Literature DB >> 18755304

CLCN7 polymorphisms and bone mineral density in healthy premenopausal white women and in white men.

Kang Chu1, Daniel L Koller, Shoji Ichikawa, Richard Snyder, Leah Curry, Dongbing Lai, Anthony Austin, Xiaoling Xuei, Howard J Edenberg, Siu L Hui, Tatiana M Foroud, Munro Peacock, Michael J Econs.   

Abstract

INTRODUCTION: Mutations in the chloride channel 7 gene (CLCN7) cause osteopetrosis, and polymorphisms of CLCN7 in the non-disease allele are associated with penetrance of the autosomal dominant osteopetrosis (ADO) phenotype. Studies have also shown an association between CLCN7 polymorphisms and bone mineral density (BMD) in women. However, there is no study to date that has examined whether CLCN7 polymorphisms underlie normal variation of peak BMD in healthy premenopausal white women and in white men.
METHODS: Six single nucleotide polymorphisms (SNPs) and one variable number tandem repeat (VNTR) polymorphism in the CLCN7 gene were genotyped. Association was tested between CLCN7 gene polymorphisms and both lumbar spine and femoral neck BMD. Healthy premenopausal white sisters (age 33.1+/-7.2, n=1692) and healthy white brothers (age 33.6+/-10.9, n=715) were studied.
RESULTS: No significant association between CLCN7 gene polymorphisms and BMD at the lumbar spine or femoral neck was found in white women or white men.
CONCLUSIONS: Genetic variation in the CLCN7 gene is not a major contributor to the variability in peak BMD at the femoral neck and lumber spine in healthy premenopausal white women and in white men.

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Year:  2008        PMID: 18755304      PMCID: PMC2657035          DOI: 10.1016/j.bone.2008.07.249

Source DB:  PubMed          Journal:  Bone        ISSN: 1873-2763            Impact factor:   4.398


  14 in total

1.  False positive rates in association studies as a function of degree of stratification.

Authors:  Daniel L Koller; Munro Peacock; Dongbing Lai; Tatiana Foroud; Michael J Econs
Journal:  J Bone Miner Res       Date:  2004-04-19       Impact factor: 6.741

2.  Haploview: analysis and visualization of LD and haplotype maps.

Authors:  J C Barrett; B Fry; J Maller; M J Daly
Journal:  Bioinformatics       Date:  2004-08-05       Impact factor: 6.937

3.  Analysis of variation in expression of autosomal dominant osteopetrosis type 2: searching for modifier genes.

Authors:  Kang Chu; Daniel L Koller; Richard Snyder; Tonya Fishburn; Dongbing Lai; Steven G Waguespack; Tatiana Foroud; Michael J Econs
Journal:  Bone       Date:  2005-08-24       Impact factor: 4.398

Review 4.  Mechanisms of anabolic therapies for osteoporosis.

Authors:  Ernesto Canalis; Andrea Giustina; John P Bilezikian
Journal:  N Engl J Med       Date:  2007-08-30       Impact factor: 91.245

5.  Loss of the ClC-7 chloride channel leads to osteopetrosis in mice and man.

Authors:  U Kornak; D Kasper; M R Bösl; E Kaiser; M Schweizer; A Schulz; W Friedrich; G Delling; T J Jentsch
Journal:  Cell       Date:  2001-01-26       Impact factor: 41.582

6.  Albers-Schönberg disease (autosomal dominant osteopetrosis, type II) results from mutations in the ClCN7 chloride channel gene.

Authors:  E Cleiren; O Bénichou; E Van Hul; J Gram; J Bollerslev; F R Singer; K Beaverson; A Aledo; M P Whyte; T Yoneyama; M C deVernejoul; W Van Hul
Journal:  Hum Mol Genet       Date:  2001-12-01       Impact factor: 6.150

7.  Polymorphisms of the CLCN7 gene are associated with BMD in women.

Authors:  Ulrika Pettersson; Omar M E Albagha; Max Mirolo; Anna Taranta; Annalisa Frattini; Fiona E A McGuigan; Paolo Vezzoni; Anna Teti; Wim van Hul; David M Reid; Anna Villa; Stuart H Ralston
Journal:  J Bone Miner Res       Date:  2005-07-18       Impact factor: 6.741

Review 8.  Genetics of osteoporosis.

Authors:  Munro Peacock; Charles H Turner; Michael J Econs; Tatiana Foroud
Journal:  Endocr Rev       Date:  2002-06       Impact factor: 19.871

9.  Chloride channel 7 (ClCN7) gene mutations and autosomal dominant osteopetrosis, type II.

Authors:  Steven G Waguespack; Daniel L Koller; Kenneth E White; Tonya Fishburn; Gwenaelle Carn; Kenneth A Buckwalter; Michelle Johnson; Maureen Kocisko; Wayne E Evans; Tatiana Foroud; Michael J Econs
Journal:  J Bone Miner Res       Date:  2003-08       Impact factor: 6.741

10.  Chloride channel ClCN7 mutations are responsible for severe recessive, dominant, and intermediate osteopetrosis.

Authors:  Annalisa Frattini; Alessandra Pangrazio; Lucia Susani; Cristina Sobacchi; Massimiliano Mirolo; Mario Abinun; Marino Andolina; Adrienne Flanagan; Edwin M Horwitz; Ercan Mihci; Luigi D Notarangelo; Ugo Ramenghi; Anna Teti; Johan Van Hove; Dragana Vujic; Terri Young; Alberto Albertini; Paul J Orchard; Paolo Vezzoni; Anna Villa
Journal:  J Bone Miner Res       Date:  2003-10       Impact factor: 6.741

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  2 in total

Review 1.  Molecular genetic studies of gene identification for osteoporosis: the 2009 update.

Authors:  Xiang-Hong Xu; Shan-Shan Dong; Yan Guo; Tie-Lin Yang; Shu-Feng Lei; Christopher J Papasian; Ming Zhao; Hong-Wen Deng
Journal:  Endocr Rev       Date:  2010-03-31       Impact factor: 19.871

Review 2.  Genetics of osteoporosis: accelerating pace in gene identification and validation.

Authors:  Wen-Feng Li; Shu-Xun Hou; Bin Yu; Meng-Meng Li; Claude Férec; Jian-Min Chen
Journal:  Hum Genet       Date:  2009-12-12       Impact factor: 4.132

  2 in total

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