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Statin Therapy and the Development of Cerebral Amyloid Angiopathy--A Rodent in Vivo Approach.
Reuter, Björn; Venus, Alexander; Grudzenski, Saskia; Heiler, Patrick; Schad, Lothar; Staufenbiel, Matthias; Hennerici, Michael G; Fatar, Marc.
Afiliação
  • Reuter B; Department of Neurology and Neurophysiology, University Freiburg, 79106 Freiburg, Germany. bjoern.reuter@uniklinik-freiburg.de.
  • Venus A; Department of Neurology, Universitätsmedizin Mannheim, Heidelberg University, 68167 Mannheim, Germany. venus.alexander@gmx.de.
  • Grudzenski S; Department of Neurology, Universitätsmedizin Mannheim, Heidelberg University, 68167 Mannheim, Germany. grudzenski@neuro.ma.uni-heidelberg.de.
  • Heiler P; Computer Assisted Clinical Medicine, Heidelberg University, 68167 Mannheim, Germany. patrick.heiler@siemens.com.
  • Schad L; Computer Assisted Clinical Medicine, Heidelberg University, 68167 Mannheim, Germany. lothar.schad@medma.uni-heidelberg.de.
  • Staufenbiel M; Nervous System Department, Novartis Institutes for Biomedical Research, 4002 Basel, Switzerland. staufenbiel.m@gmail.com.
  • Hennerici MG; Department of Neurology, Universitätsmedizin Mannheim, Heidelberg University, 68167 Mannheim, Germany. m.g.hennerici@eurostroke.eu.
  • Fatar M; Department of Neurology, Universitätsmedizin Mannheim, Heidelberg University, 68167 Mannheim, Germany. fatar@neuro.ma.uni-heidelberg.de.
Int J Mol Sci ; 17(1)2016 Jan 19.
Article em En | MEDLINE | ID: mdl-26797603
BACKGROUND: Cerebral amyloid angiopathy (CAA) is characterized by vascular deposition of amyloid ß (Aß) with a higher incidence of cerebral microbleeds (cMBs) and spontaneous hemorrhage. Since statins are known for their benefit in vascular disease we tested for the effect on CAA. METHODS: APP23-transgenic mice received atorvastatin-supplemented food starting at the age of eight months (n = 13), 12 months (n = 7), and 16 months (n = 6), respectively. Controls (n = 16) received standard food only. At 24 months of age cMBs were determined with T2*-weighted 9.4T magnetic resonance imaging and graded by size. RESULTS: Control mice displayed an average of 35 ± 18.5 cMBs (mean ± standard deviation), compared to 29.3 ± 9.8 in mice with eight months (p = 0.49), 24.9 ± 21.3 with 12 months (p = 0.26), and 27.8 ± 15.4 with 16 months of atorvastatin treatment (p = 0.27). In combined analysis treated mice showed lower absolute numbers (27.4 ± 15.6, p = 0.16) compared to controls and also after adjustment for cMB size (p = 0.13). CONCLUSION: Despite to a non-significant trend towards fewer cMBs our results failed to provide evidence for beneficial effects of long-term atorvastatin treatment in the APP23-transgenic mouse model of CAA. A higher risk for bleeding complications was not observed.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hemorragia Cerebral / Angiopatia Amiloide Cerebral / Atorvastatina / Anticolesterolemiantes Limite: Animals Idioma: En Revista: Int J Mol Sci Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hemorragia Cerebral / Angiopatia Amiloide Cerebral / Atorvastatina / Anticolesterolemiantes Limite: Animals Idioma: En Revista: Int J Mol Sci Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Alemanha