<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">JDM</journal-id><journal-title-group><journal-title>Journal of Diabetes Mellitus</journal-title></journal-title-group><issn pub-type="epub">2160-5831</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/jdm.2015.54029</article-id><article-id pub-id-type="publisher-id">JDM-60665</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Factors Affecting Clinical Depression in Diabetic Geriatric Population
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>hailesh</surname><given-names>Jain</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Bhavana</surname><given-names>Mocharla</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Yulia</surname><given-names>Belopolsky</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Jamal</surname><given-names>Islam</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib></contrib-group><aff id="aff3"><addr-line>Texas Tech University Health Sciences Center, Odessa, USA</addr-line></aff><aff id="aff1"><addr-line>Department of Psychiatry, Texas Tech University Health Sciences Center, Odessa, USA</addr-line></aff><aff id="aff2"><addr-line>Department of Family and Community Medicine, Texas Tech University Health Sciences Center, Odessa, USA</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>bobby.jain@ttuhsc.edu(HJ)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>21</day><month>09</month><year>2015</year></pub-date><volume>05</volume><issue>04</issue><fpage>238</fpage><lpage>244</lpage><history><date date-type="received"><day>17</day>	<month>August</month>	<year>2015</year></date><date date-type="rev-recd"><day>accepted</day>	<month>25</month>	<year>October</year>	</date><date date-type="accepted"><day>28</day>	<month>October</month>	<year>2015</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Introduction: Diabetes mellitus is a common metabolic disorder affecting about 10% - 25% of the elderly population. The mechanisms, linking diabetes and major depressive disorders are unknown. Obesity is the risk factor for both diabetes mellitus and depression. The goal of this study was to explore if BMI of elderly diabetic patients with depression differed from BMI of the diabetic 
  individuals without depression. Further, we aimed to explore the association of age, gender, 
  health insurance status, ethnicity influence and systolic blood pressure (SBP) and diastolic blood pressure (DBP) with clinical depression in geriatric diabetics. Methods: Nursing home residents were recruited from an outpatient internal medicine clinic in a teaching university setting. After given 
  written consent, patients received Public Health Questionnaire-9 (PHQ-9) in either English or 
  Spanish language. Results: While the clinically depressed diabetic participants did not differ from that of the non-depressed diabetic participants with respect to age (70.6 &#177; 6.1 vs. 72.1 &#177; 4.8; 
  p
   = 0.111), gender (47.2% of males vs. 57.1% of females; 
  p
   = 0.754), or ethnicity (69% explain vs. 71%, 
  p
   = 1.000), race did appear to differ in depression status: Caucasian, African-American, and others 
  were respectively 37%, 48%, and 15% vs. 32%, 16%, 52%, p = 0.0003). Neither the BMI (p &gt; 0.499) 
  nor Hemoglobin A1c (
  p
   &gt; 0.839) differed between the clinically depressed and non-depressed participants when controlled for these race differences. Conclusion: In our sample, diabetic African Americans are three times more likely to be depressed. Diabetic Caucasians also experience higher rates of clinical depression. However, diabetics with depression did not differ from diabetics without depression with regard to their age, gender, BMI, HbA1C, health insurance status, systolic blood pressure or diastolic blood pressure.
 
</p></abstract><kwd-group><kwd>Geriatric Depression</kwd><kwd> Diabetes Mellitus</kwd><kwd> Ethnicity</kwd><kwd> BMI</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Diabetes mellitus―a common metabolic disorder affecting about 10% - 25% of the elderly population [<xref ref-type="bibr" rid="scirp.60665-ref1">1</xref>] is frequently associated with psychiatric disturbances [<xref ref-type="bibr" rid="scirp.60665-ref2">2</xref>] . Patients with diabetes mellitus are 2 - 4 times more likely to be diagnosed with major depressive disorder [<xref ref-type="bibr" rid="scirp.60665-ref3">3</xref>] . In elderly diabetic patients the risk of depressive mood symptoms is increased by 30 % (HR 1.31 (95% CI: 1.07 - 1.61)) [<xref ref-type="bibr" rid="scirp.60665-ref4">4</xref>] . The adjusted odds ratio (OR) for functional disability is 7.9 per subject with diabetes and depression, whereas OR is 2.4 for subjects with diabetes alone and three for subjects who have major depression alone [<xref ref-type="bibr" rid="scirp.60665-ref5">5</xref>] . The mechanisms, linking diabetes and major depressive disorders are unknown. Obesity is the risk factor for both diabetes mellitus and depression. However, data-ex- ploring association of body mass index (BMI) in diabetic patients, suffering from depression, is sparse.</p><p>Background: people with diabetes have an increased risk of developing depressive symptoms and people with depression also have an increased risk of developing diabetes [<xref ref-type="bibr" rid="scirp.60665-ref6">6</xref>] . It is estimated that about one third of diabetics suffer from clinical depression [<xref ref-type="bibr" rid="scirp.60665-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.60665-ref6">6</xref>] . The prognosis of both diabetes and depression in terms of severity of disease, complications, treatment resistance and mortality is worse for either diseases when they are comorbid than when they occur separately [<xref ref-type="bibr" rid="scirp.60665-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.60665-ref7">7</xref>] . Besides clinical depression, diabetes mellitus has also been an established risk factor for cardiovascular diseases [<xref ref-type="bibr" rid="scirp.60665-ref8">8</xref>] , metabolic syndrome, stroke, retinopathy and obesity [<xref ref-type="bibr" rid="scirp.60665-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.60665-ref10">10</xref>] .</p><p>However, the epidemiological data-linking diabetes with such risk factors, including obesity, smoking, and perceived burden of diabetes treatment, particularly in the genetic population, remains sparse.</p><p>A number of studies have reported prevalence rates of depression markedly and inconsistently high in people with type II diabetes compared to those without type II diabetes [<xref ref-type="bibr" rid="scirp.60665-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.60665-ref12">12</xref>] . Such rates have varied between 17.8% and 39%. However, certain European and Canadian studies have reported lower prevalence rates of depression in people with type II diabetes [<xref ref-type="bibr" rid="scirp.60665-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.60665-ref14">14</xref>] . Other studies, including that of Holt et al. (2009), have reported lower rates of depression in both people with and without type II diabetes (5% versus 3.8%) but they find a statistically significant association between depression and diabetes. Icks et al. [<xref ref-type="bibr" rid="scirp.60665-ref15">15</xref>] have suggested that there is no significant association between diabetes and depressive symptoms in women after controlling for comorbidities. For diabetes mellitus type I, the prevalence of clinical depression and controlled studies was 12% (5.8% - 43.3%) for people with diabetes compared with 3.2% (2.7% - 11.4%) for control subjects [<xref ref-type="bibr" rid="scirp.60665-ref16">16</xref>] . In contrast, other studies [<xref ref-type="bibr" rid="scirp.60665-ref17">17</xref>] reported significant high prevalence rates of depressive symptoms in both men and women with type I diabetes compared to individuals without diabetes (men: 25.5 versus 11.6%; women:37.9 versus 20.5%). Through a more recent cross-sectional study involving out-patients with diabetes in the Netherlands, it was observed that about one third of the sample reported elevated depression scores, and that eight―24% were diagnosed with a depressive disorder [<xref ref-type="bibr" rid="scirp.60665-ref10">10</xref>] .</p><p>Most studies considering race or ethnicity only analyzed ethnicity as an associate variable of depression and/or diabetes. Studies with African-American participants have shown a mixed picture in terms of rates of diabetes and depression [<xref ref-type="bibr" rid="scirp.60665-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.60665-ref18">18</xref>] . Katon et al. [<xref ref-type="bibr" rid="scirp.60665-ref19">19</xref>] reported that depressed individuals were less likely to be African-American, and were more likely to be Hispanic (African-American 13%; Asian American 15.2%; white Americans 15.5%; Hispanic 21.8%). However, Lin et al. [<xref ref-type="bibr" rid="scirp.60665-ref20">20</xref>] found no difference in rates between White Americans and non-White Americans for either minor depression of a major depression. European studies have reported higher levels of depressive symptoms or depressive effects in non-Dutch patients with type II diabetes compared with Dutch patients. However, they found no ethnic differences in depression in patients with type I diabetes [<xref ref-type="bibr" rid="scirp.60665-ref10">10</xref>] . Ali et al. [<xref ref-type="bibr" rid="scirp.60665-ref11">11</xref>] have found that the United Kingdom reports lower levels of diagnosed depressive disorder than their White European counterparts.</p><p>A number of studies have found diabetic women to have higher rates of depression than their men counterparts with similar findings in type I diabetes mellitus and type II diabetes mellitus [<xref ref-type="bibr" rid="scirp.60665-ref16">16</xref>] [<xref ref-type="bibr" rid="scirp.60665-ref21">21</xref>] [<xref ref-type="bibr" rid="scirp.60665-ref20">20</xref>] . However, Holt et al. [<xref ref-type="bibr" rid="scirp.60665-ref22">22</xref>] found diabetic men to have more depression rates than diabetic women.</p><p>In regards to age, a number of community-based studies in the US have reported an increase prevalence of psychological morbidity in younger adults with type II diabetes. Most studies have reported age as a risk factor for depression. However, depression has been found to be less common in older cohorts would depression [<xref ref-type="bibr" rid="scirp.60665-ref23">23</xref>] . Collins et al. [<xref ref-type="bibr" rid="scirp.60665-ref9">9</xref>] have reported lower rates of depression in older individuals with type I diabetes mellitus, suggesting that age may have a protective effect.</p><p>The goal of this study was to explore if BMI of elderly patients with diabetes differed from BMI of the individuals without depression. Further, we aimed to explore the association of age, gender, health insurance status, ethnicity influence and systolic blood pressure (SBP) and diastolic blood pressure (DBP) with clinical depression in geriatric diabetics.</p></sec><sec id="s2"><title>2. Methods</title><sec id="s2_1"><title>2.1. Study Design</title><p>This was a cross-sectional analytic comparative non-interventional study.</p></sec><sec id="s2_2"><title>2.2. Subjects’ Recruitment and Characteristics</title><p>Nursing home residents were recruited from outpatient internal medicine clinics at the Texas Tech Health Science Center at Permian Basin between 2012 and 2013. All consenting diabetics with duration of diagnoses more than one year, irrespective of type I or type II over the age of 65 were eligible for the study. Relevant information was collected including independent variables: age, gender, ethnicity, Systolic and Diastolic blood pressure, BMI and latest HbA1c. The dependent variable was assessed with Patients received Public Health Questionnaire-9 (PHQ-9) in either English or Spanish language. The PHQ is based on DSM-IV (Diagnostic and statistical Manual -IV) criteria and has a 88% sensitivity and 88% specificity for diagnosis of major depression (PHQ score ≥ 10) in comparison to interview by mental health professionals.</p></sec><sec id="s2_3"><title>2.3. Statistical Method</title><p>Univariate analysis was conducted to compare depressed and non-depressed nursing home residents with respect to the primary outcome measures of BMI and HgA1c along with secondary outcomes of SBP and DBP. In the absence of any statistical significance (alpha = 0.05) between primary outcomes of the two groups, the age, race, ethnicity, gender, and insurance status between groups were compared in a similar fashion to probe for confounding. A post-hoc analysis was conducted comparing HgA1c and BMI between the depressed and non-de- pressed groups after adjusting for significant race differences between the two groups.</p></sec></sec><sec id="s3"><title>3. Results</title><p>There was no statistical difference between the depressed (n = 67) and non-depressed (n = 32) participants in their assessment of primary outcomes of HbA1C (7.5 &#177; 1.6 vs. 7.4 &#177;1.4; p = 0.447) or BMI ( 31.4 &#177;5.8 vs. 32.8 &#177; 5.3; p = 0.254), nor did the secondary outcomes: systolic blood pressure (142 &#177; 18.4 vs. 143 &#177; 25.8; p = 0.823) or diastolic blood pressure ( 77.6 &#177;9.4, 75.1 &#177; 11.1; p = 0.240) differ by depression status (<xref ref-type="table" rid="table1">Table 1</xref> and <xref ref-type="table" rid="table2">Table 2</xref>). While the clinically depressed diabetic participants did not differ to that of the non-depressed diabetic participants with respect to age (70.6 &#177; 6.1 vs. 72.1 &#177; 4.8; p = 0.111); gender (47.2% of males vs. 57.1% of females ; p = 0.754), or ethnicity (69% explain vs. 71%, p = 1.000), race did appear to differ by depression status: Caucasian, African-American, and other were respectively 37%, 48%, and 15% vs. 32%, 16%, 52%, p = 0.0003). Neither the BMI (p &gt; 0.499) nor Hemoglobin A1c (p &gt; 0.839) differed between the clinically depressed and non-depressed participants when controlled for these race differences (<xref ref-type="fig" rid="fig1">Figure 1</xref>).</p></sec><sec id="s4"><title>4. Discussion</title><p>In our sample, diabetic African Americans are three times more likely to be depressed. Diabetic Caucasians also experience higher rates of clinical depression. However, diabetics with depression did not differ from diabetics without depression with regards to their age, gender, BMI, HbA1C, health insurance status, systolic blood pressure or diastolic blood pressure.</p><p>Diabetes is a risk factor for high prevalence of depression [<xref ref-type="bibr" rid="scirp.60665-ref24">24</xref>] . It is possible that stress-associated hypothamamic-pituitary adrenal axis reaction with lowered hippocampal volume, upregulation of serotonin receptors (5 HT-2A receptors), decreased BDNF (Brain Derived Neurotropic Factor) and elevated inflammatory cytokines in diabetes may be directly related to the depression in diabetes. Our findings are in agreement with data, reporting higher incidence of depression in African American patients with diabetes [<xref ref-type="bibr" rid="scirp.60665-ref25">25</xref>] [<xref ref-type="bibr" rid="scirp.60665-ref26">26</xref>] . However, unlike the previous studies [<xref ref-type="bibr" rid="scirp.60665-ref27">27</xref>] [<xref ref-type="bibr" rid="scirp.60665-ref28">28</xref>] , presence of clinical depression did not influence HbA1C levels. Similar to Munshi et al. [<xref ref-type="bibr" rid="scirp.60665-ref29">29</xref>] , Engum [<xref ref-type="bibr" rid="scirp.60665-ref30">30</xref>] and Lin et al. [<xref ref-type="bibr" rid="scirp.60665-ref20">20</xref>] we did not find an association between the presence of depression and glycemic control. Knol et al. [<xref ref-type="bibr" rid="scirp.60665-ref8">8</xref>] in the cross-sectional study also demonstrated that impaired fasting glucose was not associated with depression in people with diabetes. Only one longitudinal study observed a significant association between elevated mean HbA1c values and a history of depression among participants with diabetes [<xref ref-type="bibr" rid="scirp.60665-ref31">31</xref>] . In a more recent cross-sectional study involving outpatients with any form of diabetes, Pouwer et al. [<xref ref-type="bibr" rid="scirp.60665-ref32">32</xref>] found that</p><fig id="fig1"  position="float"><label><xref ref-type="fig" rid="fig1">Figure 1</xref></label><caption><title> Difference between mean hemoglobin A1c levels between depressed and non-depressed diabetics</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/6-4300312x7.png"/></fig><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Association of confounding factors (BM1, age, ethnicity, gender, race and health insurance status) for depressed and non-depressed diabetics</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  colspan="4"  >Confounders</th><th align="center" valign="middle" ></th></tr></thead><tr><td align="center" valign="middle" >BMI</td><td align="center" valign="middle" >Mean</td><td align="center" valign="middle" >SD</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >p-value</td></tr><tr><td align="center" valign="middle" >Depressed</td><td align="center" valign="middle" >31.4</td><td align="center" valign="middle" >5.8</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >0.254</td></tr><tr><td align="center" valign="middle" >Not depressed</td><td align="center" valign="middle" >32.8</td><td align="center" valign="middle" >5.3</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Age</td><td align="center" valign="middle" >Mean</td><td align="center" valign="middle" >SD</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >p-value</td></tr><tr><td align="center" valign="middle" >Depressed</td><td align="center" valign="middle" >70.6</td><td align="center" valign="middle" >6.1</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >0.111</td></tr><tr><td align="center" valign="middle" >Not depressed</td><td align="center" valign="middle" >72.1</td><td align="center" valign="middle" >4.8</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Ethnicity</td><td align="center" valign="middle" >Non-hispanic</td><td align="center" valign="middle" >Hispanic</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >p-value</td></tr><tr><td align="center" valign="middle" >Depressed</td><td align="center" valign="middle" >29</td><td align="center" valign="middle" >37</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >1.000</td></tr><tr><td align="center" valign="middle" >Non-depressed</td><td align="center" valign="middle" >13</td><td align="center" valign="middle" >15</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >42</td><td align="center" valign="middle" >52</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Percentage</td><td align="center" valign="middle" >45%</td><td align="center" valign="middle" >55%</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Gender</td><td align="center" valign="middle" >Male</td><td align="center" valign="middle" >Female</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >p-value</td></tr><tr><td align="center" valign="middle" >Depressed</td><td align="center" valign="middle" >29</td><td align="center" valign="middle" >30</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >0.665</td></tr><tr><td align="center" valign="middle" >Non-depressed</td><td align="center" valign="middle" >14</td><td align="center" valign="middle" >18</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >43</td><td align="center" valign="middle" >48</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Percentage</td><td align="center" valign="middle" >47%</td><td align="center" valign="middle" >53%</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Race</td><td align="center" valign="middle" >White</td><td align="center" valign="middle" >Black</td><td align="center" valign="middle" >Other</td><td align="center" valign="middle" >p-value</td></tr><tr><td align="center" valign="middle" >Depressed</td><td align="center" valign="middle" >25</td><td align="center" valign="middle" >32</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >0.0003</td></tr><tr><td align="center" valign="middle" >Non-depressed</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >16</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >35</td><td align="center" valign="middle" >37</td><td align="center" valign="middle" >26</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Percentage</td><td align="center" valign="middle" >36%</td><td align="center" valign="middle" >38%</td><td align="center" valign="middle" >27%</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Insurance</td><td align="center" valign="middle" >Medicaid</td><td align="center" valign="middle" >Medicare</td><td align="center" valign="middle" >Self</td><td align="center" valign="middle" >p-value</td></tr><tr><td align="center" valign="middle" >Depressed</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >7</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >0.600</td></tr><tr><td align="center" valign="middle" >Non-depressed</td><td align="center" valign="middle" >31</td><td align="center" valign="middle" >30</td><td align="center" valign="middle" >16</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >35</td><td align="center" valign="middle" >37</td><td align="center" valign="middle" >18</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Percentage</td><td align="center" valign="middle" >39%</td><td align="center" valign="middle" >41%</td><td align="center" valign="middle" >20%</td><td align="center" valign="middle" ></td></tr></tbody></table></table-wrap><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Showing outcome measures for Hemoglobin A1c (HA1c), Systolic Blood Pressure (SBP) and Diastolic Blood Pressure (DBP) for diabetics with and without depressive symptoms</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  colspan="4"  >Outcome measures</th></tr></thead><tr><td align="center" valign="middle" >HA1c</td><td align="center" valign="middle" >Mean</td><td align="center" valign="middle" >SD</td><td align="center" valign="middle" >p-value</td></tr><tr><td align="center" valign="middle" >Depressed</td><td align="center" valign="middle" >7.5</td><td align="center" valign="middle" >1.6</td><td align="center" valign="middle" >0.447</td></tr><tr><td align="center" valign="middle" >Not depressed</td><td align="center" valign="middle" >7.4</td><td align="center" valign="middle" >1.4</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >SBP</td><td align="center" valign="middle" >Mean</td><td align="center" valign="middle" >SD</td><td align="center" valign="middle" >p-value</td></tr><tr><td align="center" valign="middle" >Depressed</td><td align="center" valign="middle" >142.0</td><td align="center" valign="middle" >18.4</td><td align="center" valign="middle" >0.823</td></tr><tr><td align="center" valign="middle" >Not depressed</td><td align="center" valign="middle" >143.2</td><td align="center" valign="middle" >25.8</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >DBP</td><td align="center" valign="middle" >Mean</td><td align="center" valign="middle" >SD</td><td align="center" valign="middle" >p-value</td></tr><tr><td align="center" valign="middle" >Depressed</td><td align="center" valign="middle" >77.6</td><td align="center" valign="middle" >9.4</td><td align="center" valign="middle" >0.240</td></tr><tr><td align="center" valign="middle" >Not depressed</td><td align="center" valign="middle" >75.1</td><td align="center" valign="middle" >11.1</td><td align="center" valign="middle" ></td></tr></tbody></table></table-wrap><p>depressive effect was associated with poor glycemic control for type 1 DM only.</p><p>Depressed diabetic patients in our study did not differ in their BMI compared to non-depressed diabetic participants. This is contrast to other studies [<xref ref-type="bibr" rid="scirp.60665-ref33">33</xref>] who found increased BMI in the patients with diabetes and depression.</p><p>The gender has been reported to play an important role in the psychiatric disorders. Women with diabetes have consistently shown higher rates of depression than men [<xref ref-type="bibr" rid="scirp.60665-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.60665-ref31">31</xref>] [<xref ref-type="bibr" rid="scirp.60665-ref34">34</xref>] [<xref ref-type="bibr" rid="scirp.60665-ref35">35</xref>] . However, in our study we did not find any gender difference in diabetic patients with or without clinical depression. Our results are in line with the findings of one study [<xref ref-type="bibr" rid="scirp.60665-ref36">36</xref>] where, when controlled for BMI, age, race, there was no gender difference in presence of clinical depression, in diabetic patients</p><p>Age is associated with the clinical symptoms of depression. Studies found that younger patients with diabetic tend to experience more clinical depression than elderly population with diabetes [<xref ref-type="bibr" rid="scirp.60665-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.60665-ref20">20</xref>] [<xref ref-type="bibr" rid="scirp.60665-ref23">23</xref>] . In fact, Collins et al. [<xref ref-type="bibr" rid="scirp.60665-ref9">9</xref>] have reported lower rates of depression in older individuals, suggesting that age might be a protective factor.</p><p>It has been argued that diabetes precedes depression and leads to depression either through a direct effect of hyper glycaemia, possibly leading to altered glucose transport in the brain, or as a result of the psychological stress resulting from the knowledge of the diagnosis or from the rigorour treatment, throught the both?lifestyle corrections and pharmacological interventions [<xref ref-type="bibr" rid="scirp.60665-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.60665-ref30">30</xref>] [<xref ref-type="bibr" rid="scirp.60665-ref37">37</xref>] . However, this assumption has been challenged by several recent cohort studies that have suggested that depression may be a risk factor for diabetes [<xref ref-type="bibr" rid="scirp.60665-ref30">30</xref>] [<xref ref-type="bibr" rid="scirp.60665-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.60665-ref36">36</xref>] while diabetes does not necessarily predict depression or is associated with only a modest risk of development of depression [<xref ref-type="bibr" rid="scirp.60665-ref30">30</xref>] .</p><p>There are a number of limitations of this study. The design of the study gives only a snap shot of the symptoms experiencing by the participants in the previous two weeks. A prospective case controlled study would have been informative. We took one-year duration of diabetes as a cut off point for inclusion in this study. Hence this study does not provide information about effect of new onset of diabetes on mood symptoms. We also did not take into consideration if the diabetics had any comorbid complications of diabetes such as diabetic retinopathy or neuropathy, which can cause severe limitations and hence influence mood symptoms. Most importantly, we had assessment of depressive symptoms through one time evaluation through PHQ-9 in lieu of a comprehensive clinical depression assessment. However in spite of the limitations as this is first study in our knowledge that has tried to assess the effect of such confounding factors (age, gender, ethnicity, race, health insurance status, SBP/DBP, BMI and HbA1c) on development of depression in geriatric population.</p><p>Future studies may need further exploration of the association of such factors in a prospective case controlled design.</p></sec><sec id="s5"><title>5. Conclusion</title><p>In summary, despite being cross-sectional, our study is significant for its unexpected findings.</p></sec><sec id="s6"><title>Addendum</title><p>CRI contributed to the collection and analysis of the data.</p></sec><sec id="s7"><title>Cite this paper</title><p>ShaileshJain,BhavanaMocharla,YuliaBelopolsky,JamalIslam, (2015) Factors Affecting Clinical Depression in Diabetic Geriatric Population. Journal of Diabetes Mellitus,05,238-244. doi: 10.4236/jdm.2015.54029</p></sec><sec id="s8"><title>NOTES</title></sec></body><back><ref-list><title>References</title><ref id="scirp.60665-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Fagot-Campagna, A., Bourdel-Marchasson, I. and Simon, D. (2005) Burden of Diabetes in an Aging Population: Prevalence, Incidence, Mortality, Characteristics and Quality of Care. 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