Genetic Influences on Trajectories of Systolic Blood Pressure Across Childhood and Adolescence

被引:25
|
作者
Howe, Laura D. [1 ,2 ]
Parmar, Priyakumari G. [3 ]
Paternoster, Lavinia [1 ,2 ]
Warrington, Nicole M. [3 ]
Kemp, John P. [1 ,2 ]
Briollais, Laurent [5 ]
Newnham, John P. [3 ]
Timpson, Nicholas J. [1 ,2 ]
Smith, George Davey [1 ,2 ]
Ring, Susan M. [1 ,2 ]
Evans, David M. [1 ,2 ]
Tilling, Kate [2 ]
Pennell, Craig E. [3 ]
Beilin, Lawrie J. [4 ]
Palmer, Lyle J. [6 ]
Lawlor, Debbie A. [1 ,2 ]
机构
[1] Univ Bristol, MRC Integrat Epidemiol Unit, Bristol, Avon, England
[2] Univ Bristol, Sch Social & Community Med, Bristol, Avon, England
[3] Univ Western Australia, Sch Womens & Infants Hlth, Perth, WA 6009, Australia
[4] Univ Western Australia, Sch Med & Pharmacol, Royal Perth Hosp Unit, Perth, WA 6009, Australia
[5] Univ Toronto, Samuel Lunenfeld Res Inst, Toronto, ON M5S 1A1, Canada
[6] Univ Toronto, Ontario Inst Canc Res, Toronto, ON M5S 1A1, Canada
基金
英国惠康基金; 英国医学研究理事会;
关键词
adolescent; blood pressure; genetics; humans; CARDIOVASCULAR RISK-FACTORS; VARIANTS; COHORT; ASSOCIATION; ADULTHOOD;
D O I
10.1161/CIRCGENETICS.113.000197
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Blood pressure (BP) tends to increase across childhood and adolescence, but the genetic influences on rates of BP change are not known. Potentially important genetic influences could include genetic variants identified in genome-wide association studies of adults as being associated with BP, height, and body mass index. Understanding the contribution of these genetic variants to changes in BP across childhood and adolescence could yield understanding into the life course development of cardiovascular risk. Methods and Results Pooling data from 2 cohorts (the Avon Longitudinal Study of Parents and Children [n=7013] and the Western Australian Pregnancy Cohort [n=1459]), we examined the associations of allelic scores of 29 single-nucleotide polymorphisms (SNPs) for adult BP, 180 height SNPs, and 32 body mass index SNPs, with trajectories of systolic BP (SBP) from 6 to 17 years of age, using linear spline multilevel models. The allelic scores of BP and body mass index SNPs were associated with SBP at 6 years of age (per-allele effect sizes, 0.097 mm Hg [SE, 0.039 mm Hg] and 0.107 mm Hg [SE, 0.037 mm Hg]); associations with age-related changes in SBP between 6 and 17 years of age were of small magnitude and imprecisely estimated. The allelic score of height SNPs was only weakly associated with SBP changes. No sex or cohort differences in genetic effects were observed. Conclusions Allelic scores of BP and body mass index SNPs demonstrated associations with SBP at 6 years of age with a similar magnitude but were not strongly associated with changes in SBP with age between 6 and 17 years. Further work is required to identify variants associated with changes with age in BP.
引用
收藏
页码:608 / 614
页数:7
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