AI Article Synopsis

  • The study investigates gene polymorphisms in COVID-19 patients with lung involvement who initially tested negative for the virus using PCR.
  • It includes 79 COVID-19 patients and 100 healthy controls, revealing that specific gene variations (AB genotype) were more common in PCR-positive patients compared to those who tested negative but had lung issues.
  • The absence of the AB genotype significantly increases the risk of detecting lung involvement through CT scans, suggesting its potential use for early identification of affected individuals despite negative PCR results.

Article Abstract

For COVID-19 (Coronavirus Disease-2019) cases, detecting host-based factors that predispose to infection is a very important research area. In this study, the aim is to investigate the and gene polymorphisms in COVID-19 patients with lung involvement, whose first nasopharyngeal PCR results were negative. Seventy-nine patients diagnosed with COVID-19 between April-June 2020 who were admitted to a university hospital, and 100 healthy controls were included. In the first statistical analysis performed between PCR-positive, CT-negative and PCR-negative, CT-positive patients; the AB of genotype was significantly higher in the first group (p = 0.049). The B allele was also significantly higher in the same subgroup (p = 0.001). The absence of the AB genotype was found to increase the risk of CT positivity by 6.9 times. The AB genotype of was higher in healthy controls (p = 0.006). The absence of the AB genotype was found to increase the risk of CT positivity; also, it can be used for early detection and isolation of patients with typical lung involvement who had enough viral loads, but whose initial PCR results were negative.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8477587PMC
http://dx.doi.org/10.1080/20477724.2021.1984726DOI Listing

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