Skip to main content
The BMJ logoLink to The BMJ
. 2002 Oct 5;325(7367):749. doi: 10.1136/bmj.325.7367.749

Association between psychological symptoms in adults and growth in early life: longitudinal follow up study

Y B Cheung a, K S Khoo b, J Karlberg c, D Machin d
PMCID: PMC128376  PMID: 12364303

Abstract

Objectives

To test the hypothesis that birth weight for gestational age and weight gain in early childhood have a long term association with psychological distress in adults.

Design

Longitudinal study of 1958 birth cohort followed to age 42 years.

Setting

Population based birth cohort study.

Participants

9731 cohort members with valid perinatal, postnatal, and adult data.

Main outcome measures

Malaise inventory scores measured at ages 23, 33, and 42 years. Generalised estimating equations approach used to analyse repeated measures.

Results

Psychological distress score was inversely related to birthweight z score and weight gain from birth to the age of 7 years. A unit increase in birthweight z score or childhood weight gain was associated with a mean reduction in psychological distress score of 0.10 (95% confidence interval 0.05 to 0.15) and 0.06 (0.02 to 0.10), respectively. Birth weight and weight gain were also inversely related to the odds of having a high level of psychological distress, with odds ratios being 0.90 (0.85 to 0.95) and 0.93 (0.89 to 0.98), respectively.

Conclusions

Psychological health in adults is related to fetal growth and growth in early childhood.

What is already known on this topic

Psychological outcomes in children are related to fetal growth and postnatal growth

Size at birth is also associated with psychological outcomes in adolescents and young adults

What this study adds

Both birthweight z score and weight gain in early childhood are associated with psychological distress at ages 23 to 42

The impact of a smaller size at birth may be compensated for by a higher postnatal weight gain

Introduction

Although numerous studies have shown that fetal and postnatal growth can affect psychological and developmental outcomes in children, it is uncertain whether the influence persists into adulthood. A study of Swedish conscripts showed an inverse relation between birth weight and susceptibility to stress at age 18.1 A study of British people born in 1970 showed that birth weight for gestational age is associated with the psychological but not somatic score of the malaise inventory at age 26 years.2 In contrast, one study found no association between fetal growth retardation and psychological outcomes in adolescents3; another found no association between birth weight and life satisfaction in young adults.4 Several investigators have suggested the relevancy of postnatal growth to hormone concentration, metabolism, and blood pressure.5,6

We tested the hypothesis that small size at birth and slow growth in early childhood are associated with higher levels of psychological distress in adults. We used data from the UK national child development study, which followed a cohort of people born in 1958 from birth to age 42.

Methods

Participants

The national child development study (NCDS) is a cohort study of about 17 000 people born in England, Wales, and Scotland in one week in March 1958. Data were collected at birth and then at ages 7, 11, 16, 23, 33, and 42 years from medical records, clinical examinations, and face to face as well as self administered interviews. The samples have been shown to be representative of the national population in a similar age range. Details of the cohort study have been reported elsewhere.7,8

Data collected at birth included birth weight; gestational age in weeks determined by last menstrual period; mother's parity, smoking habit during pregnancy, and marital status; and father's social class defined according to the registrar general's classification. Data collected at age 7 years included body weight and housing tenure. The categorisations of the variables are shown in table 1.

Table 1.

 Descriptive summary of explanatory variables measured at birth and 7 years. Figures are mean (SD) or percentage distribution

Variables
Men (n=4925)
Women (n=4806)
Gestational age (weeks) 39.7 (1.7) 39.8 (1.7)
Birth weight (g) 3417 (521) 3273 (504)
Birthweight z score 0.02 (1.00) 0.01 (1.00)
Father's social class:
 I  4.7  4.4
 II 13.4 13.6
 III 59.9 59.5
 IV 11.3 11.8
 V  8.7  8.3
 Others  2.0  2.4
Mother's marital status:
 Married 97.4 96.8
 Unmarried  2.6  3.2
Parity:
 1 36.2 36.9
 2-3 48.1 47.4
 ⩾4 15.7 15.7
Maternal smoking:
 Non-smoker 60.5 58.7
 Not during pregnancy  6.3  8.2
 <5 cigarettes/day  7.5  7.7
 5-14 cigarettes/day 21.3 21.1
 ⩾15 cigarettes/day  4.5  4.3
Housing tenure at 7 years:
 Owner occupier 43.7 43.5
 Council tenant 39.0 39.6
 Private tenant 11.4 11.2
 Others  5.9  5.7
Weight gain (change in z score) 0.01 (1.17) 0.01 (1.20)

At ages 23, 33, and 42 participants filled in a questionnaire for the malaise inventory. The inventory was developed by Rutter et al,9 based on the Cornell medical index. It consists of a 15 item subscale of psychological symptoms and an eight item subscale of somatic symptoms.10,11 There is a nine item variant of the somatic symptom scale, but the cohort study suggests the eight item version is used (NCDS user manual). A total of at least eight (psychological plus somatic) symptoms indicates a high risk of psychiatric morbidity.8

Current study

The present study was approved by the ethics committee, National Cancer Centre Singapore.

We proportionally assigned the cut-off point of eight symptoms to the psychological and somatic subscales to indicate the high level of distress in each—that is, at least five psychological symptoms and at least three somatic symptoms. To quantify intrauterine growth retardation we standardised birth weight for gestational age separately for each sex, giving a birth weight SD score or z score.12 The procedure involves a Box-Cox transformation towards a normal distribution and then standardisation of the transformed values within each gestational age.12,13 A unit increase in birthweight z score is an increase of 1 SD of birth weight for gestational age. Body size measured at age 7 formed the basis of the childhood growth variable. The data collection at age 7 took about one year to complete so the age (in months) at body size measurement was variable. Weight at this measurement was standardised similarly for age and sex. Weight gain in childhood was measured as the difference in weight z scores at 7 years and at birth. Cohort members with missing growth data at birth or 7 years were not included in the main analyses.

Analysis

We used a logistic regression model to examine if growth data were related to the four socioeconomic and maternal variables measured at birth. We also used t tests to compare the malaise inventory subscale scores between members included and excluded due to missing growth data. We used analysis of variance to compare the rates of fetal and childhood growth of cohort members by levels of participation 23, 33, and 42 years.

For the main analyses we used the generalised estimating equations approach to analyse psychological and somatic scores at age 23, 33, and 42 in relation to birthweight z score and weight gain, with adjustment for covariates.14,15 We used an exchangeable correlation structure to adjust for the correlation between repeated measurements. One set of models estimated the difference in mean score (linear regression) and one estimated the odds ratio for a high level of distress (logistic regression). We first fitted a model with birthweight z score and all covariates except weight gain as explanatory variables (model I). In a second model we added weight gain (model II). A comparison of the difference in regression coefficients shows whether the influence of birthweight z score is mediated by weight gain in childhood.16 The analyses were performed with Stata (release 6.0; StataCorp, College Station, TX). To examine the importance of the growth variables in relation to others we took plus or minus 1.28 z score as an indication of high (about 90th centile) and low (10th centile) growth rates and multiplied the coefficients in the regression models by 2.56.

Results

Characteristics of non-participants

After we excluded stillbirths, infant deaths, and twin births we had complete information at birth and at 7 years on 11 115 (67%) cohort members. Of these, 9731 (88%) participated in at least one of the follow up assessments at ages 23, 33, or 42. Overall 59% of the eligible cohort members were involved in the present analysis.

Most (94%) of the cases with missing data at birth or 7 years had incomplete information on birthweight z score (due to missing gestational age or birthweight data) or weight at 7 years. In a multivariable logistic regression that estimated the odds of having missing anthropometric data at birth or 7 years, all four dichotomous variables included in the model were significant: cohort members whose mothers smoked during pregnancy (odds ratio 1.07; 95% confidence interval 1.00 to 1.14), whose mothers were unmarried (1.87; 1.58 to 2.20), whose father's social class was IV or V or others (1.22; 1.13 to 1.32), and who had three or more older siblings (1.19; 1.09 to 1.30) had an increased odds of having missing growth data. Furthermore, among cohort members who at any time completed the malaise inventory, those with missing data at birth or 7 years had higher levels of psychological and somatic distress. For instance, at age 23 the difference in mean in psychological score of was 0.19 (0.09 to 0.27).

Modelling of psychosomatic distress

The subsequent analyses included only cohort members in the main analysis set—that is, members with valid data at birth and 7 years and who participated in at least one adult follow up. Table 1 gives a summary of the birth, maternal, and socioeconomic variables. Table 2 shows a comparison of the key explanatory variables according to participation in the adult follow up. For both men and women, non-participants and those who took part in one, two, or three follow ups had essentially the same mean birthweight z score and weight gain. Table 3 shows the number of cohort members and mean (SD) malaise inventory subscale scores, as well as the proportions with high scores, by sex and age. Women had higher psychological and somatic scores at all ages. Somatic subscale scores increased steadily with age. Psychological subscale scores were lower at age 33 than 23, suggesting transition into adulthood (age 23) was a relatively stressful stage.

Table 2.

 Comparison of mean (SD) birthweight z score and weight gain by level of participation in follow up at ages 23, 33, and 42 years in national child development study

Participation
No participation
Partial (1 or 2 follow ups)
Full (3 follow ups)
P value
Men
No 818 2167 2758
Birthweight z score 0.03 (0.99) 0.00 (1.01) 0.03 (0.99) 0.45
Weight gain (change in z score) −0.07 (1.23) 0.01 (1.17) 0.01 (1.16) 0.16
Women
No 566 1787 3019
Birthweight z score 0.03 (1.00) −0.03 (0.98) 0.03 (1.00) 0.18
Weight gain (change in z score) −0.07 (1.23) 0.01 (1.21) 0.01 (1.20) 0.83

Table 3.

 Psychological and somatic subscale scores of malaise inventory by sex and age at follow up

Men
Women
Psychological score
Somatic score
Psychological score
Somatic score
At age 23 years
No 4211 4212 4240 4239
Mean (SD) 1.33 (1.77) 0.62 (0.99) 2.43 (2.45) 0.87 (1.14)
High distress (%) 6.3 5.9 18.3 9.4
At age 33 years
No 3721 3728 3809 3809
Mean (SD) 1.20 (1.89) 0.73 (1.10) 1.85 (2.32) 0.86 (1.15)
High distress (%) 6.3 8.2 12.5 9.5
At age 42 years
No 3780 3780 3889 3889
Mean (SD) 2.12 (2.50) 0.92 (1.24) 2.81 (2.78) 1.07 (1.30)
High distress (%) 15.5 10.1 22.2 12.6

Table 4 presents the summary findings of the multiple regression analyses of psychological score. Full details of model II are given in table 5. In model I a unit increase in birthweight z score was associated with a reduction of 0.05 (0.01 to 0.09) in mean psychological score. The odds ratio for a high level of psychological distress was 0.95 (0.92 to 0.99). When we added weight gain to the variables of model I (model II) the reduction in mean psychological score increased to 0.10 (0.05 to 0.14). A higher weight gain was also associated with a lower mean psychological score, the reduction being 0.06 (0.02 to 0.10). The odds ratios were 0.90 (0.85 to 0.95) and 0.93 (0.89 to 0.98) for birthweight z score and weight gain, respectively.

Table 4.

 Summary of findings in generalised estimating equations multiple linear regression (mean scores) and logistic regression (odds ratios) models of psychological scores measured at three adult ages*

One unit increase in variable
Difference in mean (95% confidence interval)
Odds ratio (95% confidence interval)
Model I
Model II
Model I
Model II
Birthweight z score −0.05 (−0.09 to −0.01) −0.10 (−0.14 to −0.05) 0.95 (0.92 to 0.99) 0.90 (0.85 to 0.95)
Weight gain (change in z score) NA −0.06 (−0.10 to −0.02) NA 0.93 (0.89 to 0.98)

NA=not applicable. 

*

Adjusted for sex, age at follow up, and covariates in table 1

Table 5.

 Details of generalised estimating equations multiple linear regression (mean score) and logistic regression (odds ratio) models of psychological score measured at three adult ages (summary of key findings given in models II of table 4)

Regressor
Difference in mean (95% CI)
Odds ratio (95% CI)
Birthweight z score −0.10 (−0.14 to −0.05) 0.90 (0.85 to 0.95)
Weight gain (change in z score) −0.06 (−0.10 to −0.02) 0.93 (0.89 to 0.98)
Sex:
 Male 0 1
 Female 0.82 (0.75 to 0.90) 2.08 (1.90 to 2.29)
Follow up:
 At age 23 0 1
 At age 33 −0.34 (−0.39 to −0.28) 0.75 (0.68 to 0.82)
 At age 42 0.61 (0.56 to 0.66) 1.72 (1.58 to 1.84)
Gestational age (weeks) −0.00 (−0.02 to 0.02) 1.00 (0.98 to 1.03)
Father's social class:
 I 0 1
 II −0.01 (−0.22 to 0.20) 0.94 (0.71 to 1.23)
 III 0.20 (0.01 to 0.39) 1.14 (0.89 to 1.47)
 IV 0.31 (0.09 to 0.52) 1.29 (0.98 to 1.70)
 V 0.48 (0.25 to 0.71) 1.48 (1.11 to 1.97)
 Others −0.11 (−0.58 to 0.36) 0.98 (0.58 to 1.66)
Mother's marital status:
 Married 0 1
 Unmarried 0.62 (0.24 to 1.00) 1.66 (1.13 to 2.44)
Parity:
 1 0 1
 2-3 0.13 (0.04 to 0.21) 1.16 (1.04 to 1.29)
 ⩾4 0.37 (0.25 to 0.50) 1.39 (1.21 to 1.58)
Maternal smoking:
 Non-smoker 0 1
 Not during pregnancy 0.07 (−0.09 to 0.22) 1.04 (0.87 to 1.25)
 <5 cigarettes/day 0.13 (−0.02 to 0.28) 1.15 (0.97 to 1.36)
 5-14 cigarettes/day 0.26 (0.16 to 0.36) 1.27 (1.13 to 1.42)
 ⩾15 cigarettes/day 0.39 (0.20 to 0.59) 1.32 (1.07 to 1.63)
Housing tenure at age 7 years:
 Owner occupier 0 1
 Council tenant 0.30 (0.21 to 0.39) 1.35 (1.21 to 1.51)
 Private tenant 0.33 (0.20 to 0.47) 1.36 (1.17 to 1.60)
 Others 0.13 (−0.04 to 0.30) 1.22 (0.99 to 1.49)

We found no association between somatic distress and birthweight z score and weight gain (details not shown). All mean differences were close to zero and the odds ratios were close to one.

Comparison of clinical importance

On the basis of the regression coefficients in table 5, the reduction in mean psychological score between having a high or low fetal growth was 0.10×2.56 or 0.26. This reduction is comparable with that between social classes I and IV, between owner occupier and council tenants, and between being a non-smoker and smoking 5-14 cigarettes per day during pregnancy (table 5). Similarly, the possible impact of weight gain in childhood is −0.06×2.56 or −0.15. This is comparable with the difference between social classes I and III or between being a non-smoker and smoking 1-5 cigarettes per day during pregnancy.

Discussion

This study of the early origins of psychological distress in the 1958 British birth cohort is unique in that the sample size was large, members were followed up to 42 years of age, and growth in childhood was measured. The analyses adjusted for major potential confounders, such as father's social class and maternal smoking. Loss to follow up in a longitudinal study over 40 years is inevitable. However, nearly three fifths of the cohort members were available for the main analyses. This proportion is much higher than in other studies with shorter follow up times. Our analysis showed that participation in adult follow up was unrelated to birthweight z score and postnatal weight gain among those with valid growth data. Missing growth data tended to correlate with a disadvantaged socioeconomic and maternal health background as well as a higher level of distress in adults. As such, the available data tended to emphasise members with relatively good growth and psychological health status. Therefore the real magnitude of the effect of growth failure may be stronger than that estimated here.17 Whether this is indeed the case remains to be verified by further studies. In 1958 gestation was estimated from the date of the last menstrual period, which might make the birthweight z score imprecise. Studies with data from discordant twins will be useful to confirm our findings because they have the same gestational duration.

Our findings are consistent with those from a previous study of people followed to age 26 in that a higher birthweight z score is associated with a reduction in the psychological, but not the somatic, subscale score of the malaise inventory.2 As the psychological subscale is closely related to stress,10,11,18 the finding is in line with the hypothesis that people with impaired growth in early life will become more susceptible to stress.1 It is of interest that the association between one unit increase in birthweight z score and the reduction in psychological score strengthened from 0.05 to 0.10 when we adjusted for weight gain in childhood. Small size at birth is usually followed by some degree of postnatal catch up. Our results suggest that the impact of a smaller size at birth is partly compensated by a higher weight gain in infancy.

Conclusions

We conclude that the association of size at birth and psychological distress persists into middle age. Previous studies could only demonstrate such a relation up to the age of 18 or 26 years. Secondly, growth rate from birth to the age of 7 years was also associated with the psychological outcome. Thirdly, the potential impact of small size at birth may be partly compensated for by a faster weight gain in early childhood.

Acknowledgments

We thank the UK Data Archive and the Centre for Longitudinal Studies, London, for providing data from the national child development study.

Footnotes

Funding: YBC and DM were supported by the National Medical Research Council of Singapore.

Competing interests: None declared.

References

  • 1.Nilsson PM, Nyberg P, Ostergren PO. Increased susceptibility to stress at a psychological assessment of stress tolerance is associated with impaired fetal growth. Int J Epidemiol. 2001;30:75–80. doi: 10.1093/ije/30.1.75. [DOI] [PubMed] [Google Scholar]
  • 2.Cheung YB. Early origins and adult correlates of psychosomatic distress. Soc Sci Med. 2002;55:937–948. doi: 10.1016/s0277-9536(01)00225-8. [DOI] [PubMed] [Google Scholar]
  • 3.Lagerstrom M, Bremme K, Eneroth P, Janson CG. Long-term development for girls and boys at age 16-18 as related to birthweight and gestational age. Int J Psychophysiology. 1994;17:175–180. doi: 10.1016/0167-8760(94)90033-7. [DOI] [PubMed] [Google Scholar]
  • 4.Strauss RS. Adult functional outcome of those born small for gestational age. JAMA. 2000;283:625–632. doi: 10.1001/jama.283.5.625. [DOI] [PubMed] [Google Scholar]
  • 5.Cianfarani S, Germani D, Branca F. Low birthweight and adult insulin resistance: the “catch-up growth” hypothesis. Arch Dis Child Fetal Neonat Ed. 1999;81:F71–F73. doi: 10.1136/fn.81.1.f71. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Cheung YB, Low LCK, Osmond C, Barker DJP, Karlberg JPE. Fetal growth and early postnatal growth are related to blood pressure in adults. Hypertension. 2000;36:795–800. doi: 10.1161/01.hyp.36.5.795. [DOI] [PubMed] [Google Scholar]
  • 7.Ferri E. Life at 33: the fifth follow-up of the National Child Development Study. London: National Children's Bureau; 1993. [Google Scholar]
  • 8.Power C, Manor O, Fox J. Health and class: the early years. London: Chapman and Hall; 1991. [Google Scholar]
  • 9.Rutter M, Tizard J, Whitmore K. Education, health and behaviour. London: Longmans; 1970. [Google Scholar]
  • 10.Grant G, Nolan M, Ellis N. A reappraisal of the malaise inventory. Soc Psychiatry Psychiatr Epidemiol. 1990;25:170–178. doi: 10.1007/BF00782957. [DOI] [PubMed] [Google Scholar]
  • 11.Rodgers B, Pickles A, Power C, Collishaw S, Maughan B. Validity of the malaise inventory in general population samples. Soc Psychiatry Psychiatr Epidemiol. 1999;34:333–341. doi: 10.1007/s001270050153. [DOI] [PubMed] [Google Scholar]
  • 12.Niklasson A, Ericson A, Fryer JG, Karlberg J, Lawrence C, Karlberg P. An update of the Swedish reference standards for weight, length and head circumference at birth for given gestational age (1977-1981) Acta Paediatr Scand. 1991;80:756–762. doi: 10.1111/j.1651-2227.1991.tb11945.x. [DOI] [PubMed] [Google Scholar]
  • 13.Box GEP, Cox DR. An analysis of transformations. J Roy Stat Soc Series B. 1964;26:211–243. [Google Scholar]
  • 14.Liang KY, Zeger SL. Longitudinal data analysis using generalized linear models. Biometrika. 1986;73:13–22. [Google Scholar]
  • 15.Fayers PM, Machin D. Quality of life: assessment, analysis and interpretation. Chichester: Wiley; 2000. [Google Scholar]
  • 16.Lucas A, Fewtrell MS, Cole TJ. Fetal origin of adult disease: the hypothesis revisited. BMJ. 1999;319:245–249. doi: 10.1136/bmj.319.7204.245. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Cheung YB. Adjustment for selection bias in cohort studies: an application of a probit model with selectivity to life course epidemiology. J Clin Epidemiol. 2001;54:1238–1243. doi: 10.1016/s0895-4356(01)00403-6. [DOI] [PubMed] [Google Scholar]
  • 18.Hirst MA, Bradshaw JR. Evaluating the malaise inventory: a comparison of measures of stress. J Psychosom Res. 1983;27:193–199. doi: 10.1016/0022-3999(83)90022-3. [DOI] [PubMed] [Google Scholar]

Articles from BMJ : British Medical Journal are provided here courtesy of BMJ Publishing Group

RESOURCES