Bibliographic Details
Title: |
Genetic Variations of the Vitamin D Metabolic Pathway and COVID-19 Susceptibility and Severity: Current Understanding and Existing Evidence |
Authors: |
Nipith Charoenngam, Aunchalee Jaroenlapnopparat, Sofia K. Mettler, Ashna Grover |
Source: |
Biomedicines, Vol 11, Iss 2, p 400 (2023) |
Publisher Information: |
MDPI AG, 2023. |
Publication Year: |
2023 |
Collection: |
LCC:Biology (General) |
Subject Terms: |
vitamin D, 25-hydroxyvitamin D, vitamin D receptor, vitamin D-binding protein, DBP, GC protein, Biology (General), QH301-705.5 |
More Details: |
The immunomodulatory and metabolic effects of vitamin D receptor (VDR) activation have been considered beneficial in mitigating the susceptibility and severity of COVID-19 infection. Furthermore, vitamin D-binding protein (DBP) has pleiotropic effects on the immune system that may influence inflammation associated with COVID-19. Multiple observational studies have demonstrated an association between low levels of serum 25-hydroxyvitamin D and risk and the severity of COVID-19 infection. However, the impact of vitamin D supplementation as an adjunctive treatment for COVID-19 based on evidence from randomized clinical trials is unclear. Equally important is that certain variations of the genes involved in the vitamin D metabolic pathway have been shown to affect immune function and linked with various clinical outcomes, including cardio-metabolic disorders, autoimmune diseases, infections, and cancers. This indicates inter-individual difference in body response to vitamin D. There is also emerging evidence that common polymorphisms of these genes may influence the susceptibility and severity of COVID-19, although the confidence of these findings is limited by a small number of studies and participants. Further studies are needed to address the potential role of VDR activation and DBP in the pathophysiology of COVID-19 which take into account the genetic variations of vitamin D metabolic pathway. |
Document Type: |
article |
File Description: |
electronic resource |
Language: |
English |
ISSN: |
2227-9059 |
Relation: |
https://www.mdpi.com/2227-9059/11/2/400; https://doaj.org/toc/2227-9059 |
DOI: |
10.3390/biomedicines11020400 |
Access URL: |
https://doaj.org/article/7dec968b4bf94b339fb05d902152aec3 |
Accession Number: |
edsdoj.7dec968b4bf94b339fb05d902152aec3 |
Database: |
Directory of Open Access Journals |