Evidence map›Paper›PMID 40702130›Full record

ArticleScientific reports2025

Association between vitamin D receptor gene variants and the risk of type 2 diabetes mellitus in a Ghanaian population.

Freeman Arhin-Aidoo, Linda Ahenkorah Fondjo, Christian Obirikorang, Eddie-Williams Owiredu, Ebenezer Senu, Samuel Kwame Sopuruchi Agomuo, Edwin F Laing

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Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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7 authors.

Freeman Arhin-AidooDepartment of Molecular Medicine, SMS, KNUST, Kumasi, Ghana.
Linda Ahenkorah FondjoDepartment of Molecular Medicine, SMS, KNUST, Kumasi, Ghana. linda.ahenkorahfondjo@yahoo.com.
Christian ObirikorangDepartment of Molecular Medicine, SMS, KNUST, Kumasi, Ghana.
Eddie-Williams OwireduDepartment of Molecular Medicine, SMS, KNUST, Kumasi, Ghana.
Ebenezer SenuDepartment of Molecular Medicine, SMS, KNUST, Kumasi, Ghana.
Samuel Kwame Sopuruchi AgomuoDepartment of Molecular Medicine, SMS, KNUST, Kumasi, Ghana.
Edwin F LaingDepartment of Molecular Medicine, SMS, KNUST, Kumasi, Ghana.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gene variants of the vitamin D receptor (VDR) have been linked to the alterations of the vitamin D metabolic pathway and thus a candidate risk gene for developing type 2 diabetes mellitus (T2DM). However, the association between VDR gene variants and vitamin D status as well as susceptibility to T2DM in the Ghanaian population have not been explored. This study assessed VDR gene variants, vitamin D status and susceptibility to T2DM. In a 1:1 matched case-control study, 100 clinically diagnosed T2DM patients visiting the Greenshield Hospital at Sefwi Bekwai and 100 apparently healthy non-diabetic controls living in same environs were recruited. Venous blood samples were obtained for biochemical analyses. Lipid profile was estimated spectrophotometrically and serum vitamin D was determined by enzyme linked immunosorbent assay. The variants of the VDR gene were determined using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). Logistic regression models were used to assess the associations between single nucleotide polymorphisms and T2DM. The prevalence of vitamin D deficiency (28.0%) and insufficiency (70.0%) was higher in T2DM than in non-diabetics (5.3% and 44.2%), respectively (p < 0.0001). rs10735810 and rs7975232 was found to increase risk of T2DM under the codominant model (OR = 1.93 (95% CI = 0.69-5.46) and OR = 1.81 (95% CI = 0.51-6.38), respectively), and additive model 1 (OR = 2.02 (95% CI = 0.68-5.98) and OR = 1.29 (95% CI = 0.34-4.84), respectively) whereas rs10735810 and rs7975232 was found to decrease risk of T2DM under the recessive model (OR = 0.96 (95% CI = 0.55-1.67) and OR = 0.58 (95% CI = 0.32-1.02), respectively). Besides, rs7975232 variant was associated with hypertension among individuals with T2DM (p = 0.033). Low vitamin D levels are common in T2DM. There is no association between variants rs10735810 and rs7975232 of VDR gene and T2DM; however, rs7975232 was associated with hypertension and that the 'A' allele of rs7975232 variant seems to be protective against hypertension among T2DM.

Indexed as

Diabetes Mellitus, Type 2Genetic Predisposition to DiseasePolymorphism, Single NucleotideReceptors, CalcitriolAdultAgedCase-Control StudiesFemaleGhanaHumansMaleMiddle AgedPolymorphism, Restriction Fragment LengthRisk FactorsVitamin DVitamin D DeficiencyReceptors, CalcitriolVDR protein, humanVitamin DGene variantsGenotypesrs10735810rs7975232 vitamin D receptorSingle nucleotide polymorphismssub-Saharan AfricaType 2 diabetes mellitus

Identifiers

PMID40702130
PMCPMC12287319

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