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Published Online First: 2 May 2008. doi:10.1136/adc.2007.129122
Archives of Disease in Childhood 2008;93:760-767
Copyright © 2008 BMJ Publishing Group Ltd & Royal College of Paediatrics and Child Health.

Original articles

Association between birth weight and adolescent systolic blood pressure in a caucasian birth cohort differs according to skin type, CRH promoter or 11β-HSD2 genotype

T Dwyer1,2, L Blizzard1, B Patterson1, A-L Ponsonby1,2, K Martin1, S Quinn1, M M Sale1,3, S M Richards1, R Morley2,4, S Rich1,3, J L Dickinson1

1 Menzies Research Institute, University of Tasmania, Hobart, Tasmania, Australia
2 Murdoch Childrens Research Institute, Royal Children’s Hospital, Parkville, Victoria, Australia
3 Department of Public Health Sciences University of Virginia School of Medicine Charlottesville, VA, USA
4 University of Melbourne Department of Paediatrics, Royal Children’s Hospital, Parkville, Victoria, Australia

Professor T Dwyer, Murdoch Childrens Research Institute, Royal Children’s Hospital, Parkville, Victoria 3052, Australia; terry.dwyer{at}mcri.edu.au

Objective: To examine whether the inverse association between birth weight and blood pressure varies by skin pigmentation and/or related genotypes.

Study design: 671 children from a predominantly caucasian birth cohort were followed-up to adolescence (mean (SD) age 14.4 (0.64)).

Methods: Data on birth weight, socioeconomic status, maternal antenatal smoking, adolescent blood pressure and polymorphisms of candidate genes were obtained and analysed by multiple linear regression.

Results: An increase in birth weight of 1 kg was associated with an non-significant difference in adolescent systolic blood pressure of –0.53 mm Hg (95% CI –1.72 to 0.66) per kg after adjustment for child age and cohort entry criteria. The inverse association between birth weight and systolic blood pressure was stronger for those with darker skin (>=2% melanin) (difference in effect, p = 0.02), those with more copies of the C allele of corticotropin-releasing hormone (CRH) +T1273C (p = 0.06), and those with more copies of the short (<=236 bp) form of the 11β-HSD2{CA}nrepeat microsatellite (p = 0.03).

Conclusions: These findings add to the evidence that cortisol-related pathways may account for at least part of the observed birth weight–blood pressure associations.


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