Genetic Risk Factors for End-Stage Hip Osteoarthritis Treated With Total Hip Arthroplasty: A Genome-wide Association Study.

epidemiology genetics genome wide association study genomics hip osteoarthritis total hip arthroplasty

Journal

The Journal of arthroplasty
ISSN: 1532-8406
Titre abrégé: J Arthroplasty
Pays: United States
ID NLM: 8703515

Informations de publication

Date de publication:
10 2023
Historique:
received: 20 01 2023
revised: 28 04 2023
accepted: 03 05 2023
medline: 25 9 2023
pubmed: 14 5 2023
entrez: 13 5 2023
Statut: ppublish

Résumé

Although a genetic component to hip osteoarthritis (OA) has been described, focused evaluation of the genetic components of end-stage disease is limited. We present a genomewide association study for patients undergoing total hip arthroplasty (THA) to characterize the genetic risk factors associated with end-stage hip osteoarthritis (ESHO), defined as utilization of the procedure. Patients who underwent primary THA for hip OA were identified in a national patient data repository using administrative codes. Fifteen thousand three hundred and fifty-five patients with ESHO and 374,193 control patients were identified. Whole genome regression of genotypic data for patients who underwent primary THA for hip OA corrected for age, sex, and body mass index (BMI) was performed. Multivariate logistic regression models were used to evaluate the composite genetic risk from the identified genetic variants. There were 13 significant genes identified. Composite genetic factors resulted in an odds ratio 1.04 for ESHO (P < .001). The effect of genetics was lower than that of age (Odds Ratio (OR): 2.38; P < .001) and BMI (1.81; P < .001). Multiple genetic variants, including 5 novel loci, were associated with end-stage hip OA treated with primary THA. Age and BMI were associated with greater odds of developing end-stage disease when compared to genetic factors.

Sections du résumé

BACKGROUND
Although a genetic component to hip osteoarthritis (OA) has been described, focused evaluation of the genetic components of end-stage disease is limited. We present a genomewide association study for patients undergoing total hip arthroplasty (THA) to characterize the genetic risk factors associated with end-stage hip osteoarthritis (ESHO), defined as utilization of the procedure.
METHODS
Patients who underwent primary THA for hip OA were identified in a national patient data repository using administrative codes. Fifteen thousand three hundred and fifty-five patients with ESHO and 374,193 control patients were identified. Whole genome regression of genotypic data for patients who underwent primary THA for hip OA corrected for age, sex, and body mass index (BMI) was performed. Multivariate logistic regression models were used to evaluate the composite genetic risk from the identified genetic variants.
RESULTS
There were 13 significant genes identified. Composite genetic factors resulted in an odds ratio 1.04 for ESHO (P < .001). The effect of genetics was lower than that of age (Odds Ratio (OR): 2.38; P < .001) and BMI (1.81; P < .001).
CONCLUSION
Multiple genetic variants, including 5 novel loci, were associated with end-stage hip OA treated with primary THA. Age and BMI were associated with greater odds of developing end-stage disease when compared to genetic factors.

Identifiants

pubmed: 37179025
pii: S0883-5403(23)00471-0
doi: 10.1016/j.arth.2023.05.006
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2149-2153.e1

Informations de copyright

Copyright © 2023 Elsevier Inc. All rights reserved.

Auteurs

Scott Kulm (S)

Weill Cornell Medicine, New York, New York; Englander Institute for Precision Medicine, New York, New York.

Austin C Kaidi (AC)

Adult Reconstruction and Joint Replacement, Hospital for Special Surgery, New York, New York.

David Kolin (D)

Adult Reconstruction and Joint Replacement, Hospital for Special Surgery, New York, New York.

Mark T Langhans (MT)

Adult Reconstruction and Joint Replacement, Hospital for Special Surgery, New York, New York.

Mathias P Bostrom (MP)

Adult Reconstruction and Joint Replacement, Hospital for Special Surgery, New York, New York.

Olivier Elemento (O)

Weill Cornell Medicine, New York, New York; Englander Institute for Precision Medicine, New York, New York.

Tony S Shen (TS)

Adult Reconstruction and Joint Replacement, Hospital for Special Surgery, New York, New York.

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