Arthritis Research UK Primary Care Centre, Research Institute for Primary Care & Health Sciences, Keele University, Staffordshire, ST5 5BG, UK.
Haywood Academic Rheumatology Centre, Staffordshire and Stoke-on-Trent Partnership Trust, Stoke-on-Trent, UK.
Osteoporos Int. 2018 Jul;29(7):1659-1664. doi: 10.1007/s00198-018-4491-z. Epub 2018 Mar 24.
This study aimed to examine fracture risk in patients with late-onset psoriasis. A cohort study was conducted using primary care records from the Clinical Practice Research Datalink. Psoriasis patients had a 10% increased risk of fracture compared to matched controls (hazard ratio (HR) = 1.10; 95% confidence interval (CI) 1.04, 1.16).
This study aimed to examine fracture risk in patients with late-onset psoriasis and investigate the effect of methotrexate on fracture risk.
A cohort study was conducted using primary care records from the UK-based Clinical Practice Research Datalink. Individuals aged 40 years and over, with incident (new onset) diagnoses of psoriasis, were identified from 1990 to 2004 and followed up until 2015. For each exposed individual, up to four age-, gender-, and practice-matched controls were randomly selected. Incidence rates of fragility fracture (hip, vertebral, spine, radius or unspecified site) per 10,000 person-years were calculated and hazard rates were compared to the unexposed using Cox regression models. The risk of fracture was also estimated, within the exposed group for patients receiving/not receiving methotrexate.
Twenty-four thousand two hundred nineteen patients with psoriasis and 94,820 controls were identified. The absolute rate of fracture in psoriasis patients was 58 per 10,000 person-years (95% CI 55, 61) and 53 per 10,000 person-years in the matched controls (CI 52, 54). Psoriasis patients had a 10% increased risk of fracture compared to their matched controls (HR = 1.10; 95% CI 1.04, 1.16). Methotrexate use was not associated with increased risk (HR = 0.91; 95% CI 0.72, 1.15).
Identifying additional clinical factors associated with increased fracture risk is important in improving fracture risk stratification. Further work is needed to determine the relationship between age of onset of psoriasis and fracture risk, explore causative explanations, and identify if existing fracture risk stratification tools underestimate fracture risk in patients with psoriasis.
本研究旨在探讨晚发性银屑病患者的骨折风险,并研究甲氨蝶呤对骨折风险的影响。
采用英国临床实践研究数据链中的初级保健记录进行队列研究。1990 年至 2004 年间,确定了年龄在 40 岁及以上、新发(新发病例)银屑病诊断的个体,并随访至 2015 年。对于每个暴露个体,随机选择最多 4 名年龄、性别和实践匹配的对照者。每 10000 人年的脆性骨折(髋部、椎体、脊柱、桡骨或未指定部位)发生率计算,并使用 Cox 回归模型比较暴露组与未暴露组的危险率。还在接受/未接受甲氨蝶呤的暴露组内估计了骨折风险。
确定了 24219 例银屑病患者和 94820 例对照者。银屑病患者的骨折绝对发生率为 58/10000 人年(95%CI 55,61),匹配对照者为 53/10000 人年(CI 52,54)。与匹配对照组相比,银屑病患者骨折风险增加 10%(HR=1.10;95%CI 1.04,1.16)。甲氨蝶呤的使用与风险增加无关(HR=0.91;95%CI 0.72,1.15)。
确定与骨折风险增加相关的其他临床因素对于改善骨折风险分层很重要。需要进一步研究以确定银屑病发病年龄与骨折风险之间的关系,探讨因果关系,并确定现有的骨折风险分层工具是否低估了银屑病患者的骨折风险。