Snapshots of neuronal activation due to visual and ... · PROTOCOL DETAILS - EXCLUSION CRITERIA...
Transcript of Snapshots of neuronal activation due to visual and ... · PROTOCOL DETAILS - EXCLUSION CRITERIA...
SNAPSHOTS OF NEURONAL ACTIVATION DUE TO VISUAL
AND AUDITORY STIMULI UNDER AGE, GENDER AND
NEURODEGENERATION EFFECT. HIGH- DENSITY EEG
STUDIES
ANTHOULA C. TSOLAKI, MD
NEUROLOGY CLINIC, G.H. “AGIOS PAVLOS”, THESSALONIKI, GREECE
INFORMATION TECHNOLOGIES INSTITUTE (ITI), CENTRE FOR RESEARCH & TECHNOLOGY HELLAS
10th Panhellenic Conference of Alzheimer's Disease and Related Disorders (PICAD) and
2nd Mediterranean Conference of Neurodegenerative Diseases (MeCOND)
COGNITIVE BRAIN SIGNAL PROCESSING LAB, (CBP)
Information Technologies Institute
3 Neurophysiological Studies using HD- EEG recordings
EGI 300 Geodesic EEG system (GES 300) using a 256-channel HydroCel GeodesicSensorNet (HCGSN)
Study of neuronal response in different age groups, in healthy and neurodegenerative disease.
Event related potentials MMN, P300, N400, N170
Brain source localization
HD-EEG
PROTOCOL DETAILS - EXCLUSION CRITERIA
Participants
volunteers from the Centre for Research & Technology Hellas,
the dementia outpatient clinic of the 3rd Neurology department of Aristotle University of Thessaloniki
from personal inquiry and emails in social networks
120 participants are recruited, divided in three groups: a) 30 young healthy participants aged 25-40 years old, b) 30 healthy elderly greater than 65 years old d) 30 MCI subjects and d) 30 mild AD patients aged greater than 65 years old
The study protocol has been approved by the Ethics Committee of the Centre for Research & Technology Hellas and the Ethics Committee of Aristotle University (Protocol No 69/29.12.2013)
Exclusion criteria:
any severe physical illness
current psychiatric or neurological disorder
history of drug or alcohol abuse
recent start (less than 15 days) of acethylcholinesterase inhibitors medication or other neuromodifying drugs
other types of dementia
Participants reported normal or corrected-to-normal vision and audition
Neuropsycological evaluation: MMSE , MoCA, TRAIL B, BDI, GDS, IADL, and FRSSD
Blood tests and brain MRI, qualitative EEG evaluation
Diagnosis of mild AD or mild cognitive impairment is according DSM-V criteria
1ST STUDY, HEALTHY POPULATION, AGE AND GENDER DIFFERENCE
PARTICIPANTS - PROTOCOL
27 young (14F/13M) and 18 elderly (9F/8M)
Active Two- tone oddball experiment, Standard tone (250Hz, probability 0,8), Target tone (4000Hz, probability 0,2)
All stimuli:150ms duration, 5ms rise/fall time and 75dB SPL, ISI of 2 sec
Total number of tones: 250
The subject was asked to identify the target tone by clicking the left button of the mouse with the Right hand.
RESULTS (1)
RESULTS (2)
RESULTS (3)
RESULTS (4)
MMN BA Lobe
Young 47 Frontal
Elderly 47 Frontal
P300 BA Lobe
Young 11 Frontal
Elderly 38 Temporal
N400 BA Lobe
Young 11 Frontal
Elderly 11 Frontal
2ND STUDY, AGE EFFECT IN EMOTIONAL PROCESSING, HEALTHY
POPULATION
PARTICIPANTS
Ηealthy female (11 young (25-40 years old) and 11 elderly (>60 years old))
right-handed volunteers Α subgroup of the sample recruited for the project CBP: Cognitive Brain Signal
Processing Lab (Kosmidou et al., 2014).
Νormal or corrected-to-normal vision and audition.
Νeuropsychological evaluation -blood tests - brain MRI
All participants with depression (BDI >9/63 score, and GDS >4/15) were excluded,
Participants provided written informed consent.
PROTOCOL
RESULTS
Anger Fear
latency
(ms)
amplitude (μV) latency
(ms)
amplitude (μV)
Young 156 -2.02a 156 -1.84a
Elderly 168 -6.13a 176 -4.68a
RESULTS (2)
RESULTS (3)
ID Location Intensity
(nA)
BA Gyri Lobe
Anger
Young 576 (-45, 45, -13) 0.30 47 Inferior Frontal Frontal
Elderly 191 (-10, 31,-27) 0.30 11 Rectal Frontal
Fear
Young 38 (-31, 17, -41) 0.33 38 Superior Temporal Temporal
Elderly 38 (-31, 17, -41) 0.34 38 Superior Temporal Temporal
RESULTS (4)
ID Location Intensity
(nA)
BA Gyri Lobe
Young vs
Elderly
Anger 24 (18, 3, -41) 0.18 36 Uncus Limbic
Fear 5 (32, -11,-41) 0.28 20 Uncus Limbic
3RD STUDY, AUDIO ERPS IN HEALTHY, MCI & AD
Brain source localization of MMN and P300 ERPs in Mild
Cognitive Impairment and Alzheimer's disease: A High Density
EEG approach
Anthoula C. Tsolaki, Vasiliki Kosmidou, Ioannis (Yiannis) Kompatsiaris, Chrysa Papadaniil, Leontios Hadjileontiadis,
Katerina Adam,Magda Tsolaki.
Under Revision in Neurobiology of Aging
PARTICIPANTS
Group # of Participants (Female/Male) Age (years) MMSE score Education level (years) Error on standard tone Error on target tone Response time (ms)
Control21 (13/8) 67 (±2.7) 28.81*
(±0.9)
14** (±5) 0.50 (±0.19) 1.02* (±0.26) 645 (±71)
MCI21 (14/7) 72 (±4.7) 27* (±1.4) 10 (±5) 1.01 (±1.4) 9.32* (±24.95) 667 (±253)
AD21 (14/7) 70 (±6.8) 22.6* (±3.4) 8 (±6) 2.5* (±2.31) 22.56* (±22.78) 957* (±162)
*p<0.005, **p<0.01, no super-script indicates no statistical significance between the groups
PROTOCOL
Active Two- tone oddball experiment, Standard tone (250Hz, probability 0,8), Target
tone (4000Hz, probability 0,2)
All stimuli:150ms duration, 5ms rise/fall time and 75dB SPL, ISI of 2 sec
Total number of tones: 250
The subject was asked to identify the target tone by clicking the left button of the
mouse with the Right hand.
RESULTS
MMN P300
RESULTS (2)
ID Location Intensity
(nA)
Brodmann
Area
Gyri Lobe
P300
Control 40 (39,17,-41) 0.13 38 Superior Temporal Temporal
MCI 603 (39, 59,-13) 0.14 11 Middle Frontal Frontal
AD 603 (39,59,-13) 0.18 11 Middle Frontal Frontal
ID Location Intensity
(nA)
Brodmann
Area
Gyri Lobe
MMN
Control 189 (4,24,-27) 0.11 11 Rectal Frontal
MCI 595 (-38,59,-13) 0.14 11 Middle Frontal Frontal
AD 240 (25,-39,-20) 0.12 37 Fusiform Gyrus Temporal
RESULTS (3)
MMN P300
CONCLUSIONS
Brain source localization is achieved with high density EEG
Results reveal changes in N170 with aging for two negative emotional stimuli
Differences in brain neural activation at the ‘anger’ and ‘fear’ face processing
Higher negativity in the occipito-temporal electrode sites in case of elderly
Aging appears to affect the limbic area neural activation at emotional processing
Brain source localization of ERPs is proposed as prognostic tool in neurodegeneration.
Early change of neuronal activation is revealed even in preclinical stages.
Frontal lobe is revealed to play an important role both in MCI and AD.
Group- based Results
ACKNOWLEDGMENTS
This work was funded by the GSRT Research Excellent Grant ARISTEIA,
within the 4th Strategic Objective of the operational program “Education
and Lifelong Learning” entitled ‘Supporting the Human Capital in order
Promote Research and Innovation’, under grant agreement 440
Dr. Vasiliki Kosmidou,
Post-doctoral Researcher
Information Technologies Institute
(ITI), Centre for Research &
Technology Hellas
Dr. Chrysa Papadanii,Department of Electrical & Computer Engineering, AristotleUniversity of Thessaloniki.Doctoral grant- holder
Katerina Adam,
Information Technologies Institute
(ITI), Centre for Research &
Technology Hellas
Dr. Ioannis (Yiannis) KompatsiarisResearcher A,
Information Technologies Institute
(ITI), Centre for Research &
Technology Hellas
Dr. Leontios Hadjileontiadis,
Professor of Department of Electrical& Computer Engineering, AristotleUniversity of Thessaloniki.& Department of Electrical and Computer Engineering, KhalifaUniversity, PO BOX 127788, AbuDhabi, UAE.
Dr. Magdalini Tsolaki
Professor of Neurology,
3rd Department of Neurology,
Aristotle University of Thessaloniki
Pressident og Panhellenic Federation
of Alzheimer’s Disease
SPECIAL THANKS
Thank you for your attention!