PMID- 33161057 OWN - NLM STAT- MEDLINE DCOM- 20210125 LR - 20210125 IS - 1879-0038 (Electronic) IS - 0378-1119 (Linking) VI - 768 DP - 2021 Feb 5 TI - SLC30A8 gene polymorphism rs13266634 associated with increased risk for developing type 2 diabetes mellitus in Jordanian population. PG - 145279 LID - S0378-1119(20)30948-3 [pii] LID - 10.1016/j.gene.2020.145279 [doi] AB - BACKGROUND: Several genome-wide association studies (GWAS) have identified the single nucleotide polymorphism (SNP) rs13266634 in the Solute carrier family 30 member 8 (SLC30A8) gene as a risk factor to type 2 diabetes mellitus (T2DM). Nevertheless, other studies reported controversial findings of no significant association between the rs13266634 with T2DM. In this study, we aimed to investigate the association of this SNP with T2DM among Jordanian population in addition to define its corresponding allelic and genotypic frequencies. METHOD: This case-control study enrolled 358 T2DM patients and 326 healthy controls who fulfilled the inclusion criteria. Blood samples were collected from all participants and were used for the rs13266634 SNP genotyping by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) technique. RESULTS: We demonstrated a significant association between the C/T rs13266634 SNP and T2DM among Jordanian population. A significant difference was found between the cases and controls regarding the allelic (P = 0.003) distribution. Compared to people having T allele, those with C allele had higher risk of T2DM (OR = 1.47 ; 95% CI: 1.14 - 1.89; P = 0.003). Having a CC genotype versus TT genotype was significantly associated with increased risk to T2DM (OR = 2.44; 95% CI: 1.16 - 5.12; P = 0.019) after adjusting for age, gender, and BMI. Under the recessive model, subjects with CC genotype were more likely to have T2DM compared to those with CT or TT genotypes, (OR = 1.64; 95% CI: 1.18 - 2.26; P = 0.003) after adjusting for age, gender and BMI. CONCLUSION: The rs13266634 SNP is significantly associated with T2DM susceptibility among Jordanian Population. CI - Copyright (c) 2020. Published by Elsevier B.V. FAU - Mashal, Safaa AU - Mashal S AD - Department of Pathology, Microbiology and Forensic Medicine, School of Medicine, University of Jordan, PO Box: 13617, Queen Rania St., Amman 11942, Jordan. FAU - Khanfar, Mariam AU - Khanfar M AD - Department of Medical Laboratory Sciences, Jordan University of Science and Technology, P.O.Box 3030, Irbid 22110, Jordan. FAU - Al-Khalayfa, Sawsan AU - Al-Khalayfa S AD - Department of Pathology, Microbiology and Forensic Medicine, School of Medicine, University of Jordan, PO Box: 13617, Queen Rania St., Amman 11942, Jordan. FAU - Srour, Luma AU - Srour L AD - Department of Pathology, Microbiology and Forensic Medicine, School of Medicine, University of Jordan, PO Box: 13617, Queen Rania St., Amman 11942, Jordan. FAU - Mustafa, Lina AU - Mustafa L AD - Department of Pathology, Microbiology and Forensic Medicine, School of Medicine, University of Jordan, PO Box: 13617, Queen Rania St., Amman 11942, Jordan. FAU - Hakooz, Nancy M AU - Hakooz NM AD - Department of Biopharmaceutics and Clinical Pharmacy, School of Pharmacy, University of Jordan, PO Box: 13617, Queen Rania St., Amman 11942, Jordan. FAU - Zayed, Ayman A AU - Zayed AA AD - Division of Endocrinology, Diabetes, and Metabolism, Department of Internal Medicine, School of Medicine, The University of Jordan, Jordan University Hospital, PO Box: 13617, Queen Rania St., Amman 11942, Jordan. FAU - Khader, Yousef S AU - Khader YS AD - Department of Community Medicine, Public Health and Family Medicine, Faculty of Medicine, Jordan University of Science and Technology, P.O.Box 3030, Irbid 22110, Jordan. FAU - Azab, Bilal AU - Azab B AD - Department of Pathology, Microbiology and Forensic Medicine, School of Medicine, University of Jordan, PO Box: 13617, Queen Rania St., Amman 11942, Jordan; Department of Human and Molecular Genetics, School of Medicine, Virginia Commonwealth University, United States. Electronic address: azabbm@mymail.vcu.edu. LA - eng PT - Journal Article DEP - 20201105 PL - Netherlands TA - Gene JT - Gene JID - 7706761 RN - 0 (SLC30A8 protein, human) RN - 0 (Zinc Transporter 8) SB - IM MH - Case-Control Studies MH - Diabetes Mellitus, Type 2/*genetics MH - Female MH - Gene Frequency/genetics MH - Genetic Predisposition to Disease/*genetics MH - Genome-Wide Association Study MH - Genotype MH - Humans MH - Jordan MH - Male MH - Middle Aged MH - Polymerase Chain Reaction MH - Polymorphism, Restriction Fragment Length/genetics MH - Polymorphism, Single Nucleotide/genetics MH - Zinc Transporter 8/*genetics OTO - NOTNLM OT - Polymerase chain reaction-restriction fragment length polymorphism OT - SLC30A8 OT - Solute carrier family 30 member 8 OT - Type 2 diabetes mellitus OT - rs13266634 EDAT- 2020/11/09 06:00 MHDA- 2021/01/26 06:00 CRDT- 2020/11/08 20:27 PHST- 2020/07/01 00:00 [received] PHST- 2020/10/08 00:00 [revised] PHST- 2020/10/23 00:00 [accepted] PHST- 2020/11/09 06:00 [pubmed] PHST- 2021/01/26 06:00 [medline] PHST- 2020/11/08 20:27 [entrez] AID - S0378-1119(20)30948-3 [pii] AID - 10.1016/j.gene.2020.145279 [doi] PST - ppublish SO - Gene. 2021 Feb 5;768:145279. doi: 10.1016/j.gene.2020.145279. Epub 2020 Nov 5.