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Home » Major Depressive Disorder

Psychiatric Times. Vol. 30 No. 1
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COMORBIDITIES 

Treatment Implications for Comorbid Diabetes Mellitus and Depression

By Shane M. Coleman, MD and Wayne Katon, MD | January 18, 2013
Dr Coleman is a Senior Fellow at the University of Washington, School of Medicine, Seattle. Dr Katon is Professor, Vice-Chair, and Director of the Division of Health Services and Psychiatric Epidemiology at the University of Washington, School of Medicine. Dr Coleman reports no conflicts of interest concerning the subject matter of this article. Dr Katon reports that he has received CME honoraria from Lilly, Pfizer, and Forest, and that he is on the Advisory Board for Lilly.

These symptoms are also more specific when they develop in conjunction with at least 1 of the 2 cardinal symptoms of depression, so understanding the timing or onset of somatic symptoms is informative. Considering the etiology of the symptom, or whether the somatic symptom could be caused by diabetes can be helpful because symptoms unrelated to medical illness are more likely due to depression. And finally, if the somatic symptom is out of proportion to the illness, medication, or another relevant factor, it may be more likely due to depression.

Despite challenges associated with diagnosing depression in the medically ill, studies performed in ambulatory diabetic cohorts have been encouraging. In general, they have shown that common depression screening scales, including the BDI and Patient Health Questionnaire-9 (PHQ-9), retain both their sensitivity and specificity in identifying depression when administered in outpatient settings.15,16

TABLE

Clinical tips and implications for treating depression in patients with diabetes
(MORE: Comorbid Movement and Psychiatric Disorders)

Treatment

Many studies have examined the effectiveness of treatment for depression in diabetic patients. This has included the examination of evidence-based psychotherapy; psychopharmacology; mixed-treatment modalities; and systems-based approaches, such as those using collaborative depression care models to treat depression in primary care (Table). Cognitive-behavioral therapy (CBT) with added emphasis on diabetes self-management can be effective at treating depression and may also help reduce HbA1c levels.

Psychopharmacological approaches have proved effective for treating acute depressive episodes, for maintenance therapy for MDD, and for successfully preventing relapse of depressive episodes. Moreover, there is observational evidence that antidepressant use may increase the risk of type 2 diabetes mellitus.17

Collaborative depression care programs have successfully improved depression outcomes. However, only multicondition collaborative care programs, such as TEAM-care, have demonstrated the ability to improve depression as well as diabetes-related measures such as blood pressure and HbA1c and low-density lipoprotein cholesterol levels.18

Choice of psychopharmacological agents in the treatment of depression in diabetic patients deserves special attention because depression in these patients is complicated not only by the adverse effects of medication but also by the effects of diabetes. For instance, some SSRIs may cause weight gain, which will exacerbate insulin resistance and may contribute to sexual dysfunction, worsening a common, long-term complication of diabetes. SSRIs may also cause drug-drug interactions via their effects on the cytochrome P-450 (CYP) isoenzymes by interfering with the metabolism of diabetes medications. For example, fluoxetine(Drug information on fluoxetine), fluvoxamine(Drug information on fluvoxamine), and sertraline may inhibit the CYP2C9 isoenzyme and affect the metabolism of the sulfonylureas tolbutamide(Drug information on tolbutamide) and glimepiride(Drug information on glimepiride).

TCAs, while effective for treating depression in diabetes, have unique properties that limit their usefulness. First, TCAs may cause elevations in fasting blood glucose levels and they are more likely to cause weight gain than other, newer antidepressants. Second, many adverse effects associated with TCAs, such as orthostasis and arrhythmia, are particularly problematic when diabetes itself targets the nervous and cardiovascular systems.

Bupropion, in particular, possesses many qualities attractive for treatment of the diabetic patient, and it has been found to be efficacious for depression in this population.19 This drug is weight-neutral (or may even help diabetic patients lose weight); it is associated with less sexual dysfunction; it can be effective for smoking cessation (a common and costly comorbidity in depressed diabetic patients); and it has shown efficacy in treating neuropathic pain.16,19 However, bupropion is ineffective for treating co-occurring anxiety disorders. Venlafaxine and duloxetine(Drug information on duloxetine), which have shown efficacy in treating depression and neuropathic pain, may also be useful in diabetic patients with depression.

CASE VIGNETTE

Mr M, a 54-year-old with diabetes and hypertension, was referred for evaluation by his primary care physician. During the interview, Mr M rated his mood as “fair,” but he is experiencing decreased interest in leisurely activities, such as hiking and cigar smoking, as well as decreased motivation for self-care, including eating a healthy diet and taking regular blood sugar readings. He describes frequent nighttime waking, with no more than 3 hours of uninterrupted sleep; normal appetite, with a recent 5-lb weight gain; normal concentration; and decreased energy. He denies hopelessness but endorses feelings of guilt and describes himself as a bad partner to his wife because he’s currently unable to work and no longer engages in physical activity with her. When asked if he ever has thoughts of hurting himself or others, he replies, “Yeah, sometime I think I’m no good and people might be better off without me.”

Mr M is clearly depressed; he has decreased interest, guilty thoughts, feelings of being ineffective, and intermittent suicidal ideation. He’s not sleeping well (possibly because of polydipsia) and has decreased energy as well as a recent 5-lb weight gain. Additional history about the duration of both his depression and diabetes may be helpful, as would specific symptoms that the patient attributes to his diabetes, including the severity of these symptoms. Knowing the time of onset of his decreased interest and somatic symptoms may be useful. Direct inquiry into whether the patient suffers from anxiety, sexual dysfunction, or neuropathy may also help guide treatment.

We recommend administering the PHQ-9 and Montreal Cognitive Assessment during the initial patient evaluation. These examinations should be repeated regularly over time to track the patient’s progress and response to treatment. Additional history can be obtained from the patient’s primary care physician. Pending further history, CBT with an emphasis on diabetes self-care should be discussed as a possible option, as should treatment with bupropion, an SSRI, or a dual-acting agent.

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by The Editors | March 14, 2013 11:35 AM EDT

Editor's note: The quiz question referenced in Dr Pies' note can be found at http://www.psychiatrictimes.com/mdd/content/article/10168/2130035. Thanks to Dr Pies for his compelling question.

by Ronald Pies | February 26, 2013 10:20 PM EST

This quiz question based on this very interesting article presents the quiz-taker with a difficult choice--between
"c"and "d". The reference supporting choice "c" is the 1992 study, by Katon
& Schulberg (Gen Hosp Psychiatry. 1992 Jul;14(4):237-47) This study found that,


"Major depression is a common illness among persons in the community,
in ambulatory medical clinics, and in inpatient medical care. Studies
have estimated that major depression occurs in 2%-4% of persons in the
community, in 5%-10% of primary care patients, and 10%-14% of medical
inpatients. In each setting there are two to three times as many persons
with depressive symptoms that fall short of
major depression criteria."

In contrast, the DSM-IV text from 1994 indicated that "the lifetime risk for Major depressive disorder
in community samples has varied from 10%-25% for women and from 5%-12% for men. The
point prevalence for Major Depressive Disorder in adults in community samples has
varied from 5%-9% for women and from 2% to 3% for men."


On average, then (men and women), for lifetime MDD prevalence, the figure would be
about 13% in the general community, based on those DSM-IV figures. Indeed,
in the PT poll, 49% of respondents (N=57) are indicating choice "d" (10-12%) vs.
35% selecting choice "c", 5-10%, ostensibly the "correct" choice. My own choice,
in fact, was "d".

On the other hand, a review of the English language literature (1980-2000) found a
1 year MDD prevalance of about 4%, and a lifetime prevalence of about 6.7%--
corresponding to choice "c" in the quiz. Notably, the authors concluded that,

"The prevalence of mood disorders reported in high-quality studies is
generally lower than rates commonly reported in the general psychiatric
literature. When controlled for common methodological confounds, variation
in prevalence rates persists across studies and deserves continued study.
Methodological variation among studies that have examined the prevalence of
depression in primary health care services is so large that comparative
analyses cannot be achieved." [Waraich et al, Can J Psychiatry. 2004 Feb;49(2)
:124-38.]

Bottom line: I think either choice "c" or "d" could be considered correct, depending
on the study methods and population, as well as whether "point prevalence" or lifetime
prevalence is considered. Any epidemiologists care to comment?

Best regards,

Ron Pies MD

Also in this Special Report

Introduction: The Integrated Approach to Addressing Comorbidities—Part 1

Comorbidities in Borderline Personality Disorder

Identifying and Treating Common Psychiatric Conditions Comorbid with Myalgic Encephalomyelitis and/or Fibromyalgia

Migraine and Psychiatric Comorbidity

Treatment Implications for Comorbid Diabetes Mellitus and Depression

Comorbid Movement and Psychiatric Disorders





References

1. Katon W, Schulberg H. Epidemiology of depression in primary care. Gen Hosp Psychiatry. 1992;14:237-247.
2. American Diabetes Association. Diabetes Statistics, 2011. http://www.diabetes.org/diabetes-basics/diabetes-statistics. Accessed December 6, 2012.
3. Ali S, Stone MA, Peters JL, et al. The prevalence of co-morbid depression in adults with type 2 diabetes: a systematic review and meta-analysis. Diabet Med. 2006;23:1165-1173.
4. Anderson RJ, Freedland KE, Clouse RE, Lustman PJ. The prevalence of comorbid depression in adults with diabetes: a meta-analysis. Diabetes Care. 2001;24:1069-1078.
5. Eaton WW, Armenian H, Gallo J, et al. Depression and risk for onset of type II diabetes: a prospective population-based study. Diabetes Care. 1996;19:1097-1102.
6. Gonder-Frederick LA, Cox DJ, Bobbitt SA, Pennebaker JW. Mood changes associated with blood glucose fluctuations in insulin-dependent diabetes mellitus. Health Psychol. 1989;8:45-59.
7. Katon WJ, Von Korff M, Lin EH, et al. The Pathways Study: a randomized trial of collaborative care in patients with diabetes and depression. Arch Gen Psychiatry. 2004;61:1042-1049.
8. Lustman PJ, Griffith LS, Freedland KE, Clouse RE. The course of major depression in diabetes. Gen Hosp Psychiatry. 1997;19:138-143.
9. Ciechanowski PS, Katon WJ, Russo JE. Depression and diabetes: impact of depressive symptoms on adherence, function, and costs. Arch Intern Med. 2000;160:3278-3285.
10. de Groot M, Anderson R, Freedland KE, et al. Association of depression and diabetes complications: a meta-analysis. Psychosom Med. 2001;63:619-630.
11. Egede LE, Zheng D, Simpson K. Comorbid depression is associated with increased health care use and expenditures in individuals with diabetes. Diabetes Care. 2002;25:464-470.
12. Cassem EH. Depressive disorders in the medically ill: an overview. Psychosomatics. 1995;36(2):S2-S10.
13. Cavanaugh S, Clark DC, Gibbons RD. Diagnosing depression in the hospitalized medically ill. Psychosomatics. 1983;24:809-815.
14. Cavanaugh SV. Diagnosing depression in the hospitalized patient with chronic medical illness. J Clin Psychiatry. 1984;45(3, pt 2):13-17.
15. Lustman PJ, Freedland KE, Carney RM, et al. Similarity of depression in diabetic and psychiatric patients. Psychosom Med. 1992;54:602-611.
16. Katon WJ. The comorbidity of diabetes mellitus and depression. Am J Med. 2008;121(11 suppl 2):S8-S15.
17. Andersohn F, Schade R, Suissa S, Garbe E. Long-term use of antidepressants for depressive disorders and the risk of diabetes mellitus. Am J Psychiatry. 2009;166:591-598.
18. Katon WJ, Lin EH, Von Korff M, et al. Collaborative care for patients with depression and chronic illnesses. N Engl J Med. 2010;363:2611-2620.
19. Lustman PJ, Williams MM, Sayuk GS, et al. Factors influencing glycemic control in type 2 diabetes during acute- and maintenance-phase treatment of major depressive disorder with bupropion. Diabetes Care. 2007;30:459-466.


 
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