Research on EEG Neurofeedback for Anxiety
Society for Neuronal Regulation
9th Annual Conference
Monterey, CA 27-30 October 2001
Anterior Alpha Asymmetry in Anxiety and Depression
Robert Lawson and Eugenia Bodenhamer-Davis
University of North Texas, Denton, TX
Many studies have found that people with depression have less activity
in the left frontal region than healthy normals. An EEG correlate of this
relative reduced activity is left side alpha asymmetry. It is not known,
however, if there are frontal alpha asymmetry variations between individuals
with depression only compared to persons with anxious depression.
This
exploratory study compared QEEG records of frontal alpha of a group of
seven depressed persons with those of a group of nine anxious depressed.
Based on clinical observations, it was hypothesized that the depressed
group would have more left side alpha asymmetry than the anxious depressed
group.
Membership in the depressed group was defined as having an MMPI2 Scale
2 Depression score => 60 and a Scale 7 Psychasthenia score =< 60.
The anxious depressed group membership consisted of individuals whose
MMPI2 Depression scores were => 60 and Psychasthenia scores >60.
Asymmetry was calculated with the following equation: (F3-F4)/(F3+F4)
(magnitude, not power, voltage was used). EEG data were recorded on a
Lexicor NRS 24 with a linked ear reference and remontaged to a Cz reference.
Results of comparing the QEEG records of the two groups of individuals
revealed that 85% of the depressed only group and 55% of the anxious depressed
group had left side asymmetry. The depressed only mean asymmetry = -.043;
the anxious depressed mean asymmetry = -.0052. The depressed only group
had significantly more left side asymmetry (p=. 023). A surprising finding
was that the anxious depressed group had higher alpha on both sides than
did the depressed only group (p=. 029). The mean frontal alpha, (F3 alpha
+ F4 alpha)/2, of the depressed only group was 11.8, and 18.0 for the
anxious depressed group.
This increased alpha suggests that, relative
to the depressed only group, persons who are anxious depressed have reduced
frontal activation in both hemispheres.
Roshi Compared with the Rosenfeld Depression Protocol: A Case
Report
D. Corydon Hammond, Ph.D., University of Utah, School of Medicine
The Rosenfeld depression protocol for modifying frontal alpha asymmetry
is soundly based theoretically on substantial research that finds an alpha
asymmetry in depression. Preliminary results on its use are quite encouraging.
There are, however, other ways of correcting such a frontal alpha asymmetry
and treating depression through neurofeedback. A case report will detail
the treatment with neurofeedback of a severely depressed man. His alpha
asymmetry was congruent with experimental evidence as measured with the
Rosenfeld protocol.
In his initial three sessions following informed consent
and using the Rosenfeld protocol, he was, however, unable to demonstrate
any improvements during the course of the session. In fact, the asymmetry
increased in two of the three sessions. Subsequently, we switched treatment
and began using the Roshi, a neurofeedback system utilizing photic stimulation
which can be set so that the frequency of photic stimulation varies depending
on the patient's existing dominant brainwave.
Electrodes continued to
be placed at F3 and F4, and we were reinforcing 15-18 Hz with the patient
simultaneously seeking to inhibit alpha and theta frequencies. For the
initial 8-10 minutes of a session, we used "complex-adaptive" light stimulation. This consisted of feeding back to the left eye (through
varying the frequencies of photic stimulation) information from the F3
(left) electrode site, and vice versa.
The theory is that each eye sees
separate EEG information which causes the brain to seek to correct for
the apparent error, increasing brain flexibility. It is usually found
that the result is a flattening of the spectrum. Following this brief
stimulation, the photic stimulation was set to vary so as to pulse on
the peak frequency within the 15-18 Hz range, while the patient continued
to seek to inhibit slow frequencies and to enhance this beta activity.
Results were rapid and fairly dramatic. After 5 sessions the patient was
reporting that he didn't really feel depressed any longer. He received
subsequent reinforcing sessions, periodically having him simultaneously
hooked to a Lexicor unit, measuring alpha asymmetry using the Rosenfeld
protocol, without receiving any feedback linked to the Rosenfeld protocol.
These periodic EEG follow-up evaluations revealed positive physiologic
changes in baseline and training measures of alpha asymmetry references
to Cz. Psychometric evaluation with 5 measures likewise confirmed the
effectiveness of treatment. It thus appears that other neurofeedback protocols
are capable to effectively treating depression.
QEEG Relationships With the MMPI-2 Depression Scale and Subscales
Roger deBeus, M.S. University of North Texas, Neurotherapy Lab
Introduction: Depression is a heterogeneous disorder.
One demonstration of this is the different classes of antidepressants
used to treat it, many with different modes of action. However, most published
literature examining QEEG and depression have used measurements with only
a single composite score (e.g., the Beck Depression Inventory, Hamilton
Depression Rating Scale), and combined genders.
One benefit of utilizing
the MMPI-2 is that it considers several factors contributing to depression
symptomology. For example, the Harris and Lingoes (1955) subscales include
Subjective Depression (D1), Psychomotor Retardation (D2), Physical Malfunctioning
(D3), Mental Dullness (D4), and Brooding (D5). Examining these scales
in relationship to QEEG measures will help generate a better understanding
of this multifaceted disorder.
The hypothesis for this study was that
males and females would have different QEEG profiles in relation to their
depression scores.
Methods: Participants were part of the patient pool
who presented to the UNT Neurotherapy Lab for treatment between 1996 and
1999. As part of the intake procedure, each client participated in a QEEG
and completed an MMPI-2. QEEG was collected on the Cadwell Spectrum 32
digital EEG machine. One of the QEEG conditions collected was eyes-closed,
which was then analyzed through the NYU database.
Resulting QEEG parameters
included absolute power, relative power, asymmetry, and coherence referenced
to the ears. Bandwidths examined were Delta (1.5-3.5 Hz), Theta (3.5-7.5
Hz), Alpha (7.5-12.5 Hz), and Beta (12.5-25.0 Hz). The MMPI-2 scales considered
for this study included clinical scale Depression, content scale Depression,
D1 (Subjective Depression), D2 (Psychomotor Retardation), D3 (Physical
Malfunctioning), D4 (Mental Dullness), and D5 (Brooding).
Twenty males
and 20 females were analyzed separately by gender. Nonparametric correlations
were performed between QEEG parameters and MMPI-2 depression scales.
Findings: The analyses identified distinctive patterns
for each QEEG parameter and depression scale for both genders. Overall,
the females showed almost four times more significant correlations than
the males. For QEEG parameters, the significant findings for females showed
more correlations in relative power in the Theta and Alpha bands, and
coherence in the Alpha and Delta bands.
Results with the males showed
more significant associations with asymmetry involving the Delta, Theta,
and Alpha bands. For the depression scales, the females showed the most
significant correlations with D4, D5, D1, Depression, and content Depression
in descending order. The males showed the most significant correlations
with subscales D1, D5, and D3.
More specifically, QEEG correlates with the clinical Depression scale
for the female group showed absolute power in frontal Alpha, relative
power in frontal Theta and Alpha, and frontal, temporal, and occipital
Beta, asymmetry in occipital Beta, coherence in temporal and parietal-occipital
Delta, temporal Theta, frontal and frontal-occipital Alpha, and central-parietal
Beta. The males showed asymmetry in frontal Theta and temporal Alpha.
Correlations with the content Depression scale for the females showed
relative Theta over most of the head; asymmetry in temporal Delta, temporal
Alpha, and frontal, central, and temporal Beta; coherence in frontal-temporal
Delta, and parietal-occipital and frontal-occipital Alpha. The male group
showed relative power in frontal Alpha, and asymmetry in parietal Delta
and frontal Theta.
QEEG correlates with the Subjective Depression (D1) subscale for the
females showed absolute power in parietal and occipital Theta; relative
Theta over most of the head; asymmetry in temporal Alpha and frontal Beta;
coherence with temporal and frontal-occipital Delta, frontal-occipital
Alpha, and central-parietal Beta. The male group showed correlations with
absolute power in parietal and temporal Beta, relative frontal Beta, and
asymmetry in frontal Delta, Theta, and Alpha.
Correlations with the Psychomotor Retardation (D2) subscale for the female
group showed coherence in frontal Delta and frontal-occipital Alpha. The
males showed absolute parietal Delta, asymmetry in temporal Alpha and
frontal Beta, and coherence in central Beta.
The Physical Malfunctioning (D3) subscale for the females was associated
with relative temporal and occipital Beta; and coherence in frontal, temporal,
and parietal-occipital Delta, and frontal-occipital Alpha. The male group
showed relative frontal Alpha and Beta, asymmetry in frontal Delta, and
coherence in frontal Alpha and Beta.
The Mental Dullness (D4) aspect of depression for the females was correlated
with absolute frontal and central Alpha; relative Theta and Alpha over
the entire head; asymmetry in frontal Beta; coherence in frontal-temporal
Delta, and frontal and frontal-occipital Alpha. The male group showed
associations with absolute parietal Delta, and relative frontal Alpha.
The Brooding (D5) component of depression for the female group was related
with absolute occipital Theta; relative Theta over most of the head; asymmetry
in temporal Delta, frontal, temporal, and occipital Alpha, and frontal
and central Beta; coherence in frontal-temporal and frontal-occipital
Delta, temporal Theta, frontal-occipital and temporal Alpha, and central-parietal
and temporal Beta. The male group showed absolute parietal and temporal
Beta, and asymmetry in central, parietal, and temporal Delta, and frontal
Theta and Alpha.
Discussion: The results showed (1) unique relationships
between QEEG parameters and the depression scales of the MMPI-2, and (2)
male and female differences. Each cluster of depression questions elicited
a different QEEG profile. Examining subscales or items can aid in the
interpretation of diverse depression symptomology and QEEG correlates.
Furthermore, this suggests that treatment options are also heterogeneous
and that careful assessment should be done to determine which factors
contribute most to a client's depression.
Therefore, appropriate electrode
sites and modalities can be selected for EEG biofeedback treatment. Another
finding was that the males and females had different QEEG profiles for
each depression scale although the MMPI-2 profiles were relatively homogeneous
for both groups. One interpretation may be that male and female brains
experience depression in a different way.
The presence of four times more
correlations of the female group compared with males corresponds to the
gender effect of two to three times more depression for women found in
the general population. Although these findings are preliminary, they
support the heterogeneity and complexity of depression.
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