Lifetime eating disorder comorbidity associated with delayed depressive recovery in bipolar disorder
Balzafiore et al. Int J Bipolar Disord (2017) 5:25
DOI 10.1186/s40345-017-0094-4
Open Access
RESEARCH
Lifetime eating disorder comorbidity
associated with delayed depressive recovery
in bipolar disorder
Danielle R. Balzafiore1,2, Natalie L. Rasgon1, Laura D. Yuen1, Saloni Shah1, Hyun Kim3, Kathryn C. Goffin1,
Shefali Miller1, Po W. Wang1 and Terence A. Ketter1*
Abstract
Background: Although eating disorders (EDs) are common in bipolar disorder (BD), little is known regarding their
longitudinal consequences. We assessed prevalence, clinical correlates, and longitudinal depressive severity in BD
patients with vs. without EDs.
Methods: Outpatients referred to Stanford University BD Clinic during 2000–2011 were assessed with the Systematic
Treatment Enhancement Program for BD (STEP-BD) affective disorders evaluation, and while receiving naturalistic
treatment for up to 2 years, were monitored with the STEP-BD clinical monitoring form. Patients with vs. without
lifetime EDs were compared with respect to prevalence, demographic and unfavorable illness characteristics/current
mood symptoms and psychotropic use, and longitudinal depressive severity.
Results: Among 503 BD outpatients, 76 (15.1%) had lifetime EDs, which were associated with female gender, and
higher rates of lifetime comorbid anxiety, alcohol/substance use, and personality disorders, childhood BD onset, episode accumulation (≥10 prior mood episodes), prior suicide attempt, current syndromal/subsyndromal depression,
sadness, anxiety, and antidepressant use, and earlier BD onset age, and greater current overall BD severity. Among currently depressed patients, 29 with compared to 124 without lifetime EDs had significantly delayed depressive recovery. In contrast, among currently recovered (euthymic ≥8 weeks) patients, 10 with compared to 95 without lifetime
EDs had only non-significantly hastened depressive recurrence.
Limitations: Primarily Caucasian, insured, suburban, American specialty clinic-referred sample limits generalizability. Small number of recovered patients with EDs limited statistical power to detect relationships between EDs and
depressive recurrence.
Conclusions: Further studies are warranted to explore the degree to which EDs impact longitudinal depressive illness burden in BD.
Keywords: Bipolar disorders, Eating disorders, Comorbidity, Characteristics, Recovery, Recurrence
Background
High rates of co-occurrence of bipolar disorder (BD)
and eating disorders (EDs) are well documented (Jen
et al. 2013; McElroy et al. 2011, 2013, 2016; Wildes et al.
*Correspondence:
1
Department of Psychiatry and Behavioral Sciences, Stanford University
School of Medicine, 401 Quarry Road, Room 2124, Stanford, CA
94305‑5723, USA
Full list of author information is available at the end of the article
2008). EDs are more prevalent among females compared
to males with BD (Jen et al. 2013; McElroy et al. 2011,
2016; Seixas et al. 2012) and have been associated with
more challenging bipolar course, including earlier onset
age (Brietzke et al. 2011; Jen et al. 2013; Lunde et al.
2009; McElroy et al. 2011, 2016), more depressive and
mood episodes (Brietzke et al. 2011; Lunde et al. 2009;
McElroy et al. 2011), rapid cycling (Fornaro et al. 2010;
McElroy et al. 2011, 2016), depressive symptoms (Jen
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Balzafiore et al. Int J Bipolar Disord (2017) 5:25
et al. 2013; Seixas et al. 2012; Wildes et al. 2007, 2008),
suicide attempts (Brietzke et al. 2011; McElroy et al. 2011,
2013, 2016), weight disturbance (McElroy et al. 2011,
2013, 2016; Wildes et al. 2007, 2008), and psychiatric
comorbidities (Seixas et al. 2012), including lifetime
anxiety (Brietzke et al. 2011; Jen et al. 2013; McElroy
et al. 2013, 2016) and alcohol/substance use disorders
(Brietzke et al. 2011; Fornaro et al. 2010; Jen et al. 2013;
McElroy et al. 2013).
Although EDs, considered cross-sectionally, have been
associated with higher rates of multiple unfavorable BD
illness characteristics, the longitudinal consequences of
comorbid EDs in BD remain to be definitively established.
In the Systematic Treatment Enhancement Program for
BD (STEP-BD), one of the largest prospective naturalistic
studies to examine longitudinal outcome in BD patients,
lifetime comorbid EDs appeared to increase the risk for
depressive recurrence (Perlis et al. 2006). Similarly, in
unipolar depression comorbid EDs appeared to increase
risks of depressive recurrence and poor antidepressant
response (Jang et al. 2013; Mischoulon et al. 2011). In
contrast, data are lacking regarding whether or not a
lifetime history of ED affects time to recovery from
mood episodes. Clearly, additional research is needed to
ascertain the influence of lifetime comorbid EDs on BD
illness longitudinal outcome. Enhanced understanding of
how BD course is influenced by lifetime comorbid EDs
is imperative to permit early identification of patients
at risk for poor outcomes and could lead to improved
treatment for patients with comorbid EDs.
Therefore, among BD outpatients, we assessed the
prevalence of lifetime EDs and relationships between
lifetime EDs and demographics, baseline illness
characteristics/current mood states/current mood
symptoms/current psychotropic use, and longitudinal
depressive outcomes.
Methods
We included outpatients with bipolar I disorder or
bipolar II disorder referred by community practitioners
(primarily psychiatrists) to the Stanford University
Bipolar Disorder Clinic between 2000 and 2011.
Patients were assessed with the Systematic Treatment
Enhancement Program for Bipolar Disorder (STEP-BD)
affective disorders evaluation (ADE) (Sachs et al. 2003),
which included the structured clinical interview for the
diagnostic and statistical manual of mental disorders,
4th edition (SCID-IV) (First et al. 1996) mood disorders
module, as well as the anxiety/eating disorder subtype
screening questions from the mini international
neuropsychiatric interview (MINI) (Sheehan et al. 1998),
and clinical global impression for bipolar disorderoverall severity (CGI-BP-OS) score (Spearing et al. 1997).
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Bipolar and comorbid (including anxiety/eating disorder
subtype) Axis I psychiatric disorder diagnoses were
determined by clinician consensus of results of the ADE
and MINI (which was administered by trained research
staff and assessed EDs and subtypes) as well as available
medical records. Axis II psychiatric disorder diagnoses
were determined by unstructured clinician DSM-IV
assessment as well as assessing available medical records.
Due to limited numbers, patients with lifetime EDs (...truncated)