Common variation in the lipoprotein lipase gene: effects on plasma lipids and risk of atherosclerosis

被引:142
作者
Fisher, RM
Humphries, SE
Talmud, PJ
机构
[1] Division of Cardiovascular Genetics, Department of Medicine, Univ. College London Medical School, London, WC1E 6JJ
关键词
genetic variation; triacylglycerol; body mass index;
D O I
10.1016/S0021-9150(97)00199-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The importance of the enzyme lipoprotein lipase (LPL) in the development of dyslipidaemia and atherosclerosis is increasingly recognised. Variations in the LPL gene which are common in the general population have been shown to be associated with alterations in plasma lipids. D9N and N291S both occur at carrier frequencies of up to about 5% and have been associated with increased plasma triacylglycerol and decreased high density lipoprotein cholesterol concentrations, effects which seem to be magnified in mon obese individuals. S447X carrier frequency is approximately 20%, but unlike carriers of N9 or S291, X447 carriers appear to have a more favourable lipid profile. A transition within the LPL promoter at position-93 may lead to increased LPL activity and have a beneficial effect on plasma lipids. Greater knowledge of the underlying mechanisms of these variations within the LPL gene may be of considerable importance in understanding genetic predisposition to atherosclerosis and heart disease. (C) 1997 Elsevier Science Ireland Ltd.
引用
收藏
页码:145 / 159
页数:15
相关论文
共 87 条
  • [1] AHN YI, 1993, J LIPID RES, V34, P421
  • [2] [Anonymous], CURR OPIN LIPIDOL
  • [3] INHERITANCE OF LOW-DENSITY-LIPOPROTEIN SUBCLASS PATTERNS IN FAMILIAL COMBINED HYPERLIPIDEMIA
    AUSTIN, MA
    BRUNZELL, JD
    FITCH, WL
    KRAUSS, RM
    [J]. ARTERIOSCLEROSIS, 1990, 10 (04): : 520 - 530
  • [4] FAMILIAL COMBINED HYPERLIPIDEMIA AND ABNORMAL LIPOPROTEIN-LIPASE
    BABIRAK, SP
    BROWN, BG
    BRUNZELL, JD
    [J]. ARTERIOSCLEROSIS AND THROMBOSIS, 1992, 12 (10): : 1176 - 1183
  • [5] A SUGGESTED NOMENCLATURE FOR DESIGNATING MUTATIONS
    BEAUDET, AL
    TSUI, LC
    [J]. HUMAN MUTATION, 1993, 2 (04) : 245 - 248
  • [6] Brunzell JD, 1989, The Metabolic Basis of Inherited Disease, P1165
  • [7] THE MUTANT ASN(291)-]SER HUMAN LIPOPROTEIN-LIPASE IS ASSOCIATED WITH REDUCED CATALYTIC ACTIVITY AND DOES NOT INFLUENCE BINDING TO HEPARIN
    BUSCA, R
    PEINADO, J
    VILELLA, E
    AUWERX, J
    DEEB, SS
    VILARO, S
    REINA, M
    [J]. FEBS LETTERS, 1995, 367 (03) : 257 - 262
  • [8] THE TRIGLYCERIDE ISSUE - A VIEW FROM FRAMINGHAM
    CASTELLI, WP
    [J]. AMERICAN HEART JOURNAL, 1986, 112 (02) : 432 - 437
  • [9] DNA POLYMORPHISMS AT THE LIPOPROTEIN-LIPASE GENE - ASSOCIATIONS IN NORMAL AND HYPERTRIGLYCERIDEMIC SUBJECTS
    CHAMBERLAIN, JC
    THORN, JA
    OKA, K
    GALTON, DJ
    STOCKS, J
    [J]. ATHEROSCLEROSIS, 1989, 79 (01) : 85 - 91
  • [10] CHATURVEDI N, 1994, DIABETOLOGIA, V37, P765, DOI 10.1007/BF00404333