<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wu Y</submitter><funding>the Special Project of Contingency Research for COVID-19 at Hubei University of Medicine</funding><funding>the Cultivating Project for Young Scholar at Hubei University of Medicine</funding><pagination>57</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8558762</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>8(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Mitochondria have been shown to play vital roles during severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and coronavirus disease 2019 (COVID-19) development. Currently, it is unclear whether mitochondrial DNA (mtDNA) variants, which define mtDNA haplogroups and determine oxidative phosphorylation performance and reactive oxygen species production, are associated with COVID-19 risk.&lt;h4>Methods&lt;/h4>A population-based case-control study was conducted to compare the distribution of mtDNA variations defining mtDNA haplogroups between healthy controls (n = 615) and COVID-19 patients (n = 536). COVID-19 patients were diagnosed based on molecular diagnostics of the viral genome by qPCR and chest X-ray or computed tomography scanning. The exclusion criteria </pubmed_abstract><journal>Military Medical Research</journal><pubmed_title>Common mtDNA variations at C5178a and A249d/T6392C/G10310A decrease the risk of severe COVID-19 in a Han Chinese population from Central China.</pubmed_title><pmcid>PMC8558762</pmcid><funding_grant_id>№: 2018QDJZR01</funding_grant_id><funding_grant_id>№:2020XGFYZR11</funding_grant_id><funding_grant_id>№:2020XGFYZR03</funding_grant_id><pubmed_authors>Peng CY</pubmed_authors><pubmed_authors>Fang ZC</pubmed_authors><pubmed_authors>Yu SL</pubmed_authors><pubmed_authors>Wang YF</pubmed_authors><pubmed_authors>Wang XH</pubmed_authors><pubmed_authors>Li XH</pubmed_authors><pubmed_authors>Cheng W</pubmed_authors><pubmed_authors>Liu YQ</pubmed_authors><pubmed_authors>Ma HC</pubmed_authors><pubmed_authors>Zhang SY</pubmed_authors><pubmed_authors>Tang JM</pubmed_authors><pubmed_authors>Song LY</pubmed_authors><pubmed_authors>Wang LF</pubmed_authors><pubmed_authors>Ji FY</pubmed_authors><pubmed_authors>Wu Y</pubmed_authors><pubmed_authors>Yuan LY</pubmed_authors></additional><is_claimable>false</is_claimable><name>Common mtDNA variations at C5178a and A249d/T6392C/G10310A decrease the risk of severe COVID-19 in a Han Chinese population from Central China.</name><description>&lt;h4>Background&lt;/h4>Mitochondria have been shown to play vital roles during severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and coronavirus disease 2019 (COVID-19) development. Currently, it is unclear whether mitochondrial DNA (mtDNA) variants, which define mtDNA haplogroups and determine oxidative phosphorylation performance and reactive oxygen species production, are associated with COVID-19 risk.&lt;h4>Methods&lt;/h4>A population-based case-control study was conducted to compare the distribution of mtDNA variations defining mtDNA haplogroups between healthy controls (n = 615) and COVID-19 patients (n = 536). COVID-19 patients were diagnosed based on molecular diagnostics of the viral genome by qPCR and chest X-ray or computed tomography scanning. The exclusion criteria </description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Nov</publication><modification>2026-05-08T05:42:35.142Z</modification><creation>2022-02-11T12:26:36.033Z</creation></dates><accession>S-EPMC8558762</accession><cross_references><pubmed>34724985</pubmed><doi>10.1186/s40779-021-00351-2</doi></cross_references></HashMap>