A Bivariate Whole Genome Linkage Study Identified Genomic Regions Influencing Both BMD and Bone Structure

被引:12
作者
Liu, Xiao-Guang [1 ,2 ,3 ]
Liu, Yong-Jun [3 ]
Liu, Jianfeng [3 ]
Pei, Yufang [1 ,2 ,3 ]
Xiong, Dong-Hai [4 ,5 ]
Shen, Hui [3 ]
Deng, Hong-Yi [3 ]
Papasian, Christopher J. [3 ]
Drees, Betty M. [3 ]
Hamilton, James J. [3 ]
Recker, Robert R. [4 ,5 ]
Deng, Hong-Wen [1 ,2 ,3 ,6 ]
机构
[1] Xi An Jiao Tong Univ, Key Lab Biomed Informat Engn, Minist Educ, Xian 710049, Peoples R China
[2] Xi An Jiao Tong Univ, Sch Life Sci & Technol, Inst Mol Genet, Xian 710049, Peoples R China
[3] Univ Missouri, Sch Med, Kansas City, MO 64108 USA
[4] Creighton Univ, Osteoporosis Res Ctr, Omaha, NE 68178 USA
[5] Creighton Univ, Dept Biomed Sci, Omaha, NE 68178 USA
[6] Hunan Normal Univ, Coll Lifc Sci, Lab Mol & Stat Genet, Changsha, Hunan, Peoples R China
基金
美国国家科学基金会;
关键词
BMD; bone structure; bone size; whole genome linkage scan; bivariate;
D O I
10.1359/JBMR.080614
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
Areal BMD (aBMD) and areal bone size (ABS) are biologically correlated traits and are each important determinants of bone Strength and risk of fractures. Studies showed that aBMD and ABS are Genetically correlated, indicating that they may share some common genetic factors. which, however, are largely unknown. To study the genetic factors-influencing both aBMD and ABS, bivariate whole genome linkage analyses were conducted for aBMD-ABS at the femoral neck (FN), lumbar spine (LS), and ultradistal (UD)-forearm in a large sample of 451 white pedigrees made up of 4498 individuals. We detected significant linkage oil chromosome Xq27 (LOD = 4.89) for LS aBMD-ABS. In addition, we detected suggestive linkages at 20q11 (LOD = 3.65) and Xp11 (LOD = 2.96) for FN aBMD-ABS; at 12p11 (LOD = 3.39) and 17q21 (LOD = 2.94) for LS aBMD-ABS: and at 5q23 (LOD = 3.54), 7p15 (LOD = 3.45), Xq27 (LOD = 2.93) and 12p11 (LOD = 2.92) for UD-forearm aBMD-ABS. Subsequent discrimination analyses indicated that quantitative trait loci (QTLs) at 12p11 and 17q21 may have pleiotropic effects on aBMD and ABS. This Study identified several genomic regions that may contain QTLs important for both aBMD and ABS. Further endeavors are necessary to follow these regions to eventually pinpoint the genetic variants affecting bone strength and risk of fractures.
引用
收藏
页码:1806 / 1814
页数:9
相关论文
共 35 条
[1]
SUSPECTS: enabling fast and effective prioritization of positional candidates [J].
Adie, EA ;
Adams, RR ;
Evans, KL ;
Porteous, DJ ;
Pickard, BS .
BIOINFORMATICS, 2006, 22 (06) :773-774
[2]
Gene prioritization through genomic data fusion [J].
Aerts, S ;
Lambrechts, D ;
Maity, S ;
Van Loo, P ;
Coessens, B ;
De Smet, F ;
Tranchevent, LC ;
De Moor, B ;
Marynen, P ;
Hassan, B ;
Carmeliet, P ;
Moreau, Y .
NATURE BIOTECHNOLOGY, 2006, 24 (05) :537-544
[3]
Almasy L, 1997, GENET EPIDEMIOL, V14, P953, DOI 10.1002/(SICI)1098-2272(1997)14:6<953::AID-GEPI65>3.0.CO
[4]
2-K
[5]
Multipoint quantitative-trait linkage analysis in general pedigrees [J].
Almasy, L ;
Blangero, J .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (05) :1198-1211
[6]
Differences in bone mineral density, bone mineral content, and bone areal size in fracturing and non-fracturing women, and their interrelationships at the spine and hip [J].
Deng, HW ;
Xu, FH ;
Davies, KM ;
Heaney, R ;
Recker, RR .
JOURNAL OF BONE AND MINERAL METABOLISM, 2002, 20 (06) :358-366
[7]
A genomewide linkage scan for quantitative-trait loci for obesity phenotypes [J].
Deng, HW ;
Deng, HY ;
Liu, YJ ;
Liu, YZ ;
Xu, FH ;
Shen, H ;
Conway, T ;
Li, JL ;
Huang, QY ;
Davies, KM ;
Recker, RR .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 70 (05) :1138-1151
[8]
Univariate and bivariate variance component linkage analysis of a whole-genome scan for loci contributing to bone mineral density [J].
Devoto, M ;
Spotila, LD ;
Stabley, DL ;
Wharton, GN ;
Rydbeck, H ;
Korkko, J ;
Kosich, R ;
Prockop, D ;
Tenenhouse, A ;
Sol-Church, K .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2005, 13 (06) :781-788
[9]
A strategy to search for common obesity and type 2 diabetes genes [J].
Elbers, Clara C. ;
Onland-Moret, N. Charlotte ;
Frankel, Lude ;
Niehoff, Anne G. ;
van der Schouw, Yvonne T. ;
Wijmenga, Cisca .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2007, 18 (01) :19-26
[10]
Cartilage-derived morphogenetic proteins and osteogenic protein-1 differentially regulate osteogenesis [J].
Erlacher, L ;
Mccartney, J ;
Piek, E ;
Ten Dijke, P ;
Yanagishita, M ;
Oppermann, H ;
Luyten, FP .
JOURNAL OF BONE AND MINERAL RESEARCH, 1998, 13 (03) :383-392