Musculoskeletal Biology I, Institute of Ageing and Chronic Disease, University of Liverpool, Liverpool, UK.
Department of Academic Rheumatology, Aintree University Hospital, Liverpool, UK.
Arthritis Res Ther. 2019 Jul 22;21(1):177. doi: 10.1186/s13075-019-1958-z.
The impact of smoking on TNF inhibition (TNFi) therapy is unclear. We examined the effect of smoking on all-cause and cause-specific TNFi discontinuation in axial spondyloarthritis (axSpA).
We used longitudinal data from the British Society for Rheumatology Biologics Register for Ankylosing Spondylitis (BSRBR-AS). Patients fulfilling the ASAS criteria for axSpA, who started their first TNFi, were eligible for analysis. Inverse-probability weights were used to balance differences in baseline disease severity and other confounders. We used marginal structural Cox proportional hazard models to estimate hazard ratios (HR) for TNFi discontinuation according to smoking status. In analyses of cause-specific discontinuation, competing risk events were considered as censoring, using inverse-probability weights.
A total of 758 participants were included in the analysis (66% male, mean age 45 years), providing 954 patient-years of follow-up. TNFi was discontinued in 174 (23%) patients, among whom 26% stopped due to infections, 20% due to other adverse events and 44% due to inefficacy or other reasons. Thirty-four percent were current smokers and 30% ex-smokers. Compared to never smokers, current smokers' risk of TNFi discontinuation was HR 0.79 (95%CI 0.53 to 1.20) and ex-smokers HR 0.68 (95%CI 0.45 to 1.04). Our data did not show evidence that current smoking influenced discontinuation due to infections (HR 0.79, 95%CI 0.40 to 1.54), other adverse events (HR 0.86, 95%CI 0.41 to 1.78) or inefficacy/other causes (HR 1.44, 95%CI 0.86 to 2.41).
Baseline smoking status did not impact TNFi discontinuation in this UK cohort of axSpA participants.
吸烟对 TNF 抑制剂(TNFi)治疗的影响尚不清楚。我们研究了吸烟对轴性脊柱关节炎(axSpA)患者全因和特定原因 TNFi 停药的影响。
我们使用英国风湿病学会生物制剂登记处用于强直性脊柱炎(BSRBR-AS)的纵向数据。符合 ASAS 轴性 SpA 标准、开始使用首次 TNFi 的患者有资格进行分析。使用逆概率权重来平衡基线疾病严重程度和其他混杂因素的差异。我们使用边缘结构 Cox 比例风险模型根据吸烟状况估计 TNFi 停药的危险比(HR)。在特定原因停药的分析中,将竞争风险事件视为截尾,使用逆概率权重。
共纳入 758 名患者(66%为男性,平均年龄 45 岁),随访 954 患者-年。174 名(23%)患者停用 TNFi,其中 26%因感染停药,20%因其他不良事件停药,44%因疗效不佳或其他原因停药。34%为当前吸烟者,30%为曾吸烟者。与从不吸烟者相比,当前吸烟者 TNFi 停药的风险比(HR)为 0.79(95%CI 0.53 至 1.20),曾吸烟者 HR 为 0.68(95%CI 0.45 至 1.04)。我们的数据没有证据表明当前吸烟会影响因感染(HR 0.79,95%CI 0.40 至 1.54)、其他不良事件(HR 0.86,95%CI 0.41 至 1.78)或疗效不佳/其他原因(HR 1.44,95%CI 0.86 至 2.41)而停药。
在这项英国 axSpA 参与者队列研究中,基线吸烟状况并未影响 TNFi 的停药。