the combined csd and fpca method: improves topographic specificity over eeg field potentials

1
The combined CSD and fPCA method: Improves topographic specificity over EEG field potentials Yields reference-free spectral measures similar in form to those used in conventional EEG analyses Yields orthogonal Spectral Factors Spectral Factors consistent with the analyzed data as opposed to simple, predetermined rectangular frequency bands Automatically removes EMG, EOG and electrical artifacts Provides replicable Alpha Factors Alpha Factors with characteristic peaks and topographies Allows anatomical interpretations of regional findings that are impossible with conventional EEG measures Conclusions Conclusions •The volume conduction of field potentials from neuronal generators approximates Ohm’s Law for a conductive medium, varying linearly over distance •Concurrent generators produce additive field potential effects •Linear EEG properties are preserved in the frequency domain: Fourier transformation is linear and reversible, but complex-valued Linear Properties of EEG Linear Properties of EEG •Based on simplifications of Poisson's equation, relating current generators to the negative spatial derivative of the field potential in a conductive medium •Removes volume-conducted activity •Provides a concise, reference-free simplification of a field topography •Indicates neuronal depolarization as a current sink (negativity), repolarization or hyperpolarization as a current source (positivity) •Estimates are real (magnitude and sign) Properties of CSD Properties of CSD I I dentification and separation of reference-free spectral EEG components: Combining Current Source Density (CSD) and frequency dentification and separation of reference-free spectral EEG components: Combining Current Source Density (CSD) and frequency Principal Components Analysis (fPCA) Principal Components Analysis (fPCA) Craig E. Tenke and Jürgen Kayser Craig E. Tenke and Jürgen Kayser Department of Biopsychology, New York State Psychiatric Institute, New York Impact of Reference on Frequency Spectra Impact of Reference on Frequency Spectra Reversible Transformation ourier transformation Pz Pz Fourier Spectrum [uV] Cz Pz Pz Amplitude Spectrum Irreversible Transformation Cz F z Fpz Absolute Amplitude [uV] Freq [Hz] Freq [Hz] Freq [Hz] Freq [Hz] [complex numbers] [Fourier Map at 10 Hz] Fpz Fpz Fpz F z F z F z Cz Cz Pz Pz Pz Pz - 2 0 +3 - 2 0 +3 [Amplitude Map at 10 Hz] Reference Electrode Fpz Cz EEG Time series Signal Amplitude [uV] Time [ms] Time [ms] Pz Pz Cz F z Fpz Fpz F z Cz Pz Pz [real numbers] EEG Time Series: A single cosine wave topography that varies linearly across the midline sites (Fpz, Fz, Cz, Pz), shown for a Fpz and Cz reference. Fourier Transformation: Fourier spectra are linearly and reversibly related to the temporal data. Since the simulated data are simple cosines, the complex spectra consist of real numbers. Color maps show spherical spline interpolations for a 12-channel EEG montage with lateral activity identical to midline sites. Amplitude Spectrum: Amplitude of Fourier Spectra (i.e., amplitude of frequency spectrum via Pythagorean Fourier Maps (data w/o asymmetry) Reference Electrode Fpz Cz Fpz Cz Field Potential Topographies CSD Topographies -2 0 +3 -7 0 +7 Fourier Maps (asymmetric data) Amplitude Maps (asymmetric data) Irreversible nonlinear Transformation Linear midline gradient Lateral = midline Linear midline gradient Asymmetry added to mid-frontal sites: F3 = F3 - .5 µV F4 = F4 + .5 µV Impact of Reference on Spectral Topographies of Field Potential and Impact of Reference on Spectral Topographies of Field Potential and CSD CSD -2 0 +3 -7 0 +7 Fourier Maps (data w/o asymmetry): While field potentials of Fourier maps shift in amplitude and sign depending on the chosen reference, both produce identical CSD maps (approximately zero due to the linear gradient). Fourier Maps (asymmetric data): When a hemispheric asymmetry is added to mid- frontal sites (left < right), it is evident in the field potential Fourier maps for both reference schemes. The “frontal generators” of the asymmetry are evident from the CSD maps. Amplitude Maps (asymmetric data): Nonlinear transformations commonly used in spectral analysis (power or absolute value) may distort a field topography and even reverse the direction of an asymmetry. In contrast, the equivalent transformation of CSD data preserves all information about the location of current generators without distortion. Only phase information related to concurrent source/sink properties is lost. Amplitude spectra of CSD from resting EEG: •Clarify and separate key features of the resting EEG, including: (1) Alpha Alpha peak that is largest at posterior posterior sites (eyes closed) (2) Low frequency EOG artifacts Low frequency EOG artifacts, largest near eyes (eyes closed) (3) EMG artifacts EMG artifacts largest near face (e.g., Fp1/2, eyes open) (4) Electrical artifacts at 60 60 and 70 Hz 70 Hz (at Fz) Waveform Comparison: Overview of Amplitude Spectra of CSD Overview of Amplitude Spectra of CSD Amplitude Spectra of CSD from Resting EEG Amplitude Spectra of CSD from Resting EEG nose Fp1 Fp2 Fz Cz Pz Oz F4 F8 F3 F7 FC5 FT9 FC6 FT10 TP10 CP6 CP5 TP9 C3 T7 Cz C4 T8 P3 P7 P9 P4 P8 P10 O1 O2 eyes eyes 0 7.8 15.6 23.4 31.2 39.0 46.8 54.6 62.4 70.2 78. 0 3 6 9 12 eyes closed eyes closed: Pz Pz, P8 P8, Fz Fz eyes open: eyes open: Fz Fz Frequency Frequency [Hz] Waveform Comparison Waveform Comparison •Fourier Spectra are complex, with both amplitude (Pythagorean Theorem) and phase (angle from real axis) •Power Spectra simplify EEG variance, integrating squared amplitudes over frequency (i.e., Mean Squared) •Power Spectra have empirical and theoretical value independent of the Properties of EEG Power Spectra Properties of EEG Power Spectra •Factors derived from dataset • PCA uses a linear statistical model to produce orthogonal components •Factors are useful for identifying and defining temporal measures Properties of PCA Properties of PCA Power Spectra impede inferences about underlying EEG generators, because information is lost when the data are squared (i.e., linear volume conduction properties not preserved) CSD calculation (Laplacian, Hjorth, etc.) is impossible after nonlinear transformation (i.e., the measure is physiologically unintelligible) Power estimates are not proportional to the underlying (linear) EEG field potentials Logarithmic transformations correct skew of Power Spectrum, but exaggerate systematic, low amplitude noise Problems with EEG Power Spectra Problems with EEG Power Spectra Subjects: Subjects: N =143 right-handed adults (n = 63 healthy adults and n = 82 clinically depressed outpatients, pooled across two separate studies) Recordings Recordings: Resting 30-channel EEG from four 2-min time periods (order of eyes open/closed counterbalanced as OCCO or COOC across subjects), referenced to nose tip (Grass, 10K gain; 0.1 - 30 Hz band pass; recorded using NeuroScan at 200 samples/s); vertical and horizontal EOG recorded differentially Signal processing: Signal processing: Data were segmented into 1.28 s epochs (50% overlap), yielding a frequency resolution of 0.78 Hz; artifactual data eliminated from epoched data under visual guidance (semi-automated procedure) CSD: CSD: CSD waveforms were computed for each accepted epoch using the spherical spline method of Perrin et al. (1989) [lambda = 10 -5 ; 50 iterations; m = 4) Spectral Analysis: Spectral Analysis: Hanning window (50%) applied to each CSD epoch; mean Power Spectra (PS) computed across epochs for each condition (i.e., eyes open/ closed), and subsequently converted to a RMS Amplitude Spectra (square root of Power Spectra, proportional to the amplitude of an underlying sinusoid) fPCA: fPCA: Amplitude Spectrum data from 0-77.2 Hz (100 points = 100 variables) submitted to unrestricted covariance-based Principal Components Analysis, using electrodes (31) x Conditions (2) x participants (145) as 8990 cases, followed by unscaled Varimax rotation (Kayser & Tenke, in press) Methods Methods 4.5 4.0 3.5 3.0 2.5 2.0 1.5 1.0 0.5 0.0 -.5 0.0 10.0 20.0 30.0 40.0 50.0 60.0 70.0 Frequency [Hz] Unscaled Varimax Rotated Factor Loadings for fPCA Computed from RMS Amplitude Spectra of temporal CSD Results Results -.6 +.6 Topographies of first nine fPCA Factor Scores (96.14% variance of Amplitude Spectra) Low Alpha Low Alpha High Alpha High Alpha Alpha Alpha EOG Artifact EOG Artifact EMG Artifact EMG Artifact High Variance (88.59% total) Factors 6-9 (additional 7.55%) 60 Hz 60 Hz Low Beta Low Beta Alpha Residual Alpha Residual High Beta High Beta •First five factors accounted for almost 90% of the variance of the CSD Amplitude Spectra; Alpha Alpha activity was represented by Factors 1, 3 and 5 Factors 1, 3 and 5 •Factors 2 and 4 extracted known physiological physiological artifacts artifacts (EMG, EOG) •Factors 6-9 each accounted for less than 2% of the variance (60.16 Hz: 1.98%; low beta: 17.97 Hz, 1.94%; 8.59 Hz, 1.92%; high beta: 23.44 Hz) Overview of fPCA solution Overview of fPCA solution Factor 1 Factor 1 is a prominent (26.53% variance) low alpha factor that overlaps theta. It has a posterior/inferior topography, as well as a secondary topography on the frontal midline. Factor 3 Factor 3 is a prominent (18.11%) high alpha factor with a medial parietal topography. Factor 5 Factor 5 also has a medial parietal topography, is intermediate in frequency, and less prominent than the others (7.43%). •These three alpha factors showed a condition condition dependence dependence and consistent topographies across four groups consistent topographies across four groups of participants [i.e., two independent samples of healthy adults (DC,CE) and depressed patients (DD,DE)]. Alpha Factor Topographies Alpha Factor Topographies Grouped by Factor 1 at Fz: Low Alpha (Factor 1) had a secondary Fz maximum. The secondary frontal topography was seen for individuals in both two replications using two groups. A consistent topography was also observed for subjects with high, medium or low Factor 1 scores at Fz. Single Epoch for Representative High Fz Subject: Posterior and frontal midline Alpha topographies of Factor reflect linked, inverted current generators. The sharpness of the frontal midline topography suggests local field closure, as would be produced by an opposed pair of simultaneous regional dipoles. Inferior and Frontal Generators? CET Inferior and Frontal Generators? CET Amplitude Spectrum of CSD Epoch [Hz] Black = Fz Black = Fz 1200 1000 800 600 400 200 0 6.2 6.2 Single Epoch for Representative High Fz Subject Lowpass filtered (15 Hz) CSD waveforms at Fz Fz (black line) and P8 P8 (red) from a representative epoch in a subject with high factor scores for Factor 1. Waveform peaks at Fz Fz and P8 P8 show current sources (warm colors) alternating with sinks (cold colors) between the two sites. The topography of the Amplitude Spectrum of this epoch reflects both midline frontal and posterior/inferior foci described by Factor 1. A single Red = P8 Red = P8 Grouped by Factor 1 at Fz Low Med High -1 +1 0 2 -1 +1 0 -1 +1 0 anxiety, and melancholic features. Biol Psychiatry, 2002, 52, 73- 85. Perrin, F., Pernier, J., Bertrand, O. and Echallier, J.F. Spherical splines for scalp potential and current source density mapping. Electroencephalog. clin. Neurophysiol., 1989, 72, 184-187. Pivik R.T., Broughton R.J., Coppola R., Davidson R.J., Fox, N., and Nuwer, M.R.. Guidelines for the recording and quantitative analysis of electroencephalographic activity in research contexts. Psychophysiology, 1993, 30,547-58. Nunez, P.L. Electric Fields of the Brain: The neurophysics of EEG, New York: Oxford, 1981. Tenke,C.E. Statistical characterization of the EEG: the use of the power spectrum as a measure of ergodicity. Electroencephalog. References References Bendat, J.S., and Piersol, A.G. Random Data: Analysis and measurement procedures. Wiley-Interscience, New York, 1971. Goncharova, I.I., McFarland, D.J., Vaughan, T.M., and Wolpaw, J.R. EMG contamination of EEG: spectral and topographic characteristics. Clin. Neurophysiol., 2003, 114, 1580-1593. Kayser, J., Tenke, C.E. Optimizing PCA methodology for ERP component identification and measurement: Theoretical rationale and empirical evaluation. Clin. Neurophysiol., in press. Kayser, J., Tenke, C.E., Debener, S. Principal components analysis (PCA) as a tool for identifying EEG frequency bands: I. Methodological considerations and preliminary findings. Psychophysiology, 2000, 37, S54. Pizzagalli, D.A., Nitschke, J.B., Oakes, T.R., Hendrick, A.M., Electrophysiologic measures may provide useful information about the anatomical origin and physiological significance of an experi- mental finding. However, certain methodological choices severely limit the capacity for such inferences. Notable issues concern the impact of the (1) recording reference recording reference and the (2) quantification method quantification method itself (i.e., defining and measuring a component or frequency band). (1) The reference problem has been addressed by the parallel application of different reference schemes. As an alternative, CSD methods (Laplacian, Hjorth, etc.) can be used as a true reference-free measure with a known correspondence to neuronal current generators. (2) The quantification problem has been addressed by defining multiple, more loosely defined frequency bands tailored to the data. These problems are exacerbated in quantitative EEG studies that apply nonlinear transformations to the data (e.g., logarithmic transformations, power or amplitude spectra, and asymmetry measures derived from them). We now describe a general, reference-free, data-driven method for simplifying and quantifying EEG CSD spectra using frequency PCA. Introduction Introduction http://psychophysiology.cpmc.columbia.edu 7.0 7.0 7.8 7.8 8.6 8.6 9.4 9.4 10.1 10.1 11.0 11.0 0.0 +0.4 Consistency of Factor Topography across Groups and Studies Closed Closed Closed Open Open Open Controls Depressed Controls Depressed Controls Depressed DC (24) CE (27) DD (58) DE (36) DC (24) CE (27) DD (58) DE (36) DC (24) CE (27) DD (58) DE (36) Factor 1 Factor 3 Factor 5 -0.5 0.0 +1.0 -0.5 0.0 +1.0 -0.5 0.0 +1.0 -0.5 0.0 +1.0 -0.5 0.0 +1.0 -0.5 0.0 +1.0 Eyes Eyes Eyes

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I dentification and separation of reference-free spectral EEG components: Combining Current Source Density (CSD) and frequency Principal Components Analysis (fPCA) Craig E. Tenke and Jürgen Kayser Department of Biopsychology, New York State Psychiatric Institute, New York. - PowerPoint PPT Presentation

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Page 1: The combined CSD and fPCA method: Improves topographic specificity over EEG field potentials

The combined CSD and fPCA method:• Improves topographic specificity over EEG field potentials• Yields reference-free spectral measures similar in form to those used in

conventional EEG analyses• Yields orthogonal Spectral FactorsSpectral Factors consistent with the analyzed data as

opposed to simple, predetermined rectangular frequency bands• Automatically removes EMG, EOG and electrical artifacts• Provides replicable Alpha FactorsAlpha Factors with characteristic peaks and

topographies• Allows anatomical interpretations of regional findings that are

impossible with conventional EEG measures

ConclusionsConclusions

• The volume conduction of field potentials from neuronal generators approximates Ohm’s Law for a conductive medium, varying linearly over distance

• Concurrent generators produce additive field potential effects

• Linear EEG properties are preserved in the frequency domain: Fourier transformation is linear and reversible, but complex-valued

Linear Properties of EEGLinear Properties of EEG

• Based on simplifications of Poisson's equation, relating current generators to the negative spatial derivative of the field potential in a conductive medium

• Removes volume-conducted activity• Provides a concise, reference-free simplification of a field

topography• Indicates neuronal depolarization as a current sink

(negativity), repolarization or hyperpolarization as a current source (positivity)

• Estimates are real (magnitude and sign)

Properties of CSD Properties of CSD

IIdentification and separation of reference-free spectral EEG components: Combining Current Source Density (CSD) and frequency Principal Components Analysis (fPCA)dentification and separation of reference-free spectral EEG components: Combining Current Source Density (CSD) and frequency Principal Components Analysis (fPCA) Craig E. Tenke and Jürgen KayserCraig E. Tenke and Jürgen Kayser

Department of Biopsychology, New York State Psychiatric Institute, New York

Impact of Reference on Frequency SpectraImpact of Reference on Frequency Spectra

ReversibleTransformation

Fourier transformation PzPz

Fo

uri

er

Sp

ect

rum

[u

V]

CzPzPz

Amplitude Spectrum

IrreversibleTransformation

CzFzFpz

Ab

so

lute

A

mp

litu

de

[u

V]

Freq [Hz]

Freq [Hz]

Freq [Hz]

Freq [Hz]

[complex numbers]

[Fourier Map at 10 Hz]

Fpz

Fpz

Fpz

Fz

Fz FzCz CzPzPz PzPz

-2

0

+3

-2

0

+3

[Amplitude Map at 10 Hz]

Reference Electrode Fpz Cz

EEG Time series

Sig

na

l A

mp

litu

de

[u

V]

Time [ms]Time [ms]

PzPzCz

Fz

Fpz

Fpz

Fz

CzPzPz

[real numbers]

EEG Time Series: A single cosine wave topography that varies linearly across the midline sites (Fpz, Fz, Cz, Pz), shown for a Fpz and Cz reference. Fourier Transformation: Fourier spectra are linearly and reversibly related to the temporal data. Since the simulated data are simple cosines, the complex spectra consist of real numbers. Color maps show spherical spline interpolations for a 12-channel EEG montage with lateral activity identical to midline sites. Amplitude Spectrum: Amplitude of Fourier Spectra (i.e., amplitude of frequency spectrum via Pythagorean Theorem). The amplitude spectrum is identical to the Fourier spectrum when and only when components are real and positive (FPz reference), but differs markedly when they are not (Cz reference).

Fourier Maps(data w/o asymmetry)

Reference Electrode Fpz Cz Fpz Cz

Field Potential Topographies CSD Topographies

-2

0

+3

-7

0

+7

Fourier Maps(asymmetric data)

Amplitude Maps(asymmetric data)

IrreversiblenonlinearTransformation

Linear midline gradientLateral = midline

Linear midline gradientAsymmetry added to mid-frontal sites: F3 = F3 - .5 µV F4 = F4 + .5 µV

Impact of Reference on Spectral Topographies of Field Potential and CSDImpact of Reference on Spectral Topographies of Field Potential and CSD

-2

0

+3

-7

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+7

Fourier Maps (data w/o asymmetry): While field potentials of Fourier maps shift in amplitude and sign depending on the chosen reference, both produce identical CSD maps (approximately zero due to the linear gradient). Fourier Maps (asymmetric data): When a hemispheric asymmetry is added to mid-frontal sites (left < right), it is evident in the field potential Fourier maps for both reference schemes. The “frontal generators” of the asymmetry are evident from the CSD maps.Amplitude Maps (asymmetric data): Nonlinear transformations commonly used in spectral analysis (power or absolute value) may distort a field topography and even reverse the direction of an asymmetry. In contrast, the equivalent transformation of CSD data preserves all information about the location of current generators without distortion. Only phase information related to concurrent source/sink properties is lost.

Amplitude spectra of CSD from resting EEG:

• Clarify and separate key features of the resting EEG, including:

(1) AlphaAlpha peak that is largest at posteriorposterior sites (eyes closed)(2) Low frequency EOG artifactsLow frequency EOG artifacts, largest near eyes (eyes closed)(3) EMG artifactsEMG artifacts largest near face (e.g., Fp1/2, eyes open)(4) Electrical artifacts at 6060 and 70 Hz70 Hz (at Fz)

Waveform Comparison:

• CSD Alpha peak at inferior sites (P8P8) has a lower peak frequency and includes more theta (4-8 Hz) than the midline (PzPz) alpha peak

• Alpha is also seen at Fz (eyes closed), and is partially separable from a lower frequency peak

Overview of Amplitude Spectra of CSD Overview of Amplitude Spectra of CSD

Amplitude Spectra of CSD from Resting EEG Amplitude Spectra of CSD from Resting EEG

nose

Fp1 Fp2

Fz

Cz

Pz

Oz

F4 F8F3F7

FC5FT9 FC6 FT10

TP10CP6CP5TP9

C3T7 Cz C4 T8

P3P7P9 P4 P8 P10

O1 O2

eyeseyes

0 7.8 15.6 23.4 31.2 39.0 46.8 54.6 62.4 70.2 78.0

3

6

9

12

eyes closedeyes closed: PzPz, P8P8, FzFz eyes open:eyes open: FzFz

FrequencyFrequency [Hz]

Waveform Comparison Waveform Comparison

• Fourier Spectra are complex, with both amplitude (Pythagorean Theorem) and phase (angle from real axis)

• Power Spectra simplify EEG variance, integrating squared amplitudes over frequency (i.e., Mean Squared)

• Power Spectra have empirical and theoretical value independent of the EEG applications (e.g., random process models, systems theory, etc.)

Properties of EEG Power SpectraProperties of EEG Power Spectra

• Factors derived from dataset• PCA uses a linear statistical model to produce orthogonal

components• Factors are useful for identifying and defining temporal

measures

Properties of PCAProperties of PCA

• Power Spectra impede inferences about underlying EEG generators, because information is lost when the data are squared (i.e., linear volume conduction properties not preserved)

• CSD calculation (Laplacian, Hjorth, etc.) is impossible after nonlinear transformation (i.e., the measure is physiologically unintelligible)

• Power estimates are not proportional to the underlying (linear) EEG field potentials

• Logarithmic transformations correct skew of Power Spectrum, but exaggerate systematic, low amplitude noise

Problems with EEG Power SpectraProblems with EEG Power Spectra

Subjects:Subjects: N =143 right-handed adults (n = 63 healthy adults and n = 82 clinically depressed outpatients, pooled across two separate studies)

RecordingsRecordings: Resting 30-channel EEG from four 2-min time periods (order of eyes open/closed counterbalanced as OCCO or COOC across subjects), referenced to nose tip (Grass, 10K gain; 0.1 - 30 Hz band pass; recorded using NeuroScan at 200 samples/s); vertical and horizontal EOG recorded differentially

Signal processing:Signal processing: Data were segmented into 1.28 s epochs (50% overlap), yielding a frequency resolution of 0.78 Hz; artifactual data eliminated from epoched data under visual guidance (semi-automated procedure)

CSD:CSD: CSD waveforms were computed for each accepted epoch using the spherical spline method of Perrin et al. (1989) [lambda = 10-5; 50 iterations; m = 4)

Spectral Analysis:Spectral Analysis: Hanning window (50%) applied to each CSD epoch; mean Power Spectra (PS) computed across epochs for each condition (i.e., eyes open/ closed), and subsequently converted to a RMS Amplitude Spectra (square root of Power Spectra, proportional to the amplitude of an underlying sinusoid)

fPCA:fPCA: Amplitude Spectrum data from 0-77.2 Hz (100 points = 100 variables) submitted to unrestricted covariance-based Principal Components Analysis, using electrodes (31) x Conditions (2) x participants (145) as 8990 cases, followed by unscaled Varimax rotation (Kayser & Tenke, in press)

MethodsMethods

4.5

4.0

3.5

3.0

2.5

2.0

1.5

1.0

0.5

0.0

-.5

0.0 10.0 20.0 30.0 40.0 50.0 60.0 70.0

Frequency [Hz]

Unscaled Varimax Rotated Factor Loadings for fPCA Computed from RMS Amplitude Spectra of temporal CSD

ResultsResults

-.6

+.6

Topographies of first nine fPCA Factor Scores(96.14% variance of Amplitude Spectra)

Low AlphaLow Alpha High AlphaHigh Alpha AlphaAlphaEOG ArtifactEOG ArtifactEMG ArtifactEMG Artifact

High Variance(88.59% total)

Factors 6-9(additional 7.55%)

60 Hz60 Hz Low BetaLow Beta Alpha ResidualAlpha Residual High BetaHigh Beta

• First five factors accounted for almost 90% of the variance of the CSD Amplitude Spectra; AlphaAlpha activity was represented by Factors 1, 3 and 5Factors 1, 3 and 5

• Factors 2 and 4 extracted known physiological physiological artifactsartifacts (EMG, EOG)• Factors 6-9 each accounted for less than 2% of the variance (60.16 Hz: 1.98%; low

beta: 17.97 Hz, 1.94%; 8.59 Hz, 1.92%; high beta: 23.44 Hz)

Overview of fPCA solutionOverview of fPCA solution

• Factor 1Factor 1 is a prominent (26.53% variance) low alpha factor that overlaps theta. It has a posterior/inferior topography, as well as a secondary topography on the frontal midline.

• Factor 3Factor 3 is a prominent (18.11%) high alpha factor with a medial parietal topography.

• Factor 5Factor 5 also has a medial parietal topography, is intermediate in frequency, and less prominent than the others (7.43%).

• These three alpha factors showed a condition dependencecondition dependence and consistent consistent topographies across four groupstopographies across four groups of participants [i.e., two independent samples of healthy adults (DC,CE) and depressed patients (DD,DE)].

Alpha Factor TopographiesAlpha Factor Topographies

Grouped by Factor 1 at Fz: Low Alpha (Factor 1) had a secondary Fz maximum. The secondary frontal topography was seen for individuals in both two replications using two groups. A consistent topography was also observed for subjects with high, medium or low Factor 1 scores at Fz.

Single Epoch for Representative High Fz Subject: Posterior and frontal midline Alpha topographies of Factor reflect linked, inverted current generators. The sharpness of the frontal midline topography suggests local field closure, as would be produced by an opposed pair of simultaneous regional dipoles.

Inferior and Frontal Generators? CETInferior and Frontal Generators? CET

Amplitude Spectrum of CSD Epoch [Hz]

Black = FzBlack = Fz

12001000800600400200 0

6.26.2

Single Epoch for Representative High Fz Subject

Lowpass filtered (15 Hz) CSD waveforms at FzFz (black line) and P8P8 (red) from a representative epoch in a subject with high factor scores for Factor 1. Waveform peaks at FzFz and P8P8 show current sources (warm colors) alternating with sinks (cold colors) between the two sites. The topography of the Amplitude Spectrum of this epoch reflects both midline frontal and posterior/inferior foci described by Factor 1. A single generator (or pair) is unlikely, since CSDs of dipolar ERP generators are less focal at a distance (e.g., N1).

Red = P8Red = P8

Grouped by Factor 1 at Fz

Low

Med

High

-1

+1

0

2

-1

+1

0

-1

+1

0

anxiety, and melancholic features. Biol Psychiatry, 2002, 52, 73-85. Perrin, F., Pernier, J., Bertrand, O. and Echallier, J.F. Spherical splines for scalp potential and current source density mapping. Electroencephalog. clin. Neurophysiol., 1989, 72, 184-187. Pivik R.T., Broughton R.J., Coppola R., Davidson R.J., Fox, N., and Nuwer, M.R.. Guidelines for the recording and quantitative analysis of electroencephalographic activity in research contexts. Psychophysiology, 1993, 30,547-58.Nunez, P.L. Electric Fields of the Brain: The neurophysics of EEG, New York: Oxford, 1981. Tenke,C.E. Statistical characterization of the EEG: the use of the power spectrum as a measure of ergodicity. Electroencephalog. Clin. Neurophysiol., 1986, 63, 488-493. Tenke,C.E., Schroeder, C.E., Arezzo, J.C. and Vaughan, H.G., Jr. Interpretation of high- resolution current source density profiles: a simulation of sublaminar contributions to the visual evoked potential. Exp. Brain Res., 1993, 94,183-192.

ReferencesReferences Bendat, J.S., and Piersol, A.G. Random Data: Analysis and measurement procedures. Wiley-Interscience, New York, 1971. Goncharova, I.I., McFarland, D.J., Vaughan, T.M., and Wolpaw, J.R. EMG contamination of EEG: spectral and topographic characteristics. Clin. Neurophysiol., 2003, 114, 1580-1593. Kayser, J., Tenke, C.E. Optimizing PCA methodology for ERP component identification and measurement: Theoretical rationale and empirical evaluation. Clin. Neurophysiol., in press. Kayser, J., Tenke, C.E., Debener, S. Principal components analysis (PCA) as a tool for identifying EEG frequency bands: I. Methodological considerations and preliminary findings. Psychophysiology, 2000, 37, S54. Pizzagalli, D.A., Nitschke, J.B., Oakes, T.R., Hendrick, A.M., Horras, K.A., Larson, C.L., Abercrombie, H.C., Schaefer, S.M., Koger, J.V., Benca, R.M., Pascual-Marqui, R.D., and Davidson, R.J. Brain electrical tomography in depression: the importance of symptom severity,

Electrophysiologic measures may provide useful information about the anatomical origin and physiological significance of an experi-mental finding. However, certain methodological choices severely limit the capacity for such inferences. Notable issues concern the impact of the (1) recording referencerecording reference and the (2) quantification quantification methodmethod itself (i.e., defining and measuring a component or frequency band).(1) The reference problem has been addressed by the parallel

application of different reference schemes. As an alternative, CSD methods (Laplacian, Hjorth, etc.) can be used as a true reference-free measure with a known correspondence to neuronal current generators.(2) The quantification problem has been addressed by defining

multiple, more loosely defined frequency bands tailored to the data.These problems are exacerbated in quantitative EEG studies that

apply nonlinear transformations to the data (e.g., logarithmic transformations, power or amplitude spectra, and asymmetry measures derived from them). We now describe a general, reference-free, data-driven method for simplifying and quantifying EEG CSD spectra using frequency PCA.

IntroductionIntroduction

http://psychophysiology.cpmc.columbia.edu

7.07.0 7.87.8 8.68.6 9.49.4 10.110.1 11.011.0

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+0.4

Consistency of Factor Topography across Groups and Studies

Closed

Closed

Closed

Open

Open

Open

Controls Depressed

Controls Depressed

Controls Depressed

DC (24) CE (27) DD (58) DE (36)

DC (24) CE (27) DD (58) DE (36)

DC (24) CE (27) DD (58) DE (36)

Factor 1

Factor 3

Factor 5

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