Division of Rheumatology, Allergy and Immunology, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Clinical Epidemiology Unit, Boston University School of Medicine, Boston, Massachusetts, USA.
Ann Rheum Dis. 2017 Oct;76(10):1737-1742. doi: 10.1136/annrheumdis-2017-211253. Epub 2017 Jul 11.
Recent studies have shown an increase in both cardiovascular and all-cause mortality in ankylosing spondylitis (AS). We examined the potential survival benefit of statin use in AS within a general population context.
We performed an incident user cohort study with time-stratified propensity score matching using a UK general population database between 1 January 2000 and 31 December 2014. To account for potential confounders, we compared propensity score-matched cohorts of statin initiators and non-initiators using 1-year cohort accrual blocks. The variables used to create the propensity score model included disease duration, body mass index, lifestyle factors, comorbidities and medication use.
Using unmatched AS cohorts, statin initiators (n=1430) showed a 43% higher risk of mortality than non-initiators (n=1430) (HR=1.43; 95% CI 1.12 to 1.84). After propensity score matching, patients with AS who initiated statins (n=1108) had 96 deaths, and matched non-initiators (n=1108) had 134 deaths over a mean follow-up of 5.3 and 5.1 years, respectively. This corresponded to mortality rates of 16.5 and 23.8 per 1000 person-years (PY), respectively, resulting in an HR of 0.63 (95% CI 0.46 to 0.85) and an absolute mortality rate difference of 7.3 deaths per 1000 PY (95% CI 2.1 to 12.5).
This general population-based cohort study suggests that statin initiation is associated with a substantially lower risk of mortality among patients with AS. The magnitude of the inverse association appears to be larger than that observed in randomised trials of the general population and in population-based cohort studies of patients with rheumatoid arthritis.
最近的研究表明,强直性脊柱炎(AS)患者的心血管和全因死亡率均有所上升。我们在一般人群背景下研究了他汀类药物在 AS 中的潜在生存获益。
我们在 2000 年 1 月 1 日至 2014 年 12 月 31 日期间,使用英国一般人群数据库进行了一项以事件为基础的使用者队列研究,并进行了时间分层倾向评分匹配。为了考虑潜在的混杂因素,我们使用 1 年队列累积块比较了他汀类药物起始者和非起始者的倾向评分匹配队列。用于创建倾向评分模型的变量包括疾病持续时间、体重指数、生活方式因素、合并症和药物使用情况。
在未匹配的 AS 队列中,他汀类药物起始者(n=1430)的死亡率比非起始者(n=1430)高 43%(HR=1.43;95%CI 1.12 至 1.84)。在进行倾向评分匹配后,接受他汀类药物治疗的 AS 患者(n=1108)有 96 人死亡,匹配的非起始者(n=1108)有 134 人死亡,平均随访时间分别为 5.3 年和 5.1 年。这相当于死亡率分别为每 1000 人年 16.5 人和 23.8 人(每 1000 人年分别为 0.63(95%CI 0.46 至 0.85)和 0.73 人(95%CI 0.21 至 1.25),绝对死亡率差异为每 1000 人年 7.3 人。
这项基于一般人群的队列研究表明,他汀类药物的起始治疗与 AS 患者的死亡率显著降低相关。这种负相关的幅度似乎大于一般人群随机试验和类风湿关节炎患者基于人群的队列研究中观察到的幅度。