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dc.contributor.authorUlgen, Ayse
dc.contributor.authorCetin, Sirin
dc.contributor.authorCetin, Meryem
dc.contributor.authorSivgin, Hakan
dc.contributor.authorLi, Wentian
dc.date.accessioned2024-03-12T19:29:05Z
dc.date.available2024-03-12T19:29:05Z
dc.date.issued2022
dc.identifier.issn1476-9271
dc.identifier.issn1476-928X
dc.identifier.urihttps://doi.org/10.1016/j.compbiolchem.2022.107681
dc.identifier.urihttps://hdl.handle.net/20.500.12450/2183
dc.description.abstractHaving a complete and reliable list of risk factors from routine laboratory blood test for COVID-19 disease severity and mortality is important for patient care and hospital management. It is common to use meta-analysis to combine analysis results from different studies to make it more reproducible. In this paper, we propose to run multiple analyses on the same set of data to produce a more robust list of risk factors. With our time-to-event survival data, the standard survival analysis were extended in three directions. The first is to extend from tests and corresponding p-values to machine learning and their prediction performance. The second is to extend from single-variable to multiple-variable analysis. The third is to expand from analyzing time-to-decease data with death as the event of interest to analyzing time-to-hospital-release data to treat early recovery as a meaningful event as well. Our extension of the type of analyses leads to ten ranking lists. We conclude that 20 out of 30 factors are deemed to be reliably associated to faster-death or faster-recovery. Considering correlation among factors and evidenced by stepwise variable selection in random survival forest, 10 ~ 15 factors seem to be able to achieve the optimal prognosis performance. Our final list of risk factors contain calcium, white blood cell and neutrophils count, urea and creatine, D-dimer, red cell distribution widths, age, ferritin, glucose, lactate dehydrogenase, lymphocyte, basophils, anemia related factors (hemoglobin, hematocrit, mean corpuscular hemoglobin concentration), sodium, potassium, eosinophils, and aspartate aminotransferase.en_US
dc.description.sponsorshipRobert S Boas Center for Genomics and Human Geneticsen_US
dc.description.sponsorshipWL thanks the support from the Robert S Boas Center for Genomics and Human Genetics.en_US
dc.language.isoengen_US
dc.publisherElsevier Sci Ltden_US
dc.relation.ispartofComputational Biology And Chemistryen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectCOVID-19en_US
dc.subjectSurvival analysisen_US
dc.subjectCompeting risksen_US
dc.subjectComposite rankingen_US
dc.titleA composite ranking of risk factors for COVID-19 time-to-event data from a Turkish cohorten_US
dc.typearticleen_US
dc.departmentAmasya Üniversitesien_US
dc.authoridLi, Wentian/0000-0003-1155-110X
dc.identifier.volume98en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.scopus2-s2.0-85130110187en_US
dc.identifier.doi10.1016/j.compbiolchem.2022.107681
dc.department-temp[Ulgen, Ayse] Girne Amer Univ, Fac Med, Dept Biostat, Karmi, Cyprus; [Cetin, Sirin] Tokat Gaziosmanpasa Univ, Fac Med, Dept Biostat, Tokat, Turkey; [Cetin, Meryem] Amasya Univ, Fac Med, Dept Med Microbiol, Amasya, Turkey; [Sivgin, Hakan] Tokat Gaziosmanpasa Univ, Fac Med, Dept Internal Med, Tokat, Turkey; [Li, Wentian] Northwell Hlth, Robert S Boas Ctr Genom & Human Genet, Feinstein Inst Med Res, Manhasset, NY USAen_US
dc.identifier.wosWOS:000797961000008en_US
dc.identifier.pmid35487152en_US
dc.authorwosidcet, sir/GXG-3814-2022


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