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Original Research Depressive Symptomatology in the Immediate Postnatal Period: Identifying Maternal Characteristics Related to True- and False-Positive Screening Scores
Cindy-Lee Dennis, Lori E Ross

(PDF)

Obesity in Bipolar Disorder and Major Depressive Disorder: Results from a National Community Health Survey on Mental Health and Well-Being
Roger S McIntyre, Jakub Z Konarski, Kathryn Wilkins, Joanna K Soczynska, Sidney H Kennedy

(PDF)

Agreement Between Staff and Service Users Concerning the Clientele’s Mental Health Needs: A Quebec Study
Marie-Josée Fleury, Guy Grenier, Alain Lesage

(PDF)

Sedative Hypnotic Use in Alberta
Aliya Kassam, Brian Carter, Scott B Patten

(PDF)


Review Paper
Androgen Treatment of Depressive Symptoms in Older Men: A Systematic Review of Feasibility and Effectiveness

Nathalie T Shamlian, Martin G Cole

(PDF)

Systematic Overview of Drug Interactions With Antidepressant Medications
Carmine Nieuwstraten, N Renee Labiris, Anne Holbrook

(PDF)


Research Methods
Building a Better Model: An Introduction to Structural Equation Modelling

David L Streiner

(PDF)


Brief Communication
The Parent Interview for Child Symptoms: A Situation-Specific Clinical Research Interview for Attention-Deficit Hyperactivity and Related Disorders

Abel Ickowicz, Russell J Schachar, Richard Sugarman, Shirley X Chen, Claude Millette, Lisa Cook

(PDF)


Book Reviews
(PDF)

Sexual Abuse of Males: The SAM Model of Theory and Practice *
Review by
Harvey Armstrong


Clinical Work with Substance-Abusing Clients
Review by
Ewa Swoboda


Understanding and Treating Borderline Personality Disorder: A Guide for Professionals and Families
Review by
John Livesley


Insomnia: Principles and Management
Review by
Alan Douglass



Letters to the Editor
(PDF)

Re: Day Treatment for Personality Disorders

Re: Recent Advances in the Treatment of Borderline Personality Disorder

Reply: Recent Advances in the Treatment of Borderline Personality Disorder


Original Research

Obesity in Bipolar Disorder and Major Depressive Disorder: Results from a National Community Health Survey on Mental Health and Well-Being

Roger S McIntyre, MD, FRCPC1, Jakub Z Konarski, MSc2, Kathryn Wilkins, MSc3, Joanna K Soczynska, BSc4, Sidney H Kennedy, MD, FRCPC5

 

Objective: We aimed to ascertain the prevalence of obesity in individuals with a mood disorder (MD) (that is, bipolar disorder or major depressive disorder), compared with the general population. We further aimed to examine the likelihood of an association between obesity and MD, while controlling for the influence of sociodemographic variables.

Method: The analysis was based on data from Statistics Canada’s Canadian Community Health Survey: Mental Health and Well-Being (CCHS 1.2), conducted in 2002. The sample (n = 36 984; ≥ aged 15 years) was drawn from the Canadian household-dwelling population. The CCHS used diagnostic criteria outlined in the DSM-IV to screen respondents.

Results: Individuals with a lifetime history of MD were more likely to be obese (body mass index [BMI] > 30) than were individuals without lifetime MD (19%, compared with 15%, respectively; P < 0.001). In sex-specific multivariate analysis, lifetime MD was associated with elevated odds of obesity in female respondents (95%CI, 1.03 to 1.46, odds ratio 1.22), but not in male respondents. Antipsychotic pharmacotherapy was also associated with obesity.

Conclusions: This is the first Canadian epidemiologic investigation to specifically evaluate anthropometric indices and associated factors in people with MDs. The results herein supplement substantial clinical evidence documenting the association between MDs and stress-sensitive somatic disorders (for example, obesity). These data also underscore the metabolic consequences of some psychotropic agents.

(Can J Psychiatry 2006;51:274–280)

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Clinical Implications

  • Women with an MD may be more likely to experience metabolic abnormalities.

  • Practitioners should screen for metabolic disorders in all MD patients.

  • Patients receiving antipsychotics need to be closely monitored for weight gain and metabolic consequences.

Limitations

  • These data are cross-sectional and do not permit a determination of direction or causality.

  • The diagnosis of an MD and obesity was not clinically confirmed.

  • The CCHS collected information only from the household-dwelling population.

Key Words: major depressive disorder, bipolar disorder, overweight, obesity, depression, epidemiology, population

Résumé : L’obésité dans le trouble bipolaire et le trouble dépressif majeur : résultats de l’Enquête nationale sur la santé dans les collectivités, santé mentale et bien-être 



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The prevalence and public health implications of being overweight and obese constitute a national health priority. Most North American adults are overweight, and a rising proportion are categorically obese (1). MDD and BD are also highly prevalent chronic medical disorders with an estimated combined lifetime prevalence of 10% to 15% (2). Both MDD and BD are associated with an increased prevalence of somatic disorders (for example, diabetes mellitus and coronary artery disease) (3).

Obesity and MDs are clinically and pathoetiologically heterogeneous (5). Over the past several decades, the lifetime prevalence for obesity and MDs has significantly increased in both children and adults (6). This rapid increase in the estimated lifetime prevalence for each chronic disorder offers epidemiologic support for shared environmental risks (7).

Results from several cross-sectional and longitudinal studies indicate that obesity and MDs frequently cooccur (8). Moreover, several obesity-associated medical disorders may occur more frequently and manifest at a relatively earlier age in individuals with MDs (compared with the general population) (9,10). The association between obesity and MDs strengthens support for common moderating and mediating variables for both phenotypes (11).

To our knowledge, there are no previous population-based investigations attempting to simultaneously estimate the prevalence of obesity in both BD and MDD. We hypothesized that indices of excess weight would be more prevalent in individuals screening positive for an MDE or an ME. We further aimed to examine factors that may moderate the obesity–MD covariation.

Methods

The CCHS 1.2 was conducted by Statistics Canada (www.statcan.ca/english/freepub/82-617-XIE). Respondents were residents of private dwellings. Dwellings were sampled with a multistage stratified cluster design. Most interviews (86%) were conducted in person, the remainder by telephone. The responding sample totaled 36 984 people aged 15 years or over. The response rate was 77%. The data were weighted to represent the household population in the 10 Canadian provinces in 2002.

The survey collected information on lifetime and past 12-month prevalence of various mental disorders, using the WMH-CIDI. The WMH-CIDI was designed to be administered by lay interviewers and is generally based on diagnostic criteria outlined in the DSM-IV (1). (The questionnaire used for the CCHS is available at www.statcan.ca/English/concepts/heatlh/cycle1.2/index.htm). Details of the specific algorithms used to define MDD and BD are available in a published report (12). The survey collected information on self-reported height and weight, previously diagnosed medical disorders, access to and use of mental health care services, admissions to hospitals and use of medications, and disability associated with mental health.

The survey also collected information on determinants and correlates of mental health, such as sociodemographic information, income, and level of education, and level of leisure time physical activity.

According to DSM-IV-TR criteria, MD was defined as a lifetime occurrence of either an MDE or an ME. The prevalence of MD in the household population aged 15 years or over was estimated by appropriately weighting the sample proportion screening positive for MD. The association of MD with obesity was examined with weighted bivariate tabulations using BMI cutpoints established by the WHO (13). Sex-specific multivariate regression models were fitted to further examine the relation between obesity and MD while controlling for other demographic variables (for example, sex, age, education, income, marital status, level of leisure time physical activity, illicit drug dependency, alcohol dependency, functional dependency [that is, dependency on help from others to carry out activities of daily living], and hospitalization for a mental health problem within the past year). Further analyses explored the possible relations between MD and selected classes of psychotropic medication.

All statistical analyses were performed with SAS statistical software, release 9.1. To account for the complex sampling design of the CCHS, coefficients of variation were calculated on estimates and significance of differences between estimates according to the bootstrap technique. The level of statistical significance was defined as P < 0.05.

Results

Data from the CCHS indicate that 13% of Canadians aged 15 years or over screen positive for an MD (that is, symptoms consistent with an MDE or an ME) (Table 1). This proportion of positive screens extrapolates to about 3.3 million Canadians. The prevalence of MD among individuals who were categorically obese was higher in married individuals than in those who were single, divorced, separated, or widowed. MD also varied with income: individuals at the lowest level of income had nearly twice the likelihood (22%) of MD, compared with those at the highest level (12%).

Table 1  Percentage of Canadian household population aged 15 years or over in 2002 experiencing lifetime MD (MDE or ME)  and percentage classified as obese by sociodemographic characteristic 


 

Lifetime MDE or ME 


Obese class I–III 

 

 

No lifetime MD 

Lifetime MD 


Total 

13.3 

15.4 

19.0c 

Sex 

 

   

     Male 

10.4a 

15.9 

18.5 

     Female 

16.0a 

13.9 

19.3

Age group (years) 

 

   

     15 to 29 

12.5 

8.6 

9.2 

     30 to 44 

15.0a 

15.7 

19.8

     45 to 64 

15.3a 

19.8 

24.3b 

     65+ 

6.7a 

13.8 

20.1

Marital status 

 

   

     Married or living with partner 

11.5a 

16.7 

20.8

     Single, divorced, separated, or
     widowed 

16.0a 

11.8 

17.0

Level of education 

 

   

     Less than secondary school
     graduation 

11.4a 

15.7 

22.5

     Secondary school graduation 

12.6 

16.1 

21.4

     Some postsecondary 

15.0a 

14.0 

19.0 

     Postsecondary graduation 

14.1a 

14.2 

17.0

Level of income 

 

   

     Lowest 

22.3a 

14.3 

25.9

     Lower-middle 

15.9 

16.3 

28.6a,c 

     Middle 

13.0 

14.6 

20.1

     Upper-middle 

13.4 

16.2 

20.4c 

     Highest 

12.4a 

14.7 

14.2 


Data source:  2002 CCHS 

aDiffers significantly from estimate for total population (P < 0.05) 

bCoefficient of variation between 16.6% and 33.3%; interpret with caution 

cDiffers significantly from corresponding estimate for population with no lifetime MD (P < 0.05) 

Individuals screening positive for an MD were more likely to be obese than the general population: 19% of people with an MD were obese, compared with 15% without an MD (P < 0.05). The average BMI for the general population was 25.53. For individuals screening positive for MDE or ME, the average BMI was 25.96 (P < 0.001) (data not shown).

In nearly all examined subpopulations, the likelihood of obesity was higher in individuals with lifetime MD (Table 1). Differences were especially pronounced in individuals at lower socioeconomic levels. For example, in the lowest level of income group, the prevalence of obesity was nearly 26% in individuals with lifetime MD, compared with 14% in those without MD.

Sex-specific tabulations revealed that within all 3 obesity classes the prevalence of obesity was higher for female respondents with MD. In male respondents, however, no significant differences emerged in obesity with MD (Figures 1 and 2).

Figure 1 Prevalence of obesity by BMI class and presence of MD in male respondents aged 15 years or over in 2002

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Figure 2 Prevalence of obesity by BMI class and presence of MD in female respondents aged 15 years or over in 2002

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*Significantly higher than estimate for female respondents without MD (P < 0.01)

To study the relation between MD and obesity while controlling for sociodemographics, we employed multiple logistic regression. In preliminary analysis, the OR differed significantly by sex, and consequently, separate models were fitted for the sexes. In male respondents, once we controlled for the effects of sociodemographic factors, chronic disease, alcohol dependency, illicit drug dependency, recent hospitalization, functional dependency, and physical activity level, the odds of obesity showed no significant association with MD (Table 2).

Table 2 Adjusted ORs relating lifetime MD and other selected characteristics to obesity in Canadian respondents aged 15 years or over in 2002 


 

Male sex 
Female  sex 

 

OR 

95% CI 

OR 

95%CI 


Lifetime mood disorderb 

1.10 

(0.85–1.42) 

1.22a 

(1.03-1.46) 

Age group (years) 

 

     

     15 to 29b 

1.00 

— 

1.00 

— 

     30 to 44 

1.60a 

(1.31–1.95) 

1.64a 

(1.35–2.00) 

     45 to 64 

1.78a 

(1.44–2.20) 

1.76a 

(1.44–2.14) 

     65+ 

0.77a 

(0.60–0.98) 

0.84 

(0.67–1.05) 

Level of education 

 

     

     Less than secondary graduation 

1.28a 

(1.08–1.51) 

1.41a 

(1.19–1.67) 

     Secondary graduation 

1.32a 

(1.11–1.57) 

1.08 

(0.93–1.26) 

     Some postsecondary 

1.36a 

(1.07–1.74) 

1.06 

(0.85–1.33) 

     Postsecondary graduation

1.00 

— 

1.00 

— 

Marital status 

 

     

     Single, widowed, divorced, or
     separated

1.00 

— 

1.00 

— 

     Married  or living with partner 

1.17a 

(1.02–1.35) 

1.14a 

(1.00–1.30) 

Number of diagnosed chronic conditionsc 

1.30a 

(1.23–1.37) 

1.30a 

(1.24–1.35) 

Alcohol dependentb 

0.87 

(0.63–1.21) 

1.01 

(0.62–1.64) 

Illicit drug dependentb 

0.47a 

(0.23–0.97) 

0.35a 

(0.13–0.97) 

Hospitalized within past yearb 

0.56 

(0.24–1.32) 

1.11 

(0.62–2.00) 

Activity restriction (activities of daily living)b 

0.84 

(0.69–1.04) 

1.26a 

(1.08–1.48) 

Moderate or active level of physical activityb 

0.88a 

(0.77–0.99) 

0.75a 

(0.67–0.85) 


Data source:  2002 CCHS 

Model based on records for 15 447 male and 18 278 female respondents.  

aDiffers significantly from estimate for reference category (P < 0.05) 

bReference category.  When not noted, reference category is absence of characteristic; for example, reference category for alcohol-dependent is not alcohol-dependent. 

cUsed as continuous variable in model 

Significant associations emerged for level of education. Male respondents without a college or university education had higher odds of obesity, compared with postsecondary graduates. The odds of obesity were elevated in relation to prevalent chronic disease, but lowered in relation to illicit drug dependency in male respondents. As expected, moderate or intense physical activity was negatively related to obesity.

In female respondents, the odds of obesity were modestly, but significantly, elevated in relation to the presence of an MD (95%CI, 1.0 to 1.5, OR 1.2) (Table 2). Associations between education and obesity, however, were less powerful in female respondents than in male respondents. Chronic disease and activities of daily living dependency were positively associated with obesity, while illicit drug dependency and physical activity were negatively associated with obesity.

Further analyses studied the possible relation between psychotropic medication use and obesity. The CCHS asked respondents about their use of selected categories of medications in the past year, including hypnotics, anxiolytics, mood stabilizers, antidepressants, and antipsychotics. As indicated in Table 3, in individuals screening positive for lifetime MD, antidepressants, followed by anxiolytics, were used most commonly. Under 2% of individuals with MD reported using antipsychotic medication.

Table 3 Past-12-month medication use in Canadian lifetime MD population aged 15 years or over in 2002 


Type of medication 

Percentage of population
using medication 


Sleeping pills 

22.1 

Antianxiety medication 

16.4 

Mood stabilizers 

6.0 

Antidepressants 

24.2 

Antipsychotics 

1.7 


Data source:  2002 CCHS   

We examined use of each of these drug categories in relation to obesity in multiple logistic regression modelling. Only antipsychotics were significantly associated with obesity (P < 0.05). In female respondents, in the fully controlled model (as shown in Table 2), the odds of obesity in association with this class of drugs was 3.1 (95%CI,1.7 to 5.7, P < 0.05) (data not shown). In male respondents, the data suggested a similar relation (95%CI, 1.0 to 5.5, OR 2.3), with a trend toward statistical significance (P = 0.06).

Discussion

This is the first investigation evaluating excess weight among respondents in Canada who screen positive for an MD. Results indicate that female respondents who screen positive for MD have a significantly higher likelihood of being obese. The use of antipsychotic medications was also associated with obesity (14).

A significant database documents similarities between obesity and MDs in phenomenology, comorbidity, family history, and pharmacologic treatment response (2,3). Recent reviews of this topic have concluded that MDs and obesity are separate but related disorders, with distinct but overlapping pathophysiologies. There are likely multiple affective disorder–obesity covariations in the population (5,6). For example, both conditions are more frequently reported in individuals with lower socioeconcomic status and lower levels of education (7–10).

Neither the guidelines for the treatment of MDs nor those for the treatment of obesity disorders contain any specific recommendations for screening of the other condition. The presence of obesity in MD populations, notably in individuals with BD, is associated with a more severe illness, as indicated by more frequent affective episodes, greater severity of index presentation, higher recurrence vulnerability, comorbid medical disorders, and suicidal behaviour (11,15–17). This investigation was unable to address the association of obesity with illness course variables (2).

This investigation has several methodologic factors that limit interpretations and inferences that can be drawn from it. The WMH-CIDI is a validated screening tool for psychopathology in population-based epidemiologic studies. It was devised for use in epidemiologic and transcultural fields, can be used by nonmedical staff, has a modular structure, and simultaneously gives diagnoses according to the ICD-10 and the DSM-IV-TR, covering 39 and 32 diagnoses respectively on Axis I (18). A clinical reappraisal study suggested that the WMH-CIDI was able to detect an ME characterized by euphoria, grandiosity and the ability to maintain energy without sleep; however, it was less sensitive at detecting irritable and dysphoric forms of mania (that is, mixed states) (19). This suggests that the WMH-CIDI may underestimate the overall prevalence of BD. The proportion of individuals screening positive for an MDE or an ME is commensurate with other recently conducted regional and crossnational studies with lifetime aggregate estimates of about 10% to 25% (20–23).

Most respondents screening positive for an MD were not taking psychotropic medications. These results are consistent with medication compliance studies, which indicate that a relatively small proportion of diagnosed and treated MD patients will be compliant with medication for at least 1 year (24–27). Our data also indicate that MDs with comorbid obesity are more frequent in married individuals, compared with single, widowed, divorced, and separated individuals. This is inconsistent with other epidemiologic studies. We also report on the lifetime occurrence of an MD and current presence of obesity. We have no way of knowing whether the individuals screening positive for MD were currently affectively ill.

Anthropometric indices were determined by self-report. In general, respondents, particularly women, tend to underestimate their actual weight and overestimate their height (28). This reporting bias suggests that our estimates of obesity may be conservative. Analyses were not adjusted for the potential presence of psychiatric disorders in the general population control group. Given the methodology of this study, we were unable to determine the directionality of the association between affective disorders and obesity (29–31).

Although it is likely that the prevalence of mental disorders is higher in individuals who are institutionalized or homeless, the CCHS only collected information from the household-dwelling population. Therefore, estimates of prevalence can only be generalized to this population and probably underestimate the prevalence in the entire population. The extent to which such underascertainment may have biased the results of the analysis is unknown. While it is preferable to stratify respondents according to the elapsed interval since their last affective episode, it was not possible to do so with the CCHS data.

We agree with other commentators, that clinicians should be encouraged to screen for indices of excess weight and associated morbidity (for example, diabetes mellitus) in patients (notably women) who screen positive for an affective disorder (33). Although not the focus of this investigation, other study results support routine screening of psychiatric disorders in individuals who are obese (32–35). There is a need to develop and test specific interventions for individuals with comorbid affective disorders and obesity. The field would also benefit from research attempting to ascertain the mediators and moderators of the association between MDs and excess weight (5).

Funding and Support

This research received no funding or support.


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Author(s)

Manuscript received October 2005, revised, and accepted January 2006.

1.Assistant Professor, Department of Psychiatry and Pharmacology, University of Toronto, Toronto, Ontario; Head, Mood Disorders Psychopharmacology Unit, University Health Network, Toronto, Ontario.

2.PhD Candidate, Institute of Medical Science, University of Toronto, Toronto, Ontario.

3.Senior Analyst, Health Statistics Division, Statistics Canada, Ottawa, Ontario.

4.Research Coordinator, Mood Disorders Psychopharmacology Unity, University Health Network, Toronto, Ontario.

5.Psychiatrist in Chief, Department of Psychiatry, University Health Network, Toronto Ontario; Professor, Department of Psychiatry, University of Toronto, Toronto, Ontario; Institute of Medical Science, University of Toronto, Toronto, Ontario.

Address for correspondence: Dr RS McIntyre, Department of Psychiatry, University of Toronto, 399 Bathurst Street, Toronto, ON, M5T 2S8

e-mail: roger.mcintyre@uhn.on.ca

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