Girls-2.53 [-4.32, -0.73] b
MGFTotal IQ at 15All-1.07 [-2.13, -0.02] d
Girls-1.61 [-2.98, -0.24] d
Performance IQAll-2.03 [-3.30, -0.76] b
Boys-2.92 [-4.69, -1.14] c
Girls-1.87 [-3.50, -0.25] d
Grandmother smoked when pregnantPGMVerbal IQ at 8Boys -2.51 [-2.36, -0.66] c
PGMPerformance IQAll-2.67 [-4.00, -1.34] a
Boys-2.01 [-3.63, -0.39] d
Girls-1.79 [-3.52, -0.06] d

aP<0.0001; bP<0.001; cP<0.01; dP<0.05. ytrend in IQ per standardised GDP per year.

MGM = maternal grandmother; MGF = maternal grandfather; PGM = paternal grandmother; PGF = paternal grandfather.

Summary of all adjusted results with potential transgenerational associations associated with 8-year-old grandchild’s total IQ.

See Extended data, Tables S1–S27 ( Iles Caven ) for details of analyses. aP<0.0001; bP<0.001; cP<0.01; dP<0.05. ytrend in IQ per standardised GDP per year. MGM = maternal grandmother; MGF = maternal grandfather; PGM = paternal grandmother; PGF = paternal grandfather.

Total IQ at age 15

Results for the relationships between the characteristics of the grandparents and the grandchild’s Total IQ at age 15 are shown in Extended data, Tables S5–S12 ( Iles Caven ). In summary these show that two possible transgenerational associations were retained in the model concerning the maternal line: the GDP trend level at maternal grandmother’s year of birth and whether the maternal grandfather was a smoker ( Extended data, Table S7) ( Iles Caven ). When the grandsons were analysed separately, the trend in the maternal grandmother’s GDP trend level was retained, but not the grandfather’s smoking. For the granddaughters, whether the maternal grandfather was a smoker was retained but not the maternal grandmother’s GDP trend level at birth ( Table 7 and Extended data, Tables S8 and S9) ( Iles Caven ). Overall, for the paternal line, the only potential transgenerational association retained was whether the grandfather was a smoker ( Extended data, Table S8) ( Iles Caven ). Separate analysis for grandsons resulted in no potential transgenerational associations remaining in the model ( Extended data, Table S11), but for the granddaughters both the GDP trend level in the paternal grandfather’s year of birth and whether he smoked were retained ( Table 7 and Extended data, Table S12) ( Iles Caven ).

Verbal and performance IQs at age 8

The data concerning the verbal and performance subgroups of the total IQ measure were analysed in a similar way (see Extended data, Tables S13–S27) ( Iles Caven ) and are summarised below. Unadjusted associations for the variables in the maternal line were apparent for all the variables considered with the exception of the business cycle at the year of birth, maternal parity and the ethnic group of the maternal grandfather ( Extended data, Tables S13 and S14) ( Iles Caven ). Adjusted analysis revealed the same five variables being retained in the model as found for the Total IQ at 8 – none of these variables were potential transgenerational associations; similar results were found for grandsons and granddaughters when analysed separately ( Extended data, Tables S15, S17 and S18) ( Iles Caven ). For the paternal line, adjusted analysis of all grandchildren resulted in four variables being retained, one of which was a possible transgenerational association: GDP trend in year of birth of the paternal grandmother ( Extended data, Table S16) ( Iles Caven ). There were different results for the grandsons (where the smoking of the paternal grandmother in the pregnancy resulting in the father was retained, but not the trend in GDP), and the granddaughters (with the trend in GDP as well as the business cycle prevailing in the year of birth of the paternal grandmother) ( Table 7 and Extended data, Tables S19 and S20) ( Iles Caven ). For the maternal line, all variables had unadjusted associations with the exception of the business cycles, ethnic groups and parity ( Extended data, Tables S21 and S22) ( Iles Caven ). Upon adjustment, two potential transgenerational associations were retained – the trend in GDP with maternal grandmother’s year of birth and whether the maternal grandfather was a smoker. The same association with the paternal grandfather being a smoker was apparent for both grandsons and granddaughters, but the association with the trend in GDP of birth year of the maternal grandmother was only retained in the grandson’s model ( Extended data, Tables S24 and S25) ( Iles Caven ). Among the variables describing the paternal line, neither the paternal grandfather smoking nor any variables associated with GDP entered, but there was an association with the paternal grandmother smoking in the pregnancy that resulted in the birth of the study father ( Extended data, Table S23) ( Iles Caven ). This exposure was retained in the model for the grandsons but not the granddaughters. For the granddaughters the trend in GDP when the paternal grandmother was born was retained ( Extended data, Tables S26 and S27) ( Iles Caven ).

Discussion

This paper follows on from our earlier studies showing differing associations between the grandmother smoking in pregnancy and the outcome of the grandchild, often depending on the grandchild’s sex. We previously demonstrated clear associations between grand-maternal prenatal smoking and intrauterine growth (including head circumference at birth); child growth and increasing body mass index (BMI) in adolescence; asthma; autism and autistic traits. We had, therefore, hypothesised that there would be associations between the grandmaternal smoking in pregnancy and the IQ of the grandchild. Unlike our previous studies, we decided here to include other exposures of the grandparents that might exhibit associations in later generations. We highlighted for consideration, among the variables collected, the smoking habit of each grandfather, and the GDP at the year of birth of each grandparent as potential exposures that might show transgenerational associations (this was analysed as a trend as well as a component of the business cycle). We used the social variables available concerning the grandparents as confounders since it was likely that the social circumstances and education would be passed from one generation to another by social patterning rather than by genetic or transgenerational non-genetic inheritance. Our research questions were largely hypothesis generating. We did not specify the direction in which associations might be found, but we did predict that associations were likely to be specific to the sex of the grandparent exposed and/or the sex of the affected grandchild. We found 25 significant associations with these variables: 9 down the female line, and 16 down the male line ( Figure 1 and Table 7). The results are summarised below.
Figure 1.

The adjusted associations at P<0.05 between grandparental exposures and grandchild IQ.

( A) Grandmother smoking during pregnancy. ( B) Grandfather being a smoker. ( C) GDP when the grandmother was born. ( D) GDP when grandfather was born. MGM=Maternal grandmother; MGF=Maternal grandfather; PGM=Paternal grandmother; PGF=Paternal grandfather.

The adjusted associations at P<0.05 between grandparental exposures and grandchild IQ.

( A) Grandmother smoking during pregnancy. ( B) Grandfather being a smoker. ( C) GDP when the grandmother was born. ( D) GDP when grandfather was born. MGM=Maternal grandmother; MGF=Maternal grandfather; PGM=Paternal grandmother; PGF=Paternal grandfather.

Grandmother smoking in the pregnancy resulting in the birth of the parent

We found no significant associations with a history of the maternal grandmother smoking when pregnant with the study mother. For the paternal grandmother smoking in the pregnancy resulting in the birth of the study father, there were associations with a lower Performance IQ for all 8-year-old grandchildren as well as for grandsons and granddaughters when analysed separately; there was also an association with a lower verbal IQ for the grandsons. There were no associations with the Total IQ at either age 8 or age 15 ( Figure 1A; Table 7).

Grandparents’ smoking habit

There were no adjusted associations with the grandmother smoking, other than when she had smoked during pregnancy as described above. Grandfather’s smoking, however, was associated down the maternal line with Performance IQ for all grandchildren, grandsons only and granddaughters only, and with Total IQ at 15 with granddaughters only and with all grandchildren. Down the male line, grandfather smoking was associated with Total IQ at 15, especially in granddaughters rather than grandsons ( Figure 1B).

Trends in GDP in the year of birth of the grandmothers and grandfathers

The trend in the GDP present during the year of birth of each grandparent showed different adjusted associations with the IQ outcomes: (a) that of the maternal grandmother was associated with the Total IQ at age 15 for all grandchildren and particularly for the grandsons; (b) that of the paternal grandmother was associated with the Total IQ at 8, and the verbal IQ for all grandchildren as well as for the grandsons and granddaughters considered separately – in addition the granddaughters (but not grandsons) had a lower performance IQ when the paternal grandmother had been born in a year with a higher GDP; (c) the trend in the GDP for the years of birth of the maternal grandfather was associated with the performance IQ among all grandchildren, but not statistically significant at P<0.05 among either the grandsons or granddaughters when analysed separately; (d) the trend among the offspring of the paternal grandfathers was associated with Total IQ at 15 for all grandchildren, and for granddaughters when analysed separately ( Table 7 and Figure 1C, D).

GDP business cycle at birth of grandparents

Only one association with business cycle survived adjustment (positive association between paternal grandmother business cycle and verbal IQ of granddaughters) ( Extended data, Table S20) ( Iles Caven ).

Adjusting for multiple tests

The study was designed to develop hypotheses rather than to test them. We carried out a total of 12 tests for each of four exposures and four outcomes – i.e. 192 tests. Chance would dictate that there would be at least two results with a P value <0.01, and 0.2 at P<0.001. The current adjusted analyses identified 15 results at P<0.001, 13 of which had a P<0.0001. Thus, there are many more associations than would be expected by chance. However, that does not, at this stage, imply causal effects – even though some of the features were hypothesised (i.e. that the results would differ according to whether the maternal or paternal line, and whether grandson or granddaughter was considered). It should be acknowledged that, although the numbers of individual grandparent/grandchild pairs were larger than in other studies, they are still smaller than would be required to demonstrate significance for any other than large effect sizes. Importantly, although the numbers considered down the paternal line were only about half of those considered down the female line, it was the paternal line that showed more significant associations.

Could grandparental smoking have a transgenerational effect?

We have shown an association here between the paternal grandmother smoking in the pregnancy resulting in the father and performance and verbal IQ, especially in the grandsons. This mirrors a study that we had published earlier looking at fetal growth when the paternal grandmother and the study mother had both smoked in pregnancy - this showed a deficit in head circumference at birth among the grandsons, with an accompanying reduction in IQ at 8 years. In that study we controlled for social circumstances present at the time of birth of the grandchild ( Miller ). Here we have controlled for social circumstances present at the time of birth and childhood of the grandparents. Both methods of analysis have shown an association between paternal (but not maternal) grandmother smoking prenatally and a deficit in IQ of the grandchildren, especially the grandsons. This was independent of whether the study mother had smoked or not (data not shown). We have not examined possible effects of the grandfather smoking prior to the pregnancy, although we have shown associations between the father starting to smoke regularly in mid-childhood and his son’s obesity, which increased with age ( Golding ; Northstone ). Here if the grandfather was reported to be a smoker, we have assumed that he was likely to have smoked before the study parent was conceived, since past population survey data indicate that the commencement of smoking whilst a teenager was particularly high, and in the 1920s–1930s there is substantial evidence that the prevalence of smoking was approximately 90% of men in the UK ( Forey ). In this study, we have shown associations between Total IQ at age 15 with both the maternal and paternal grandfathers being smokers. The effect sizes were larger for the granddaughters than the grandsons. There was also an association between the maternal grandfather being a smoker and performance IQ for both grandsons and granddaughters. There were no associations, however, with Total IQ at 8 or verbal IQ at 8.

GDP in the year of birth of the grandparents

Of the 96 tests carried out, 13 demonstrated an association between increasing levels of GDP at the time of a grandparent’s birth and a reduction in the IQ of their grandchild. This was particularly true for the years of birth of the grandmothers as opposed to grandfathers (10 and 3 respectively). However, the trends in year of birth of the grandparents and the trends in GDP were strongly correlated ( Extended data, Table S28a, b) ( Iles Caven ), and it is possible that the trend in GDP was measuring the same construct as the trend in year of birth. We did not force the two variables into the same regressions because of the collinearity that would result.

Strengths and limitations of the study

Among the strengths are the following: (a) The data on the grandparents were collected at the time the study mother was pregnant, and therefore could not be biased by knowledge of the IQ of the offspring. (b) There was unlikely to be gross misreporting of the smoking habits of the grandparents – the parents were likely to know their parents’ smoking habits. (c) It is noteworthy that the grandmothers would mostly have been pregnant with the study parents long before the health message concerning the disadvantages to the unborn baby of maternal smoking were known. Consequently, it is unlikely there would be biases concerning those grandmothers who were health conscious and those who were not in regard to smoking. (d) Although the information concerning whether the grandmother (F0) smoked during the pregnancy resulting in the birth of the parent (F1) was sometimes missing, we have assumed she did smoke prenatally if she smoked but it was not known if this occurred during pregnancy. There is evidence that this was an appropriate assumption since the mean birthweights of the parents were reduced to the extent that one would expect if smoking had occurred ( Pembrey ). (e) The proportion of the offspring for whom a valid measure of IQ was available was reasonably consistent for the different grandparent measures ( Table 2). There are several limitations: (i) There are no replication studies currently published to confirm (or refute) these findings. (ii) Information on the grandparents’ environments relied on reports from the parents – although these are unlikely to be 100% accurate, others have shown that parental report of their parents smoking in pregnancy has a high reliability (kappa = 0.61; Pape ). (iii) It could be argued that the factors controlled for in this study were inappropriate, or that key covariates were missing. We deliberately controlled for the social and demographic variables current at the time of the grandmother’s pregnancy or earlier, rather than social factors operating at the time of the birth of the grandchild, since there is evidence, for example, that prenatal smoke exposure is linked to a variety of poor outcomes which could influence the development and achievements of the subsequent generation (i.e. F1). Thus, controlling for F1 factors such as their education or social status might be an over-control. (iv) Selective fertility among F0 and F1 is an additional limitation of this study (as it is for any intergenerational study). For example, those in F0 exposed to adverse conditions might be less fertile and hence be less likely to generate any F2 offspring. This could lead to a bias in interpretation.

Conclusions

In line with our other studies, we find that smoking of the grandparents is associated with demonstrable changes in the grandchild, this time involving IQ; and similar to our other studies, we found that the associations were stronger in one sex than the other. If substantiated in other studies this raises the question as to what the mechanism might be. IQ is a composite measure, combining a number of different features, and we hypothesise that there are likely to be different mechanisms in consequence. We have argued elsewhere ( Hall ), ‘At present we are largely ignorant of the causal pathways underpinning this and similar intergenerational responses to grandmaternal smoking in pregnancy. As indicated in the Introduction, the exposure of either (F1) parent to tobacco as a fetus may have resulted in a direct xenobiotic exposure to both their developing somatic tissues and their emerging germline, ultimately destined for any (F2) grandchildren. Alternatively, it may be the generalised DNA damage caused by (F0) grandmaternal smoking and/or the consequent DNA damage response of the fetus that modifies the emerging germline and alters F2 embryonic brain development. Clearly very complex, it is premature to speculate further.’

Data availability

Underlying data

ALSPAC data access is through a system of managed open access. The steps below highlight how to apply for access to the data included in this data note and all other ALSPAC data: Please read the ALSPAC access policy ( http://www.bristol.ac.uk/media-library/sites/alspac/documents/researchers/data-access/ALSPAC_Access_Policy.pdf) which describes the process of accessing the data and samples in detail, and outlines the costs associated with doing so. You may also find it useful to browse our fully searchable research proposals database ( https://proposals.epi.bristol.ac.uk/?q=proposalSummaries), which lists all research projects that have been approved since April 2011. Please submit your research proposal ( https://proposals.epi.bristol.ac.uk/) for consideration by the ALSPAC Executive Committee. You will receive a response within 10 working days to advise you whether your proposal has been approved.

Extended data

Figshare: Supplementary data on grandparental smoking and environmental exposures and IQ in grandchildren.pdf. https://doi.org/10.6084/m9.figshare.12789359 ( Iles Caven ). File ‘Additional data.pdf’ contains Tables S1–S28. Extended data are available under the terms of the Creative Commons Attribution 4.0 International license (CC-BY 4.0). The authors have responded to our comments and suggestions and we agree that you can change the status to “approved” on our part. Upon re-reading the manuscript, we noted these errors: To improve clarity, we would also like to encourage the authors to specify the linear regression method used (i.e., Ordinary Least Squares or Maximum Likelihood estimation). Our approval is however not conditional on a response to these remarks. Table S10 has a point-estimate (-8.84) which is outside of its confidence interval (-4.99, -2.68). In Table S26, there is a numerical error of “1-0.11” instead of “-0.11”. Is the work clearly and accurately presented and does it cite the current literature? Partly If applicable, is the statistical analysis and its interpretation appropriate? Partly Are all the source data underlying the results available to ensure full reproducibility? Yes Is the study design appropriate and is the work technically sound? Yes Are the conclusions drawn adequately supported by the results? Yes Are sufficient details of methods and analysis provided to allow replication by others? Partly Reviewer Expertise: Statistics, Neuroscience. We confirm that we have read this submission and believe that we have an appropriate level of expertise to confirm that it is of an acceptable scientific standard. No further comments, approved. Is the work clearly and accurately presented and does it cite the current literature? Yes If applicable, is the statistical analysis and its interpretation appropriate? I cannot comment. A qualified statistician is required. Are all the source data underlying the results available to ensure full reproducibility? Yes Is the study design appropriate and is the work technically sound? Yes Are the conclusions drawn adequately supported by the results? Yes Are sufficient details of methods and analysis provided to allow replication by others? Yes Reviewer Expertise: Multi-generation research in humans, mainly in asthma/allergies. I confirm that I have read this submission and believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard. In their paper, Golding and co-workers explore the potential associations between environmental exposures in grandparents (UK gross domestic product, GDP, at their time of birth and their smoking history) and performance of their grandchildren on tests of intelligence. The primary objective was to generate support for the very interesting hypothesis that such exposures have transgenerational, sex-specific, effects detectable at the level of cognitive performance. To this end the authors explore multi-generational data available in ALSPAC. In their introduction, the authors cite relevant literature including some of the many studies to date that have reported on the high, and increasing, degree of heritability of adult intelligence and the contribution of common genetic variation to this complex trait. The authors could also acknowledge the large degree of genetic correlation that has been reported between intelligence and many mental and somatic disorders and traits. Of relevance to the current study is the highly significant inverse genetic correlation between general cognitive ability and smoking history reported by Trampush et al. (Trampush, 2017) [1]. Such data suggests that a phenotypic association between smoking and intelligence observed among related individuals is expected on a purely genetic basis. The authors could also elaborate a bit more on the rationale for choosing GDP as an exposure in the introduction. The authors used questionnaire data on exposures; grandparental smoking history (provided by parent) and the gross domestic product of the UK (GDP) at the time of birth of the grandparent along with the co-variates grandparental educational level, social class, birth-year, age at birth of parent (all provided by parents). The authors suggest that associations with grandparental smoking history and/or GDP are likely to represent inter/transgenerational effects and investigate these using multiple stepwise regression models including the co-variates. We suggest that the authors mention what type of regression model they are using along with a clarification of the inconsistent reporting of p-values, exact vs. e.g. <0.001. While the authors use a continuous outcome, there is no information on the nature of a possibly non-linear relationship between GDP and IQ, which contradicts the authors’ aim to “determine the relationships between different aspects of the environment of the grandparents (F0) of the study children (F2)”. We would also like the authors to explain their statement “taking care to ensure that we avoided Type I errors as much as possible”, in more detail. It has been reported that the heritability of smoking habits varies between men and women and between environments that are more or less permissive to smoking (Li, 2003) [2]. We would therefore like the authors to provide a more justifiable rationale than “hypothesis generation” for omitting parental co-variates from the current study, pending that such data is available. The discussion would benefit from less repetition of the results section and more of actual discussion of the potential mechanisms underlying the results and suggestions for future studies of this complex issue. Is the work clearly and accurately presented and does it cite the current literature? Partly If applicable, is the statistical analysis and its interpretation appropriate? Partly Are all the source data underlying the results available to ensure full reproducibility? Yes Is the study design appropriate and is the work technically sound? Yes Are the conclusions drawn adequately supported by the results? Yes Are sufficient details of methods and analysis provided to allow replication by others? Partly Reviewer Expertise: Statistics, Neuroscience. We confirm that we have read this submission and believe that we have an appropriate level of expertise to confirm that it is of an acceptable scientific standard, however we have significant reservations, as outlined above. We are grateful to the reviewers for their comments. Our responses are below. They suggest that the correlation between intelligence and many different disorders such as those indicated by Trampush and colleagues (2017) indicates that one would expect an association between smoking and intelligence purely on genetic grounds. If this were an explanation of our findings, we would surely expect similar associations between paternal grandparents’ smoking habits with IQ and those between maternal grandparents’ smoking habits and IQ. We agree that the discussion of the use of GDP as an exposure should be expanded, and this we have now done at the end of the second paragraph of the Introduction. We have expanded the description of the statistical methods used to encompass: (i) our use of stepwise multiple regression in order to disentangle the collinear factors that are independently associated with each outcome. (ii)  In regard to the possible non-linear nature of a GDP effect, the additional factor ‘business cycle’ identified the years where the GDP did not fall within a linear trajectory and was included along with the variable indicating the trend in GDP. (iii) we have expanded the sentence on avoiding Type I errors to include the reason for not taking account of multiple testing. The issue of how the P values are presented is noted. Different methods are used, but we argue that the meaning is clear throughout. We will not change on this occasion, but take note for further manuscripts. We have added some suggestions as to mechanisms at the end of the paper. Alessie, R. J., Angelini, V., van den Berg, G. J., Mierau, J. O., & Viluma, L. (2019). Economic conditions at birth and cardiovascular disease risk in adulthood: Evidence from post-1950 cohorts. Social Science & Medicine, 224, 77-84. van den Berg, G. J., Paul, A., & Reinhold, S. (2020). Economic conditions and the health of newborns: Evidence from comprehensive register data. Labour Economics, 63, 101795. This paper presents an important hypothesis-generating analysis of a highly relevant topic, addressing potential associations of grandparental environmental factors (Gross Domestic Product measures, grandparental smoking) with measures of IQ, with focus on sex-specific patterns. Overall, the work is well presented, the authors guide the reader very well through complex issues, and the conclusions are appropriately cautious but still very valuable. The paper cites relevant literature related to the outcome IQ as far as I can appreciate, but limits literature related to the exposures mainly to publications from their own study. I suggest to add a reference validating offspring’s reporting of parental smoking (Pape K et al. 2019 [1]). About the statistical methods, the argument that correction for multiple testing is not done in this hypothesis generating analysis is sound. The assumptions underlying the analyses are clearly presented to the reader. I am not convinced about the appropriateness of using a backwards step-wise approach but on the other hand acknowledge the complexity of these analyses; I suggest that a statistician with some experience with multi-generation analyses comments on this. For the discussion, I would have liked more speculation with regard to potential underlying biological mechanisms. Considering the terminology, the authors state that they will use the term “transgenerational” whether inter- or transgenerational mechanisms are assumed. One may hope that the field is becoming somewhat more familiar to readers and that one may distinguish between these in near future. Two details as to the exposure description, (i) with the term “smoking history” I would expect more than a question on whether a parent smoked, and suggest to merely give the wording of the question; ii) last sentence “This assumption was validated…” Showing lower birthweight in mothers reported to have smoked hardly “validates” exposure during pregnancy, this should be worded more carefully. Is the work clearly and accurately presented and does it cite the current literature? Yes If applicable, is the statistical analysis and its interpretation appropriate? I cannot comment. A qualified statistician is required. Are all the source data underlying the results available to ensure full reproducibility? Yes Is the study design appropriate and is the work technically sound? Yes Are the conclusions drawn adequately supported by the results? Yes Are sufficient details of methods and analysis provided to allow replication by others? Yes Reviewer Expertise: Multi-generation research in humans, mainly in asthma/allergies. I confirm that I have read this submission and believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard. Thank you for the Pape reference – We were not aware of it until now, and have now referred to it in this paper. You ask for more discussion about possible mechanisms. We have added a section at the end of the Conclusions that answers this. You also ask for the actual wording of the smoking in pregnancy question – and this is now included in the Methodology section. You pointed out that showing that exposed mothers had lower birthweight was not, strictly speaking, a validation. Rather, as we now state more accurately, it provides face validity to the claim.
  29 in total

Review 1.  Heritability estimates versus large environmental effects: the IQ paradox resolved.

Authors:  W T Dickens; J R Flynn
Journal:  Psychol Rev       Date:  2001-04       Impact factor: 8.934

Review 2.  An Expanded View of Complex Traits: From Polygenic to Omnigenic.

Authors:  Evan A Boyle; Yang I Li; Jonathan K Pritchard
Journal:  Cell       Date:  2017-06-15       Impact factor: 41.582

Review 3.  The Flynn effect: a meta-analysis.

Authors:  Lisa H Trahan; Karla K Stuebing; Jack M Fletcher; Merrill Hiscock
Journal:  Psychol Bull       Date:  2014-06-30       Impact factor: 17.737

4.  Cohort Profile: the Avon Longitudinal Study of Parents and Children: ALSPAC mothers cohort.

Authors:  Abigail Fraser; Corrie Macdonald-Wallis; Kate Tilling; Andy Boyd; Jean Golding; George Davey Smith; John Henderson; John Macleod; Lynn Molloy; Andy Ness; Susan Ring; Scott M Nelson; Debbie A Lawlor
Journal:  Int J Epidemiol       Date:  2012-04-16       Impact factor: 7.196

5.  Large-Scale Cognitive GWAS Meta-Analysis Reveals Tissue-Specific Neural Expression and Potential Nootropic Drug Targets.

Authors:  Max Lam; Joey W Trampush; Jin Yu; Emma Knowles; Gail Davies; David C Liewald; John M Starr; Srdjan Djurovic; Ingrid Melle; Kjetil Sundet; Andrea Christoforou; Ivar Reinvang; Pamela DeRosse; Astri J Lundervold; Vidar M Steen; Thomas Espeseth; Katri Räikkönen; Elisabeth Widen; Aarno Palotie; Johan G Eriksson; Ina Giegling; Bettina Konte; Panos Roussos; Stella Giakoumaki; Katherine E Burdick; Antony Payton; William Ollier; Ornit Chiba-Falek; Deborah K Attix; Anna C Need; Elizabeth T Cirulli; Aristotle N Voineskos; Nikos C Stefanis; Dimitrios Avramopoulos; Alex Hatzimanolis; Dan E Arking; Nikolaos Smyrnis; Robert M Bilder; Nelson A Freimer; Tyrone D Cannon; Edythe London; Russell A Poldrack; Fred W Sabb; Eliza Congdon; Emily Drabant Conley; Matthew A Scult; Dwight Dickinson; Richard E Straub; Gary Donohoe; Derek Morris; Aiden Corvin; Michael Gill; Ahmad R Hariri; Daniel R Weinberger; Neil Pendleton; Panos Bitsios; Dan Rujescu; Jari Lahti; Stephanie Le Hellard; Matthew C Keller; Ole A Andreassen; Ian J Deary; David C Glahn; Anil K Malhotra; Todd Lencz
Journal:  Cell Rep       Date:  2017-11-28       Impact factor: 9.995

6.  The anthropometry of children and adolescents may be influenced by the prenatal smoking habits of their grandmothers: a longitudinal cohort study.

Authors:  Jean Golding; Kate Northstone; Steven Gregory; Laura L Miller; Marcus Pembrey
Journal:  Am J Hum Biol       Date:  2014-08-18       Impact factor: 1.937

7.  Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index.

Authors:  Jian Yang; Andrew Bakshi; Zhihong Zhu; Gibran Hemani; Anna A E Vinkhuyzen; Sang Hong Lee; Matthew R Robinson; John R B Perry; Ilja M Nolte; Jana V van Vliet-Ostaptchouk; Harold Snieder; Tonu Esko; Lili Milani; Reedik Mägi; Andres Metspalu; Anders Hamsten; Patrik K E Magnusson; Nancy L Pedersen; Erik Ingelsson; Nicole Soranzo; Matthew C Keller; Naomi R Wray; Michael E Goddard; Peter M Visscher
Journal:  Nat Genet       Date:  2015-08-31       Impact factor: 38.330

Review 8.  Genetics and intelligence differences: five special findings.

Authors:  R Plomin; I J Deary
Journal:  Mol Psychiatry       Date:  2014-09-16       Impact factor: 15.992

9.  Do grandmaternal smoking patterns influence the etiology of childhood asthma?

Authors:  Laura L Miller; John Henderson; Kate Northstone; Marcus Pembrey; Jean Golding
Journal:  Chest       Date:  2014-06       Impact factor: 10.262

10.  Prepubertal start of father's smoking and increased body fat in his sons: further characterisation of paternal transgenerational responses.

Authors:  Kate Northstone; Jean Golding; George Davey Smith; Laura L Miller; Marcus Pembrey
Journal:  Eur J Hum Genet       Date:  2014-04-02       Impact factor: 4.246

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1.  Nicotine and the developing brain: Insights from preclinical models.

Authors:  Deirdre M McCarthy; Lin Zhang; Bradley J Wilkes; David E Vaillancourt; Joseph Biederman; Pradeep G Bhide
Journal:  Pharmacol Biochem Behav       Date:  2022-02-14       Impact factor: 3.697

Review 2.  Ancestral smoking and developmental outcomes: a review of publications from a population birth cohort†.

Authors:  Jean Golding; Marcus Pembrey; Yasmin Iles-Caven; Sarah Watkins; Matthew Suderman; Kate Northstone
Journal:  Biol Reprod       Date:  2021-09-14       Impact factor: 4.285

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