Luque C A, Rey J A
Department of Pharmacy Practice, College of Pharmacy, Nova Southeastern University, Fort Lauderdale, FL 33328, USA.
Ann Pharmacother. 1999 Sep;33(9):968-78. doi: 10.1345/aph.18319.
To review the pharmacology, pharmacokinetics, efficacy data, adverse effects, and drug interactions of sibutramine as a treatment for obesity.
English-language clinical studies, abstracts, and review articles were identified using MEDLINE, EMBASE, and a manual search from January 1980 through December 1998. References were also obtained from the reference section of published articles.
All articles identified were evaluated for possible inclusion in this review. Evaluative and comparative data from prospective, open-label, double-blind, and controlled studies were reviewed.
Sibutramine is a serotonin-norepinephrine reuptake-inhibitor effective in the treatment of obesity. It does not act as a releasing agent of these neurotransmitters. Sibutramine undergoes extensive metabolism in the liver via CYP3A4, forming two pharmacologically active metabolites. This agent has demonstrated efficacy superior to placebo in reducing weight when used as part of an integrated regimen involving behavior modification, physical activity, and a reduced-calorie intake. The most frequently reported adverse effects include dry mouth, anorexia, headache, insomnia, and constipation. Sibutramine has also been shown to substantially increase blood pressure and heart rate in some patients.
Based on anorectic efficacy data, sibutramine, a serotonin-norepinephrine reuptake-inhibitor, is a viable therapeutic option for the treatment of obesity. Recommended candidates for this medication are patients with a body mass index (BMI) > or = 30 kg/m2 without concomitant risk factors or patients with a BMI > or = 27 kg/m2 with concomitant risk factors. Sibutramine should be used with caution in patients with a history of hypertension and should not be used in those with uncontrolled hypertension and concomitant cardiovascular disease. Further studies need to be conducted in order to identify long-term outcomes beyond one year.
综述西布曲明治疗肥胖症的药理学、药代动力学、疗效数据、不良反应及药物相互作用。
通过检索1980年1月至1998年12月期间的MEDLINE、EMBASE并进行手工检索,确定英文临床研究、摘要及综述文章。还从已发表文章的参考文献部分获取相关文献。
对所有检索到的文章进行评估,以确定是否可能纳入本综述。对前瞻性、开放标签、双盲及对照研究的评估性和比较性数据进行了综述。
西布曲明是一种5-羟色胺-去甲肾上腺素再摄取抑制剂,对治疗肥胖症有效。它并非这些神经递质的释放剂。西布曲明在肝脏中通过CYP3A4进行广泛代谢,形成两种具有药理活性的代谢产物。当作为包括行为矫正、体育活动及减少热量摄入的综合方案的一部分使用时,该药物在减轻体重方面已显示出优于安慰剂的疗效。最常报告的不良反应包括口干、厌食、头痛、失眠及便秘。在一些患者中,西布曲明还显示会大幅升高血压及心率。
基于食欲抑制疗效数据,5-羟色胺-去甲肾上腺素再摄取抑制剂西布曲明是治疗肥胖症的一种可行治疗选择。推荐使用此药物的患者为体重指数(BMI)≥30 kg/m²且无并发危险因素的患者,或BMI≥27 kg/m²且有并发危险因素的患者。有高血压病史的患者应谨慎使用西布曲明,未控制的高血压患者及并发心血管疾病的患者不应使用。需要进行进一步研究以确定超过一年的长期疗效。