عبير محمد راوى عبد المنعم
أستاذ
FokI polymorphism of the vitamin D receptor gene: Linking COVID-19 risk to genetic susceptibility in children
• 2025
معلومات البحث
المؤلفون
Amal Ahmed Mohamed a,1
, Abdullah Taher Alanazi b
, Hoda H. Ahmed c
, Samar Elfiky d
Muhammad T Abdel Ghafar e
, Ingy Maherf
, Sherin A. Taha g
Mohammed Zakaria Ali AbuRahma h
, Waleed Elagawy i
, Dina A. Mohareb j
, Abeer M. Rawy k
الكلمات المفتاحية
Not Available
المجلة العلمية
Not Available
الناشر
Not Available
المجلد
Not Available
العدد
Not Available
الصفحات
Not Available
publication.type
International
رابط البحث
Not Available
المواد المرفقة
Not Available
الملخص
Background: Vitamin D receptor (VDR), influenced by gene polymorphisms like FokI, may affect susceptibility to
infections, including coronavirus disease 2019 (COVID-19). Since studies in children are limited, we aimed to
analyze the correlation between the VDR FokI variant and both the incidence and severity of COVID-19 in
Egyptian children.
Methods: Seventy-seven COVID-19-positive and 107 COVID-19-negative pediatric patients were included. Participants’ serum 25(OH)D levels, inflammatory biomarkers, and demographics were evaluated. Real-time polymerase chain reaction (PCR) was used for genotyping the VDR FokI (rs2228570) polymorphism.
Results: Absolute lymphocyte count (ALC) was significantly lower in COVID-19 patients than in controls, while
interleukin-6 (IL-6), erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), procalcitonin, and D-dimer
were significantly higher (all p < 0.001). Vitamin D insufficiency was significantly more common in COVID-19
cases (18.2 % versus 3.7 %, p = 0.002). Male sex, increased tumor necrosis factor-alpha (TNF-α), and CRP were
significantly associated with severe COVID-19 (p = 0.032, 0.029, < 0.001, respectively). The FokI TT genotype in
codominant and recessive models and the T allele in the multiplicative model were significantly correlated with
2.4, 3.0, and 1.8 folds increased COVID-19 risk (p = 0.043, < 0.001, and 0.004, respectively). However, VDR FokI
variants did not significantly associate with severe COVID-19.
Conclusion: The T allele and TT genotype of the FokI variant in the VDR gene increase susceptibility to COVID-19
but not its severity in Egyptian children. Additional research is required to validate the potential role of vitamin
D and its receptor polymorphism in COVID-19
infections, including coronavirus disease 2019 (COVID-19). Since studies in children are limited, we aimed to
analyze the correlation between the VDR FokI variant and both the incidence and severity of COVID-19 in
Egyptian children.
Methods: Seventy-seven COVID-19-positive and 107 COVID-19-negative pediatric patients were included. Participants’ serum 25(OH)D levels, inflammatory biomarkers, and demographics were evaluated. Real-time polymerase chain reaction (PCR) was used for genotyping the VDR FokI (rs2228570) polymorphism.
Results: Absolute lymphocyte count (ALC) was significantly lower in COVID-19 patients than in controls, while
interleukin-6 (IL-6), erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), procalcitonin, and D-dimer
were significantly higher (all p < 0.001). Vitamin D insufficiency was significantly more common in COVID-19
cases (18.2 % versus 3.7 %, p = 0.002). Male sex, increased tumor necrosis factor-alpha (TNF-α), and CRP were
significantly associated with severe COVID-19 (p = 0.032, 0.029, < 0.001, respectively). The FokI TT genotype in
codominant and recessive models and the T allele in the multiplicative model were significantly correlated with
2.4, 3.0, and 1.8 folds increased COVID-19 risk (p = 0.043, < 0.001, and 0.004, respectively). However, VDR FokI
variants did not significantly associate with severe COVID-19.
Conclusion: The T allele and TT genotype of the FokI variant in the VDR gene increase susceptibility to COVID-19
but not its severity in Egyptian children. Additional research is required to validate the potential role of vitamin
D and its receptor polymorphism in COVID-19
