2011
DOI: 10.1016/j.joca.2011.01.020
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Osteoarthritis year 2010 in review: genetics

Abstract: At the 2010 Osteoarthritis Research Society International (OARSI) congress in Brussels I was asked to present on "Genetics" in the "Year in Review" session. This gave me an opportunity to reflect on the talk that I gave on the same topic at the 2007 OARSI congress in Ft Lauderdale, Florida. My 2007 talk was very upbeat and ended with the hostage to fortune statement "The next few years will provide tremendous clarity in our genetic understanding of osteoarthritis".

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Cited by 23 publications
(14 citation statements)
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“…Most genes identified have not been consistently replicated in later studies or in cohorts from different geographical regions. An exception is growth/differentiation factor 5 (GDF‐5), a protein involved in joint formation from the bone morphogenic protein family [24]. GDF‐5 has shown consistent associations with knee OA in both East Asian and white European cohorts, reaching genome‐wide significance in the latter; less consistent associations have been seen with hip OA [25].…”
Section: Risk Factors For Oamentioning
confidence: 99%
“…Most genes identified have not been consistently replicated in later studies or in cohorts from different geographical regions. An exception is growth/differentiation factor 5 (GDF‐5), a protein involved in joint formation from the bone morphogenic protein family [24]. GDF‐5 has shown consistent associations with knee OA in both East Asian and white European cohorts, reaching genome‐wide significance in the latter; less consistent associations have been seen with hip OA [25].…”
Section: Risk Factors For Oamentioning
confidence: 99%
“…Investigation of the genetic component of osteoarthritis (OA) susceptibility has yielded the identification of several loci achieving genome-wide significance or consistent replication [1-3]. These loci are insufficient to account for the heritability of OA, which has been estimated as 49 to 78% for knee OA in twin and family studies [4-6].…”
Section: Introductionmentioning
confidence: 99%
“…Multiple possible causes of this discrepancy, which has become known as the missing heritability problem of complex diseases, have been discussed [7]. Some have a particular importance in OA, like the difficulties in discriminating between cases and controls, the variability in phenotype definitions and the relatively small size of genome wide association studies (GWAS) in which OA has been studied in comparison with other diseases [3,8]. Other causes are shared by most complex diseases.…”
Section: Introductionmentioning
confidence: 99%
“…So sind unterschiedliche Signalkaskaden der Skelettentwicklung, der extrazellulären Matrixproteine, der Chondrozytenphänotypen, der Apoptose als auch inflammatorischer Moleküle, wie des Zytokin-, Prostaglandin, Arachidonsäure-Stoffwechsels als auch der Proteaseninteraktion beschrieben worden [46,47]. Genetische Faktoren sind ebenso in die Entwicklung einer Arthrose (Osteoarthritis; OA) involviert [28], wie Vitamin-D-Mangel und Adipositas als einflussgebende Prädiktoren beschrieben wurden [6]. Insgesamt wird von einer Interaktion sowohl angeborener, erworbener als auch Umweltfaktoren ausgegangen [6].…”
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