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  <front>
    <journal-meta>
      <journal-id journal-id-type="publisher-id">JDT</journal-id>
      <journal-title-group>
        <journal-title>Journal of Depression And Therapy</journal-title>
      </journal-title-group>
      <issn pub-type="epub">2476-1710</issn>
      <publisher>
        <publisher-name>Open Access Pub</publisher-name>
        <publisher-loc>United States</publisher-loc>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="publisher-id">JDT-16-1260</article-id>
      <article-id pub-id-type="doi">10.14302/issn.2476-1710.jdt-16-1260</article-id>
      <article-categories>
        <subj-group>
          <subject>editorial</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Depression and Dementia</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Ladislav</surname>
            <given-names>Volicer</given-names>
          </name>
          <xref ref-type="aff" rid="idm1815606924">1</xref>
          <xref ref-type="aff" rid="idm1815608364">2</xref>
          <xref ref-type="aff" rid="idm1815609012">*</xref>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Hana</surname>
            <given-names>Vaňková</given-names>
          </name>
          <xref ref-type="aff" rid="idm1815606924">1</xref>
        </contrib>
      </contrib-group>
      <aff id="idm1815606924">
        <label>1</label>
        <addr-line>3rd Medical Faculty, Charles University, Prague, Czech Republic and</addr-line>
      </aff>
      <aff id="idm1815608364">
        <label>2</label>
        <addr-line>School of Aging Studies, University of South Florida, Tampa, FL, USA</addr-line>
      </aff>
      <aff id="idm1815609012">
        <label>*</label>
        <addr-line>corresponding author</addr-line>
      </aff>
      <contrib-group>
        <contrib contrib-type="editor">
          <name>
            <surname>Kwok</surname>
            <given-names>Lai Yuk Ching</given-names>
          </name>
          <xref ref-type="aff" rid="idm1815467020">1</xref>
        </contrib>
      </contrib-group>
      <aff id="idm1815467020">
        <label>1</label>
        <addr-line>Associate Professor, Department of Applied Social Studies, City University of Hong Kong</addr-line>
      </aff>
      <author-notes>
        <corresp>
  Ladislav Volicer, <addr-line>School of Aging Studies, University of South Florida, Tampa, FL, USA.</addr-line> Email: <email>lvolicer@usf.edu</email></corresp>
        <fn fn-type="conflict" id="idm1815875108">
          <p>The authors have declared that no competing interests exist.</p>
        </fn>
      </author-notes>
      <pub-date pub-type="epub" iso-8601-date="2016-12-12">
        <day>12</day>
        <month>12</month>
        <year>2016</year>
      </pub-date>
      <volume>1</volume>
      <issue>2</issue>
      <fpage>1</fpage>
      <lpage>7</lpage>
      <history>
        <date date-type="received">
          <day>14</day>
          <month>08</month>
          <year>2016</year>
        </date>
        <date date-type="accepted">
          <day>17</day>
          <month>11</month>
          <year>2016</year>
        </date>
        <date date-type="online">
          <day>12</day>
          <month>12</month>
          <year>2016</year>
        </date>
      </history>
      <permissions>
        <copyright-statement>© </copyright-statement>
        <copyright-year>2016</copyright-year>
        <copyright-holder>Ladislav Volicer, et al.</copyright-holder>
        <license xlink:href="http://creativecommons.org/licenses/by/4.0/" xlink:type="simple">
          <license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</license-p>
        </license>
      </permissions>
      <self-uri xlink:href="http://openaccesspub.org/jdt/article/390">This article is available from http://openaccesspub.org/jdt/article/390</self-uri>
      <abstract>
        <p>Relationship between dementia is very complex and individual. There are some pathogenetic processes that may be common to both conditions: neurotransmitter deficits, vascular changes and beta amyloid deposits. Presence of depression in persons with dementia have serious consequences on progression of dementia, quality of life and behavioral symptoms of dementia. Therefore, it is important to treat effectively even minor depressive symptoms.</p>
      </abstract>
      <kwd-group>
        <kwd>Depression</kwd>
        <kwd>dementia</kwd>
        <kwd>behavior</kwd>
        <kwd>caregivers</kwd>
      </kwd-group>
      <counts>
        <fig-count count="0"/>
        <table-count count="0"/>
        <page-count count="7"/>
      </counts>
    </article-meta>
  </front>
  <body>
    <sec id="idm1815470836" sec-type="intro">
      <title>Introduction</title>
      <p>Depression is the most common psychiatric condition in people with dementia. It occurs already in 16.9% of people with “cognitive impairment no dementia” (CIND, a clinical syndrome consisting of measurable decline in memory / cognition with little effect on day-to-day functioning that does not meet criteria for dementia listed by DSM-IVTR) <xref ref-type="bibr" rid="ridm1816294620">1</xref>. In people with mild cognitive impairment (MCI), prevalence of depression is 44% in hospital-based studies and 16% in population-based studies <xref ref-type="bibr" rid="ridm1816359724">2</xref>. Prevalence of depression increases with severity of depression, reaching 42.5% in institutionalized people with severe dementia <xref ref-type="bibr" rid="ridm1816370420">3</xref>. Depression is often underdiagnosed in people with cognitive impairment. Using Geriatric Depression Scale in people with MCI or moderate dementia to compare different sources of depression diagnosis, it was found that only 11% of people had clinical diagnosis, while information from collateral sources indicated that 49% of them were depressed <xref ref-type="bibr" rid="ridm1816159196">4</xref>.</p>
      <sec id="idm1815472132">
        <title>Similarities of Pathogeneses in Depression and Dementia.</title>
        <p>The high prevalence of depression in people with cognitive impairment could be due to some similarities of pathological processes between depression and dementia. These similarities include changes in neurotransmitters, especially serotonin, brain vascular changes and beta amyloid deposits as will be explained in the following paragraphs.</p>
      </sec>
      <sec id="idm1815470548">
        <title>Neurotransmitters.</title>
        <p>Alzheimer’s disease causes serotoninergic and noradrenergic denervation <xref ref-type="bibr" rid="ridm1816164380">5</xref><xref ref-type="bibr" rid="ridm1816161500">6</xref> and loss of serotonin receptors <xref ref-type="bibr" rid="ridm1816145988">7</xref>. Serotonin is involved in sexual behavior, appetite and aggression and together with norepinephrine in mood state, irritability and thought processes. High prevalence of depression in individuals with Alzheimer’s disease can be expected because of these monoaminergic deficits. The importance of serotonin for depression is supported by the most effective medications which are selective serotonin reuptake inhibitors (SSRIs). Treatment with antidepressants that potentiate the effect of serotonin may be similar to treatment with cholinesterase inhibitors that potentiate the effect of acetylcholine.</p>
      </sec>
      <sec id="idm1815469540">
        <title>Vascular Changes</title>
        <p>Vascular etiology of depression was proposed already 20 years ago <xref ref-type="bibr" rid="ridm1816141596">8</xref>. Recent studies found that white matter hyperintensities increase the risk of depression development 8.1 times during 3-year follow up study <xref ref-type="bibr" rid="ridm1816136604">9</xref> and it is proposed that the damage of brain structure reflected by these hyperintensities, indicating reduced white matter microstructural integrity, is a pathophysiological mechanism of late-life major depressive disorder <xref ref-type="bibr" rid="ridm1816132860">10</xref>. Presence of white matter hyperintensities also predicted development of functional disability in depressed individuals <xref ref-type="bibr" rid="ridm1816124940">11</xref>. Vascular etiology of depression is supported by association of depression with hypertension in a large epidemiological study <xref ref-type="bibr" rid="ridm1816119540">12</xref>. White matter hyperintensities are also hallmarks of one type of vascular dementia – Binswanger disease <xref ref-type="bibr" rid="ridm1816119180">13</xref><xref ref-type="bibr" rid="ridm1816112916">14</xref>.</p>
      </sec>
      <sec id="idm1815469252">
        <title>Beta Amyloid Deposits. </title>
        <p>Availability of detection of beta amyloid levels in the brain in vivo, opened another avenue for investigation of relationship between Alzheimer’s disease and depression. A recent review reported that out of 19 studies investigating beta amyloid levels in people with depression, 15 found significant differences between depressed and non-depressed older adults <xref ref-type="bibr" rid="ridm1816127820">15</xref>. Another more recent study also found correlation between depressive symptoms and mean cortical beta amyloid burden in older cognitively normal persons <xref ref-type="bibr" rid="ridm1816101636">16</xref>. A longitudinal study found that elevated beta amyloid levels are associated with a 4.5-fold increase likelihood of developing significant depressive symptoms during the 54-months follow-up <xref ref-type="bibr" rid="ridm1816097748">17</xref>. Therefore, it was proposed that late-life depression could be considered as predementia state and the persons with this condition could be candidates for participation in anti-amyloid drug trials <xref ref-type="bibr" rid="ridm1816096452">18</xref>. However, beta amyloid may not be always involved because one study found that people with subjective and mild cognitive impairments and depressive symptoms did not have pathological and biochemical biomarkers of Alzheimer’s disease <xref ref-type="bibr" rid="ridm1816091844">19</xref>.</p>
      </sec>
      <sec id="idm1815469108">
        <title>Consequences of Depression in People with Dementia</title>
        <p>Unrecognized and/or untreated depression has serious effects on people with dementia that include increased dementia progression, decreased quality of life and increased risk of developing behavioral symptoms of dementia. Depression in patients also increases burden of their caregivers. Unfortunately, depression in people with dementia is often unrecognized and even when it is recognized and treated the treatment is not always effective. Using Minimum Data Set (MDS) information, clinical and MDS-based diagnoses of depression were compared in 1851 residents of 8 Dutch nursing homes 3. A clinical diagnosis of depression was present only in 14.4% of residents while 42.5% had an MDS diagnosis. This difference was mainly due to decreased prevalence of clinical diagnosis of depression in persons with more advanced dementia. Antidepressants were used only in 33.9% of residents with an MDS diagnosis of severe depression and symptoms of depression were present even in residents treated with antidepressants. Antidepressants were also used less often in older residents with a clinical diagnosis of depression. There is some evidence that the use of antidepressants in persons with dementia is increasing <xref ref-type="bibr" rid="ridm1816048404">20</xref> but it is not clear if the treatment is completely effective.</p>
      </sec>
      <sec id="idm1815469396">
        <title>Dementia Progression. </title>
        <p>There is an evidence that treatment of depression in people with dementia delays progression of dementia, while untreated depression increases the rate of dementia progression. A study comparing 13 hospitalized older adults with dementia syndrome of depression (DSD) with 14 adults with Alzheimer's dementia with a concurrent major depression on a battery of neuropsychological tests found that successful treatment of depression delayed progression of dementia for up to 3 years <xref ref-type="bibr" rid="ridm1816047036">21</xref>. Another study, however, found that successful treatment of depression improved only processing speed and attention and that development of depression exacerbated cognitive decline in dementia-free persons 60 years old and older <xref ref-type="bibr" rid="ridm1816057332">22</xref>. A three year follow-up study found that 43% of patients with depression and cognitive impairment, whose cognitive impairment improved by antidepressant treatment, and therefore could be considered having reversible dementia, eventually developed irreversible dementia <xref ref-type="bibr" rid="ridm1816054236">23</xref>. Thirteen-year follow-up study found that the effect on dementia progression differ according to the type of depression. Surprisingly, persons who had initially nondysphoric depression were more cognitively impaired, and impaired in basic and instrumental activity of daily living at the follow-up than persons who had initially major depression <xref ref-type="bibr" rid="ridm1816050564">24</xref>. This may be partially explained by 8-10% of persons with subthreshold depression who develop major depression per year, and by a low remission rate <xref ref-type="bibr" rid="ridm1816030276">25</xref>. Depressive symptoms also increase risk of progression of mild cognitive impairment into dementia <xref ref-type="bibr" rid="ridm1816024660">26</xref>.</p>
      </sec>
      <sec id="idm1815470116">
        <title>Quality of Life. </title>
        <p>Presence of depression decreases significantly quality of life of elderly persons even when the depression is minor <xref ref-type="bibr" rid="ridm1816037764">27</xref>. Depression is also associated with disability <xref ref-type="bibr" rid="ridm1816035100">28</xref>, decreased active life expectancy <xref ref-type="bibr" rid="ridm1816015468">29</xref>, worsened outcomes of comorbid chronic medical diseases <xref ref-type="bibr" rid="ridm1816013164">30</xref>, and may even cause nocturia <xref ref-type="bibr" rid="ridm1816008412">31</xref>. Geriatric depression amplifies physical/somatic complaints and pain, increases outpatient visits, prescription medications, risk of hip fracture due to falls, and admission to nursing homes. Depressive symptoms also increase mortality in both the whole community based sample of older persons, and in persons with incident Alzheimer’s disease <xref ref-type="bibr" rid="ridm1816003516">32</xref>.</p>
      </sec>
      <sec id="idm1815469972">
        <title>Behavioral Symptoms of Dementia. </title>
        <p>The most common behavioral symptoms are agitation and rejection of care, that may result in reactive aggression. Agitation may be defined as a motor restlessness, heightened responsivity to stimuli, irritability, inappropriate and/or purposeless verbal or motor activity, decreased sleep, with fluctuation of symptoms over time <xref ref-type="bibr" rid="ridm1816000060">33</xref> (p.6). It is often caused by boredom and is ameliorated by meaningful activities <xref ref-type="bibr" rid="ridm1815998836">34</xref>. In people with dementia who were depressed there was a significant correlation between depression and agitation scores. Depression scores increased in residents whose agitation worsened and decreased in residents whose agitation improved <xref ref-type="bibr" rid="ridm1815994588">35</xref>. These results indicate that depression is an important factor associated with agitation in nursing home residents with dementia.</p>
        <p>Rejection of care is a very common and the most disturbing behavioral symptom of dementia <xref ref-type="bibr" rid="ridm1815989980">36</xref>. It is caused mostly by the lack of understanding by persons with dementia of intentions of a care provider. The persons with dementia defend themselves against unwanted attention and this defense may escalate into combativeness and reactive aggression (called behaviors directed towards others in MDS 3.0). Depression is the second most important factor for development of rejection of care which may result in behaviors directed towards others <xref ref-type="bibr" rid="ridm1815987964">37</xref>. Depression was also found to be the most important factor increasing risk for development of physical and verbal aggression in 3 national samples of nursing home residents (&gt;500,000 total) in &gt;9,000 facilities <xref ref-type="bibr" rid="ridm1815976572">38</xref>. Another study found that physically aggressive behavior is associated with depression, male gender, impairment in ADLs after adjustment for delusions, hallucinations, sleep disturbances and severity of dementia. After adjustment for depression, gender and impairment in ADLs there was no association with either delusions or hallucinations indicating that depression was the most important factor <xref ref-type="bibr" rid="ridm1815975348">39</xref>. Antidepressant treatment decreases behavioral symptoms of dementia, but only if it is successful in treatment of depression <xref ref-type="bibr" rid="ridm1815969084">40</xref>.</p>
      </sec>
      <sec id="idm1815448532">
        <title>Treatment of Geriatric Depression.</title>
        <p>Antidepressant treatment may need to be long-term because the underlying conditions are not improving with progression of dementia. Treatment of depression in elderly individuals may not be effective because of several reasons: underrecognition of depression, inadequate doses of antidepressants, inadequate duration of treatment, failure to recognize and treat relapse, failure to recognize and treat comorbid conditions, and patient noncompliance <xref ref-type="bibr" rid="ridm1815964188">41</xref>. A single antidepressant may not be always effective in resolving depressive symptoms because single antidepressant treatment is effective only in one third of even cognitively intact patients <xref ref-type="bibr" rid="ridm1815963684">42</xref> and may require augmentation by an atypical antipsychotic <xref ref-type="bibr" rid="ridm1815958644">43</xref>.</p>
      </sec>
      <sec id="idm1815447452">
        <title>Caregiver´s Burden and Morbidity.</title>
        <p>Behavioral symptoms in dementia patients are associated with increased caregiver´s burden <xref ref-type="bibr" rid="ridm1815953172">44</xref><xref ref-type="bibr" rid="ridm1815949356">45</xref> carer depression and increased rates of institutionalization of patients <xref ref-type="bibr" rid="ridm1815979020">46</xref><xref ref-type="bibr" rid="ridm1815928292">47</xref>. One study explicitly confirmed that clinician-rated patient depression scores are independently and significantly associated with caregiver psychological morbidity <xref ref-type="bibr" rid="ridm1815923252">48</xref>. In conclusion, treatment of depression in dementia patients provides benefits not only for patients but it is very important also for their caregivers.</p>
      </sec>
    </sec>
    <sec id="idm1815448028" sec-type="conclusions">
      <title>Conclusions.</title>
      <p>Relationship of depression and dementia is complex because both of these conditions have multiple causes and risk factors, and their combination may be very individual in a particular patient. From the clinical point of view, it is possible to consider depression and dementia as a continuum, with depression without cognitive impairment on one end and dementia without depressive symptoms on the other end <xref ref-type="bibr" rid="ridm1816359724">2</xref><xref ref-type="bibr" rid="ridm1815921164">49</xref>. It is important to treat even subthreshold depressive symptoms because they could have serious consequences for dementia progression, quality of life and behavioral symptoms of dementia. </p>
    </sec>
  </body>
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