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COVID-19 as a worldwide selective event and bitter taste receptor polymorphisms: An ecological correlational study
Given the observed olfactory and gustatory dysfunctions in patients with COVID-19 and recent findings on taste receptors possible important activities in the immune system, we elected to estimate the correlation between COVID-19 mortality and polymorphism of a particular type of bitter taste recepto...
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Published in: | International journal of biological macromolecules 2021-04, Vol.177, p.204-210 |
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creator | Parsa, Shima Mogharab, Vahid Ebrahimi, Mohsen Ahmadi, Sayyed Reza Shahi, Behzad Mehramiz, Neema John Foroughian, Mahdi Zarenezhad, Mohammad Kalani, Navid Abdi, Mohammad Hashem Javdani, Farshid Keshavarz, Pouyan Hatami, Naser |
description | Given the observed olfactory and gustatory dysfunctions in patients with COVID-19 and recent findings on taste receptors possible important activities in the immune system, we elected to estimate the correlation between COVID-19 mortality and polymorphism of a particular type of bitter taste receptor gene called TAS2R38, in a worldwide epidemiological point of view.
Pooled rate of each of the rs713598, rs1726866, rs10246939, and PAV/AVI polymorphisms of the TAS2R38 gene was obtained in different countries using a systematic review methodology and its relationship with the mortality of COVID-19. Data were analyzed by the comprehensive meta-analysis software and SPSS.
There was only a significant reverse Pearson correlation in death counts and PAV/AVI ratio, p = 0.047, r = −0.503. Also, a significant reverse correlation of PAV/AVI ratio and death rate was seen, r = −0.572 p = 0.021. rs10246939 ratio had a significant positive correlation with death rate, r = 0.851 p = 0.031. Further analysis was not significant. Our results showed that the higher presence of PAV allele than AVI, and a higher rate of G allele than A in rs10246939 polymorphism in a country, could be associated with lower COVID-19 mortality. While assessing all three polymorphisms showed a huge diversity worldwide.
Due to extraoral activities of bitter taste receptor genes, especially in mucosal immunity, this gene seems to be a good candidate for future studies on COVID-19 pathophysiology. Also, the high worldwide diversity of TAS2R38 genes polymorphism and its possible assassination with mortality raises concerns about the efficiency of vaccine projects in different ethnicities. |
doi_str_mv | 10.1016/j.ijbiomac.2021.02.070 |
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Pooled rate of each of the rs713598, rs1726866, rs10246939, and PAV/AVI polymorphisms of the TAS2R38 gene was obtained in different countries using a systematic review methodology and its relationship with the mortality of COVID-19. Data were analyzed by the comprehensive meta-analysis software and SPSS.
There was only a significant reverse Pearson correlation in death counts and PAV/AVI ratio, p = 0.047, r = −0.503. Also, a significant reverse correlation of PAV/AVI ratio and death rate was seen, r = −0.572 p = 0.021. rs10246939 ratio had a significant positive correlation with death rate, r = 0.851 p = 0.031. Further analysis was not significant. Our results showed that the higher presence of PAV allele than AVI, and a higher rate of G allele than A in rs10246939 polymorphism in a country, could be associated with lower COVID-19 mortality. While assessing all three polymorphisms showed a huge diversity worldwide.
Due to extraoral activities of bitter taste receptor genes, especially in mucosal immunity, this gene seems to be a good candidate for future studies on COVID-19 pathophysiology. Also, the high worldwide diversity of TAS2R38 genes polymorphism and its possible assassination with mortality raises concerns about the efficiency of vaccine projects in different ethnicities.</description><identifier>ISSN: 0141-8130</identifier><identifier>EISSN: 1879-0003</identifier><identifier>DOI: 10.1016/j.ijbiomac.2021.02.070</identifier><identifier>PMID: 33582215</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Alleles ; Correlation of Data ; COVID-19 ; COVID-19 - genetics ; COVID-19 - mortality ; Databases, Factual ; Genetic Association Studies ; Genetic Predisposition to Disease ; Genotype ; Humans ; Mortality ; Polymorphism ; Polymorphism, Single Nucleotide ; Receptors, G-Protein-Coupled - genetics ; TAS2R38 gene ; Taste - genetics</subject><ispartof>International journal of biological macromolecules, 2021-04, Vol.177, p.204-210</ispartof><rights>2021 Elsevier B.V.</rights><rights>Copyright © 2021 Elsevier B.V. All rights reserved.</rights><rights>2021 Elsevier B.V. All rights reserved. 2021 Elsevier B.V.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c471t-c01d4857daf2637a8aeff8ee2f4d0e9328c2edbd8b5df68b1a94897778325e073</citedby><cites>FETCH-LOGICAL-c471t-c01d4857daf2637a8aeff8ee2f4d0e9328c2edbd8b5df68b1a94897778325e073</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33582215$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Parsa, Shima</creatorcontrib><creatorcontrib>Mogharab, Vahid</creatorcontrib><creatorcontrib>Ebrahimi, Mohsen</creatorcontrib><creatorcontrib>Ahmadi, Sayyed Reza</creatorcontrib><creatorcontrib>Shahi, Behzad</creatorcontrib><creatorcontrib>Mehramiz, Neema John</creatorcontrib><creatorcontrib>Foroughian, Mahdi</creatorcontrib><creatorcontrib>Zarenezhad, Mohammad</creatorcontrib><creatorcontrib>Kalani, Navid</creatorcontrib><creatorcontrib>Abdi, Mohammad Hashem</creatorcontrib><creatorcontrib>Javdani, Farshid</creatorcontrib><creatorcontrib>Keshavarz, Pouyan</creatorcontrib><creatorcontrib>Hatami, Naser</creatorcontrib><title>COVID-19 as a worldwide selective event and bitter taste receptor polymorphisms: An ecological correlational study</title><title>International journal of biological macromolecules</title><addtitle>Int J Biol Macromol</addtitle><description>Given the observed olfactory and gustatory dysfunctions in patients with COVID-19 and recent findings on taste receptors possible important activities in the immune system, we elected to estimate the correlation between COVID-19 mortality and polymorphism of a particular type of bitter taste receptor gene called TAS2R38, in a worldwide epidemiological point of view.
Pooled rate of each of the rs713598, rs1726866, rs10246939, and PAV/AVI polymorphisms of the TAS2R38 gene was obtained in different countries using a systematic review methodology and its relationship with the mortality of COVID-19. Data were analyzed by the comprehensive meta-analysis software and SPSS.
There was only a significant reverse Pearson correlation in death counts and PAV/AVI ratio, p = 0.047, r = −0.503. Also, a significant reverse correlation of PAV/AVI ratio and death rate was seen, r = −0.572 p = 0.021. rs10246939 ratio had a significant positive correlation with death rate, r = 0.851 p = 0.031. Further analysis was not significant. Our results showed that the higher presence of PAV allele than AVI, and a higher rate of G allele than A in rs10246939 polymorphism in a country, could be associated with lower COVID-19 mortality. While assessing all three polymorphisms showed a huge diversity worldwide.
Due to extraoral activities of bitter taste receptor genes, especially in mucosal immunity, this gene seems to be a good candidate for future studies on COVID-19 pathophysiology. Also, the high worldwide diversity of TAS2R38 genes polymorphism and its possible assassination with mortality raises concerns about the efficiency of vaccine projects in different ethnicities.</description><subject>Alleles</subject><subject>Correlation of Data</subject><subject>COVID-19</subject><subject>COVID-19 - genetics</subject><subject>COVID-19 - mortality</subject><subject>Databases, Factual</subject><subject>Genetic Association Studies</subject><subject>Genetic Predisposition to Disease</subject><subject>Genotype</subject><subject>Humans</subject><subject>Mortality</subject><subject>Polymorphism</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Receptors, G-Protein-Coupled - genetics</subject><subject>TAS2R38 gene</subject><subject>Taste - genetics</subject><issn>0141-8130</issn><issn>1879-0003</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNqFkU9P3DAQxa2qqGxpvwLysZcE_0lip4eqaCktEhIX2qvl2BPwyolT27tov32NFlA5cbLGfvPeeH4InVJSU0K7s03tNoMLkzY1I4zWhNVEkHdoRaXoK0IIf49WhDa0kpSTY_QxpU257VoqP6BjzlvJGG1XKK5v_lxdVLTHOmGNH0L09sFZwAk8mOx2gGEHc8Z6tnhwOUPEWacMOIKBJYeIl-D3U4jLvUtT-orPZwwm-HDnjPbYhBjB6-zCXKqUt3b_CR2N2if4_HSeoN-XP27Xv6rrm59X6_PryjSC5soQahvZCqtH1nGhpYZxlABsbCyBnjNpGNjByqG1YycHqvtG9kIIyVkLRPAT9O3gu2yHCawpv4jaqyW6Sce9Ctqp1y-zu1d3YackabjoumLw5ckghr9bSFlNLhnwXs8QtkmxkteRVjRNkXYHqYkhpQjjSwwl6hGY2qhnYOoRmCJMFWCl8fT_IV_angkVwfeDAMqqdg6iSsbBbMC6QiArG9xbGf8AwhStkA</recordid><startdate>20210430</startdate><enddate>20210430</enddate><creator>Parsa, Shima</creator><creator>Mogharab, Vahid</creator><creator>Ebrahimi, Mohsen</creator><creator>Ahmadi, Sayyed Reza</creator><creator>Shahi, Behzad</creator><creator>Mehramiz, Neema John</creator><creator>Foroughian, Mahdi</creator><creator>Zarenezhad, Mohammad</creator><creator>Kalani, Navid</creator><creator>Abdi, Mohammad Hashem</creator><creator>Javdani, Farshid</creator><creator>Keshavarz, Pouyan</creator><creator>Hatami, Naser</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20210430</creationdate><title>COVID-19 as a worldwide selective event and bitter taste receptor polymorphisms: An ecological correlational study</title><author>Parsa, Shima ; 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Pooled rate of each of the rs713598, rs1726866, rs10246939, and PAV/AVI polymorphisms of the TAS2R38 gene was obtained in different countries using a systematic review methodology and its relationship with the mortality of COVID-19. Data were analyzed by the comprehensive meta-analysis software and SPSS.
There was only a significant reverse Pearson correlation in death counts and PAV/AVI ratio, p = 0.047, r = −0.503. Also, a significant reverse correlation of PAV/AVI ratio and death rate was seen, r = −0.572 p = 0.021. rs10246939 ratio had a significant positive correlation with death rate, r = 0.851 p = 0.031. Further analysis was not significant. Our results showed that the higher presence of PAV allele than AVI, and a higher rate of G allele than A in rs10246939 polymorphism in a country, could be associated with lower COVID-19 mortality. While assessing all three polymorphisms showed a huge diversity worldwide.
Due to extraoral activities of bitter taste receptor genes, especially in mucosal immunity, this gene seems to be a good candidate for future studies on COVID-19 pathophysiology. Also, the high worldwide diversity of TAS2R38 genes polymorphism and its possible assassination with mortality raises concerns about the efficiency of vaccine projects in different ethnicities.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>33582215</pmid><doi>10.1016/j.ijbiomac.2021.02.070</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Alleles Correlation of Data COVID-19 COVID-19 - genetics COVID-19 - mortality Databases, Factual Genetic Association Studies Genetic Predisposition to Disease Genotype Humans Mortality Polymorphism Polymorphism, Single Nucleotide Receptors, G-Protein-Coupled - genetics TAS2R38 gene Taste - genetics |
title | COVID-19 as a worldwide selective event and bitter taste receptor polymorphisms: An ecological correlational study |
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