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
相关论文
共 30 条
  • [1] AMGRIMSSON R, 1993, NAT GENET, V4, P114
  • [2] GENETIC AND FAMILIAL PREDISPOSITION TO ECLAMPSIA AND PREECLAMPSIA IN A DEFINED POPULATION
    ARNGRIMSSON, R
    BJORNSSON, S
    GEIRSSON, RT
    BJORNSSON, H
    WALKER, JJ
    SNAEDAL, G
    [J]. BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 1990, 97 (09): : 762 - 769
  • [3] Evidence for a familial pregnancy-induced hypertension locus in the eNOS-gene region
    Arngrimsson, R
    Hayward, C
    Nadaud, S
    Baldursdottir, A
    Walker, JJ
    Liston, WA
    Bjarnadottir, RI
    Brock, DJH
    Geirsson, RT
    Connor, JM
    Soubrier, F
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (02) : 354 - 362
  • [4] ANALYSIS OF DIFFERENT INHERITANCE PATTERNS IN PREECLAMPSIA/ECLAMPSIA SYNDROME
    ARNGRIMSSON, R
    BJORNSSON, H
    GEIRSSON, RT
    [J]. HYPERTENSION IN PREGNANCY, 1995, 14 (01) : 27 - 38
  • [5] Optimal ascertainment strategies to detect linkage to common disease alleles
    Badner, JA
    Gershon, ES
    Goldin, LR
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (03) : 880 - 888
  • [6] Comprehensive human genetic maps: Individual and sex-specific variation in recombination
    Broman, KW
    Murray, JC
    Sheffield, VC
    White, RL
    Weber, JL
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (03) : 861 - 869
  • [7] GENETICS OF HYPERTENSION IN PREGNANCY - POSSIBLE SINGLE GENE-CONTROL OF PREECLAMPSIA AND ECLAMPSIA IN THE DESCENDANTS OF ECLAMPTIC WOMEN
    CHESLEY, LC
    COOPER, DW
    [J]. BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 1986, 93 (09): : 898 - 908
  • [8] THE CLASSIFICATION AND DEFINITION OF THE HYPERTENSIVE DISORDERS OF PREGNANCY
    DAVEY, DA
    MACGILLIVRAY, I
    [J]. AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1988, 158 (04) : 892 - 898
  • [9] UNDERLYING DISORDERS ASSOCIATED WITH SEVERE EARLY-ONSET PREECLAMPSIA
    DEKKER, GA
    DEVRIES, JIP
    DOELITZSCH, PM
    HUIJGENS, PC
    VONBLOMBERG, BME
    JAKOBS, C
    VANGEIJN, HP
    [J]. AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1995, 173 (04) : 1042 - 1048
  • [10] A comprehensive genetic map of the human genome based on 5,264 microsatellites
    Dib, C
    Faure, S
    Fizames, C
    Samson, D
    Drouot, N
    Vignal, A
    Millasseau, P
    Marc, S
    Hazan, J
    Seboun, E
    Lathrop, M
    Gyapay, G
    Morissette, J
    Weissenbach, J
    [J]. NATURE, 1996, 380 (6570) : 152 - 154