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The early course of affective and cognitive symptoms in de novo patients with Parkinson’s disease
Neuropsychiatric and cognitive symptoms are common in patients with Parkinson’s disease (PD) from the early stage of the disease but their course is still unclear. In this study we investigated prospectively the progression of affective and cognitive symptoms and disorders in de novo idiopathic PD p...
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Published in: | Journal of neurology 2014-06, Vol.261 (6), p.1126-1132 |
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creator | Spalletta, Gianfranco Robinson, Robert G. Cravello, Luca Pontieri, Francesco E. Pierantozzi, Mariangela Stefani, Alessandro Long, Jeffrey D. Caltagirone, Carlo Assogna, Francesca |
description | Neuropsychiatric and cognitive symptoms are common in patients with Parkinson’s disease (PD) from the early stage of the disease but their course is still unclear. In this study we investigated prospectively the progression of affective and cognitive symptoms and disorders in de novo idiopathic PD patients. Twenty-four de novo drug naïve PD patients underwent a comprehensive neurological, psychopathological and neuropsychological evaluation at the first diagnostic visit (OFF), after 4−6 months when the antiparkinsonian therapy regimen was stabilized (ON-1), and at one year following the ON-1 follow-up visit (ON-2). Generalized least squares analysis revealed a significant improvement over time in the depressive mood, short and long term episodic verbal memory, visual memory, and the motor symptoms. Pairwise comparisons showed a significant change from OFF to ON-1 for all the aforementioned variables, except for short term episodic verbal memory which approached significance. A significant improvement from ON-1 to ON-2, however, was shown for short term episodic verbal memory. An ancillary analysis indicated that overall level and change in a number of cognitive variables, but not depression, was conditional upon age of onset, education, and sometime gender. In conclusion, early stage PD is not associated with affective and cognitive deterioration. On the contrary, very specific neuropsychiatric and cognitive symptoms may improve. This study provides Class III evidence that antiparkinsonian treatment commonly used in the clinical practice improves memory performance and depression severity in de novo patients with PD. |
doi_str_mv | 10.1007/s00415-014-7327-6 |
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In this study we investigated prospectively the progression of affective and cognitive symptoms and disorders in de novo idiopathic PD patients. Twenty-four de novo drug naïve PD patients underwent a comprehensive neurological, psychopathological and neuropsychological evaluation at the first diagnostic visit (OFF), after 4−6 months when the antiparkinsonian therapy regimen was stabilized (ON-1), and at one year following the ON-1 follow-up visit (ON-2). Generalized least squares analysis revealed a significant improvement over time in the depressive mood, short and long term episodic verbal memory, visual memory, and the motor symptoms. Pairwise comparisons showed a significant change from OFF to ON-1 for all the aforementioned variables, except for short term episodic verbal memory which approached significance. A significant improvement from ON-1 to ON-2, however, was shown for short term episodic verbal memory. An ancillary analysis indicated that overall level and change in a number of cognitive variables, but not depression, was conditional upon age of onset, education, and sometime gender. In conclusion, early stage PD is not associated with affective and cognitive deterioration. On the contrary, very specific neuropsychiatric and cognitive symptoms may improve. This study provides Class III evidence that antiparkinsonian treatment commonly used in the clinical practice improves memory performance and depression severity in de novo patients with PD.</description><identifier>ISSN: 0340-5354</identifier><identifier>EISSN: 1432-1459</identifier><identifier>DOI: 10.1007/s00415-014-7327-6</identifier><identifier>PMID: 24695996</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Age Factors ; Aged ; Antiparkinson Agents - therapeutic use ; Anxiety ; Apathy ; Cognition Disorders - diagnosis ; Cognition Disorders - etiology ; Cognitive ability ; Disease Progression ; Educational Status ; Female ; Humans ; Longitudinal Studies ; Male ; Medicine ; Medicine & Public Health ; Memory ; Mental disorders ; Mental Status Schedule ; Middle Aged ; Mood Disorders - diagnosis ; Mood Disorders - etiology ; Movement disorders ; Neurologic Examination ; Neurology ; Neuropsychological Tests ; Neuropsychology ; Neuroradiology ; Neurosciences ; Original Communication ; Parkinson Disease - complications ; Parkinson Disease - drug therapy ; Parkinson's disease ; Psychopathology</subject><ispartof>Journal of neurology, 2014-06, Vol.261 (6), p.1126-1132</ispartof><rights>Springer-Verlag Berlin Heidelberg 2014</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c475t-1bf0d92fa1704e05f6f1b7bacd89c7aad228b976cbd491b3890933528403f1c73</citedby><cites>FETCH-LOGICAL-c475t-1bf0d92fa1704e05f6f1b7bacd89c7aad228b976cbd491b3890933528403f1c73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24695996$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Spalletta, Gianfranco</creatorcontrib><creatorcontrib>Robinson, Robert G.</creatorcontrib><creatorcontrib>Cravello, Luca</creatorcontrib><creatorcontrib>Pontieri, Francesco E.</creatorcontrib><creatorcontrib>Pierantozzi, Mariangela</creatorcontrib><creatorcontrib>Stefani, Alessandro</creatorcontrib><creatorcontrib>Long, Jeffrey D.</creatorcontrib><creatorcontrib>Caltagirone, Carlo</creatorcontrib><creatorcontrib>Assogna, Francesca</creatorcontrib><title>The early course of affective and cognitive symptoms in de novo patients with Parkinson’s disease</title><title>Journal of neurology</title><addtitle>J Neurol</addtitle><addtitle>J Neurol</addtitle><description>Neuropsychiatric and cognitive symptoms are common in patients with Parkinson’s disease (PD) from the early stage of the disease but their course is still unclear. In this study we investigated prospectively the progression of affective and cognitive symptoms and disorders in de novo idiopathic PD patients. Twenty-four de novo drug naïve PD patients underwent a comprehensive neurological, psychopathological and neuropsychological evaluation at the first diagnostic visit (OFF), after 4−6 months when the antiparkinsonian therapy regimen was stabilized (ON-1), and at one year following the ON-1 follow-up visit (ON-2). Generalized least squares analysis revealed a significant improvement over time in the depressive mood, short and long term episodic verbal memory, visual memory, and the motor symptoms. Pairwise comparisons showed a significant change from OFF to ON-1 for all the aforementioned variables, except for short term episodic verbal memory which approached significance. A significant improvement from ON-1 to ON-2, however, was shown for short term episodic verbal memory. An ancillary analysis indicated that overall level and change in a number of cognitive variables, but not depression, was conditional upon age of onset, education, and sometime gender. In conclusion, early stage PD is not associated with affective and cognitive deterioration. On the contrary, very specific neuropsychiatric and cognitive symptoms may improve. This study provides Class III evidence that antiparkinsonian treatment commonly used in the clinical practice improves memory performance and depression severity in de novo patients with PD.</description><subject>Age Factors</subject><subject>Aged</subject><subject>Antiparkinson Agents - therapeutic use</subject><subject>Anxiety</subject><subject>Apathy</subject><subject>Cognition Disorders - diagnosis</subject><subject>Cognition Disorders - etiology</subject><subject>Cognitive ability</subject><subject>Disease Progression</subject><subject>Educational Status</subject><subject>Female</subject><subject>Humans</subject><subject>Longitudinal Studies</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Memory</subject><subject>Mental disorders</subject><subject>Mental Status Schedule</subject><subject>Middle Aged</subject><subject>Mood Disorders - diagnosis</subject><subject>Mood Disorders - etiology</subject><subject>Movement disorders</subject><subject>Neurologic Examination</subject><subject>Neurology</subject><subject>Neuropsychological Tests</subject><subject>Neuropsychology</subject><subject>Neuroradiology</subject><subject>Neurosciences</subject><subject>Original Communication</subject><subject>Parkinson Disease - complications</subject><subject>Parkinson Disease - drug therapy</subject><subject>Parkinson's disease</subject><subject>Psychopathology</subject><issn>0340-5354</issn><issn>1432-1459</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqNkcuKFDEUhoMoTtv6AG4k4MZN6cmtUlnK4A0GdDGuQyqVzGTsStqc6hl652v4ej6J6elRRBDcJCTny3_I-Qh5yuAlA9CvEEAy1QGTnRZcd_09smJS8I5JZe6TFQgJnRJKnpBHiFcAMLTCQ3LCZW-UMf2K-PPLQIOrmz31ZVcx0BKpizH4JV0H6vLU7i9yuj3hft4uZUaaMp0CzeW60K1bUsgL0pu0XNJPrn5JGUv-8e070ilhcBgekwfRbTA8udvX5PPbN-en77uzj-8-nL4-67zUaunYGGEyPDqmQQZQsY9s1KPz02C8dm7ifBiN7v04ScNGMRgwQig-SBCReS3W5MUxd1vL113Axc4JfdhsXA5lh5YpJY3ivZH_gQrVC2BtWZPnf6FXbVC5feSWatMFKRrFjpSvBbGGaLc1za7uLQN7kGWPsmyTZQ-y7CH52V3ybpzD9PvFLzsN4EcAWylfhPpH63-m_gT4DZ-S</recordid><startdate>20140601</startdate><enddate>20140601</enddate><creator>Spalletta, Gianfranco</creator><creator>Robinson, Robert G.</creator><creator>Cravello, Luca</creator><creator>Pontieri, Francesco E.</creator><creator>Pierantozzi, Mariangela</creator><creator>Stefani, Alessandro</creator><creator>Long, Jeffrey D.</creator><creator>Caltagirone, Carlo</creator><creator>Assogna, Francesca</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20140601</creationdate><title>The early course of affective and cognitive symptoms in de novo patients with Parkinson’s disease</title><author>Spalletta, Gianfranco ; 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In this study we investigated prospectively the progression of affective and cognitive symptoms and disorders in de novo idiopathic PD patients. Twenty-four de novo drug naïve PD patients underwent a comprehensive neurological, psychopathological and neuropsychological evaluation at the first diagnostic visit (OFF), after 4−6 months when the antiparkinsonian therapy regimen was stabilized (ON-1), and at one year following the ON-1 follow-up visit (ON-2). Generalized least squares analysis revealed a significant improvement over time in the depressive mood, short and long term episodic verbal memory, visual memory, and the motor symptoms. Pairwise comparisons showed a significant change from OFF to ON-1 for all the aforementioned variables, except for short term episodic verbal memory which approached significance. A significant improvement from ON-1 to ON-2, however, was shown for short term episodic verbal memory. An ancillary analysis indicated that overall level and change in a number of cognitive variables, but not depression, was conditional upon age of onset, education, and sometime gender. In conclusion, early stage PD is not associated with affective and cognitive deterioration. On the contrary, very specific neuropsychiatric and cognitive symptoms may improve. This study provides Class III evidence that antiparkinsonian treatment commonly used in the clinical practice improves memory performance and depression severity in de novo patients with PD.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>24695996</pmid><doi>10.1007/s00415-014-7327-6</doi><tpages>7</tpages></addata></record> |
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subjects | Age Factors Aged Antiparkinson Agents - therapeutic use Anxiety Apathy Cognition Disorders - diagnosis Cognition Disorders - etiology Cognitive ability Disease Progression Educational Status Female Humans Longitudinal Studies Male Medicine Medicine & Public Health Memory Mental disorders Mental Status Schedule Middle Aged Mood Disorders - diagnosis Mood Disorders - etiology Movement disorders Neurologic Examination Neurology Neuropsychological Tests Neuropsychology Neuroradiology Neurosciences Original Communication Parkinson Disease - complications Parkinson Disease - drug therapy Parkinson's disease Psychopathology |
title | The early course of affective and cognitive symptoms in de novo patients with Parkinson’s disease |
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