Exploring the efficacy of a 5-day course of transcranial direct current stimulation (TDCS) on depression and memory function in patients with well-controlled temporal lobe epilepsy
Depression and memory dysfunction significantly impact the quality of life of patients with epilepsy. Current therapies for these cognitive and psychiatric comorbidities are limited. We explored the efficacy and safety of transcranial direct current stimulation (TDCS) for treating depression and mem...
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Published in | Epilepsy & behavior Vol. 55; pp. 11 - 20 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
Elsevier Inc
01.02.2016
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Online Access | Get full text |
ISSN | 1525-5050 1525-5069 1525-5069 |
DOI | 10.1016/j.yebeh.2015.10.032 |
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Abstract | Depression and memory dysfunction significantly impact the quality of life of patients with epilepsy. Current therapies for these cognitive and psychiatric comorbidities are limited. We explored the efficacy and safety of transcranial direct current stimulation (TDCS) for treating depression and memory dysfunction in patients with temporal lobe epilepsy (TLE).
Thirty-seven (37) adults with well-controlled TLE were enrolled in a double-blinded, sham-controlled, randomized, parallel-group study of 5days of fixed-dose (2mA, 20min) TDCS. Subjects were randomized to receive either real or sham TDCS, both delivered over the left dorsolateral prefrontal cortex. Patients received neuropsychological testing and a 20-minute scalp EEG at baseline immediately after the TDCS course and at 2- and 4-week follow-up.
There was improvement in depression scores immediately after real TDCS, but not sham TDCS, as measured by changes in the Beck Depression Inventory (BDI change: −1.68 vs. 1.27, p<0.05) and NDDI-E (−0.83 vs. 0.9091, p=0.05). There was no difference between the groups at the 2- or 4-week follow-up. There was no effect on delayed or working memory performance. Transcranial direct current stimulation was well-tolerated and did not increase seizure frequency or interictal discharge frequency. Transcranial direct current stimulation induced an increase in delta frequency band power over the frontal region and delta, alpha, and theta band power in the occipital region after real stimulation compared to sham stimulation, although the difference did not reach statistical significance.
This study provides evidence for the use of TDCS as a safe and well-tolerated nonpharmacologic approach to improving depressive symptoms in patients with well-controlled TLE. However, there were no changes in memory function immediately following or persisting after a stimulation course. Further studies may determine optimal stimulation parameters for maximal mood benefit.
•A five-day course of TDCS has a modest but significant benefit in improving depressive symptoms in adult patients with well controlled TLE, but the effects did not persist to the 2- and 4- week follow up.•There is no effect on delayed recall or working memory function after a 5-day course of TDCS.•TDCS does not increase seizure frequency or interictal discharge frequency, and is well tolerated among patients.•TDCS induced an increase in delta frequency power over the frontal region and delta, theta, and alpha power in the occipital region, immediately after stimulation, compared to sham stimulation, although this did not reach statistical significance. |
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AbstractList | Introduction: Depression and memory dysfunction significantly impact the quality of life of patients with epilepsy. Current therapies for these cognitive and psychiatric comorbidities are limited. We explored the efficacy and safety of transcranial direct current stimulation (TDCS) for treating depression and memory dysfunction in patients with temporal lobe epilepsy (TLE). Methods: Thirty-seven (37) adults with well-controlled TLE were enrolled in a double-blinded, sham-controlled, randomized, parallel-group study of 5 days of fixed-dose (2 mA, 20 min) TDCS. Subjects were randomized to receive either real or sham TDCS, both delivered over the left dorsolateral prefrontal cortex. Patients received neuropsychological testing and a 20-minute scalp EEG at baseline immediately after the TDCS course and at 2- and 4-week follow-up. Results: There was improvement in depression scores immediately after real TDCS, but not sham TDCS, as measured by changes in the Beck Depression Inventory (BDI change: - 1.68 vs. 1.27, p < 0.05) and NDDI-E (- 0.83 vs. 0.9091, p = 0.05). There was no difference between the groups at the 2- or 4-week follow-up. There was no effect on delayed or working memory performance. Transcranial direct current stimulation was well-tolerated and did not increase seizure frequency or interictal discharge frequency. Transcranial direct current stimulation induced an increase in delta frequency band power over the frontal region and delta, alpha, and theta band power in the occipital region after real stimulation compared to sham stimulation, although the difference did not reach statistical significance. Discussion This study provides evidence for the use of TDCS as a safe and well-tolerated nonpharmacologic approach to improving depressive symptoms in patients with well-controlled TLE. However, there were no changes in memory function immediately following or persisting after a stimulation course. Further studies may determine optimal stimulation parameters for maximal mood benefit. Abstract Introduction Depression and memory dysfunction significantly impact the quality of life of patients with epilepsy. Current therapies for these cognitive and psychiatric comorbidities are limited. We explored the efficacy and safety of transcranial direct current stimulation (TDCS) for treating depression and memory dysfunction in patients with temporal lobe epilepsy (TLE). Methods Thirty-seven (37) adults with well-controlled TLE were enrolled in a double-blinded, sham-controlled, randomized, parallel-group study of 5 days of fixed-dose (2 mA, 20 min) TDCS. Subjects were randomized to receive either real or sham TDCS, both delivered over the left dorsolateral prefrontal cortex. Patients received neuropsychological testing and a 20-minute scalp EEG at baseline immediately after the TDCS course and at 2- and 4-week follow-up. Results There was improvement in depression scores immediately after real TDCS, but not sham TDCS, as measured by changes in the Beck Depression Inventory (BDI change: − 1.68 vs. 1.27, p < 0.05) and NDDI-E (− 0.83 vs. 0.9091, p = 0.05). There was no difference between the groups at the 2- or 4-week follow-up. There was no effect on delayed or working memory performance. Transcranial direct current stimulation was well-tolerated and did not increase seizure frequency or interictal discharge frequency. Transcranial direct current stimulation induced an increase in delta frequency band power over the frontal region and delta, alpha, and theta band power in the occipital region after real stimulation compared to sham stimulation, although the difference did not reach statistical significance. Discussion This study provides evidence for the use of TDCS as a safe and well-tolerated nonpharmacologic approach to improving depressive symptoms in patients with well-controlled TLE. However, there were no changes in memory function immediately following or persisting after a stimulation course. Further studies may determine optimal stimulation parameters for maximal mood benefit. Depression and memory dysfunction significantly impact the quality of life of patients with epilepsy. Current therapies for these cognitive and psychiatric comorbidities are limited. We explored the efficacy and safety of transcranial direct current stimulation (TDCS) for treating depression and memory dysfunction in patients with temporal lobe epilepsy (TLE). Thirty-seven (37) adults with well-controlled TLE were enrolled in a double-blinded, sham-controlled, randomized, parallel-group study of 5 days of fixed-dose (2 mA, 20 min) TDCS. Subjects were randomized to receive either real or sham TDCS, both delivered over the left dorsolateral prefrontal cortex. Patients received neuropsychological testing and a 20-minute scalp EEG at baseline immediately after the TDCS course and at 2- and 4-week follow-up. There was improvement in depression scores immediately after real TDCS, but not sham TDCS, as measured by changes in the Beck Depression Inventory (BDI change: -1.68 vs. 1.27, p<0.05) and NDDI-E (-0.83 vs. 0.9091, p=0.05). There was no difference between the groups at the 2- or 4-week follow-up. There was no effect on delayed or working memory performance. Transcranial direct current stimulation was well-tolerated and did not increase seizure frequency or interictal discharge frequency. Transcranial direct current stimulation induced an increase in delta frequency band power over the frontal region and delta, alpha, and theta band power in the occipital region after real stimulation compared to sham stimulation, although the difference did not reach statistical significance. This study provides evidence for the use of TDCS as a safe and well-tolerated nonpharmacologic approach to improving depressive symptoms in patients with well-controlled TLE. However, there were no changes in memory function immediately following or persisting after a stimulation course. Further studies may determine optimal stimulation parameters for maximal mood benefit. Depression and memory dysfunction significantly impact the quality of life of patients with epilepsy. Current therapies for these cognitive and psychiatric comorbidities are limited. We explored the efficacy and safety of transcranial direct current stimulation (TDCS) for treating depression and memory dysfunction in patients with temporal lobe epilepsy (TLE).INTRODUCTIONDepression and memory dysfunction significantly impact the quality of life of patients with epilepsy. Current therapies for these cognitive and psychiatric comorbidities are limited. We explored the efficacy and safety of transcranial direct current stimulation (TDCS) for treating depression and memory dysfunction in patients with temporal lobe epilepsy (TLE).Thirty-seven (37) adults with well-controlled TLE were enrolled in a double-blinded, sham-controlled, randomized, parallel-group study of 5 days of fixed-dose (2 mA, 20 min) TDCS. Subjects were randomized to receive either real or sham TDCS, both delivered over the left dorsolateral prefrontal cortex. Patients received neuropsychological testing and a 20-minute scalp EEG at baseline immediately after the TDCS course and at 2- and 4-week follow-up.METHODSThirty-seven (37) adults with well-controlled TLE were enrolled in a double-blinded, sham-controlled, randomized, parallel-group study of 5 days of fixed-dose (2 mA, 20 min) TDCS. Subjects were randomized to receive either real or sham TDCS, both delivered over the left dorsolateral prefrontal cortex. Patients received neuropsychological testing and a 20-minute scalp EEG at baseline immediately after the TDCS course and at 2- and 4-week follow-up.There was improvement in depression scores immediately after real TDCS, but not sham TDCS, as measured by changes in the Beck Depression Inventory (BDI change: -1.68 vs. 1.27, p<0.05) and NDDI-E (-0.83 vs. 0.9091, p=0.05). There was no difference between the groups at the 2- or 4-week follow-up. There was no effect on delayed or working memory performance. Transcranial direct current stimulation was well-tolerated and did not increase seizure frequency or interictal discharge frequency. Transcranial direct current stimulation induced an increase in delta frequency band power over the frontal region and delta, alpha, and theta band power in the occipital region after real stimulation compared to sham stimulation, although the difference did not reach statistical significance.RESULTSThere was improvement in depression scores immediately after real TDCS, but not sham TDCS, as measured by changes in the Beck Depression Inventory (BDI change: -1.68 vs. 1.27, p<0.05) and NDDI-E (-0.83 vs. 0.9091, p=0.05). There was no difference between the groups at the 2- or 4-week follow-up. There was no effect on delayed or working memory performance. Transcranial direct current stimulation was well-tolerated and did not increase seizure frequency or interictal discharge frequency. Transcranial direct current stimulation induced an increase in delta frequency band power over the frontal region and delta, alpha, and theta band power in the occipital region after real stimulation compared to sham stimulation, although the difference did not reach statistical significance.This study provides evidence for the use of TDCS as a safe and well-tolerated nonpharmacologic approach to improving depressive symptoms in patients with well-controlled TLE. However, there were no changes in memory function immediately following or persisting after a stimulation course. Further studies may determine optimal stimulation parameters for maximal mood benefit.DISCUSSIONThis study provides evidence for the use of TDCS as a safe and well-tolerated nonpharmacologic approach to improving depressive symptoms in patients with well-controlled TLE. However, there were no changes in memory function immediately following or persisting after a stimulation course. Further studies may determine optimal stimulation parameters for maximal mood benefit. Depression and memory dysfunction significantly impact the quality of life of patients with epilepsy. Current therapies for these cognitive and psychiatric comorbidities are limited. We explored the efficacy and safety of transcranial direct current stimulation (TDCS) for treating depression and memory dysfunction in patients with temporal lobe epilepsy (TLE). Thirty-seven (37) adults with well-controlled TLE were enrolled in a double-blinded, sham-controlled, randomized, parallel-group study of 5days of fixed-dose (2mA, 20min) TDCS. Subjects were randomized to receive either real or sham TDCS, both delivered over the left dorsolateral prefrontal cortex. Patients received neuropsychological testing and a 20-minute scalp EEG at baseline immediately after the TDCS course and at 2- and 4-week follow-up. There was improvement in depression scores immediately after real TDCS, but not sham TDCS, as measured by changes in the Beck Depression Inventory (BDI change: −1.68 vs. 1.27, p<0.05) and NDDI-E (−0.83 vs. 0.9091, p=0.05). There was no difference between the groups at the 2- or 4-week follow-up. There was no effect on delayed or working memory performance. Transcranial direct current stimulation was well-tolerated and did not increase seizure frequency or interictal discharge frequency. Transcranial direct current stimulation induced an increase in delta frequency band power over the frontal region and delta, alpha, and theta band power in the occipital region after real stimulation compared to sham stimulation, although the difference did not reach statistical significance. This study provides evidence for the use of TDCS as a safe and well-tolerated nonpharmacologic approach to improving depressive symptoms in patients with well-controlled TLE. However, there were no changes in memory function immediately following or persisting after a stimulation course. Further studies may determine optimal stimulation parameters for maximal mood benefit. •A five-day course of TDCS has a modest but significant benefit in improving depressive symptoms in adult patients with well controlled TLE, but the effects did not persist to the 2- and 4- week follow up.•There is no effect on delayed recall or working memory function after a 5-day course of TDCS.•TDCS does not increase seizure frequency or interictal discharge frequency, and is well tolerated among patients.•TDCS induced an increase in delta frequency power over the frontal region and delta, theta, and alpha power in the occipital region, immediately after stimulation, compared to sham stimulation, although this did not reach statistical significance. |
Author | Schachter, Steven Friedman, Daniel Bryant, Andrew Shafi, Mouhsin Devinsky, Orrin Minhas, Preet Liu, Anli Barr, William Pascual-Leone, Alvaro Herman, Susan Jefferson, Ashlie Thesen, Thomas O'Connor, Margaret Barnard, Sarah |
Author_xml | – sequence: 1 givenname: Anli surname: Liu fullname: Liu, Anli email: Anli.liu@nyumc.org organization: NYU Comprehensive Epilepsy Center, USA – sequence: 2 givenname: Andrew orcidid: 0000-0002-5615-803X surname: Bryant fullname: Bryant, Andrew organization: NYU Comprehensive Epilepsy Center, USA – sequence: 3 givenname: Ashlie surname: Jefferson fullname: Jefferson, Ashlie organization: NYU Comprehensive Epilepsy Center, USA – sequence: 4 givenname: Daniel surname: Friedman fullname: Friedman, Daniel organization: NYU Comprehensive Epilepsy Center, USA – sequence: 5 givenname: Preet surname: Minhas fullname: Minhas, Preet organization: NYU Comprehensive Epilepsy Center, USA – sequence: 6 givenname: Sarah surname: Barnard fullname: Barnard, Sarah organization: NYU Comprehensive Epilepsy Center, USA – sequence: 7 givenname: William surname: Barr fullname: Barr, William organization: NYU Comprehensive Epilepsy Center, USA – sequence: 8 givenname: Thomas surname: Thesen fullname: Thesen, Thomas organization: NYU Comprehensive Epilepsy Center, USA – sequence: 9 givenname: Margaret surname: O'Connor fullname: O'Connor, Margaret organization: Beth Israel Deaconess Medical Center, USA – sequence: 10 givenname: Mouhsin surname: Shafi fullname: Shafi, Mouhsin organization: Beth Israel Deaconess Medical Center, USA – sequence: 11 givenname: Susan surname: Herman fullname: Herman, Susan organization: Beth Israel Deaconess Medical Center, USA – sequence: 12 givenname: Orrin surname: Devinsky fullname: Devinsky, Orrin organization: NYU Comprehensive Epilepsy Center, USA – sequence: 13 givenname: Alvaro surname: Pascual-Leone fullname: Pascual-Leone, Alvaro organization: Beth Israel Deaconess Medical Center, USA – sequence: 14 givenname: Steven surname: Schachter fullname: Schachter, Steven organization: Beth Israel Deaconess Medical Center, USA |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/26720704$$D View this record in MEDLINE/PubMed |
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Keywords | Neurostimulation Temporal lobe epilepsy Depression Stimulation safety Transcranial direct current stimulation Memory |
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Snippet | Depression and memory dysfunction significantly impact the quality of life of patients with epilepsy. Current therapies for these cognitive and psychiatric... Abstract Introduction Depression and memory dysfunction significantly impact the quality of life of patients with epilepsy. Current therapies for these... Introduction: Depression and memory dysfunction significantly impact the quality of life of patients with epilepsy. Current therapies for these cognitive and... |
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SubjectTerms | Adult Depression Depressive Disorder - etiology Depressive Disorder - psychology Depressive Disorder - therapy Double-Blind Method Electroencephalography Epilepsy, Temporal Lobe - complications Epilepsy, Temporal Lobe - psychology Epilepsy, Temporal Lobe - therapy Female Follow-Up Studies Humans Male Memory Memory Disorders - etiology Memory Disorders - psychology Memory Disorders - therapy Memory, Short-Term Middle Aged Neurology Neuropsychological Tests Neurostimulation Prefrontal Cortex Psychiatric Status Rating Scales Psychomotor Performance Quality of Life Stimulation safety Temporal lobe epilepsy Transcranial direct current stimulation Transcranial Direct Current Stimulation - adverse effects |
Title | Exploring the efficacy of a 5-day course of transcranial direct current stimulation (TDCS) on depression and memory function in patients with well-controlled temporal lobe epilepsy |
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