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The Relationship between Birthweight and Longitudinal Changes of Blood Pressure Is Modulated by Beta-Adrenergic Receptor Genes: The Bogalusa Heart Study

机译:出生体重与血压的纵向变化之间的关系是由β-肾上腺素能受体基因调节的:Bogalusa心脏研究

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摘要

This study examines the genetic influence of β-adrenergic receptor gene polymorphisms (β2-AR Arg16Gly and β3-AR Trp64Arg) on the relationship of birthweight to longitudinal changes of blood pressure (BP) from childhood to adulthood in 224 black and 515 white adults, aged 21–47 years, enrolled in the Bogalusa Heart Study. Blacks showed significantly lower birthweight and frequencies of β2-AR Gly16 and β3-AR Trp64 alleles and higher BP levels and age-related trends than whites. In multivariable regression analyses using race-adjusted BP and birthweight, low birthweight was associated with greater increase in age-related trend of systolic BP (standardized regression coefficient β = −0.09, P = .002) and diastolic BP (β = −0.07, P = .037) in the combined sample of blacks and whites, adjusting for the first BP measurement in childhood, sex, age, and gestational age. Adjustment for the current body mass index strengthened the birthweight-BP association. Importantly, the strength of the association, measured as regression coefficients, was modulated by the combination of β2-AR and β3-AR genotypes for systolic (P = .042 for interaction) and diastolic BP age-related trend (P = .039 for interaction), with blacks and whites showing a similar trend in the interaction. These findings indicate that the intrauterine programming of BP regulation later in life depends on β-AR genotypes.
机译:这项研究调查了224名黑人和515名白人成年人中,β-肾上腺素能受体基因多态性(β2-ARArg16Gly和β3-ARTrp64Arg)对出生体重与从童年到成年血压纵向变化(BP)的关系的遗传影响,年龄在21-47岁之间,参加了Bogalusa心脏研究。与白人相比,黑人的出生体重和β2-ARGly16和β3-ARTrp64等位基因的频率显着降低,并且BP水平和与年龄有关的趋势更高。在使用种族调整后的BP和出生体重进行的多变量回归分析中,低出生体重与年龄相关的收缩压(标准化回归系数β= -0.09,P = .002)和舒张压BP(β= -0.07, P = 0.037)在黑人和白人的混合样本中,调整了儿童,性别,年龄和胎龄的首次血压测量值。当前体重指数的调整加强了出生体重-血压关联。重要的是,通过β2-AR和β3-AR基因型的收缩压(相互作用P = .042)和舒张性BP年龄相关趋势(对于P = 0.039)的组合,以回归系数来衡量的关联强度受到调节。互动),而黑人和白人的互动趋势相似。这些发现表明,在生命的后期,宫腔内对BP调节的编程取决于β-AR基因型。

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