Efficacy and Safety of Coadministration of Rosuvastatin , Ezetimibe , and Colestimide in Heterozygous Familial Hypercholesterolemia

Aggressive low-density lipoprotein (LDL) cholesterol-lowering therapy is important for high-risk patients. However, sparse data exist on the impact of combined aggressive LDL cholesterol-lowering therapy in familial hypercholesterolemia (FH), particularly on side effects to changes in plasma coenzym...

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Veröffentlicht in:The American journal of cardiology 2012-02, Vol.109 (3), p.364-369
Hauptverfasser: Kawashiri, Masa-aki, MD, Nohara, Atsushi, MD, Noguchi, Tohru, PhD, Tada, Hayato, MD, Nakanishi, Chiaki, MD, Mori, Mika, MD, Konno, Tetsuo, MD, Hayashi, Kenshi, MD, Fujino, Noboru, MD, Inazu, Akihiro, MD, Kobayashi, Junji, MD, Mabuchi, Hiroshi, MD, Yamagishi, Masakazu, MD
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Sprache:eng
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Zusammenfassung:Aggressive low-density lipoprotein (LDL) cholesterol-lowering therapy is important for high-risk patients. However, sparse data exist on the impact of combined aggressive LDL cholesterol-lowering therapy in familial hypercholesterolemia (FH), particularly on side effects to changes in plasma coenzyme Q10 and proprotein convertase subtilisin/kexin type 9 levels. We enrolled 17 Japanese patients with heterozygous FH (12 men, 63.9 ± 7.4 years old) with single LDL receptor gene mutations in a prospective open randomized study. Permitted maximum doses of rosuvastatin (20 mg/day), ezetimibe (10 mg/day), and granulated colestimide (3.62 g/day) were introduced sequentially. Serum levels of LDL cholesterol decreased significantly by −66.4% (p
ISSN:0002-9149
1879-1913
DOI:10.1016/j.amjcard.2011.09.019