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HMG CoA还原酶抑制剂对慢性肺移植功能障碍发展的影响。

Effect of HMG CoA reductase inhibitors on the development of chronic lung allograft dysfunction.

作者信息

Szczepanik Amanda, Hulbert Amanda, Lee Hui-Jie, Benedetti Clark, Snyder Laurie, Byrns Jennifer

机构信息

Department of Pharmacy, Duke University Hospital, Durham, NC, USA.

Department of Biostatistics and Bioinformatics, Duke University Hospital, Durham, NC, USA.

出版信息

Clin Transplant. 2018 Jan;32(1). doi: 10.1111/ctr.13156. Epub 2017 Dec 8.

Abstract

Lung transplant recipients (LRs) have a reduced median 5-year survival of approximately 55% primarily due to chronic lung allograft dysfunction (CLAD). Statins have anti-inflammatory and immunomodulatory effects that may facilitate CLAD prevention. This study sought to evaluate statin effect on CLAD development. Adult bilateral LRs from January 2004 to October 2013 were included. Statin group included recipients with early statin use and continued for minimum 6 months. Propensity score matching was performed for age, gender, and native lung disease to select matched nonstatin group. Competing risk approach was used to evaluate statin effect on CLAD development at 3 years while controlling for acute rejection and CMV pneumonitis. A total of 130 patients were included in each group. CLAD cumulative incidence at 3 years for statin and nonstatin groups was 20.6% (CI: 11.8%-33.5%) and 22.4% (CI: 12.2%-27.3%). Statin use was not associated with a decreased risk of CLAD (subdistribution hazard ratio [SHR]: 0.93, 95% CI: 0.55-1.59, P = .80) but was associated with a decreased risk of death (SHR: 0.45, CI: 0.22-0.90, P = .024). At 3 years, patient survival was 81.7% in statin group and 68.3% in nonstatin group (P = .012). Statins did not significantly delay the time to development of CLAD in LR but did demonstrate a benefit in patient survival.

摘要

肺移植受者(LRs)的5年中位生存率约为55%,有所降低,主要原因是慢性肺移植功能障碍(CLAD)。他汀类药物具有抗炎和免疫调节作用,可能有助于预防CLAD。本研究旨在评估他汀类药物对CLAD发生发展的影响。纳入了2004年1月至2013年10月的成年双侧LRs。他汀类药物组包括早期使用他汀类药物且持续至少6个月的受者。对年龄、性别和原生肺部疾病进行倾向评分匹配,以选择匹配的非他汀类药物组。采用竞争风险方法评估他汀类药物在3年时对CLAD发生发展的影响,同时控制急性排斥反应和巨细胞病毒性肺炎。每组共纳入130例患者。他汀类药物组和非他汀类药物组3年时CLAD的累积发病率分别为20.6%(CI:11.8%-33.5%)和22.4%(CI:12.2%-27.3%)。使用他汀类药物与CLAD风险降低无关(亚分布风险比[SHR]:0.93,95%CI:0.55-1.59,P = 0.80),但与死亡风险降低有关(SHR:0.45,CI:0.22-0.90,P = 0.024)。3年时,他汀类药物组的患者生存率为81.7%,非他汀类药物组为68.3%(P = 0.012)。他汀类药物并未显著延迟LRs中CLAD的发生时间,但确实显示出对患者生存有益。

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