Genetic effects on blood pressure localized to chromosomes 6 and 7

被引:16
作者
Adeyemo, A
Luke, A
Wu, XD
Cooper, RS
Kan, D
Omotade, A
Zhu, XF
机构
[1] Loyola Univ, Ctr Med, Dept Prevent Med & Epidemiol, Maywood, IL 60153 USA
[2] Univ Ibadan, Coll Med, Inst Child Hlth, Dept Pediat, Ibadan, Nigeria
关键词
genome wide scan; QTDT; African population;
D O I
10.1097/01.hjh.0000173519.06353.8b
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Objective To identify quantitative trait loci (QTL) contributing to the variation in blood pressure in a west African population. Methods We conducted a multi-stage genome scan in a population sample from rural Nigeria. A 10 centimorgan genome-wide screen for log-transformed systolic blood pressure (SBP) and diastolic blood pressure (DBP) was first performed based on 1054 individuals from 188 families. In the second phase we performed a similar analysis in an independent sample of 621 individuals from 101 families. In a third follow-up fine mapping phase we genotyped 25 additional markers in the three regions identified in the first two phases. Results Genome-wide significant linkage evidence was found for SBP on chromosome 7p (lod = 4.73, genome wide P <= 0.01, point-wise P = 1.53 X 10(-6)) in the combined sample. Suggestive linkage evidence was also detected on 6q (lod = 2.9, point-wise P = 0.00013) and 7q (lod = 2.6, point-wise P = 0.00027) for SBP, and 7q (lod = 1.6, point-wise P = 0.003) for DBP. Conclusions This study has identified several regions that may harbor genetic variants affecting the variation in blood pressure. Further association mapping under the linkage peaks will be required to refine the linkage evidence that has emerged from our analysis. (c) 2005 Lippincott Williams & Wilkins.
引用
收藏
页码:1367 / 1373
页数:7
相关论文
共 20 条
[1]   A general test of association for quantitative traits in nuclear families [J].
Abecasis, GR ;
Cardon, LR ;
Cookson, WOC .
AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 66 (01) :279-292
[2]   Merlin-rapid analysis of dense genetic maps using sparse gene flow trees [J].
Abecasis, GR ;
Cherny, SS ;
Cookson, WO ;
Cardon, LR .
NATURE GENETICS, 2002, 30 (01) :97-101
[3]   Genome-wide mapping of human loci for essential hypertension [J].
Caulfield, M ;
Munroe, P ;
Pembroke, J ;
Samani, N ;
Dominiczak, A ;
Brown, M ;
Benjamin, N ;
Webster, J ;
Ratcliffe, P ;
O'Shea, S ;
Papp, J ;
Taylor, E ;
Dobson, R ;
Knight, J ;
Newhouse, S ;
Hooper, J ;
Lee, W ;
Brain, N ;
Clayton, D ;
Lathrop, GM ;
Farrall, M ;
Connell, J .
LANCET, 2003, 361 (9375) :2118-2123
[4]   The genetic basis of plasma variation in adiponectin, a global endophenotype for obesity and the metabolic syndrome [J].
Comuzzie, AG ;
Funahashi, T ;
Sonnenberg, G ;
Martin, LJ ;
Jacob, HJ ;
Black, AEK ;
Maas, D ;
Takahashi, M ;
Kihara, S ;
Tanaka, S ;
Matsuzawa, Y ;
Blangero, J ;
Cohen, D ;
Kissebah, A .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2001, 86 (09) :4321-4325
[5]  
Cooper, 1997, Blood Press Monit, V2, P35
[6]   The prevalence of hypertension in seven populations of West African origin [J].
Cooper, R ;
Rotimi, C ;
Ataman, S ;
McGee, D ;
Osotimehin, B ;
Kadiri, S ;
Muna, W ;
Kingue, S ;
Fraser, H ;
Forrester, T ;
Bennett, F ;
Wilks, R .
AMERICAN JOURNAL OF PUBLIC HEALTH, 1997, 87 (02) :160-168
[7]   Genome scan among Nigerians linking blood pressure to chromosomes 2, 3, and 19 [J].
Cooper, RS ;
Luke, A ;
Zhu, XF ;
Kan, DH ;
Adeyemo, A ;
Rorimi, C ;
Bouzekri, N ;
Ward, R .
HYPERTENSION, 2002, 40 (05) :629-633
[8]   Antihypertensive treatments obscure familial contributions to blood pressure variation [J].
Cui, JSS ;
Hopper, JL ;
Harrap, SB .
HYPERTENSION, 2003, 41 (02) :207-210
[9]  
EXCOFFIER L, 1995, MOL BIOL EVOL, V12, P921
[10]   Ignoring linkage disequilibrium among tightly linked markers induces false-positive evidence of linkage for affected sib pair analysis [J].
Huang, QQ ;
Shete, S ;
Amos, CI .
AMERICAN JOURNAL OF HUMAN GENETICS, 2004, 75 (06) :1106-1112