Repetitive Transcranial Repetitive Transcranial Magnetic Stimulation (rTMS) Magnetic Stimulation (rTMS) Tung-Ping Su, MD Tung-Ping Su, MD Department of Psychiatry Department of Psychiatry Taipei-Veterans General Hospital Taipei-Veterans General Hospital National Yang-Ming University National Yang-Ming University Dec. 09, 2009 for IBS Dec. 09, 2009 for IBS
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Repetitive Transcranial Magnetic Stimulation (rTMS) Tung-Ping Su, MD Department of Psychiatry Taipei-Veterans General Hospital National Yang-Ming University.
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Repetitive Transcranial Magnetic Repetitive Transcranial Magnetic Stimulation (rTMS)Stimulation (rTMS)
Tung-Ping Su, MDTung-Ping Su, MDDepartment of PsychiatryDepartment of Psychiatry
Taipei-Veterans General HospitalTaipei-Veterans General Hospital
National Yang-Ming UniversityNational Yang-Ming UniversityDec. 09, 2009 for IBSDec. 09, 2009 for IBS
History of NeuromodulationHistory of Neuromodulation
• DBS: deep brain stimulationDBS: deep brain stimulation
• MST: magnetic seizure therapyMST: magnetic seizure therapy
Electro-chemical communicationElectro-chemical communication
Electrical brain:
Excitatory (glutamate) and Inhibitory (GABA)neurons
Introduction to TMSIntroduction to TMS(Transcranial Magnetic (Transcranial Magnetic
Stimulation)Stimulation)
First Patent of TMS First Patent of TMS
for Depression--1902for Depression--1902
• The 1902 patent was issued The 1902 patent was issued to Pollocsek and Beer for an to Pollocsek and Beer for an electromagnetic device to electromagnetic device to treat depression and treat depression and neuroses.neuroses.
• Source: Library of Mark S. GeorgeSource: Library of Mark S. George
Early TMS Early TMS
• Sylvanius Sylvanius P.Thompson and his P.Thompson and his apparatus to produce apparatus to produce phosphenes using phosphenes using magnetic stimulationmagnetic stimulation
Modern TMSModern TMS
• A.T barker with his A.T barker with his TMS machine in TMS machine in 1985, which set the 1985, which set the stage for much of stage for much of today’s work with today’s work with TMSTMS
TMS HistoryTMS History
• 19951995 – First therapeutic cases reported in – First therapeutic cases reported in depression depression (Mark George et al, Neuroreport)(Mark George et al, Neuroreport)
Rapid increase in publications Rapid increase in publications concerning rTMSconcerning rTMS
• • Brain Behavior ResearchBrain Behavior Research• • Translation to TherapiesTranslation to Therapies• • Interface with CAIRInterface with CAIR
Started in 1995,Assembled grant by grant
Transcranial Magnetic Stimulation (TMS)
Time-Varying Electrical Current in a Coil Produces
Focal 2 Tesla Magnetic FieldPasses Unimpeded ThroughSkull
Induces Current in Neurons
Behavioral Change
TMS is TMS is ‘Electrodeless’ Electrical Stimulation‘Electrodeless’ Electrical Stimulation
1) Electrical Energy in CoilInduces2) Magnetic Field (right handRule, Maxwell’s Equations)3) Passes unimpeded through theSkull4) Induces an electrical current inThe brainFrom TMS Review in Science, June 18, 2001
Understanding TMS Effects on NeuronsUnderstanding TMS Effects on Neurons
Critical Variables Include:• fiber orientation• intensity (submotor likely more inhibitory interneurons)• frequency• region• Distance into cortex
Using Phase Maps to Determine The Using Phase Maps to Determine The Exact Magnetic FieldExact Magnetic Field
Structural Scan with TMS Coil Phase Map of Exact Magnetic Field
Approximate Depth Limit of Direct Approximate Depth Limit of Direct Stimulation with Current TMS CoilsStimulation with Current TMS CoilsApproximate Depth Limit of Direct Approximate Depth Limit of Direct Stimulation with Current TMS CoilsStimulation with Current TMS Coils
TMS as a Brain Circuit ProbeTMS as a Brain Circuit Probe• ProsPros
– Relatively non-invasive– Good spatial and temporal resolution
• ConsCons– Unclear knowledge of effects on neurons (local
or secondary), especially as a function of• Frequency,• Duration• Brain region• Intensity
Hughlings Jackson - “Is TMS irritative (augment) or ablative?”
Applications of TMSApplications of TMS• Anticonvulsant(<1 HZ) or proconvulsant (fast)
• Mapping the cortex of the brain
• Probing neural networks by stimulation or inhibition at different places and times
• Measuring cortical excitability in health and in disease, and in response to drugs
• Modulating brain function to study the pathophysiology of a variety of neuropsychiatric conditions, and possibly treat them
• Sadness Induction in Healthy Adults, O15 PET, Sadness Induction in Healthy Adults, O15 PET, (George et al, Am J Psych, (George et al, Am J Psych, 1995)1995)
• Pros - Great potentialPros - Great potential– Non-invasive– Potential for pushing and pulling circuits
• Therapeutics - Therapeutics - – Still Experimental– Repeated stimulation over 2-3 weeks treats depression
• Problems - Problems - basic effectsbasic effects on neuronal function are on neuronal function are largely unknownlargely unknown– Intensity, frequency, location, trains, dose– Currently limited to cortex
Safety Concerns of Safety Concerns of Transcranial Magnetic StimulationTranscranial Magnetic Stimulation
rTMS Parameters Important for safetyrTMS Parameters Important for safety
• Intensity (strength of voltage; %MT)Intensity (strength of voltage; %MT)
• versusversus
• Frequency (how fast; Hz)Frequency (how fast; Hz)
Current rTMS safety guidelines Current rTMS safety guidelines ::
maximum safe duration (seconds) for single trains of rTMS based on the National maximum safe duration (seconds) for single trains of rTMS based on the National
Institute of Neurological Disorders and Stroke experience(NINDS)Institute of Neurological Disorders and Stroke experience(NINDS)
Conclusions: side effectsConclusions: side effects
• Both Single-pulse TMS / rTMSBoth Single-pulse TMS / rTMS can cause can cause• Headache:Headache:
local discomfortlocal discomfort
muscle tension headachemuscle tension headache• Temporary Temporary increase in auditory thresholdincrease in auditory threshold without without
earplugsearplugs• Heating of metallic objectsHeating of metallic objects within head,on scalp within head,on scalp• Malfunction Malfunction of very close electronic/magnetic devicesof very close electronic/magnetic devices
Effect of Repetitive Transcranial Magnetic Effect of Repetitive Transcranial Magnetic Stimulation (rTMS)Stimulation (rTMS)
on Mood and Cognition on Mood and Cognition
Tung-Ping Su, MDTung-Ping Su, MD
Department of PsychiatryDepartment of Psychiatry
Taipei-Veterans General HospitalTaipei-Veterans General Hospital
April, 23, 2002April, 23, 2002
The five major regions of dysfunction in depressed brains
and Nu. Accumbens are underactivity and HPA axis: overactivity
Amygdala:Emotional recognition of facesLt Amygdala activated during sadness
• Personality change
• ResultsResults
Hamilton Depressive Rating Scale
0
5
10
15
20
25
30
35
40
Baseline 1st week 2nd week 3rd week 4th week
Time
Add-on rTMS for medication-resistant Add-on rTMS for medication-resistant depression:depression:
a randomized, double-blind, sham-a randomized, double-blind, sham-controlled trial in Chinese patientscontrolled trial in Chinese patients
Tung-Ping Su, Chih-Chia HuangTung-Ping Su, Chih-Chia Huang
J of Clinical Psychiatry 2005:66:930-937J of Clinical Psychiatry 2005:66:930-937
Effect of Age, Gender, Menopausal Status, and Ovarian Hormonal Level
on rTMS in Treatment-Resistant Depression
Chih-Chia Huanga, I-Hua Weid, Yuan-Hwa Choua, Tung-Ping Su
Psychoneuroendocrinology, 2007
post-menopausal women
Age
80706050403020
perc
enta
ge H
AM
-D r
educ
tion
100
80
60
40
20
0
- 20
pre-menopausal women
Age
80706050403020
perc
enta
ge H
AM
-D r
educ
tion
100
80
60
40
20
0
-20
N=47
Responder: 23
Non-responder: 24
N=17
Responder: 12
Non-responder: 5
N=14
Responder: 0
Non-responder: 14
N=16
Responder: 11
Non-responder: 5
N=31
Responder: 12
Non-responder: 19
Pearson’s correlation test
r = -0.276
P = 0.061
Pearson’s correlation test
r = -0.322
P = 0.207
Pearson’s correlation test
r = 0.35
P = 0.184
Pearson’s correlation test
r = 0.117
P = 0.691
Pearson’s correlation test
r = -0.646
P < 0.001
men
Age
80706050403020
perc
enta
ge H
AM
-D r
educ
tion
100
80
60
40
20
0
-20
Fig. 1 Relationship of reduction of percent HAM-D Score with Age in the Whole Group of Depressed Patients, between Genders, and Premenopausal and Postmenopausal Females
all subjects
Age
80706050403020
perc
enta
ge H
AM
-D r
educ
tion
100
80
60
40
20
0
- 20
women
Age
80706050403020
per
cen
tage
HA
M-D
red
uct
ion 100
80
60
40
20
0
- 20
Fig. 2 Percentage HAM-D reduction vs. E2/P ratio
N=16
r = -0.11
P = 0.968
N=17
r = 0.563
P = 0.019
N=14
r = 0.158
P = 0.590
N=31
r = 0.527
P = 0.002
men
E2/P ratio
3000200010000
per
cen
tag
e H
AM
-D r
edu
ctio
n 100
80
60
40
20
0
-20
pre-menopausal women
E2/P ratio
1000080006000400020000-2000
per
cen
tag
e H
AM
-D r
edu
ctio
n
100
80
60
40
20
0
post-menopausal women
E2/P ratio
3000200010000
perc
enta
ge H
AM
-D r
educ
tion
50
40
30
20
10
0
- 10
women
E2/P ratio
1000080006000400020000- 2000
per
cen
tag
e H
AM
-D r
edu
ctio
n
100
80
60
40
20
0
- 20
Table 3 Stepwise Multiple Linear Regression Analysis of Factors Correlated to Percentage HAM-D Reduction After rTMS in Female Patients
Variables
Percentage HAM-D reduction
β t P Adjusted r2
Menopausal status(pre=1; post = 0)
0.728 6.334 <0.001 0.525
P -0.266 -2.350 0.026 0.630
E2/P ratio 0.257 2.248 0.033 0.677
LOCF was applied.E2, estradiol; P, progesterone; pre, premenopausal status; post, postmenopausal status.
Prediction of antidepressant efficacy of a 2-week add-on trial rTMS
in Medication-Resistant Depression: a 18F-FDG PET study
Tung-Ping Su, MDDepartment of Psychiatry
National Yang-Ming UniversityTaipei Veterans General Hospital
2nd WCAP, Taipei, Nov. 9, 2009
Introduction
• Impaired reciprocal function relationship of limbic amygdala &
hippocampus - cortical dorsolateral, medical and ventral prefrontal circuit—thought to correlate with emotional dysregulation and depression– Inconsistent results from imaging studies (PET or SPECT) in exact
location and direction of regional cerebral metabolism in depression, suggesting possible roles of using pre-Tx regional metabolic activities in various parts of the brain to predict tx response from antidepressants (Mayberg 2000, Little 2005,Milak, 2009)
– Medication-resistant depression (MRD) is a unique model for study as if underlying pathophysiology is different from pharmaco-responsive major depression (MDD).
Hypotheses and Aims
• Responders are different from non-responders in resting brain metabolism– Differences may account for core antidepressant mechanism of
rTMS
• Pre-rTMS regional brain glucose uptake in DLPFC, ACC, hippocampus and brainstem may – Predict rTMS effectiveness in medicated MRD patients.
• Is underlying pathophysiology of MRD different from other depressives ?– Compare with previous hypothesis of depression
Methods• Criteria for MRD (N=20)
– MDD dx through MINI and history taking– MRD dx, a hx of failing to respond to at least 2 different antidepressant trials and
with severity of scores >=18 of Hamilton Depression Rating Scale (HRDS-17)– No alcohol or substance abuse history, no major medical and neurological
disorders, no comorbidity of schizophrenia, bipolar disorder, OCD, PTSD or cluster–B personality d/o
• A 2-week of daily rTMS administration with continuation of the current antidepressant medications
• Responders (HDRS-17 score >= 50% reduction) vs. non-responders• PET and MRI procedures
– Healthy control subjects (N=20)
Setting for Repetitive transcranial stimulation, r-TMSm using Brainsight(MRI DLPFC localization)
Study designStudy design
ResultsResults
Treatment-Resistant MDD (20) vs. NC (20) Treatment-Resistant MDD (20) vs. NC (20)
NC < MDDNC > MDD
•Global variance across scans: removed by analysis of covariance (ANCOVA)•Btw-gp comparison: ANCOVA, Controlling for age and gender•Cluster level, corrected p <0.001
Treatment-Resistant MDD (20) vs. NC (20) Treatment-Resistant MDD (20) vs. NC (20) A cortico-limbal dysregulationA cortico-limbal dysregulation
• MDDMDDBil DLPFCBil DLPFCBil OFCBil OFCBil Med. PFC Bil Med. PFC Bil Ant. Insula - IFABil Ant. Insula - IFAAnterior CingulumAnterior CingulumMiddle CingulumMiddle Cingulum
Bil AmygdalaBil AmygdalaBil Putamen/GP Bil Putamen/GP Bil InsulaBil InsulaHippo/ParahipHippo/ParahipRaphe nu. Raphe nu. CerebellumCerebellum
Less hypoactive in ACC, bilateral medial prefrontal Less hypoactive in ACC, bilateral medial prefrontal gyrusgyrus
Responder > N-R
•Global variance across scans: removed by analysis of covariance (ANCOVA)•Btw-gp comparison: ANCOVA, Controlling for age and gender•Using NC vs. MDD mask•Cluster level, k=2000,uncorrected p <0.05
Less hyperactive in Less hyperactive in left hippocampus and fusiform gyrusleft hippocampus and fusiform gyrus
Responder < N-R
•Global variance across scans: removed by analysis of covariance (ANCOVA)•Btw-gp comparison: ANCOVA, Controlling for age and gender•Using MDD vs NC mask•Cluster level, k=1000,uncorrected p <0.10
Pre-tx areas predicting treatment responses Pre-tx areas predicting treatment responses (≥50% decreases in HDRS)(≥50% decreases in HDRS)
•Higher pre-tx metabolism in ACC •Cluster level, k=1000, uncorrected, p = 0.089 (trend-significance)
•Lower pre-tx metabolism in Left fusiform/hippo/parahippocamcal gyri •Cluster level, k=1000, uncorrected, p = 0.004
ACC Left fusiform/hippocamcal gyri
(Paper in submission, 2009)
SummarySummary• Medicated M-R MDD patients vs. normal subjectsMedicated M-R MDD patients vs. normal subjects
– Lower metabolism in both L and R DLPFC
– Also in the status of limbic-cortical dysregulation
• Patients who responded well to rTMS Patients who responded well to rTMS – Not that severe in limbic-corticol dysregulation
– Higher pre-tx ACC and lower left Hippocampal/Fusiform activities could predict rTMS responses
• rTMS mechanism: stimulate L DLPFCrTMS mechanism: stimulate L DLPFC– By reverse metabolism of L DLPFC activities only ?
– Might have an effect of normalizing limbal-cortical dysregulation
There is an explosion of new techniques for There is an explosion of new techniques for stimulating the brain stimulating the brain (TMS, MST, VNS (TMS, MST, VNS and DBS)and DBS)
These new tools will drastically change These new tools will drastically change neuropsychiatry researchneuropsychiatry research and therapies and therapies in the in the next 20 yearsnext 20 years