Obesity, Weight Loss, and Progression of Disability in Rheumatoid Arthritis.
Obesity, Weight Loss, and Progression of Disability in Rheumatoid Arthritis.
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DOI:
10.1002/acr.23579
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发表时间:
2018-12
影响因子:
4.7
通讯作者:
Michaud K
中科院分区:
文献类型:
--
作者:
Baker JF;England BR;Mikuls TR;Sayles H;Cannon GW;Sauer BC;George MD;Caplan L;Michaud K
Obese patients with rheumatoid arthritis (RA) report greater disability in cross-sectional studies. The longitudinal effects of obesity, however, are not well-characterized. We evaluated associations between obesity, weight loss, and worsening of disability in two large registry studies with long-term follow-up. This study included patients with RA from the National Data Bank of Rheumatic Diseases (Forward) (N=23,323) and the Veterans Affairs RA (VARA) registry study (N=1,697). Results of the Health Assessment Questionnaire (HAQ) or Multi-Dimensional (MD)-HAQ were recorded over follow-up. Significant worsening was defined as an increase of HAQ or MD-HAQ of >0.2. Cox proportional hazards models evaluated the risk of worsening from baseline, adjusting for demographics, baseline disability, comorbidity, disease duration, and other disease features. At enrollment, disability scores were higher among severely obese patients compared to overweight in both Forward [B: 0.17 (0.14, 0.20) p<0.001] and VARA [B: 0.17 (0.074, 0.27) p=0.001]. In multivariable models, patients who were severely obese at enrollment had a greater risk of progressive disability compared to overweight patients in Forward [HR 1.25 (1.18, 1.33) p<0.001] and VARA [HR 1.33 (1.07, 1.66) p=0.01]. Weight loss following enrollment was also associated with a greater risk in both cohorts. Associations were independent of other clinical factors including time-varying CRP and swollen joint count in VARA. Severe obesity is associated with more rapid progression of disability in RA. Weight loss is also associated with worsening disability, possibly by identifying individuals with chronic illness and the development of age-related or disease-related frailty.
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影响因子:
4.7
作者:
Cannon GW;Mikuls TR;Hayden CL;Ying J;Curtis JR;Reimold AM;Caplan L;Kerr GS;Richards JS;Johnson DS;Sauer BC
通讯作者:
Sauer BC
影响因子:
4.7
作者:
Baker JF;Von Feldt J;Mostoufi-Moab S;Noaiseh G;Taratuta E;Kim W;Leonard MB
通讯作者:
Leonard MB
影响因子:
4.9
作者:
Mikuls TR;Gould KA;Bynoté KK;Yu F;Levan TD;Thiele GM;Michaud KD;O'Dell JR;Reimold AM;Hooker R;Caplan L;Johnson DS;Kerr G;Richards JS;Cannon GW;Criswell LA;Noble JA;Bridges SL Jr;Hughes L;Gregersen PK
通讯作者:
Gregersen PK
DOI:
10.1093/gerona/60.8.1007
发表时间:
2005-08-01
影响因子:
5.1
作者:
Lee, JS;Kritchevsky, SB;Newman, AB
通讯作者:
Newman, AB
影响因子:
4.7
作者:
Ajeganova, Sofia;Andersson, Maria L.;Hafstrom, Ingiald
通讯作者:
Hafstrom, Ingiald