Metabolomic Profiling Of Active And İnactive Liver Cystic Echinococcosis
Date
2021Author
Doğrul, Ahmet Bülent
Turkmen T. Ciftci
Samiye Yabanoglu-Ciftci
Emre Unal
Devrim Akinci
Ipek Baysal
Gokhan Yuce
Serra Orsten
Okan Akhan
Emirhan Nemutlu
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Show full item recordAbstract
Cystic 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.