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Hypercholesterolemia, HMG-CoA reductase inhibitors, and risk of intracerebral hemorrhage: a case-control study
Daniel Woo1, Brett M Kissela, Jane C Khoury
1Department of Neurology and the Neuroscience Institute, University of Cincinnati, College of Medicine, 231 Bethesda Avenue ML 0525, Cincinnati, Ohio 45267-0525, USA. Daniel.woo@uc.edu
Insights
Hypercholesterolemia, or high cholesterol, was linked to a reduced risk of intracerebral hemorrhage (ICH). Statin use did not increase ICH risk in this population-based study.
Area of Science:
- Neurology
- Cardiovascular Science
- Epidemiology
Background:
- Intracerebral hemorrhage (ICH) risk factors are crucial for prevention.
- Previous studies suggest a link between low cholesterol and ICH.
- The role of high cholesterol and statin use in ICH remains unclear.
Purpose of the Study:
- To investigate the association between hypercholesterolemia and intracerebral hemorrhage (ICH).
- To determine if HMG-CoA reductase inhibitor (statin) use is associated with ICH risk.
- To test the hypothesis that hypercholesterolemia or statin use, or both, are independent risk factors for ICH.
Main Methods:
- Population-based case-control study design.
- Conditional stepwise logistic regression modeling used for analysis.
- Inclusion of 188 ICH cases and 366 matched controls.
Main Results:
- Hypercholesterolemia was less common in ICH cases (25%) than controls (38%).
- Statin use was also less frequent in ICH cases (9%) compared to controls (17%).
- Hypercholesterolemia combined with statin use showed a significantly reduced risk of ICH (OR=0.30).
Conclusions:
- Hypercholesterolemia is associated with a lower risk of intracerebral hemorrhage.
- Widespread statin use in the population was not found to increase ICH risk.
- Further research is needed to clarify the relationship between statin-induced cholesterol reduction and ICH risk.
Background And Purpose:
Several studies have demonstrated an association between hypocholesterolemia and intracerebral hemorrhage (ICH). We tested the hypothesis that hypercholesterolemia or use of HMG-CoA reductase inhibitors (statin) agents, or both, are associated with ICH.
Methods:
This study was part of the preplanned midway analysis of an ongoing, population-based, case-control study of the genetic and environmental risk factors of hemorrhagic stroke. Conditional stepwise logistic regression modeling was used to determine if self-reported hypercholesterolemia or statin use, or both, were independent risk factors for ICH.
Results:
Between December 1, 1997, and June 30, 2000, 188 cases of ICH and 366 age-, race-, and gender-matched controls were enrolled. Hypercholesterolemia and statin use were less common among cases than controls: 25% versus 38% (P=0.003) and 9% versus 17% (P=0.03), respectively. Hypercholesterolemia with statin use was associated with less risk of ICH (OR=0.30; P=0.0008) in multivariable analysis after controlling for alcohol use, hypertension, previous stroke, first-degree relative with ICH, education level, and apolipoprotein E alleles.
Conclusions:
Hypercholesterolemia was associated with a lower risk of ICH. We have not found an increased risk of ICH with the widespread use of statins in our population. Given the lack of cholesterol levels in the current study, further studies are needed to determine if lower cholesterol levels secondary to statin use bear the same risk as low cholesterol levels for ICH.
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