A genome-wide scan reveals a maternal susceptibility locus for pre-eclampsia on chromosome 2p13

被引:151
|
作者
Arngrímsson, R
Siguróardóttir, S
Frigge, ML
Bjarnadóttir, RI
Jónsson, T
Stefánsson, H
Baldursdóttir, A
Einarsdóttir, AS
Palsson, B
Snorradóttir, S
Lachmeijer, AMA
Nicolae, D
Kong, A
Bragason, BT
Gulcher, JR
Geirsson, RT
Stefánsson, K
机构
[1] Univ Iceland, Fac Med, Med Genet Unit, IS-101 Reykjavik, Iceland
[2] DeCODE Genet, IS-110 Reykjavik, Iceland
[3] Natl Univ Hosp, Dept Obstet & Gynecol, IS-101 Reykjavik, Iceland
[4] Univ Chicago, Dept Human Genet, Chicago, IL 60637 USA
[5] Univ Chicago, Dept Stat, Chicago, IL 60637 USA
基金
英国惠康基金;
关键词
D O I
10.1093/hmg/8.9.1799
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pre-eclampsia is a common and serious disease and a major cause of maternal and infant mortality, Antenatal care systems world-wide screen for signs of the disease such as hypertension and proteinuria. Unlike most other human disorders it impacts two individuals, the mother and the child, both of whom can be severely affected. The pathophysiology of the disorder is incompletely understood, but familial clustering of the disease is apparent, Here we report the results of a genome-wide screen of Icelandic families representing 343 affected women. Including those patients with nonproteinuric pre-eclampsia (gestational hypertension), proteinuric pre-eclampsia and eclampsia, we detected a significant locus on 2p13 with a lod score of 4.70 (single point P < 3.49 x 10(-6)). This is the first reported locus for pre-eclampsia meeting the criteria for genome-wide significance.
引用
收藏
页码:1799 / 1805
页数:7
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