Faculty of Pharmaceutical Sciences, Teikyo Heisei University, 4-21-2, Nakano, Nakano-ku, Tokyo, 164-8530, Japan.
Faculty of Pharmaceutical Sciences, Teikyo Heisei University, 4-21-2, Nakano, Nakano-ku, Tokyo, 164-8530, Japan.
Pulm Pharmacol Ther. 2018 Jun;50:88-92. doi: 10.1016/j.pupt.2018.04.003. Epub 2018 Apr 5.
This study aimed to determine the frequency and risk factors for statin-induced interstitial pneumonia (IP).
We conducted a retrospective cohort study using a large Japanese health insurance claims database. We determined the statin-induced IP incidence in patients treated with statins for hyperlipidemia (n = 194,814) with 12-month screening and 3-month observation periods. Statin-induced IP was defined as: (1) diagnosis with IP (ICD-10 codes: J70.2-J70.4, J84.1, and J84.9) within 3 months after starting statins; (2) steroid administration starts after starting statins; (3) undergoing laboratory tests for sialylated carbohydrate antigen Krebs von den Lungen-6 or pulmonary surfactant protein-D; and (4) undergoing high-resolution computed tomography (HRCT). Risk factors for IP were defined as presence of lung-related diseases including lung cancer and IP (ICD-10 codes: A15-16, J12-18, 43-46, 60-70, and 80-99) that were known to the risk factors inducing IP during the screening period.
Cohort 1 had no IP-inducing risk factors; based on lung-related disease history, we identified 4 cases (male/female: 0/4, 61 ± 2.5 years) and 46,574 controls (male/female: 29,677/16,897, 51.3 ± 9.5 years). In cohort 1, all cases were female and average age was older than that of controls (p < 0.01). Cohort 2 had lung-related disease history that were known to the risk factors inducing IP; we identified 25 cases (male/female: 11/14, 52.8 ± 11.3 years) and 4005 controls (male/female: 2305/1,700, 51.0 ± 10.4 years). IP incidence was higher in cohort 2 than in cohort 1, who had no IP risk factors (0.6% vs. 0.009%, p < 0.01). The adjusted case/control odds ratio in cohort 2 was 3.8 (1.7-8.5) in patients who had taken atorvastatin and 2.5 (1.1 - 5.6) with diabetes mellitus.
We clarified the incidence (0.009% and 0.6% in patients without and with lung-related disease history that were known to the risk factors inducing IP, respectively) and risk factors for statin-induced IP (elderly females without lung-related disease history; atorvastatin administration in those with lung-related disease history). Physicians and pharmacists should pay close attention to female patients starting atorvastatin, especially those with past histories of lung-related diseases that were known to the risk factors for IP.
本研究旨在确定他汀类药物诱导的间质性肺炎(IP)的频率和危险因素。
我们使用大型日本健康保险索赔数据库进行了回顾性队列研究。我们确定了在接受他汀类药物治疗高脂血症的患者(n=194814)中,经过 12 个月的筛查和 3 个月的观察期,他汀类药物诱导的 IP 的发生率。他汀类药物诱导的 IP 定义为:(1)在开始使用他汀类药物后 3 个月内诊断为 IP(ICD-10 代码:J70.2-J70.4、J84.1 和 J84.9);(2)开始使用皮质类固醇;(3)进行唾液酸化碳水化合物抗原 Krebs von den Lungen-6 或肺表面活性蛋白-D 的实验室检测;和(4)进行高分辨率计算机断层扫描(HRCT)。IP 的危险因素定义为存在与肺部相关的疾病,包括肺癌和 IP(ICD-10 代码:A15-16、J12-18、43-46、60-70 和 80-99),这些疾病在筛查期间已知会引起 IP。
队列 1 没有 IP 诱导的危险因素;根据肺部相关疾病史,我们确定了 4 例(男/女:0/4,61±2.5 岁)和 46574 例对照(男/女:29677/16897,51.3±9.5 岁)。在队列 1 中,所有病例均为女性,平均年龄大于对照组(p<0.01)。队列 2 有肺部相关疾病史,这些疾病与已知的 IP 危险因素有关;我们确定了 25 例(男/女:11/14,52.8±11.3 岁)和 4005 例对照(男/女:2305/1700,51.0±10.4 岁)。与无 IP 危险因素的队列 1 相比,队列 2 的 IP 发生率更高(0.6% vs. 0.009%,p<0.01)。队列 2 中使用阿托伐他汀的病例/对照比值比为 3.8(1.7-8.5),患有糖尿病的比值比为 2.5(1.1-5.6)。
我们阐明了他汀类药物诱导的 IP 的发生率(无肺部相关疾病史的患者为 0.009%,有肺部相关疾病史且已知与 IP 危险因素相关的患者为 0.6%)和危险因素(无肺部相关疾病史的老年女性;有肺部相关疾病史且正在服用阿托伐他汀的患者)。医生和药剂师应密切关注开始使用阿托伐他汀的女性患者,特别是那些有肺部相关疾病史且已知与 IP 危险因素相关的患者。