| Literature DB >> 20949129 |
Dorly J H Deeg, Martijn Huisman.
Abstract
Midlife is a period during which ageing-related health problems first emerge. In view of increasing life expectancy, it is of great importance that people in midlife adapt to possible health problems, to be able to lead productive and engaged lives as long as possible. It may be expected that given the better circumstances in which more recent cohorts grew up, they are better equipped to adapt to health problems than earlier cohorts. This study addresses the question if the way people in midlife adapt to health problems is or is not improving in the Netherlands. The study is based on the nationally representative 1992-1993 and 2002-2003 cohorts of the Longitudinal Aging Study Amsterdam (ages 55-64 years), with follow-up cycles in 1995-1996 (n = 811) and 2005-2006 (n = 829), respectively. Mastery is considered as a measure of adaptation, and 3-year change in mastery is compared in subjects without and with health problems at baseline. A rise was observed in the prevalence of diabetes, chronic lung disease, arthritis, subthreshold depression, and disability. Subjects without health problems in the recent cohort had better mastery than their counterparts in the early cohort. Regardless of cohort membership, mastery declined over 3 years for those with subthreshold depression, mild disability, chronic lung disease, and stroke. In the recent cohort only, mastery declined for those with cognitive impairment, but improved for those with heart disease. These findings do not support the expectation that recent cohorts are better equipped to deal with health problems for conditions other than heart disease.Entities:
Year: 2010 PMID: 20949129 PMCID: PMC2950078 DOI: 10.1007/s10433-010-0157-1
Source DB: PubMed Journal: Eur J Ageing ISSN: 1613-9372
Baseline characteristics of early and recent cohorts, 1992–1993 and 2002–2003, continuing participants Longitudinal Aging Study Amsterdam
| Cohort 1928–1937 in 1992–1993 | Cohort 1938–1947 in 2002–2003#
| Chi-square test (df) | ||
|---|---|---|---|---|
| Age (M, sd) | 60.1 (2.8) | 59.9 (2.9) | 1.78 | |
| Gender (% female) | 52.9 | 52.3 | 0.07 (1) | |
| Education (%) | 38.55 (2) | |||
| Low | 31.1 | 18.6 | ||
| Middle | 50.9 | 55.9 | ||
| High | 18.0 | 25.5** | ||
| Partner (%) | 83.0 | 85.1 | 1.34 (1) | |
| Paid job (%) | 29.3 | 43.9** | 38.08 (1) | |
| Somatic diseases (%) | 8.72 (2) | |||
| One | 33.3 | 38.7 | ||
| Two or more | 14.2 | 16.3* | ||
| Specific diseases (%) | ||||
| Heart disease | 13.2 | 11.0 | 1.88 (1) | |
| Peripheral artery disease | 6.1 | 5.1 | 0.72 (1) | |
| Stroke | 1.2 | 2.5 | 3.53 (1) | |
| Diabetes | 3.4 | 6.5* | 8.33 (1) | |
| Chronic lung disease | 7.2 | 9.8 | 3.48 (1) | |
| Cancer | 6.0 | 8.0 | 2.58 (1) | |
| Arthritis | 28.6 | 34.1* | 5.56 (1) | |
| Subthreshold depression (%) | 10.5 | 13.4+ | 3.32 (1) | |
| Cognitive impairment (%) | 7.2 | 8.8 | 1.42 (1) | |
| Disability longer than 3 months (%) | 18.35 (2) | |||
| Mild | 14.2 | 20.7 | ||
| Severe | 6.8 | 9.5** | ||
| Mastery (M, sd) | 18.1 (3.3) | 18.2 (3.5) | −1.01 | |
#Data of 2002–2003 weighted to age–sex distribution of 1992–1993
Significant cohort difference: + p < 0.10, * p < 0.05, ** p < 0.001
Explanatory factors for baseline mastery and change in mastery, full model
| Baseline masterya | Change in masteryb | |||
|---|---|---|---|---|
| Standardised Beta coefficient | Standardised Beta coefficient | |||
| Baseline mastery (one point higher) | – | – | −0.52 | <0.001 |
| Cohort (recent vs. early) | 0.05 | 0.05 | −0.01 | 0.60 |
| Age (1 year higher) | −0.03 | 0.29 | −0.02 | 0.56 |
| Gender (female vs. male) | −0.05 | 0.06 | −0.03 | 0.27 |
| Education (one point higher) | 0.02 | 0.33 | 0.08 | 0.001 |
| Partner (yes vs. no) | 0.05 | 0.05 | 0.02 | 0.40 |
| Paid work (yes vs. no) | 0.05 | 0.04 | 0.03 | 0.27 |
| Somatic diseases | ||||
| One | −0.04 | 0.09 | −0.03 | 0.18 |
| Two or more | −0.04 | 0.15 | −0.05 | 0.03 |
| Subthreshold depression (yes vs. no) | −0.28 | <0.001 | −0.08 | 0.001 |
| Cognitive impairment (yes vs. no) | −0.08 | <0.001 | −0.02 | 0.44 |
| Disability longer than 3 months | ||||
| Mild | −0.07 | 0.01 | −0.06 | 0.04 |
| Severe | −0.07 | 0.01 | 0.03 | 0.29 |
aMultivariable regression model with the continuous baseline score of mastery as the dependent variable
bMultivariable regression model with the continuous change score of mastery (= T2 score − T1 score) as the dependent variable
Specific conditions: direct effect on change in masterya and interaction with cohort, each specific condition in a separate modelb
| Unstandardised B coefficient | Model improvement with interaction condition * cohort ( | ||
|---|---|---|---|
| Heart disease | 0.13 | 0.55 | 0.02 |
| Peripheral artery disease | 0.05 | 0.87 | 0.18 |
| Stroke | −0.76 | 0.12 | 0.64 |
| Diabetes | 0.07 | 0.82 | 0.21 |
| Chronic lung disease | −0.43 | 0.08 | 0.32 |
| Cancer | −0.18 | 0.50 | 0.61 |
| Arthritis | −0.18 | 0.26 | 0.26 |
| Subthreshold depression | −0.89 | <0.001 | 0.68 |
| Cognitive impairment | −0.24 | 0.34 | 0.03 |
| Disability longer than 3 months | |||
| Mild | −0.41 | 0.03 | 0.52 |
| Severe | 0.29 | 0.32 | 0.05 |
aChange in mastery = T2 score − T1 score
bEach model adjusted for baseline mastery, age, sex, education, and somatic and mental comorbidity (multivariable regression models)
Specific conditions with interaction effects: association with change in mastery in early and recent cohort, adjusted models
| Cohort 1928–1937 in 1992–1993 | Cohort 1938–1947 in 2002–2003 | |||
|---|---|---|---|---|
| Unstandardised B coefficient | Unstandardised B coefficient | |||
| Heart disease | −0.34 | 0.24 | 0.67 | 0.03 |
| Cognitive impairment | 0.37 | 0.32 | −0.74 | 0.03 |
| Disability longer than 3 months | ||||
| Severe | 0.54 | 0.16 | −0.37 | 0.24 |