<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-05-22T00:53:39Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/23440" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/23440</identifier><datestamp>2024-11-28T20:17:15Z</datestamp><setSpec>com_20.500.12105_15322</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>col_20.500.12105_16967</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Torrens-Mas, Margalida</subfield>
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      <subfield code="a">Galmes-Panades, Aina Maria</subfield>
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      <subfield code="a">Sanchez-Polo, Andrés</subfield>
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      <subfield code="a">Pierola Lopetegui, Javier</subfield>
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      <subfield code="a">Barceló, Carles</subfield>
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      <subfield code="a">Gonzalez-Freire, Marta</subfield>
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      <subfield code="a">Coronavirus disease 19 (COVID-19) is a persistent global pandemic with a very heterogeneous disease presentation ranging from a mild disease to dismal prognosis. Early detection of sensitivity and severity of COVID-19 is essential for the development of new treatments. In the present study, we measured the levels of circulating growth differentiation factor 15 (GDF15) and angiotensin-converting enzyme 2 (ACE2) in plasma of severity-stratified COVID-19 patients and uninfected control patients and characterized the in vitro effects and cohort frequency of ACE2 SNPs. Our results show that while circulating GDF15 and ACE2 stratify COVID-19 patients according to disease severity, ACE2 missense SNPs constitute a risk factor linked to infection susceptibility.</subfield>
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      <subfield code="a">Torrens-Mas M, Perelló-Reus CM, Trias-Ferrer N, Ibargüen- González L, Crespí C, Galmes-Panades AM, et al. GDF15 and ACE2 stratify COVID-19 patients according to severity while ACE2 mutations increase infection susceptibility. Front Cell Infect Microbiol. 2022 Jul 22;12:942951.</subfield>
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      <subfield code="a">GDF15 and ACE2 stratify COVID-19 patients according to severity while ACE2 mutations increase infection susceptibility</subfield>
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