Publication:
Mitochondrial haplogroup H is related to CD4+ T cell recovery in HIV infected patients starting combination antiretroviral therapy

dc.contributor.authorMedrano, Luz Maria
dc.contributor.authorGutiirrez-Rivas, Monica
dc.contributor.authorBlanco, Julià
dc.contributor.authorGarcía, Marcial
dc.contributor.authorJimenez-Sousa, Maria Angeles
dc.contributor.authorPacheco, Yolanda María
dc.contributor.authorMontero, Marta
dc.contributor.authorIribarren, José Antonio
dc.contributor.authorBernal, Enrique
dc.contributor.authorMartínez, Onofre Juan
dc.contributor.authorBenito, José Miguel
dc.contributor.authorRallón, Norma
dc.contributor.authorResino, Salvador
dc.contributor.funderInstituto de Salud Carlos III
dc.contributor.funderUnión Europea. Fondo Europeo de Desarrollo Regional (FEDER/ERDF)
dc.contributor.funderFundación para la Investigación y la Prevención del Sida en España
dc.contributor.funderRed de Investigación Cooperativa en Investigación en Sida (España)
dc.date.accessioned2019-05-28T09:45:24Z
dc.date.available2019-05-28T09:45:24Z
dc.date.issued2018
dc.description.abstractBACKGROUND: 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+ < 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+ < 200 cells/mm3.es_ES
dc.description.peerreviewedes_ES
dc.description.sponsorshipThis work has been (partially) funded by Grants RD12/0017/0024 and RD16CIII/0002/0002 to SR, and RD12/0017/0031 and RD16/0025/0013 to JMB as part of the Health Research and Development Strategy, State Plan for Scientific and Technical Research and Innovation (2008–2011; 2013–2016) and co-financed by Institute of Health Carlos III, ISCIII–Sub-Directorate General for Research Assessment and Promotion and European Regional Development Fund (ERDF). Luz Mª Medrano is supported by Spanish Carlos III Institute of Health (ISCIII) Madrid, Spain [Grant Number CD14/00002]. N Rallón is a Miguel Servet investigator from the ISCIII [Grant Number CP14/00198]; M. García is a predoctoral student co-funded by CP14/00198 Grant and Intramural Research Scholarship from IIS-FJD. The authors would like to thank the Spanish National Genotyping Center (CEGEN-PRB2-ISCIII) for providing SNP genotyping services (http://www.cegen.org). CEGEN is supported by grant PT13/0001, ISCIII-SGEFI/FEDER. We also acknowledge the patients in this study for their participation and the Centro de Transfusión of Comunidad de Madrid for the healthy donor blood samples provided. We acknowledge the Spanish HIV-1 BioBank integrated into the Spanish AIDS Research Network (RIS) and collaborating centers for the clinical samples provided. The HIV BioBank, integrated in the Spanish AIDS Research Network, is supported by ISCIII, Spanish Health Ministry (Grant nº RD06/0006/0035 and RD12/0017/0037) as part of the State Plan for Scientific and Technical Research and Innovation and co-financed by ISCIII–Sub-Directorate General for Research Assessment and Promotion and European Regional Development Fund (ERDF) and Foundation for Research and Prevention of AIDS in Spain (FIPSE). The RIS Cohort (CoRIS) is funded by the ISCIII through the Spanish AIDS Research Network (RISC03/173 and RD12/0017/0018) as part of the State Plan for Scientific and Technical Research and Innovation and co-financed by ISCIII–Sub-Directorate General for Research Assessment and Promotion and European Regional Development Fund (ERDF).es_ES
dc.format.number1es_ES
dc.format.page343es_ES
dc.format.volume16es_ES
dc.identifier.citationJ Transl Med. 2018 Dec 6;16(1):343.es_ES
dc.identifier.doi10.1186/s12967-018-1717-yes_ES
dc.identifier.e-issn1479-5876es_ES
dc.identifier.issn1479-5876es_ES
dc.identifier.journalJournal of translational medicinees_ES
dc.identifier.pubmedID30522500es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/7686
dc.language.isoenges_ES
dc.publisherBioMed Central (BMC)
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/RD12/0017/0024es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/RD16CIII/0002/0002es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/RD12/0017/0031es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/RD16/0025/0013es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/CD14/00002es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/CP14/00198es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/PT13/0001es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/RD06/0006/0035es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/RD12/0017es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/RISC03/173es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/RD12/0017/0018es_ES
dc.relation.publisherversionhttps://doi.org/10.1186/s12967-018-1717-yes_ES
dc.repisalud.centroISCIII::Centro Nacional de Microbiologíaes_ES
dc.repisalud.institucionISCIIIes_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectHIVes_ES
dc.subjectHaplogroupses_ES
dc.subjectImmune reconstitutiones_ES
dc.subjectMitochondriaes_ES
dc.subjectcARTes_ES
dc.subjectmtDNAes_ES
dc.titleMitochondrial haplogroup H is related to CD4+ T cell recovery in HIV infected patients starting combination antiretroviral therapyes_ES
dc.typeresearch articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
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