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Coronary artery disease risk factors in patients with schizophrenia: Effects of short term antipsychotic treatment

dc.contributor.buuauthorSarandöl, Aslı
dc.contributor.buuauthorKirli, Selçuk
dc.contributor.buuauthorAkkaya, Cengiz
dc.contributor.buuauthorOcak, Nihal
dc.contributor.buuauthorErol, Esma
dc.contributor.buuauthorSarandöl, Emre
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentBiyokimya Ana Bilim Dalı
dc.contributor.departmentPsikiyatri Bölümü
dc.contributor.orcid0000-0002-2593-7196
dc.contributor.researcheridABE-1716-2020
dc.contributor.scopusid14020405100
dc.contributor.scopusid14019745700
dc.contributor.scopusid14061855100
dc.contributor.scopusid23989248600
dc.contributor.scopusid22950749100
dc.contributor.scopusid55943324800
dc.date.accessioned2022-09-07T13:11:23Z
dc.date.available2022-09-07T13:11:23Z
dc.date.issued2007-11
dc.description.abstractThe aim of the present study was to investigate serum paraoxonase/ arylesterase activities and oxidation/ oxidizability of apolipoprotein B- containing lipoproteins and several coronary artery disease risk factors, including homocysteine, high sensitive C- reactive protein, tumour necrosis factor- alpha, leptin and adiponectin in patients with schizophrenia. Oxidation of lipoproteins plays an important role in atherogenesis, and the enzyme paraoxonase has been shown to prevent lipoprotein oxidation. Furthermore, low paraoxonase activity has been suggested to predict coronary artery disease. Forty patients who fully met the fourth Diagnostic and Statistical Manual of Mental Disorders criteria for schizophrenia and 35 healthy control subjects were included in the study. Serum paraoxonase/ arylesterase activities were determined spectrophotometrically. Malondialdehyde levels of apolipoprotein B- containing lipoproteins were determined before and after incubation with copper- sulphate, which yielded basal- and Delta- malondialdehyde values, respectively. Homocysteine and highly sensitive C- reactive protein levels were determined using a fluorescence- polarization immunoassay and immunonephelometry, respectively. Leptin and adiponectin levels were measured with radioimmunoassay and tumour necrosis factor-alpha was determined by enzyme linked immunosorbent assay. Serum paraoxonase and arylesterase activities were significantly lower and Delta- malondialdehyde levels were significantly higher in the schizophrenia group compared with the control group. However, there were not any significant differences in other parameters of the study between the study groups. There was a significant increase in body mass index and serum triglyceride and very low density lipoprotein cholesterol levels in the schizophrenic group after 6 weeks of treatment. These parameters were significantly increased in patients treated with atypical antipsychotics but not in patients treated with typic or long acting antipsychotics. The results of the present study suggest that patients with schizophrenia might have increased risk for coronary artery disease related to reduced serum paraoxonase activity and increased oxidizability of apolipoprotein B- containing lipoproteins.
dc.identifier.citationSarandöl, A. vd. (2007). "Coronary artery disease risk factors in patients with schizophrenia: Effects of short term antipsychotic treatment". Journal of Psychopharmacology, 21(8), 857-863.
dc.identifier.doi10.1177/0269881107077609
dc.identifier.endpage863
dc.identifier.issn1461-7285
dc.identifier.issn0269-8811
dc.identifier.issue8
dc.identifier.pubmed17715203
dc.identifier.scopus2-s2.0-35649003173
dc.identifier.startpage857
dc.identifier.urihttps://doi.org/10.1177/0269881107077609
dc.identifier.urihttps://journals.sagepub.com/doi/10.1177/0269881107077609
dc.identifier.urihttp://hdl.handle.net/11452/28547
dc.identifier.volume21
dc.identifier.wos000251688800012
dc.indexed.scopusScopus
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherSage Publications
dc.relation.journalJournal of Psychopharmacology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectAdiponectin
dc.subjectLow-density-lipoprotein
dc.subjectAntipsychotic
dc.subjectHigh sensitive C-reactive protein
dc.subjectHomocysteine
dc.subjectLeptin
dc.subjectLipoprotein oxidation
dc.subjectParaoxonase
dc.subjectSchizophrenia
dc.subjectTumour necrosis factor-α
dc.subjectSerum paraoxonase arylesterase
dc.subjectIschemic-heart-disease
dc.subjectNecrosis-factor-alpha
dc.subjectCardiovascular-disease
dc.subjectMethylenetetrahydrofolate reductase
dc.subjectAtypical antipsychotics
dc.subjectInsulin-resistance
dc.subjectAdiponectin levels
dc.subjectPromising marker
dc.subject.emtreeControlled study
dc.subject.emtreeAdult
dc.subject.emtreeAnalytic method
dc.subject.emtreeArticle
dc.subject.emtreeAtherogenesis
dc.subject.emtreeBody mass
dc.subject.emtreeCardiovascular risk
dc.subject.emtreeClinical article
dc.subject.emtreeComparative study
dc.subject.emtreeFemale
dc.subject.emtreeTumor necrosis factor alpha
dc.subject.emtreeCoronary artery disease
dc.subject.emtreeDiagnostic and statistical manual of mental disorders
dc.subject.emtreeEnzyme activity
dc.subject.emtreeEnzyme linked immunosorbent assay
dc.subject.emtreeMale
dc.subject.emtreeFluorescence polarization immunoassay
dc.subject.emtreeLipid peroxidation
dc.subject.emtreeHuman
dc.subject.emtreePriority journal
dc.subject.emtreeTriacylglycerol blood level
dc.subject.emtreeNephelometry
dc.subject.emtreeOxidation
dc.subject.emtreeRadioimmunoassay
dc.subject.emtreeNeuroleptic agent
dc.subject.emtreeSchizophrenia
dc.subject.emtreeSpectrophotometry
dc.subject.emtreeLipoprotein
dc.subject.emtreeLow density lipoprotein cholesterol
dc.subject.emtreeClozapine
dc.subject.emtreeAdiponectin
dc.subject.emtreeAmisulpride
dc.subject.emtreeApolipoprotein B
dc.subject.emtreeAryldialkylphosphatase
dc.subject.emtreeArylesterase
dc.subject.emtreeAtypical antipsychotic agent
dc.subject.emtreeC reactive protein
dc.subject.emtreeHomocysteine
dc.subject.emtreeCopper sulfate
dc.subject.emtreeHaloperidol
dc.subject.emtreeLeptin
dc.subject.emtreeMalonaldehyde
dc.subject.emtreeOlanzapine
dc.subject.emtreeQuetiapine
dc.subject.emtreeRisperidone
dc.subject.emtreeTriacylglycerol
dc.subject.meshAdult
dc.subject.meshAntipsychotic agents
dc.subject.meshAryldialkylphosphatase
dc.subject.meshC-Reactive protein
dc.subject.meshFemale
dc.subject.meshCarboxylic ester hydrolases
dc.subject.meshCoronary artery disease
dc.subject.meshHumans
dc.subject.meshLeptin
dc.subject.meshOxidation-reduction
dc.subject.meshLipoproteins
dc.subject.meshMale
dc.subject.meshMalondialdehyde
dc.subject.meshRisk factors
dc.subject.meshSchizophrenia
dc.subject.meshTriglycerides
dc.subject.meshTumor necrosis factor-alpha
dc.subject.scopusAryldialkylphosphatase; Arylesterase; Human PON1 Protein
dc.subject.wosClinical neurology
dc.subject.wosNeurosciences
dc.subject.wosPharmacology & pharmacy
dc.subject.wosPsychiatry
dc.titleCoronary artery disease risk factors in patients with schizophrenia: Effects of short term antipsychotic treatment
dc.typeArticle
dc.wos.quartileN/A
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Psikiyatri Bölümü
local.contributor.departmentTıp Fakültesi/Biyokimya Ana Bilim Dalı
local.indexed.atPubMed
local.indexed.atWOS
local.indexed.atScopus

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