Avaliação da fração de plaquetas imaturas no diagnóstico da trombocitopenia imune e sua relação com a gravidade da Covid-19

Detalhes bibliográficos
Autor(a) principal: Pereira, Karla Nunes
Data de Publicação: 2022
Tipo de documento: Tese
Idioma: por
Título da fonte: Manancial - Repositório Digital da UFSM
dARK ID: ark:/26339/001300000g458
Texto Completo: http://repositorio.ufsm.br/handle/1/27403
Resumo: Platelets are cytoplasmic fragments of megakaryocytes, cells present in the bone marrow, which are key players in hemostasis. Adequate platelet kinetics, with a balance between production, activation, and apoptosis, is essential to maintain the stability of this process. Hemostasis imbalance due to different causes results in changes in the number and/or function of platelets. In immune thrombocytopenia (ITP), this imbalance leads to a reduction in the number of platelets. In COVID-19, the imbalance results in platelet hyperactivation with consequent immunothrombotic dysregulation. Recently, in addition to counting the number of platelets, the analysis of other platelet parameters, including mean platelet volume (MPV), immature platelet fraction (IPF), absolute number of platelets, immature platelets (AIPC), platelet cell count (PCT), large platelet ratio (P-LCR), and PDW (platelet distribution amplitude) are performed using more advanced automated equipment. The aim of this study was to evaluate IPF (%), AIPC (× 109 /L), and MPV (fL) in ITP diagnosis and platelet changes present in the pathophysiology of COVID-19. EDTA-containing whole blood samples from patients diagnosed with ITP (41 patientes) and from patients diagnosed with COVID-19 (152 patients) were analyzed for the determination of these markers in the XE5000 analyzer. Samples from blood donors were used as the healthy control group. Results showed that a cutoff of 6.4% for IPF can be used as a laboratory marker for the diagnosis of ITP. In the case of COVID-19, results showed that patients requiring intensive care had a median of 6.20% (4.70–8.53) and 14.98x109 /L (11.15–21.25) for IPF and AIPC, respectively. For patients with COVID-19 without intensive treatment, the values obtained were 5.30% (3.20–6.80) and 13.39x109 /L (8.64–18.93). For the control group without COVID-19, the values were 3.40% (2.55–4.85) and 7.78x109 /L (5.58–9.97). The MPV values were 10.4 fL (9.90–11.10), 9.80 fL (9.30–10.40), and 10.1 fL (9.65–11.00) for the control group, patients with COVID-19 without intensive treatment, and those in need of intensive treatment, respectively. The results suggest that these markers can be used to assess the severity of COVID-19. Our results show that once platelet parameters are standardized with defined reference values, they can be useful in clinical practice for confirmatory diagnostic purposes in the case of ITP or for the assessment of the severity and follow-up of the disease in the case of COVID19.
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spelling Avaliação da fração de plaquetas imaturas no diagnóstico da trombocitopenia imune e sua relação com a gravidade da Covid-19Evaluation of the fraction immature platelets in the diagnosis of immune trombocytopenia and and its relationship with the severity of Covid-19Índices plaquetáriosTrombocitopenia imuneCovid-19PlaquetasFração de plaquetas imaturasPlatelet indicesImmune thrombocytopeniaPlateletsImmature platelets fractionCNPQ::CIENCIAS DA SAUDE::FARMACIAPlatelets are cytoplasmic fragments of megakaryocytes, cells present in the bone marrow, which are key players in hemostasis. Adequate platelet kinetics, with a balance between production, activation, and apoptosis, is essential to maintain the stability of this process. Hemostasis imbalance due to different causes results in changes in the number and/or function of platelets. In immune thrombocytopenia (ITP), this imbalance leads to a reduction in the number of platelets. In COVID-19, the imbalance results in platelet hyperactivation with consequent immunothrombotic dysregulation. Recently, in addition to counting the number of platelets, the analysis of other platelet parameters, including mean platelet volume (MPV), immature platelet fraction (IPF), absolute number of platelets, immature platelets (AIPC), platelet cell count (PCT), large platelet ratio (P-LCR), and PDW (platelet distribution amplitude) are performed using more advanced automated equipment. The aim of this study was to evaluate IPF (%), AIPC (× 109 /L), and MPV (fL) in ITP diagnosis and platelet changes present in the pathophysiology of COVID-19. EDTA-containing whole blood samples from patients diagnosed with ITP (41 patientes) and from patients diagnosed with COVID-19 (152 patients) were analyzed for the determination of these markers in the XE5000 analyzer. Samples from blood donors were used as the healthy control group. Results showed that a cutoff of 6.4% for IPF can be used as a laboratory marker for the diagnosis of ITP. In the case of COVID-19, results showed that patients requiring intensive care had a median of 6.20% (4.70–8.53) and 14.98x109 /L (11.15–21.25) for IPF and AIPC, respectively. For patients with COVID-19 without intensive treatment, the values obtained were 5.30% (3.20–6.80) and 13.39x109 /L (8.64–18.93). For the control group without COVID-19, the values were 3.40% (2.55–4.85) and 7.78x109 /L (5.58–9.97). The MPV values were 10.4 fL (9.90–11.10), 9.80 fL (9.30–10.40), and 10.1 fL (9.65–11.00) for the control group, patients with COVID-19 without intensive treatment, and those in need of intensive treatment, respectively. The results suggest that these markers can be used to assess the severity of COVID-19. Our results show that once platelet parameters are standardized with defined reference values, they can be useful in clinical practice for confirmatory diagnostic purposes in the case of ITP or for the assessment of the severity and follow-up of the disease in the case of COVID19.As plaquetas são fragmentos citoplasmáticos dos megacariócitos, células presentes na medula óssea, as quais são peças-chave na hemostasia. A adequada cinética plaquetária, com equilíbrio entre produção, ativação e apoptose é fundamental para manutenção da estabilidade desse processo. O desequilíbrio da hemostasia por diferentes causas, resulta em prejuízo na quantidade e/ou função das plaquetas. Na trombocitopenia imune (PTI) esse desequilíbrio leva a uma redução no número de plaquetas, enquanto na COVID-19 ocorre uma hiperativação plaquetária com consequente desregulação imunotrombótica. Atualmente, em adição a avaliação do número de plaquetas, os equipamentos automatizados permitem também realizar a análise de outros parâmetros plaquetários, entre eles o volume plaquetário médio (VPM), a fração de plaquetas imaturas (IPF), o número absoluto de plaquetas imaturas (AIPC), o plaquetócrito (PCT), a razão de grandes plaquetas (P-LCR), e a amplitude de distrubuição das plaquetas (PDW). O objetivo deste estudo foi avaliar IPF, AIPC e o VPM no diagnóstico da PTI e nas alterações plaquetárias presentes na fisiopatologia da COVID-19. Foram analisadas amostras de sangue total com EDTA proveniente de pacientes diagnosticados com PTI (41 indivíduos) e de pacientes diagnosticados com COVID-19 (152 indivíduos), para a determinação destes marcadores no equipamento XE5000 da Sysmex. Como grupo controle saudável foram utilizadas amostras de doadores de sangue. Nossos resultados mostraram que um ponto de corte de 6,4% para o IPF pode ser utilizado como marcador laboratorial para diagnóstico de PTI. No caso da COVID-19, nossos resultados mostraram que pacientes com COVID-19 que necessitaram de tratamento intensivo apresentaram uma mediana de 6,20% (4,70- 8,53) e 14,98x109 /L (11,15-21,25) para IPF e AIPC, respectivamente. Para os pacientes com COVID-19 sem necessidade de tratamento intensivo os valores obtidos foram de 5,30 % (3,20–6,80) e 13,39 x109 /L (8,64-18,93). Já para o grupo controle, sem COVID-19, os valores foram de 3,40% (2,55 – 4,85) e 7,78 x109 /L (5,58-9,97). Os valores de VPM foram de 10,40 fL (9,90 – 11,10), 9,80 fL (9,30-10,40) e 10,10 fL (9,65 – 11,00), para grupo controle, pacientes com COVID-19 sem e com necessidade de tratamento intensivo, respectivamente. Esses resultados sugerem que esses marcadores possam ser utilizados como auxiliares na avaliação da gravidade da COVID-19. Nossos resultados mostram que esses parâmetros plaquetários, uma vez padronizados e com valores de referência definidos, possam ser úteis na prática clínica com finalidade diagnóstica confirmatória no caso da PTI ou para avaliação da gravidade e acompanhamento da COVID-19.Universidade Federal de Santa MariaBrasilAnálises Clínicas e ToxicológicasUFSMPrograma de Pós-Graduação em Ciências FarmacêuticasCentro de Ciências da SaúdeSilva, José Edson Paz dahttp://lattes.cnpq.br/1177504021154172Carvalho, José Antonio Mainardi deMachado, Michel MansurBochi, Guilherme VargasSantos, Magnun Nueldo Nunes dosPilger, Diogo AndréPereira, Karla Nunes2022-12-26T14:37:22Z2022-12-26T14:37:22Z2022-11-25info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisapplication/pdfhttp://repositorio.ufsm.br/handle/1/27403ark:/26339/001300000g458porAttribution-NonCommercial-NoDerivatives 4.0 Internationalhttp://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessreponame:Manancial - Repositório Digital da UFSMinstname:Universidade Federal de Santa Maria (UFSM)instacron:UFSM2022-12-26T14:37:22Zoai:repositorio.ufsm.br:1/27403Biblioteca Digital de Teses e Dissertaçõeshttps://repositorio.ufsm.br/ONGhttps://repositorio.ufsm.br/oai/requestatendimento.sib@ufsm.br||tedebc@gmail.comopendoar:2022-12-26T14:37:22Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)false
dc.title.none.fl_str_mv Avaliação da fração de plaquetas imaturas no diagnóstico da trombocitopenia imune e sua relação com a gravidade da Covid-19
Evaluation of the fraction immature platelets in the diagnosis of immune trombocytopenia and and its relationship with the severity of Covid-19
title Avaliação da fração de plaquetas imaturas no diagnóstico da trombocitopenia imune e sua relação com a gravidade da Covid-19
spellingShingle Avaliação da fração de plaquetas imaturas no diagnóstico da trombocitopenia imune e sua relação com a gravidade da Covid-19
Pereira, Karla Nunes
Índices plaquetários
Trombocitopenia imune
Covid-19
Plaquetas
Fração de plaquetas imaturas
Platelet indices
Immune thrombocytopenia
Platelets
Immature platelets fraction
CNPQ::CIENCIAS DA SAUDE::FARMACIA
title_short Avaliação da fração de plaquetas imaturas no diagnóstico da trombocitopenia imune e sua relação com a gravidade da Covid-19
title_full Avaliação da fração de plaquetas imaturas no diagnóstico da trombocitopenia imune e sua relação com a gravidade da Covid-19
title_fullStr Avaliação da fração de plaquetas imaturas no diagnóstico da trombocitopenia imune e sua relação com a gravidade da Covid-19
title_full_unstemmed Avaliação da fração de plaquetas imaturas no diagnóstico da trombocitopenia imune e sua relação com a gravidade da Covid-19
title_sort Avaliação da fração de plaquetas imaturas no diagnóstico da trombocitopenia imune e sua relação com a gravidade da Covid-19
author Pereira, Karla Nunes
author_facet Pereira, Karla Nunes
author_role author
dc.contributor.none.fl_str_mv Silva, José Edson Paz da
http://lattes.cnpq.br/1177504021154172
Carvalho, José Antonio Mainardi de
Machado, Michel Mansur
Bochi, Guilherme Vargas
Santos, Magnun Nueldo Nunes dos
Pilger, Diogo André
dc.contributor.author.fl_str_mv Pereira, Karla Nunes
dc.subject.por.fl_str_mv Índices plaquetários
Trombocitopenia imune
Covid-19
Plaquetas
Fração de plaquetas imaturas
Platelet indices
Immune thrombocytopenia
Platelets
Immature platelets fraction
CNPQ::CIENCIAS DA SAUDE::FARMACIA
topic Índices plaquetários
Trombocitopenia imune
Covid-19
Plaquetas
Fração de plaquetas imaturas
Platelet indices
Immune thrombocytopenia
Platelets
Immature platelets fraction
CNPQ::CIENCIAS DA SAUDE::FARMACIA
description Platelets are cytoplasmic fragments of megakaryocytes, cells present in the bone marrow, which are key players in hemostasis. Adequate platelet kinetics, with a balance between production, activation, and apoptosis, is essential to maintain the stability of this process. Hemostasis imbalance due to different causes results in changes in the number and/or function of platelets. In immune thrombocytopenia (ITP), this imbalance leads to a reduction in the number of platelets. In COVID-19, the imbalance results in platelet hyperactivation with consequent immunothrombotic dysregulation. Recently, in addition to counting the number of platelets, the analysis of other platelet parameters, including mean platelet volume (MPV), immature platelet fraction (IPF), absolute number of platelets, immature platelets (AIPC), platelet cell count (PCT), large platelet ratio (P-LCR), and PDW (platelet distribution amplitude) are performed using more advanced automated equipment. The aim of this study was to evaluate IPF (%), AIPC (× 109 /L), and MPV (fL) in ITP diagnosis and platelet changes present in the pathophysiology of COVID-19. EDTA-containing whole blood samples from patients diagnosed with ITP (41 patientes) and from patients diagnosed with COVID-19 (152 patients) were analyzed for the determination of these markers in the XE5000 analyzer. Samples from blood donors were used as the healthy control group. Results showed that a cutoff of 6.4% for IPF can be used as a laboratory marker for the diagnosis of ITP. In the case of COVID-19, results showed that patients requiring intensive care had a median of 6.20% (4.70–8.53) and 14.98x109 /L (11.15–21.25) for IPF and AIPC, respectively. For patients with COVID-19 without intensive treatment, the values obtained were 5.30% (3.20–6.80) and 13.39x109 /L (8.64–18.93). For the control group without COVID-19, the values were 3.40% (2.55–4.85) and 7.78x109 /L (5.58–9.97). The MPV values were 10.4 fL (9.90–11.10), 9.80 fL (9.30–10.40), and 10.1 fL (9.65–11.00) for the control group, patients with COVID-19 without intensive treatment, and those in need of intensive treatment, respectively. The results suggest that these markers can be used to assess the severity of COVID-19. Our results show that once platelet parameters are standardized with defined reference values, they can be useful in clinical practice for confirmatory diagnostic purposes in the case of ITP or for the assessment of the severity and follow-up of the disease in the case of COVID19.
publishDate 2022
dc.date.none.fl_str_mv 2022-12-26T14:37:22Z
2022-12-26T14:37:22Z
2022-11-25
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
format doctoralThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://repositorio.ufsm.br/handle/1/27403
dc.identifier.dark.fl_str_mv ark:/26339/001300000g458
url http://repositorio.ufsm.br/handle/1/27403
identifier_str_mv ark:/26339/001300000g458
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade Federal de Santa Maria
Brasil
Análises Clínicas e Toxicológicas
UFSM
Programa de Pós-Graduação em Ciências Farmacêuticas
Centro de Ciências da Saúde
publisher.none.fl_str_mv Universidade Federal de Santa Maria
Brasil
Análises Clínicas e Toxicológicas
UFSM
Programa de Pós-Graduação em Ciências Farmacêuticas
Centro de Ciências da Saúde
dc.source.none.fl_str_mv reponame:Manancial - Repositório Digital da UFSM
instname:Universidade Federal de Santa Maria (UFSM)
instacron:UFSM
instname_str Universidade Federal de Santa Maria (UFSM)
instacron_str UFSM
institution UFSM
reponame_str Manancial - Repositório Digital da UFSM
collection Manancial - Repositório Digital da UFSM
repository.name.fl_str_mv Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)
repository.mail.fl_str_mv atendimento.sib@ufsm.br||tedebc@gmail.com
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