Δημοσίευση

Aggressive statin treatment, very low serum cholesterol levels and haemorrhagic stroke: is there an association?

ΤίτλοςAggressive statin treatment, very low serum cholesterol levels and haemorrhagic stroke: is there an association?
Publication TypeJournal Article
Year of Publication2010
AuthorsAthyros, V. G., Tziomalos K., Karagiannis A., Wierzbicki A. S., & Mikhailidis D. P.
JournalCurr Opin Cardiol
Volume25
Issue4
Pagination406-10
Date Published2010 Jul
ISSN1531-7080
Λέξεις κλειδιάAnticholesteremic Agents, Brain Ischemia, Cholesterol, LDL, Coronary Artery Disease, Heptanoic Acids, Humans, Hydroxymethylglutaryl-CoA Reductase Inhibitors, Hypercholesterolemia, Intracranial Hemorrhages, Primary Prevention, Pyrroles, Risk Factors, Secondary Prevention, Stroke
Abstract

PURPOSE OF REVIEW: To assess the potential association between haemorrhagic stroke and achieving very low serum cholesterol levels with aggressive statin treatment.RECENT FINDINGS: The Stroke Prevention by Aggressive Reduction in Cholesterol Levels (SPARCL) study showed a reduction in both fatal and nonfatal stroke but an increase in the risk for haemorrhagic stroke during high-dose atorvastatin treatment. However, post-hoc analyses of this trial showed that this increased risk is primarily observed in elderly men with a history of haemorrhagic stroke. In addition, there was no relationship between baseline or on-treatment low-density lipoprotein cholesterol (LDL-C) levels and haemorrhagic stroke.SUMMARY: Existing data suggest that low LDL-C levels during intensive statin treatment are not associated with an increased risk for haemorrhagic stroke, except in patients with a history of intracerebral haemorrhage. In patients with a history of ischaemic stroke, intensive statin treatment substantially reduces the risk for both recurrent ischaemic stroke and for coronary heart disease (CHD) events. Any possible excess of haemorrhagic stroke is greatly outweighed by the protective effect against ischaemic stroke and CHD events.

DOI10.1097/HCO.0b013e3283393c1a
Alternate JournalCurr. Opin. Cardiol.
PubMed ID20375883

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