The 103I variant of the melanocortin 4 receptor is associated with low serum triglyceride levels

被引:25
作者
Brönner, G
Sattler, AM
Hinney, A
Soufi, M
Geller, F
Schäfer, H
Maisch, B
Hebebrand, J
Schaefer, JR
机构
[1] Univ Duisburg Gesamthsch, Dept Child & Adolescent Psychiat & Psychotherapy, D-45147 Essen, Germany
[2] Univ Marburg, Inst Med Biometry & Epidemiol, D-35037 Marburg, Germany
[3] Univ Marburg, Dept Internal Med & Cardiol, D-35037 Marburg, Germany
[4] deCODE Genet, Reykjavik, Iceland
关键词
D O I
10.1210/jc.2005-0919
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context: The melanocortin 4 receptor (MC4R) is an essential regulator of energy intake and body weight. Recently, the V103I polymorphism of MC4R has been shown to be negatively associated with body mass index. This suggests that serum lipids and blood pressure in individuals carrying the 103I allele might be influenced as well. Objective: The objective of this study was to determine whether the most common polymorphism of the MC4R, V103I, affects serum lipid levels and/or blood pressure. Design, Setting, and Participants: The study participants were 1173 consecutive patients undergoing cardiac catheterization; they were genotyped for the rs2229616 G -> A substitution at codon 103 (V103I polymorphism) of the MC4R gene. Patients had strictly fasted for at least 12 h before blood samples were drawn. The average age of the patients was 60.9 yr; 72% were males. Results: Heterozygous carriers of the 103I allele had significantly lower triglyceride levels than individuals homozygous for the wildtype allele (127 vs. 168 mg/dl mean total triglyceride; P = 0.001 or 0.009 after Bonferroni adjustment for seven tests). No homozygous carriers of the 103I allele were present in the study population. Conclusions: Our study suggests an influence of MC4R activity on triglyceride levels in cardiovascular patients.
引用
收藏
页码:535 / 538
页数:4
相关论文
共 27 条
[1]   Genetic causes of monogenic heterozygous familial hypercholesterolemia: A HuGE prevalence review [J].
Austin, MA ;
Hutter, CM ;
Zimmern, RL ;
Humphries, SE .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 2004, 160 (05) :407-420
[2]   Abdominal obesity and dyslipidemia in the metabolic syndrome: Importance of type 2 diabetes and familial combined hyperlipidemia in coronary artery disease risk [J].
Carr, MC ;
Brunzell, JD .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (06) :2601-2607
[3]   Liver denervation affects hepatocyte mitochondrial fatty acid transport capacity [J].
Carreño, FR ;
Seelaender, MCL .
CELL BIOCHEMISTRY AND FUNCTION, 2004, 22 (01) :9-17
[4]   Role for stearoyl-CoA desaturase-1 in leptin-mediated weight loss [J].
Cohen, P ;
Miyazaki, M ;
Socci, ND ;
Hagge-Greenberg, A ;
Liedtke, W ;
Soukas, AA ;
Sharma, R ;
Hudgins, LC ;
Ntambi, JM ;
Friedman, JM .
SCIENCE, 2002, 297 (5579) :240-243
[5]   Upstream stimulatory factor 1 associated with familial combined hyperlipidemia, LDL cholesterol, and triglycerides [J].
Coon, H ;
Xin, YP ;
Hopkins, PN ;
Cawthon, RM ;
Hasstedt, SJ ;
Hunt, SC .
HUMAN GENETICS, 2005, 117 (05) :444-451
[6]   Clinical spectrum of obesity and mutations in the melanocortin 4 receptor gene [J].
Farooqi, IS ;
Keogh, JM ;
Yeo, GSH ;
Lank, EJ ;
Cheetham, T ;
O'Rahilly, S .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (12) :1085-1095
[7]  
FRIEDEWALD WT, 1972, CLIN CHEM, V18, P499
[8]   Melanocortin-4 receptor gene variant I103 is negatively associated with obesity [J].
Geller, F ;
Reichwald, K ;
Dempfle, A ;
Illig, T ;
Vollmert, C ;
Herpertz, S ;
Siffert, W ;
Platzer, M ;
Hess, C ;
Gudermann, T ;
Biebermann, H ;
Wichmann, HE ;
Schäfer, H ;
Hinney, A ;
Hebebrand, J .
AMERICAN JOURNAL OF HUMAN GENETICS, 2004, 74 (03) :572-581
[9]   Molecular screening of the human melanocortin-4 receptor gene: Identification of a missense variant showing no association with obesity, plasma glucose, or insulin [J].
Gotoda, T ;
Scott, J ;
Aitman, TJ .
DIABETOLOGIA, 1997, 40 (08) :976-979
[10]   Identification and functional analysis of novel human melanocortin-4 receptor variants [J].
Gu, W ;
Tu, ZM ;
Kleyn, PW ;
Kissebah, A ;
Duprat, L ;
Lee, J ;
Chin, W ;
Maruti, S ;
Deng, NH ;
Fisher, SL ;
Franco, LS ;
Burn, P ;
Yagaloff, KA ;
Nathan, J ;
Heymsfield, S ;
Albu, J ;
Pi-Sunyer, FX ;
Allison, DB .
DIABETES, 1999, 48 (03) :635-639