Genome scan among Nigerians linking blood pressure to chromosomes 2, 3, and 19
Document Type
Article
Publication Date
11-1-2002
Abstract
An understanding of the genetic influences on hypertension would help unravel the pathophysiology of this complex disorder and improve our understanding of causal mechanisms. Contemporary technology makes it possible to examine enough genetic markers to support a generalized search across the entire genome for candidate regions. In the present study, a family set was recruited from southwest Nigeria, and 378 microsatellite markers were typed on 792 individuals in 196 families. Multipoint variance component analysis identified linkage signals (logarithm of the odds [LOD]>1.74, P<0.0023) for systolic blood pressure on 19p (D19S714) and 19q (D19S246), whereas for diastolic blood pressure, linkage was observed on 2p (D2S1790), 3p (D3S1304), 5q (D5S1462), 7p (D7S3046), 7q (D7S821), and 10q (D10S1221). Other regions of interest (1.18
Publication Source (Journal or Book title)
Hypertension
First Page
629
Last Page
633
Recommended Citation
Cooper, R., Luke, A., Zhu, X., Kan, D., Adeyemo, A., Rorimi, C., Bouzekri, N., & Ward, R. (2002). Genome scan among Nigerians linking blood pressure to chromosomes 2, 3, and 19. Hypertension, 40 (5), 629-633. https://doi.org/10.1161/01.HYP.0000035708.02789.39