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dc.contributor.authorWozniak, Gretaen
dc.contributor.authorGeorgoulias, Panagiotisen
dc.contributor.authorIliadis, Charalambosen
dc.contributor.authorValotassiou, Varvaraen
dc.contributor.authorPapadopoulos, G.en
dc.contributor.authorBagiatis, Vasilisen
dc.contributor.authorTsougos, Ioannisen
dc.contributor.authorPaterakis, K. N.en
dc.contributor.authorFountas, Kostas N.en
dc.creatorWozniak, Gretaen
dc.creatorGeorgoulias, Panagiotisen
dc.creatorIliadis, Charalambosen
dc.creatorValotassiou, Varvaraen
dc.creatorPapadopoulos, G.en
dc.creatorBagiatis, Vasilisen
dc.creatorTsougos, Ioannisen
dc.creatorPaterakis, K. N.en
dc.creatorFountas, Kostas N.en
dc.date.accessioned2018-06-22T09:53:28Z
dc.date.available2018-06-22T09:53:28Z
dc.date.issued2010
dc.identifier.urihttps://gnosis.library.ucy.ac.cy/handle/7/41851
dc.description.abstractOBJECTIVES: To investigate the association between serotonin (SER), cholesterol, and neuron-specific enolase (NSE) serum levels with depression after traumatic brain injury (TBI). MATERIALS AND METHODS: Seventy-four patients with the diagnosis of TBI were included in our study. Admission computed tomography scans of all patients were analyzed. Serum concentrations of SER, NSE, low-density lipoprotein, and cholesterol were measured within on admission. Serum levels of SER and NSE were also measured at discharge and at the 6-month follow-up evaluation. In addition, serum NSE and SER levels were measured in a control group of 44 healthy volunteers. The TBI patients in our cohort were divided into 3 groups according to their admitting Glasgow Coma Scale and their discharging Glasgow Outcome Scale scores. Likewise, depressive symptoms were characterized using the Diagnostic and Statistical Manual of Mental Disorders criteria and the Mini-International Neuropsychiatric Interview. RESULTS: The measured SER serum levels were significantly lower (P<0.01) in TBI patients compared with the normal controls. Analysis of our data showed no correlation between the levels of SER, NSE, cholesterol, and low-density lipoprotein. The NSE serum levels were found to be elevated in our TBI group. However, these levels were not different between patients with depressive symptomatology. SER and cholesterol serum levels were lower in TBI patients developing depressive symptoms compared with those with no depression in a statistically significant manner. Fifty-seven percent of our patients developed depressive symptomatology. CONCLUSIONS: Decreased serum SER concentration may serve as an additional biochemical risk marker of posttraumatic mental disturbances. Copyright © 2010 by Lippincott Williams & Wilkins.en
dc.language.isoengen
dc.sourceNeurosurgery Quarterlyen
dc.subjectChilden
dc.subjectArticleen
dc.subjectHumanen
dc.subjectAdulten
dc.subjectAgeden
dc.subjectControlled studyen
dc.subjectFemaleen
dc.subjectMajor clinical studyen
dc.subjectFollow upen
dc.subjectPriority journalen
dc.subjectAdolescenten
dc.subjectMaleen
dc.subjectEnzyme blood levelen
dc.subjectDepressionen
dc.subjectCholesterolen
dc.subjectCholesterol blood levelen
dc.subjectLipoprotein blood levelen
dc.subjectNeuron specific enolaseen
dc.subjectSchool childen
dc.subjectLow density lipoproteinen
dc.subjectNeuron-specific enolaseen
dc.subjectSerotoninen
dc.subjectSerotonin blood levelen
dc.subjectSerumen
dc.subjectTraumatic brain injuryen
dc.titleSerotonin and neuron-specific enolase: Serum acute and mid-term levels and their association with posttraumatic depressionen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1097/WNQ.0b013e3181732399
dc.description.volume20
dc.description.issue4
dc.description.startingpage297
dc.description.endingpage303
dc.author.facultyΙατρική Σχολή / Medical School
dc.author.departmentΙατρική Σχολή / Medical School
dc.type.uhtypeArticleen
dc.contributor.orcidWozniak, Greta [0000-0002-8939-0927]
dc.contributor.orcidGeorgoulias, Panagiotis [0000-0002-6493-705X]
dc.contributor.orcidTsougos, Ioannis [0000-0002-5204-5273]
dc.contributor.orcidFountas, Kostas N. [0000-0002-3415-3799]
dc.gnosis.orcid0000-0002-8939-0927
dc.gnosis.orcid0000-0002-6493-705X
dc.gnosis.orcid0000-0002-5204-5273
dc.gnosis.orcid0000-0002-3415-3799


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