Differences in parental bonding between schizophrenia and bipolar disorder: Evidence of prodromal symptoms?
Introduction
Bipolar disorder types I and II affect about 2% of the world's population, with subthreshold forms of the disorder affecting another 2% (Merikangas et al., 2007). Even with treatment, about 37% of patients relapse into depression or mania within 1 year, and 60% within 2 years (Gitlin et al., 1995). On the other hand, the prevalence of schizophrenia (SCZ) is estimated to be around 1% worldwide (Saha et al., 2005). SCZ follows a course characterized by prodromal symptoms in early adolescence, illness onset around 20s with several recurrence and exacerbations, resulting in chronic state of residual symptoms and functional impairment (Saha et al., 2005, Lieberman et al., 2013). Both disorders have been described as a life shortening condition (Hoang et al., 2011). Patients with a diagnosis of SCZ die 12–15 years before the average population while life expectancy has been reported to be decreased 9 years for patients with bipolar disorder (BD) (Saha et al., 2007, Crump et al., 2013). Given these findings, a thorough understanding of the early course of these diseases is important for timely accurate diagnosis and therapeutic intervention, as well as for the prevention of substantial burden of illness progression (Post and Kalivas, 2013, Carlborg et al., 2014), comorbidities (Young, 2009, Kredentser et al., 2014) and suicide attempts (Saha et al., 2007, Ishii et al., 2014).
Many patients with BD and SCZ are initially misdiagnosed especially in the early stages of both disorders (Young, 2009). The diagnostic difficulties between them are common (Vieta, 2010). The consequences of misdiagnosis can include worsening of manic or depression symptoms, increased drug resistance, reduced quality of life, and increased risk of suicide (Young, 2009). Early detection and appropriate differential diagnosis has potentially great benefits for prognosis and specific treatments preventing functional impairment (Hill et al., 2013).
The relationships with parents during childhood seem to have an important role in the children's psychosocial development (Ramchandani and Psychogiou, 2009) and could directly influence the ability to overcome a traumatic situation (Sagi-Schwartz et al., 2003, Lima et al., 2014). The study of parental bonding and its particularities in patients with SCZ and BD may shed some light to clarify the prodromal symptoms of each disorder, and helps in early differential diagnosis. Disturbances in this relationship have been associated with increased risk for a number of mental disorders and neurobiological dysfunctions (Enns et al., 2002, Klier and Muzik, 2004, Tyrka et al., 2008). For instance, low maternal warmth is one of the leading risk factors associated with the risk of mania relapse after recovery in child BD subjects (Geller et al., 2008, Geller et al., 2004).
Parental bonding characterizes a two-way process in which the child becomes emotionally attached to parents (Bowlby, 1977). The Parental Bonding Instrument (PBI) was developed to investigate parental behavior and healthy parent–child bonds during the first 16 years (Parker, 1979). PBI has two dimensions: care and overprotection (Parker, 1979). Previous PBI studies revealed that patients with several psychiatric disorders, such as major depressive disorder and obsessive compulsive disorder, are likely to have a low parental care score or a high overprotection score for the first 16 years (Narita et al., 2000, Wilcox et al., 2008, Willinger et al., 2002).
Our study aims to compare the parental bonding features among three groups: patients with BD and SCZ, and healthy controls. Our hypothesis is that there may be a difference in the quality of the bond between these two disorders, given the opposite clinical feature of BD and SCZ regarding affect modulation, which might be crucial for attachment and bonding development. This is the first study to perform such comparison.
Section snippets
Subjects
Fifty-nine patients with SCZ, thirty-six patients with BD and fifty-two healthy controls were enrolled in this study. The inclusion criteria for the patients were the following: diagnosis of BD or SCZ according to the Structured Clinical Interview for DSM-IV Axis I Disorders (SCID-1); to be literate; and to be euthymic if it was a BD patient, or out of the psychotic episode if it was a SCZ patient. The exclusion criteria were a) parentless patients; b) genetic, neurologic or autoimmune
Results
Demographic variables and PBI mean scores are shown in Table 1. Variables, including gender, years of education, and age were significantly different among three groups.
Discussion
There were significant differences in the perception of attachment by patients during the first 16 years between SCZ and BD. The parental bonds of BD patients when compared to patients with SCZ were characterized by lower care (maternal and paternal score have shown 36% and 42% less care respectively) and higher control (maternal and paternal scores have shown 38% and 32% more overprotection respectively). Moreover, no significant difference was observed between patients with SCZ and healthy
Role of funding source
Dr. Passos, Dr. Belmonte-de-Abreu, Dr. Kapczinski, and Dr. Kauer-Santa'Anna received funding resources from the institutions CAPES and CNPq belonging to the Brazilian Government.
Contributors
Authors Gomes, Kauer-Sant’Anna, Kapczinski, Vasconcelos-Moreno and Belmonte-de-Abreu designed and wrote the protocol. Authors Gomes, Passos, Krolow, Reckziegel, and Sparemberg managed the literature searches and analyses. Authors Passos and Reckziegel undertook the statistical analysis, and authors Gomes and Passos wrote the first draft of the manuscript. All authors contributed to and have approved the final manuscript.
Conflict of interest
Dr. Gomes, Dr. Passos, Dr. Krolow, Dr. Reckziegel, Dr. Vasconcelos-Moreno Dr. Spanemberg, and Dr. Belmonte-de-Abreu reported no biomedical financial interests or potential conflicts of interest. Dr. Kauer-Sant’Anna is on speaker/advisory boards for, or has received research grants, from NARSAD, Stanley Medical Research Institute, CNPq-Universal, CNPq/INCT-TM, CNPq productivity award II, FIPE-HCPA and Eli-Lilly. Dr Kapczinski has received grants/research support from AstraZeneca, Eli Lilly,
Acknowledgment
We thank the Bipolar Disorder Program team from Hospital de Clinicas de Porto Alegre (HCPA) that help us to include patients.
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