Age-dependent association of apolipoprotein E genotype with coronary and aortic atherosclerosis in middle-aged men -: An autopsy study

被引:140
作者
Ilveskoski, E
Perola, M
Lehtimäki, T
Laippala, P
Savolainen, V
Pajarinen, J
Penttilä, A
Lalu, KH
Männikkö, A
Liesto, KK
Koivula, T
Karhunen, PJ
机构
[1] Univ Tampere, Sch Med, FIN-33101 Tampere, Finland
[2] Tampere Univ Hosp, Tampere, Finland
[3] Natl Publ Hlth Inst, Dept Human Mol Genet, Helsinki, Finland
[4] Tampere Univ Hosp, Dept Clin Chem, FIN-33521 Tampere, Finland
[5] Lab Atherosclerosis Genet, Tampere, Finland
[6] Univ Tampere, Tampere Sch Publ Hlth, FIN-33101 Tampere, Finland
[7] Univ Helsinki, Dept Forens Med, SF-00300 Helsinki, Finland
关键词
apolipoproteins; atherosclerosis; coronary disease;
D O I
10.1161/01.CIR.100.6.608
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-Apolipoprotein E (apoE) polymorphism is one of the genetic determinants of serum cholesterol values, The apoE epsilon 4 allele has been associated with advanced coronary heart disease (CHD) diagnosed by angiography, but the role of the apoE genotype in atherosclerosis has not been confirmed at vessel-wall level, nor is any age-dependent effect of the apoE genotype on the development of CHD known. Methods and Results-The right and left anterior descending coronary arteries (RCA and LAD) and the aorta from 700 male autopsy cases (Helsinki Sudden Death Study) in 1981-1982 and 1991-1992 (average age 53 years, range 33 to 70 years) were stained for fat, and all areas covered with fatty streaks, fibrotic plaques, and complicated lesions were measured, In the RCA and LAD, the apoE genotype was significantly associated with the area of total atherosclerotic lesions in men <53 years old but not with that in older men (P = 0.0085 and P=0.041, respectively, fir age-by-genotype interaction). Men <53 years old with the E4/3 genotype showed 61% larger total atherosclerotic lesion area in the RCA (P=0.0027) and 26% larger area in the LAD (P=0.12) than did men with the epsilon 3/3. The apoE epsilon 4/3 was also associated with atherosclerotic lesions in the abdominal (P=0.014) and thoracic (P=0.12) aorta, but this effect, unlike that of the coronary arteries, was not age-related. Conclusions-In men, the apoE epsilon 4 allele is a significant genetic risk factor for coronary atherosclerosis in early middle age. This suggests that at older age, other known risk factors of CHD play a more important role in the atherosclerotic process than apoE polymorphisms.
引用
收藏
页码:608 / 613
页数:6
相关论文
共 32 条
[1]  
DALLONGEVILLE J, 1992, J LIPID RES, V33, P447
[2]   APOLIPOPROTEIN-E POLYMORPHISM AND ATHEROSCLEROSIS [J].
DAVIGNON, J ;
GREGG, RE ;
SING, CF .
ARTERIOSCLEROSIS, 1988, 8 (01) :1-21
[3]  
EHNHOLM C, 1986, J LIPID RES, V27, P227
[4]   RELATION OF APOLIPOPROTEIN E PHENOTYPE TO MYOCARDIAL-INFARCTION AND MORTALITY FROM CORONARY-ARTERY DISEASE [J].
EICHNER, JE ;
KULLER, LH ;
ORCHARD, TJ ;
GRANDITS, GA ;
MCCALLUM, LM ;
FERRELL, RE ;
NEATON, JD .
AMERICAN JOURNAL OF CARDIOLOGY, 1993, 71 (02) :160-165
[5]  
GUZMAN MA, 1968, LAB INVEST, V18, P479
[6]   APOLIPOPROTEIN-E POLYMORPHISMS AFFECT ATHEROSCLEROSIS IN YOUNG MALES [J].
HIXSON, JE .
ARTERIOSCLEROSIS AND THROMBOSIS, 1991, 11 (05) :1237-1244
[7]  
HIXSON JE, 1990, J LIPID RES, V31, P545
[8]  
ISOLA J, 1994, AM J PATHOL, V145, P1301
[9]   Evidence that the apolipoprotein E genotype effects on lipid levels can change with age in males: A longitudinal analysis [J].
Jarvik, GP ;
Goode, EL ;
Austin, MA ;
Auwerx, J ;
Deeb, S ;
Schellenberg, GD ;
Reed, T .
AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (01) :171-181
[10]   APOPROTEIN-E POLYMORPHISM AND CORONARY-ARTERY DISEASE - INCREASED PREVALENCE OF APOLIPOPROTEIN E-4 IN ANGIOGRAPHICALLY VERIFIED CORONARY PATIENTS [J].
KUUSI, T ;
NIEMINEN, MS ;
EHNHOLM, C ;
YKIJARVINEN, H ;
VALLE, M ;
NIKKILA, EA ;
TASKINEN, MR .
ARTERIOSCLEROSIS, 1989, 9 (02) :237-241