Adjusting MtDNA quantification in whole blood for peripheral blood platelet and leukocyte counts

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Show simple item record Hurtado-Roca, Yamilee Ledesma, Marta González-Lázaro, Mónica Moreno-Loshuerto, Raquel Fernández-Silva, Patricio Enriquez, José Antonio Laclaustra, Martín
dc.contributor.other UAM. Departamento de Medicina Preventiva y Salud Pública y Microbiología es_ES 2017-04-24T17:36:37Z 2017-04-24T17:36:37Z 2016-10-01
dc.identifier.citation PLOS ONE 11.10 (2016): e016377 es_ES
dc.identifier.issn 1932-6203 es_ES
dc.description.abstract This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.Alterations of mitochondrial DNA copy number (mtDNAcn) in the blood (mitochondrial to nuclear DNA ratio) appear associated with several systemic diseases, including primary mitochondrial disorders, carcinogenesis, and hematologic diseases. Measuring mtDNAcn in DNA extracted from whole blood (WB) instead of from peripheral blood mononuclear cells or buffy coat may yield different results due to mitochondrial DNA present in platelets. The aim of this work is to quantify the contribution of platelets to mtDNAcn in whole blood [mtDNAcn(WB)] and to propose a correction formula to estimate leukocytes' mtDNAcn [mtDNAcn(L)] from mtDNAcn(WB). Blood samples from 10 healthy adults were combined with platelet-enriched plasma and saline solution to produce artificial blood preparations. Aliquots of each sample were combined with five different platelet concentrations. In 46 of these blood preparations, mtDNAcn was measured by qPCR. MtDNAcn(WB) increased 1.07 (95%CI 0.86, 1.29; p<0.001) per 1000 platelets present in the preparation. We proved that leukocyte count should also be taken into account as mtDNAcn(WB) was inversely associated with leukocyte count; it increased 1.10 (95%CI 0.95, 1.25, p<0.001) per unit increase of the ratio between platelet and leukocyte counts. If hematological measurements are available, subtracting 1.10 the platelets/leukocyte ratio from mtDNAcn(WB) may serve as an estimation for mtDNAcn(L). Both platelet and leukocyte counts in the sample are important sources of variation if comparing mtDNAcn among groups of patients when mtDNAcn is measured in DNA extracted from whole blood. Not taking the platelet/leukocyte ratio into account in whole blood measurements, may lead to overestimation and misclassification if interpreted as leukocytes' mtDNAcn. en_US
dc.description.sponsorship This work was supported by Grants PI10/00021 and PI14/00009 (which include FEDER funding) from Instituto de Salud Carlos III supported for research material; FINCyT Science and Technology Program (Scholarships Nº088-FINCyT-BDE-2014 from agreement 1663/OC-PE, between the Republic of Peru and the Inter-American Development Bank) provided support in the form of salaries for author [YHR]. es_ES
dc.format.extent 14 pag. es_ES
dc.format.mimetype application/pdf en
dc.language.iso eng en
dc.publisher Public Library of Science en_US
dc.relation.ispartof PLoS ONE en_US
dc.rights © 2016 Hurtado-Roca et al. es_ES
dc.subject.other Mitochondrial DNA en_US
dc.subject.other Blood en_US
dc.subject.other Systemic diseases en_US
dc.subject.other Platelet-enriched plasma en_US
dc.subject.other Leukocytes en_US
dc.title Adjusting MtDNA quantification in whole blood for peripheral blood platelet and leukocyte counts en_US
dc.type article en
dc.subject.eciencia Medicina es_ES
dc.relation.publisherversion es_ES
dc.identifier.doi 10.1371/journal.pone.0163770 es_ES
dc.identifier.publicationfirstpage e016377-1 es_ES
dc.identifier.publicationissue 10 es_ES
dc.identifier.publicationlastpage e016377-14 es_ES
dc.identifier.publicationvolume 11 es_ES
dc.type.version info:eu-repo/semantics/publishedVersion en Reconocimiento es_ES
dc.rights.accessRights openAccess en
dc.authorUAM Laclaustra Gimeno, Martín (262750)

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