Causal association between subtypes of osteoarthritis and common comorbidities: A Mendelian randomisation study

被引:3
作者
Thompson, Will [1 ]
Swain, Subhashisa [1 ,2 ]
Zhao, Sizheng Steven [3 ]
Kamps, Anne [4 ]
Coupland, Carol [5 ]
Kuo, Changfu [6 ]
Bierma-Zeinstra, Sita [4 ]
Runhaar, Jos [4 ]
Doherty, Michael [1 ]
Zhang, Weiya [1 ]
机构
[1] Nottingham City Hosp, Acad Rheumatol, Clin Sci Bldg,Hucknall Rd, Nottingham, England
[2] Radcliffe Observ Quarter, Nuffield Dept Primary Care Hlth Sci, Radcliffe Primary Care Bldg,Woodstock Rd, Oxford, England
[3] Univ Manchester, Ctr Epidemiol Versus Arthrit, Div Musculoskeletal & Dermatol Sci, Manchester, England
[4] Erasmus MC Univ Med Ctr Rotterdam, Dept Gen Practice, Dr Molewaterpl 40, NL-3015 GD Rotterdam, Netherlands
[5] Ctr Acad Primary Care, Sch Med, Univ Pk, Nottingham NG7 2RD, England
[6] Chang Gung Mem Hosp, Div Rheumatol Allergy & Immunol, 5 Fu Hsing St, Taoyuan 333, Taiwan
来源
OSTEOARTHRITIS AND CARTILAGE OPEN | 2023年 / 5卷 / 04期
基金
英国医学研究理事会;
关键词
OA; GO consortium; UK biobank; MR; Comorbidities; KNEE OSTEOARTHRITIS; PRIMARY-CARE; CHRONIC PAIN; FIBROMYALGIA; IMPACT; SLEEP; BIAS;
D O I
10.1016/j.ocarto.2023.100414
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Objective: To investigate the causal association between Osteoarthritis (OA) and five comorbidities: depression, tiredness, multisite chronic pain, irritable bowel syndrome (IBS) and gout. Design:This study used two-sample Mendelian Randomisation (MR). To select the OA genetic instruments, we used data from the largest recent genome-wide association study (GWAS) of OA (GO Consortium), with a focus on OA of the knee (62,497 cases, 333,557 controls), hip (35,445 cases, 316,943 controls) and hand (20,901 cases, 282,881 controls). Genetic associations for comorbidities were selected from GWAS for depression (246,363 cases, 561,190 controls), tiredness (449,019 participants), multisite chronic pain (387,649 participants), IBS (53,400 cases, 433,201 controls) and gout (6543 cases, 456,390 controls). We performed a bidirectional MR analysis using the inverse variance weighted method, for both joint specific and overall OA. Results: Hip OA had a causal effect on multisite chronic pain (per unit change 0.02, 95% CI 0.01 to 0.04). Multisite chronic pain had a causal effect on knee (odd ratio (OR) 2.74, 95% CI 2.20 to 3.41), hip (OR 2.12, 95% CI 1.54 to 2.92), hand (OR 2.24, 95% CI 1.59 to 3.16) and overall OA (OR 2.44, 95% CI, 2.06 to 2.86). In addition, depression and tiredness had causal effects on knee and hand, but not hip, OA. Conclusions: Apart from Hip OA to multisite chronic pain, other joint OA did not have causal effects on these comorbidities. In contrast, multisite chronic pain had a causal effect on any painful OA.
引用
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页数:11
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