PMID- 31004714 OWN - NLM STAT- MEDLINE DCOM- 20190610 LR - 20190613 IS - 1879-0038 (Electronic) IS - 0378-1119 (Linking) VI - 705 DP - 2019 Jul 15 TI - BDNF Val66Met genetic variation and its plasma level in patients with morbid obesity: A case-control study. PG - 51-54 LID - S0378-1119(19)30398-1 [pii] LID - 10.1016/j.gene.2019.04.045 [doi] AB - Obesity is a major public health concern worldwide. Genetic, behavioral, and environmental factors contribute to the multifactorial etiology of obesity. Evidence suggests an association between human Brain-Derived Neurotrophic Factor (BDNF) Val66Met single nucleotide polymorphism (SNP) and obesity. Reduced plasma BDNF levels have also been reported in patients with eating disorders and obesity. We aimed to evaluate the BDNF Val66Met (rs6265) SNP and also plasma BDNF levels in morbidly obese patients compared with healthy normal controls in southern Iran. One hundred morbidly obese patients and one hundred eight healthy normal controls were enrolled. Blood-derived DNA samples were genotyped using the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method and confirmed by DNA sequencing. Plasma BDNF levels were evaluated using a commercially available sandwich enzyme-linked immunosorbent assay (ELISA) kit for human BDNF. Data analysis was performed by SPSS software, version 18.0. Genotype distribution was not significantly different between obese patients and controls. However, plasma BDNF levels were significantly lower in obese patients compared with controls. Interestingly, a significant association was found between BDNF Val66Met SNP and plasma BDNF levels. No relationship was observed between BDNF Val66Met SNP and all assessed demographic and clinical characteristics of obese patients. It seems that plasma BDNF levels were associated with both obesity and BDNF Val66Met SNP. However, this association was not found between BDNF Val66Met SNP and obesity. Further studies with larger sample sizes are needed for more detailed assessment of this genetic variation as a potential biomarker for obesity. CI - Copyright (c) 2019 Elsevier B.V. All rights reserved. FAU - Zamani, Mozhdeh AU - Zamani M AD - Colorectal Research Center, Shiraz University of Medical Sciences, Shiraz, Iran. FAU - Hosseini, Seyed Vahid AU - Hosseini SV AD - Colorectal Research Center, Shiraz University of Medical Sciences, Shiraz, Iran. FAU - Behrouj, Hamid AU - Behrouj H AD - Department of Biochemistry, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran. FAU - Erfani, Mehran AU - Erfani M AD - Department of Biochemistry, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran. FAU - Dastghaib, Sanaz AU - Dastghaib S AD - Department of Biochemistry, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran. FAU - Ahmadi, Mojtaba AU - Ahmadi M AD - Department of Biochemistry, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran. FAU - Shamsdin, Seyedeh Azra AU - Shamsdin SA AD - Gastroenterohepatology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran. FAU - Mokarram, Pooneh AU - Mokarram P AD - Department of Biochemistry, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran. Electronic address: mokaram2@gmail.com. LA - eng PT - Journal Article DEP - 20190417 PL - Netherlands TA - Gene JT - Gene JID - 7706761 RN - 0 (Brain-Derived Neurotrophic Factor) RN - 7171WSG8A2 (BDNF protein, human) RN - AE28F7PNPL (Methionine) RN - HG18B9YRS7 (Valine) SB - IM MH - Adult MH - *Amino Acid Substitution MH - Brain-Derived Neurotrophic Factor/*blood/*genetics MH - Case-Control Studies MH - Down-Regulation MH - Female MH - Genetic Association Studies MH - Genetic Predisposition to Disease MH - Humans MH - Iran MH - Male MH - Methionine/*genetics MH - Middle Aged MH - Obesity, Morbid/blood/*genetics MH - Polymorphism, Restriction Fragment Length MH - Sequence Analysis, DNA MH - Valine/*genetics OTO - NOTNLM OT - Brain-derived neurotrophic factor OT - Obesity OT - Polymorphism EDAT- 2019/04/21 06:00 MHDA- 2019/06/14 06:00 CRDT- 2019/04/21 06:00 PHST- 2018/11/20 00:00 [received] PHST- 2019/03/23 00:00 [revised] PHST- 2019/04/16 00:00 [accepted] PHST- 2019/04/21 06:00 [pubmed] PHST- 2019/06/14 06:00 [medline] PHST- 2019/04/21 06:00 [entrez] AID - S0378-1119(19)30398-1 [pii] AID - 10.1016/j.gene.2019.04.045 [doi] PST - ppublish SO - Gene. 2019 Jul 15;705:51-54. doi: 10.1016/j.gene.2019.04.045. Epub 2019 Apr 17.