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Arthritis Rheumatol. 2019 Jan 7. doi: 10.1002/art.40812. [Epub ahead of print]

Cardiometabolic polygenic risk scores and osteoarthritis outcomes: a Mendelian randomization study from the Malmӧ Diet and Cancer Study and the UK Biobank.

Author information

1
Department of Clinical Sciences in Malmö, Lund University, Sweden.
2
Program in Medical and Population Genetics and the Cardiovascular Disease Initiative, Broad Institute, Cambridge, Massachusetts, USA.
3
Center for Genomic Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
4
Diabetes Research Centre and Department of Health Sciences, University of Leicester, UK.

Abstract

OBJECTIVE:

To investigate the causal role of cardiometabolic risk factors in osteoarthritis (OA) using associated genetic variants.

METHODS:

We studied 27691 adults from the Malmö Diet and Cancer Study (MDCS) and replicated novel findings among 376435 adults from the UK Biobank. Trait-specific polygenic risk scores for LDL- and HDL-cholesterol (LDLC, HDLC), triglycerides (TG), BMI, fasting plasma glucose (FPG) and systolic blood pressure (SBP) were used to test the associations of genetically predicted elevations in each trait with incident OA-diagnosis (n=3559), OA-joint replacement (n=2780), or both (total-OA, n=4226) in Mendelian randomization (MR) analyses in MDCS, and with self-reported and/or hospital diagnosed OA (n=65213) in the UK Biobank. Multivariable MR, MR-Egger and weighted-median MR were used to adjust for potential pleiotropic biases.

RESULTS:

In MDCS, genetically predicted higher LDLC was associated with lower risk of OA-diagnosis (OR: 0.83; 95% CI: 0.73-0.95 per 1-SD) and total-OA (0.87; 0.78-0.98) which was supported by multivariable MR for OA-diagnosis (0.84; 0.75-0.95) and total-OA (0.87; 0.78-0.97), and by conventional two-sample MR for OA-diagnosis (0.86; 0.75-0.98). MR-Egger indicated no pleiotropic bias. Genetically predicted higher BMI was associated with increased risk for OA-diagnosis (1.65; 1.14-2.41), while MR-Egger indicated pleiotropic bias and larger association with OA-diagnosis (3.25; 1.26-8.39), OA-joint replacement (3.81; 1.39-10.4) and total-OA (3.41; 1.43-8.15). No associations were observed between genetically predicted HDLC, TG, FPG or SBP and OA outcomes. The LDLC associations were replicated in the UK Biobank (0.95; 0.93-0.98).

CONCLUSION:

Our MR study provides evidence for causal role of lower LDLC and higher BMI in OA. This article is protected by copyright. All rights reserved.

PMID:
30615301
DOI:
10.1002/art.40812

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