Investigation of MBL2 and NOS3 functional gene variants in suspected COVID-19 PCR (–) patients

Pehlivan, Sacide; Köse, Murat; Mese, Sevim; Serin, Istemi; Senkal, Naci; Oyacı, Yasemin; Medetalibeyoglu, Alpay; Pehlivan, Mustafa; Sayın, Gözde Yesil; Isoglu-Alkac, Ummihan; Tukek, Tufan

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 MBL2 and NOS3 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 MBL2 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 MBL2 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.