Article

Elevated Prevalence of Obesity, Metabolic Syndrome, and Cardiovascular Risk Factors in Bipolar Disorder

Department of Psychiatry, Roy J and Lucille A Carver College of Medicine, The University of Iowa, Iowa City, Iowa, USA.
Annals of Clinical Psychiatry (Impact Factor: 2.36). 07/2008; 20(3):131-7. DOI: 10.1080/10401230802177722
Source: PubMed

ABSTRACT

Bipolar disorder is associated with excess cardiovascular mortality. We hypothesized outpatients with bipolar disorder would exhibit excess cardiovascular risk factors, particularly among prevalent users of the second-generation antipsychotics associated with weight gain and valproic acid derivatives.
This chart review of 217 patients with bipolar disorder examined cardiovascular risk factors of the metabolic syndrome. We also evaluated if certain medications were cross-sectionally associated with metabolic syndrome.
Fifty-six patients were not weighed and many did not have available lipid profiles. Over three-quarters of those with available data (n = 161) were overweight or obese (body mass index >or= 25) and nearly half were obese (body mass index >or= 30). A prevalence exceeding general population estimates was also observed for hypertriglyceridemia, elevated blood pressure/hypertension, and elevated fasting glucose/diabetes. Among those with all requisite data (n = 60), over 50% met criteria for National Cholesterol Education Program-defined metabolic syndrome, nearly double the expected prevalence. A trend toward greater prevalence of metabolic syndrome among prevalent users of the second-generation antipsychotics associated with weight gain was observed.
Obesity and the metabolic syndrome were common in patients with bipolar disorder. These patients may be under-evaluated for cardiovascular risk and warrant screening and early intervention.

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    • "Nonetheless, there is a " dose–response " relationship between BMI and health outcomes, and the adverse health consequences of increased weight are even greater in obese individuals (Guh et al., 2009). Obesity rates increase with illness duration in BD, and up to 75% of patients become overweight or obese as the illness progresses (Wang et al., 2006; Fiedorowicz et al., 2008; Bond et al., 2010). BMI-related inflammation is thus relevant to the vast majority of people with BD, and its impact likely increases with illness duration. "

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    • "Furthermore, the loss of functional capacity cognitive impairment, and risk of developing rapid cycling bipolar disorder (RC-BD) appear to be enhanced by the presence of metabolic disturbances [1] [13]. Nevertheless, it is still unclear whether metabolic disturbances are the consequences or the leading factors of some of the health problems and maladaptive behaviors observed in BD [10] [11] [12]. "
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    ABSTRACT: Recent evidence shows an important relationship between metabolic disturbances and bipolar disorder (BD). However, it is still unclear whether such metabolic disturbances are only a consequence or to some extent the precipitating factors for health problems and maladaptive behaviors observed in BD. Because both metabolic disturbances and BD are medical conditions sharing common alterations in multiple biomarkers, it is plausible to hypothesize that metabolic disturbances may be considered to some extent as a major vulnerability factor in the latent phase of BD for some young adults. In line with this hypothesis , obesity may be regarded as a major driving force for prevalent cardio-metabolic disorders encountered within the early stages of BD. Likewise, premorbid metabolic disturbances as a whole may be considered as a potential source for vulnerability to develop BD. In addition, a synergistic relationship between obesity and metabolic disturbances associated with a premorbid disruption of biological rhythms may also lead to BD. Therefore, we postulate that metabolic disturbances may serve as a specific marker of premorbid illness activity in some people at risk for BD. Future prospective studies should focus on validating metabolic disturbances as vulnerability factors within the staging model of BD.
    Full-text · Article · Jan 2015 · Iranian Journal of Medical Hypotheses and Ideas
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    • "Comorbid medical conditions are frequent, long time hospitalization is common and suicide risk is high (20%) in bipolar disorder. Overall, the illness is an important socio-economic burden on the individual, family members and society (Fagiolini and Goracci, 2009; Fiedorowicz et al., 2008; Goldberg and Harrow, 2004; Kemp et al., 2014; McIntyre et al., 2008; Young and Grunze, 2013). BD is a highly heritable disease. "
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    ABSTRACT: Introduction: Glial Derived Neurotrophic Factor (GDNF) plays an important role in the survival and differentiation of neurons. We examined 5'upstream and 3' untranslated region of the GDNF gene by PCR amplification and direct sequencing to explore the effect of alteration in the potentially regulated part of GDNF in bipolar disorder. Materials and methods: Sixty-six patients with bipolar disorder, 27 first degree relatives of these patients and 56 healthy volunteers were screened for mutations and polymorphisms in GDNF gene. Results: Seven previously reported polymorphisms and additional three novel allele variants of GDNF were detected. Association test of rs2075680 C > A SNP showed significant difference between patients and healthy subjects with higher allele frequency in healthy subjects performing Chi-square test. However, there was no significant difference after multiple test corrections between groups. There were no significant differences in association test of rs2075680 C > A SNP between first degree relatives and healthy volunteers/patients. rs142426358 T > C SNP was seen only in one patient with an early age of illness onset. New T > A alterations were found in chromosome locations 5:37812784 and 5:37812782 in two male bipolar disorder patients with age of illness onset 12 and 24 years. Limitations: The sample size was relatively small. Discussion: Our study proposes the suggestive association between polymorphisms in the potential regulatory sites of GDNF and bipolar disorder.
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