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

• Published in: BioMed research international 2010-01, Vol.2010 (2010), p.1-8
• Main Authors: Chen, Wei, Srinivasan, Sathanur R., Hallman, D. Michael, Berenson, Gerald S.
• Format: Article
• Language: English
• Subjects: Adolescent; Adult; African Americans; Area Under Curve; Biomedical research; Birth Weight; Black or African American; Black People - genetics; Blood pressure; Blood Pressure - genetics; Child; Child, Preschool; Cohort Studies; Female; Genotype & phenotype; Health sciences; Humans; Hypertension; Louisiana - epidemiology; Male; Middle Aged; Polymorphism, Genetic; Public health; Receptors, Adrenergic, beta - genetics; Regression Analysis; Sex Factors; Statistical methods; Studies; White people; White People - genetics
• ISSN: 1110-7243; 2314-6133; 1110-7251; 1110-7251; 2314-6141
• DOI: 10.1155/2010/543514

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.