PMID- 31886290 OWN - NLM STAT- MEDLINE DCOM- 20200609 LR - 20200609 IS - 2314-6753 (Electronic) IS - 2314-6745 (Print) VI - 2019 DP - 2019 TI - Association Study between BGLAP Gene HindIII Polymorphism and Type 2 Diabetes Mellitus Development in Ukrainian Population. PG - 9302636 LID - 10.1155/2019/9302636 [doi] LID - 9302636 AB - Type 2 diabetes mellitus (T2DM) belongs to the diseases with hereditary predisposition, so both environmental and genetic factors contribute to its development. Recent studies have demonstrated that the skeleton realizes systemic regulation of energy metabolism through the secretion of osteocalcin (OCN). Thus, the association analysis between HindIII single nucleotide polymorphism of OCN gene (BGLAP) promoter region and T2DM development in Ukrainian population was carried out. 153 individuals diagnosed with T2DM and 311 control individuals were enrolled in the study. The genotyping was performed using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method. The lack of association between BGLAP HindIII single nucleotide polymorphism (SNP) and T2DM development among Ukrainians was found. Further studies with extended groups of comparison are needed to confirm the obtained results. CI - Copyright (c) 2019 Yaroslav D. Chumachenko et al. FAU - Chumachenko, Yaroslav D AU - Chumachenko YD AUID- ORCID: 0000-0002-4803-5435 AD - Scientific Laboratory of Molecular Genetic Studies, Medical Institute of the Sumy State University, 40007, Ukraine. FAU - Harbuzova, Viktoriia Yu AU - Harbuzova VY AD - Scientific Laboratory of Molecular Genetic Studies, Medical Institute of the Sumy State University, 40007, Ukraine. FAU - Ataman, Alexander V AU - Ataman AV AD - Department of Physiology and Pathophysiology with Medical Biology Course, Medical Institute of the Sumy State University, 40018, Ukraine. LA - eng PT - Journal Article DEP - 20191127 PL - England TA - J Diabetes Res JT - Journal of diabetes research JID - 101605237 RN - 0 (BGLAP protein, human) RN - 104982-03-8 (Osteocalcin) SB - IM MH - Aged MH - Case-Control Studies MH - Diabetes Mellitus, Type 2/diagnosis/epidemiology/*genetics MH - Female MH - Genetic Association Studies MH - Genetic Predisposition to Disease MH - Humans MH - Male MH - Middle Aged MH - Osteocalcin/*genetics MH - Phenotype MH - *Polymorphism, Single Nucleotide MH - Promoter Regions, Genetic MH - Risk Factors MH - Ukraine/epidemiology PMC - PMC6900942 COIS- There is no conflict of interests. EDAT- 2019/12/31 06:00 MHDA- 2020/06/10 06:00 PMCR- 2019/11/27 CRDT- 2019/12/31 06:00 PHST- 2019/09/01 00:00 [received] PHST- 2019/10/16 00:00 [revised] PHST- 2019/11/01 00:00 [accepted] PHST- 2019/12/31 06:00 [entrez] PHST- 2019/12/31 06:00 [pubmed] PHST- 2020/06/10 06:00 [medline] PHST- 2019/11/27 00:00 [pmc-release] AID - 10.1155/2019/9302636 [doi] PST - epublish SO - J Diabetes Res. 2019 Nov 27;2019:9302636. doi: 10.1155/2019/9302636. eCollection 2019.