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dc.contributor.authorDoğrul, Ahmet Bülent
dc.contributor.authorTurkmen T. Ciftci
dc.contributor.authorSamiye Yabanoglu-Ciftci
dc.contributor.authorEmre Unal
dc.contributor.authorDevrim Akinci
dc.contributor.authorIpek Baysal
dc.contributor.authorGokhan Yuce
dc.contributor.authorSerra Orsten
dc.contributor.authorOkan Akhan
dc.contributor.authorEmirhan Nemutlu
dc.date.accessioned2024-11-21T07:31:08Z
dc.date.available2024-11-21T07:31:08Z
dc.date.issued2021
dc.identifier.citationhttps://doi.org/10.1016/j.actatropica.2021.105985tr_TR
dc.identifier.urihttps://doi.org/10.1016/j.actatropica.2021.105985
dc.identifier.urihttps://hdl.handle.net/11655/36160
dc.description.abstractCystic Echinococcosis (CE) is one of the life-threatening diseases worldwide. It is a parasitic zoonosis caused by tapeworms of the species Echinococcus granulosus sensu lato (s.l). The treatment options of CE vary from simple “watch and wait” approach to invasive treatment, based on the type and especially the nature of the cyst (active/ inactive). Serological tests are inadequate to distinguish between active and inactive CE. A diagnostic reference that can determine whether the cyst is active or inactive can easily guide the treatment strategy. We aimed to test whether gas chromatography-mass spectrometry (GC-MS) and liquid chromatographyquadropole time of flight mass spectrometry (LC-qTOF-MS) based metabolomics can establish a plasma meta bolic fingerprint of CE patients and identify a diagnostic reference to discriminate active and inactive CE cysts. Metabolite concentrations were measured in plasma samples of 36 active CE patients, 17 inactive CE patients and 31 healthy controls. Multivariate statistical analysis on 232 identified metabolites obtained from two analytical platforms was performed by using principle component analysis (PCA) and partial least squarediscriminant analysis (PLS-DA) methods. The PLS-DA scores plot of the combined data set demonstrated a good separation between the groups. Compared to the healthy control group, decreased levels of squalene and increased levels of glyceric acid, 3-phosphoglycerate, glutamic acid, palmitoleic acid and oleic acid were determined in the CE patients. However, decreased levels of 3-phosphoglycerate and increased levels of 4- hydroxyphenylacetylglutamine, docosahexanoic acid were determined in active CE patients compared to the inactive CE patients. Determination of differences in metabolites may provide detailed understandings of potential metabolic process associated with active and inactive CE patients, and altered specific metabolic changes may provide some clues to obtain diagnostic reference for CE. This study has certain limitations: a. various factors affecting results of metabolomic studies such as lifestyle and dietary habits of the patients could not be fully controlled b. other infectious or malignant diseases of the liver should also be included as a positive control to evaluate the spec ificity of the diagnostic references.tr_TR
dc.language.isoentr_TR
dc.publisherSCİENCEDİRECTtr_TR
dc.relation.isversionof10.1016/j.actatropica.2021.105985tr_TR
dc.rightsinfo:eu-repo/semantics/openAccesstr_TR
dc.subjectcystic echinococcosis liver GC-MS LC-qTOF-MS diagnostic referencetr_TR
dc.titleMetabolomic Profiling Of Active And İnactive Liver Cystic Echinococcosistr_TR
dc.typeinfo:eu-repo/semantics/articletr_TR
dc.relation.journalACTA TROPICAtr_TR
dc.contributor.departmentGenel Cerrahitr_TR
dc.identifier.volume105895tr_TR
dc.identifier.issue221tr_TR
dc.identifier.startpage1tr_TR
dc.identifier.endpage8tr_TR
dc.description.indexWoStr_TR
dc.fundingYoktr_TR
dc.subtypeworkingPapertr_TR


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