INSERTION/DELETION POLYMORPHISM OF THE ANGIOTENSIN-CONVERTING ENZYME GENE IS STRONGLY ASSOCIATED WITH CORONARY HEART-DISEASE IN NON-INSULIN-DEPENDENT DIABETES-MELLITUS

被引:237
作者
RUIZ, J
BLANCHE, H
COHEN, N
VELHO, G
CAMBIEN, F
COHEN, D
PASSA, P
FROGUEL, P
机构
[1] FDN JEAN DAUSSET,CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
[2] HOP ST LOUIS,DEPT ENDOCRINOL,F-75010 PARIS,FRANCE
[3] INSERM,U358,F-75010 PARIS,FRANCE
[4] INSERM,F-75005 PARIS,FRANCE
关键词
D O I
10.1073/pnas.91.9.3662
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Non-insulin-dependent diabetes mellitus (NIDDM) is considered a model of premature atherosclerosis with a strong genetic component. We have investigated the role of angiotensin-converting enzyme (ACE; EC 3.4.15.1) gene in 316 unrelated NIDDM individuals, 132 who had myocardial infarction or significant coronary stenoses and 184 with no history of coronary heart disease (CHD). A deletion-polymorphism in the ACE gene was recently reported to be associated with myocardial infarction especially in people classified as low risk. Here we report that the D allele of the ACE gene is a strong and independent risk factor for CHD in NIDDM patients. The D allele is associated with early-onset CHD in NIDDM, independently of hypertension and lipid values. A progressively increasing relative risk in individuals heterozygous and homozygous for the D allele was observed (odds ratios of 1.41 and 2.35, respectively; P < 0.007), suggesting a codominant effect on the cardiovascular risk. The percentage of CHD attributable to the ACE deletion allele was 24% in this NIDDM population. Identification of NIDDM patients carrying this putative CHD-susceptibility genotype would help early detection and treatment of CHD.
引用
收藏
页码:3662 / 3665
页数:4
相关论文
共 23 条
  • [1] DELETION POLYMORPHISM IN THE GENE FOR ANGIOTENSIN-CONVERTING ENZYME IS A POTENT RISK FACTOR FOR MYOCARDIAL-INFARCTION
    CAMBIEN, F
    POIRIER, O
    LECERF, L
    EVANS, A
    CAMBOU, JP
    ARVEILER, D
    LUC, G
    BARD, JM
    BARA, L
    RICARD, S
    TIRET, L
    AMOUYEL, P
    ALHENCGELAS, F
    SOUBRIER, F
    [J]. NATURE, 1992, 359 (6396) : 641 - 644
  • [2] CHATELLIER G, 1992, PRESSE MED, V21, P1250
  • [3] DISEASE ASSOCIATIONS - CHANCE, ARTIFACT, OR SUSCEPTIBILITY GENES
    COX, NJ
    BELL, GI
    [J]. DIABETES, 1989, 38 (08) : 947 - 950
  • [4] FAMILIAL CLUSTERING OF CARDIOVASCULAR-DISEASE IN PATIENTS WITH INSULIN-DEPENDENT DIABETES AND NEPHROPATHY
    EARLE, K
    WALKER, J
    HILL, C
    VIBERTI, G
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1992, 326 (10) : 673 - 677
  • [5] STRATEGIES FOR THE COLLECTION OF SIBLING-PAIR DATA FOR GENETIC-STUDIES IN TYPE-2 (NON-INSULIN-DEPENDENT) DIABETES-MELLITUS
    FROGUEL, P
    VELHO, G
    COHEN, D
    PASSA, P
    [J]. DIABETOLOGIA, 1991, 34 (09) : 685 - 685
  • [7] NEOINTIMA FORMATION AFTER VASCULAR INJURY IS ANGIOTENSIN-II MEDIATED
    LAPORTE, S
    ESCHER, E
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 187 (03) : 1510 - 1516
  • [8] LESAGE S, 1993, DIABETOLOGIA, V36, P72
  • [9] MARRE M, 1994, IN PRESS DIABETES
  • [10] NAKA M, 1992, AM HEART J, V23, P46