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Validating Diagnostic Markers That May Predict the Outcome of Ebola Virus Disease Patients.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Validating Diagnostic Markers That May Predict the Outcome of Ebola Virus Disease Patients./
作者:
Lazo, Jocelyn Ginette Perez .
出版者:
Ann Arbor : ProQuest Dissertations & Theses, : 2020,
面頁冊數:
282 p.
附註:
Source: Dissertations Abstracts International, Volume: 83-04, Section: B.
Contained By:
Dissertations Abstracts International83-04B.
標題:
Tumor necrosis factor-TNF. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=28671113
ISBN:
9798544200123
Validating Diagnostic Markers That May Predict the Outcome of Ebola Virus Disease Patients.
Lazo, Jocelyn Ginette Perez .
Validating Diagnostic Markers That May Predict the Outcome of Ebola Virus Disease Patients.
- Ann Arbor : ProQuest Dissertations & Theses, 2020 - 282 p.
Source: Dissertations Abstracts International, Volume: 83-04, Section: B.
Thesis (Ph.D.)--The University of Liverpool (United Kingdom), 2020.
This item must not be sold to any third party vendors.
Ebola virus disease (EVD) is one of the deadliest viral infections in humans, with case fatality rates recorded between 50 to 70%. Despite the ongoing efforts to control disease transmission using a recently licensed vaccine, no licensed treatments and prognostic tests are available that could improve the outcome of acute EVD patients and survivors. In the search for prognostic tools, different markers have been proposed. However, to date Ebola virus (EBOV) viral load measured as Ct value is currently the most reliable predictor of the clinical outcome, particularly in the context of defining survivors (Ct > 22) or fatal cases (Ct < 20). However, the viral load cannot predict accurately the clinical outcome in patients with Ct values between this range since the outcome is approximately equal between survival and a fatal infection. In a previous study 10 genes were identified by machine-learning of transcriptome data from EBOV patients as being potential prognostic markers. This study investigates whether this set of host-based response markers can predict the outcome of infection at the acute phase specially in situations where viral load gives little predictive value. Quantitative reverse transcription PCR (RT-qPCR) assays were developed for each gene transcripts and analysed in 39 clinical samples collected by the European Mobile Laboratory during the 2013-16 West Africa outbreak. A subset of the gene transcripts was used to generate machine learning models with or without EBOV Ct values to predict the outcome of a second group of 64 EVD patient samples using a blind-coded approach. The best discriminating model had a greater overall predictive accuracy (68.4%) compared to a model that only used EBOV Ct as a predictor variable (54.3%). These findings were ratified in a larger sample size, the prediction performance of the models was enhanced when a subset of the gene transcripts was combined with EBOV Ct (90-100%) than EBOV Ct alone (87%). Furthermore, a multiplex RT-qPCR assay for a subset of the gene transcripts was developed. This study proposes a novel approach that highly predictsthe risk of Ebola virus disease mortality at the time of diagnosis, which could be used to speed up the triage and clinical management of patients in future outbreaks.
ISBN: 9798544200123Subjects--Topical Terms:
3560383
Tumor necrosis factor-TNF.
Validating Diagnostic Markers That May Predict the Outcome of Ebola Virus Disease Patients.
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Ebola virus disease (EVD) is one of the deadliest viral infections in humans, with case fatality rates recorded between 50 to 70%. Despite the ongoing efforts to control disease transmission using a recently licensed vaccine, no licensed treatments and prognostic tests are available that could improve the outcome of acute EVD patients and survivors. In the search for prognostic tools, different markers have been proposed. However, to date Ebola virus (EBOV) viral load measured as Ct value is currently the most reliable predictor of the clinical outcome, particularly in the context of defining survivors (Ct > 22) or fatal cases (Ct < 20). However, the viral load cannot predict accurately the clinical outcome in patients with Ct values between this range since the outcome is approximately equal between survival and a fatal infection. In a previous study 10 genes were identified by machine-learning of transcriptome data from EBOV patients as being potential prognostic markers. This study investigates whether this set of host-based response markers can predict the outcome of infection at the acute phase specially in situations where viral load gives little predictive value. Quantitative reverse transcription PCR (RT-qPCR) assays were developed for each gene transcripts and analysed in 39 clinical samples collected by the European Mobile Laboratory during the 2013-16 West Africa outbreak. A subset of the gene transcripts was used to generate machine learning models with or without EBOV Ct values to predict the outcome of a second group of 64 EVD patient samples using a blind-coded approach. The best discriminating model had a greater overall predictive accuracy (68.4%) compared to a model that only used EBOV Ct as a predictor variable (54.3%). These findings were ratified in a larger sample size, the prediction performance of the models was enhanced when a subset of the gene transcripts was combined with EBOV Ct (90-100%) than EBOV Ct alone (87%). Furthermore, a multiplex RT-qPCR assay for a subset of the gene transcripts was developed. This study proposes a novel approach that highly predictsthe risk of Ebola virus disease mortality at the time of diagnosis, which could be used to speed up the triage and clinical management of patients in future outbreaks.
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