Key result
Prior statin use fails to reduce AKI risk in community-acquired pneumonia.
Why the study?
Animal studies suggest statins may reduce risk of AKI and mortality in sepsis, but their association with pneumonia-induced AKI and mortality in humans is unclear.
Does statin use before hospitalization reduce the risk of acute kidney injury and 1-year mortality in patients hospitalized with community-acquired pneumonia?
Cohort (n=1,836)
Yes
Does statin use before hospitalization reduce the risk of acute kidney injury and 1-year mortality in patients hospitalized with community-acquired pneumonia?
Odds Ratio: 1.32 (95% CI 1.02–1.69)
p-value: p=0.05
In patients hospitalized with community-acquired pneumonia, prior statin use does not reduce the risk of developing acute kidney injury or significantly improve 1-year mortality among those who develop AKI.
Prior statin use was not linked to lower AKI risk in pneumonia; this Level 3 finding leaves open any causal effect and requires RCT confirmation.
BACKGROUND AND OBJECTIVES: Sepsis is a leading cause of AKI. Animal studies suggest that the pleiotropic effect of statins attenuates the risk for AKI and decreases mortality. This study examined whether statin use was associated with a lower risk for pneumonia-induced AKI and 1-year and cause-specific mortality in patients with AKI. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: Multicenter, prospective cohort study of 1836 patients hospitalized with community-acquired pneumonia. RESULTS: Baseline characteristics differed among statin users and nonusers. Of the 413 patients (22.5%) who received a statin before hospitalization, statin treatment, when adjusted for differences in age, severity of pneumonia, admission from nursing home, health insurance, and propensity for statin use, did not reduce the risk for AKI (odds ratio [OR], 1.32 [95% confidence interval (CI), 1.02-1.69]; P=0.05). Of patients with AKI (n=631), statin use was associated with a lower risk for death at 1 year (27.8% versus 38.8%; P=0.01), which was not significant when adjusted for differences in age, severity of pneumonia and AKI, use of mechanical ventilation, and propensity score (OR, 0.72 [95% CI, 0.50-1.06]; P=0.09). Among patients with AKI, cardiovascular disease accounted for one third of all deaths. CONCLUSIONS: In a large cohort of patients hospitalized with pneumonia, statins did not reduce the risk for AKI. Among patients with AKI, statin use was not associated with lower risk for death at 1 year. The higher risk for AKI observed among statin users may be due to indication bias.
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Murugan et al. (2012) conducted a cohort in Community-acquired pneumonia (n=1,836). Statin use vs. Nonusers was evaluated on Acute kidney injury (OR 1.32, 95% CI 1.02-1.69, p=0.05). Statin use prior to hospitalization for community-acquired pneumonia did not reduce the risk for acute kidney injury (OR 1.32; 95% CI 1.02-1.69; P=0.05).
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