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Blood group O is associated with post-COVID-19 syndrome in outpatients with a low comorbidity index
ABO blood group system modulates the inflammatory response and has been implicated in COVID-19. Group O protects against SARS-CoV-2 infection, but there are no data regarding post-COVID-19 syndrome (PCS). Our aim was to assess this possible association. Case-control study in a community setting, wit...
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Published in: | Infectious diseases (London, England) England), 2022-12, Vol.54 (12), p.897-908 |
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creator | Díaz-Salazar, Sara Navas, Raquel Sainz-Maza, Laura Fierro, Patricia Maamar, Meryam Artime, Arancha Basterrechea, Héctor Petitta, Benedetta Pini, Stefanie Olmos, José Manuel Ramos, Carmen Pariente, Emilio Hernández, José Luis |
description | ABO blood group system modulates the inflammatory response and has been implicated in COVID-19. Group O protects against SARS-CoV-2 infection, but there are no data regarding post-COVID-19 syndrome (PCS). Our aim was to assess this possible association.
Case-control study in a community setting, with subjects who had experienced mild COVID-19. Cases were PCS+, controls were PCS-, and the exposure variable, group O. We collected age, sex, BMI, smoking, comorbidities, inflammatory markers, anti-SARS-CoV-2 IgG antibodies, blood type and clinical data. Five composite inflammatory indices were developed. Multivariate analyses were performed.
We analysed 121 subjects (56.2% women), mean age 45.7 ± 16 years. Blood group frequencies were 41.5%, 7.9%, 5.9%, and 44.5% for A, B, AB and O, respectively. Thirty-six patients were PCS+, without significant differences between cases and controls. Compared to non-O, a higher prevalence of PCS (p = .036), and number of symptoms of PCS (p = .017) were noted in group O. Concerning biomarkers, PCS + and PCS- showed no differences in A, B, and AB groups. In contrast, group O PCS + patients had significantly lower albumin-to-globulin ratio and higher lymphocyte count, fibrinogen, CRP levels, and higher percentages of 3 composite indices, than PCS- subjects. Group O showed a 6-fold increased risk of PCS, compared to non-O (adjusted OR = 6.25 [95%CI, 1.6-23]; p = .007).
Group O has shown a consistent relationship with PCS, characterised by a more intense inflammatory burden than the other blood groups. Blood group O could be part of the immunological link between acute COVID-19 and PCS. |
doi_str_mv | 10.1080/23744235.2022.2115548 |
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Case-control study in a community setting, with subjects who had experienced mild COVID-19. Cases were PCS+, controls were PCS-, and the exposure variable, group O. We collected age, sex, BMI, smoking, comorbidities, inflammatory markers, anti-SARS-CoV-2 IgG antibodies, blood type and clinical data. Five composite inflammatory indices were developed. Multivariate analyses were performed.
We analysed 121 subjects (56.2% women), mean age 45.7 ± 16 years. Blood group frequencies were 41.5%, 7.9%, 5.9%, and 44.5% for A, B, AB and O, respectively. Thirty-six patients were PCS+, without significant differences between cases and controls. Compared to non-O, a higher prevalence of PCS (p = .036), and number of symptoms of PCS (p = .017) were noted in group O. Concerning biomarkers, PCS + and PCS- showed no differences in A, B, and AB groups. In contrast, group O PCS + patients had significantly lower albumin-to-globulin ratio and higher lymphocyte count, fibrinogen, CRP levels, and higher percentages of 3 composite indices, than PCS- subjects. Group O showed a 6-fold increased risk of PCS, compared to non-O (adjusted OR = 6.25 [95%CI, 1.6-23]; p = .007).
Group O has shown a consistent relationship with PCS, characterised by a more intense inflammatory burden than the other blood groups. Blood group O could be part of the immunological link between acute COVID-19 and PCS.</description><identifier>ISSN: 2374-4235</identifier><identifier>EISSN: 2374-4243</identifier><identifier>DOI: 10.1080/23744235.2022.2115548</identifier><language>eng</language><publisher>Taylor & Francis</publisher><subject>ABO blood group ; Blood group O ; COVID-19 ; inflammatory markers ; post-COVID-19 syndrome</subject><ispartof>Infectious diseases (London, England), 2022-12, Vol.54 (12), p.897-908</ispartof><rights>2022 Society for Scandinavian Journal of Infectious Diseases 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c390t-a1cf7aa9de3f3fdbfd9f38f16edcfb02726b49e4fd373eea6a09463b89555f013</citedby><cites>FETCH-LOGICAL-c390t-a1cf7aa9de3f3fdbfd9f38f16edcfb02726b49e4fd373eea6a09463b89555f013</cites><orcidid>0000-0002-7765-0891 ; 0000-0003-0035-3298 ; 0000-0002-6585-8847 ; 0000-0003-1970-1627</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,786,790,27957,27958</link.rule.ids></links><search><creatorcontrib>Díaz-Salazar, Sara</creatorcontrib><creatorcontrib>Navas, Raquel</creatorcontrib><creatorcontrib>Sainz-Maza, Laura</creatorcontrib><creatorcontrib>Fierro, Patricia</creatorcontrib><creatorcontrib>Maamar, Meryam</creatorcontrib><creatorcontrib>Artime, Arancha</creatorcontrib><creatorcontrib>Basterrechea, Héctor</creatorcontrib><creatorcontrib>Petitta, Benedetta</creatorcontrib><creatorcontrib>Pini, Stefanie</creatorcontrib><creatorcontrib>Olmos, José Manuel</creatorcontrib><creatorcontrib>Ramos, Carmen</creatorcontrib><creatorcontrib>Pariente, Emilio</creatorcontrib><creatorcontrib>Hernández, José Luis</creatorcontrib><title>Blood group O is associated with post-COVID-19 syndrome in outpatients with a low comorbidity index</title><title>Infectious diseases (London, England)</title><description>ABO blood group system modulates the inflammatory response and has been implicated in COVID-19. Group O protects against SARS-CoV-2 infection, but there are no data regarding post-COVID-19 syndrome (PCS). Our aim was to assess this possible association.
Case-control study in a community setting, with subjects who had experienced mild COVID-19. Cases were PCS+, controls were PCS-, and the exposure variable, group O. We collected age, sex, BMI, smoking, comorbidities, inflammatory markers, anti-SARS-CoV-2 IgG antibodies, blood type and clinical data. Five composite inflammatory indices were developed. Multivariate analyses were performed.
We analysed 121 subjects (56.2% women), mean age 45.7 ± 16 years. Blood group frequencies were 41.5%, 7.9%, 5.9%, and 44.5% for A, B, AB and O, respectively. Thirty-six patients were PCS+, without significant differences between cases and controls. Compared to non-O, a higher prevalence of PCS (p = .036), and number of symptoms of PCS (p = .017) were noted in group O. Concerning biomarkers, PCS + and PCS- showed no differences in A, B, and AB groups. In contrast, group O PCS + patients had significantly lower albumin-to-globulin ratio and higher lymphocyte count, fibrinogen, CRP levels, and higher percentages of 3 composite indices, than PCS- subjects. Group O showed a 6-fold increased risk of PCS, compared to non-O (adjusted OR = 6.25 [95%CI, 1.6-23]; p = .007).
Group O has shown a consistent relationship with PCS, characterised by a more intense inflammatory burden than the other blood groups. Blood group O could be part of the immunological link between acute COVID-19 and PCS.</description><subject>ABO blood group</subject><subject>Blood group O</subject><subject>COVID-19</subject><subject>inflammatory markers</subject><subject>post-COVID-19 syndrome</subject><issn>2374-4235</issn><issn>2374-4243</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kMtKxDAUhoMoOIzzCEKWbjrm0lt26ngbGJiNug1pLhppm5qkjH17Wzq6dHUOh-__4XwAXGK0xqhE14QWaUpotiaIkDXBOMvS8gQspnuSkpSe_u00OwerED4RQpgyNrILIO9q5xR8967v4B7aAEUITloRtYIHGz9g50JMNvu37X2CGQxDq7xrNLQtdH3sRLS6jWFGBazdAUrXOF9ZZeMwUkp_X4AzI-qgV8e5BK-PDy-b52S3f9pubneJpAzFRGBpCiGY0tRQoyqjmKGlwblW0lSIFCSvUqZTo2hBtRa5QCzNaVWyLMvM-NISXM29nXdfvQ6RNzZIXdei1a4PnBSoKIsixxOazaj0LgSvDe-8bYQfOEZ88sp_vfLJKz96HXM3c862xvlGHJyvFY9iqJ03XrTSBk7_r_gBSu1_sw</recordid><startdate>20221202</startdate><enddate>20221202</enddate><creator>Díaz-Salazar, Sara</creator><creator>Navas, Raquel</creator><creator>Sainz-Maza, Laura</creator><creator>Fierro, Patricia</creator><creator>Maamar, Meryam</creator><creator>Artime, Arancha</creator><creator>Basterrechea, Héctor</creator><creator>Petitta, Benedetta</creator><creator>Pini, Stefanie</creator><creator>Olmos, José Manuel</creator><creator>Ramos, Carmen</creator><creator>Pariente, Emilio</creator><creator>Hernández, José Luis</creator><general>Taylor & Francis</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-7765-0891</orcidid><orcidid>https://orcid.org/0000-0003-0035-3298</orcidid><orcidid>https://orcid.org/0000-0002-6585-8847</orcidid><orcidid>https://orcid.org/0000-0003-1970-1627</orcidid></search><sort><creationdate>20221202</creationdate><title>Blood group O is associated with post-COVID-19 syndrome in outpatients with a low comorbidity index</title><author>Díaz-Salazar, Sara ; Navas, Raquel ; Sainz-Maza, Laura ; Fierro, Patricia ; Maamar, Meryam ; Artime, Arancha ; Basterrechea, Héctor ; Petitta, Benedetta ; Pini, Stefanie ; Olmos, José Manuel ; Ramos, Carmen ; Pariente, Emilio ; Hernández, José Luis</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c390t-a1cf7aa9de3f3fdbfd9f38f16edcfb02726b49e4fd373eea6a09463b89555f013</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>ABO blood group</topic><topic>Blood group O</topic><topic>COVID-19</topic><topic>inflammatory markers</topic><topic>post-COVID-19 syndrome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Díaz-Salazar, Sara</creatorcontrib><creatorcontrib>Navas, Raquel</creatorcontrib><creatorcontrib>Sainz-Maza, Laura</creatorcontrib><creatorcontrib>Fierro, Patricia</creatorcontrib><creatorcontrib>Maamar, Meryam</creatorcontrib><creatorcontrib>Artime, Arancha</creatorcontrib><creatorcontrib>Basterrechea, Héctor</creatorcontrib><creatorcontrib>Petitta, Benedetta</creatorcontrib><creatorcontrib>Pini, Stefanie</creatorcontrib><creatorcontrib>Olmos, José Manuel</creatorcontrib><creatorcontrib>Ramos, Carmen</creatorcontrib><creatorcontrib>Pariente, Emilio</creatorcontrib><creatorcontrib>Hernández, José Luis</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Infectious diseases (London, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Díaz-Salazar, Sara</au><au>Navas, Raquel</au><au>Sainz-Maza, Laura</au><au>Fierro, Patricia</au><au>Maamar, Meryam</au><au>Artime, Arancha</au><au>Basterrechea, Héctor</au><au>Petitta, Benedetta</au><au>Pini, Stefanie</au><au>Olmos, José Manuel</au><au>Ramos, Carmen</au><au>Pariente, Emilio</au><au>Hernández, José Luis</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Blood group O is associated with post-COVID-19 syndrome in outpatients with a low comorbidity index</atitle><jtitle>Infectious diseases (London, England)</jtitle><date>2022-12-02</date><risdate>2022</risdate><volume>54</volume><issue>12</issue><spage>897</spage><epage>908</epage><pages>897-908</pages><issn>2374-4235</issn><eissn>2374-4243</eissn><notes>ObjectType-Article-1</notes><notes>SourceType-Scholarly Journals-1</notes><notes>ObjectType-Feature-2</notes><notes>content type line 23</notes><abstract>ABO blood group system modulates the inflammatory response and has been implicated in COVID-19. Group O protects against SARS-CoV-2 infection, but there are no data regarding post-COVID-19 syndrome (PCS). Our aim was to assess this possible association.
Case-control study in a community setting, with subjects who had experienced mild COVID-19. Cases were PCS+, controls were PCS-, and the exposure variable, group O. We collected age, sex, BMI, smoking, comorbidities, inflammatory markers, anti-SARS-CoV-2 IgG antibodies, blood type and clinical data. Five composite inflammatory indices were developed. Multivariate analyses were performed.
We analysed 121 subjects (56.2% women), mean age 45.7 ± 16 years. Blood group frequencies were 41.5%, 7.9%, 5.9%, and 44.5% for A, B, AB and O, respectively. Thirty-six patients were PCS+, without significant differences between cases and controls. Compared to non-O, a higher prevalence of PCS (p = .036), and number of symptoms of PCS (p = .017) were noted in group O. Concerning biomarkers, PCS + and PCS- showed no differences in A, B, and AB groups. In contrast, group O PCS + patients had significantly lower albumin-to-globulin ratio and higher lymphocyte count, fibrinogen, CRP levels, and higher percentages of 3 composite indices, than PCS- subjects. Group O showed a 6-fold increased risk of PCS, compared to non-O (adjusted OR = 6.25 [95%CI, 1.6-23]; p = .007).
Group O has shown a consistent relationship with PCS, characterised by a more intense inflammatory burden than the other blood groups. Blood group O could be part of the immunological link between acute COVID-19 and PCS.</abstract><pub>Taylor & Francis</pub><doi>10.1080/23744235.2022.2115548</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-7765-0891</orcidid><orcidid>https://orcid.org/0000-0003-0035-3298</orcidid><orcidid>https://orcid.org/0000-0002-6585-8847</orcidid><orcidid>https://orcid.org/0000-0003-1970-1627</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | ABO blood group Blood group O COVID-19 inflammatory markers post-COVID-19 syndrome |
title | Blood group O is associated with post-COVID-19 syndrome in outpatients with a low comorbidity index |
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