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Interpersonal and Social Rhythm Therapy: Managing the Chaos of Bipolar Disorder Ellen Frank, Holly A. Swartz, and David J. Kupfer Interpersonal and social rhythm therapy is an individual patients with bipolar disorder recover fully from mania or psychotherapy designed specifically for the treatment for depression, remain asymptomatic between episodes, and bipolar disorder. Interpersonal and social rhythm therapy experience no decline in functional status over time. grew from a chronobiological model of bipolar disorder Psychotherapy for bipolar disorder was considered super- postulating that individuals with bipolar disorder have a fluous and was largely neglected as a treatment strategy genetic predisposition to circadian rhythm and sleep– for many years (Benson 1975). Beginning in the 1980s, wakecycle abnormalities that may be responsible, in part, however, reports appeared in the literature suggesting that for the symptomatic manifestations of the illness. In our outcomeswithlithium alone were suboptimal. Cumulative model, life events (both negative and positive) may cause data suggest that pharmacotherapy alone fails to prevent disruptions in patients’ social rhythms that, in turn, recurrence in 50 to 70% of patients over a 2- to 3-year perturb circadian rhythms and sleep–wake cycles and lead to the development of bipolar symptoms. Administered in period (Markar and Mander 1989; Prien et al 1984) and concert with medications, interpersonal and social rhythm that overall functioning of bipolar patients remains low therapy combines the basic principles of interpersonal even after the resolution of fully syndromal episodes psychotherapy with behavioral techniques to help patients (Coryell et al 1993; Goldberg et al 1995). Researchers and regularize their daily routines, diminish interpersonal clinicians became increasingly cognizant that the chronic problems, and adhere to medication regimens. It modu- course of bipolar disorder may, in the absence of appro- lates both biological and psychosocial factors to mitigate priate interventions, lead to unremitting symptoms and a patients’ circadian and sleep–wake cycle vulnerabilities, downward psychosocial spiral. improve overall functioning, and better manage the po- tential chaos of bipolar disorder symptomatology. Biol A Disorderly Disorder Psychiatry 2000;48:593–604 © 2000 Society of Biologi- As depicted in Figure 1, the course of recurrent unipolar cal Psychiatry disorder, although often debilitating, is unidirectional and Key Words: Psychotherapy, bipolar disorder, mood dis- relatively easy to describe: patients become depressed, orders, circadian rhythms, life events, interpersonal recover, have a period of remission, and then may or may psychotherapy not become depressed again at some point in the future (Kupfer 1991). Although a small percentage of the popu- lation experiences refractory depression, most patients, in Introduction the absence of significant comorbidity, eventually respond uring the second half of the 20th century, new to treatment and achieve a euthymic state. By contrast, the Dtreatments for bipolar disorder focused primarily on course of bipolar disorder is typically hectic and variable. somatic therapies. The discovery of lithium carbonate as a A“roller coaster” for both patients and clinicians, extreme treatment for “psychotic excitement” by Cade in 1949 highs and lows intermingle with mixed states and subsyn- (Cade 1949) and advances in research supporting the dromal symptom flurries to create hybrid symptom states heritability of bipolar disorder led investigators to concep- that defy easy labels. As depicted in Figure 2, hypomania tualize bipolar disorder as a purely biological process can surge into a fully syndromal mania and then plummet amenable to pharmacotherapy alone. Furthermore, clinical into a debilitating major depression. A fall from mania can lore mistakenly led practitioners to believe that most lead to endless months of major depression, with brief excursions into minor depression providing only relative relief from unrelenting dysphoria, anergia, and hypersom- From the Department of Psychiatry, University of Pittsburgh, Western Psychiatric nia. Treatments for those intolerable depressions may send Institute and Clinic, Pittsburgh, Pennsylvania. a patient’s mood back into the manic range, only to plunge Address reprint request to Ellen Frank, Ph.D., University of Pittsburgh Medical Center, Western Psychiatric Institute and Clinic, 3811 O’Hara Street, Pitts- back down into depression. Although we distinguish burgh PA 15213-2593. Received March 3, 2000; revised June 14, 2000; accepted June 22, 2000. between the treatment of acute symptomatology (labeled ©2000 Society of Biological Psychiatry 0006-3223/00/$20.00 PII S0006-3223(00)00969-0 594 BIOL PSYCHIATRY E. Frank et al 2000;48:593–604 biology to create three probable pathways to recurrence of bipolar illness: 1) stressful life events; 2) disruptions in social rhythms; and 3) medication nonadherence. As envisioned by Goodwin and Jamison, these routes to illness are interconnected. Their model suggests that individuals with bipolar disorder are fundamentally vul- nerable to disruptions in circadian rhythms. Psychosocial stressors then interact with this biological vulnerability to cause symptoms. For instance, stressful life events disrupt Figure 1. Response, remission recovery, relapse, and recurrence: social rhythms, which causes disturbances in circadian phases of treatment in unipolar disorder. (Reproduced with integrity, which, in turn, may lead to recurrence. Alter- permission from Kupfer 1991.) nately, problematic interpersonal relationships or disor- dered schedules contribute to a patient’s difficulty adher- ing to a medication regimen which, again, may lead to Preliminary Phase in Figure 2) and prophylactic treatment recurrence. As a direct consequence of this model, one following remission (labeled Preventative Phase), we would assume that helping patients learn to take their recognize that these distinctions are often arbitrary and medication regularly, lead more orderly lives, and resolve inaccurate. In fact, patients in a nonacute phase of treat- interpersonal problems more effectively would promote ment often experience on-going symptom fluctuations. circadian integrity and minimize risk of recurrence. Depressive symptoms, in particular, seem especially dif- ficult to eradicate completely (Hlastala et al 1997). Thus, Treating Bipolar Disorder the holy grail of sustained euthymia in bipolar disorder As depicted in Figure 2, bipolar illness is a disorderly mayremainanelusivegoalintheabsenceofsophisticated disorder. Characterized by erratic sleep–wake cycles and treatments that address both the biological and psycholog- dramatic symptom fluctuations, the clinical course is ical aspects of this disorder. unpredictable and rarely static. Needless to say, treating this “moving target” creates many interesting—and some- Pathways to Recurrence times problematic—challenges. For instance, lithium Goodwin and Jamison’s definitive textbook on bipolar monotherapy is still considered the “gold standard” of disorder (Goodwin and Jamison 1990) acknowledges the pharmacotherapy for bipolar disorder. As patients move important interplay between biological and psychosocial through the various phases of the disorder, however, most factors in determining the course of bipolar disorder. psychiatrists find themselves treating patients with a range Recognizing the primacy of biology, they hypothesized of mood stabilizers in combination with neuroleptics, that “the genetic defect in manic depressive illness in- sedative-hypnotics, and antidepressants (Sachs et al 2000). volves the circadian pacemaker or systems that modulate Efforts to simplify regimens are often thwarted by unsat- it” (Goodwin and Jamison 1990, 589) but then further isfactory treatment response, resulting in years of complex postulated that psychosocial factors will interact with polypharmacy. Vacillating symptomatology, impaired psychosocial functioning, and problematic medication side effects converge to create unique clinical challenges for both patients and health care professionals. Considering the complexities of this illness, it is not surprising that pharmacotherapy alone does not address the multiple needs of patients with bipolar disorder. Although there are many excellent review papers discussing extant psychos- ocial approaches to bipolar disorder (Colom et al 1998; Johnson et al 2000; Miklowitz and Frank 1999), there are surprisingly few data supporting their efficacy (Craighead et al 1998; Swartz and Frank, in press). The absence of well-designed, empirically tested psychotherapies in the literature led us to develop and test a model of individual psychotherapy that would be used in conjunction with Figure 2. Response, remission, recovery, relapse, and recur- medication to enhance functioning and diminish recur- rence: phases of treatment of bipolar disorder. rences in patients with bipolar I disorder. Interpersonal and Social Rhythm Therapy BIOL PSYCHIATRY 595 2000;48:593–604 Theoretical Context for Interpersonal and could trigger an episode by causing the dysregulation of Social Rhythm Therapy biological rhythms. For instance, the loss of a spouse Interpersonal and social rhythm therapy (IPSRT) is a through death or divorce results in the loss of a social treatment that is specifically designed for patients with Zeitgeber that may have previously determined sleep– bipolar disorder. As elaborated below, the genesis of wake times, rest periods, and meal times. In an individual IPSRT rests in a psycho-chronobiological theory of affec- with the genetic predisposition to depression, the physio- tive illness that we articulated in a series of papers in the logic and chronobiological disturbances produced by los- 1980s and early 1990s (Ehlers et al 1988, 1993; Monk et ing the social cues for sleep and meal times could be as al 1991, 1990). Its design was also strongly influenced by important in the genesis of an episode as the psychologic the instability model of bipolar disorder proposed by distress generated by the event. Goodwin and Jamison (1990) and our evolving under- We subsequently extended this model of mood disor- standing of the relationship between stressful life events ders to include the concept of Zeitsto¨rers (time disturbers; and bipolar episodes. Ehlers et al 1993). As defined above, social Zeitgebers are persons, social demands, or tasks that set the biological clock. By contrast, Zeitsto¨rers are physical, chemical, or Circadian Rhythms, Sleep–Wake Cycles, and Mood psychosocial events that disturb the biological clock. For Disorders instance, travel across time zones represents a prototypical Researchers have identified reciprocal relationships Zeitsto¨rer. The abrupt change in the timing of light among circadian rhythms, sleep–wake cycles and mood. exposure, meal times, and sleep times can produce a range Wehr and colleagues have demonstrated that sleep reduc- of symptoms from mild “jet lag” to a full-blown affective tion can lead to mania in bipolar subjects (Leibenluft et al episode in predisposed individuals. Other examples of 1996; Wehr et al 1987). Sleep deprivation has significant potential Zeitsto¨rers include newborn babies, marital sep- (if transient) antidepressant effects in both unipolar and arations, work deadlines (e.g., a college student who stays bipolar depressed subjects (Barbini et al 1998; Leibenluft up all night to complete a term paper), and rotating shift et al 1993; Leibenluft and Wehr 1992), and PET studies work. Each of these disruptions has the potential to havedemonstratedlocalized effects of sleep deprivation in significantly alter an individual’s circadian and sleep– the medial prefrontal cortex (Wu et al 1999). The purpose wake rhythms that we argue, in turn, could result in an of IPSRT is to regulate both circadian rhythms and affective episode. In the context of our exploration of sleep–wake cycles. It must be noted, however, that the social Zeitgebers and Zeitsto¨rers, our group developed an relationship between bipolar disorder and circadian instrument to quantify an individual’s social rhythms rhythms is less well characterized than its relationship to (Monketal 1990). The Social Rhythm Metric (SRM) was sleep–wake disturbances. By targeting social factors that designed as both a means of categorizing interindividual modulate these rhythms, IPSRT is presumed to alter the differences in social rhythm regularity and as a therapeutic underlying neuronal circuitry involved in the pathogenesis tool to track decline into and recovery from an affective of bipolar symptomatology. episode. We hypothesized that a psychotherapy that helps The theoretical underpinnings of IPSRT began with our regulate social rhythms could help a vulnerable individual efforts to better understand the psycho-chronobiological reduce the risk of developing mood symptoms. determinants of unipolar disorder. In 1988, we proposed Stressful Life Events and Mood an etiologic model of major depression that focused on the role of disrupted social rhythms in the emergence of a We formulated IPSRT at a time when there was a great depressive episode in biologically vulnerable individuals deal of interest in the relationship between stressful life (Ehlers et al 1988). Noting that the established biological events and bipolar episode onset (Ellicott et al 1990). correlates of affective disorder include disrupted sleep Given the probable role of circadian rhythm disruption in electroencephalogram recordings (Kupfer et al 1991) and the genesis of bipolar episodes, our research group was phasic changes in the circadian secretions of pituitary particularly interested in the effects of those life events hormones (Carroll et al 1980), we hypothesized that that caused a significant disruption in social rhythms. disruptions in the social cues that entrain these cycles may These theories, however, had not been subject to method- act as triggers for mood episodes. We argued that social ologically rigorous testing at the inception of IPSRT. Zeitgebers, that is, personal relationships, social demands, Therefore, simultaneous with our early testing of IPSRT, or tasks that entrain biological rhythms, may serve as the we began an on-going study to assess the relationship link between the biological and psychosocial processes between life events and bipolar episode onset with a that place an individual at risk for developing mood reliable and valid life stress instrument, the Bedford symptoms. We hypothesized that losing a social Zeitgeber College Life Event and Difficulty Schedule (LEDS). 596 BIOL PSYCHIATRY E. Frank et al 2000;48:593–604 In our research program, each life event of any severity individuals, stressful interpersonal events may contribute identified by LEDS criteria was subject to an additional to the onset of depression. It also argues that depressive rating devised by our group to reflect the degree to which symptoms can interfere with an individual’s capacity to any given event is likely to have an acute effect on social successfully negotiate interpersonal conflict or find con- routines, particularly those that might disrupt the sleep– structive solutions to interpersonal dilemmas. Interper- wakecycle. The Social Rhythm Disruption (SRD) ratings, sonal psychotherapy is a “here and now” treatment that like the LEDS rating, were contextually determined by focuses on the relationship between the patient’s current consensus panel and guided by clearly delineated criteria interpersonal milieu and his or her depressive symptoms. and a dictionary of examples. In an initial report based on TreatmentfocusesononeoffourIPTproblemareas:grief, 39subjects with bipolar I disorder who were assessed with role disputes, role transitions, or interpersonal deficits. the LEDS/SRD protocol, we found evidence that life events (regardless of severity of threat) characterized by a Integrating the Behavioral, Interpersonal, and high degree of social disruption were associated with the Psychoeducational Models onset of manic but not depressive episodes (Malkoff- Schwartz et al 1998). Severely stressful life events (re- In the context of adapting IPT for the maintenance treatment gardless of SRD rating) were related to the onset of both of recurrent unipolar depression, we saw the potential utility manic and depressive bipolar episodes. In a follow-up of this treatment for another highly recurrent affective illness, study, we interviewed bipolar subjects with purely manic bipolar disorder. We established that patients with recurrent (n 5 21), purely depressed (n 5 21), and mixed or cycling unipolar disorder could recover from depression with an (n 5 24) episodes and compared this bipolar sample with acute course of IPT and then decrease the risk of having 44 patients with recurrent unipolar depression (Malkoff- another episode by receiving monthly sessions of mainte- Schwartz et al 2000). We again found that life events nance IPT (Frank et al 1990). We began to conceptualize a associated with a high degree of social disruption occur- similar kind of maintenance treatment for bipolar I disorder; ring in the 8 weeks before the onset of an episode were however, given extant theories about the relationship be- more frequently associated with the onset of manic epi- tweencircadianrhythmsandbipolarepisodesandsubsequent sodes relative to bipolar cycling, bipolar depressed, or data linking SRD events to mania (Malkoff-Schwartz et al unipolar depressive episodes. Severely life-threatening 1998, 2000), we decided to augment IPT with behavioral events were more frequently associated with the onset of strategies designed to stabilize daily routines. We borrowed manic episodes relative to bipolar cycling episodes. We traditional cognitive-behavioral techniques such as self-mon- conclude that SRD and severe events are associated with itoring, realistic goal-setting, and graded task assignment to manic episode onsets in a manner distinct from the help patients follow more consistent patterns of eating, association between SRD and severe events in bipolar sleeping, and social stimulation. depressed, bipolar cycling, and unipolar depressed onsets. Weexpected IPT to contribute a specific antidepressant effect and hypothesized that helping patients stabilize their Origins of Interpersonal and Social Rhythm social rhythms would decrease the risk of new affective Therapy (especially manic) episodes. Nonetheless, we were aware that there is tremendous overlap between interpersonal Interpersonal Psychotherapy of Depression stress and social rhythm disruption: a disturbance in the Interpersonal psychotherapy (IPT) is a time-limited, fo- social milieu (such as a new job or conflict with a spouse) cused psychotherapy developed in the 1970s by Klerman, often acts as a Zeitsto¨rer which, in turn, can lead to Weissman, and colleagues for the treatment of unipolar changes in daily routines. We therefore envisioned IPSRT depression (Klerman et al 1984). Unlike many other as a truly integrated therapy that would allow these psychotherapies, IPT is designed to treat a specific disor- strategies to function synergistically. Thus, we expected der (depression) and has been systematically evaluated in that the IPT-induced resolution of interpersonal conflict several randomized, controlled research trials. IPT was would also contribute to more stable rhythms and more envisioned as an acute (12–16 weeks) treatment for stable daily routines would promote more stable life depression but has also been tested in an 8-month contin- circumstances (jobs, relationships, etc.). uation study (Klerman et al 1974) and as a long-term The third component of IPSRT is psychoeducation. maintenance strategy for patients with recurrent depres- Recalling that the Goodwin and Jamison model (Goodwin sion (Frank et al 1990). The basis of IPT is the premise and Jamison 1990) predicts three probable pathways to that depression occurs in a psychosocial and interpersonal recurrence in bipolar disorder, including medication non- context. Akin to the social Zeitgeber hypothesis, the adherence, a cogent psychotherapy for bipolar disorder philosophy of IPT posits that in biologically vulnerable also necessarily addresses medical issues such as side
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