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Genome-wide association meta-analysis of knee and hip osteoarthritis uncovers genetic differences between patients treated with joint replacement and patients without joint replacement.
Henkel, Cecilie; Styrkársdóttir, Unnur; Thorleifsson, Gudmar; Stefánsdóttir, Lilja; Björnsdóttir, Gyda; Banasik, Karina; Brunak, Søren; Erikstrup, Christian; Dinh, Khoa Manh; Hansen, Thomas Folkmann; Nielsen, Kaspar René; Bruun, Mie Topholm; Dowsett, Joseph; Brodersen, Thorsten; Thorgeirsson, Thorgeir E; Gromov, Kirill; Boesen, Mikael Ploug; Ullum, Henrik; Ostrowski, Sisse Rye; Pedersen, Ole Birger; Stefánsson, Kári; Troelsen, Anders.
Afiliação
  • Henkel C; Clinical Orthopaedic Research Hvidovre (CORH), Department of Orthopaedic Surgery, Copenhagen University Hospital Hvidovre, Hvidovre, Denmark cecilie.henkel@regionh.dk.
  • Styrkársdóttir U; deCODE genetics/Amgen, Reykjavik, Iceland.
  • Thorleifsson G; deCODE genetics/Amgen, Reykjavik, Iceland.
  • Stefánsdóttir L; deCODE genetics/Amgen, Reykjavik, Iceland.
  • Björnsdóttir G; deCODE genetics/Amgen, Reykjavik, Iceland.
  • Banasik K; Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Brunak S; Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Erikstrup C; Department of Clinical Immunology, Aarhus University Hospital, Aarhus, Denmark.
  • Dinh KM; Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.
  • Hansen TF; Department of Clinical Immunology, Aarhus University Hospital, Aarhus, Denmark.
  • Nielsen KR; Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Bruun MT; Danish Headache Center, Department of Neurology, Rigshospitalet Glostrup, Glostrup, Denmark.
  • Dowsett J; Department of Clinical Immunology, Aalborg University Hospital, Aalborg, Denmark.
  • Brodersen T; Department of Clinical Immunology, Odense University Hospital, Odense, Denmark.
  • Thorgeirsson TE; Department of Clinical Immunology, Zealand University Hospital Køge, Køge, Denmark.
  • Boesen MP; deCODE genetics/Amgen, Reykjavik, Iceland.
  • Ullum H; Clinical Orthopaedic Research Hvidovre (CORH), Department of Orthopaedic Surgery, Copenhagen University Hospital Hvidovre, Hvidovre, Denmark.
  • Ostrowski SR; Clinical Academic Group: Research OsteoArthritis Denmark (CAG ROAD), Greater Copenhagen Health Science Partners, Copenhagen, Denmark.
  • Pedersen OB; Clinical Academic Group: Research OsteoArthritis Denmark (CAG ROAD), Greater Copenhagen Health Science Partners, Copenhagen, Denmark.
  • Stefánsson K; Department of Radiology, Bispebjerg Hospital, Copenhagen, Denmark.
  • Troelsen A; Statens Serum Institut, Copenhagen, Denmark.
Ann Rheum Dis ; 82(3): 384-392, 2023 03.
Article em En | MEDLINE | ID: mdl-36376028
ABSTRACT

OBJECTIVES:

Osteoarthritis is a common and severe, multifactorial disease with a well-established genetic component. However, little is known about how genetics affect disease progression, and thereby the need for joint placement. Therefore, we aimed to investigate whether the genetic associations of knee and hip osteoarthritis differ between patients treated with joint replacement and patients without joint replacement.

METHODS:

We included knee and hip osteoarthritis cases along with healthy controls, altogether counting >700 000 individuals. The cases were divided into two groups based on joint replacement status (surgical vs non-surgical) and included in four genome-wide association meta-analyses surgical knee osteoarthritis (N = 22 525), non-surgical knee osteoarthritis (N = 38 626), surgical hip osteoarthritis (N = 20 221) and non-surgical hip osteoarthritis (N = 17 847). In addition, we tested for genetic correlation between the osteoarthritis groups and the pain phenotypes intervertebral disc disorder, dorsalgia, fibromyalgia, migraine and joint pain.

RESULTS:

We identified 52 sequence variants associated with knee osteoarthritis (surgical 17, non-surgical 3) or hip osteoarthritis (surgical 34, non-surgical 1). For the surgical phenotypes, we identified 10 novel variants, including genes involved in autophagy (rs2447606 in ATG7) and mechanotransduction (rs202127176 in PIEZO1). One variant, rs13107325 in SLC39A8, associated more strongly with non-surgical knee osteoarthritis than surgical knee osteoarthritis. For all other variants, significance and effect sizes were higher for the surgical phenotypes. In contrast, genetic correlations with pain phenotypes tended to be stronger in the non-surgical groups.

CONCLUSIONS:

Our results indicate differences in genetic associations between knee and hip osteoarthritis depending on joint replacement status.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Osteoartrite do Quadril / Artroplastia de Quadril / Artroplastia do Joelho / Osteoartrite do Joelho Tipo de estudo: Risk_factors_studies / Systematic_reviews Limite: Humans Idioma: En Revista: Ann Rheum Dis Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Dinamarca

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Osteoartrite do Quadril / Artroplastia de Quadril / Artroplastia do Joelho / Osteoartrite do Joelho Tipo de estudo: Risk_factors_studies / Systematic_reviews Limite: Humans Idioma: En Revista: Ann Rheum Dis Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Dinamarca