Genetic epidemiology of age-related osteoporosis and its clinical applications

Technological innovations have contributed greatly to advancing our knowledge of the genetic basis of osteoporosis. This article reviews the current understanding of osteoporosis genetics with a focus on developments since 2007. The potential clinical implications of this information and future dire...

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Published inNature reviews. Rheumatology Vol. 6; no. 9; pp. 507 - 517
Main Authors Cheung, Ching-Lung, Xiao, Su-Mei, Kung, Annie W. C.
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 01.09.2010
Nature Publishing Group
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Online AccessGet full text
ISSN1759-4790
1759-4804
1759-4804
DOI10.1038/nrrheum.2010.106

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Abstract Technological innovations have contributed greatly to advancing our knowledge of the genetic basis of osteoporosis. This article reviews the current understanding of osteoporosis genetics with a focus on developments since 2007. The potential clinical implications of this information and future directions for research are also discussed. Osteoporosis is an important and complex disorder that is highly prevalent worldwide. This disease poses a major challenge to modern medicine and its treatment is associated with high costs. Numerous studies have endeavored to decipher the pathogenesis of this disease. The clinical assessment of patients often incorporates information about a family history of osteoporotic fractures. Indeed, the observation of an increased risk of fracture in an individual with a positive parental history of hip fracture provides strong evidence for the heritability of osteoporosis. The onset and progression of osteoporosis are generally controlled by multiple genetic and environmental factors, as well as interactions between them, with rare cases determined by a single gene. In an attempt to identify the genetic markers of complex diseases such as osteoporosis, there has been a move away from traditional linkage mapping studies and candidate gene association studies to higher-density genome-wide association studies. The advent of high-throughput technology enables genotyping of millions of DNA markers in the human genome, and consequently the identification and characterization of causal variants and loci that underlie osteoporosis. This Review presents an overview of the major findings since 2007 and clinical applications of these genome-wide linkage and association studies. Key Points Osteoporosis is a complex disease and bone mineral density (BMD) and osteoporotic fractures are highly heritable traits Genetic studies using linkage and association approaches have identified a number of osteoporosis susceptibility genes and loci that are associated with low BMD and fracture risk The loci identified by candidate gene association and genome-wide association studies are involved in several well-defined biological pathways related to bone metabolism This genetic information has potential clinical applications in terms of nosology, risk prediction, pharmacogenetics, and the development of biomarkers and therapeutic agents
AbstractList Technological innovations have contributed greatly to advancing our knowledge of the genetic basis of osteoporosis. This article reviews the current understanding of osteoporosis genetics with a focus on developments since 2007. The potential clinical implications of this information and future directions for research are also discussed. Osteoporosis is an important and complex disorder that is highly prevalent worldwide. This disease poses a major challenge to modern medicine and its treatment is associated with high costs. Numerous studies have endeavored to decipher the pathogenesis of this disease. The clinical assessment of patients often incorporates information about a family history of osteoporotic fractures. Indeed, the observation of an increased risk of fracture in an individual with a positive parental history of hip fracture provides strong evidence for the heritability of osteoporosis. The onset and progression of osteoporosis are generally controlled by multiple genetic and environmental factors, as well as interactions between them, with rare cases determined by a single gene. In an attempt to identify the genetic markers of complex diseases such as osteoporosis, there has been a move away from traditional linkage mapping studies and candidate gene association studies to higher-density genome-wide association studies. The advent of high-throughput technology enables genotyping of millions of DNA markers in the human genome, and consequently the identification and characterization of causal variants and loci that underlie osteoporosis. This Review presents an overview of the major findings since 2007 and clinical applications of these genome-wide linkage and association studies. Key Points Osteoporosis is a complex disease and bone mineral density (BMD) and osteoporotic fractures are highly heritable traits Genetic studies using linkage and association approaches have identified a number of osteoporosis susceptibility genes and loci that are associated with low BMD and fracture risk The loci identified by candidate gene association and genome-wide association studies are involved in several well-defined biological pathways related to bone metabolism This genetic information has potential clinical applications in terms of nosology, risk prediction, pharmacogenetics, and the development of biomarkers and therapeutic agents
Osteoporosis is an important and complex disorder that is highly prevalent worldwide. This disease poses a major challenge to modern medicine and its treatment is associated with high costs. Numerous studies have endeavored to decipher the pathogenesis of this disease. The clinical assessment of patients often incorporates information about a family history of osteoporotic fractures. Indeed, the observation of an increased risk of fracture in an individual with a positive parental history of hip fracture provides strong evidence for the heritability of osteoporosis. The onset and progression of osteoporosis are generally controlled by multiple genetic and environmental factors, as well as interactions between them, with rare cases determined by a single gene. In an attempt to identify the genetic markers of complex diseases such as osteoporosis, there has been a move away from traditional linkage mapping studies and candidate gene association studies to higher-density genome-wide association studies. The advent of high-throughput technology enables genotyping of millions of DNA markers in the human genome, and consequently the identification and characterization of causal variants and loci that underlie osteoporosis. This Review presents an overview of the major findings since 2007 and clinical applications of these genome-wide linkage and association studies. Cheung, C.-L. et al. Nat. Rev. Rheumatol. 6, 507-517 (2010); published online 3 August 2010; doi: 10.1038/nrrheum.2010.106
Osteoporosis is an important and complex disorder that is highly prevalent worldwide. This disease poses a major challenge to modern medicine and its treatment is associated with high costs. Numerous studies have endeavored to decipher the pathogenesis of this disease. The clinical assessment of patients often incorporates information about a family history of osteoporotic fractures. Indeed, the observation of an increased risk of fracture in an individual with a positive parental history of hip fracture provides strong evidence for the heritability of osteoporosis. The onset and progression of osteoporosis are generally controlled by multiple genetic and environmental factors, as well as interactions between them, with rare cases determined by a single gene. In an attempt to identify the genetic markers of complex diseases such as osteoporosis, there has been a move away from traditional linkage mapping studies and candidate gene association studies to higher-density genome-wide association studies. The advent of high-throughput technology enables genotyping of millions of DNA markers in the human genome, and consequently the identification and characterization of causal variants and loci that underlie osteoporosis. This Review presents an overview of the major findings since 2007 and clinical applications of these genome-wide linkage and association studies.
Osteoporosis is an important and complex disorder that is highly prevalent worldwide. This disease poses a major challenge to modern medicine and its treatment is associated with high costs. Numerous studies have endeavored to decipher the pathogenesis of this disease. The clinical assessment of patients often incorporates information about a family history of osteoporotic fractures. Indeed, the observation of an increased risk of fracture in an individual with a positive parental history of hip fracture provides strong evidence for the heritability of osteoporosis. The onset and progression of osteoporosis are generally controlled by multiple genetic and environmental factors, as well as interactions between them, with rare cases determined by a single gene. In an attempt to identify the genetic markers of complex diseases such as osteoporosis, there has been a move away from traditional linkage mapping studies and candidate gene association studies to higher-density genome-wide association studies. The advent of high-throughput technology enables genotyping of millions of DNA markers in the human genome, and consequently the identification and characterization of causal variants and loci that underlie osteoporosis. This Review presents an overview of the major findings since 2007 and clinical applications of these genome-wide linkage and association studies.Osteoporosis is an important and complex disorder that is highly prevalent worldwide. This disease poses a major challenge to modern medicine and its treatment is associated with high costs. Numerous studies have endeavored to decipher the pathogenesis of this disease. The clinical assessment of patients often incorporates information about a family history of osteoporotic fractures. Indeed, the observation of an increased risk of fracture in an individual with a positive parental history of hip fracture provides strong evidence for the heritability of osteoporosis. The onset and progression of osteoporosis are generally controlled by multiple genetic and environmental factors, as well as interactions between them, with rare cases determined by a single gene. In an attempt to identify the genetic markers of complex diseases such as osteoporosis, there has been a move away from traditional linkage mapping studies and candidate gene association studies to higher-density genome-wide association studies. The advent of high-throughput technology enables genotyping of millions of DNA markers in the human genome, and consequently the identification and characterization of causal variants and loci that underlie osteoporosis. This Review presents an overview of the major findings since 2007 and clinical applications of these genome-wide linkage and association studies.
Audience Academic
Author Kung, Annie W. C.
Xiao, Su-Mei
Cheung, Ching-Lung
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  fullname: Xiao, Su-Mei
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  surname: Kung
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/20683440$$D View this record in MEDLINE/PubMed
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Snippet Technological innovations have contributed greatly to advancing our knowledge of the genetic basis of osteoporosis. This article reviews the current...
Osteoporosis is an important and complex disorder that is highly prevalent worldwide. This disease poses a major challenge to modern medicine and its treatment...
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SubjectTerms 631/208/205/2138
692/699/1670/316/801
692/700/478/174
Bone density
Collaboration
Complications and side effects
Development and progression
Disease
Epidemiology
Fractures
Gene loci
Genetic aspects
Genetic Linkage
Genetic markers
Genetic Predisposition to Disease
Genomes
Genomics
Geometry
High-Throughput Nucleotide Sequencing
Hip joint
Humans
Medicine
Medicine & Public Health
Meta-Analysis as Topic
Molecular Epidemiology
Osteoporosis
Osteoporosis - epidemiology
Osteoporosis - genetics
Osteoporosis - therapy
Physiological aspects
Polymorphism, Single Nucleotide
review-article
Rheumatology
Risk factors
Ultrasonic imaging
Title Genetic epidemiology of age-related osteoporosis and its clinical applications
URI https://link.springer.com/article/10.1038/nrrheum.2010.106
https://www.ncbi.nlm.nih.gov/pubmed/20683440
https://www.proquest.com/docview/1790189757
https://www.proquest.com/docview/754001180
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