A haemochromatosis-causing HFE mutation is associated with SARS-CoV-2 susceptibility in the Czech population
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00064190%3A_____%2F22%3AN0000055" target="_blank" >RIV/00064190:_____/22:N0000055 - isvavai.cz</a>
Alternative codes found
RIV/00216224:14110/23:00130381 RIV/00216208:11110/23:10452023 RIV/00216208:11120/23:43924470 RIV/00064190:_____/23:10000992 and 2 more
Result on the web
<a href="https://doi.org/10.1016/j.cca.2022.12.025" target="_blank" >https://doi.org/10.1016/j.cca.2022.12.025</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.cca.2022.12.025" target="_blank" >10.1016/j.cca.2022.12.025</a>
Alternative languages
Result language
angličtina
Original language name
A haemochromatosis-causing HFE mutation is associated with SARS-CoV-2 susceptibility in the Czech population
Original language description
Background: Coronavirus disease (COVID-19), which is caused by the SARS-CoV-2 virus, has become a global pandemic. While susceptibility to COVID-19 is subject to several external factors, including hypertension, BMI, and the presence of diabetes, it is also genetically determined to a significant extent. Infectious agents require iron (Fe) for proper functioning. Carriers of mutations resulting in increased iron concentrations are understood to be at increased risk of COVID-19.Methods: We examined HFE genotypes associated with hereditary haemochromatosis (rs1800562 and rs1799945 SNPs) in 617 COVID-19 patients (166 asymptomatic, 246 symptomatic and 205 hospitalised survivors) and 2 559 population-based controls.Results: We found a higher frequency of the minor allele (Tyr282) of the rs1800562 polymorphism (P < 0.002) in patients compared to controls (8.5 % vs 5.5 %). Non-carriers of the minor allele were protected against SARS-Cov-2 infection (OR, 95 %CI; 0.59, 0.42-0.82). The frequency of minor allele carriers was almost identical across asymptomatic, symptomatic, and hospitalised survivors. The rs1799945 variant did not affect disease severity and its occurrence was almost identical in patients and controls (P between 0.58 and 0.84).Conclusions: In conclusion, our results indicate that presence of the rs1800562 minor allele, which is associated with hereditary haemochromatosis (thus increased levels of plasma Fe), increases susceptibility to SARS-CoV-2.
Czech name
—
Czech description
—
Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
—
OECD FORD branch
20602 - Medical laboratory technology (including laboratory samples analysis; diagnostic technologies) (Biomaterials to be 2.9 [physical characteristics of living material as related to medical implants, devices, sensors])
Result continuities
Project
—
Continuities
V - Vyzkumna aktivita podporovana z jinych verejnych zdroju
Others
Publication year
2022
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Clinica Chimica Acta
ISSN
0009-8981
e-ISSN
1873-3492
Volume of the periodical
538
Issue of the periodical within the volume
12/2022
Country of publishing house
NL - THE KINGDOM OF THE NETHERLANDS
Number of pages
6
Pages from-to
211-215
UT code for WoS article
000923428500001
EID of the result in the Scopus database
2-s2.0-85145304911