PMID- 22539584 OWN - NLM STAT- MEDLINE DCOM- 20120926 LR - 20131121 IS - 1945-7197 (Electronic) IS - 0021-972X (Linking) VI - 97 IP - 7 DP - 2012 Jul TI - Dynamic change of serum FGF21 levels in response to glucose challenge in human. PG - E1224-8 LID - 10.1210/jc.2012-1132 [doi] AB - AIMS: Fibroblast growth factor 21 (FGF21), an endocrine factor predominantly secreted from liver, possesses multiple beneficial effect on energy metabolism and insulin sensitivity in animals. This study aimed to investigate the acute change of serum FGF21 in response to glucose challenge in humans. METHODS: A 75-g oral glucose tolerance test was performed among 20 healthy subjects, 18 with impaired glucose tolerance (IGT) and 21 with type 2 diabetes mellitus (T2DM). Blood samples were collected for measurement of FGF21 and other biochemical parameters. The associations of FGF21 with insulin and other metabolic parameters were analyzed. RESULTS: Fasting serum FGF21 levels increased progressively from healthy, IGT to T2DM subjects (P < 0.05 for global trend). After oral glucose administration, the serum FGF21 level showed a similar biphasic change in all three groups. It declined to a nadir level at 60 min and then increased gradually to its peak level at 180 min. FGF21 levels at different time points of oral glucose tolerance test negatively correlated with glucose levels in all subjects, and the fold change of serum FGF21 at different time points (compared with the basal level) were inversely associated with fold changes of insulin (P = 0.012) and C-peptide (P = 0.043) levels in healthy subjects but not in IGT and T2DM patients. CONCLUSIONS: The dynamic change of circulating FGF21 was associated with alterations in insulin levels in response to glucose challenge in humans. These findings support the role of FGF21 as a potential regulator of insulin secretion and glucose metabolism in humans. FAU - Lin, Zhuofeng AU - Lin Z AD - Metabolism Disease Research Center, the 2nd Affiliated Hospital, Wenzhou Medical College, Zhejiang 325035, China. FAU - Gong, Qi AU - Gong Q FAU - Wu, Chaoming AU - Wu C FAU - Yu, Jiawen AU - Yu J FAU - Lu, Tingting AU - Lu T FAU - Pan, Xuebo AU - Pan X FAU - Lin, Shaoqiang AU - Lin S FAU - Li, Xiaokun AU - Li X LA - eng PT - Controlled Clinical Trial PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20120426 PL - United States TA - J Clin Endocrinol Metab JT - The Journal of clinical endocrinology and metabolism JID - 0375362 RN - 0 (Blood Glucose) RN - 0 (C-Peptide) RN - 0 (Insulin) RN - 0 (fibroblast growth factor 21) RN - 62031-54-3 (Fibroblast Growth Factors) RN - IY9XDZ35W2 (Glucose) SB - IM MH - Adult MH - Blood Glucose/metabolism MH - C-Peptide/blood/metabolism MH - Diabetes Mellitus, Type 2/blood/metabolism MH - Female MH - Fibroblast Growth Factors/*blood/metabolism/physiology MH - Glucose/administration & dosage/*pharmacology MH - Glucose Intolerance/blood/metabolism MH - Glucose Tolerance Test MH - Health MH - Humans MH - Insulin/blood/metabolism MH - Insulin Resistance/physiology MH - Male MH - Matched-Pair Analysis EDAT- 2012/04/28 06:00 MHDA- 2012/09/27 06:00 CRDT- 2012/04/28 06:00 PHST- 2012/04/28 06:00 [entrez] PHST- 2012/04/28 06:00 [pubmed] PHST- 2012/09/27 06:00 [medline] AID - jc.2012-1132 [pii] AID - 10.1210/jc.2012-1132 [doi] PST - ppublish SO - J Clin Endocrinol Metab. 2012 Jul;97(7):E1224-8. doi: 10.1210/jc.2012-1132. Epub 2012 Apr 26.