A sib-pair analysis study of 15 candidate genes in French families with morbid obesity -: Indication for linkage with islet 1 locus on chromosome 5q

被引:40
作者
Clément, K
Dina, C
Basdevant, A
Chastang, N
Pelloux, V
Lahlou, N
Berlan, M
Langin, D
Guy-Grand, B
Froguel, P
机构
[1] Inst Pasteur, CNRS EP 10, F-59019 Lille, France
[2] Hop Hotel Dieu, Dept Nutr, F-75181 Paris, France
[3] Inst Biol, Lille, France
[4] Louis Bugnard Inst, Toulouse, France
[5] Hop St Vincent de Paul, F-75674 Paris, France
[6] Serv Endocrinol Diabete Enfant, Paris, France
关键词
D O I
10.2337/diabetes.48.2.398
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
As part of an ongoing search for susceptibility genes in obese families, we performed linkage analyses in 101 French families between qualitative and quantitative traits related to morbid obesity and polymorphisms located in or near 15 candidate genes whose products are involved in body weight regulation. These included cholecystokinin A and B receptors (CCK-AR and CCK-BR), glucagon-like peptide 1 receptor (GLP-1R), the LIM/homeodomain islet-l gene (Isl-l), the caudal-type homeodomain 3 (CDX-3), the uncoupling protein 1 (UCP-1), the beta(3)-adrenoceptor (beta(3)-AR), the fatty acid-binding protein 2 (FABP-2), the hormone-sensitive Lipase (HSL), the lipoprotein lipase (LPL), the apoprotein-C2 (apo-C2), the insulin receptor substrate-1 (IRS-1) the peroxisome proliferator-activated receptor-gamma (PPAR-gamma), tumor necrosis factor-alpha (TNF-alpha), and the liver carnitine palmitoyltransferase-1 (CPT-1). Phenotypes related to obesity such as EMI, adult life body weight gain, fasting leptin, insulin, fasting glycerol, and free fatty acids were used for nonparametric sib-pair analyses. A weak indication for linkage was obtained between the Isl-l locus and obesity status defined by a z score over one SD of BMI (n = 226 sib pairs, pi = 0.54 +/- 0.02, P = 0.03). Moreover, a suggestive indication for linkage was found between the Isl-l locus and BMI and leptin values (P = 0.001 and 0.0003, respectively) and leptin adjusted for BMI (P = 0.0001), Multipoint analyses for leptin trait with Isl-1 and two flanking markers (D5S418 and D5S407) showed that the logarithm of odds (LOD) score is 1.73, coinciding with the Isl-l locus. Although marginally positive indications for linkage in subgroups of families were found with IRS-I, CPT-I, and HSL loci, our data suggested that these genes are not major contributors to obesity. Whether an obesity susceptibility gene (Isl-l itself or another nearby gene) lies on chromosome 5q should be determined by further analyses.
引用
收藏
页码:398 / 402
页数:5
相关论文
共 42 条
[1]   Independent requirement for ISL1 in formation of pancreatic mesenchyme and islet cells [J].
Ahlgren, U ;
Pfaff, SL ;
Jessell, TM ;
Edlund, T ;
Edlund, H .
NATURE, 1997, 385 (6613) :257-260
[2]   AN AMINO-ACID SUBSTITUTION IN THE HUMAN INTESTINAL FATTY-ACID-BINDING PROTEIN IS ASSOCIATED WITH INCREASED FATTY-ACID-BINDING, INCREASED FAT OXIDATION, AND INSULIN-RESISTANCE [J].
BAIER, LJ ;
SACCHETTINI, JC ;
KNOWLER, WC ;
EADS, J ;
PAOLISSO, G ;
TATARANNI, PA ;
MOCHIZUKI, H ;
BENNETT, PH ;
BOGARDUS, C ;
PROCHAZKA, M .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (03) :1281-1287
[3]   Chromosomal localization and partial genomic structure of the human peroxisome proliferator activated receptor-gamma (hPPAR gamma) gene [J].
Beamer, BA ;
Negri, C ;
Yen, CJ ;
Gavrilova, O ;
Rumberger, JM ;
Durcan, MJ ;
Yarnall, DP ;
Hawkins, AL ;
Griffin, CA ;
Burns, DK ;
Roth, J ;
Reitman, M ;
Shuldiner, AR .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 233 (03) :756-759
[4]   RADIOMETRIC ASSAYS FOR GLYCEROL, GLUCOSE, AND GLYCOGEN [J].
BRADLEY, DC ;
KASLOW, HR .
ANALYTICAL BIOCHEMISTRY, 1989, 180 (01) :11-16
[5]   Fine chromosome mapping of the genes for human liver and muscle carnitine palmitoyltransferase I (CPT1A and CPT1B) [J].
Britton, CH ;
Mackey, DW ;
Esser, V ;
Foster, DW ;
Burns, DK ;
Yarnall, DP ;
Froguel, P ;
McGarry, JD .
GENOMICS, 1997, 40 (01) :209-211
[6]  
Clement K, 1996, INT J OBESITY, V20, P1062
[7]   GENETIC-VARIATION IN THE BETA(3)-ADRENERGIC RECEPTOR AND AN INCREASED CAPACITY TO GAIN WEIGHT IN PATIENTS WITH MORBID-OBESITY [J].
CLEMENT, K ;
VAISSE, C ;
MANNING, BS ;
BASDEVANT, A ;
GUYGRAND, B ;
RUIZ, J ;
SILVER, KD ;
SHULDINER, AR ;
FROGUEL, P ;
STROSBERG, AD .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (06) :352-354
[8]   Indication for linkage of the human OB gene region with extreme obesity [J].
Clement, K ;
Garner, C ;
Hager, J ;
Philippi, A ;
LeDuc, C ;
Carey, A ;
Harris, TJR ;
Jury, C ;
Cardon, LR ;
Basdevant, A ;
Demenais, F ;
GuyGrand, B ;
North, M ;
Froguel, P .
DIABETES, 1996, 45 (05) :687-690
[9]   A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction [J].
Clément, K ;
Vaisse, C ;
Lahlou, N ;
Cabrol, S ;
Pelloux, V ;
Cassuto, D ;
Gourmelen, M ;
Dina, C ;
Chambaz, J ;
Lacorte, JM ;
Basdevant, A ;
Bougneres, P ;
Lebouc, Y ;
Froguel, P ;
Guy-Grand, B .
NATURE, 1998, 392 (6674) :398-401
[10]   A major quantitative trait locus determining serum leptin levels and fat mass is located on human chromosome 2 [J].
Comuzzie, AG ;
Hixson, JE ;
Almasy, L ;
Mitchell, BD ;
Mahaney, MC ;
Dyer, TD ;
Stern, MP ;
MacCluer, JW ;
Blangero, J .
NATURE GENETICS, 1997, 15 (03) :273-276