Simvastatin Improves Neutrophil Function and Clinical Outcomes in Pneumonia A Pilot Randomized Controlled Clinical Trial

被引:71
|
作者
Sapey, Elizabeth [1 ]
Patel, Jaimin M. [1 ]
Greenwood, Hannah [1 ]
Walton, Georgia M. [1 ]
Grudzinska, Frances [1 ]
Parekh, Dhruv [1 ]
Mahida, Rahul Y. [1 ]
Dancer, Rachel C. A. [1 ]
Lugg, Sebastian T. [1 ]
Howells, Philip A. [1 ]
Hazeldine, Jon [1 ]
Newby, Paul [1 ]
Scott, Aaron [1 ]
Nightingale, Peter [2 ]
Hill, Adam T. [3 ]
Thickett, David R. [1 ]
机构
[1] Univ Birmingham, Queen Elizabeth Hosp Birmingham, Inst Inflammat & Ageing, Birmingham Acute Care Res Grp, Mindelsohn Way, Birmingham B12 2GW, W Midlands, England
[2] Univ Hosp Birmingham, Natl Hlth Serv Fdn Trust, Birmingham, W Midlands, England
[3] Royal Infirm Edinburgh NHS Trust, Dept Resp Med, Med Res Council, Ctr Inflammat Res, Edinburgh, Midlothian, Scotland
基金
英国医学研究理事会;
关键词
innate immunity; sepsis; pneumonia; statin; elderly care; COMMUNITY-ACQUIRED PNEUMONIA; EXTRACELLULAR TRAPS; STATIN THERAPY; FREE SURVIVAL; SEPTIC SHOCK; SEPSIS; MANAGEMENT; MORTALITY; CLARITHROMYCIN; POPULATION;
D O I
10.1164/rccm.201812-2328OC
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Rationale: Population studies suggest improved sepsis outcomes with statins, but the results of randomized controlled trials in patients with sepsis and organ dysfunction in critical care settings have broadly been negative. In vitro data suggest that statins modulate age-related neutrophil functions, improving neutrophil responses to infection, but only in older patients and at high doses. Objectives: To determine if high-dose simvastatin improves neutrophil functions and is safe and tolerated in hospitalized older adults with community-acquired pneumonia with sepsis (CAP+S) not admitted to critical care. Methods: We conducted a randomized, double-blind, placebo-controlled pilot study of simvastatin 80 mg or placebo for 7 days for patients with CAP+S aged 55 years or older admitted to a secondary care hospital. The Day 4 primary endpoint was change in neutrophil extracellular trap formation (NETosis). Day 4 secondary endpoints included neutrophil chemotaxis, safety and tolerability, Sequential Organ Failure Assessment score, mortality, readmission, and markers of tissue degradation/inflammation. Measurements and Main Results: Four days of simvastatin adjuvant therapy in patients with CAP+S was associated with improvements in systemic neutrophil function (NETosis and chemotaxis), a reduction in systemic neutrophil elastase burden, and improved Sequential Organ Failure Assessment scores compared with placebo. A post hoc analysis demonstrated that simvastatin therapy was associated with improved hospitalization-free survival compared with placebo. Simvastatin was well tolerated in this elderly and multimorbid patient group with common coprescription of macrolide antibiotics. Conclusions: This pilot study supports high-dose simvastatin as an adjuvant therapy for CAP + Sin an older and milder disease cohort than assessed previously. A definitive multicenter study is now warranted in this population to assess the likelihood of benefit and harm.
引用
收藏
页码:1282 / 1293
页数:12
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