Association between Interleukin-6 Gene Polymorphism (rs1800795 and rs1800796) and Type 2 Diabetes Mellitus in a Ghanaian Population: A Case-Control Study in the Ho Municipality

Author:

Obirikorang Christian1ORCID,Lokpo Sylvester Yao12ORCID,Owiredu William K. B. A.1,Ahenkorah-Fondjo Linda1ORCID,Osei-Yeboah James3ORCID,Duedu Kwabena Obeng45ORCID,Adejumo Esther Ngozi6,Ametepe Samuel7,Asamoah Evans Adu8ORCID,Coffie Shadrack Asiedu9,Mawuli Emmanuel Nattah10ORCID,Essandoh Priscilla4ORCID,Kwadzokpui Precious Kwablah11ORCID

Affiliation:

1. Department of Molecular Medicine, School of Medicine and Dentistry, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana

2. Department of Medical Laboratory Sciences, School of Allied Health Sciences, University of Health and Allied Sciences, Ho, Ghana

3. Department of Global and International Health, School of Public Health, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana

4. Department of Biomedical Sciences, School of Basic and Biomedical Sciences, University of Health and Allied Sciences, Ho, Ghana

5. College of Life Sciences, Birmingham City University, City South Campus, Birmingham, UK

6. Department of Medical Laboratory Science, School of Public and Allied Health, Babcock University, Ilishan-Remo, Ogun State, Nigeria

7. Faculty of Allied Health Sciences, Koforidua Technical University, Koforidua, Greater Eastern Region, Ghana

8. Kumasi Centre for Collaborative Research, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana

9. Biotechnology Laboratory, University of Ghana, Legon, Ghana

10. Department of Molecular Diagnostics, Claron Health International, Accra, Ghana

11. Laboratory Department, Ho Teaching Hospital, Ho, Ghana

Abstract

Background. There is no conclusive evidence on the association between interleukin- (IL-) 6 gene polymorphism and type 2 diabetes mellitus (type 2 DM). Thus, this study is aimed at evaluating the role of rs1800795 and rs1800796 polymorphisms in the pathogenesis of type 2 DM among Ghanaians in the Ho Municipality. Materials and Methods. We recruited into this hospital-based case-control study 174 patients with type 2 DM (75 DM alone and 99 with DM+HTN) and 149 healthy individuals between 2018 and 2020. Demographic, lifestyle, clinical, anthropometric, and haemodynamic variables were obtained. Fasting blood samples were collected for haematological, biochemical, and molecular analyses. Genomic DNA was extracted, amplified using Tetra-primer amplification refractory mutation system-polymerase chain reaction (T-ARMS-PCR) technique, and genotyped for IL-6 gene polymorphism. Logistic regression analyses were performed to assess the association between IL-6 gene polymorphism and type 2 DM. Results. The minor allele frequency (MAF) of the rs1800795 and rs1800796 polymorphisms was higher in DM alone (57.5%, 62.0%) and DM with HTN groups (58.3%, 65.3%) than controls (33.1%, 20.0%). Carriers of the rs1800795GC genotype (aOR=2.35, 95% CI: 1.13-4.90, p=0.022) and mutant C allele (aOR=2.41, 95% CI: 1.16-5.00, p=0.019) as well as those who carried the rs1800796GC (aOR=8.67, 95% CI: 4.00-18.90, p<0.001) and mutant C allele (aOR=8.84, 95% CI: 4.06-19.26, p=0.001) had increased odds of type 2 DM. For both polymorphisms, carriers of the GC genotype had comparable levels of insulin, HOMA-IR, and fasting blood glucose (FBG) with those who carried the GG genotype. IL-6 levels were higher among carriers of the rs1800796GC variant compared to carriers of the rs1800796GG variant (p=0.023). The rs1800796 polymorphism, dietary sugar intake, and exercise status, respectively, explained approximately 3% (p=0.046), 3.2% (p=0.038, coefficient=1.456), and 6.2% (p=0.004, coefficient=2.754) of the variability in IL-6 levels, suggesting weak effect sizes. Conclusion. The GC genotype and mutant C allele are risk genetic variants associated with type 2 DM in the Ghanaian population. The rs1800796 GC variant, dietary sugar intake, and exercise status appear to contribute significantly to the variations in circulating IL-6 levels but with weak effect sizes.

Publisher

Hindawi Limited

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