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    <title>AMA Publishing Group: Mild Cognitive Impairment Topic Collection</title>
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    <pubDate>Wed, 01 May 2013 00:00:00 GMT</pubDate>
    <lastBuildDate>Mon, 13 May 2013 16:45:13 GMT</lastBuildDate>
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      <title>Prognosis of Mild Cognitive Impairment in Early Parkinson Disease The Norwegian ParkWest Study  Cognitive Impairment in Early Parkinson Disease </title>
      <link>http://pubs.jamanetwork.com/article.aspx?articleID=1671737</link>
      <pubDate>Wed, 01 May 2013 00:00:00 GMT</pubDate>
      <author>Pedersen K, Larsen J, Tysnes O, et al. </author>
      <description>&lt;span class="paragraphSection"&gt;&lt;div class="boxTitle"&gt;Importance&lt;/div&gt;Mild cognitive impairment (MCI) is common in Parkinson disease (PD), but the prognostic value of MCI in early PD is unknown.&lt;div class="boxTitle"&gt;Objective&lt;/div&gt;To examine the course of MCI and its progression to dementia in an incident PD cohort.&lt;div class="boxTitle"&gt;Design&lt;/div&gt;Prospective longitudinal cohort study.&lt;div class="boxTitle"&gt;Setting&lt;/div&gt;The Norwegian ParkWest study, an ongoing population-based study of the incidence, neurobiology, and prognosis of PD in western and southern Norway.&lt;div class="boxTitle"&gt;Participants&lt;/div&gt;A population-based cohort of 182 patients with incident PD monitored for 3 years.&lt;div class="boxTitle"&gt;Main Outcomes and Measures&lt;/div&gt;Serial neuropsychological tests of attention, executive function, verbal memory, and visuospatial skills were administered at baseline, 1 year, and 3 years. Patients were classified as having MCI and received a diagnosis of dementia according to published consensus criteria.&lt;div class="boxTitle"&gt;Results&lt;/div&gt;Significantly more patients with MCI than without MCI at baseline (10 of 37 [27.0%] vs 1 of 145 [0.7%]; relative risk, 39.2 [95% CI, 5.2-296.5]; P &lt; .001) progressed to dementia during follow-up. Of those with MCI at baseline, 8 of 37 (21.6%) had MCI that reverted to normal cognition during follow-up. Mild cognitive impairment at the 1-year visit was associated with a similar progression rate to dementia (10 of 36 patients [27.8%]) and reversion rate to normal cognition (7 of 36 [19.4%]). However, among the 22 patients with persistent MCI at baseline and the 1-year visit, 10 (45.5%) developed dementia and only 2 (9.1%) had MCI that reverted to normal cognition by the end of study.&lt;div class="boxTitle"&gt;Conclusions and Relevance&lt;/div&gt;Mild cognitive impairment at PD diagnosis predicts a highly increased risk for early dementia. Repeated neuropsychological testing increases the prognostic accuracy of MCI with respect to early dementia development in PD.&lt;/span&gt;</description>
      <prism:volume xmlns:prism="prism">70</prism:volume>
      <prism:number xmlns:prism="prism">5</prism:number>
      <prism:startingPage xmlns:prism="prism">580</prism:startingPage>
      <prism:endingPage xmlns:prism="prism">586</prism:endingPage>
      <prism:doi xmlns:prism="prism">10.1001/jamaneurol.2013.2110</prism:doi>
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      <title>Can Mild Cognitive Impairment in Parkinson Disease Predict the Development of Dementia? MCI in PD and the Development of Dementia </title>
      <link>http://pubs.jamanetwork.com/article.aspx?articleID=1671738</link>
      <pubDate>Wed, 01 May 2013 00:00:00 GMT</pubDate>
      <author>Copeland BJ, Schiess MC. </author>
      <description>&lt;span class="paragraphSection"&gt;The term mild cognitive impairment (MCI) emerged in the 1990s, defining a transition state from normal cognitive function and forcing our appreciation of cognitive changes not attributable to age, education, sex, race, ethnicity, language, or culture, but rather to a well-defined disease process or related pathology. The acceptance of MCI as a precursor to dementia and its use in predicting progression to Alzheimer dementia, by identifying a profile of cognitive dysfunction unique to Alzheimer dementia and attributable to the disease process and related pathology, is well substantiated. Recently, subtypes of MCI have been described that may have individual predilections for various dementia types.&lt;/span&gt;</description>
      <prism:volume xmlns:prism="prism">70</prism:volume>
      <prism:number xmlns:prism="prism">5</prism:number>
      <prism:startingPage xmlns:prism="prism">553</prism:startingPage>
      <prism:endingPage xmlns:prism="prism">555</prism:endingPage>
      <prism:doi xmlns:prism="prism">10.1001/jamaneurol.2013.260</prism:doi>
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