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	<title>The Longevity Project &#187; depression</title>
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	<link>http://thelongevityproject.com</link>
	<description>Prevention, cognition, sustainable aging</description>
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		<title>Successful aging and longevity in older old women: the role of depression and cognition</title>
		<link>http://thelongevityproject.com/successful-aging-and-longevity-in-older-old-women-the-role-of-depression-and-cognition/</link>
		<comments>http://thelongevityproject.com/successful-aging-and-longevity-in-older-old-women-the-role-of-depression-and-cognition/#comments</comments>
		<pubDate>Thu, 11 Aug 2011 10:27:11 +0000</pubDate>
		<dc:creator>TLP</dc:creator>
				<category><![CDATA[Abstracts]]></category>
		<category><![CDATA[Cognitive activity]]></category>
		<category><![CDATA[Psychology]]></category>
		<category><![CDATA[aging]]></category>
		<category><![CDATA[cerebrovascular burden]]></category>
		<category><![CDATA[cognition]]></category>
		<category><![CDATA[depression]]></category>
		<category><![CDATA[successful aging theory]]></category>
		<category><![CDATA[terminal cognitive drop]]></category>

		<guid isPermaLink="false">http://thelongevityproject.com/?p=1029</guid>
		<description><![CDATA[Based in successful aging theory and terminal cognitive drop research, this paper investigates cerebrovascular burden (CVB), depressive symptoms, and cognitive decline as threats to longevity. A subsample of stroke-free women over the age of 80 was identified in the Health and Retirement Survey (years 2000-2008). Mortality at 2, 6, and 8 year intervals was predicted [...]]]></description>
			<content:encoded><![CDATA[<p>Based  in successful aging theory and terminal cognitive drop research, this  paper investigates cerebrovascular burden (CVB), depressive symptoms,  and cognitive decline as threats to <strong>longevity</strong>. A subsample of  stroke-free women over the age of 80 was identified in the Health and  Retirement Survey (years 2000-2008). Mortality at 2, 6, and 8 year  intervals was predicted using CVB (diabetes, heart disease,  hypertension), depressive symptoms (Center for Epidemiological Studies  Depression Scale), and cognitive decline (decline of 1 standard  deviation or more on the 35-point Telephone Interview for Cognitive  Status over 2 years). At most waves (2002, 2004, and 2006) mortality was  predicted by CVB, depressive symptoms, and cognitive drop measured 2  years prior. CVB and depressive symptoms at the 2000 wave predicted  mortality at 6 and 8 years. Older women with the greatest <strong>longevity</strong> had low CVB, robust cognitive functioning, and few depression symptoms,  supporting successful aging theory and terminal cognitive drop.</p>
<div>
<div><a title="Journal of aging research." href="http://www.ncbi.nlm.nih.gov/pubmed/21766034#">J Aging Res.</a> 2011;2011:912680. Epub  2011 Jul 9.</div>
<div>Paulson D, Bowen ME, Lichtenberg PA.</div>
<div>Department of Psychology and Institute of Gerontology, Wayne State University, Detroit, MI 48202-3801, USA.</div>
<p><a href="http://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21766034/?tool=pubmed" target="_blank">Free PMC Article</a></p>
</div>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Bright light treatment in elderly patients with nonseasonal major depressive disorder: a randomized placebo-controlled trial.</title>
		<link>http://thelongevityproject.com/bright-light-treatment-in-elderly-patients-with-nonseasonal-major-depressive-disorder-a-randomized-placebo-controlled-trial/</link>
		<comments>http://thelongevityproject.com/bright-light-treatment-in-elderly-patients-with-nonseasonal-major-depressive-disorder-a-randomized-placebo-controlled-trial/#comments</comments>
		<pubDate>Sun, 13 Feb 2011 20:47:30 +0000</pubDate>
		<dc:creator>CL</dc:creator>
				<category><![CDATA[Abstracts]]></category>
		<category><![CDATA[Environment]]></category>
		<category><![CDATA[Longevity]]></category>
		<category><![CDATA[Studies]]></category>
		<category><![CDATA[depression]]></category>
		<category><![CDATA[elderly]]></category>
		<category><![CDATA[light]]></category>
		<category><![CDATA[treatment]]></category>

		<guid isPermaLink="false">http://thelongevityproject.com/?p=713</guid>
		<description><![CDATA[Arch Gen Psychiatry. 2011 Jan;68(1):61-70. Lieverse R , Van Someren EJ , Nielen MM , Uitdehaag BM , Smit JH , Hoogendijk WJ . Department of Psychiatry, VU University Medical Center, Amsterdam, the Netherlands. ritsaert.lieverse@gmail.com Abstract CONTEXT: Major depressive disorder (MDD) in elderly individuals is prevalent and debilitating. It is accompanied by circadian rhythm disturbances [...]]]></description>
			<content:encoded><![CDATA[<p>Arch Gen Psychiatry. 2011 Jan;68(1):61-70.</p>
<p>Lieverse R , Van Someren EJ , Nielen MM , Uitdehaag BM , Smit JH , Hoogendijk WJ .</p>
<p>Department of Psychiatry, VU University Medical Center, Amsterdam, the Netherlands. ritsaert.lieverse@gmail.com</p>
<p>Abstract</p>
<p>CONTEXT: Major depressive disorder (MDD) in elderly individuals is prevalent and debilitating. It is accompanied by circadian rhythm disturbances associated with impaired functioning of the suprachiasmatic nucleus, the biological clock of the brain. Circadian rhythm disturbances are common in the elderly. Suprachiasmatic nucleus stimulation using bright light treatment (BLT) may, therefore, improve mood, sleep, and hormonal rhythms in elderly patients with MDD.</p>
<p>OBJECTIVE: To determine the efficacy of BLT in elderly patients with MDD.</p>
<p>DESIGN: Double-blind, placebo-controlled randomized clinical trial.</p>
<p>SETTING: Home-based treatment in patients recruited from outpatient clinics and from case-finding using general practitioners&#8217; offices in the Amsterdam region.</p>
<p>PARTICIPANTS: Eighty-nine outpatients 60 years or older who had MDD underwent assessment at baseline (T0), after 3 weeks of treatment (T1), and 3 weeks after the end of treatment (T2). Intervention Three weeks of 1-hour early-morning BLT (pale blue, approximately 7500 lux) vs placebo (dim red light, approximately 50 lux).</p>
<p>MAIN OUTCOME MEASURES: Mean improvement in Hamilton Scale for Depression scores at T1 and T2 using parameters of sleep and cortisol and melatonin levels.</p>
<p>RESULTS: Intention-to-treat analysis showed Hamilton Scale for Depression scores to improve with BLT more than placebo from T0 to T1 (7%; 95% confidence interval, 4%-23%; P = .03) and from T0 to T2 (21%; 7%-31%; P = .001). At T1 relative to T0, get-up time after final awakening in the BLT group advanced by 7% (P &lt; .001), sleep efficiency increased by 2% (P = .01), and the steepness of the rise in evening melatonin levels increased by 81% (P = .03) compared with the placebo group. At T2 relative to T0, get-up time was still advanced by 3% (P = .001) and the 24-hour urinary free cortisol level was 37% lower (P = .003) compared with the placebo group. The evening salivary cortisol level had decreased by 34% in the BLT group compared with an increase of 7% in the placebo group (P = .02).</p>
<p>CONCLUSIONS: In elderly patients with MDD, BLT improved mood, enhanced sleep efficiency, and increased the upslope melatonin level gradient. In addition, BLT produced continuing improvement in mood and an attenuation of cortisol hyperexcretion after discontinuation of treatment.</p>
<p>TRIAL REGISTRATION: clinicaltrials.gov Identifier NCT00332670.</p>
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		<item>
		<title>Dietary pattern and depressive symptoms in middle age</title>
		<link>http://thelongevityproject.com/dietary-pattern-and-depressive-symptoms-in-middle-age/</link>
		<comments>http://thelongevityproject.com/dietary-pattern-and-depressive-symptoms-in-middle-age/#comments</comments>
		<pubDate>Thu, 05 Nov 2009 15:12:36 +0000</pubDate>
		<dc:creator>TLP</dc:creator>
				<category><![CDATA[Abstracts]]></category>
		<category><![CDATA[depression]]></category>
		<category><![CDATA[diet]]></category>
		<category><![CDATA[dietary pattern]]></category>
		<category><![CDATA[fish]]></category>
		<category><![CDATA[fruits]]></category>
		<category><![CDATA[vegetable]]></category>

		<guid isPermaLink="false">http://thelongevityproject.com/?p=512</guid>
		<description><![CDATA[BACKGROUND: Studies of diet and depression have focused primarily on individual nutrients. AIMS: To examine the association between dietary patterns and depression using an overall diet approach. METHOD: Analyses were carried on data from 3486 participants (26.2% women, mean age 55.6 years) from the Whitehall II prospective cohort, in which two dietary patterns were identified: [...]]]></description>
			<content:encoded><![CDATA[<p>BACKGROUND: Studies of diet and depression have focused primarily on individual nutrients. AIMS: To examine the association between dietary patterns and depression using an overall diet approach. METHOD: Analyses were carried on data from 3486 participants (26.2% women, mean age 55.6 years) from the Whitehall II prospective cohort, in which two dietary patterns were identified: &#8216;whole food&#8217; (heavily loaded by vegetables, fruits and fish) and &#8216;processed food&#8217; (heavily loaded by sweetened desserts, fried food, processed meat, refined grains and high-fat dairy products). Self-reported depression was assessed 5 years later using the Center for Epidemiologic Studies &#8211; Depression (CES-D) scale. RESULTS: After adjusting for potential confounders, participants in the highest tertile of the whole food pattern had lower odds of CES-D depression (OR = 0.74, 95% CI 0.56-0.99) than those in the lowest tertile. In contrast, high consumption of processed food was associated with an increased odds of CES-D depression (OR = 1.58, 95% CI 1.11-2.23). CONCLUSIONS: In middle-aged participants, a processed food dietary pattern is a risk factor for CES-D depression 5 years later, whereas a whole food pattern is protective.</p>
<p class="citation">Br J Psychiatry. 2009 Nov;195(5):408-13.</p>
<p class="auth_list">Akbaraly TN, Brunner EJ, Ferrie JE, Marmot MG, Kivimaki M, Singh-Manoux A.</p>
<p class="aff">Department of Epidemiology and Public Health, University College London, London WC1E 6BT, UK. tasnime.akbaraly@inserm.fr</p>
<div class="icons"><a href="http://www.ncbi.nlm.nih.gov/entrez/utils/fref.fcgi?PrId=3051&amp;itool=Abstract-def&amp;uid=19880930&amp;nlmid=0342367&amp;db=pubmed&amp;url=http://bjp.rcpsych.org/cgi/pmidlookup?view=long&amp;pmid=19880930" target="_blank"><img id="linkout-icon-def-entrez" src="http://www.ncbi.nlm.nih.gov/corehtml/query/egifs/http:--highwire.stanford.edu-icons-externalservices-pubmed-notfree-bjprcpsych-entrez.gif" border="0" alt="Click here to read" /></a></div>
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