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Are H1 and H3 haplotypes of endothelial protein C receptor (PROCR) an important factor in contracting COVID-19?
Mehmet Reşat Ceylan1, Nazım Kankılıç2, Özlem Öz3
1Department of Infectious Diseases and Clinical Microbiology, Faculty of Medicine, Campus of Osmanbey, University of Harran, Şanlıurfa, Turkey.
Insights
Genetic factors influence COVID-19 susceptibility. Specific endothelial protein C receptor (PROCR) haplotypes, PROCR H1 and PROCR H3, were found to be associated with increased risk of contracting COVID-19 infection.
Area of Science:
- Cardiovascular Genetics
- Infectious Disease Epidemiology
Background:
- COVID-19 (coronavirus 2019) infection can lead to cardiovascular disease and myocardial damage.
- Understanding the interplay between genetic predispositions and COVID-19 infection is crucial for risk assessment.
Purpose of the Study:
- To investigate the relationship between genetic cardiovascular risk factors and COVID-19 infection.
- To identify specific genetic markers associated with COVID-19 susceptibility and severity.
Main Methods:
- Study included 135 patients: 27 COVID-19 negative and 108 COVID-19 positive.
- Patients were categorized into three groups: COVID-19 negative, asymptomatic COVID-19 positive, and symptomatic COVID-19 positive with pulmonary involvement.
- New generation sequencing was used to analyze genetic cardiovascular risk factors in blood samples.
Main Results:
- No significant differences in several genetic factors (fibrinogen, HPA1, ACE, AGT, AGTR1, Apo E, eNOS) were found across the groups.
- Significant differences were observed in endothelial protein C receptor (PROCR) gene variants: PROCR H3 haplotype/G (A3 haplotype) and PROCR H1 haplotype/C (A1 haplotype).
- COVID-19 positivity was more common in individuals with PROCR H1 haplotype/C and PROCR H3 haplotype/G genotypes.
Conclusions:
- PROCR H1 and PROCR H3 haplotypes may play a significant role in susceptibility to COVID-19 infection.
- Identifying PROCR genetic variations and measuring soluble EPCR (sEPCR) levels could aid in managing COVID-19 patients.
Abstract:
The development of cardiovascular disease shows increase after contracting coronavirus 2019 (COVID-19) disease and myocardial damage is observed in patients who have had the disease severely. The relationship between genetic cardiovascular risk factors with COVID-19 infection was investigated in our study. One hundred thirty-five patients, 27 of whom were COVID-19 (-) and 108 were COVID-19 (+) patients, were included in the study. Patients were divided into three groups ([COVID-19 [-], COVID-19 [+] asymptomatic, and COVID-19 [+] symptomatic + patients with pulmonary involvement]). Genetic cardiovascular risk factors were examined in blood samples taken from the patients with new generation sequencing analysis. In the clinical classification, there were no significant differences between the three groups in fibrinogen beta chain-455G>A, human platelet antigen 1 (HPA1b)/platelet receptor GPIIIa/(ITGB3) (HPA1a/b; GpIIIa; integrin beta 3 L33P), ACE I/D, AGT (M268T), AGTR1 (1166A>C), Apo E (E2/E3/E4) (rs7412, rs429358), eNOS (786T>C), eNOS (894G>T) genes (p > 0.05). However, significant differences were observed in PROCR H3 haplotype/G (endothelial protein C receptor gene [EPCR] 4600A>G [A3 haplotype]), PROCR H1 haplotype/C (EPCR 4678G>C [A1 haplotype]) genes (p < 0.05). When COVID-19 (+) and COVID-19 (-) groups were compared, it was observed that the infection was more common in people with PROCR H1 haplotype/C and PROCR H3 haplotype/G genotypes (p < 0.05). PROCR H1 and PROCR H3 haplotypes may be an important factor in contracting COVID-19 disease. In people with COVID-19 disease, revealing PROCR genetic differences and measuring sEPCR levels will be beneficial in the follow-up of the disease.
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