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. Author manuscript; available in PMC: 2016 Jan 31.
Published in final edited form as: Clin Geriatr Med. 2014 Nov 15;31(1):117–137. doi: 10.1016/j.cger.2014.08.022

Depression among older adults with diabetes mellitus

Mijung Park 1, Charles F Reynolds III 2
PMCID: PMC4254540  NIHMSID: NIHMS626700  PMID: 25453305

Synopsis

Depression is among the leading causes of decreased disability-adjusted life years in the world1 and a serious public health problem.2 Older adults with DM experience greater risk for comorbid depression compared to those who do not have DM.3 Having DM increases the risk of subsequent development or recurrence of depression. Conversely, history of depression increases the risk for new onset DM.4 As an unwanted co-traveler of DM, undetected, untreated or undertreated depression impinges an individual’s ability to manage their DM successfully, hindering their adherence to treatment regime.5 It also undermines the effectiveness of provider-patient communication and decays therapeutic relationships. Thus, in the context of caring for older adults with DM, comorbid depression presents special challenges and opportunities for clinicians. Moreover, recent studies have suggested that co-occurring depression and DM may accelerate cognitive decline, highlighting the importance of treating depression and DM. Several treatment modalities are available, which can be used to treat and manage depression in primary care settings: pharmaceutical, brief psychotherapeutic, behavioral and life style interventions, and combination therapies. An evidence-based health care delivery model is also available for treating depression in primary care settings. In this article, we summarize the clinical presentation of late-life depression, potential mechanisms of comorbidity of depression and DM, importance of depression in the successful management of DM, and available best practice models for depression treatment.

Keywords: Diabetes, Depression, Mood disorders, Aging, Collaborative Care

Introduction

Diabetes mellitus (DM) is one of the most common chronic conditions among older adults. About 26.9%, or 10.9 million U.S. residents aged 65 years and older had diabetes in 2010.6 Depressive disorders are serious chronic diseases that increase morbidity and mortality,7 erode quality of life,8 and increase medical expenditure. Depression and DM often co-occur. Data from a range of settings suggest that the prognosis of both DM and depression—in terms of severity of disease, complications, treatment resistance and mortality—is worse for either disease when they are co-morbid than when they occur separately. Comorbid depression in patients with DM is strongly associated with increased burdens of DM symptoms9, poor self-management and treatment adherence10, increase in health care services utilization and medical expenditures11 and an increased risk of DM complications.12 DM complications such as myocardial infarction, amputation or loss of vision can in turn precipitate or worsen depressive episodes. Yet, few studies have extensively examined the associations between depression and DM in the older adults populations. Also, recent studies have found that combination of DM and depression may increase the risk for dementia, suggesting increased brain toxicity.13 The purpose of this review is to summarize the clinical presentation of late-life depression among older adults with DM, potential mechanisms of comorbidity of depression and DM, importance of depression in the successful management of DM, and available best practice models for depression treatment.

Disease description

Depression is a mood disorder that causes a persistent feeling of sadness and loss of interest. To be diagnosed with major depression, a patient must have depressed mood or anhedonia and at least 5 of the following 9 symptoms nearly every day for at least 2 weeks:

  • Depressed mood

  • Marked diminished interest/pleasure

  • Sleep disturbance (increased or decreased sleep)

  • Appetite disturbance (increased or decreased appetite; typically with weight change)

  • Fatigue/loss or energy

  • Diminished concentration or indecisiveness

  • Feelings of worthlessness or excessive or inappropriate guilt

  • Psychomotor retardation or agitation (a change in mental and physical speed perceived by other people)

  • Recurrent thoughts of death or suicide (not just fear of dying)

They must also experience functional impairment related to these depressive symptoms.

Older adults, however, do not always present with the typical symptoms of depression. In particular, depressed or sad mood may be less evident or not even present. In these cases, anhedonia may be better indicator for depression.14,15 Depressed older adults may experience sleep disturbances (sleeping too much or too little) or changes in appetite (eating too much or too little). Decrease in self-efficacy, motivation, and ability to participate in self-care may also indicate underlying depressive symptoms. Signs of such symptoms can be subtle. Older adults may reply with “I don’t know” to simple questions, decline to participate in physical, speech or occupational therapy, and feeling negative or hopeless about treatments offered. Some may easily give up tasks during these therapies. Older adult who experience loss of self-worth or sense of loneliness due to depression, may complain “nobody needs me,” or “I feel I am just in everyone’s way.” The symptoms of late-life depression are often attributed to normal aging, grief, physical illness or dementia and providers and patients miss important opportunities to initiate treatment for what is an treatable health problem.16

The majority of older adults with clinically significant depressive symptoms do not meet standard diagnostic criteria for major depression or dysthymic disorder.17,18 Patients in this group fall short of meeting diagnostic criteria for major depression because of fewer or limited duration of depression symptoms. Nonetheless, studies suggest that these patients carry similar disease burden: poorer health outcomes, functional impairment, and higher health utilization and treatment costs.19-21 Moreover, these patients are at very high risk for subsequently developing major depression and may also develop suicidal ideation.22-24

Although depression can be successfully treated,25 many older adult suffer from a chronic or recurrent depression.26 In a prospective study about courses of major depression, approximately 85% of individuals who recover from depression experience recurrence within 15 years.27 Findings meta-analyses of chronic depression in primary care and community sample suggests that about one in three depressed older adults experience chronic and persist course.28,29 Depressed patients with DM are at greater risk for a chronic course of depression or less complete recovery.30 Such chronicity, in turn, makes it more difficult for older adults and their family caregivers to optimally self-manage DM.

In the older adults with DM, depressive symptoms may be overlooked because they are assumed to be due to concurrent DM and other medical illnesses. Many of the symptoms of depression such as lower energy, fatigue, loss of appetite, and sleep disturbance are also associated with DM. Thus differentiating stress related to DM self-management and depression can be challenging.31 Somatic complaints may suggest presence of depression, especially if they are out of proportion to underling physical disorders.32 Only 25-30% of primary care patients present with purely affective or cognitive symptoms of depression.33

Risk factors

Risk factors for developing depression after age 65 are similar to those in younger individuals and include being female, unmarried, low socioeconomic status, having chronic physical illness, social isolation, a history of depression, and a family history. The risk of major depression increases up to three-fold if a first-degree relative has the illness.34 Additional risk factors that are particularly important in older adults include loss and grief,35 social isolation or limited social support,36 high degrees of family conflict,37,38 and care-taking responsibilities.39 Other risk factors that increase the likelihood of depression in the medically ill elderly include presence of cognitive impairment, age greater than 75, active alcohol abuse, and lower educational attainment.40-49 Table 1 summarized the risk factors for depression in older adults.

Table 1.

Risk Factors for Depression in Older Adults

Authors, year Sample Finding
Age
Cole et al (2003)152 Age≥50 Meta-analysis of epidemiological studies. Pooled OR for depression associated with age: 1.2 (95% CI: 0.9-1.7)
Snowden (2008)153 Mixed age Comprehensive review of epidemiological studies: Depression is as common in older age as in earlier life.

Being Female
Cole et al (2003)152 Age≥50 Meta-analysis of epidemiological studies. Pooled OR for depression associated with being female: 1.4 (95% CI: 1.2-1.8)
Sonnenberg et al
(2001)154
55≤Age≤85 A random, age and sex-stratified community sample of 3056 older Dutch people; Prevalence of depression in women was almost twice as high as in men.

Grief and Loss
Zisook et al (1991)155 Mixed age Major depression and anxiety disorders are common within the first year of the spouse’s death: 29-58% meet criteria for major depression at one month, 24-30% at two months, and 25% at three months.
Cole et al (2003)152 Age≥50 Meta-analysis of epidemiological studies. Pooled OR for depression associated with recent bereavement: 3.3 (95% CI: 1.7-4.9)
Turkey et al (1999)156 Age≥70 The rate of syndromal depression in the newly bereaved was nearly nine times as high as the rate for married individuals, and the rate of depressive symptoms was nearly four times as high.

Social Isolation
Cole et al (2003)152 Age≥50 Meta-analysis of epidemiological studies. Pooled OR for depression associated with living alone: 1.7 (95% CI: 0.6-4.7)
Prince et al (1998)157 Age≥65 Prospective epidemiological study. Lack of contact with friends was a direct risk factor but also modified the association between handicap and depression.
Cacioppo et al (2006)158 Age≥55 There is a reciprocal relationship between loneliness depressive symptomatology and over time

Cognitive impairment
Cole et al (2003)152 Age≥50 Meta-analysis of epidemiological studies. Pooled OR for depression associated with recent bereavement: 2.1 (95% CI: 0.6-8.6)

Protective factors

Strong and supportive social context has been identified as a protective factor. A compelling body of evidence has shown that social support decreases the risks for depression50,51 and for depression relapse,52 increases adherence to depression treatment, 53,54 and improves treatment outcomes. Social support may have positive effects on psychological wellbeing independent of whether or not individuals are exposed to stress.55,56 Social support may also promote wellbeing through modulation of neuro-endocrine response to stress.57

Social activities, such as volunteering suggested to have positive effect on depression outcomes in older adults.58 Studies have also suggested that religion and spirituality may play an important part in many older adults’ lives and social connectedness and support are an important part of organized religion.59 Religion may allow older adults to experience life as meaningful despite losses and challenges and, thereby, reduce the risk of depression. It is also possible that the positive effect of religion on mental health is mediated by the social connectedness and the social support derived from taking part in religious activities.

Prevalence/Incidence

Depression is one of the most common mental disorders in late-life.60 About one in four U.S. resident projected to experience major depression by age 75.61 In community settings, about 5% of adults aged 65 and older meet research diagnostic criteria of major depression,62,63 with rates of subsyndromal, clinically significant depression estimated at 8% -16%.64 The rates of geriatric depression increase to 12-30% in institutional settings, and up to 50% for residents in long-term care facilities.65,66 Approximately 5-10% of older adults seen in primary care settings have clinically significant depression.67

Variations in prevalence in late-life depression across racial/ethnic group are rarely examined and existing literature present mixed findings. However, given that differences in diabetes prevalence exist by racial/ethnic group, these may be important to appreciate. Cross-sectional and longitudinal epidemiological study showed that Non-Hispanic White and Latino older adults have higher rates of depression.68-70 A longitudinal population study of community-dwelling Hispanic older adults showed approximately 9% of sample met the criteria for lifetime diagnosis of major depression, while 24% of sample reported minor depression.70 The prevalence of depression in African American is generally lower than their White counterparts.71

Minority older adults are less likely to be diagnosed with or treated for depression than their white counterparts.72,73 These health service disparities in minority populations become increasingly complicated when considering cultural beliefs and attitudes towards depression care. Culture influences how individuals experience and express depression.74,75 Minority patients from certain ethnic groups may express their depression somatically than psychologically.33,76 Such somatic presentations may reduce the recognition of depression by primary care providers or leads to the perception of a patient as ‘difficult.’77 Some minorities may also have less faith in the biological etiology of depression, be more skeptical about antidepressant use, and show stronger preferences for counseling than their White counterparts.78,79 When pharmaceutical treatment is the only available option, minority older adults may be less likely to engage in treatment and more likely to be non-adherent. The present primary care systems that focus primarily on pharmacological treatment without considering the unique barriers faced by ethnic and racial minority populations may not affect the pattern of disparities observed.80

Scant information on the cross-national prevalence of late-life depression is available. A report from a World Health Organization concluded that older adults in developed countries had relatively low average depression rates of 2.6% while those in developing countries had an average rate almost three times higher (7.5%).81 The rapid increase in diabetes across the world, particularly in developing countries,82,83 indicate that these international discrepancies are critical to understand.

Among older adults with DM, depression is highly prevalent.84 Up to 30% of individuals with DM have a significant number of depressive symptoms and 12 to 18% meet diagnostic criteria for major depression.3,85 Patients with DM experience significantly higher rates of depression compared with their age- and gender-matched counterparts.84 A meta-analysis of ten studies showed that the prevalence of depression was significantly higher in patients with DM compared with those without (17.6 vs. 9.8%).84 The prevalence of depression was higher in females with diabetes (23.8%) compared with males (12.8%); however, the odds ratio for depression in patients with Type 2 DM compared with those without was higher in males (OR = 1.9, 95% CI 1.7-2.1) than females (OR = 1.3, 95% CI 1.2-1.4).

Depression and mortality in individuals with DM

Based on several meta-analyses, depression is associated 1.5- to 2.6-fold increase of mortality among individuals with in DM.7,86,87 Few studies have examined if treating depression may decrease mortality among individuals with depression. Data from a large clinical trial of collaborative late-life depression treatment program in primary care setting (PROSPECT) showed that evidence-based treatment of depression can reduce mortality rates among those with DM (adjusted hazard ratio 0.49, 95% CI: 0.24-0.98).88 Another study of all cause mortality with same sample also found that patients with major depression in intervention practice were 24% less likely to have died, compared to depressed older adults in usual primary care practices.89

Underlying mechanisms of comorbidity of depression and DM

Katon90 proposed a complex bidirectional relationship between depression and type 2 DM (Figure 1). Depression early in adult life is a risk factor for subsequent development of DM.91 The increased risk of DM in patients with depression has been hypothesized to be the result of maladaptive health risk behaviors associated with depression such as smoking, obesity and lack of physical exercise90 as well as psychobiologic factors such as increased cortisol levels, increased inflammatory factors92 and insulin resistance.93

Figure 1. A conceptual model of interaction between major depression and medical illness.

Figure 1

Reproduced from Katon, Wayne J. "Clinical and Health Services Relationships between Major Depression, Depressive Symptoms, and General Medical Illness." Biological Psychiatry 54, no. 3 (2003): 216-26.

On the other hand, DM may increase risk of depression or worsen the depression symptoms due to increased symptom burden, DM complications causing functional impairment and decreased quality of life, as well as vascular brain changes secondary to DM. Comorbid depression has been found to impair the ability to perform self-care activities necessary to control DM by affecting memory, energy level, and executive function.94-96 Lack of self-care and the psychobiologic changes associated with comorbid depression may explain why individuals with comorbid depression experience increased risk of macro- and micro-vascular complications12 and dementia.13

While DM and depression independently associated with memory and cognitive impairment,97-99 recent clinical epidemiological studies found that concurrent DM and depression may have synergistic negative effect on brain health, posing greater risk for developing dementia and Alzheimer’s disease.13 There are several biological mechanisms that can explain such a toxic effect of the DM and depression combination on brain health. First, DM and depression are risk factors for cardiovascular and cerebrovascular diseases (e.g., vascular dementia and Alzheimer’s disease). Concurrent DM and depression may increase risk for cardiovascular and cerebrovascular events in additive fashion.13 Secondly, depression is associated with dysregulation of the hypothalamic-pituitary axis,100,101 which increases glucocorticoid production, and impairs negative feedback. Hypercortisolemia is associated with metabolic syndrome—a risk factor for vascular dementia and Alzheimer’s disease.102-104 Finally, chronic or recurrent depression is associated with hippocampal atrophy.105,106

The temporal relationship between depression and DM has not been fully established. Existing evidence suggests that the association between history of depression and subsequent development of DM is stronger than that between history DM and subsequent development of depression.107 Several prospective epidemiological studies have found that having depression increased risk for developing DM subsequent years by 1.62-to 2.52-fold: Demakakos and colleagues108 analyzed data of 6,111 individuals who reported not having doctor-diagnosed DM at baseline in 2002-2003 and concluded that, after adjusting for several demographic and clinical characteristics, individuals who had greater depressive symptomatology at baseline experienced 1.62-fold increased risk for developing DM in the subsequent 45.8 months. In another longitudinal study of community-residing adult population by Camethon et al, after adjusting for age, race, and gander, the adjusted risk of developing DM in subsequent years are 2.52-fold higher among those with greater depressive symptoms than those with low depressive symptoms.109 A prospective epidemiological study of 1,715 residents of Baltimore Catchment area showed that having major depressive disorder was associated with more than 2-fold increase in risk (adjusted odds ratio: 2.23; 95% CI 0.90-5.55) for developing DM in the subsequent 13 years.110 However, this was not statistically significant.

Having DM increases the risk for developing depression subsequently. A meta-analysis of 11 epidemiological studies concluded that individuals who had Type 2 DM without depression at baseline experienced 1.24-fold increased risk (95% CI 1.09-1.40) for subsequently developing or recurring depression in subsequent years.111 Data from the study of 5,201 multi-racial participants of Women’s Health Across the Nation (SWAN) concluded that having DM increase the odds for developing DM in the subsequent 2 years by 2.8-fold (95% CI: 1.2-6.4) among depressed African American Women.91 Therefore, older adults with diabetes should be considered at higher risk for future depression.

Prevention and early treatment

Prevention and early treatment of depression matter to providers who treat individuals with DM for several reasons. First, as mentioned earlier, having depression may increase the risk for subsequently developing DM. Thus, prevention and early treatment of depression may lower the incidence of DM. Second, having comorbid depression decreases individuals’ ability to successfully self-manage DM and increases likelihood for poor DM outcomes. Thirdly, depression is treatable and several treatment approaches are developed for primary care settings. In a recent clinical trial with 247 older adults112 suggests that both problem solving therapy for primary care (PST-PC) and coaching in health dietary practices could effectively reduce the incidence of major depression in older adults, including in older black adults with high BMI. Despite the fact that black participants in the trial carried a greater risk for depression than did their white counterparts – including obesity –the interventions were equally effective in reducing the incidence of major depression from an expected rate of 20-25% over 2 years to only 8-9%, in both black older adults and white older adults. Thus, given the challenges of treating prevalent depression in people living with both depression an DM mellitus, especially in minority populations –where stigma represents an important barrier, it seems particularly important to develop depression prevention strategies that utilize, variously, active coping strategies and life style interventions that promote health and protective factors.

The U.S. Preventive Services Task Force found at least fair evidence that screening adults for depression improves health outcomes and that benefits outweigh harms (B rating), and recommends screening for depression if practices have systems in place to assure accurate diagnosis, effective treatment, and follow-up.113 Based on these recommendations, the Centers for Medicare & Medicaid Services recently determined to cover annual screening for depression for Medicare beneficiaries in primary care settings with staff-assisted depression care supports.

Treatment strategies

In managing DM, clinicians use several clinical data to establish a baseline and treatment goals – e.g. fasting serum glucose level and HgA1C. The same stepped, measurement-based treatment principles can be applied to treating depression: establishing a baseline; setting clinical and functional goal for depression; and assessing patient’s progress accordingly. Figure 2 illustrates one of widely used clinical guidelines for depression treatment.

Figure 2.

Figure 2

Algorithm for Screening and Treating Depression in Primary Care Setting

Various treatment options are available for late-life depression: antidepressant medications, psychotherapy, or a combination. Other options include exercise programs or other life-style modifying interventions and electroconvulsive therapy (ECT). Several meta-analyses showed that combination therapy is more efficacious than monotherapeutic approaches in treating and in preventing relapse.114-117 In a recent meta-analysis of 14 RCTs of intervention for depression among patient with diabetes, all treatments have shown to be effective in reduction of depressive symptoms (g=−0.51, 95% CI: −0.63, −0.39).118 The pooled effect size was large in psychotherapeutic interventions combined with diabetes self-management education (g= −0.58, 95% CI −0.77, −0.39); and pharmacological treatment showed moderate pooled effect size (g=−0.47; 95% CI −0.67 to −0.27).118 Unlike major depression, subsyndromal depressive conditions have a relatively small evidence base regarding treatments; existing data suggest that available therapies have modest effect sizes when compared to usual care or placebo.16,119,120

Targeting interventions for patients with minor and subsyndromal depression may prove useful as both primary and secondary prevention strategies and clinicians should watch such patients carefully because of the high risk of worsening depression, especially if patients have experienced prior episodes of major depression. Psychosocial treatments may be more helpful than medications for older adults with less severe forms of depression.121

Treatment delivery model for comorbid depression and DM

To date, more than 40 randomized controlled trials have established a robust evidence base for an approach called ’collaborative care models (also called integrated care models).122-125 Recently, several trials of collaborative care model have documented the effectiveness of treating comorbid depression and DM125,126 (e.g., PATHWAY126) and comorbid depression, and DM and/or coronary heart disease (TEAMcare127). In such programs, a depression care manager (usually a nurse or clinical social worker) supports medication management prescribed by PCPs through patient education, close and proactive follow-up, and brief, evidence-based psychosocial treatments such as behavioral activation or problem solving treatment in primary care. The care manager may also facilitate referrals to additional services as needed. A psychiatric consultant regularly (usually weekly) reviews all patients in the care manager’s caseload who are not improving as expected and provides focused treatment recommendations to the patient’s PCP.122,128-130

Tools for assessing and tracking depression

Several tools for assessing depression severity are available and can be easily administered by office staff or physicians during a clinic care visit. The most frequently used tool is the 9-item Patient Health Questionnaire (PHQ-9)131, which systematically explores the 9 DSM-IV132 symptoms of major depression. A score of 10 or greater on the PHQ-9 indicates an elevated level of depressive symptomatology and increased risk of clinically significant depression. PHQ-9 have good sensitivity and specificity (both about 88%) for detecting depressive disorders.133,131

Pharmacological management

Approximately 80% of antidepressant prescribed in the U.S. is prescribed in primary care settings. More than 20 antidepressant medications have been approved by the FDA for treatment of depression in older adults. Newer generations of antidepressants such as SSRIs and SNRIs have more tolerable side effect profile compared to tricyclic antidepressants (TCAs).134,135 Comparing second generation antidepressants, studies found no evidence that specific medications are more effective than others.136 Thus, physicians may discuss the choice of medication with patients and their family. Because of the changes in pharmacokinetics (e.g., decreased renal or hepatic clearance), older adults may require lower doses of medications than their younger counterparts. Furthermore, considering high rates of multimorbidity and polypharmacy among older adults, drug-drug interactions are particular concern in this population. On the other hand, medication doses should be titrated upwards to full adult doses in patients who experience partial responses without substantial side effects. Table 2 summarizes common antidepressant medications.

Table 2.

Commonly used antidepressant for late-life depression

Medication Starting
dose
Common Therapeutic Doses Half-life
(hour)
Common side effects Comments
SSRI (Selective serotonin-reuptake inhibitors): Nausea, dyspepsia, anorexia, tremors,
anxiety, insomnia, sexual dysfunction,
jitteriness, hyponatremia
Risk of serotonin syndrome if
combined with certain drugs.
Fluoxetine 5 mg 10 – 40 mg once daily 70-80 Very long acting.
Sertraline 12.5 mg 50 – 200 mg once daily 25-30 Loose stools, diarrhea
Citalopram 10 mg 20 – 40 mg once daily 40-50
Escitalopram 2.5 mg 10– 30 mg once daily 40-50
Paroxetine 10 mg 20 – 50 mg once daily 10-20 Dry mouth, drowsiness, fatigue, weight
gain,
More anticholinergic side effects.
High risk of discontinuation
syndrome if drug stopped abruptly.
SNRIs (Serotonin-norepinephrine reuptake inhibitors) Nausea, drowsiness, fatigue, weight gain,
hyponatremia, diastolic hypertension at
higher doses
Risk of serotonin syndrome if
combined with certain drugs. High
risk of discontinuation syndrome if
medication stopped abruptly.
Venlafaxine XR 37.5 mg 75-225g once daily 5 – 9
Duloxetine 20 mg 20-60mg once daily 8 – 17
Other newer antidepressants
Mirtazapine 15mg 15-45mg at bedtime 20 -40 Sedation, increased appetite / weight gain No sexual side effects.
Bupropion SR 100mg 100-150 mg twice daily 15 No sexual side effects.
Contraindicated in patients with
seizures. Not recommended for
patients with comorbid anxiety.
TCAs (Tricyclic antidepressants) Sedation, weight gain, dry mouth, urinary
retention, constipation, blurry vision,
orthostatic hypotension, impairment of
cardiac conduction
High risk in overdose: 10 days of
typical daily dose may result in a
fatal cardiac arrhythmia. Get baseline
ECG and follow-up ECG at steady
state or if new cardiac symptoms
occur.
Nortriptyline 10mg 50-125mg every night 18–56 Fatigue Therapeutic blood levels range from
50 to 150 ng/mL
Desipramine 25mg 100-200mg once daily 12–28 Insomnia, agitation

Psychological management

Older adults patients with depression tend to prefer psychotherapy over medications.137 Several psychotherapeutic modalities are effective for late-life depression138-140: cognitive behavioral therapy (CBT),121,141 interpersonal therapy (IPT),142 problem solving treatment (PST),143 and Behavioral Activation and Pleasant Activity Scheduling (BA).144-146 A recent meta-analysis of 44 studies comparing psychotherapies and control conditions,140 concluded that the overall effect size of psychotherapy over control group were g = 0.64 (95% CI: 0.47-0.80). Although such treatments can be effectively provided to older adults in primary care,147,148 they are not widely available in most primary care settings today and we encourage clinicians to develop relationships with mental health specialists who can offer such treatments or to train a staff member in the clinic to provide evidence-based brief psychotherapies. Table 3 summarizes brief- and evidence –based psychotherapeutic approaches that can be easily administered in the primary care context and by nurses, social workers, or other licensed psychotherapists.

Table 3. Efficacious non-pharmacologic treatments for late-life depression.

Treatment type Studies Level of evidence Comments
Cognitive Behavioral Therapy
(CBT)
Gould et al 2012159 Meta-analysis of RCTs CBT significantly more efficacious at reducing depressive symptoms
Combination with pharmacotherapy more efficacious than CBT alone

Cuijpers et al 2014140 Meta-analysis of RCTs Older adults populations studies

Behavior activation (BA) Cuijpers et al 2007160 Meta-analysis of RCTs Mixed population studies
Effect is weaker in older adults

Ekers et al, 2014161 Meta-analysis of RCTs Mixed population studies

Samad et al162 Meta-analysis of RCTs Older adults populations studies

Problem solving therapy (PST) Bell et al 2009163 Meta-analysis of RCTs Mixed population studies

Interpersonal psychotherapy (IPT) Beekman et al 2006164 Pragmatic RCT Older adults populations studies

Bohlmeijer et al 2003165 Meta-analysis of RCTs Older adults populations studies

Reminiscence (life review) Pinquart & Forstmeier166 Meta-analysis of RCTs Efficacious for broad range of outcomes, and therapeutic as
well as preventive effects are similar to those observed in
other frequently used interventions.

Electroconvulsive Treatment (ECT)

ECT is an important and viable treatment option for severely depressed older adults. ECT should be strongly considered for patients who have severe, persistent depression that does not respond to several trials of antidepressant medications or psychotherapy and/or puts patient at high risk of harm (e.g. severe weight loss, malnutrition, refusal of food, suicidal ideation). Poor tolerance or limited response to medications and a history of successful treatment with ECT are also indications for ECT. Rates of ECT use in depressed adults vary substantially.149,150 Older adults are more likely to receive ECT than younger adults, African Americans are less likely to receive ECT than Whites and individuals with poor health insurance or living in rural areas are also less likely to receive ECT.149

Summary/Discussion

DM and depression is frequently comorbid in older adult patients. Considering the negative synergistic effects on range of health outcomes resulted by comorbid depression and DM, prevention and early treatment of comorbid depression are a critical component of successful health management in older adult patients with DM.

Key Points.

  1. Depression is highly prevalent in the general population and increases the risk for type 2 DM 2.

  2. Comorbid depression and DM is associated negative health outcomes, such as accelerated cognitive decline and increased mortality.

  3. Depression impinges the patient and the family caregiver’s ability to effectively manage DM, decreases adherence to treatment, and undermines successful physician-patient relationship

  4. Effective models for treating comorbid depression and DM exists and some components of these models are implementable in individual clinics.

Footnotes

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Contributor Information

Mijung Park, Department of Health and Community Systems, University of Pittsburgh, School of Nursing, 3500 Victoria Street, 421 Victoria building, Pittsburgh, PA 15213.

Charles F. Reynolds, III, NIMH Center of Excellence in Late Life Depression Prevention and Treatment, Hartford Center of Excellence in Geriatric Psychiatry, and Aging Institute of UPMC Senior Services and the University of Pittsburgh, 3811 O’Hara Street, Pittsburgh, PA 15213-2582, Telephone: 412-246-5991, ReynoldsCF@upmc.edu.

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