Bivariate whole genome linkage analysis for femoral neck geometric parameters and total body lean mass

被引:21
作者
Deng, Fei-Yan
Xiao, Peng
Lei, Shu-Feng
Zhang, Lei
Yang, Fang
Tang, Zi-Hui
Liu, Peng-Yuan
Liu, Yong-Jun
Recker, Robert R.
Deng, Hong-Wen [1 ]
机构
[1] Hunan Normal Univ, Coll Life Sci, Minist Educ, Lab Mol & Stat Genet, Changsha, Hunan, Peoples R China
[2] Hunan Normal Univ, Coll Life Sci, Key Lab Prot Chem & Dev Bio, Minist Educ, Changsha, Hunan, Peoples R China
[3] Creighton Univ, Med Ctr, Osteoporosis Res Ctr, Dept Biomed Sci, Omaha, NE 68178 USA
[4] Xi An Jiao Tong Univ, Sch Life Sci & Technol, Inst Genet Mol, Minist Educ, Xian 710049, Peoples R China
[5] Xi An Jiao Tong Univ, Sch Life Sci & Technol, Key Lab Biomed Informat Engn, Xian 710049, Peoples R China
[6] Univ Missouri, Dept Orthoped Surg, Kansas City, MO 64110 USA
[7] Univ Missouri, Dept Basic Med Sci, Kansas City, MO 64110 USA
关键词
bivariate analysis; whole genome scan; geometric parameters; lean mass; sex-specific;
D O I
10.1359/JBMR.070303
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
A genome-wide bivariate analysis was conducted for femoral neck GPs and TBLM in a large white sample. We found QTLs shared by GPs and TBLM in the total sample and the sex-specific samples. QTLs with potential pleiotropy were also disclosed. Introduction: Previous studies have suggested that femoral neck cross-section geometric parameters (FNCSGPs), including periosteal diameter (W), cross-sectional area (CSA), cortical thickness (CT), buckling ratio (BR), and section modulus (Z), are genetically correlated with total body lean mass (TBLM). However, the shared genetic factors between them are unknown. Materials and Methods: To identify the specific QTLs shared by FNCS-GPs and TBLM, we performed bivariate whole genome linkage analysis (WGLA) in a large sample of 451 white families made up of 4498 subjects. Results: Multipoint bivariate linkage analyses for 22 autosomes showed evidence of suggestive or significant linkages (thresholds of LOD = 2.3 and 3.7, respectively) to chromosomes 3q12 and 20q13 in the entire sample, 6p25 and 10q24 in women, and 4p15, 5q34-35 and 7q21 in men. Two-point linkage analyses for chromosome X showed strong linkage to Xp22.13, Xp11.4, Xq22.3, Xq23-24, and Xq25. Complete pleiotropy was identified on 10q24 and 5q35 for TBLM and BR in women and for TBLM and CT in men, respectively. Furthermore, chromosomes 5q34-35, 7q21, 10q24, 20q13, Xp22.13, Xpl 1.4, and Xq25 are also of importance because of their linkage to multiple trait pairs. For example, linkage to chromosome 10q24 was found for TBLM x W (LOD = 2.31), TBLM x CT (LOD = 2.51), TBLM x CSA (LOD = 2.51), TBLM x BR (LOD = 2.64), and TBLM x Z (LOD = 2.55) in women. Conclusions: In this study, we identified several genomic regions (e.g., 3q12 and 20q13) that seem to be linked to both FNCS-GPs and TBLM. These regions are of interesting because they may harbor genes that may contribute to variation in both FNCS-GPs and TBLM.
引用
收藏
页码:808 / 816
页数:9
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