Literature DB >> 22574949

Lifestyle interventions for overweight and obese pregnant women to improve pregnancy outcome: systematic review and meta-analysis.

Eugene Oteng-Ntim1, Rajesh Varma, Helen Croker, Lucilla Poston, Pat Doyle.   

Abstract

BACKGROUND: Overweight and obesity pose a big challenge to pregnancy as they are associated with adverse maternal and perinatal outcome. Evidence of lifestyle intervention resulting in improved pregnancy outcome is conflicting. Hence the objective of this study is to determine the efficacy of antenatal dietary, activity, behaviour or lifestyle interventions in overweight and obese pregnant women to improve maternal and perinatal outcomes.
METHODS: A systematic review and meta-analyses of randomised and non-randomised clinical trials following prior registration (CRD420111122 http://www.crd.york.ac.uk/PROSPERO) and PRISMA guidelines was employed. A search of the Cochrane Library, EMBASE, MEDLINE, CINAHL, Maternity and Infant care and eight other databases for studies published prior to January 2012 was undertaken. Electronic literature searches, study selection, methodology and quality appraisal were performed independently by two authors. Methodological quality of the studies was assessed according to Cochrane risk of bias tool. All appropriate randomised and non-randomised clinical trials were included while exclusions consisted of interventions in pregnant women who were not overweight or obese, had pre-existing diabetes or polycystic ovarian syndrome, and systematic reviews. Maternal outcome measures, including maternal gestational weight gain, gestational diabetes and Caesarean section, were documented. Fetal outcomes, including large for gestational age and macrosomia (birth weight > 4 kg), were also documented.
RESULTS: Thirteen randomised and six non-randomised clinical trials were identified and included in the meta-analysis. The evidence suggests antenatal dietary and lifestyle intervention in obese pregnant women reduces maternal pregnancy weight gain (10 randomised clinical trials; n = 1228; -2.21 kg (95% confidence interval -2.86 kg to -1.59 kg)) and a trend towards a reduction in the prevalence of gestational diabetes (six randomised clinical trials; n = 1,011; odds ratio 0.80 (95% confidence interval 0.58 to 1.10)). There were no clear differences reported for other outcomes such as Caesarean delivery, large for gestational age, birth weight or macrosomia. All available studies were assessed to be of low to medium quality.
CONCLUSION: Antenatal lifestyle intervention is associated with restricted gestational weight gain and a trend towards a reduced prevalence of gestational diabetes in the overweight and obese population. These findings need to be interpreted with caution as the available studies were of poor to medium quality.

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Mesh:

Year:  2012        PMID: 22574949      PMCID: PMC3355057          DOI: 10.1186/1741-7015-10-47

Source DB:  PubMed          Journal:  BMC Med        ISSN: 1741-7015            Impact factor:   8.775


Background

Both developed and developing countries are experiencing a rapid increase in the prevalence of obesity [1-3]. In the UK, 24% of women of reproductive age are now obese (body mass index (BMI) equal or greater than 30 kg/m2) and the prevalence appears to be increasing [4]. Studies in UK women show that the rates of obesity in pregnancy have almost doubled in the last two decades [5,6]. Recent estimates suggest the prevalence of obesity in pregnancy in the UK is at least 20% with 5% having severe or morbid obesity [7,8]. Observational study data has linked obesity in pregnancy with adverse maternal and infant outcomes [7-10]. Obesity increases the risks of gestational diabetes [8,10-12], hypertensive disease (including pre-eclampsia) [8,13,14], thromboembolism [15,16], infection [14,17], Caesarean section [8,18], congenital fetal anomalies [19], macrosomia [13], induction [20], stillbirth [12], shoulder dystocia [14] and preterm delivery [21]. Moreover, maternal obesity may impact on long-term outcomes such as the increasing weight of the child in infancy and the severity of obesity in future generations [10,22,23]. As most of the adverse outcomes of obese pregnancies show strong associations with pre-pregnancy BMI, it is reasonable to assume that the ideal intervention would be to reduce obesity prior to pregnancy [24]. However, this is difficult to achieve because 50% of pregnancies in the UK are unplanned and a recent study concluded that only a small proportion of women planning pregnancy follow nutrition and lifestyle recommendations [25]. As such, an intervention pre-pregnancy may reach only a small proportion of the intended women. Alternatively, pregnancy itself may represent an ideal opportunity to target lifestyle change as women have increased motivation to maximise their own health and that of their unborn child [25]. However, evidence of benefit from published intervention studies appears limited and inconsistent [26-44]. We therefore sought to determine the efficacy of combined dietary activity and behaviour support interventions in overweight and obese pregnant women by undertaking a systematic review and meta-analysis according to PRISMA (Transparent Reporting of Systematic Reviews and Meta-analyses) criteria for maternal clinical outcomes of weight gain, gestational diabetes and Caesarean section and infant outcomes, such as large for gestational age and macrosomia. Our aim was to generate data of the highest statistical power and sensitivity. Hence, in comparison with previous similar themed systematic reviews [45-48], we chose to interrogate multiple databases (not restricted to English) and also separately meta-analyse randomised clinical trials (RCTs) and non-RCTs evaluating relevant clinical outcomes, including gestational diabetes and Caesarean section, which had not been attempted in prior meta-analyses.

Methods

Eligibility criteria

The eligible studies included RCTs and non-RCTs that evaluated antenatal dietary and lifestyle interventions in obese and overweight pregnant women whose outcome measures included quantitative maternal and fetal health outcomes. Systematic reviews and trials of women with existing gestational diabetes, or trials of pre-conception or postpartum interventions, were not included. Inclusion of trials was not restricted by language, publication date or country. Systematic reviews and observational studies were excluded.

Information sources

Literature searches were performed using five mainstream electronic databases (Cochrane Library, MEDLINE, EMBASE, CINAHL, Maternity and Infant care), and eight other databases (PsyclINFO via OVID SP, PyscLNFO via OVID SP, Science Citation Index via Web of Science, Social Science Citation Index via Web of Science, Global Health, Popline, Medcarib, Nutrition database).

Search strategy

The following MeSH terms, words and combinations of words, were used in constructing the systematic search: overweight OR obesity; pregnancy OR pregnancy complications OR pregnancy outcome OR prenatal care, prenatal, antenatal, intervention, randomised controlled trial, life style, "early intervention (education)", health education, education, patient education handout, patient education, exercise, exercise therapy, health promotion, diet, carbohydrate-restricted, diet, fat-restricted, diet, reducing, diet therapy, weight loss. Full details of the search strategy are shown in Table 1. The searches were unlimited by time up to January 2012 and limited to human studies and clinical trials. The systematic search was undertaken in the mainstream databases and targeted searches were conducted in the other databases.
Table 1

Search strategy utilised for MEDLINE 1946 to January 2012

BatchSearch term (MESH)CombinationResult
1Pregnancy Complications/OR Pregnancy/OR Pregnancy Outcome/OR Pregnancy, High Risk/646,055
2Prenatal Care/OR Pregnancy/OR Pregnancy Complications647,726
3Antenatal.mp.18,393
4Gestation intervention.mp.4
51 OR 2 OR 3 OR 4651,321
6Overweight.mp. OR Obesity/OR Overweight/OR Body Weight/249,097
7Obesity/OR Obesity, Morbid/or Obesity.mp.145,882
8Body Weight/OR Obesity/OR Body Mass Index/or BMI.mp. OR Overweight/293,584
96 OR 7 OR 8328,089
105 AND 921,583
11Diet, Fat-Restricted/OR Diet/OR Diet, Protein-Restricted/OR Diet, Carbohydrate-Restricted/OR Diet.mp. OR Diet, Reducing/OR Diet Therapy/255,985
12Life Style/36,837
13Health Education/48,625
14Patient Education as Topic/63,238
15Exercise.mp. OR Exercise/OR Exercise, Therapy/192,937
16Health Promotion/43,967
17Weight Loss/19,434
1811 OR 12 OR 13 OR 14 OR 15 OR 16 OR 17601,919
1910 AND 183,769
20LIMIT 19 TO ((female or humans or pregnancy) and (clinical trial, all OR clinical trial, phase i OR clinical trial, phase ii OR clinical trial, phase iii OR clinical trial, phase iv OR clinical trial OR controlled clinical trial OR randomized controlled trial))154
Search strategy utilised for MEDLINE 1946 to January 2012

Study selection

Electronic literature searches, study selection, methodology, appropriateness for inclusion and quality appraisal were performed independently and in duplicate by two authors (E-ON and RV). Disagreements between reviewers were resolved by consensus. Included studies were divided into two groups (RCTs and non-RCTs) and separately meta-analysed.

Data collection process

Two independent reviewers extracted the data. As a first step, each paper was screened using the title and the abstract. In the next round, studies were assessed for methodological quality and appropriateness for inclusion by two reviewers working independently from the full text of the manuscript. This was done without consideration of the results.

Data items

For each included trial, data was extracted on maternal gestational weight gain; gestational diabetes; Caesarean section; large for gestational age baby (> 4 kg); and birth weight. The included studies have been summarised in Tables 2 and 3.
Table 2

A summary of the studies that met the criteria of the systematic review on lifestyle interventions in overweight and obese pregnant women: randomised trials

Author (year)Ethnic group/CountryParticipant/settingSample sizeInterventionOutcome measure(s)Conclusion
Polley et al. (2002) [32]31% black and 61% white/USARecruited before 20 weeks of pregnancy (normal BMI > 19.5 to 24.9; overweight BMI ≥ 25 to < 30 kg/m2)/Hospital based120, including 49 overweight59 in control arm; 61 in intervention armExercise and nutrition information (oral and newsletter) Personalised graphs and behavioural counselling.Gestational weight gain; gestational diabetes; Caesarean section; birthweightNo statistically significant reduction in gestational weight, prevalence of gestational diabetes, Caesarean section, or large for gestational age baby
Hui et al. (2006) [33]Predominantly Caucasian/CanadaLess than 26 weeks pregnant (community based and antenatal clinics). All BMI categories. Mean BMI of non-intervention arm = 25.7 (SD = 6.3) and for intervention arm = 23.4(SD = 3.9)4521 in non-intervention arm; 24 in intervention armPhysical exercise (group-sessions home-based exercise)Individualized nutrition plansGestational weight gainNo statistically significant reduction in gestational weight gain
Wolff et al., 2008 [30]100% Caucasian/DenmarkObese (BMI ≥ 30 kg/m2) women enrolled at 15 weeks' gestation50 analysed23 in control arm; 27 in intervention armIntensive intervention with 10 one-hour visits with a dietician at each antenatal visit, dietary guidance providedGestational weight gain; gestational diabetes; Caesarean section; birthweightStatistically significant reduction in gestational weight gain, no statistically significant reduction in prevalence of gestational diabetes or Caesarean section, or birthweight
Jeffries et al., 2009 [28]> 90% Caucasian/AustraliaWomen at or below 14 weeks' gestation. All BMI categories included286138 in control arm; 148 in intervention armPersonalised weight measurement card (based on Institute of Medicine guidelines). Control had only single measurement at enrolmentGestational weight gainNo statistically significant reduction in gestational weight gain.
Ong et al., 2009 [42]Predominantly Caucasian/AustraliaPregnant obese women recruited at 18 weeks' gestation12six in control arm; six in intervention armPersonalised 10 weeks of home-based supervised exercise (three sessions per week)Maternal aerobic fitness and gestational diabetesNo statistically significant difference in aerobic fitness or gestational diabetes
Barakat et al., 2011 [41]100% Caucasian/SpainAll BMI categories16080 in control arm; 80 in intervention armThree group-based sessions per week, light resistance and toning exercise from the second trimesterGestational weight gain and birthweightNo statistically significant difference in gestational weight gain and birth weight. Exercise intervention might attenuate adverse consequences of maternal BMI on newborn birth size
Asbee et al., 2009 [27]26% African American/USAPregnant women recruited before 16 weeks' gestation. All BMI categories except those of BMI > 40 kg/m210043 in control arm; 53 in intervention armOne session of dietetic counselling and activityGestational weight gain; pregnancy outcomeStatistically significant reduction in gestational weight gain. No effect on pregnancy outcome
Thornton et al., 2009 [29]41% African American/USAObese pregnant women (BMI ≥ 30 kg/m2) recruited between 12 and 28 weeks' gestation257 randomised.25 lost to follow up. 116 in control arm; 116 in intervention armNutritional regime for gestational diabetesGestational weight gain; gestational diabetes; Caesarean section; pregnancy outcomeStatistically significant reduction in gestational weight gain, no statistically significant reduction in prevalence of gestational diabetes, Caesarean section or birthweight
Guelinckx et al., 2010 [26]100% Caucasian/BelgiumObese (BMI > 30 kg/m2) women enrolled at 15 weeks' gestation.195 randomised85 analysed65 in control arm; 65 in passive arm, 65 in intervention armThree arms: group sessions with a dietician; written brochures; and standard careDietary and physical activity guidance provided by dietician and in written brochuresNutritional habits; gestational weight gain; gestational diabetes; Caesarean section; birthweightImproved nutritional habits; no statistically significant reduction in gestational weight gain, prevalence of gestational diabetes, Caesarean section or birthweight.
Phelan et al., 2011 [34]67% White/USAPregnant women BMI between 19.8 and 40 kg/m2 recruited between 10 and 16 weeks' gestation401 randomised.201 in non-intervention arm; 200 in intervention armExercise and nutrition information (oral and newsletter) Personalised graphs and behavioural counsellingGestational weight gain; gestational diabetes; Caesarean section; pregnancy outcomeSignificant reduction in gestational weight gain; no statistically significant reduction in prevalence of gestational diabetes, Caesarean section or birthweight
Quinlivan et al., 2011 [59]73% white, 19% Asian/AustraliaPregnant women: overweight (BMI 25 to 29.9 kg/m2) and obese (BMI ≥ 30 kg/m2)132 randomised.65 in non-intervention arm; 67 in intervention armAttended a study- specific antenatal clinic providing continuity of care, weighing on arrival, brief dietary intervention by food technologist and psychological assessment and intervention if indicatedGestational weight gain; gestational diabetes; birthweightStatistically significant reduction in gestational weight gain and prevalence of gestational weight gain. No statistically significant reduction in birthweight.
Luoto et al., 2011 [43]Predominantly white/FinlandPregnant women at risk of gestational diabetes. All BMI ranges399 cluster randomised.219 in non-intervention arm; 180 in intervention armAttended a study-specific individual antenatal lifestyle counselling clinic including group exerciseGestational diabetes; gestational weight gain; birthweightStatistically significant reduction in birthweight and macrosomia but no statistically significant difference in gestational diabetes
Nascimento et al., 2011 [44]Predominantly white/BrazilPregnant women of all BMI categories82 randomised.42 in non-intervention arm; 40 in intervention armAttended a group-based exercise under supervision and received a home exercise counsellingGestational weight gain; raised blood pressure; perinatal outcomeNo statistically significant difference in gestational weight gain in terms of gestational weight gain, raised blood pressure or perinatal outcome

BMI: body mass index; SD: standard deviation

Table 3

Summary of the studies that met the criteria of the systematic review on lifestyle interventions in overweight and obese pregnant women: non-randomised trials

Author (year)Ethnic group/countryParticipants/settingSample sizeInterventionOutcome measure(s)Conclusion
Gray-Donald et al. (2000) [38]Native Americans/CanadaRecruited before the 26th week of pregnancy, non-parallel recruitment of control and intervention arms.Mean BMI = 29.6 kg/m2 (SD = 6.45) in non-intervention arm and mean BMI = 30.8 kg/m2 (SD = 6.85) in intervention arm at baseline.219107 in non-intervention arm; 112 in intervention armDietary and weight counsellingExercise groups providedGestational weight gain; gestational diabetes;Caesarean section;birthweight;postpartum weight retentionNo statistically significant difference in gestational weight gain, prevalence of gestational diabetes, Caesarean section or large for gestational age baby
Olson et al. (2004) [51]96% white/USARecruited before third trimester. Hospital and clinic settingBMI range: 19.8 to 29 kg/m2498381 in non-intervention arm; 117 in the intervention armUsed the Institute of Medicine recommended guidelines on weight gain; 'health book' used to record diet and exercise and contained healthy eating and exercise informationGestational weight gain; birthweightNo statistically significant reduction in gestational weight gain or prevalence of large for gestational age baby
Claesson et al. (2007) [36]Not stated. Predominantly Caucasian/SwedenObese and registered at antenatal care clinic.BMI ≥ 30 kg/m2348193 in non-intervention arm; 155 in intervention armNutritional habits interview, weekly counselling and aqua aerobic sessionsGestational weight gain; Caesarean section.Statistically significant reduction in gestational weight gain; no difference in prevalence of Caesarean section
Kinnunen et al. (2007) [37]Over 90% Caucasian/FinlandFirst-time pregnant women who were obese (BMI ≥ 30 kg/m2)19695 in non-intervention arm; 101 in intervention armIndividual counselling at each antenatal visits. Dietary guidance and optional activity sessions.Gestational weight gain; diet change; birthweightNo statistically significant reduction in gestational weight gain or prevalence of large for gestational age baby. Statistically significant reduction in dietary glycaemic load.
Shirazian et al., 2010 [39]33% blacks; 67% Latino/USASingleton obese (≥ 30 kg/m2) pregnant women recruited in the first trimester. Historical non-intervention group.5428 in non-parallel control arm; 28 in intervention arm)One-to-one counselling; six structured seminars on healthy living (healthy eating and walking)Gestational weight gain; gestational diabetes; Caesarean sectionStatistically significant reduction in gestational weight gain; no difference in prevalence of gestational diabetes
Mottola et al., (2010) [35]Not stated/CanadaOverweight (BMI ≥ 25 to 29.9 kg/m2) and obese (BMI ≥ 30 kg/m2) pregnant women recruited before 16 weeks' gestation; historical non-intervention group.65 matched non-parallel control of 260Individualised nutrition plan; exercise consisted of walking (three to four times per week, used pedometers)Gestational weight gain; Caesarean section; birthweight; peripartum weight retentionPossible reduction in gestational weight gain; no difference in prevalence of Caesarean section or large for gestational age baby; minimal effect on peripartum weight retention

BMI: body mass index; SD: standard deviation.

A summary of the studies that met the criteria of the systematic review on lifestyle interventions in overweight and obese pregnant women: randomised trials BMI: body mass index; SD: standard deviation Summary of the studies that met the criteria of the systematic review on lifestyle interventions in overweight and obese pregnant women: non-randomised trials BMI: body mass index; SD: standard deviation.

Risk of bias in individual studies

The quality of studies was assessed based on how the studies had minimised bias and error in their methods. We categorised the studies according to criteria based on PRISMA guidelines [49] and the Cochrane Library [50]. For example, high quality trials reported study aims; control comparison similar to the intervention group; relevant population demographics pre- and post-intervention; and data on each outcome. These study characteristics are tabulated in Tables 4 and 5. A final assessment categorised the studies as high, medium or low quality.
Table 4

Assessment of the quality of the included trials: non-randomised trials

Author (year)Population representativenessAdequacy of sequence generationMasking/selection biasIncomplete outcome dataContaminationSample sizeGrade of quality
Gray-Donald et al. (2000) [38]Yes: Registered from clinicNoNoNoNo: non-parallel control219Low
Olson et al. (2004) [51]YesNoNoNoNo: non-parallel control560Low
Claesson et al. (2007) [36]Yes: Registered from clinicNoNoYesNo: selected from nearby city315Low
Kinnunen et al. (2007) [37]YesNoNoNoYes55Low
Shirazian et al., (2010) [39]YesNoNoYesNo: non-parallel control28Low
Mottola et al., (2010) [35]YesNoNoYesNo: non-parallel control65Low
Table 5

Assessment quality of included trials: randomised trials

Author (year)Population representativenessAdequacy of sequence generationMasking/selection biasIntention to treatIncomplete outcome dataLoss to follow upSample sizeGrade of quality
Polley et al. 2002 [32]YesYes:NoNot reportedNoYes120Low
Hui et al. (2006) [33]Yes: from clinicExact method not describedNoNot reportedNoYes52Low
Wolff et al., 2008 [30]YesYes: computer generatedNoNot reportedYesYes50Low
Jeffries et al., 2009 [28]YesYes: Opaque envelopeYesNot reportedYesYes286Low
Ong et al., 2009 [42]YesExact method not describedNoNot reportedNoNo12Low
Barakat et al., 2011 [41]YesYesYesYesYesYes160Medium
Asbee et al. 2009 [27]YesYesNoNot reportedYesNo100Low
Thornton et al., 2009 [29]YesYesYesNot reportedYesYes257Medium
Guelinckx et al., 2010 [26]Not reportedRandomised but not reported howNot reportedNot reportedYesNot reported99Low
Phelan et al., 2011 [34]YesYes: Opaque envelopeYesYesYesYes401Medium,
Quinlivan et al., 2011 [59]YesYes: Opaque envelopeYesYesYesYes124Medium
Luoto et al., 2011 [43]YesYesYesYesYesYes399Medium
Nascimento et al., 2011 [44]YesYes: Opaque envelopeYesYesYesYes82Low
Assessment of the quality of the included trials: non-randomised trials Assessment quality of included trials: randomised trials

Summary and analysis of studies that meet the criteria

This is shown in Figure 1 and in a tabulated format contained within Table 2 and 3.
Figure 1

Flow diagram of study selection.

Flow diagram of study selection.

Summary measures and data synthesis

The main measure of effect of the meta-analysis was the odds ratio or standardised mean difference. The data syntheses were conducted according to the Cochrane methodology [50]. First, we used statistical meta-analysis techniques to assess the efficacy of the interventions of controlled trials. Chi-square statistics tests were used to test for heterogeneity (Q statistics) between controlled trials. When there was no significant heterogeneity, we combined effect sizes in a fixed effect statistical meta-analysis using Review Manager (RevMan; Version 5.0, Copenhagen: The Nordic Cochrane Centre, The Cochrane Collaboration, 2008). The meta-analyses were performed by calculating the odds ratios (for proportion data) or standardised mean differences (for scale data) using a fixed effects model. Quantitative analysis was performed on an intention-to-treat basis focused on data derived from the period of follow-up. There was heterogeneity between studies because of the smaller sample size of some of the studies (poor quality), variation of the study population and the intensity and duration of the interventional strategies being evaluated. A random effects model was used to adjust for heterogeneity.

Results

Study characteristics

The review process is outlined in Figure 1 and the selected papers summarised in Tables 2 and 3. Fifteen trials met the inclusion criteria: 13 RCTs [26-34] and six non-RCTs [35,36,38,39,51,52]. All 19 trials were performed in developed countries: five in the USA, three in Canada, three in Australia, two in Finland and one in Denmark, Netherlands, Sweden, Spain, Brazil and Belgium (Tables 2 and 3). Five RCTs were judged to be of medium quality [27,29,34]. The rest were deemed low quality (Tables 4 and 5). The pooled RCTs included a total of 1,228 participants and the pooled non-RCTs included 1,534 participants. Participants were predominantly white except in the studies by Asbee et al. [27], Gray-Donald et al. [38] and Hui et al. [33]. In the Asbee et al. study, the majority were described as being of Hispanic ethnicity [27]. For all included RCTs, the control group received no intervention or standard care. In the non-RCTs, most used non-parallel controls [35,38,39,51] or controls from another centre [36]. The outcomes investigated in the trials were gestational weight gain, gestational diabetes, Caesarean section delivery, large for gestational age baby and birth weight.

Effects of the intervention on outcomes

Of the 19 controlled trials, 16 measured gestational weight gain (10 randomised, 6 non-randomised); 8 recorded gestational diabetes (6 randomised, 2 non-randomised); 10 recorded Caesarean delivery (6 randomised, 4 non-randomised); 10 measured large for gestational age (6 randomised, 4 non-randomised); and 7 measured birth weight (7 randomised). Meta-analyses for the different outcomes are shown in Tables 6 and 7, and Figures 2, 3, 4, 5, 6, 7, 8, 9 and 10.
Table 6

Effect estimates for randomised trials of lifestyle advice versus standard care

Outcome or subgroupStudiesParticipantsStatistical methodEffect estimate
Large for gestational age61,008Odds ratio (Fixed, 95% CI)0.91 (0.62, 1.32)
Caesarean delivery6663Odds ratio (Fixed, 95% CI)0.96 (0.68, 1.36)
Gestational diabetes61,017Odds ratio (M-H, Fixed, 95% CI)0.80 (0.58, 1.10)a
Gestational weight gain (kg)101,228Mean difference (Fixed, 95% CI)-2.21 (-2.86, -1.57)a
Birth weight (g)71,133Mean difference (Fixed, 95% CI)-56.64 (-120.15, 6.88)

aStatistically significant pooled estimates. CI: confidence interval

Table 7

Effect estimates for non-randomised trials of lifestyle advice versus standard care

Outcome or subgroupStudiesParticipantsStatistical methodEffect estimate
Large for gestational age41,199Odds ratio (Fixed, 95% CI)0.85 (0.63, 1.16)
Caesarean delivery41,246Odds ratio (Fixed, 95% CI)1.13 (0.78, 1.64)
Gestational diabetes2233Odds ratio (Fixed, 95% CI)1.51 (0.72, 3.16)
Gestational weight gain (kg)61,534Mean difference (Fixed, 95% CI)-0.42 (-1.03, 0.19)

CI: confidence interval

Figure 2

Forest plot of randomised trials investigating the effect of lifestyle advice versus standard care on gestational weight gain (kg).

Figure 3

Forest plot of randomised trials investigating the effect of lifestyle advice versus standard care on risk of gestational diabetes.

Figure 4

Forest plot of randomised trials investigating the effect of lifestyle advice versus standard care on risk of Caesarean delivery.

Figure 5

Forest plot of randomised trials investigating the effect of lifestyle advice versus standard care on risk of large for gestational age baby.

Figure 6

Forest plot of randomised trials investigating the effect of lifestyle advice versus standard care on birthweight.

Figure 7

Forest plot of non-randomised trials investigating the effect of lifestyle advice versus standard care on risk of large for gestational age baby.

Figure 8

Forest plot of non-randomised trials investigating the effect of lifestyle advice versus standard care on risk of Caesarean section.

Figure 9

Forest plot of non-randomised trials investigating the effect of lifestyle advice versus standard care on risk of gestational diabetes.

Figure 10

Forest plot of non-randomised trials investigating the effect of lifestyle advice versus standard care on gestational weight gain (kg).

Effect estimates for randomised trials of lifestyle advice versus standard care aStatistically significant pooled estimates. CI: confidence interval Effect estimates for non-randomised trials of lifestyle advice versus standard care CI: confidence interval Forest plot of randomised trials investigating the effect of lifestyle advice versus standard care on gestational weight gain (kg). Forest plot of randomised trials investigating the effect of lifestyle advice versus standard care on risk of gestational diabetes. Forest plot of randomised trials investigating the effect of lifestyle advice versus standard care on risk of Caesarean delivery. Forest plot of randomised trials investigating the effect of lifestyle advice versus standard care on risk of large for gestational age baby. Forest plot of randomised trials investigating the effect of lifestyle advice versus standard care on birthweight. Forest plot of non-randomised trials investigating the effect of lifestyle advice versus standard care on risk of large for gestational age baby. Forest plot of non-randomised trials investigating the effect of lifestyle advice versus standard care on risk of Caesarean section. Forest plot of non-randomised trials investigating the effect of lifestyle advice versus standard care on risk of gestational diabetes. Forest plot of non-randomised trials investigating the effect of lifestyle advice versus standard care on gestational weight gain (kg). Meta-analysis of RCTs showed that combined antenatal lifestyle, dietary and activity intervention restricts gestational weight gain (Table 6 and Figure 2) and there was a trend towards reduction in the prevalence of gestational diabetes in overweight and obese women (Table 6 and Figure 3). However, meta-analysis of non-RCTs only showed weak evidence that lifestyle intervention reduces gestational weight gain (Table 7 and Figure 7) and there was no evidence for a reduction in prevalence of gestational diabetes (Table 7 and Figure 8). There was no robust evidence that lifestyle intervention is associated with a lower prevalence of Caesarean delivery or macrosomia or any alteration in birth weight (Tables 6 and 7, Figures 4,5, 6, 8, 9 and 10).

Intervention characteristics

The nature of the interventions varied widely between studies and some of the key features of the interventions are outlined in Tables 2 and 3. In summary, for the six non-RCTs, three of the interventions comprised individual and group or seminar components [36,38,39,53], two were individual [35,52] and one was unclear [51]. Of the 13 RCTs, one comprised individual and group components [33], eight were individual [27-30,32,34] and three were group-based [26]. Where there were individual and group components, the latter were usually physical activity sessions. All of the non-RCTs included dietary and physical activity guidance, as did the majority of the randomised studies. Exceptions were two studies which included only nutritional guidance [29,30] and one which included guidelines about weight gain and weight monitoring only [28]. The majority of studies included dietary or physical activity guidance, with one of the non-RCTs [35] and three of the RCTs [29,32-34] specifying that guidance was personalised.

Discussion

Summary of main findings

Antenatal lifestyle, dietary and activity advice for overweight and obese pregnant women restricts maternal weight gain during pregnancy and lowers the prevalence of gestational diabetes in women who are overweight or obese. However, the quality of the study designs was generally poor. The reduction in gestational weight gain was observed to be statistically significant in the meta-analysis of randomised trials (10 RCTs; n = 1,228; -2.21 kg (95% CI, -2.86 to -1.57 kg)) but non-significant in the meta-analysis of non-randomised trials (six non-RCTs; n = 1,534). No effects of antenatal lifestyle interventions were identified in obese and overweight pregnant women in relation to Caesarean delivery, large for gestational age, birth weight and macrosomia (> 4 kg).

Interpretation

There is evidence to suggest antenatal lifestyle interventions may restrict gestational weight gain and a trend towards a reduced prevalence of gestational diabetes, but there was no statistical effect on other important clinical outcomes, possibly due to inadequate power of the combined sample size. The effect on restricted weight gain and gestational diabetes was not consistent across all the trial populations and therefore cannot be generalised. There was also wide variation in the types of interventions evaluated in the studies. The majority were individual-based and most provided generic guidance comprising mainly dietary and physical activity information, with few tailoring guidelines. There was considerable heterogeneity in intervention design and no obvious patterns between intervention type and study outcomes. For the gestational weight gain and gestational diabetes outcomes, both the successful and non-successful studies included those which were personalised, combined physical activity and dietary guidance and were individual-based. Moreover, degrees of weight gain restriction achieved were modest overall. It is even harder to make conclusions regarding the specific behaviour change strategies included (for example, monitoring and goal setting) or theoretical basis of interventions since these were typically poorly reported. Identifying specific components of successful interventions aids understanding of how interventions are having an effect and clear reporting of intervention design allows for easier replication [54]. Previous reviews have attempted to make conclusions regarding specific effective components of interventions. Suggestions that weight monitoring and setting weight goals could be useful [46] and also monitoring along with education counselling and physical activity sessions [51,55] have been made. Another review suggested that interventions should be based on the Theory of Planned Behaviour, but the rationale for using this model over others in this population was unclear [56]. None of these reviews examined intervention components systematically. A more recent review by Gardner et al. assessed interventions targeting gestational weight gain from a psychological perspective and specifically examined intervention content and delivery methods [57]. This review comprised 10 controlled trials, all included in the current review; only two of the studies reported basing interventions on theory and the studies used, on average, five behaviour change strategies (self-monitoring, feedback provision and setting behavioural goals were the most common), but no conclusions could be drawn as to their contribution to study outcomes. Broadly consistent with this were the four studies in the current review which were not included in the review by Gardner et al. [57]. Their review questioned the evidence supporting the benefits of weight monitoring, but tentatively suggested that information provision had been underused and that it might be of benefit to have a narrower focus of intervention targets [57].

Comparison with other systematic reviews and strengths

Our study adds to a growing body of evidence that aims to evaluate lifestyle intervention as a means to minimise the adverse outcome associated with obesity in pregnancy. In comparison to other published reviews [45,46,56], we have adopted an original approach by broadening the literature source (multiple data sources, no language restriction), focusing on relevant clinical outcomes (such as Caesarean section, gestational diabetes, macrosomia), and improving our sensitivity by meta-analysing both RCTs and non-RCTs. Furthermore, to minimise bias, the review methodology was registered a priori (Prospero number CRD420111122 http://www.crd.york.ac.uk/PROSPERO). We therefore believe our review provides a comprehensive and reliable analysis of the current evidence and for the first time highlights that lifestyle intervention in pregnancy may reduce the prevalence of gestational diabetes.

Limitations of this systematic review

The evidence summarised in this work comes from available studies of which most are of low quality, with only four studies fulfilling a medium quality score. Hence, the evidence base is weak and calls for more robust studies. Our trial population is relatively small, the intensity and duration of the interventions of trials varied and trials were predominantly USA in origin; a phenomenon common to many public health reviews, especially on obesity. Although our focus was on antenatal lifestyle intervention for obese and overweight pregnant women, our search yielded some studies that contained a mixed group of obese and normal weight women and we excluded all the non-obese participants from our analysis. Still, this may lead to inconsistencies in measuring the effect of the intervention as well as under- or overestimating the treatment effect. Furthermore, even though our search was systematic and rigorous, we could have missed eligible studies inadvertently.

Conclusions

This review reveals that lifestyle interventions for obese and overweight women during pregnancy restrict gestational weight gain and a trend was evident towards reducing the prevalence of gestational diabetes. However, the quality of the published studies is mainly poor. This then highlights a paradox. At a time when solutions to address adverse outcome associated with maternal overweight and obesity are identified as a public health priority, we find that most of the research evidence lacks robustness to inform future evidence-based lifestyle interventions for obese pregnant women. There is thus a research gap regarding the effectiveness of lifestyle intervention in pregnancy. It is unlikely that further meta-analysis will help to refine the quality of evidence because studies demonstrated significant heterogeneity in relation to demography, outcome measurement, follow-up and degree of intervention. Hence, we conclude that there is the need for a well-designed large-scale prospective trial which examines combined antenatal lifestyle interventions in obese pregnant women that is suitably powered and incorporates robust methodology in accordance with standards set by Medical Research Council's framework for evaluating complex interventions [58]. There are two such studies which are currently ongoing called LIMIT (ACTRN 12607000161426) and UPBEAT (ISRCTN89971375). Both of these studies are appropriately powered to show convincingly whether lifestyle intervention is most likely to improve pregnancy outcome or not.

Competing interests

The authors declare that they have no competing interests.

Authors' contributions

The idea was conceived by PD and EO-N. The literature search and meta-analysis were by RV and EO-N and all contributed to the write up. All authors read and approved the final version of the manuscript.

Pre-publication history

The pre-publication history for this paper can be accessed here: http://www.biomedcentral.com/1741-7015/10/47/prepub
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