The FOXC2 C-512T polymorphism is associated with obesity and dyslipidemia

被引:13
作者
Carlsson, E [1 ]
Almgren, P
Hoffstedt, J
Groop, L
Ridderstråle, M
机构
[1] Lund Univ, Univ Hosp MAS, Dept Endocrinol, Wallenberg Lab, S-20502 Malmo, Sweden
[2] Huddinge Univ Hosp, Dept Med, Stockholm, Sweden
来源
OBESITY RESEARCH | 2004年 / 12卷 / 11期
关键词
forkhead transcription factor; dysmetabolic syndrome; case-control association study; dyslipidemia;
D O I
10.1038/oby.2004.215
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
The transcription factor FOXC2 has been implicated in resistance to diet-induced obesity and insulin resistance. To investigate the possible role for FOXC2 in obesity and related phenotypes, we performed two association studies for obesity using unrelated case-control materials by genotyping the FOXC2 C-512T polymorphism. In the first study (127 obese and 127 normal-weight nondiabetic subjects matched for age and sex), the C-allele showed association with obesity, odds, ratio 1.74 (1.12 to 2.73; p < 0.01) for the C- vs. T-allele and 1.81 (1.04 to 3.25; p < 0.05) for the C/C and C/T vs. T/T genotype. BMI was higher in carriers of the C/C and C/T genotype in normal weight [adjusted p value (p(adj)) = 0.02] but not in obese subjects (p(adj) = 0.1). In the replication study (223 obese and 231 nonobese subjects), subjects with the C/C genotype exhibited an increased risk for obesity, odds ratio 2.01 (1.15 to 3.52; p = 0.01). Obese carriers of the C-allele had lower high-density lipoprotein-cholesterol [1.1 (0.9 to 1.3) vs. 1.2 (1.0 to 1.4) mM, p(adj) = 0.006] and increased triglyceride levels (1.95 [1.30 to 2.68] vs. 1.60 [1.10 to 2.40] mM, p(adj) = 0.02) compared with obese carriers of the T/T, genotype. Our data suggest that FOXC2 is a weak but consistent candidate gene for obesity and dyslipidemia.
引用
收藏
页码:1738 / 1743
页数:6
相关论文
共 20 条
[1]
Candidate gene association study in type 2 diabetes indicates a role for genes involved in β-cell function as well as insulin action [J].
Barroso, I ;
Luan, J ;
Middelberg, RPS ;
Harding, AH ;
Franks, PW ;
Jakes, RW ;
Clayton, D ;
Schafer, AJ ;
O'Rahilly, S ;
Wareham, NJ .
PLOS BIOLOGY, 2003, 1 (01) :41-55
[2]
METABOLIC AND GENETIC-CHARACTERIZATION OF PREDIABETIC STATES - SEQUENCE OF EVENTS LEADING TO NON-INSULIN-DEPENDENT DIABETES-MELLITUS [J].
BECKNIELSEN, H ;
GROOP, LC .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (05) :1714-1721
[3]
Carey DGP, 1996, INT J OBESITY, V20, P722
[4]
FOXC2 is a winged helix gene that counteracts obesity, hypertriglyceridemia, and diet-induced insulin resistance [J].
Cederberg, A ;
Gronning, LM ;
Ahrén, B ;
Taskén, K ;
Carlsson, P ;
Enerbäck, S .
CELL, 2001, 106 (05) :563-573
[5]
Insulin and TNFα induce expression of the forkhead transcription factor gene Foxc2 in 3T3-L1 adipocytes via PI3K and ERK 1/2-dependent pathways [J].
Gronning, LM ;
Cederberg, A ;
Miura, N ;
Enerbäck, S ;
Taskén, K .
MOLECULAR ENDOCRINOLOGY, 2002, 16 (04) :873-883
[6]
Metabolic consequences of a family history of NIDDM (The Botnia Study) - Evidence for sex-specific parental effects [J].
Groop, L ;
Forsblom, C ;
Lehtovirta, M ;
Tuomi, T ;
Karanko, S ;
Nissen, M ;
Ehrnstrom, BO ;
Forsen, B ;
Isomaa, B ;
Snickars, B ;
Taskinen, MR .
DIABETES, 1996, 45 (11) :1585-1593
[7]
The dysmetabolic syndrome [J].
Groop, L ;
Orho-Melander, M .
JOURNAL OF INTERNAL MEDICINE, 2001, 250 (02) :105-120
[8]
Cardiovascular morbidity and mortality associated with the metabolic syndrome [J].
Isomaa, B ;
Almgren, P ;
Tuomi, T ;
Forsén, B ;
Lahti, K ;
Nissén, M ;
Taskinen, MR ;
Groop, L .
DIABETES CARE, 2001, 24 (04) :683-689
[9]
Genetic variation in the human winged helix/forkhead transcription factor gene FOXC2 in Pima Indians [J].
Kovacs, P ;
Lehn-Stefan, A ;
Stumvoll, M ;
Bogardus, C ;
Baier, LJ .
DIABETES, 2003, 52 (05) :1292-1295
[10]
Human beta-2 adrenoceptor gene polymorphisms are highly frequent in obesity and associate with altered adipocyte beta-2 adrenoceptor function [J].
Large, V ;
Hellström, L ;
Reynisdottir, S ;
Lönnqvist, F ;
Eriksson, P ;
Lannfelt, L ;
Arner, P .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (12) :3005-3013