4.7 Article

Disparities in multimorbidity and comorbidities in rheumatoid arthritis by sex across the lifespan

期刊

RHEUMATOLOGY
卷 -, 期 -, 页码 -

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OXFORD UNIV PRESS
DOI: 10.1093/rheumatology/kead454

关键词

RA; multimorbidity; comorbidity; sex; disparities

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Multimorbidity has a greater impact on women with RA, while men are more likely to have cardiovascular-related conditions. These findings suggest that research, clinical practice, and policies related to rheumatic diseases should take into account the variation in care needs by sex and gender.
Objectives: Multimorbidity is burdensome for people with RA. We investigated differences in multimorbidity and comorbidities by sex and age in the RA population. Methods: This cross-sectional analysis used national administrative claims (OptumLabs((R)) Data Warehouse) from people with RA and non-RA comparators (matched on age, sex, race, census region, index year and length of baseline insurance coverage) from 2010-2019. RA was determined using a validated algorithm. Multimorbidity was defined as >= 2 (MM2+) or >= 5 (MM5+) comorbidities from a validated set of 44 chronic conditions. We used logistic regression to assess associations between characteristics and multimorbidity. Results: The sample included 154 391 RA patients and 154 391 non-RA comparators. For people aged 18-50 years, RA women (vs RA men) had 7.5 and 4.4 (vs 3.2 and 0.9 in non-RA women vs non-RA men) percentage point increases for MM2+ and MM5+, respectively. For people aged 51thorn years, RA women (vs RA men) had 2.1 and 2.5 (vs 1.2 and 0.3 in non-RA women vs non-RA men) percentage point increases for MM2+ and MM5+, respectively. Interactions revealed that differences in multimorbidity between women and men were exacerbated by RA (vs non-RA) (P < 0.05), with more pronounced effects in people aged 18-50. Men had more cardiovascular-related conditions, whereas RA women had more psychological, neurological and general musculoskeletal conditions. Other comorbidities varied by sex and age. Conclusion: Multimorbidity disproportionately impacts women with RA. Research, clinical and policy agendas for rheumatic diseases should acknowledge and support the variation in care needs by sex and gender across the lifespan.

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