Neuropeptide Y5 receptor antagonism does not induce clinically meaningful weight loss in overweight and obese adults

被引:145
|
作者
Erondu, Ngozi
Gantz, Ira
Musser, Bret
Suryawanshi, Shailaja
Mallick, Madhuja
Addy, Carol
Cote, Josee
Bray, George
Fujioka, Ken
Bays, Harold
Hollander, Priscilla
Sanabria-Bohorquez, Sandra M.
Eng, WaiSi
Langstrom, Bengt
Hargreaves, Richard J.
Burns, H. Donald
Kanatani, Akio
Fukami, Takehiro
MacNeil, Douglas J.
Gottesdiener, Keith M.
Amatruda, John M.
Kaufman, Keith D.
Heymsfield, Steven B.
机构
[1] Merck & Co Inc, Rahway, NJ 07065 USA
[2] Merck & Co Inc, Boston, MA 02115 USA
[3] Pennington Biomed Res Ctr, Baton Rouge, LA 70808 USA
[4] Scripps Clin, San Diego, CA 92130 USA
[5] LMARC Res Ctr, Louisville, KY 40213 USA
[6] Baylor Univ, Med Ctr, Dallas, TX 75246 USA
[7] Merck & Co Inc, Imaging Res, West Point, PA 19486 USA
[8] Uppsala Univ, PET Ctr, S-75109 Uppsala, Sweden
[9] Banyu Pharmaceut Co Ltd, Tsukuba Res Inst, Tsukuba, Ibaraki, Japan
关键词
D O I
10.1016/j.cmet.2006.08.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Neuropeptide Y (NPY) is a potent orexigenic neuropeptide, and antagonism of NPY Y1 and NPY Y5 receptors (NPYxR) is considered a potentially important anti-obesity drug target. We tested the hypothesis that blockade of the NPY5R will lead to weight loss in humans using MIK-0557, a potent, highly selective, orally active NPY5R antagonist. The initial series of experiments reported herein, including a multiple-dose positron-emission tomography study and a 12 week proof-of concept/dose-ranging study, suggested an optimal MK-0557 dose of 1 mg/day. The hypothesis was then tested in a 52 week, multicenter, randomized, double-blind, placebo-controlled trial involving 1661 overweight and obese patients. Although statistically significant at 52 weeks, the magnitude of induced weight loss was not clinically meaningful. These observations provide the first clinical insight into the human NPY-energy homeostatic pathway and suggest that solely targeting the NPY5R in future drug development programs is unlikely to produce therapeutic efficacy.
引用
收藏
页码:275 / 282
页数:8
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