Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.
Rheumatology Unit, Department of Medicine, Karolinska Institutet/Karolinska University Hospital, Stockholm, Sweden.
Ann Rheum Dis. 2014 Nov;73(11):2029-33. doi: 10.1136/annrheumdis-2013-205094. Epub 2014 May 12.
To investigate whether overweight/obesity at diagnosis affects the chances of decrease in disease activity and pain in early rheumatoid arthritis (RA).
We investigated incident RA cases from the population-based Epidemiological Investigation of risk factors for Rheumatoid Arthritis (EIRA) study (2006-2009, N=495) with clinical follow-up in the Swedish Rheumatology Quality Register. At diagnosis, 93% received disease-modifying antirheumatic drugs (DMARDs) (86% methotrexate). The odds of achieving a good response according to the DAS28-based European League Against Rheumatism (EULAR) criteria, low disease activity (DAS28<3.2), remission (DAS28<2.6) or pain remission (visual analogue scale ≤20 mm) at 3-months and 6-months follow-up, were calculated using logistic regression, adjusting for potential confounders.
Significant dose-response relationships were found between Body Mass Index (BMI) and change of disease activity as well as pain at both time points. Patients with BMI ≥25 had 51% lower odds of achieving low disease activity (odds ratio (OR=0.49 (95% CI 0.31 to 0.78)) and 42% lower odds of remission (OR=0.58 (95% CI 0.37 to 0.92)) at the 6-months visit, compared to normal-weight patients. This effect was also present at 3 months, where we also found a 43% decreased odds of pain remission (OR=0.57 (95% CI 0.37 to 0.88)). No effect modification was found for anti-citrullinated protein antibody (CCP)-status, sex, prednisolone treatment or DAS28 at diagnosis.
Overweight at diagnosis significantly decreases the chance of achieving good disease control during the early phase of RA.
探讨诊断时超重/肥胖是否会影响早期类风湿关节炎(RA)患者疾病活动度和疼痛减轻的机会。
我们对基于人群的类风湿关节炎危险因素流行病学调查(EIRA)研究(2006-2009 年,N=495)中的新发 RA 病例进行了研究,这些病例在瑞典风湿病质量登记处进行了临床随访。在诊断时,93%的患者接受了疾病修饰抗风湿药物(DMARDs)(86%甲氨蝶呤)治疗。使用逻辑回归,调整潜在混杂因素后,计算了在 3 个月和 6 个月随访时达到基于 DAS28 的欧洲抗风湿病联盟(EULAR)标准的良好反应(DAS28<3.2)、低疾病活动度(DAS28<3.2)、缓解(DAS28<2.6)或疼痛缓解(视觉模拟评分≤20mm)的可能性比,根据 DAS28 计算。
在两个时间点,BMI 与疾病活动度和疼痛变化之间均存在显著的剂量反应关系。BMI≥25 的患者在 6 个月随访时达到低疾病活动度的可能性低 51%(比值比(OR)=0.49(95%CI 0.31-0.78)),达到缓解的可能性低 42%(OR=0.58(95%CI 0.37-0.92)),与正常体重患者相比。这种效应在 3 个月时也存在,我们还发现疼痛缓解的可能性降低了 43%(OR=0.57(95%CI 0.37-0.88))。抗瓜氨酸蛋白抗体(CCP)状态、性别、泼尼松龙治疗或 DAS28 在诊断时没有改变效果。
诊断时超重显著降低了 RA 早期达到良好疾病控制的机会。