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Frontal Assessment Battery to Evaluate Frontal Lobe Dysfunction in ALS Patients
Assessment of frontal lobe impairment in amyotrophic lateral sclerosis (ALS) is a matter of great importance, since it often causes ALS patients to decrease medication and nursing compliance, thus shortening their survival time. The frontal assessment battery (FAB) is a short and rapid method for as...
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Published in: | Canadian journal of neurological sciences 2011-03, Vol.38 (2), p.242-246 |
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container_title | Canadian journal of neurological sciences |
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creator | Ahn, Suk-Won Kim, Su-Hyun Kim, Jee-Eun Kim, Sung-Min Kim, Seung Hyun Sung, Jung-Joon Lee, Kwang-Woo Hong, Yoon-Ho |
description | Assessment of frontal lobe impairment in amyotrophic lateral sclerosis (ALS) is a matter of great importance, since it often causes ALS patients to decrease medication and nursing compliance, thus shortening their survival time.
The frontal assessment battery (FAB) is a short and rapid method for assessing frontal executive functions. We investigated the applicability of the FAB as a screening method for assessing cognitive impairments in 61 ALS patients. Depending on the results of the FAB, we classified patients into two subgroups: FAB-normal and FAB-abnormal. We then performed additional evaluations of cognitive function using the Korean version of the mini-mental state examination (K-MMSE), a verbal fluency test (COWAT), and a neuropsychiatric inventory (NPI). Results of these tests were compared between the two groups using Mann-Whitney U-tests, and Spearman correlation analyses were used to investigate the relationships between FAB score and disease duration and severity.
Of the 61 sporadic ALS patients included in this study, 14 were classified as FAB-abnormal and 47 were classified as FAB-normal. The FAB-normal and FAB-abnormal patients performed significantly differently in all domains of the COWAT. There was no difference in behavioral disturbance, as assessed by the NPI, between the two groups. The FAB scores were found to significantly correlate with both disease duration and severity.
The FAB shows promise as a method of screening for frontal lobe dysfunction in ALS, as it is not only quick and easy, but also reliable. Additional studies should examine how FAB performance changes as ALS progresses. |
doi_str_mv | 10.1017/S0317167100011409 |
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The frontal assessment battery (FAB) is a short and rapid method for assessing frontal executive functions. We investigated the applicability of the FAB as a screening method for assessing cognitive impairments in 61 ALS patients. Depending on the results of the FAB, we classified patients into two subgroups: FAB-normal and FAB-abnormal. We then performed additional evaluations of cognitive function using the Korean version of the mini-mental state examination (K-MMSE), a verbal fluency test (COWAT), and a neuropsychiatric inventory (NPI). Results of these tests were compared between the two groups using Mann-Whitney U-tests, and Spearman correlation analyses were used to investigate the relationships between FAB score and disease duration and severity.
Of the 61 sporadic ALS patients included in this study, 14 were classified as FAB-abnormal and 47 were classified as FAB-normal. The FAB-normal and FAB-abnormal patients performed significantly differently in all domains of the COWAT. There was no difference in behavioral disturbance, as assessed by the NPI, between the two groups. The FAB scores were found to significantly correlate with both disease duration and severity.
The FAB shows promise as a method of screening for frontal lobe dysfunction in ALS, as it is not only quick and easy, but also reliable. Additional studies should examine how FAB performance changes as ALS progresses.</description><identifier>ISSN: 0317-1671</identifier><identifier>EISSN: 2057-0155</identifier><identifier>DOI: 10.1017/S0317167100011409</identifier><identifier>PMID: 21320827</identifier><identifier>CODEN: CJNSA2</identifier><language>eng</language><publisher>New York, USA: Cambridge University Press</publisher><subject>Adult ; Aged ; Amyotrophic Lateral Sclerosis - complications ; Amyotrophic Lateral Sclerosis - pathology ; Biological and medical sciences ; Cognition Disorders - diagnosis ; Cognition Disorders - etiology ; Female ; Frontal Lobe - pathology ; Frontal Lobe - physiopathology ; Humans ; Male ; Medical sciences ; Middle Aged ; Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis ; Neurology ; Neuropsychological Tests ; Original Article ; Statistics, Nonparametric ; Young Adult</subject><ispartof>Canadian journal of neurological sciences, 2011-03, Vol.38 (2), p.242-246</ispartof><rights>Copyright © The Canadian Journal of Neurological 2011</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c515t-a8e825a35e43ea6ae6133fded430a9c3a4486ca021c0f3a70b78e722c1a93d4f3</citedby><cites>FETCH-LOGICAL-c515t-a8e825a35e43ea6ae6133fded430a9c3a4486ca021c0f3a70b78e722c1a93d4f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.cambridge.org/core/product/identifier/S0317167100011409/type/journal_article$$EHTML$$P50$$Gcambridge$$H</linktohtml><link.rule.ids>161,314,776,780,27901,27902,72931</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23943314$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21320827$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ahn, Suk-Won</creatorcontrib><creatorcontrib>Kim, Su-Hyun</creatorcontrib><creatorcontrib>Kim, Jee-Eun</creatorcontrib><creatorcontrib>Kim, Sung-Min</creatorcontrib><creatorcontrib>Kim, Seung Hyun</creatorcontrib><creatorcontrib>Sung, Jung-Joon</creatorcontrib><creatorcontrib>Lee, Kwang-Woo</creatorcontrib><creatorcontrib>Hong, Yoon-Ho</creatorcontrib><title>Frontal Assessment Battery to Evaluate Frontal Lobe Dysfunction in ALS Patients</title><title>Canadian journal of neurological sciences</title><addtitle>Can. J. Neurol. Sci</addtitle><description>Assessment of frontal lobe impairment in amyotrophic lateral sclerosis (ALS) is a matter of great importance, since it often causes ALS patients to decrease medication and nursing compliance, thus shortening their survival time.
The frontal assessment battery (FAB) is a short and rapid method for assessing frontal executive functions. We investigated the applicability of the FAB as a screening method for assessing cognitive impairments in 61 ALS patients. Depending on the results of the FAB, we classified patients into two subgroups: FAB-normal and FAB-abnormal. We then performed additional evaluations of cognitive function using the Korean version of the mini-mental state examination (K-MMSE), a verbal fluency test (COWAT), and a neuropsychiatric inventory (NPI). Results of these tests were compared between the two groups using Mann-Whitney U-tests, and Spearman correlation analyses were used to investigate the relationships between FAB score and disease duration and severity.
Of the 61 sporadic ALS patients included in this study, 14 were classified as FAB-abnormal and 47 were classified as FAB-normal. The FAB-normal and FAB-abnormal patients performed significantly differently in all domains of the COWAT. There was no difference in behavioral disturbance, as assessed by the NPI, between the two groups. The FAB scores were found to significantly correlate with both disease duration and severity.
The FAB shows promise as a method of screening for frontal lobe dysfunction in ALS, as it is not only quick and easy, but also reliable. Additional studies should examine how FAB performance changes as ALS progresses.</description><subject>Adult</subject><subject>Aged</subject><subject>Amyotrophic Lateral Sclerosis - complications</subject><subject>Amyotrophic Lateral Sclerosis - pathology</subject><subject>Biological and medical sciences</subject><subject>Cognition Disorders - diagnosis</subject><subject>Cognition Disorders - etiology</subject><subject>Female</subject><subject>Frontal Lobe - pathology</subject><subject>Frontal Lobe - physiopathology</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis</subject><subject>Neurology</subject><subject>Neuropsychological Tests</subject><subject>Original Article</subject><subject>Statistics, Nonparametric</subject><subject>Young Adult</subject><issn>0317-1671</issn><issn>2057-0155</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNqFkE1rFEEQhhuJmDX6A7xIX4Kn0ar-mJ4-rptEhYUI0fNQ21MTJsxH7O4J7L93lmziQdBTHd7nfQseId4hfERA9-kGNDosHQIAogH_QqwUWFcAWnsiVoe4OOSn4nVKdwCqtKV5JU4VagWVcitxfRWnMVMv1ylxSgOPWX6mnDnuZZ7k5QP1M2WWT9h22rG82Kd2HkPuplF2o1xvb-R3yt3STW_Ey5b6xG-P90z8vLr8sflabK-_fNust0WwaHNBFVfKkrZsNFNJXKLWbcON0UA-aDKmKgOBwgCtJgc7V7FTKiB53ZhWn4kPj7v3cfo1c8r10KXAfU8jT3OqPTj0ynv_X7Ky6LUxplxIfCRDnFKK3Nb3sRso7muE-iC8_kv40nl_XJ93AzfPjSfDC3B-BCgF6ttIY-jSH057ozWahdPH5zTsYtfccn03zXFcJP7j_W9yVpYM</recordid><startdate>20110301</startdate><enddate>20110301</enddate><creator>Ahn, Suk-Won</creator><creator>Kim, Su-Hyun</creator><creator>Kim, Jee-Eun</creator><creator>Kim, Sung-Min</creator><creator>Kim, Seung Hyun</creator><creator>Sung, Jung-Joon</creator><creator>Lee, Kwang-Woo</creator><creator>Hong, Yoon-Ho</creator><general>Cambridge University Press</general><general>Canadian Journal of Neurological Sciences</general><scope>IQODW</scope><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>7X8</scope><scope>7TK</scope></search><sort><creationdate>20110301</creationdate><title>Frontal Assessment Battery to Evaluate Frontal Lobe Dysfunction in ALS Patients</title><author>Ahn, Suk-Won ; Kim, Su-Hyun ; Kim, Jee-Eun ; Kim, Sung-Min ; Kim, Seung Hyun ; Sung, Jung-Joon ; Lee, Kwang-Woo ; Hong, Yoon-Ho</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c515t-a8e825a35e43ea6ae6133fded430a9c3a4486ca021c0f3a70b78e722c1a93d4f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Amyotrophic Lateral Sclerosis - complications</topic><topic>Amyotrophic Lateral Sclerosis - pathology</topic><topic>Biological and medical sciences</topic><topic>Cognition Disorders - diagnosis</topic><topic>Cognition Disorders - etiology</topic><topic>Female</topic><topic>Frontal Lobe - pathology</topic><topic>Frontal Lobe - physiopathology</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis</topic><topic>Neurology</topic><topic>Neuropsychological Tests</topic><topic>Original Article</topic><topic>Statistics, Nonparametric</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ahn, Suk-Won</creatorcontrib><creatorcontrib>Kim, Su-Hyun</creatorcontrib><creatorcontrib>Kim, Jee-Eun</creatorcontrib><creatorcontrib>Kim, Sung-Min</creatorcontrib><creatorcontrib>Kim, Seung Hyun</creatorcontrib><creatorcontrib>Sung, Jung-Joon</creatorcontrib><creatorcontrib>Lee, Kwang-Woo</creatorcontrib><creatorcontrib>Hong, Yoon-Ho</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Neurosciences Abstracts</collection><jtitle>Canadian journal of neurological sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ahn, Suk-Won</au><au>Kim, Su-Hyun</au><au>Kim, Jee-Eun</au><au>Kim, Sung-Min</au><au>Kim, Seung Hyun</au><au>Sung, Jung-Joon</au><au>Lee, Kwang-Woo</au><au>Hong, Yoon-Ho</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Frontal Assessment Battery to Evaluate Frontal Lobe Dysfunction in ALS Patients</atitle><jtitle>Canadian journal of neurological sciences</jtitle><addtitle>Can. J. Neurol. Sci</addtitle><date>2011-03-01</date><risdate>2011</risdate><volume>38</volume><issue>2</issue><spage>242</spage><epage>246</epage><pages>242-246</pages><issn>0317-1671</issn><eissn>2057-0155</eissn><coden>CJNSA2</coden><abstract>Assessment of frontal lobe impairment in amyotrophic lateral sclerosis (ALS) is a matter of great importance, since it often causes ALS patients to decrease medication and nursing compliance, thus shortening their survival time.
The frontal assessment battery (FAB) is a short and rapid method for assessing frontal executive functions. We investigated the applicability of the FAB as a screening method for assessing cognitive impairments in 61 ALS patients. Depending on the results of the FAB, we classified patients into two subgroups: FAB-normal and FAB-abnormal. We then performed additional evaluations of cognitive function using the Korean version of the mini-mental state examination (K-MMSE), a verbal fluency test (COWAT), and a neuropsychiatric inventory (NPI). Results of these tests were compared between the two groups using Mann-Whitney U-tests, and Spearman correlation analyses were used to investigate the relationships between FAB score and disease duration and severity.
Of the 61 sporadic ALS patients included in this study, 14 were classified as FAB-abnormal and 47 were classified as FAB-normal. The FAB-normal and FAB-abnormal patients performed significantly differently in all domains of the COWAT. There was no difference in behavioral disturbance, as assessed by the NPI, between the two groups. The FAB scores were found to significantly correlate with both disease duration and severity.
The FAB shows promise as a method of screening for frontal lobe dysfunction in ALS, as it is not only quick and easy, but also reliable. Additional studies should examine how FAB performance changes as ALS progresses.</abstract><cop>New York, USA</cop><pub>Cambridge University Press</pub><pmid>21320827</pmid><doi>10.1017/S0317167100011409</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Amyotrophic Lateral Sclerosis - complications Amyotrophic Lateral Sclerosis - pathology Biological and medical sciences Cognition Disorders - diagnosis Cognition Disorders - etiology Female Frontal Lobe - pathology Frontal Lobe - physiopathology Humans Male Medical sciences Middle Aged Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis Neurology Neuropsychological Tests Original Article Statistics, Nonparametric Young Adult |
title | Frontal Assessment Battery to Evaluate Frontal Lobe Dysfunction in ALS Patients |
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