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Dive into the research topics where Christina M. Gullion is active.

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Featured researches published by Christina M. Gullion.


Psychological Medicine | 1996

The Inventory of Depressive Symptomatology (IDS) : psychometric properties

Rush Aj; Christina M. Gullion; M. R. Basco; Robin B. Jarrett; Madhukar H. Trivedi

The psychometric properties of the 28- and 30-item versions of the Inventory of Depressive Symptomatology, Clinician-Rated (IDS-C) and Self-Report (IDS-SR) are reported in a total of 434 (28-item) and 337 (30-item) adult out-patients with current major depressive disorder and 118 adult euthymic subjects (15 remitted depressed and 103 normal controls). Cronbachs alpha ranged from 0.92 to 0.94 for the total sample and from 0.76 to 0.82 for those with current depression. Item total correlations, as well as several tests of concurrent and discriminant validity are reported. Factor analysis revealed three dimensions (cognitive/mood, anxiety/arousal and vegetative) for each scale. Analysis of sensitivity to change in symptom severity in an open-label trial of fluoxetine (N = 58) showed that the IDS-C and IDS-SR were highly related to the 17-item Hamilton Rating Scale for Depression. Given the more complete item coverage, satisfactory psychometric properties, and high correlations with the above standard ratings, the 30-item IDS-C and IDS-SR can be used to evaluate depressive symptom severity. The availability of similar item content for clinician-rated and self-reported versions allows more direct evaluations of these two perspectives.


Journal of the American Academy of Child and Adolescent Psychiatry | 1997

Recurrence of Major Depressive Disorder in Hospitalized Children and Adolescents

Graham J. Emslie; A. John Rush; Warren A. Weinberg; Christina M. Gullion; Jeanne Rintelmann; Carroll W. Hughes

OBJECTIVE To evaluate the outcome of a sample of children and adolescents hospitalized with major depressive disorder (MDD) and to assess different duration and severity criteria to define recovery and recurrence. METHOD Fifty-nine of 70 children and adolescents were reevaluated 1 to 5 years later, and the intervening course of depression and other disorders was assessed using the Kiddie-Longitudinal interval Follow-up Evaluation (K-LIFE). RESULTS Ninety-eight percent of subjects had recovered from their index MDD episode within 1 year of their initial evaluation, but 61% had at least one recurrence during the follow-up period. Of those with recurrences, 47.2% had a recurrence within 1 year and 69.4% by 2 years from the offset of the index episode. Changing the criteria for recovery by increasing the length of time required to define recovery resulted in decreases in the number of episodes of recurrence reported. CONCLUSION MDD in children and adolescents is often an episodic disorder. Difference in definitions of recovery and recurrence affect the data reported. Consistent definitions of remission, recovery, relapse, and recurrence are needed. These data suggest that recovery may be defined after two consecutive months without symptoms and that episodes of MDD may be briefer, but more frequent, in children and adolescents than in adults.


Biological Psychiatry | 1992

Low plasma γ-aminobutyric acid levels in male patients with depression ☆

Frederick Petty; Gerald L. Kramer; Christina M. Gullion; A. John Rush

Abstract Plasma levels of γ-aminobutyric acid (GABA) were significantly lower in males with primary unipolar major depressive disorder than in healthy controls. Although the difference in means between control and symptomatic depressed patient groups was small, the distribution of plasma GABA in the depressed patients was markedly different from controls. Forty percent of depressed patients had plasma GABA levels below those of controls. Plasma GABA levels correlated positively with duration of illness, and negatively with age at onset of the mood disorder and the total Endogenomorphic Symptom Score on the Hamilton Rating Scale. Plasma GABA levels may be a biochemical marker of vulnerability to depression, as opposed to a consequence of the illness. A low GABA condition in depression fits and complements the prevailing biogenic amine hypotheses of depression.


Biological Psychiatry | 1998

Toward a generalizable model of symptoms in major depressive disorder

Christina M. Gullion; A. John Rush

BACKGROUND This study has two goals: 1) to establish a generalizable model of the symptoms observed in outpatients with major depressive disorder (MDD); and 2) to compare symptom coverage of the Inventory of Depressive Symptomatology, Clinician-Rated (IDS-C) and Self-Report (IDS-SR) to that of the Hamilton Depression Rating Scale (HDRS) and Beck Depression Inventory (BDI). METHODS A factor analysis of IDS-C, IDS-SR, HDRS, and BDI items was carried out on 324 adult outpatients with MDD. Patients with coexisting Axis I or III illness or those taking psychotropic medication were excluded. RESULTS Ten primary factors were identified, six of which were substantially intercorrelated, defining a second-order factor of general depression severity. Schmid-Leiman orthogonalization identified the symptoms most associated with general severity. CONCLUSIONS The IDS provided more complete factors coverage than did the HDRS or BDI and thus may be more useful in research on symptom profiles.


Psychiatry Research-neuroimaging | 1993

Tridimensional Personality Questionnaire and serotonin in bulimia nervosa

David A. Waller; Christina M. Gullion; Frederick Petty; Bettie W. Hardy; Mary V. Murdock; A. John Rush

To determine the relationship between Tridimensional Personality Questionnaire (TPQ) scales and bulimia nervosa, TPQ scores of 27 bulimic women, age range 21-59, were compared with values for an age-matched sample of 128 normal control women drawn from the national norming sample by Przybeck. Scores for Novelty Seeking and Harm Avoidance were significantly higher, while scores for Reward Dependence were significantly lower for the bulimic women. A stepwise regression model of severity of purging on TPQ selected Novelty Seeking and a composite depression score, with Novelty Seeking being the stronger of the two predictors. Whole blood serotonin levels did not relate to TPQ scores or to purging frequency.


Neuropsychopharmacology | 1999

Effects of Fluoxetine on the Polysomnogram in Outpatients with Major Depression

Madhukar H. Trivedi; A. John Rush; Roseanne Armitage; Christina M. Gullion; Bruce D. Grannemann; Paul J. Orsulak; Howard P. Roffwarg

This study investigated the effects of open-label fluoxetine (20 mg/d) on the polysomnogram (PSG) in depressed outpatients (n = 58) who were treated for 5 weeks, after which dose escalation was available (≤40 mg/d), based on clinical judgment. Thirty-six patients completed all 10 weeks of acute phase treatment and responded (HRS-D≤ 10). PSG assessments were conducted and subjective sleep evaluations were gathered at baseline and at weeks 1, 5, and 10. Of the 36 subjects who completed the acute phase, 17 were reevaluated after 30 weeks on continuation phase treatment and 13 after approximately 7 weeks (range 6–8 weeks) following medication discontinuation. Acute phase treatment in responders was associated with significant increases in REM latency, Stage 1 sleep, and REM density, as well as significant decreases in sleep efficiency, total REM sleep, and Stage 2 sleep. Conversely, subjective measures of sleep indicated a steady improvement during acute phase treatment. After fluoxetine was discontinued, total REM sleep and sleep efficiency were found to be increased as compared to baseline.


Psychiatry Research-neuroimaging | 1993

Regional cerebral blood flow alterations in unipolar depression

Michael D. Devous; Christina M. Gullion; Bruce D. Grannemann; Madhukar H. Trivedi; A. John Rush

Forty-seven symptomatic inpatients and outpatients with major depression (13 nonendogenous, 23 endogenous, and 11 psychotic by Research Diagnostic Criteria) were compared with 138 normal control subjects. Absolute regional cerebral blood flow (rCBF, ml/minute/100 g) was measured with 133Xe single photon emission computed tomography. Flow ratios (region of interest/global flow) and residual scores (the difference between patient flow ratios and expected normal flow ratios, as derived from the control population) were also computed. Results revealed significant age x region x depression subtype interactions for absolute, ratio, and residual flow data. Consequently, a test of group means (or analysis of covariance) could not be used to examine between-group differences. Multiple regression analyses were employed to study the effects of age on rCBF. This analysis revealed that different, though sometimes overlapping, regions exhibited different age effects on rCBF in different depressive subtypes. Thus, diagnostic-subtype-dependent age effects on rCBF precluded comparisons of mean values within or across regions for subject groups, but distinguished between symptomatic depressed patients and control subjects and among patient groups. Possible causes of such effects include variations in duration of illness or medication history or sensitization phenomena.


Biological Psychiatry | 1989

Sleep EEG in bulimic, depressed, and normal subjects

David A. Waller; Bettie W. Hardy; Rekha Pole; Donna E. Giles; Christina M. Gullion; A. John Rush; Howard P. Roffwarg

Attempts to achieve a more fundamental understanding of the eating disorder bulimia have focused on its relationship to depression (Swift et al. 1986; Hudson and Pope 1987). One way to investigate a possible relationship between eating disorders and depression is by means of sleep studies (Katz et al. 1984). In this article, we report rapid eye movement (REM) latency findings in subjects with normal weight bulimia who did not have a concurrent major depression. These data and other sleep electroencephalogram (EEG) measures are compared to the REM latencies and other sleep variables of normal subjects and of endogenous depressed subjects of comparable age. Our purpose was to determine whether sleep variables for bulimics resembled those in biological depressive disease or normal sleep EEG findings and to compare certain depression parameters between bulimic subjects with reduced REM latency (<65 min) and bulimics with normal REM latency. Subjects


Biological Psychiatry | 1996

Effects of four normalizing methods on data analytic results in functional brain imaging

Christina M. Gullion; Michael D. Devous; A. John Rush

Functional brain imaging data may contain large individual differences in information about whole brain and regional levels of activity, and it is common to remove these differences using arithmetic transformation (normalization) prior to statistical analysis. As no single transformation is widely accepted, we examine the effects of four normalizing methods (ratioing, residuals from regressions on global cerebral blood flow, Z scores, and subject residual profiles) on 1) profile shape, 2) correlations between regions, 3) correlations between subjects, and 4) analysis of variance results. These effects are evaluated using an empirical data set consisting of regional cerebral blood flow values from 22 regions of interest in 46 depressed adults and 48 age-matched normal controls obtained by 133Xe single photon emission computed tomography. Results show that normalization method has substantial but different effects on characteristics of the data and statistical results. The rationing method appears to be an optimal choice for most analyses.


Journal of Affective Disorders | 1996

The effects of extended evaluation on depressive symptoms in children and adolescents

Jeanne Rintelmann; Graham J. Emslie; A. John Rush; Thomas Varghese; Christina M. Gullion; Robert A. Kowatch; Carroll W. Hughes

A sample of 137 child and adolescent outpatients with major depressive disorder were examined to identify baseline clinical characteristics that predicted symptom severity at the end of a 3-week evaluation period and to determine whether change in symptom severity between week 1 and week 2 predicted symptom severity at week three. Subjects underwent three consecutive weekly evaluations prior to being considered for entry into a double-blind, placebo-controlled treatment trial of fluoxetine. Results indicated that the combination of age, social functioning, family history, Childrens Depressive Rating Scale-Revised (CDRS-R) (Poznanski et al. (1985) Psychopharmacol. Bull. 21, 979-989) total score at visit one, and percent change in symptom severity between visit one and visit two were predictors of symptom severity at visit three. These findings suggest that (1) subjects should not be excluded from randomized controlled clinical treatment trials based solely on improvement of symptom severity between visits and (2) an extended evaluation period is warranted, especially for adolescents whose symptom severity tends to fluctuate from week to week.

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A. John Rush

University of Texas Southwestern Medical Center

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Howard P. Roffwarg

University of Mississippi Medical Center

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Madhukar H. Trivedi

University of Texas Southwestern Medical Center

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Robin B. Jarrett

University of Texas Southwestern Medical Center

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Bettie W. Hardy

University of Texas Southwestern Medical Center

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Bruce D. Grannemann

University of Texas Southwestern Medical Center

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David A. Waller

University of Texas Southwestern Medical Center

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Paul J. Orsulak

University of Texas Southwestern Medical Center

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Rush Aj

University of Texas Southwestern Medical Center

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