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Osteoarthritis year 2011 in review: genetics
1Department of Molecular Epidemiology, Leiden University Medical Center, 2300 RC Leiden, The Netherlands. i.meulenbelt@lumc.nl
Osteoarthritis and Cartilage
|January 21, 2012
Summary
Genetic studies have identified some osteoarthritis (OA) variants, but success is limited. This review focuses on genetic research up to mid-2011 to understand OA
Area of Science:
- Genetics
- Molecular Biology
- Osteoarthritis Research
Background:
- Osteoarthritis (OA) pathogenesis remains incompletely understood.
- Previous genetic studies (candidate gene, GWAS) have yielded limited success in identifying causal variants.
- Understanding molecular and cellular events initiating OA is crucial.
Purpose of the Study:
- To review genetic study designs investigating the primary molecular and cellular events in human osteoarthritis (OA) onset.
- To summarize findings from studies published until mid-2011.
- To incorporate data presented at the 2011 Osteoarthritis Research Society International (OARSI) conference.
Main Methods:
- Literature review of genetic association and linkage studies.
- Focus on studies published up to mid-2011.
- Inclusion of data presented at the OARSI 2011 meeting.
Main Results:
- Several consistent genetic variants associated with OA have been identified.
- Despite identified variants, the overall success in elucidating OA mechanisms is limited.
- The review synthesizes findings on genetic contributions to early OA molecular and cellular changes.
Conclusions:
- Genetic research has provided insights into OA but has not fully elucidated its underlying mechanisms.
- Continued genetic investigations are necessary to understand OA initiation.
- The identified genetic variants warrant further functional validation.
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