Galíndez Eva, Carmona Loreto
Servicio de Reumatología, Hospital Universitario Basurto, Bilbao, Vizcaya, España.
Instituto de Salud Musculoesquelética, Madrid, España.
Reumatol Clin. 2016 Nov-Dec;12(6):307-312. doi: 10.1016/j.reuma.2015.12.005. Epub 2016 Jan 30.
To assess the association between obesity, control of inflammatory activity and increased adverse effects in psoriatic arthritis (PsA) with disease-modifying anti-inflammatory drugs (DMARD).
A systematic literature review was performed using MEDLINE and EMBASE databases following the guidelines of the Meta-analysis Of Observational Studies in Epidemiology (MOOSE) consensus statement. Studies were selected if they included patients with PsA, obesity was studied as a predictive factor, and the outcome was adverse effects, including efficacy failure. Quality was assessed using an ad hoc risk of bias tool. A qualitative analysis was carried out by type of study and study population, quality and specific results.
We found 1043 articles, discarding most of them on the basis of title and abstract. Ten articles were studied in detail and finally excluded three. The majority concluded, with statistically significant results, that in patients with PsA and treated with TNFα inhibitors (TNFαi), obesity is associated with poorer chances of achieving and maintaining a minimal disease activity, higher treatment discontinuation rates, and lower skin response. Regarding conventional synthetic DMARD, a trend toward a moderate increase in transaminases with methotrexate (MTX) was observed in obese patients with PsA.
Obesity is a negative predictor of clinical response in patients with PsA being treated with TNFαi. Except MTX hepatotoxicity, no other adverse effects, either with TNFαi or other drugs, were found in relation to obesity in PsA.
评估银屑病关节炎(PsA)患者肥胖与疾病改善抗风湿药物(DMARD)治疗时炎症活动控制及不良反应增加之间的关联。
按照流行病学观察性研究的Meta分析(MOOSE)共识声明的指南,使用MEDLINE和EMBASE数据库进行系统的文献综述。如果研究纳入了PsA患者,将肥胖作为预测因素进行研究,且结局为不良反应(包括疗效不佳),则选择这些研究。使用专门的偏倚风险工具评估质量。按研究类型、研究人群、质量和具体结果进行定性分析。
我们找到了1043篇文章,根据标题和摘要排除了其中大部分。对10篇文章进行了详细研究,最终排除了3篇。大多数研究得出具有统计学意义的结果,即PsA患者接受肿瘤坏死因子α抑制剂(TNFαi)治疗时,肥胖与达到和维持最小疾病活动度的机会较差、治疗中断率较高以及皮肤反应较低有关。对于传统合成DMARD,在肥胖的PsA患者中观察到使用甲氨蝶呤(MTX)时转氨酶有适度升高的趋势。
肥胖是接受TNFαi治疗的PsA患者临床反应的负面预测因素。除MTX肝毒性外,未发现PsA患者使用TNFαi或其他药物时与肥胖相关的其他不良反应。