The LPL S447X cSNP is associated with decreased blood pressure and plasma triglycerides, and reduced risk of coronary artery disease

被引:44
作者
Clee, SM
Loubser, O
Collins, J
Kastelein, JJP
Hayden, MR
机构
[1] Univ British Columbia, Ctr Mol Med & Therapeut, Vancouver, BC V5Z 4H4, Canada
[2] Univ Amsterdam, Dept Vasc Med, Acad Med Ctr, Amsterdam, Netherlands
关键词
blood pressure; coronary artery disease; lipoprotein lipase; S447X; triglycerides;
D O I
10.1034/j.1399-0004.2001.600407.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Linkage of the lipoprotein lipase (LPL) gene to blood pressure levels has been reported. The LPL S447X single nucleotide polymorphism (cSNP) has been associated with decreased triglycerides (TG), increased high density lipoprotein cholesterol, and a decreased risk of coronary artery disease (CAD), which may occur independently of its beneficial lipid changes. To investigate the relationship between LPL S447X cSNP and these parameters, we studied a cohort of individuals with familial hypercholesterolemia in whom blood pressures and information regarding the use of blood pressure lowering medications were available. Carriers of the S447X variant had decreased TG (1.21 +/- 0.47 vs. 1.52 +/- 0.67, p < 0.001) and a trend towards decreased vascular disease (12.7 vs. 19.5%) compared to non-carriers. More interestingly, however, carriers of this cSNP had decreased diastolic blood pressure compared to non-carriers (78 +/- 10 vs. 82 +/- 11, p = 0.002), evident in both men and women, youths and adults, with similar trends for systolic blood pressure. Furthermore, the decrease in blood pressure appeared independent of the decrease in TG (p = 0.02), suggesting that the LPL protein may have a direct influence on the vascular wall. This suggests an additional mechanism whereby this variant may have protective effects, independent of changes in plasma lipid levels.
引用
收藏
页码:293 / 300
页数:8
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共 50 条
  • [1] Brunzell JD, 1995, METABOLIC MOL BASES, P1913
  • [2] CHAPPELL DA, 1993, J BIOL CHEM, V268, P14168
  • [3] CHAPPELL DA, 1994, J BIOL CHEM, V269, P18001
  • [4] Common variation in the lipoprotein lipase gene: effects on plasma lipids and risk of atherosclerosis
    Fisher, RM
    Humphries, SE
    Talmud, PJ
    [J]. ATHEROSCLEROSIS, 1997, 135 (02) : 145 - 159
  • [5] A common truncation variant of lipoprotein lipase (Ser447X) confers protection against coronary heart disease:: the Framingham Offspring Study
    Gagné, SE
    Larson, MG
    Pimstone, SN
    Schaefer, EJ
    Kastelein, JJP
    Wilson, PWF
    Ordovas, JM
    Hayden, MR
    [J]. CLINICAL GENETICS, 1999, 55 (06) : 450 - 454
  • [6] LIPOPROTEIN CHOLESTEROL, APOLIPOPROTEIN-A-I AND APOLIPOPROTEIN-B AND LIPOPROTEIN-(A) ABNORMALITIES IN MEN WITH PREMATURE CORONARY-ARTERY DISEASE
    GENEST, J
    MCNAMARA, JR
    ORDOVAS, JM
    JENNER, JL
    SILBERMAN, SR
    ANDERSON, KM
    WILSON, PWF
    SALEM, DN
    SCHAEFER, EJ
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1992, 19 (04) : 792 - 802
  • [7] Genetic variant showing a positive interaction with beta-blocking agents with a beneficial influence on lipoprotein lipase activity, HDL cholesterol, and triglyceride levels in coronary artery disease patients - The Ser(447)-Stop substitution in the lipoprotein lipase gene
    Groenemeijer, BE
    Hallman, MD
    Reymer, PWA
    Gagne, E
    Kuivenhoven, JA
    Bruin, T
    Jansen, H
    Lie, KI
    Bruschke, AVG
    Boerwinkle, E
    Hayden, MR
    Kastelein, JJP
    [J]. CIRCULATION, 1997, 95 (12) : 2628 - 2635
  • [8] Hall S, 2000, GENET EPIDEMIOL, V18, P203, DOI 10.1002/(SICI)1098-2272(200003)18:3<203::AID-GEPI2>3.0.CO
  • [9] 2-I
  • [10] DIRECT DETECTION AND AUTOMATED SEQUENCING OF INDIVIDUAL ALLELES AFTER ELECTROPHORETIC STRAND SEPARATION - IDENTIFICATION OF A COMMON NONSENSE MUTATION IN EXON-9 OF THE HUMAN LIPOPROTEIN-LIPASE GENE
    HATA, A
    ROBERTSON, M
    EMI, M
    LALOUEL, JM
    [J]. NUCLEIC ACIDS RESEARCH, 1990, 18 (18) : 5407 - 5411