<?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>2026-04-29T06:16:11Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/7686" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/7686</identifier><datestamp>2025-04-29T13:38:55Z</datestamp><setSpec>com_20.500.12105_2052</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>com_20.500.12105_15322</setSpec><setSpec>col_20.500.12105_19609</setSpec><setSpec>col_20.500.12105_16958</setSpec><setSpec>col_20.500.12105_16971</setSpec><setSpec>col_20.500.12105_16977</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">Medrano, Luz Maria</subfield>
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      <subfield code="a">Gutiirrez-Rivas, Monica</subfield>
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      <subfield code="a">Blanco, Julià</subfield>
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      <subfield code="a">García, Marcial</subfield>
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      <subfield code="a">Jimenez-Sousa, Maria Angeles</subfield>
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      <subfield code="a">Pacheco, Yolanda María</subfield>
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      <subfield code="a">Montero, Marta</subfield>
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      <subfield code="a">Iribarren, José Antonio</subfield>
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      <subfield code="a">Bernal, Enrique</subfield>
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      <subfield code="a">Martínez, Onofre Juan</subfield>
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      <subfield code="a">Benito, José Miguel</subfield>
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      <subfield code="a">Rallón, Norma</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Resino, Salvador</subfield>
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      <subfield code="c">2018</subfield>
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      <subfield code="a">BACKGROUND: The mitochondrial DNA (mtDNA) seems to influence in a large number of diseases, including HIV infection. Moreover, there is a substantial inter-individual variability in the CD4+ recovery in HIV-infected patients on combination antiretroviral therapy (cART). Our study aimed to analyze the association between mtDNA haplogroups and CD4+ recovery in HIV-infected patients on cART. METHODS: This is a retrospective study of 324 naïve cART patients with CD4+ &lt; 200 cells/mm3, who were followed-up during 24 months after initiating cART. All patients had undetectable HIV viral load during the follow-up. Besides, we included 141 healthy controls. MtDNA genotyping was performed by using Sequenom's MassARRAY platform. The primary outcome variable was the slope of CD4+ recovery. Patients were stratified into two groups by the median slope value of CD4+ (9.65 CD4+ cells/mm3/month). Logistic regression analyses were performed to calculate the odds of CD4+ recovery according to mtDNA haplogroups. RESULTS: Our study included European HIV-infected patients within the N macro-cluster. The baseline values of CD4+ T-cells were similar between groups of patients stratified by the P50th of the slope of CD4+ T-cells recovery. Patients in the low CD4+ T-cells recovery group were older (p = 0.001), but this variable was included in the multivariate models. When we analyzed the frequencies of mtDNA haplogroups, no significant differences between HIV-infected individuals and healthy controls were found. We did not find any significant association between mtDNA haplogroups and the slope of CD4+ T-cells recovery by linear regression analysis. However, Patients carrying haplogroup H had a higher odds of having a better CD4+ recovery (> 9.65 CD4+ cells/mm3/month) than patients without haplogroup H (p = 0.032). The adjusted logistic regression showed that patients carrying haplogroup H had a higher likelihood of achieving a CD4+ recovery > 9.65 CD4+ cells/mm3/month [adjusted odds ratio (aOR) = 1.75 (95% CI = 1.04; 2.95); p = 0.035]. CONCLUSIONS: European mitochondrial haplogroup H was associated with the improved CD4+ recovery in HIV-infected patients starting cART with CD4+ &lt; 200 cells/mm3.</subfield>
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      <subfield code="a">J Transl Med. 2018 Dec 6;16(1):343.</subfield>
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      <subfield code="a">1479-5876</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12105/7686</subfield>
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      <subfield code="a">30522500</subfield>
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      <subfield code="a">10.1186/s12967-018-1717-y</subfield>
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      <subfield code="a">1479-5876</subfield>
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      <subfield code="a">Journal of translational medicine</subfield>
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      <subfield code="a">HIV</subfield>
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      <subfield code="a">Haplogroups</subfield>
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      <subfield code="a">Immune reconstitution</subfield>
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      <subfield code="a">Mitochondria</subfield>
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      <subfield code="a">cART</subfield>
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      <subfield code="a">mtDNA</subfield>
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      <subfield code="a">Mitochondrial haplogroup H is related to CD4+ T cell recovery in HIV infected patients starting combination antiretroviral therapy</subfield>
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