Electrophysiological and neuropsychological assessment of cognition in spinocerebellar ataxia type 1 patients: a pilot study

Background Event-related potentials (ERPs) reflect cognitive processing: negative early components (N100, N200) are involved in the sensory and perceptual processing of a stimulus, whereas late positive component P300 requires conscious attention. Both neuropsychological and affective disorders are...

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Veröffentlicht in:Neurological sciences 2023-05, Vol.44 (5), p.1597-1606
Hauptverfasser: Contaldi, Elena, Sensi, Mariachiara, Colucci, Fabiana, Capone, Jay Guido, Braccia, Arianna, Nocilla, Mattia Roberto, Diozzi, Enrica, Contini, Eleonora, Pelizzari, Anna Chiara, Tugnoli, Valeria
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container_end_page 1606
container_issue 5
container_start_page 1597
container_title Neurological sciences
container_volume 44
creator Contaldi, Elena
Sensi, Mariachiara
Colucci, Fabiana
Capone, Jay Guido
Braccia, Arianna
Nocilla, Mattia Roberto
Diozzi, Enrica
Contini, Eleonora
Pelizzari, Anna Chiara
Tugnoli, Valeria
description Background Event-related potentials (ERPs) reflect cognitive processing: negative early components (N100, N200) are involved in the sensory and perceptual processing of a stimulus, whereas late positive component P300 requires conscious attention. Both neuropsychological and affective disorders are present in patients with spinocerebellar ataxia type 1 (SCA1), but the underlying mechanisms need further clarification. Materials and methods In this pilot study, we assessed cognitive processing by recording auditory ERPs in 16 consecutive SCA1 patients and 16 healthy controls (HC) matched for age and sex. Motor and nonmotor symptoms were evaluated using the Scale for the Assessment and Rating of Ataxia (SARA) and an extensive neuropsychological battery. ERPs were recorded using an oddball paradigm, and peak latency and amplitude of N100, N200, and P300 were measured in the averaged responses to target tones. Results We found in SCA1 significantly increased latencies of N200 and P300 (p=0.033, p=0.007) and decreased amplitudes of N100 and P300 (p=0.024, p=0.038) compared with HC. Furthermore, P300 latency had the highest AUC in the discrimination of SCA1 in ROC analysis. The expansion of trinucleotide repeats correlated with P300 latency (r=−0.607, p=0.048), whereas both P300 and N100 amplitudes correlated with the severity of motor symptoms (r=−0.692, p=0.003; r=−0.621; p=0.010). Significant correlations between P300 latency and the scores of Emotion Attribution Task (r=−0.633, p=0.027), as well as between N200 latency and the scores of Frontal Assessment Battery and Stroop test (r=−0.520, p=0.047; r=0.538, p=0.039), were observed. Conclusions This research provides for the first time an extensive characterization of ERPs as useful electrophysiological markers to identify early cognitive dysfunction in SCA1.
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Both neuropsychological and affective disorders are present in patients with spinocerebellar ataxia type 1 (SCA1), but the underlying mechanisms need further clarification. Materials and methods In this pilot study, we assessed cognitive processing by recording auditory ERPs in 16 consecutive SCA1 patients and 16 healthy controls (HC) matched for age and sex. Motor and nonmotor symptoms were evaluated using the Scale for the Assessment and Rating of Ataxia (SARA) and an extensive neuropsychological battery. ERPs were recorded using an oddball paradigm, and peak latency and amplitude of N100, N200, and P300 were measured in the averaged responses to target tones. Results We found in SCA1 significantly increased latencies of N200 and P300 (p=0.033, p=0.007) and decreased amplitudes of N100 and P300 (p=0.024, p=0.038) compared with HC. Furthermore, P300 latency had the highest AUC in the discrimination of SCA1 in ROC analysis. The expansion of trinucleotide repeats correlated with P300 latency (r=−0.607, p=0.048), whereas both P300 and N100 amplitudes correlated with the severity of motor symptoms (r=−0.692, p=0.003; r=−0.621; p=0.010). Significant correlations between P300 latency and the scores of Emotion Attribution Task (r=−0.633, p=0.027), as well as between N200 latency and the scores of Frontal Assessment Battery and Stroop test (r=−0.520, p=0.047; r=0.538, p=0.039), were observed. Conclusions This research provides for the first time an extensive characterization of ERPs as useful electrophysiological markers to identify early cognitive dysfunction in SCA1.</description><identifier>ISSN: 1590-1874</identifier><identifier>EISSN: 1590-3478</identifier><identifier>DOI: 10.1007/s10072-022-06597-5</identifier><identifier>PMID: 36639526</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Affective disorders ; Ataxia ; Ataxin ; Attention ; Auditory discrimination ; Auditory evoked potentials ; Cognition ; Cognitive ability ; Event-related potentials ; Event-Related Potentials, P300 - physiology ; Evoked Potentials - physiology ; Evoked Potentials, Auditory - physiology ; Humans ; Information processing ; Latency ; Medicine ; Medicine &amp; Public Health ; Neurology ; Neuropsychology ; Neuroradiology ; Neurosciences ; Neurosurgery ; Original ; Original Article ; Pilot Projects ; Psychiatry ; Reaction Time ; Sensory integration ; Spinocerebellar ataxia ; Trinucleotide repeats</subject><ispartof>Neurological sciences, 2023-05, Vol.44 (5), p.1597-1606</ispartof><rights>The Author(s) 2023</rights><rights>2023. The Author(s).</rights><rights>The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). 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Both neuropsychological and affective disorders are present in patients with spinocerebellar ataxia type 1 (SCA1), but the underlying mechanisms need further clarification. Materials and methods In this pilot study, we assessed cognitive processing by recording auditory ERPs in 16 consecutive SCA1 patients and 16 healthy controls (HC) matched for age and sex. Motor and nonmotor symptoms were evaluated using the Scale for the Assessment and Rating of Ataxia (SARA) and an extensive neuropsychological battery. ERPs were recorded using an oddball paradigm, and peak latency and amplitude of N100, N200, and P300 were measured in the averaged responses to target tones. Results We found in SCA1 significantly increased latencies of N200 and P300 (p=0.033, p=0.007) and decreased amplitudes of N100 and P300 (p=0.024, p=0.038) compared with HC. Furthermore, P300 latency had the highest AUC in the discrimination of SCA1 in ROC analysis. The expansion of trinucleotide repeats correlated with P300 latency (r=−0.607, p=0.048), whereas both P300 and N100 amplitudes correlated with the severity of motor symptoms (r=−0.692, p=0.003; r=−0.621; p=0.010). Significant correlations between P300 latency and the scores of Emotion Attribution Task (r=−0.633, p=0.027), as well as between N200 latency and the scores of Frontal Assessment Battery and Stroop test (r=−0.520, p=0.047; r=0.538, p=0.039), were observed. 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Sensi, Mariachiara ; Colucci, Fabiana ; Capone, Jay Guido ; Braccia, Arianna ; Nocilla, Mattia Roberto ; Diozzi, Enrica ; Contini, Eleonora ; Pelizzari, Anna Chiara ; Tugnoli, Valeria</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c475t-9fac8ea7e17031296300b0497a0be400eaca81759254158c88252e32f2b34bf13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Affective disorders</topic><topic>Ataxia</topic><topic>Ataxin</topic><topic>Attention</topic><topic>Auditory discrimination</topic><topic>Auditory evoked potentials</topic><topic>Cognition</topic><topic>Cognitive ability</topic><topic>Event-related potentials</topic><topic>Event-Related Potentials, P300 - physiology</topic><topic>Evoked Potentials - physiology</topic><topic>Evoked Potentials, Auditory - physiology</topic><topic>Humans</topic><topic>Information processing</topic><topic>Latency</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Neurology</topic><topic>Neuropsychology</topic><topic>Neuroradiology</topic><topic>Neurosciences</topic><topic>Neurosurgery</topic><topic>Original</topic><topic>Original Article</topic><topic>Pilot Projects</topic><topic>Psychiatry</topic><topic>Reaction Time</topic><topic>Sensory integration</topic><topic>Spinocerebellar ataxia</topic><topic>Trinucleotide repeats</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Contaldi, Elena</creatorcontrib><creatorcontrib>Sensi, Mariachiara</creatorcontrib><creatorcontrib>Colucci, Fabiana</creatorcontrib><creatorcontrib>Capone, Jay Guido</creatorcontrib><creatorcontrib>Braccia, Arianna</creatorcontrib><creatorcontrib>Nocilla, Mattia Roberto</creatorcontrib><creatorcontrib>Diozzi, Enrica</creatorcontrib><creatorcontrib>Contini, Eleonora</creatorcontrib><creatorcontrib>Pelizzari, Anna Chiara</creatorcontrib><creatorcontrib>Tugnoli, Valeria</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Health &amp; 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Medical Complete (Alumni)</collection><collection>Consumer Health Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Psychology 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>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Neurological sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Contaldi, Elena</au><au>Sensi, Mariachiara</au><au>Colucci, Fabiana</au><au>Capone, Jay Guido</au><au>Braccia, Arianna</au><au>Nocilla, Mattia Roberto</au><au>Diozzi, Enrica</au><au>Contini, Eleonora</au><au>Pelizzari, Anna Chiara</au><au>Tugnoli, Valeria</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Electrophysiological and neuropsychological assessment of cognition in spinocerebellar ataxia type 1 patients: a pilot study</atitle><jtitle>Neurological sciences</jtitle><stitle>Neurol Sci</stitle><addtitle>Neurol Sci</addtitle><date>2023-05-01</date><risdate>2023</risdate><volume>44</volume><issue>5</issue><spage>1597</spage><epage>1606</epage><pages>1597-1606</pages><issn>1590-1874</issn><eissn>1590-3478</eissn><abstract>Background Event-related potentials (ERPs) reflect cognitive processing: negative early components (N100, N200) are involved in the sensory and perceptual processing of a stimulus, whereas late positive component P300 requires conscious attention. Both neuropsychological and affective disorders are present in patients with spinocerebellar ataxia type 1 (SCA1), but the underlying mechanisms need further clarification. Materials and methods In this pilot study, we assessed cognitive processing by recording auditory ERPs in 16 consecutive SCA1 patients and 16 healthy controls (HC) matched for age and sex. Motor and nonmotor symptoms were evaluated using the Scale for the Assessment and Rating of Ataxia (SARA) and an extensive neuropsychological battery. ERPs were recorded using an oddball paradigm, and peak latency and amplitude of N100, N200, and P300 were measured in the averaged responses to target tones. Results We found in SCA1 significantly increased latencies of N200 and P300 (p=0.033, p=0.007) and decreased amplitudes of N100 and P300 (p=0.024, p=0.038) compared with HC. Furthermore, P300 latency had the highest AUC in the discrimination of SCA1 in ROC analysis. The expansion of trinucleotide repeats correlated with P300 latency (r=−0.607, p=0.048), whereas both P300 and N100 amplitudes correlated with the severity of motor symptoms (r=−0.692, p=0.003; r=−0.621; p=0.010). Significant correlations between P300 latency and the scores of Emotion Attribution Task (r=−0.633, p=0.027), as well as between N200 latency and the scores of Frontal Assessment Battery and Stroop test (r=−0.520, p=0.047; r=0.538, p=0.039), were observed. Conclusions This research provides for the first time an extensive characterization of ERPs as useful electrophysiological markers to identify early cognitive dysfunction in SCA1.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>36639526</pmid><doi>10.1007/s10072-022-06597-5</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-0218-5251</orcidid><oa>free_for_read</oa></addata></record>
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subjects Affective disorders
Ataxia
Ataxin
Attention
Auditory discrimination
Auditory evoked potentials
Cognition
Cognitive ability
Event-related potentials
Event-Related Potentials, P300 - physiology
Evoked Potentials - physiology
Evoked Potentials, Auditory - physiology
Humans
Information processing
Latency
Medicine
Medicine & Public Health
Neurology
Neuropsychology
Neuroradiology
Neurosciences
Neurosurgery
Original
Original Article
Pilot Projects
Psychiatry
Reaction Time
Sensory integration
Spinocerebellar ataxia
Trinucleotide repeats
title Electrophysiological and neuropsychological assessment of cognition in spinocerebellar ataxia type 1 patients: a pilot study
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