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Low-Frequency Repetitive Transcranial Magnetic Stimulation in the Right Prefrontal Cortex Combined With Partial Sleep Deprivation in Treatment-Resistant Depression A Randomized Sham-Controlled Trial

Authorized Users Only
2014
Authors
Krstić, Jelena
Buzadzić, Ivana
Milanović, Slađan
Ilić, Nela V.
Pajić, Sanja
Ilić, Tihomir V.
Article (Published version)
Metadata
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Abstract
Introduction: 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.

Keywords:
major depression / transcranial magnetic stimulation / sleep deprivation / BDNF
Source:
Journal of ECT, 2014, 30, 4, 325-331
Publisher:
  • Lippincott Williams & Wilkins, Philadelphia
Funding / projects:
  • Ministry of Defence of the Republic of Serbia [MFVMA/12/13-15]
  • Cellular and molecular basis of neuroinflamation: potential targets for translational medicine and therapy (RS-41014)
  • Noninvasive modulation of cortical excitability and plasticity - Noninvasive neuromodulation of the CNS in the study of physiological mechanisms, diagnosis and treatment (RS-175012)

DOI: 10.1097/YCT.0000000000000099

ISSN: 1095-0680

PubMed: 24625704

WoS: 000345432000033

Scopus: 2-s2.0-84928278612
[ Google Scholar ]
24
17
URI
http://rimi.imi.bg.ac.rs/handle/123456789/563
Collections
  • Radovi istraživača / Researchers' publications
Institution/Community
Institut za medicinska istraživanja
TY  - JOUR
AU  - Krstić, Jelena
AU  - Buzadzić, Ivana
AU  - Milanović, Slađan
AU  - Ilić, Nela V.
AU  - Pajić, Sanja
AU  - Ilić, Tihomir V.
PY  - 2014
UR  - http://rimi.imi.bg.ac.rs/handle/123456789/563
AB  - Introduction: 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.
PB  - Lippincott Williams & Wilkins, Philadelphia
T2  - Journal of ECT
T1  - Low-Frequency Repetitive Transcranial Magnetic Stimulation in the Right Prefrontal Cortex Combined With Partial Sleep Deprivation in Treatment-Resistant Depression A Randomized Sham-Controlled Trial
EP  - 331
IS  - 4
SP  - 325
VL  - 30
DO  - 10.1097/YCT.0000000000000099
UR  - conv_3379
ER  - 
@article{
author = "Krstić, Jelena and Buzadzić, Ivana and Milanović, Slađan and Ilić, Nela V. and Pajić, Sanja and Ilić, Tihomir V.",
year = "2014",
abstract = "Introduction: 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.",
publisher = "Lippincott Williams & Wilkins, Philadelphia",
journal = "Journal of ECT",
title = "Low-Frequency Repetitive Transcranial Magnetic Stimulation in the Right Prefrontal Cortex Combined With Partial Sleep Deprivation in Treatment-Resistant Depression A Randomized Sham-Controlled Trial",
pages = "331-325",
number = "4",
volume = "30",
doi = "10.1097/YCT.0000000000000099",
url = "conv_3379"
}
Krstić, J., Buzadzić, I., Milanović, S., Ilić, N. V., Pajić, S.,& Ilić, T. V.. (2014). Low-Frequency Repetitive Transcranial Magnetic Stimulation in the Right Prefrontal Cortex Combined With Partial Sleep Deprivation in Treatment-Resistant Depression A Randomized Sham-Controlled Trial. in Journal of ECT
Lippincott Williams & Wilkins, Philadelphia., 30(4), 325-331.
https://doi.org/10.1097/YCT.0000000000000099
conv_3379
Krstić J, Buzadzić I, Milanović S, Ilić NV, Pajić S, Ilić TV. Low-Frequency Repetitive Transcranial Magnetic Stimulation in the Right Prefrontal Cortex Combined With Partial Sleep Deprivation in Treatment-Resistant Depression A Randomized Sham-Controlled Trial. in Journal of ECT. 2014;30(4):325-331.
doi:10.1097/YCT.0000000000000099
conv_3379 .
Krstić, Jelena, Buzadzić, Ivana, Milanović, Slađan, Ilić, Nela V., Pajić, Sanja, Ilić, Tihomir V., "Low-Frequency Repetitive Transcranial Magnetic Stimulation in the Right Prefrontal Cortex Combined With Partial Sleep Deprivation in Treatment-Resistant Depression A Randomized Sham-Controlled Trial" in Journal of ECT, 30, no. 4 (2014):325-331,
https://doi.org/10.1097/YCT.0000000000000099 .,
conv_3379 .

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