An obesity-related locus in chromosome region 12q23-24

被引:36
作者
Li, WD
Dong, CH
Li, D
Zhao, HY
Price, RA
机构
[1] Univ Penn, Ctr Neurobiol & Behav, Dept Psychiat, Philadelphia, PA 19104 USA
[2] Yale Univ, Sch Med, Dept Epidemiol, New Haven, CT 06510 USA
[3] Yale Univ, Sch Med, Dept Publ Hlth, New Haven, CT 06510 USA
关键词
D O I
10.2337/diabetes.53.3.812
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Obesity is a growing health problem in the U.S. As a complex trait, obesity involves multiple genes and gene-gene and gene-environment interactions that contribute to its pathogenesis. Here we report significant linkage from a scan of a large sample segregating extreme obesity and normal weight. We have used 382 microsatellite markers in 1,297 individuals from 260 European-American families. We conducted nonparametric linkage (NPL) analyses for dichotomous BMI (using BMI greater than or equal to27, greater than or equal to30, greater than or equal to35, and greater than or equal to40 kg/m(2)) using Gene-hunter. We also analyzed quantitative traits (BMI, percentage of fat, and waist circumference) by the family regression method using Merlin_regress. We found evidence for linkage on chromosome 12 (125 cM, D12S2070, logarithm of odds [LOD] 3.79, P=0.00001 for percentage of fat; LOD 2.98, P=0.0001 for BMI; and LOD 2.86, P=0.00014 for waist circumference) by family regression analyses. Adding three additional markers to the intervals flanking the chromosome 12 peak yielded an LOD score of 4.08 (P=0.00001) for percentage of fat at 116 cM and LOD scores of 3.57 (P=0.00003) and 3.05 (P=0.00009) for BMI and waist circumference, respectively, at 125 cM. We also obtained other suggestive linkages on chromosomes 2, 3, 7, 8, 9, 12, 13, and 21. Our results suggest multiple loci that could influence obesity, particularly a locus in chromosome region 12q23-24.
引用
收藏
页码:812 / 820
页数:9
相关论文
共 58 条
[1]   Merlin-rapid analysis of dense genetic maps using sparse gene flow trees [J].
Abecasis, GR ;
Cherny, SS ;
Cookson, WO ;
Cardon, LR .
NATURE GENETICS, 2002, 30 (01) :97-101
[2]   Continuous fatty acid oxidation and reduced fat storage in mice lacking acetyl-CoA carboxylase 2 [J].
Abu-Elheiga, L ;
Matzuk, MM ;
Abo-Hashema, KAH ;
Wakil, SJ .
SCIENCE, 2001, 291 (5513) :2613-2616
[3]   The HDL receptor SR-BI: a new therapeutic target for atherosclerosis? [J].
Acton, SL ;
Kozarsky, KF ;
Rigotti, A .
MOLECULAR MEDICINE TODAY, 1999, 5 (12) :518-524
[4]   Multipoint quantitative-trait linkage analysis in general pedigrees [J].
Almasy, L ;
Blangero, J .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (05) :1198-1211
[5]   Genomewide scans of complex human diseases:: True linkage is hard to find [J].
Altmüller, J ;
Palmer, LJ ;
Fischer, G ;
Scherb, H ;
Wjst, M .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (05) :936-950
[6]  
Amos CI, 2001, STAT METHODS MED RES, V10, P3, DOI 10.1191/096228001677031143
[7]   Testing for population subdivision and association in four case-control studies [J].
Ardlie, KG ;
Lunetta, KL ;
Seielstad, M .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (02) :304-311
[8]   Factors of insulin resistance syndrome-related phenotypes are linked to genetic locations on chromosomes 6 and 7 in nondiabetic Mexican-Americans [J].
Arya, R ;
Blangero, J ;
Williams, K ;
Almasy, L ;
Dyer, TD ;
Leach, RJ ;
O'Connell, P ;
Stern, MP ;
Duggirala, R .
DIABETES, 2002, 51 (03) :841-847
[9]   Limits of fine-mapping a quantitative trait [J].
Atwood, LD ;
Heard-Costa, NL .
GENETIC EPIDEMIOLOGY, 2003, 24 (02) :99-106
[10]   The human obesity gene map:: The 2002 update [J].
Chagnon, YC ;
Rankinen, T ;
Snyder, EE ;
Weisnagel, SJ ;
Pérusse, LK ;
Bouchard, C .
OBESITY RESEARCH, 2003, 11 (03) :313-367