Human Ace D/I Polymorphism Could Affect the Clinicobiological Course of COVID-19

Introduction. The coronavirus disease 2019 (COVID-19), that is caused by severe acute respiratory syndrome corona virus 2 (SARS-CoV-2), has spread rapidly worldwide since December 2019. The SARS-CoV-2 virus has a great affinity for the angiotensin-converting enzyme-2 (ACE-2) receptor, which is an es...

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Veröffentlicht in:Journal of the renin-angiotensin-aldosterone system 2021-01, Vol.2021, p.5509280-5509280
Hauptverfasser: Aladag, Elifcan, Tas, Zahit, Ozdemir, Bilgesu Safak, Akbaba, Tayfun Hilmi, Akpınar, Meltem Gulsun, Goker, Hakan, Unalan-Altintop, Tugce, Inkaya, Ahmet Cagkan, Alp, Alpaslan, Metan, Gokhan, Haznedaroglu, Ibrahim Celalettin, Balci-Peynircioglu, Banu, Sayinalp, Nilgun
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Sprache:eng
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Zusammenfassung:Introduction. The coronavirus disease 2019 (COVID-19), that is caused by severe acute respiratory syndrome corona virus 2 (SARS-CoV-2), has spread rapidly worldwide since December 2019. The SARS-CoV-2 virus has a great affinity for the angiotensin-converting enzyme-2 (ACE-2) receptor, which is an essential element of the renin-angiotensin system (RAS). This study is aimed at assessing the impact of the angiotensin-converting enzyme (ACE) gene insertion (I)/deletion (D) polymorphisms, on the susceptibility and clinical outcomes of the COVID-19 immunoinflammatory syndrome. Patients and Methods. A total of 112 patients diagnosed with COVID-19 between 1 and 15 May 2020 were enrolled in the study. ACE gene allele frequencies were compared to the previously reported Turkish population comprised of 300 people. Results. The most common genotype in the patients and control group was DI with 53% and II with 42%, respectively. The difference in the presence of the D allele between the patient and control groups was statistically significant (67% vs. 42%, respectively, p
ISSN:1470-3203
1752-8976
DOI:10.1155/2021/5509280