A major predisposition locus for severe obesity, at 4p15-p14

被引:100
作者
Stone, S
Abkevich, V
Hunt, SC
Gutin, A
Russell, DL
Neff, CD
Riley, R
Frech, GC
Hensel, CH
Jammulapati, S
Potter, J
Sexton, D
Tran, T
Gibbs, D
Iliev, D
Gress, R
Bloomquist, B
Amatruda, J
Rae, PMM
Adams, TD
Skolnick, MH
Shattuck, D
机构
[1] Myriad Genet Inc, Salt Lake City, UT 84108 USA
[2] Univ Utah, Dept Med, Salt Lake City, UT 84112 USA
[3] Bayer Corp, Res Ctr, West Haven, CT USA
关键词
D O I
10.1086/340670
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Although the predisposition to morbid obesity is heritable, the identities of the disease-causing genes are largely unknown. Therefore, we have conducted a genomewide search with 628 markers, using multigenerational Utah pedigrees to identify genes involved in predisposition to obesity. In the genomewide search, we identified a highly significant linkage to high body-mass index in female patients, at D4S2632, with a multipoint heterogeneity LOD (HLOD) score of 6.1 and a nonparametric linkage (NPL) score of 5.3. To further delineate the linkage, we increased both the marker density around D4S2632 and the size of our pedigree data set. As a result, the linkage evidence increased to a multipoint HLOD score of 9.2 (at D4S3350) and an NPL score of 11.3. Evidence from almost half of the families in this analysis support this linkage, and therefore the gene in this region might account for a significant percentage of the genetic predisposition to severe obesity in females. However, further studies are necessary to clarify the effect that this gene has in males and in the general population.
引用
收藏
页码:1459 / 1468
页数:10
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