The case presented here reflects the characteristic psychiatric symptoms of vascular depression and its impact on daily life. Below, we discuss the epidemiology, clinical features, and radiographic markers of vascular depression as well as how it may relate to risk for suicide in later life. Our intention for this summary is to help illustrate the clinical features of age-related vascular disease and how it affects depression and cognition. A range of treatment strategies are then described that may be beneficial for vascular depression and may provide insights on innovations in the approach to this condition.
Age-related vascular changes have long been observed to be related to depressive syndromes in later life. The insidious role of subcortical microvascular disease was recognized initially as a critical factor in the development of neurocognitive symptoms by Binswanger in 1894 (1), but the prominent role of depressive features in this condition did not become a major focus of study until many decades later (2). In the late 1990s, investigators studying late-life mood disorders proposed the concept of “vascular depression” as a research subtype of late-life unipolar depression (3). Two pivotal papers that spurred further studies of vascular depression focused, respectively, on clinically defined and MRI-defined criteria to operationalize its features (4, 5). Subsequent research testing the “vascular depression hypothesis” (6) leveraged improvements in neuroimaging methods, and the capacity of MRI-based diffusion tensor imaging to examine white matter integrity has allowed exploration of the relationship between damage to white matter and development and maintenance of depressive symptoms (7). Despite a large volume of research, vascular depression is not represented in the DSM-5 classification, an omission that may represent a missed opportunity to increase clinical recognition and clinically informed systematic study.
“Late-life depression” is diagnosed when a major depressive episode occurs in older adults, (3, 8). This is a heterogeneous group, including individuals with “early-onset” depression that arose in adolescence or early adulthood and those with “late-onset” depression, where the initial depressive episode occurs after ages 50–55. Like other variants of late-life depression, vascular depression has unique characteristics that distinguish it from early-onset depression. Notably, vascular depression frequently develops after ages 60–65 in the absence of a prior history of affective illness, and there is often no family history of affective disorder. Depression related to vascular aging does not follow a path of clearly delineated episodes with recovery, in the way early-onset depressive disorders do. In vascular depression, there is often a more persistent character to the mood and cognitive symptoms that may fluctuate over time, without discrete episodes. This insidious and often chronic course tends to delay the recognition and necessary assessments, sometimes considerably. Patients with vascular depression also may have less insight into their mood symptoms and may be less aware of and less comfortable with mental health services. A recent consensus report on vascular depression specified key symptoms of low energy, lack of insight, anhedonia, deficits in self-initiation, psychomotor retardation, and reduced processing speed (9). As in the case of Mr. A in the vignette, patients with vascular depression may not perceive themselves to have a depressive disorder. Initial evaluation often occurs at the insistence of family members who observe a change in daily function and perhaps an increase in irritability or apathy.
Epidemiology
Vascular depression is not a distinct diagnosis in DSM-5, and it has different operational definitions in various classifications, leading to variance among estimates of its frequency. One U.S. study (10) used a national probability sample of 16,423 adults to examine the population prevalence using survey assessments. Vascular depression was defined by applying DSM-IV criteria for an episode of major depressive disorder within the preceding 12 months in adults age 50 or older with cardiovascular or cerebrovascular disease or major cardiovascular risk factors. The prevalence of major depression without vascular disease was 12.2%, and the population prevalence of vascular depression was 3.4%. Among respondents affected with depression, more than one-fifth (22.1%) of those with a lifetime history of major depressive episodes met study criteria for vascular depression. These rates were higher than those found in a Korean two-stage epidemiological study of older adults (age 65 or older) using an MRI-based definition of vascular depression (11). In that population-based survey of 783 participants, the prevalence of major depression without MRI-defined vascular disease was 2.36%, and the prevalence of major depression with MRI-defined vascular disease was 2.40%. Notably, rates of MRI-defined vascular depression increased with advanced age, so in the cohort age 75 or older with a diagnosis of major depression, all patients met radiographic criteria for vascular depression.
Cognitive Features Affecting Clinical Management
Vascular depression is often characterized as a disorder of executive dysfunction, including difficulty with task completion and decision making, both of which may increase the likelihood of experiencing irritability and social withdrawal. Additional cognitive features of vascular depression include slowed speed of information processing and impairments in concentration and attention. It is not uncommon for these cognitive complaints, rather than depressive symptoms, to be the trigger for a clinical evaluation. Given the common nature of cognitive concerns in older adults, patients and families may be more amenable to engaging in the assessment process when discussing problems with attention, concentration, reasoning, and memory. In contrast, discussing one’s mood or emotions may be more difficult for an older patient. When the treatment plan and assessment are couched in seeking to improve attention, concentration, planning, and engagement in life, the therapeutic relationship can be enhanced substantially. Moreover, an awareness of the type of cognitive deficiencies associated with vascular depression can help in finding ways to increase social engagement and understand some of the limitations that patients may be experiencing. This approach is at the heart of problem-solving therapy, a form of cognitive-behavioral therapy (CBT) that has been adapted for older depressed patients with executive impairment (12, 13). Given the predominance of difficulties with psychomotor slowing, poor initiation of thought and movement, and reduced processing speed, as well as relative impairment in insight into mood symptoms, it is not uncommon for the depressive symptoms associated with vascular depression to fall short of the DSM criteria for major depressive disorder. However, in older adults, even subthreshold depressive disorders can have a substantial impact on functional status, quality of life, and mortality (14).
Along these lines, it has also been recognized that depressive symptoms may at times be a less prominent component within vascular depression, which may be characterized as a “depression-executive dysfunction syndrome,” as proposed by Alexopoulos and colleagues (15). This conceptualization focuses on executive and information processing deficits often observed in late-life depression, with an emphasis on these deficits in the diagnostic evaluation. The depression-executive dysfunction syndrome is associated with a range of clinical symptoms, including reduced fluency, impaired visual naming, psychomotor retardation, loss of interest in activities, and paranoia. In contrast, other depressive symptoms were comparatively milder. Notably, among depressed patients without the depression-executive dysfunction syndrome, depressive symptoms appeared to have less of a disabling effect than in patients with executive dysfunction. Consequently, vascular depression and depression-executive dysfunction syndrome may be conceptualized along the same spectrum of illness, with cognitive features being particularly pronounced in the latter. Depending on methods used for diagnostic evaluation, many patients may meet criteria for both disorders, reflecting the considerable clinical and diagnostic overlap between the two.
Given the prominent cognitive features in both depression-executive dysfunction syndrome and vascular depression, it is unsurprising that depressed elders are at increased risk for progression to a major neurocognitive disorder. Multiple studies have examined populations with late-life depression (of which vascular depression is one subtype) and demonstrated an increased longitudinal risk for dementia. A meta-analysis examining 23 population-based prospective studies found that late-life depression was associated with a twofold increased risk for dementia of any type and that the increased risk for vascular dementia exceeded that for dementia of the Alzheimer’s type (16). A parallel longitudinal study of late-life depression further demonstrated that white matter hyperintensity volume was independently associated with time to dementia (17).
This complex interplay between late-life mood symptoms and cognitive deficits has been difficult to capture within diagnostic nosology, particularly if both are related to cerebrovascular pathology. However, the new criteria for the cognitive disorders in DSM-5, which include the classification of “mild” neurocognitive disorder, now permit the specification of cognitive symptoms as being due to vascular disease when they have passed the threshold of severity to qualify for mild neurocognitive disorder, in the same manner that “mild cognitive impairment” was previously employed to represent the transition phase of risk for a dementia syndrome (18). Given that cognitive symptoms other than concentration deficits are not included in the DSM-5 diagnostic criteria for major depressive disorder, we propose that mood and cognitive symptoms be evaluated and diagnosed separately according to the respective criteria. For example, if criteria are met for both mild vascular neurocognitive disorder and a DSM-5 mood disorder diagnosis such as major depressive disorder, then both disorders should be recognized, for the greatest diagnostic clarity.
Clinical Assessment and Radiographic Markers
The assessment for vascular depression ideally includes not only a review of vascular risk factors and history of vascular disease but also evidence demonstrating subcortical white matter disease. Such findings are observed on an MRI brain scan as periventricular or deep white matter hyperintensities. In the clinical setting, it is not uncommon for these findings to be noted within the narrative text of the radiology report, with the overall impression often reading as “unremarkable for age.” This may lead to a reduced awareness, clinically, of the potential relationships of these findings with the clinical syndrome. For example, one study of healthy community-dwelling adults ages 44–48 reported that white matter hyperintensities were found in 50.9% of individuals (7). However, in most cases the severity of white matter hyperintensities is mild, and MRI-based definitions of vascular depression require a minimum threshold of white matter hyperintensity severity for diagnosis (19).
Given the overwhelming frequency with which clinical radiologists see white matter hyperintensities, it may be difficult for them to raise clinical concerns unless the white matter changes are particularly severe or there is a clinical background describing cognitive changes or motor impairment. The burden may fall on the psychiatrist to bring together imaging information with the clinical features of vascular depression to help educate individual patients as to the range of symptoms experienced, their underlying causes, and the rationale for treatment. Despite the lack of clarity in general clinical practice regarding the relevance of white matter hyperintensities on MRI scans, numerous neuroimaging studies have demonstrated that a greater burden of white matter hyperintensities correlates with poor treatment response (9, 20). Consequently, the best approach for incorporating white matter hyperintensities into clinical decision making may be to consider the presence of white matter hyperintensities as a risk factor for symptoms of vascular depression as well as potentially a prognostic factor when evidence of particularly severe white matter hyperintensities is observed in the context of depression. However, the ability to quantify their precise impact on risk and outcome remains to be clarified in future research, given the multiple factors that interact in late-life disorders. Data from relatively new techniques, such as diffusion tensor imaging, which utilizes fractional anisotropy as a more sensitive measure of white matter degradation, may offer new ways to better understand white matter changes in relation to depression, although studies to date remain mixed.
Treatment Issues
Suicide Risk
As suicide risk increases in later life, it is important to consider how the presence of vascular depression may affect this risk. While there is no clear evidence to date linking vascular depression specifically to suicide mortality, there is evidence that all-cause mortality is greater in persons with vascular depression. The higher mortality risk has been attributed to accelerated frailty, general morbidity, and cardiac death (18, 21). Recent mortality data from the U.S. Census Bureau highlight a concern about increasing “deaths of despair” in middle-age individuals, relating to both suicide and “poisonings” associated with complaints of poor health (21, 22). A study examining suicide risk factors using data from the Veterans Health Administration (VHA) system (23) observed that chronic pain, sleep impairment, and traumatic brain injury were associated with a greater suicide risk, attesting to the impact of medical comorbidity. While the study did not directly compare risk between younger and older veterans, the impact of medical comorbidity is an important addressable risk factor that is highly relevant to older adults with depression. A separate VHA study similarly observed that older veterans who died by suicide were more likely to have had medical health problems (24). It further noted that nearly all the elderly decedents used firearms. A noteworthy study used data from the National Violent Death Reporting System for the years 2005–2014 to identify 16,924 suicide decedents over age 65 (25). The study noted that “physical health problems were recorded as a suicide precipitant for 50% of the older decedents.” For those decedents who disclosed intent, concerns centered on pain, cancer, fear of dementia-related decline, fear of burdening others, unwillingness to live in a nursing home, and loss of independence. Finally, the cognitive symptoms of late-life depression also increase risk. Older depressed patients with executive impairment such as poor cognitive control are at increased risk for suicide attempt. Of note, problem-solving therapy can reduce suicidal ideation in older depressed adults with executive dysfunction (13).
Treatment Issues
Management
Vascular depression not only increases the likelihood of poor response to antidepressant treatment and persistent depressive symptoms but also may contribute to poor self-management of medical comorbidities and greater impairments in daily function (26, 27). There may also be cumulative disability associated with impaired sleep, chronic pain, and use of analgesic medications, as well as complex conditions such as peripheral neuropathy and impaired mobility, all of which add to the likelihood of poor outcomes in vascular depression. Response to treatment is significantly attenuated in the context of vascular depression (9), so typical treatment strategies are often unsatisfactory and do not result in full remission of depressive symptoms. For example, one of the few randomized controlled pharmacological treatment trials of vascular depression observed the low remission rate of 33% (28), even with careful titration of the selective serotonin reuptake inhibitor (SSRI) sertraline over a 12-week period. The study highlighted the interrelationships between white matter disease and depression outcome by demonstrating that both pretreatment neuropsychological function and severity of white matter hyperintensities independently predicted treatment response over the course of the trial. Despite the poor response in this trial, there is still value in antidepressant therapy for this patient population, as even a small reduction in symptoms may enhance quality of life. Furthermore, there is intriguing evidence that SSRI use may be associated with improved neural resilience in relevant brain regions, such as the hippocampus (29, 30), as well as novel evidence of a potential reduction in amyloid production, which may have relevance in reducing cognitive decline (31).
The poor response to antidepressants in vascular depression has been well documented (9). Yet there may be potential insights from studies suggesting that cognition may be targeted by antidepressants independently of mood symptoms in the context of major depression, although vascular depression has not specifically been studied (32). Among these studies, several have reported that vortioxetine, a multimodal serotonergic compound, was associated with improvement in executive function and other cognitive domains (33–35). However, while some of these studies included older adults, the safety profile for elderly adults with vascular depression has not yet been clarified. Thus, while new pharmacologic strategies offer hope for the future, an approach that incorporates wellness and general health maintenance will likely remain essential to achieving optimal outcomes. This approach includes attending to regular sleep, exercise, healthy diet, and medication adherence to minimize the impact of hypercholesterolemia, hypertension, and glucose intolerance.
Addressing sleep may offer an important opportunity to provide some relief for older adults with depression early in the course of treatment while waiting for an eventual response to therapy or antidepressant treatment. Kay et al. (36) observed that impaired sleep may increase risk for suicidal behavior in middle-aged and older adults even after adjusting for other risk factors. Furthermore, the Established Populations for Epidemiologic Studies of the Elderly study of 14,456 older adults in the community demonstrated that poor subjective sleep quality was associated with an increase in risk of death by suicide over a 10-year period. Because of concerns regarding side effects associated with hypnotic use in the elderly as well as a potential for an independent suicide risk incurred by hypnotic medications (37), management should focus on lifestyle and general health issues while attending to risk of sleep disorders common in later life, such as sleep apnea. Sleep impairment may be related to reduced endogenous melatonin production with increasing age. Furthermore, given emerging evidence that melatonin may be advantageous for age-related brain changes, melatonin supplementation may be a useful strategy to reduce symptom burden in the context of vascular depression (38). A systematic review that synthesized 16 studies of the use of melatonin in older adults noted that low doses are recommended; dosing at no more than 1–2 mg of immediate-release melatonin is optimal, and it should be administered approximately 1 hour before bedtime for disturbed sleep in this population (39).
Given high rates of polypharmacy and limited efficacy of psychotropic treatments for lowering depression burden in vascular depression, psychotherapeutic approaches to treatment have also been explored. To address sleep disturbance, CBT for insomnia may be a useful tool. While CBT for insomnia was initially demonstrated as efficacious for primary insomnia (40), it is also effective when the insomnia is comorbid with a medical or psychiatric condition (41). Current psychotherapies often used in conjunction with other treatments to manage vascular depression have been developed to address symptoms that are more often associated with late-life onset and cognitive deficits. For example, executive dysfunction, which includes impairment in task completion and difficulty with decision making, may be addressed with skills developed through problem-solving therapy or problem adaptation therapy (42), a variant of problem-focused psychotherapy. Problem adaptation therapy is consistent with the process model of emotion regulation (12, 43), but it uses an adapted approach to these emotion and behavioral psychotherapies through distinct features, including home delivery, addressing compensatory strategies, environmental adaptations, and caregiver participation. Other related strategies may partly circumvent cognitive skills and rely on behavioral strategies and interpersonal therapy to help boost mood through caregiver engagement. Evidence-based psychotherapies have been shown to be superior to other strategies that have been used with older adults in the past, such as supportive therapy, which relies solely on empathic support without specific methods to address the needs of patients with late-onset depression, such as vascular depression. Psychotherapies such as problem adaptation therapy and problem-solving therapy as well as other behavioral and interpersonal psychotherapeutic strategies aimed at improving sleep hygiene or behavioral activation can be a flexible component to long-term treatment plans.
An additional treatment option that may bear further exploration for patients with refractory vascular depression is repetitive transcranial magnetic stimulation (rTMS). A study by Jorge and colleagues (44) examined rTMS for patients with vascular depression who had been unresponsive to at least one course of treatment with an antidepressant medication. Participants received active or sham rTMS to the left dorsolateral prefrontal cortex. While there was a significant improvement in symptoms in the active treatment group compared with the sham treatment group, the depression remission rate remained modest at 27% in the active treatment group. However, it is notable that remission was achieved in patients previously unresponsive to antidepressant medication. The study also found that improvement in depressive symptoms was negatively correlated with age, which is consistent with other treatment studies of vascular depression. Additionally, for patients with treatment-resistant or severe depression, the use of ECT is an important means of achieving remission (45). A recent study examining vascular risk factors in elderly inpatients receiving antidepressant management or ECT (46) found that ECT was significantly more effective than medications in achieving remission in elderly inpatients with depression. Furthermore, remission from depression was not influenced by the vascular risk factor burden.
Summary: Clinical Pearls
•
The presenting features of vascular depression may involve poor motivation and slowed information processing as opposed to traditional mood complaints.
•
Although there is not currently an indication to obtain neuroimaging, when records are available, the assessment includes reviewing MRI reports for findings of deep white matter and periventricular hyperintensities as well as subcortical gray matter lesions.
•
Treatment planning should recognize that there may be a modest response to antidepressants and that other treatments, such as problem-solving therapy, may offer additional benefit.
•
Sleep hygiene may be important, and the patient may benefit from treatment with low-dose melatonin if indicated.
•
Management should include active support for the patient to reduce obesity, hypertension, hyperlipidemia, and glucose intolerance and to engage in appropriate dietary and exercise strategies to reduce vascular risk.
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From the Center for Cognitive Medicine, Department of Psychiatry, Vanderbilt University Medical Center, Nashville, Tenn.; the Geriatric Research, Education, and Clinical Center, Department of Veterans Affairs Medical Center, Tennessee Valley Healthcare System, Nashville; the Center of Innovation on Disability and Rehabilitation Research, VA Health Services Research and Development Service, James A. Haley Veterans Hospital, Tampa, Fla.; the Department of Psychiatry and Behavioral Sciences and the Department of Psychology, University of South Florida, Tampa; and the Department of Psychiatry, University of Connecticut Health Center, Farmington.
From the Center for Cognitive Medicine, Department of Psychiatry, Vanderbilt University Medical Center, Nashville, Tenn.; the Geriatric Research, Education, and Clinical Center, Department of Veterans Affairs Medical Center, Tennessee Valley Healthcare System, Nashville; the Center of Innovation on Disability and Rehabilitation Research, VA Health Services Research and Development Service, James A. Haley Veterans Hospital, Tampa, Fla.; the Department of Psychiatry and Behavioral Sciences and the Department of Psychology, University of South Florida, Tampa; and the Department of Psychiatry, University of Connecticut Health Center, Farmington.
From the Center for Cognitive Medicine, Department of Psychiatry, Vanderbilt University Medical Center, Nashville, Tenn.; the Geriatric Research, Education, and Clinical Center, Department of Veterans Affairs Medical Center, Tennessee Valley Healthcare System, Nashville; the Center of Innovation on Disability and Rehabilitation Research, VA Health Services Research and Development Service, James A. Haley Veterans Hospital, Tampa, Fla.; the Department of Psychiatry and Behavioral Sciences and the Department of Psychology, University of South Florida, Tampa; and the Department of Psychiatry, University of Connecticut Health Center, Farmington.
From the Center for Cognitive Medicine, Department of Psychiatry, Vanderbilt University Medical Center, Nashville, Tenn.; the Geriatric Research, Education, and Clinical Center, Department of Veterans Affairs Medical Center, Tennessee Valley Healthcare System, Nashville; the Center of Innovation on Disability and Rehabilitation Research, VA Health Services Research and Development Service, James A. Haley Veterans Hospital, Tampa, Fla.; the Department of Psychiatry and Behavioral Sciences and the Department of Psychology, University of South Florida, Tampa; and the Department of Psychiatry, University of Connecticut Health Center, Farmington.
National Institute of Mental Health10.13039/100000025: R01 MH102246 PI: Taylor
Supported by NIMH grant R01 MH102246.The authors report no financial relationships with commercial interests.
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