A hepatic lipase gene promoter polymorphism attenuates the increase in hepatic lipase activity with increasing intra-abdominal fat in women

被引:66
作者
Carr, MC
Hokanson, JE
Deeb, SS
Purnell, JQ
Mitchell, ES
Brunzell, JD
机构
[1] Univ Washington, Dept Med, Div Metab Endocrinol & Nutr, Seattle, WA 98195 USA
[2] Univ Washington, Div Med Genet, Seattle, WA 98195 USA
[3] Univ Washington, Dept Family & Child Nursing, Seattle, WA 98195 USA
关键词
cholesterol; lipoprotein; visceral obesity; LIPC; triglyceride;
D O I
10.1161/01.ATV.19.11.2701
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
High hepatic lipase (HL) activity is associated with an atherogenic lipoprotein profile of small, dense LDL particles and lower HDL2-C. Intra-abdominal fat (IAF) is positively associated with HL activity. A hepatic lipase gene (LIPC) promoter variant (G --> A(-250)) is associated with lower HL activity, higher HDL2-C, and less dense LDL particles. To determine whether the LIPC promoter polymorphism acts independently of IAF to regulate HL, 57 healthy, premenopausal women were studied. The LIPC promoter A allele was associated with significantly lower HL activity (GA/AA = 104 +/- 34 versus GG = 145 +/- 57 nmoles.mL(-1).min(-1), P = 0.009). IAF was positively correlated with HL activity (r = 0.431, P < 0.001). Multivariate analysis revealed a strong relationship between both the LIPC promoter genotype (P = 0.001) and IAF (P < 0.001) with HL activity. The relationship between IAF and HL activity for carriers and noncarriers of the A allele was curvilinear with the carriers having a lower apparent maximum level of plasma HL activity compared with noncarriers (138 versus 218 nmoles.mL(-1).min(-1), P < 0.001). In addition, the LIPC A allele was associated with a significantly higher HDL2-C (GA/AA = 16 +/- 7 versus GG = 11 +/- 5 mg/dL, P = 0.003). We conclude that the LIPC promoter A allele attenuates the increase in HL activity due to IAF in premenopausal women.
引用
收藏
页码:2701 / 2707
页数:7
相关论文
共 57 条
[1]  
AMEIS D, 1990, J BIOL CHEM, V265, P6552
[2]   EFFECT OF ESTROGEN ON POST-HEPARIN LIPOLYTIC-ACTIVITY - SELECTIVE DECLINE IN HEPATIC TRIGLYCERIDE LIPASE [J].
APPLEBAUM, DM ;
GOLDBERG, AP ;
PYKALISTO, OJ ;
BRUNZELL, JD ;
HAZZARD, WR .
JOURNAL OF CLINICAL INVESTIGATION, 1977, 59 (04) :601-608
[3]  
AUSTIN MA, 1988, JAMA-J AM MED ASSOC, V260, P1917
[4]   ATHEROGENIC LIPOPROTEIN PHENOTYPE - A PROPOSED GENETIC-MARKER FOR CORONARY HEART-DISEASE RISK [J].
AUSTIN, MA ;
KING, MC ;
VRANIZAN, KM ;
KRAUSS, RM .
CIRCULATION, 1990, 82 (02) :495-506
[5]  
BERCHTOLD P, 1981, INT J OBESITY, V5, P1
[6]  
Bjorkelund C, 1996, INT J OBESITY, V20, P213
[7]   REGRESSION OF CORONARY-ARTERY DISEASE AS A RESULT OF INTENSIVE LIPID-LOWERING THERAPY IN MEN WITH HIGH-LEVELS OF APOLIPOPROTEIN-B [J].
BROWN, G ;
ALBERS, JJ ;
FISHER, LD ;
SCHAEFER, SM ;
LIN, JT ;
KAPLAN, C ;
ZHAO, XQ ;
BISSON, BD ;
FITZPATRICK, VF ;
DODGE, HT .
NEW ENGLAND JOURNAL OF MEDICINE, 1990, 323 (19) :1289-1298
[8]   EVIDENCE FOR A COMMON, SATURABLE, TRIGLYCERIDE REMOVAL MECHANISM FOR CHYLOMICRONS AND VERY LOW-DENSITY LIPOPROTEINS IN MAN [J].
BRUNZELL, JD ;
HAZZARD, WR ;
PORTE, D ;
BIERMAN, EL .
JOURNAL OF CLINICAL INVESTIGATION, 1973, 52 (07) :1578-1585
[9]   STRUCTURE OF THE HUMAN HEPATIC TRIGLYCERIDE LIPASE GENE [J].
CAI, SJ ;
WONG, DM ;
CHEN, SH ;
CHAN, L .
BIOCHEMISTRY, 1989, 28 (23) :8966-8971
[10]   LOW-DENSITY-LIPOPROTEIN PARTICLE-SIZE AND CORONARY-ARTERY DISEASE [J].
CAMPOS, H ;
GENEST, JJ ;
BLIJLEVENS, E ;
MCNAMARA, JR ;
JENNER, JL ;
ORDOVAS, JM ;
WILSON, PWF ;
SCHAEFER, EJ .
ARTERIOSCLEROSIS AND THROMBOSIS, 1992, 12 (02) :187-195