TY - JOUR
T1 - Characteristics of lipid-lowering effects of pitavastatin according to a survey in Japan
AU - Sogou, Taiji
AU - Mashima, Keiichi
AU - Ohnishi, Nobuhiko
AU - Shinohata, Ryoko
AU - Suezawa, Chisato
AU - Ueeda, Masayuki
AU - Tominaga, Youkou
AU - Ohnishi, Hiromachi
AU - Kusachi, Shozo
AU - Nakatsu, Takaaki
AU - Takaishi, Atsushi
AU - Iwabu, Akihiro
AU - Uesugi, Tadaichi
PY - 2009/3/31
Y1 - 2009/3/31
N2 - Objectives: We examined the clinical characteristics of the efficacy of pitavastatin in connection with gender, age and low density lipoprotein (LDL) size. Patients and Methods: A total of 112 patients were analyzed: 61 de navo patients with hyperlipidemia and 51 patients with insufficient treatment of hyperlipidemia with another statin. Pitavastatin was administered at 1-4 mg a day depending on serum lipid levels. Results: In the 61 de novo patients, pitavastatin decreased total cholesterol (TC) and low density lipoprotein cholesterol (LDL-C) by 29.7 and 42.3%, respectively, without any adverse effects (TC, from 250.5 ± 37.0 to 174.8 ± 26.6 mg/dL; LDL-C, from 155.4 ± 39.8 to 87.4 ± 23.3 mg/dL). The lipid-lowering effects were not different between men and women and were observed throughout all age groups. In patients with insufficient treatment of hyperlipidemia with another statin, replacement with pitavastatin significantly decreased serum lipid levels (TC, from 230.3 ± 35.5 to 183.6 ± 21.6 mg/dL; LDL-C, from 138.4 ± 36.8 to 99.4 ± 27.2 mg/dL). Pitavastatin significantly increased LDL particle size by approximately 1% in both de novo patients and patients with pitavastatin replacement. Conclusions: The present study revealed that pitavastatin has potent lipid-lowering effects without gender and age-group differences, and significantly increased LDL particle size.
AB - Objectives: We examined the clinical characteristics of the efficacy of pitavastatin in connection with gender, age and low density lipoprotein (LDL) size. Patients and Methods: A total of 112 patients were analyzed: 61 de navo patients with hyperlipidemia and 51 patients with insufficient treatment of hyperlipidemia with another statin. Pitavastatin was administered at 1-4 mg a day depending on serum lipid levels. Results: In the 61 de novo patients, pitavastatin decreased total cholesterol (TC) and low density lipoprotein cholesterol (LDL-C) by 29.7 and 42.3%, respectively, without any adverse effects (TC, from 250.5 ± 37.0 to 174.8 ± 26.6 mg/dL; LDL-C, from 155.4 ± 39.8 to 87.4 ± 23.3 mg/dL). The lipid-lowering effects were not different between men and women and were observed throughout all age groups. In patients with insufficient treatment of hyperlipidemia with another statin, replacement with pitavastatin significantly decreased serum lipid levels (TC, from 230.3 ± 35.5 to 183.6 ± 21.6 mg/dL; LDL-C, from 138.4 ± 36.8 to 99.4 ± 27.2 mg/dL). Pitavastatin significantly increased LDL particle size by approximately 1% in both de novo patients and patients with pitavastatin replacement. Conclusions: The present study revealed that pitavastatin has potent lipid-lowering effects without gender and age-group differences, and significantly increased LDL particle size.
KW - Hyperlipidemia
KW - Low density lipoprotein size
KW - Pitavastatin
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M3 - Article
AN - SCOPUS:63049112415
SN - 0289-8020
VL - 30
SP - 189
EP - 198
JO - Therapeutic Research
JF - Therapeutic Research
IS - 2
ER -