| Literature DB >> 26959184 |
Saswata Talukdar1, Yingjiang Zhou2, Dongmei Li2, Michelle Rossulek2, Jennifer Dong2, Veena Somayaji2, Yan Weng3, Ronald Clark2, Adhiraj Lanba2, Bryn M Owen4, Martin B Brenner2, Jeffrey K Trimmer2, Kathryn E Gropp5, Jeffrey R Chabot3, Derek M Erion2, Timothy P Rolph2, Bryan Goodwin2, Roberto A Calle6.
Abstract
FGF21 plays a central role in energy, lipid, and glucose homeostasis. To characterize the pharmacologic effects of FGF21, we administered a long-acting FGF21 analog, PF-05231023, to obese cynomolgus monkeys. PF-05231023 caused a marked decrease in food intake that led to reduced body weight. To assess the effects of PF-05231023 in humans, we conducted a placebo-controlled, multiple ascending-dose study in overweight/obese subjects with type 2 diabetes. PF-05231023 treatment resulted in a significant decrease in body weight, improved plasma lipoprotein profile, and increased adiponectin levels. Importantly, there were no significant effects of PF-05231023 on glycemic control. PF-05231023 treatment led to dose-dependent changes in multiple markers of bone formation and resorption and elevated insulin-like growth factor 1. The favorable effects of PF-05231023 on body weight support further evaluation of this molecule for the treatment of obesity. Longer studies are needed to assess potential direct effects of FGF21 on bone in humans.Entities:
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Year: 2016 PMID: 26959184 DOI: 10.1016/j.cmet.2016.02.001
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287