Angiotensinogen and angiotensin converting enzyme genotypes and carotid atherosclerosis: The atherosclerosis risk in communities and the NHLBI family heart studies

被引:34
作者
Arnett, DK
Borecki, IB
Ludwig, EH
Pankow, JS
Myers, R
Evans, G
Folsom, AR
Heiss, G
Higgins, M
机构
[1] Univ Minnesota, Sch Publ Hlth, Div Epidemiol, Minneapolis, MN 55454 USA
[2] Washington Univ, Sch Med, Div Biostat, St Louis, MO 63110 USA
[3] Univ Utah, Dept Human Genet, Salt Lake City, UT USA
[4] Univ Utah, Howard Hughes Med Inst, Salt Lake City, UT USA
[5] Boston Univ, Sch Med, Prevent Med & Epidemiol Sect, Boston, MA 02118 USA
[6] Bowman Gray Sch Med, Dept Publ Hlth Sci, Winston Salem, NC USA
[7] Univ N Carolina, Sch Publ Hlth, Dept Epidemiol, Chapel Hill, NC USA
[8] Univ Michigan, Sch Publ Hlth, Dept Epidemiol, Ann Arbor, MI 48109 USA
关键词
intima-media thickness; angiotensin; converting enzymes; ultrasound; polymorphism; angiotensinogen;
D O I
10.1016/S0021-9150(98)00009-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Polymorphisms of the renin-angiotensin system are associated with cardiovascular pathology. Therefore, the association of the insertion/deletion (I/D) polymorphism of the angiotensin converting enzyme (ACE) gene and the T235 (methionine to threonine substitution) polymorphism of the angiotensinogen (ACT) gene with intima-media thickness of the carotid artery was investigated. Methods and results: Subjects were randomly selected from two centers participating in both the Atherosclerosis Risk in Communities (ARIC) and NHLBI Family Heart Studies. Probands were 45-64 years of age who were free of cardiovascular disease and had B-mode ultrasound measured carotid intima-media thickness. Multiplex polymerase chain reaction amplification was used to evaluate the ACE I/D and AGT T235 polymorphisms: genotype information was available on 495 and 475 participants, respectively. The frequencies of the ACE D and AGT T alleles were 0.56 and 0.52, respectively; 30% were homozygous for the ACE D allele, and 29% were homozygous for the AGT T allele. After adjustment for systolic blood pressure, antihypertensive medication use, diabetes, age, sex and LDL cholesterol, the mean intima-media thickness was 0.729, 0.732 and 0.721 mm in the ACE DD, ID, and II genotypes, respectively (partial F test 1.53, P = 0.22), and 0.727, 0.732 and 0.724 mm in the AGT MM, MT, and TT genotypes, respectively (partial F test 0.91, P = 0.40). Combining the genotypes for ACE and AGT, there were also no differences in intima-media thickness across the eight joint genotypes. Conclusion: We found no evidence that the ACE I/D and AGT T235 polymorphisms of the renin-angiotensin system were associated with carotid intima-media thickness in this population-based sample of middle-aged adults with no history of cardiovascular disease. The lack of an association between these variants and intima-media thickness may indicate that early atherosclerosis is mediated by factors other than these RAS polymorphisms. (C) 1998 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:111 / 116
页数:6
相关论文
共 29 条
[1]  
[Anonymous], 1991, J Neuroimaging, V1, P68
[2]   PLASMA ANGIOTENSIN-CONVERTING ENZYME-ACTIVITY AND CAROTID WALL THICKENING [J].
BONITHONKOPP, C ;
DUCIMETIERE, P ;
TOUBOUL, PJ ;
FEVE, JM ;
BILLAUD, E ;
HERAUD, V .
CIRCULATION, 1994, 89 (03) :952-954
[3]   Associations of candidate loci angiotensinogen and angiotensin-converting enzyme with severe hypertension: The NHLBI Family Heart Study [J].
Borecki, IB ;
Province, MA ;
Ludwig, EH ;
Ellison, RC ;
Folsom, AR ;
Heiss, G ;
Lalouel, JM ;
Higgins, M ;
Rao, DC .
ANNALS OF EPIDEMIOLOGY, 1997, 7 (01) :13-21
[4]  
CAMBIEN F, 1993, LANCET, V341, P1991
[5]   ANGIOTENSIN-CONVERTING ENZYME I/D POLYMORPHISM AND ARTERIAL-WALL THICKNESS IN A GENERAL-POPULATION - THE VOBARNO STUDY [J].
CASTELLANO, M ;
MUIESAN, ML ;
RIZZONI, D ;
BESCHI, M ;
PASINI, G ;
CINELLI, A ;
SALVETTI, M ;
PORTERI, E ;
BETTONI, G ;
KREUTZ, R ;
LINDPAINTNER, K ;
ROSEI, EA .
CIRCULATION, 1995, 91 (11) :2721-2724
[6]   LINKAGE OF THE ANGIOTENSINOGEN GENE TO ESSENTIAL-HYPERTENSION [J].
CAULFIELD, M ;
LAVENDER, P ;
FARRALL, M ;
MUNROE, P ;
LAWSON, M ;
TURNER, P ;
CLARK, AJL .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 330 (23) :1629-1633
[7]  
DAHLOF B, 1992, AM J HYPERTENS, V5, P900
[8]  
FERNANDEZALFONSO MS, 1992, BASIC RES CARDIOL, V87, P173
[9]   THE ANGIOTENSIN-I CONVERTING ENZYME GENE AND PREDISPOSITION TO HIGH BLOOD-PRESSURE [J].
HARRAP, SB ;
DAVIDSON, HR ;
CONNOR, JM ;
SOUBRIER, F ;
CORVOL, P ;
FRASER, R ;
FOY, CJW ;
WATT, GCM .
HYPERTENSION, 1993, 21 (04) :455-460
[10]   A POLYMORPHISM OF THE ANGIOTENSINOGEN GENE ASSOCIATED WITH VARIATION IN BLOOD-PRESSURE IN A GENETIC ISOLATE [J].
HEGELE, RA ;
BRUNT, JH ;
CONNELLY, PW .
CIRCULATION, 1994, 90 (05) :2207-2212