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Does the strength of the association between foetal growth rate and ischaemic heart disease mortality differ by social circumstances in early or later life?
  1. K Rajaleid1,
  2. O Manor2,
  3. I Koupil1
  1. 1
    Centre for Health Equity Studies (CHESS), Stockholm University/Karolinska Institutet, Stockholm, Sweden
  2. 2
    School of Public Health, Hebrew University, Jerusalem, Israel
  1. K Rajaleid, Centre for Health Equity Studies (CHESS), Stockholm University/Karolinska Institute, 106 91 Stockholm, Sweden; kristiina.rajaleid{at}chess.su.se

Abstract

Objective: To study whether the effect of size at birth on the risk of ischaemic heart disease (IHD) death is modified by social circumstances in childhood or in adulthood.

Design: A cohort study. Data on circumstances at birth were retrieved from archived obstetric records, social characteristics in adulthood and mortality follow-up through routine registers.

Participants: 6159 men and 5663 women who were born in Uppsala University Hospital, Sweden (the Uppsala Birth Cohort) during 1915–1929, were singleton births with more than 30 weeks of gestational age and were alive in 1961. Follow-up time 1961–2002 (from age 31–46 to 73–88 years).

Main outcome measure: Death from IHD. Multivariate Cox regression with age as the time scale, controlling for year of birth and stratified by gender.

Results: The risk of IHD death was lower among men and women with higher weight for gestational age. Lower social class in adulthood was associated with a higher risk of IHD death. The effect of size at birth on IHD mortality did not appear to be modified by social class at birth but was only present in men of higher social class in adulthood (hazard ratio per 1 SD weight for gestational age 0.84, 95% CI 0.75 to 0.93).

Conclusions: Weight for gestational age was inversely associated with the risk of IHD death in men and women; this effect was present in men of non-manual adult social class only but did not appear to be modified by adult social class in women or by social class at birth in either men or women.

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Footnotes

  • Funding: The UBCoS Multigen study is supported by grants from the Swedish Council for Working Life and Social Research (FAS project no 2003-0101) and the Swedish Research Council (VR project no 345-2003-2440 ). IK is currently funded by the Swedish Council for Working Life and Social Research. The funders were not involved in the study design or execution and the views and conclusions expressed in this paper are the responsibility of the authors.

  • Competing interests: None.

  • Ethics approval: The study was approved by the Regional Ethics Committee in Stockholm.