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Effects of long-term antidepressant treatment on oxidative status in major depressive disorder: A 24-week follow-up study

dc.contributor.authorKotan, Vahap Ozan
dc.contributor.buuauthorKırhan, Emine
dc.contributor.buuauthorÖzkaya, Güven
dc.contributor.buuauthorKirli, Selçuk
dc.contributor.buuauthorSarandöl, Emre
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentPsikiyatri Ana Bilim Dalı
dc.contributor.departmentBiyoistatistik Ana Bilim Dalı
dc.contributor.departmentBiyokimya Ana Bilim Dalı
dc.contributor.orcid0000-0002-2593-7196
dc.contributor.orcid0000-0003-0297-846X
dc.contributor.researcheridABE-1716-2020
dc.contributor.researcheridA-4421-2016
dc.contributor.scopusid37104411100
dc.contributor.scopusid16316866500
dc.contributor.scopusid14019745700
dc.contributor.scopusid55943324800
dc.date.accessioned2021-11-01T11:28:30Z
dc.date.available2021-11-01T11:28:30Z
dc.date.issued2011-07-19
dc.description.abstractPurpose: Major depressive disorder (MDD) is a devastating disease that afflicts large populations and has also been accepted to be an independent risk factor for cardiovascular disease (CVD). Oxidative stress seems to play an essential role in the relationship of MOD and CVD. We aimed to determine the level of oxidative stress in patients with MOD and to investigate the effects of long-term antidepressant (AD) treatment on the oxidative-antioxidative system parameters and CVD risk factors. Method: Fifty patients who fully met the fourth Diagnostic and Statistical Manual of Mental Disorders criteria for MOD and 44 healthy control subjects were included in the study. Control visits of the patients were repeated 6 weeks, 12 weeks and 24 weeks after beginning of the AD treatment Lipid profiles, oxidation and oxidizability of apolipoprotein B-containing lipoproteins (expressed as apo B-b-MDA and apo B-Delta-MDA, respectively), levels of plasma malondialdehyde (p-MDA), total antioxidative capacity (TAOC), antioxidant molecules and antioxidant enzyme activities including paraoxonase/arylesterase, red blood cell superoxide dismutase (RBC-SOD) and glutathione peroxidase were determined during 24-week of follow-up period. Results: According to the results of the study, p-MDA, apo B-b-MDA and RBC-SOD activity were increased and arylesterase activity was decreased in MDD patients. Body mass index (BMI), vitamin A and total cholesterol levels in MDD patients increased after 24-weeks of AD treatment RBC-SOD activity, TAOC, p-MDA and apo B-b-MDA levels were decreased: paraoxonase/arylesterase activities and apo B-Delta-MDA were increased at the end of 24th week. Conclusion: Oxidative stress, demonstrated in MDD patients, was partly improved during 24 weeks of AD treatment Increase in paraoxonase/arylesterase activities and decrease in p-MDA and apo B-b-MDA levels after 24 weeks seem to be beneficial for reduction of CVD risk in MDD patients. However increased BMI and apo B-Delta-MDA levels are negative cardiovascular effects of long-term AD treatment.
dc.identifier.citationKotan, V. O. vd. (2011). “Effects of long-term antidepressant treatment on oxidative status in major depressive disorder: A 24-week follow-up study”. Progress in Neuro-Psychopharmacology & Biological Psychiatry, 35(5), 1284-1290.
dc.identifier.doi10.1016/j.pnpbp.2011.03.021
dc.identifier.endpage1290
dc.identifier.issn0278-5846
dc.identifier.issn1878-4216
dc.identifier.issue5
dc.identifier.pubmed21515329
dc.identifier.scopus2-s2.0-79957815233
dc.identifier.startpage1284
dc.identifier.urihttps://doi.org/10.1016/j.pnpbp.2011.03.021
dc.identifier.urihttp://hdl.handle.net/11452/22541
dc.identifier.volume35
dc.identifier.wos000292470800013
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherPergamon-Elsevier Science
dc.relation.bap2008/37
dc.relation.collaborationSanayi
dc.relation.journalProgress in Neuro - Psychopharmacology & Biological Psychiatry
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectAntioxidants
dc.subjectMajor depressive disorder
dc.subjectMalondialdehyde
dc.subjectOxidative stress
dc.subjectCoronary-artery-disease
dc.subjectLow-density-lipoprotein
dc.subjectSuperoxide-dismutase
dc.subjectLipid-peroxidation
dc.subjectAntioxidant status
dc.subjectNitric-oxide
dc.subjectOxidized ldl
dc.subjectRat-brain
dc.subjectStress
dc.subjectPlasma
dc.subjectNeurosciences & neurology
dc.subjectPharmacology & pharmacy
dc.subjectPsychiatry
dc.subject.emtreeAntidepressant agent
dc.subject.emtreeApolipoprotein B
dc.subject.emtreeAryldialkylphosphatase
dc.subject.emtreeArylesterase
dc.subject.emtreeCholesterol
dc.subject.emtreeCitalopram
dc.subject.emtreeEscitalopram
dc.subject.emtreeFluoxetine
dc.subject.emtreeGlutathione peroxidase
dc.subject.emtreeHigh density lipoprotein cholesterol
dc.subject.emtreeMalonaldehyde
dc.subject.emtreeMilnacipran
dc.subject.emtreeMoclobemide
dc.subject.emtreeParoxetine
dc.subject.emtreeRetinol
dc.subject.emtreeSertraline
dc.subject.emtreeSuperoxide dismutase
dc.subject.emtreeTianeptine
dc.subject.emtreeTriacylglycerol
dc.subject.emtreeAdult
dc.subject.emtreeVenlafaxine
dc.subject.emtreeArticle
dc.subject.emtreeBody mass
dc.subject.emtreeCardiovascular risk
dc.subject.emtreeClinical article
dc.subject.emtreeControlled study
dc.subject.emtreeDiagnostic and statistical manual of mental disorders
dc.subject.emtreeEnzyme activity
dc.subject.emtreeErythrocyte
dc.subject.emtreeFemale
dc.subject.emtreeFollow up
dc.subject.emtreeHuman
dc.subject.emtreeLong term care
dc.subject.emtreeMajor depression
dc.subject.emtreeMale
dc.subject.emtreeOxidation
dc.subject.emtreeOxidative stress
dc.subject.emtreeProtein expression
dc.subject.meshAdult
dc.subject.meshAntidepressive agents
dc.subject.meshAntioxidants
dc.subject.meshApolipoproteins
dc.subject.meshAryldialkylphosphatase
dc.subject.meshBlood cell count
dc.subject.meshBody mass index
dc.subject.meshCarboxylic ester hydrolases
dc.subject.meshCardiovascular diseases
dc.subject.meshDepressive disorder major
dc.subject.meshFemale
dc.subject.meshFollow-up studies
dc.subject.meshHormones
dc.subject.meshHumans
dc.subject.meshLipids
dc.subject.meshLiver function tests
dc.subject.meshLong-term care
dc.subject.meshMale
dc.subject.meshMalondialdehyde
dc.subject.meshOxidative stress
dc.subject.meshPsychiatric status rating scales
dc.subject.meshRisk factors
dc.subject.meshSuperoxide dismutase
dc.subject.meshYoung adult
dc.subject.scopusSchizophrenia; Acetylcysteine; Bipolar Disorder
dc.subject.wosClinical neurology
dc.subject.wosNeurosciences
dc.subject.wosPharmacology & pharmacy
dc.subject.wosPsychiatry
dc.titleEffects of long-term antidepressant treatment on oxidative status in major depressive disorder: A 24-week follow-up study
dc.typeArticle
dc.wos.quartileQ1 (Pharmacology & Pharmacy)
dc.wos.quartileQ2
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Biyokimya Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/Biyoistatistik Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/Psikiyatri Ana Bilim Dalı
local.indexed.atPubMed
local.indexed.atWOS

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