Genetics of pediatric bone strength.

BoneKEy reports Pub Date : 2016-07-20 eCollection Date: 2016-01-01 DOI:10.1038/bonekey.2016.50
Jonathan A Mitchell, Diana L Cousminer, Babette S Zemel, Struan F A Grant, Alessandra Chesi
{"title":"Genetics of pediatric bone strength.","authors":"Jonathan A Mitchell,&nbsp;Diana L Cousminer,&nbsp;Babette S Zemel,&nbsp;Struan F A Grant,&nbsp;Alessandra Chesi","doi":"10.1038/bonekey.2016.50","DOIUrl":null,"url":null,"abstract":"<p><p>Osteoporosis is one of the most common chronic forms of disability in postmenopausal women and represents a major health burden around the world. Bone fragility is affected by bone mineral density (BMD), and, one of the most important factors in preventing osteoporosis is optimizing peak bone mass, which is achieved during growth in childhood and adolescence. BMD is a complex trait resulting from environmental and genetic factors. Genome-wide association studies have discovered robust genetic signals influencing BMD in adults, and similar studies have also been conducted to investigate the genetics of BMD in the pediatric setting. These latter studies have revealed that many adult osteoporosis-related loci also regulate BMD during growth. These investigations have the potential to profoundly impact public health and will allow for the eventual development of effective interventions for the prevention of osteoporosis. </p>","PeriodicalId":72441,"journal":{"name":"BoneKEy reports","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2016-07-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4954586/pdf/bonekey201650.pdf","citationCount":"18","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BoneKEy reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1038/bonekey.2016.50","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2016/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 18

Abstract

Osteoporosis is one of the most common chronic forms of disability in postmenopausal women and represents a major health burden around the world. Bone fragility is affected by bone mineral density (BMD), and, one of the most important factors in preventing osteoporosis is optimizing peak bone mass, which is achieved during growth in childhood and adolescence. BMD is a complex trait resulting from environmental and genetic factors. Genome-wide association studies have discovered robust genetic signals influencing BMD in adults, and similar studies have also been conducted to investigate the genetics of BMD in the pediatric setting. These latter studies have revealed that many adult osteoporosis-related loci also regulate BMD during growth. These investigations have the potential to profoundly impact public health and will allow for the eventual development of effective interventions for the prevention of osteoporosis.

儿童骨骼强度的遗传学。
骨质疏松症是绝经后妇女最常见的慢性残疾之一,是世界各地的一个主要健康负担。骨脆弱性受骨密度(BMD)的影响,而预防骨质疏松症最重要的因素之一是优化骨量峰值,这是在儿童和青少年时期实现的。骨密度是一种由环境和遗传因素共同作用的复杂性状。全基因组关联研究已经发现了影响成人骨密度的强大遗传信号,并且也进行了类似的研究来调查儿童骨密度的遗传学。这些研究表明,许多成人骨质疏松相关的基因位点也在生长过程中调节骨密度。这些调查有可能对公众健康产生深远的影响,并将允许最终发展有效的干预措施来预防骨质疏松症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信