No evidence for an association between the chemokine receptor 5 D32 polymorphism and multiple sclerosis susceptibility: A meta-analysis

Background/Aim: Numerous reports have been published on the association of the chemokine receptor 5 D32 genetic variation (rs333) with the risk of multiple sclerosis (MS), with results that are inconsistent. The relationship between rs333 and susceptibility to MS was evaluated in this study. Methods: The PRISMA guidelines were followed in the current study. Twelve databases were used to find eligible articles. The investigators extracted the necessary information. The associations of the alleles and genotypes were evaluated in different models of inheritance: co-dominant, dominant and recessive genotype models and allele model. Results: The analysis included 14 articles reporting 16 studies involving 3265 MS patients and 3735 healthy controls. There was no substantial heterogeneity between studies for any of the comparisons. The significance level was not reached for the association between rs333 and MS susceptibility. Conclusion: The findings of this study could not confirm the relationship between the rs333 and susceptibility to multiple sclerosis.

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Publication Details

Journal
Scripta Medica
Published
2025-01-01
DOI
https://doi.org/10.5937/scriptamed56-54562
Primary Topic
Systemic Lupus Erythematosus Research
Type
article
Field-Weighted Citation Impact
0.00
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article

No evidence for an association between the chemokine receptor 5 D32 polymorphism and multiple sclerosis susceptibility: A meta-analysis

Mostafa Saadat, Nazanin Akbari
Scripta Medica
Systemic Lupus Erythematosus Research
article

No evidence for an association between the chemokine receptor 5 D32 polymorphism and multiple sclerosis susceptibility: A meta-analysis

Mostafa Saadat, Nazanin Akbari
article en

Abstract

Background/Aim: Numerous reports have been published on the association of the chemokine receptor 5 D32 genetic variation (rs333) with the risk of multiple sclerosis (MS), with results that are inconsistent. The relationship between rs333 and susceptibility to MS was evaluated in this study. Methods: The PRISMA guidelines were followed in the current study. Twelve databases were used to find eligible articles. The investigators extracted the necessary information. The associations of the alleles and genotypes were evaluated in different models of inheritance: co-dominant, dominant and recessive genotype models and allele model. Results: The analysis included 14 articles reporting 16 studies involving 3265 MS patients and 3735 healthy controls. There was no substantial heterogeneity between studies for any of the comparisons. The significance level was not reached for the association between rs333 and MS susceptibility. Conclusion: The findings of this study could not confirm the relationship between the rs333 and susceptibility to multiple sclerosis.

Scripta MedicaVol. 56(1)
Openalex Percentile: Top 93%
Systemic Lupus Erythematosus Research
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No evidence for an association between the chemokine receptor 5 D32 polymorphism and multiple sclerosis susceptibility: A meta-analysis — Mostafa Saadat, Nazanin Akbari · Scripta Medica (2025) | TGRS Research Map | TGRS