La maladie de Parkinson en France (serveur d'exploration)

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Examination of the Lille Apathy Rating Scale in Parkinson disease.

Identifieur interne : 000B99 ( PubMed/Corpus ); précédent : 000B98; suivant : 000C00

Examination of the Lille Apathy Rating Scale in Parkinson disease.

Auteurs : Laura B. Zahodne ; Shamar Young ; Lindsey Kirsch-Darrow ; Anne Nisenzon ; Hubert H. Fernandez ; Michael S. Okun ; Dawn Bowers

Source :

RBID : pubmed:19133658

English descriptors

Abstract

Apathy is a unique, multidimensional syndrome commonly encountered in patients with Parkinson disease (PD). Recently, the Lille Apathy Rating Scale (LARS), a semistructured interview yielding a global score, and composite subscores for different domains of apathy (i.e., cognitive, behavioral, affective, self awareness), was developed and given to a sample of patients with PD in France. This study is the first outside of its original developers to examine the English language version of the LARS in PD. We found the LARS to be a coherent instrument demonstrating both convergent and divergent validity, as compared to the Apathy Scale (AS) and Beck Depression Inventory (BDI-II). Using a receiver operating characteristic (ROC) analysis comparing the LARS to the AS, a validated and widely-used measure, we identified a cut-off score (sensitivity = 64%, specificity = 92%, PPV = 88%, NPV = 75%) that was higher than that proposed by the original authors, who derived their cut-off by comparing LARS global scores to clinical judgments of apathy. Although the present study does not compare the LARS to a diagnostic gold standard or promote its utility for diagnosing apathy, it provides further support for the LARS as a promising instrument to examine apathy in PD.

DOI: 10.1002/mds.22441
PubMed: 19133658

Links to Exploration step

pubmed:19133658

Le document en format XML

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<div type="abstract" xml:lang="en">Apathy is a unique, multidimensional syndrome commonly encountered in patients with Parkinson disease (PD). Recently, the Lille Apathy Rating Scale (LARS), a semistructured interview yielding a global score, and composite subscores for different domains of apathy (i.e., cognitive, behavioral, affective, self awareness), was developed and given to a sample of patients with PD in France. This study is the first outside of its original developers to examine the English language version of the LARS in PD. We found the LARS to be a coherent instrument demonstrating both convergent and divergent validity, as compared to the Apathy Scale (AS) and Beck Depression Inventory (BDI-II). Using a receiver operating characteristic (ROC) analysis comparing the LARS to the AS, a validated and widely-used measure, we identified a cut-off score (sensitivity = 64%, specificity = 92%, PPV = 88%, NPV = 75%) that was higher than that proposed by the original authors, who derived their cut-off by comparing LARS global scores to clinical judgments of apathy. Although the present study does not compare the LARS to a diagnostic gold standard or promote its utility for diagnosing apathy, it provides further support for the LARS as a promising instrument to examine apathy in PD.</div>
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<PMID Version="1">16832074</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Mov Disord. 2006 Oct;21(10):1656-62</RefSource>
<PMID Version="1">16830317</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Mov Disord. 2007 Apr 30;22(6):778-84</RefSource>
<PMID Version="1">17290451</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
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<PMID Version="1">17886475</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
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<PMID Version="1">18508589</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
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<PMID Version="1">18398913</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
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<PMID Version="1">18579165</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Mov Disord. 2008 Oct 30;23(14):2004-14</RefSource>
<PMID Version="1">18709683</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Brain Cogn. 2000 Mar;42(2):268-93</RefSource>
<PMID Version="1">10744924</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Am J Psychiatry. 2001 Jun;158(6):872-7</RefSource>
<PMID Version="1">11384893</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Mov Disord. 2002 Mar;17(2):366-71</RefSource>
<PMID Version="1">11921125</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Neuropsychologia. 2002;40(13):2257-67</RefSource>
<PMID Version="1">12417456</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>J Neurol Neurosurg Psychiatry. 2002 Dec;73(6):636-42</RefSource>
<PMID Version="1">12438462</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Psychiatry Res. 1991 Aug;38(2):143-62</RefSource>
<PMID Version="1">1754629</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>J Neurol Neurosurg Psychiatry. 1992 Mar;55(3):181-4</RefSource>
<PMID Version="1">1564476</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>J Neuropsychiatry Clin Neurosci. 1991 Summer;3(3):243-54</RefSource>
<PMID Version="1">1821241</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>J Neuropsychiatry Clin Neurosci. 1992 Spring;4(2):134-9</RefSource>
<PMID Version="1">1627973</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Clin Chem. 1993 Apr;39(4):561-77</RefSource>
<PMID Version="1">8472349</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Neurosurg Clin N Am. 1995 Jan;6(1):73-104</RefSource>
<PMID Version="1">7696876</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>J Neuropsychiatry Clin Neurosci. 1998 Summer;10(3):314-9</RefSource>
<PMID Version="1">9706539</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>J Neurol Neurosurg Psychiatry. 1999 Oct;67(4):492-6</RefSource>
<PMID Version="1">10486397</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>J Neurol Neurosurg Psychiatry. 2006 May;77(5):579-84</RefSource>
<PMID Version="1">16614016</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Mov Disord. 2006 May;21(5):668-72</RefSource>
<PMID Version="1">16450355</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Cereb Cortex. 2006 Jul;16(7):916-28</RefSource>
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