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Lesion load may predict long-term cognitive dysfunction in multiple sclerosis patients

Magnetic Resonance Imaging (MRI) techniques provided evidences into the understanding of cognitive impairment (CIm) in Multiple Sclerosis (MS). To investigate the role of white matter (WM) and gray matter (GM) in predicting long-term CIm in a cohort of MS patients. 303 out of 597 patients participat...

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Published in:PloS one 2015-03, Vol.10 (3), p.e0120754-e0120754
Main Authors: Patti, Francesco, De Stefano, Manuela, Lavorgna, Luigi, Messina, Silvia, Chisari, Clara Grazia, Ippolito, Domenico, Lanzillo, Roberta, Vacchiano, Veria, Realmuto, Sabrina, Valentino, Paola, Coniglio, Gabriella, Buccafusca, Maria, Paolicelli, Damiano, D'Ambrosio, Alessandro, Montella, Patrizia, Brescia Morra, Vincenzo, Savettieri, Giovanni, Alfano, Bruno, Gallo, Antonio, Simone, Isabella, Viterbo, Rosa, Zappia, Mario, Bonavita, Simona, Tedeschi, Gioacchino
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creator Patti, Francesco
De Stefano, Manuela
Lavorgna, Luigi
Messina, Silvia
Chisari, Clara Grazia
Ippolito, Domenico
Lanzillo, Roberta
Vacchiano, Veria
Realmuto, Sabrina
Valentino, Paola
Coniglio, Gabriella
Buccafusca, Maria
Paolicelli, Damiano
D'Ambrosio, Alessandro
Montella, Patrizia
Brescia Morra, Vincenzo
Savettieri, Giovanni
Alfano, Bruno
Gallo, Antonio
Simone, Isabella
Viterbo, Rosa
Zappia, Mario
Bonavita, Simona
Tedeschi, Gioacchino
description Magnetic Resonance Imaging (MRI) techniques provided evidences into the understanding of cognitive impairment (CIm) in Multiple Sclerosis (MS). To investigate the role of white matter (WM) and gray matter (GM) in predicting long-term CIm in a cohort of MS patients. 303 out of 597 patients participating in a previous multicenter clinical-MRI study were enrolled (49.4% were lost at follow-up). The following MRI parameters, expressed as fraction (f) of intracranial volume, were evaluated: cerebrospinal fluid (CSF-f), WM-f, GM-f and abnormal WM (AWM-f), a measure of lesion load. Nine years later, cognitive status was assessed in 241 patients using the Symbol Digit Modalities Test (SDMT), the Semantically Related Word List Test (SRWL), the Modified Card Sorting Test (MCST), and the Paced Auditory Serial Addition Test (PASAT). In particular, being SRWL a memory test, both immediate recall and delayed recall were evaluated. MCST scoring was calculated based on the number of categories, number of perseverative and non-perseverative errors. AWM-f was predictive of an impaired performance 9 years ahead in SDMT (OR 1.49, CI 1.12-1.97 p = 0.006), PASAT (OR 1.43, CI 1.14-1.80 p = 0.002), SRWL-immediate recall (OR 1.72 CI 1.35-2.20 p
doi_str_mv 10.1371/journal.pone.0120754
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To investigate the role of white matter (WM) and gray matter (GM) in predicting long-term CIm in a cohort of MS patients. 303 out of 597 patients participating in a previous multicenter clinical-MRI study were enrolled (49.4% were lost at follow-up). The following MRI parameters, expressed as fraction (f) of intracranial volume, were evaluated: cerebrospinal fluid (CSF-f), WM-f, GM-f and abnormal WM (AWM-f), a measure of lesion load. Nine years later, cognitive status was assessed in 241 patients using the Symbol Digit Modalities Test (SDMT), the Semantically Related Word List Test (SRWL), the Modified Card Sorting Test (MCST), and the Paced Auditory Serial Addition Test (PASAT). In particular, being SRWL a memory test, both immediate recall and delayed recall were evaluated. MCST scoring was calculated based on the number of categories, number of perseverative and non-perseverative errors. AWM-f was predictive of an impaired performance 9 years ahead in SDMT (OR 1.49, CI 1.12-1.97 p = 0.006), PASAT (OR 1.43, CI 1.14-1.80 p = 0.002), SRWL-immediate recall (OR 1.72 CI 1.35-2.20 p&lt;0.001), SRWL-delayed recall (OR 1.61 CI 1.28-2.03 p&lt;0.001), MCST-category (OR 1.52, CI 1.2-1.9 p&lt;0.001), MCST-perseverative error(OR 1.51 CI 1.2-1.9 p = 0.001), MCST-non perseverative error (OR 1.26 CI 1.02-1.55 p = 0.032). 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Academic</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agriculture Science Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Advanced Technologies &amp; Aerospace Database</collection><collection>ProQuest Advanced Technologies &amp; Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials Science Collection</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Patti, Francesco</au><au>De Stefano, Manuela</au><au>Lavorgna, Luigi</au><au>Messina, Silvia</au><au>Chisari, Clara Grazia</au><au>Ippolito, Domenico</au><au>Lanzillo, Roberta</au><au>Vacchiano, Veria</au><au>Realmuto, Sabrina</au><au>Valentino, Paola</au><au>Coniglio, Gabriella</au><au>Buccafusca, Maria</au><au>Paolicelli, Damiano</au><au>D'Ambrosio, Alessandro</au><au>Montella, Patrizia</au><au>Brescia Morra, Vincenzo</au><au>Savettieri, Giovanni</au><au>Alfano, Bruno</au><au>Gallo, Antonio</au><au>Simone, Isabella</au><au>Viterbo, Rosa</au><au>Zappia, Mario</au><au>Bonavita, Simona</au><au>Tedeschi, Gioacchino</au><au>Wylie, Glenn</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lesion load may predict long-term cognitive dysfunction in multiple sclerosis patients</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2015-03-27</date><risdate>2015</risdate><volume>10</volume><issue>3</issue><spage>e0120754</spage><epage>e0120754</epage><pages>e0120754-e0120754</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Magnetic Resonance Imaging (MRI) techniques provided evidences into the understanding of cognitive impairment (CIm) in Multiple Sclerosis (MS). To investigate the role of white matter (WM) and gray matter (GM) in predicting long-term CIm in a cohort of MS patients. 303 out of 597 patients participating in a previous multicenter clinical-MRI study were enrolled (49.4% were lost at follow-up). The following MRI parameters, expressed as fraction (f) of intracranial volume, were evaluated: cerebrospinal fluid (CSF-f), WM-f, GM-f and abnormal WM (AWM-f), a measure of lesion load. Nine years later, cognitive status was assessed in 241 patients using the Symbol Digit Modalities Test (SDMT), the Semantically Related Word List Test (SRWL), the Modified Card Sorting Test (MCST), and the Paced Auditory Serial Addition Test (PASAT). In particular, being SRWL a memory test, both immediate recall and delayed recall were evaluated. MCST scoring was calculated based on the number of categories, number of perseverative and non-perseverative errors. AWM-f was predictive of an impaired performance 9 years ahead in SDMT (OR 1.49, CI 1.12-1.97 p = 0.006), PASAT (OR 1.43, CI 1.14-1.80 p = 0.002), SRWL-immediate recall (OR 1.72 CI 1.35-2.20 p&lt;0.001), SRWL-delayed recall (OR 1.61 CI 1.28-2.03 p&lt;0.001), MCST-category (OR 1.52, CI 1.2-1.9 p&lt;0.001), MCST-perseverative error(OR 1.51 CI 1.2-1.9 p = 0.001), MCST-non perseverative error (OR 1.26 CI 1.02-1.55 p = 0.032). In our large MS cohort, focal WM damage appeared to be the most relevant predictor of the long-term cognitive outcome.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>25816303</pmid><doi>10.1371/journal.pone.0120754</doi><oa>free_for_read</oa></addata></record>
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identifier ISSN: 1932-6203
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1932-6203
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source Publicly Available Content Database; PubMed Central
subjects Adult
Aging
Brain - pathology
Cerebrospinal fluid
Cognition Disorders - etiology
Cognition Disorders - pathology
Cognitive ability
Cognitive disorders
Cohort Studies
Disability
Disease Progression
Female
Follow-Up Studies
Gray Matter - pathology
Hospitals
Humans
Magnetic resonance
Magnetic Resonance Imaging
Male
Medical research
Memory
Memory, Short-Term
Metabolism
Middle Aged
Multiple sclerosis
Multiple Sclerosis - complications
Multiple Sclerosis - pathology
Nerve Fibers, Myelinated - pathology
Neurology
Neuropsychological Tests
Neurosciences
NMR
Nuclear magnetic resonance
Patients
Performance prediction
Prognosis
Recall
Substantia alba
Substantia grisea
title Lesion load may predict long-term cognitive dysfunction in multiple sclerosis patients
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