¶ … Bipolar Disorder on the Routine Life of the Individual
Statement of Thesis: Bipolar disorder is an intricate physiological and psychological disorder that can control, tamper, and falsify a person's thoughts and actions in their daily life.
The work of Merikangas, et al. entitled "Lifetime and 12-month prevalence of bipolar spectrum disorder in the National Comorbidity Survey Replication" reports a growing acknowledgement that bipolar disorder has a "spectrum of expression that is substantially more common than the 1% BP-I prevalence traditionally found in population surveys." (2007) Merikangas, et al. report a study with the objective of estimating "the prevalence, correlates, and treatment patterns of bipolar spectrum disorder in the U.S. population." (2007)
The study was conducted via direct interviews in household settings in the United States. Participants are stated to have been a "nationally representative sample of 9282 English-speaking adults (aged >or=18 years)." (Merikangas, et al., 2007) Main outcome measures are stated as Version 3.0 of the World Health Organization's Composite International Diagnostic Interview, a fully structured lay-administered diagnostic interview, was used to assess DSM-IV lifetime and 12-month Axis I disorders. Subthreshold BPD was defined as recurrent hypomania without a major depressive episode or with fewer symptoms than required for threshold hypomania. Indicators of clinical severity included age at onset, chronicity, symptom severity, role impairment, co morbidity, and treatment." (Merikangas, et al., 2007)
The study results state "lifetime and 12-month prevalence estimates are 1.0% (0.6%) for BP-I, 1.1% (0.8%) for BP-II, and 2.4% (1.4%) for subthreshold BPD. Most respondents with threshold and subthreshold BPD had lifetime comorbidity with other Axis I disorders, particularly anxiety disorders. Clinical severity and role impairment are greater for threshold than for subthreshold BPD and for BP-II than for BP-I episodes of major depression, but subthreshold cases still have moderate to severe clinical severity and role impairment. Although most people with BPD receive lifetime professional treatment for emotional problems, use of antimanic medication is uncommon, especially in general medical settings." (2009) The study concludes by stating that subthreshhold BPD "is common, clinically significant, and underdetected in treatment settings. Inappropriate treatment of BPD is a serious problem in the U.S. population. Explicit criteria are needed to define subthreshold BPD for future clinical and research purposes." (Merikangas, et al., 2007)
The work of Lichenstein, et al. (2009) report in the work entitled "Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study" that they linked the "multi-generation register which contains information about all children and their parents in Sweden, and the hospital discharge register, which includes all public psychiatric inpatient admissions in Sweden. We identified 9,009,202 unique individuals in more than 2 million nuclear families between 1973 and 2004." (Lichenstein, et al., 2009)
Those who were at risk for schizophrenia, bipolar disorder and comorbidity were assessed for biological and adoptive parents, offspring, full-siblings and half-siblings of probands with one of the diseases." (Lichenstein, et al., 2009) This was accomplished through a multivariate generalised linear mixed model for analysis of genetic and environmental contributions to liability for schizophrenia, bipolar disorder, and the comorbidity." (Lichenstein, et al., 2009) Reported findings include those as follows: "First-degree relatives of probands with either schizophrenia (n=35-985) or bipolar disorder (n=40-487) were at increased risk of these disorders. Half-siblings had a significantly increased risk (schizophrenia: relative risk [RR] 3-6, 95% CI 2-3 -- 5-5 for maternal half-siblings, and 2-7, 1-9 -- 3-8 for paternal half-siblings; bipolar disorder: 4-5, 2-7 -- 7-4 for maternal half-siblings, and 2-4, 1-4 -- 4-1 for paternal half-siblings), but substantially lower than that of the full-siblings (schizophrenia: 9-0, 8-5 -- 11 6; bipolar disorder: 7-9, 7-1 -- 8-8). When relatives of probands with bipolar disorder were analyzed, increased risks for schizophrenia existed for all relationships, including adopted children to biological parents with bipolar disorder. Heritability for schizophrenia and bipolar disorder was 64% and 59%, respectively. Shared environmental effects were small but substantial (schizophrenia: 4-5%, 4-4% -- 7-4%; bipolar disorder: 3-4%, 2-3% -- 6-2%) for both disorders. The comorbidity between disorders was mainly (63%) due to additive genetic effects common to both disorders." (Lichenstein, et al., 2009) It is concluded that evidence was shown that is similar to findings in molecular genetic studies that a common genetic cause is shared and these findings are stated to present a challenge to the current "nosological dichotomy between schizophrenia and bipolar disorder, and are consistent with a reappraisal...
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