Torii Haruki, Shimizu Rumiko, Tanizaki Yuriko, Omiya Yurina, Yamamoto Miwa, Kamiike Sayaka, Yasuda Daisuke, Hiraoka Yoshinori, Hashida Tohru, Kume Noriaki
Division of Clinical Pharmacy, Faculty of Pharmaceutical Sciences, Kobe Gakuin University.
Department of Pharmacy, Kobe City Medical Center General Hospital.
Biol Pharm Bull. 2018;41(12):1778-1790. doi: 10.1248/bpb.b18-00411.
Melatonin has been suggested to play important roles in lipid metabolism as well as circadian rhythm; however, very few studies explored the effects of ramelteon, a selective melatonin receptor agonist, on serum lipid profiles. In this study effects of ramelteon on serum lipid profiles were explored, comparing to those of other sleep-promoting drugs including benzodiazepines and non-benzodiazepines, in patients with insomnia. We retrospectively reviewed medical charts of outpatients who were treated with ramelteon (8 mg/d) or other sleep-promoting drugs for no less than 8 weeks during the period between October 1st, 2011 and September 30th, 2014, and compared the changes in serum lipid profiles between the two groups. Patients with regular dialysis or malignant diseases treated with cytotoxic anti-cancer drugs, or whose lipid-lowering drugs were altered during the study period, were excluded. Among 365 or 855 outpatients treated with ramelteon or other sleep-promoting drugs, 35 or 46 patients, respectively, had complete serum low-density lipoprotein cholesterol (LDL-C) or non-high-density lipoprotein cholesterol (non-HDL-C) data. Serum LDL-C was significantly reduced from 103.1±4.4 to 94.6±4.2 mg/dL (8.2% reduction, p<0.05, n=31) in the ramelteon group, and was not significantly changed (p=0.23, n=40) in the other sleep-promoting drug group. Non-HDL-C was significantly decreased from 138.8±6.0 to 130.6±4.9 mg/dL (5.9% reduction, p<0.05, n=32) in the ramelteon group, and was not significantly altered (p=0.29, n=42) in the other sleep-promoting drug group. Ramelteon, but not other sleep-promoting drugs, specifically lowers serum LDL-C and non-HDL-C levels.
褪黑素被认为在脂质代谢以及昼夜节律中发挥重要作用;然而,很少有研究探讨选择性褪黑素受体激动剂雷美替胺对血清脂质谱的影响。在本研究中,我们探讨了雷美替胺对失眠患者血清脂质谱的影响,并与包括苯二氮䓬类和非苯二氮䓬类在内的其他促眠药物进行了比较。我们回顾性分析了2011年10月1日至2014年9月30日期间接受雷美替胺(8毫克/天)或其他促眠药物治疗不少于8周的门诊患者的病历,并比较了两组患者血清脂质谱的变化。排除接受定期透析或使用细胞毒性抗癌药物治疗的恶性疾病患者,或在研究期间改变降脂药物的患者。在365例接受雷美替胺治疗或855例接受其他促眠药物治疗的门诊患者中,分别有35例或46例患者有完整的血清低密度脂蛋白胆固醇(LDL-C)或非高密度脂蛋白胆固醇(非HDL-C)数据。雷美替胺组血清LDL-C从103.1±4.4显著降至94.6±4.2毫克/分升(降低8.2%,p<0.05,n=31),而其他促眠药物组无显著变化(p=0.23,n=40)。雷美替胺组非HDL-C从138.8±6.0显著降至130.6±4.9毫克/分升(降低5.9%,p<0.05,n=32),而其他促眠药物组无显著改变(p=0.29,n=42)。雷美替胺能特异性降低血清LDL-C和非HDL-C水平,而其他促眠药物则不能。