PMID- 27787389 OWN - NLM STAT- MEDLINE DCOM- 20170209 LR - 20210109 IS - 1536-5964 (Electronic) IS - 0025-7974 (Print) IS - 0025-7974 (Linking) VI - 95 IP - 43 DP - 2016 Oct TI - Relationship between body weight and the increment in serum brain-derived neurotrophic factor after oral glucose challenge in men with obesity and metabolic syndrome: A prospective study. PG - e5260 LID - 10.1097/MD.0000000000005260 [doi] LID - e5260 AB - Brain-derived neurotrophic factor (BDNF) plays a role in energy homeostasis. However, the postprandial BDNF change has not been well investigated. We hypothesized that the BDNF increment after oral glucose challenge is associated with body weight.To address this possibility, man adults with obesity in conjunction with metabolic syndrome were compared with normal weight controls at baseline in the initial cross-sectional protocol. The obese subjects then underwent a 12-week program for body-weight reduction in the prospective protocol. The area under the curve (AUC) of serum BDNF was recorded during a 75 g oral glucose tolerant test and the BDNF AUC index was defined as [(AUC of BDNF) - (fasting BDNF2 hours)]/(fasting BDNF2 hours).A total of 25 controls and 36 obese subjects completed the study assessments. In the cross-sectional protocol, the BDNF AUC index was significantly higher in the obese subjects than in the controls (9.0 +/- 16.5% vs. - 8.0 +/- 22.5%, P = 0.001). After weight reduction (from 97.0 +/- 12.5 kg to 88.6 +/- 12.9 kg, P < 0.001), the percentage change of body weight was significantly associated with the BDNF AUC index after the study (95% CI between 0.21 and 1.82, P = 0.015). Using 6% weight reduction as a cut-off value, a larger weight reduction was able to reliably predict a negative BDNF AUC index.In conclusion, a high BDNF AUC index was observed for obese men in this study, whereas the index value significantly decreased after body-weight reduction. These findings suggest that postprandial BDNF increment may be associated with obesity. FAU - Lee, I-Te AU - Lee IT AD - Division of Endocrinology and Metabolism, Department of Internal Medicine, Taichung Veterans General Hospital, Taichung School of Medicine, National Yang-Ming University, Taipei School of Medicine, Chung Shan Medical University Center for Geriatrics and Gerontology, Taichung Veterans General Hospital Institute of Medical Technology, National Chung-Hsing University, Taichung, Taiwan. FAU - Wang, Jun-Sing AU - Wang JS FAU - Fu, Chia-Po AU - Fu CP FAU - Lin, Shih-Yi AU - Lin SY FAU - Sheu, Wayne Huey-Herng AU - Sheu WH LA - eng PT - Journal Article PT - Observational Study PL - United States TA - Medicine (Baltimore) JT - Medicine JID - 2985248R RN - 0 (Blood Glucose) RN - 0 (Brain-Derived Neurotrophic Factor) RN - 7171WSG8A2 (BDNF protein, human) SB - IM MH - Adult MH - Aged MH - Blood Glucose/*metabolism MH - *Body Weight MH - Brain-Derived Neurotrophic Factor/*blood MH - Cross-Sectional Studies MH - Fasting/blood MH - Follow-Up Studies MH - Glucose Tolerance Test MH - Humans MH - Insulin Resistance/*physiology MH - Male MH - Metabolic Syndrome/*blood/etiology/physiopathology MH - Middle Aged MH - Obesity/blood/*complications/physiopathology MH - Prospective Studies MH - Young Adult PMC - PMC5089118 COIS- The authors have no conflicts of interest to disclose. EDAT- 2016/10/28 06:00 MHDA- 2017/02/10 06:00 PMCR- 2016/10/28 CRDT- 2016/10/28 06:00 PHST- 2016/10/28 06:00 [pubmed] PHST- 2017/02/10 06:00 [medline] PHST- 2016/10/28 06:00 [entrez] PHST- 2016/10/28 00:00 [pmc-release] AID - 00005792-201610250-00037 [pii] AID - 10.1097/MD.0000000000005260 [doi] PST - ppublish SO - Medicine (Baltimore). 2016 Oct;95(43):e5260. doi: 10.1097/MD.0000000000005260.