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dc.creatorKrstić, Jelena
dc.creatorBuzadzić, Ivana
dc.creatorMilanović, Slađan
dc.creatorIlić, Nela V.
dc.creatorPajić, Sanja
dc.creatorIlić, Tihomir V.
dc.date.accessioned2021-04-20T12:38:46Z
dc.date.available2021-04-20T12:38:46Z
dc.date.issued2014
dc.identifier.issn1095-0680
dc.identifier.urihttp://rimi.imi.bg.ac.rs/handle/123456789/563
dc.description.abstractIntroduction: Sham-controlled low-frequency repetitive transcranial magnetic stimulation (rTMS) was used in patients with pharmacoresistant major depression as an added treatment along with partial sleep deprivation (PSD). In addition, the potential predictive role of brain-derived neurotrophic factor genetic polymorphism on treatment response was analyzed. Methods: We recruited 19 female patients (48.3 +/- 8.6 years old) with treatment-resistant unipolar major depression (Hamilton Depression Rating Scale [HDRS] score gt = 20) who were on a stable antidepressant treatment. They received either 1-Hz rTMS or sham stimulation over the right dorsolateral prefrontal cortex (intensity of 110% of the threshold; 3000 stimuli per protocol; and 10 daily sessions). Additionally, PSD was applied once per week during the treatment. The patients were evaluated (HDRS and Clinical Global Impression Scale) by a blind rater at baseline (B) and after 2 and 3 weeks (W2 and W3) of treatment for short-term outcome. Long-term evaluations were performed after 12 (W12) and 24 weeks (W24) for patients who received active stimulation. Results: Eleven patients in the active group showed a significant HDRS score reduction from 30.09 +/- 3.53 (B) to 16.73 +/- 5.71 (W3) compared to the lack of therapeutic response in the sham-treated patients. The long-term follow-up for the active group included 64% of the responders at W12 and 55% at W24. Full remission (HDRS lt = 10) was achieved in 5 of 11 patients. Four of these 5 patients with long-term sustained remission expressed the Val66Val genotype. Conclusion: Our study suggests a clinically relevant response, persisting for up to 6 months, from 1-Hz rTMS over the right dorsolateral prefrontal cortex and PSD in patients with pharmacoresistant major depression. The brain-derived neurotrophic factor Val66Val homozygous genotype may be related to a better treatment outcome.en
dc.publisherLippincott Williams & Wilkins, Philadelphia
dc.relationMinistry of Defence of the Republic of Serbia [MFVMA/12/13-15]
dc.relationinfo:eu-repo/grantAgreement/MESTD/Integrated and Interdisciplinary Research (IIR or III)/41014/RS//
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/175012/RS//
dc.rightsrestrictedAccess
dc.sourceJournal of ECT
dc.subjectmajor depressionen
dc.subjecttranscranial magnetic stimulationen
dc.subjectsleep deprivationen
dc.subjectBDNFen
dc.titleLow-Frequency Repetitive Transcranial Magnetic Stimulation in the Right Prefrontal Cortex Combined With Partial Sleep Deprivation in Treatment-Resistant Depression A Randomized Sham-Controlled Trialen
dc.typearticle
dc.rights.licenseARR
dc.citation.epage331
dc.citation.issue4
dc.citation.other30(4): 325-331
dc.citation.rankM23
dc.citation.spage325
dc.citation.volume30
dc.identifier.doi10.1097/YCT.0000000000000099
dc.identifier.pmid24625704
dc.identifier.scopus2-s2.0-84928278612
dc.identifier.wos000345432000033
dc.type.versionpublishedVersion


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