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Atherosclerosis and Lipoproteins |
From the University Department of Pathological Biochemistry (N.S., D.O.R.) and Department of Obstetrics and Gynaecology (I.A.G.), Glasgow Royal Infirmary, Glasgow, UK; the University Department of General Practice (A.M., M.U., G.W.), University of Glasgow, UK; and the Department of Social Medicine (G.D.S., M.U.), University of Bristol, Canynge Hall, Bristol, UK.
Correspondence to Dr Naveed Sattar, Department of Pathological Biochemistry, Glasgow Royal Infirmary, Glasgow G31 2ER, Scotland, UK. E-mail nsattar{at}clinmed.gla.ac.uk
Objective Inflammation markers and low birth weight each predict elevated risk of cardiovascular events and type 2 diabetes. However, potential associations between the low-grade inflammatory response as represented by C-reactive protein (CRP) concentrations and low birth weight have been sparsely examined.
Methods and results In the MIDSPAN Family Study, 1663 individuals had birth weight data and CRP concentrations measured as adults (age 30 to 59). The relationship between these parameters was examined after adjusting for factors known to influence CRP concentrations inclusive of age, body mass index, smoking, socio-economic deprivation, and hormone use in women. After adjusting for potential confounders, there was a negative association between birth weight and CRP, whereby a 1-kg increase in birth weight is associated with a 10.7% decrease in CRP (95% CI: 3.0% to 17.8% decrease). There was no strong evidence that the effects differed in men and women (P=0.32).
Conclusion Low birth weight contributes to elevated CRP concentration in adult life. Future studies are required to determine to what extent this association reflects catch-up centile crossing, in utero programming, or genetic factors.
Key Words: inflammation fetal programming obesity birth weight C-reactive protein
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