Association Between the Vitamin D Receptor Polymorphism in rs7975232 with the COVID-19 Susceptibility

<b><i>Background:</i></b> Vitamin D deficiency influences the pathogenicity and severity of coronavirus disease 2019 (COVID-19), suggesting that polymorphisms in the vitamin D receptor may impact disease susceptibility and outcomes. This study aims to examine the relationship between the rs7975232 SNP and susceptibility to severe acute respiratory syndrome coronavirus 2(SARS-CoV-2) infection. <b><i>Materials and Methods:</i></b> This study compared 138 COVID-19 patients with 136 healthy individuals at Shohada-ye Ashayer Hospital in Khorramabad. The PCR-RFLP (polymerase chain reaction-restriction fragment length polymorphism) method was employed to ascertain the genotypes following the collection of blood samples. The results of PCR-RFLP method were confirmed by sequencing. IBM SPSS and SNPStats software were utilized to compare genotypes and allele frequencies, as well as to conduct odds ratio analysis. <b><i>Results:</i></b> This study's results did not demonstrate a significant association between the rs7975232 polymorphism and COVID-19 susceptibility (<i>p</i> = 0.58). Subsequent analysis revealed that individuals with low lymphocyte levels and the CC genotype exhibited increased susceptibility to COVID-19 (OR = 3.45, 95%CI: 1.18-10.11). A significant association was observed between creatinine (<i>p</i> < 0.0001), neutrophils (<i>p</i> = 0.02), and NLR (Neutrophil to Lymphocyte Ratio) (<i>p</i> = 0.0015) with rs7975232. In a comparison of AA/AC genotype cases, individuals with normal levels of ALT, CPK, creatinine, blood sugar, and hemoglobin exhibited an increased likelihood of infection. In CC genotype cases, individuals with normal neutrophil levels exhibited a reduced chance of COVID-19. <b><i>Conclusion:</i></b> The current study did not demonstrate a significant association between the examined SNP and COVID-19. The findings indicated that the standard levels of various laboratory parameters influence the likelihood of the disease. Additional studies involving larger and more diverse populations can yield more valid results.

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Journal
Genetic Testing and Molecular Biomarkers
Published
2025-08-01
DOI
https://doi.org/10.1177/19450265251366457
Primary Topic
COVID-19 Clinical Research Studies
Type
article
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article

Association Between the Vitamin D Receptor Polymorphism in rs7975232 with the COVID-19 Susceptibility

Mehdi Ajorloo, Rasool Mohammadi, Ashkan Alamdary, Zohreh Beiranvand
Genetic Testing and Molecular Biomarkers
COVID-19 Clinical Research Studies
article

Association Between the Vitamin D Receptor Polymorphism in rs7975232 with the COVID-19 Susceptibility

Mehdi Ajorloo, Rasool Mohammadi, Ashkan Alamdary, Zohreh Beiranvand
article en

Abstract

<b><i>Background:</i></b> Vitamin D deficiency influences the pathogenicity and severity of coronavirus disease 2019 (COVID-19), suggesting that polymorphisms in the vitamin D receptor may impact disease susceptibility and outcomes. This study aims to examine the relationship between the rs7975232 SNP and susceptibility to severe acute respiratory syndrome coronavirus 2(SARS-CoV-2) infection. <b><i>Materials and Methods:</i></b> This study compared 138 COVID-19 patients with 136 healthy individuals at Shohada-ye Ashayer Hospital in Khorramabad. The PCR-RFLP (polymerase chain reaction-restriction fragment length polymorphism) method was employed to ascertain the genotypes following the collection of blood samples. The results of PCR-RFLP method were confirmed by sequencing. IBM SPSS and SNPStats software were utilized to compare genotypes and allele frequencies, as well as to conduct odds ratio analysis. <b><i>Results:</i></b> This study's results did not demonstrate a significant association between the rs7975232 polymorphism and COVID-19 susceptibility (<i>p</i> = 0.58). Subsequent analysis revealed that individuals with low lymphocyte levels and the CC genotype exhibited increased susceptibility to COVID-19 (OR = 3.45, 95%CI: 1.18-10.11). A significant association was observed between creatinine (<i>p</i> < 0.0001), neutrophils (<i>p</i> = 0.02), and NLR (Neutrophil to Lymphocyte Ratio) (<i>p</i> = 0.0015) with rs7975232. In a comparison of AA/AC genotype cases, individuals with normal levels of ALT, CPK, creatinine, blood sugar, and hemoglobin exhibited an increased likelihood of infection. In CC genotype cases, individuals with normal neutrophil levels exhibited a reduced chance of COVID-19. <b><i>Conclusion:</i></b> The current study did not demonstrate a significant association between the examined SNP and COVID-19. The findings indicated that the standard levels of various laboratory parameters influence the likelihood of the disease. Additional studies involving larger and more diverse populations can yield more valid results.

Genetic Testing and Molecular BiomarkersVol. 29(8)
Lorestan University of Medical Sciences (IR), High Institute for Education and Research in Transfusion Medicine (IR)
Openalex Percentile: Top 75%
COVID-19 Clinical Research Studies
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