Kalam, Ahmed Abo and Roshanuddin, Jameela and Linga, BalaSubramani Gattu and Ibrahim, Faisal E. and Hamdan, Rand and Farrell, Thomas and Shurbak, Zeena Saeed BU and Mohamed, Wael Mohamed Yousef and Al-Dewik, Nader (2026) Associations of Vitamin D receptor (ApaI, FokI, TaqI, BsmI) polymorphisms with neurodegenerative diseases in the Middle East, North Africa and Turkiye (MENA&T) region: a systematic review and meta-analysis toward population-specific precision medicine. Journal of Personalized Medicine, 16 (6). pp. 1-26. ISSN 2075-4426
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Abstract
Background: Vitamin D receptor (VDR) polymorphisms have been widely investigated as genetic determinants of neurodegenerative diseases, yet findings remain inconsistent and population-dependent. Evidence from the Middle East, North Africa, and Türkiye (MENA&T) regions, which is characterized by widespread vitamin D deficiency and distinct genetic backgrounds, has not been comprehensively synthesized. Methods: We conducted a systematic review and meta-analysis evaluating associations between four common VDR polymorphisms (ApaI rs7975232, FokI rs2228570, TaqI rs731236, and BsmI rs1544410) and the risk of multiple sclerosis (MS), Parkinson’s disease (PD), and Alzheimer’s disease (AD) in MENA&T populations. Six databases were searched from inception to November 2025. Pooled odds ratios (ORs) with 95% confidence intervals (CIs) were estimated using fixed- and random-effects models across multiple genetic contrasts. Subgroup analyses by ethnicity were conducted for MS. Study quality was assessed using the Newcastle–Ottawa Scale (NOS), and the certainty of evidence was assessed using the Grading of Recommendations Assessment, Development, and Evaluation (GRADE). Results: Nineteen unique case–control studies (20 reports), including 4744 participants, were included. For MS, the ApaI polymorphism showed consistent associations with increased risk across genetic models (random-effects ORs = 1.4–1.9), with stronger effects in Arab and Iranian populations and no association in Turkish cohorts. FokI showed associations with MS under selected genetic models, particularly recessive and homozygous contrasts, although findings were not consistent across all analytical approaches. TaqI showed model-dependent associations with substantial heterogeneity, while BsmI showed no significant association. For AD, a meta-analysis of two studies showed no significant associations. For PD, ApaI showed associations with increased risk across several models without heterogeneity; however, these findings were based on a limited number of studies. Overall certainty of evidence ranged from very low to moderate. Conclusions: In MENA&T populations, VDR ApaI polymorphism shows consistent evidence of association with MS susceptibility, while FokI may be associated under specific genetic models; evidence for AD and PD remains limited and should be considered exploratory. These findings highlight population-specific genetic heterogeneity and underscore the need for further large-scale studies to confirm these associations. These population-specific genetic associations underscore the importance of incorporating VDR genotyping into precision medicine frameworks for neurodegenerative disease risk stratification in MENA&T populations, where vitamin D deficiency is highly prevalent.
| Item Type: | Article (Journal) |
|---|---|
| Uncontrolled Keywords: | vitamin D receptor; VDR polymorphisms; multiple sclerosis; Parkinson’s disease; Alzheimer’s disease; Middle East, North Africa, and Türkiye (MENA&T); personalized medicine; precision medicine |
| Subjects: | R Medicine > R Medicine (General) |
| Kulliyyahs/Centres/Divisions/Institutes (Can select more than one option. Press CONTROL button): | Kulliyyah of Medicine > Department of Basic Medical Kulliyyah of Medicine |
| Depositing User: | Dr Wael Mohamed |
| Date Deposited: | 10 Jun 2026 15:46 |
| Last Modified: | 10 Jun 2026 15:46 |
| Queue Number: | 2026-05-Q3563 |
| URI: | http://irep.iium.edu.my/id/eprint/129142 |
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