Chromosomal regions 22q13 and 3p25 may harbor quantitative trait loci influencing both age at menarche and bone mineral density

被引:16
|
作者
Pan, Feng [1 ,2 ,3 ]
Xiao, Peng [3 ]
Guo, Yan [1 ,2 ]
Liu, Yong-Jun [4 ,5 ]
Deng, Hong-Yi [4 ,5 ]
Recker, Robert R. [3 ]
Deng, Hong-Wen [1 ,2 ,4 ,5 ,6 ]
机构
[1] Xian Jiaotong Univ, Sch Life Sci & Technol, Minist Educ, Key Lab Biomed Informat Engn, Xian 710049, Shaanxi, Peoples R China
[2] Xian Jiaotong Univ, Sch Life Sci & Technol, Inst Mol Genet, Xian 710049, Shaanxi, Peoples R China
[3] Creighton Univ, Sch Med, Res Ctr, Dept Biomed Sci & Osteoporosis, Omaha, NE 68131 USA
[4] Univ Missouri, Sch Med, Dept Basic Med Sci, Kansas City, MO 64108 USA
[5] Univ Missouri, Sch Med, Dept Orthoped Surg, Kansas City, MO 64108 USA
[6] Hunan Normal Univ, Coll Life Sci, Lab Mol & Stat Genet, Changsha 410081, Hunan, Peoples R China
关键词
D O I
10.1007/s00439-008-0490-z
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Late age at menarche (AAM), an important type of endocrinopathy in females, is associated with lower bone mineral density (BMD), a major risk factor for osteoporosis. The correlation is mainly mediated through common genetic factors, which are largely unknown. A bivariate genome-wide linkage scan was conducted on 2,522 females from 414 Caucasian pedigrees to identify quantitative trait loci influencing both AAM and BMD. The strongest linkage signal was detected on chromosome 22q13. Other regions such as the 3q13, 3p25, 7p15, and 15q13 were also suggested. The inferred promising candidate genes in the linkage regions may contribute to our understanding of pathogenesis of endocrinopathy and osteoporosis in females.
引用
收藏
页码:419 / 427
页数:9
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