4.5 Article

Metabolic Syndrome and Osteoarthritis Distribution in the Hand Joints: A Propensity Score Matching Analysis From the Osteoarthritis Initiative

期刊

JOURNAL OF RHEUMATOLOGY
卷 48, 期 10, 页码 1608-1615

出版社

J RHEUMATOL PUBL CO
DOI: 10.3899/jrheum.210189

关键词

erosive osteoarthritis; hand; metabolic syndrome; nodal osteoarthritis; Osteoarthritis Initiative; propensity score matching

资金

  1. National Institutes of Health (NIH) National Institute on Aging [P01AG066603]
  2. Osteoarthritis Initiative (OAI) [N01-AR-2-2258, N01-AR-2-2259, N01-AR-2-2260, N01-AR-2-2261, N01-AR-2-2262]
  3. National Institutes of Health (NIH)
  4. Merck Research Laboratories
  5. Novartis Pharmaceuticals Corporation
  6. GlaxoSmithKline
  7. Pfizer Inc.

向作者/读者索取更多资源

The study found that metabolic syndrome is associated with hand radiographic osteoarthritis, predominantly in distal interphalangeal and proximal interphalangeal joints, with sparing of metacarpophalangeal and first carpometacarpal joints. Metabolic syndrome was also linked to increased longitudinal hand pain incidence and higher rates of nodal and erosive HOA phenotypes.
Objective. To investigate the metabolic syndrome (MetS) association with radiographic and symptomatic hand osteoarthritis (HOA). Methods. Using 1:2 propensity score matching for relevant confounders, we included 2509 participants (896 MetS positive and 1613 MetS negative) from the Osteoarthritis Initiative dataset. MetS and its components, according to the International Diabetes Federation criteria, were extracted from baseline data, and included hypertension, abdominal obesity, dyslipidemia, and diabetes. We scored distinct hand joints based on the modified Kellgren-Lawrence (mKL) grade of baseline radiographs, with HOA defined as mKL >= 2. In the cross-sectional analysis, we investigated the association between MetS and its components with radiographic HOA and the presence of nodal and erosive HOA phenotypes using regression models. In the longitudinal analysis, we performed Cox regression analysis for hand pain incidence in follow-up visits. Results. MetS was associated with higher odds of radiographic HOA, including the number of joints with OA (OR 1.32, 95% CI 1.08-1.62), the sum of joints mKLs (OR 2.42, 95% CI 1.24-4.71), mainly in distal interphalangeal joints (DIPs) and proximal interphalangeal joints (PIPs; OR 1.52, 95% CI 1.08-2.14 and OR 1.38, 95% CI 1.09-1.75, respectively), but not metacarpophalangeal (MCP) and first carpometacarpal (CMC1) joints. Hand pain incidence during follow-up was higher with MetS presence (HR 1.25, 95% CI 1.07-1.47). The erosive HOA phenotype and joints' nodal involvement were more frequent with MetS (OR 1.40, 95% CI 1.01-1.97 and OR 1.28, 95% CI 1.02-1.60, respectively). Conclusion. MetS, a potentially modifiable risk factor, is associated with radiographic DIP and PIP OA and longitudinal hand pain incidence while sparing MCPs and CMC1s. Nodal and erosive HOA phenotypes are associated with MetS, suggestive of possible distinct pathophysiology.

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