Bechman Katie, Russell Mark D, Biddle Kathryn, Gibson Mark, Adas Maryam, Yang Zijing, Patel Samir, Dregan Alex, Walsh Sarah, Brex Peter, Patel Amit, Myall Katherine J, Norton Sam, Birring Surinder S, Galloway James
Centre for Rheumatic Diseases, Department of Inflammation Biology, King's College London, London, UK.
Department of Dermatology, King's College Hospital, London, UK.
Lancet Reg Health Eur. 2025 Apr 4;53:101283. doi: 10.1016/j.lanepe.2025.101283. eCollection 2025 Jun.
The epidemiology of sarcoidosis in England is largely uncharted, with no population-level prevalence data and outdated incidence and mortality estimates. Our objective was to investigate contemporary trends in incidence, prevalence, and mortality.
This cohort study used primary care data from the UK Clinical Practice Research Datalink (CPRD), linked to secondary-care and national death registration. Patients aged ≥18 with sarcoidosis were identified using primary care codes. Age-and-sex standardised incidence and prevalence were calculated. Standardised mortality ratios (SMRs) compared mortality with the general population. A matched non-sarcoidosis cohort was constructed within CPRD, and Poisson regression compared all-cause mortality between incident cases and controls.
Between 2003 and 2023, 18,554 incident sarcoidosis patients were identified. The age- and sex-standardised incidence per 100,000 person-years increased from 6.65 in 2003 to 7.73 in 2023, with the most pronounced rise occurring between 2010 and 2016. Incidence rose notably among males and those over 60-year-olds. Sarcoidosis prevalence increased from 167 to 230 per 100,000 individuals. The age-and-sex standardised all-cause mortality rate was 12.2 per 1000 patients in 2023. Elevated mortality was observed in males [SMR: 1.8 (1.7-1.8)] and females [SMR: 2.1(2.0-2.2)], particularly in those aged 30-70 years old. Regression models indicated higher all-cause mortality in the incident sarcoidosis cohort compared to controls [adjusted mortality rate ratio 1.36 (95% CI 1.27-1.44)].
Sarcoidosis incidence has increased during the study period, with shifts in age-and-sex distribution and excess mortality risk. Recognising this burden is key to refining healthcare policies, optimising resources and improving patient outcomes.
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英国结节病的流行病学情况在很大程度上尚不明确,缺乏人群层面的患病率数据,发病率和死亡率估计也已过时。我们的目标是调查发病率、患病率和死亡率的当代趋势。
这项队列研究使用了来自英国临床实践研究数据链(CPRD)的初级保健数据,并与二级保健和国家死亡登记数据相链接。使用初级保健编码识别年龄≥18岁的结节病患者。计算年龄和性别标准化发病率和患病率。标准化死亡比(SMR)将死亡率与一般人群进行比较。在CPRD中构建了一个匹配的非结节病队列,并通过泊松回归比较了新发病例和对照之间的全因死亡率。
2003年至2023年期间,共识别出18554例新发性结节病患者。每10万人年的年龄和性别标准化发病率从2003年的6.65上升至2023年的7.73,最显著的上升发生在2010年至2016年之间。男性和60岁以上人群的发病率显著上升。结节病患病率从每10万人中的167例增加到230例。2023年,年龄和性别标准化全因死亡率为每1000例患者12.2例。男性[SMR:1.8(1.7 - 1.8)]和女性[SMR:2.1(2.0 - 2.2)]的死亡率升高,特别是在30 - 70岁的人群中。回归模型表明,与对照组相比,新发性结节病队列的全因死亡率更高[调整后死亡率比1.36(95% CI 1.27 - 1.44)]。
在研究期间,结节病发病率有所增加,年龄和性别分布发生变化,且存在额外的死亡风险。认识到这一负担是完善医疗政策、优化资源和改善患者结局的关键。
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