Subclinical Saccadic Eye Movement Dysfunction in Pediatric Multiple Sclerosis
Background: Efferent visual dysfunction in children could lead to impaired quality of life at home and school. Eye-tracking can detect subtle efferent dysfunction missed on bedside examination but has not been validated in the pediatric multiple sclerosis population. Objective: We sought to determin...
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Veröffentlicht in: | Journal of child neurology 2019-01, Vol.34 (1), p.38-43 |
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container_title | Journal of child neurology |
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creator | Yousef, Andrew Devereux, Michael Gourraud, Pierre-Antoine Jonzzon, Soren Suleiman, Leena Waubant, Emmanuelle Green, Ari Graves, Jennifer S. |
description | Background:
Efferent visual dysfunction in children could lead to impaired quality of life at home and school. Eye-tracking can detect subtle efferent dysfunction missed on bedside examination but has not been validated in the pediatric multiple sclerosis population.
Objective:
We sought to determine the feasibility of eye-tracking in children and associations with multiple sclerosis.
Methods:
Participants meeting criteria for pediatric multiple sclerosis without acute efferent vision abnormalities and healthy controls were recruited. Multiple sclerosis participants underwent a clinical assessment and saccade and antisaccade testing paradigms. Intraclass correlation coefficients were generated for intertest repeatability. Adjusting for age and intereye correlations, generalized estimating equations compared latencies with case status, Expanded Disability Status Scale and Symbol Digit Modalities Test (SDMT) scores.
Results:
We eye-tracked 15 children with multiple sclerosis (n = 30 eyes, mean age 15.6 ± 2.1, mean disease duration 3.9 years, median Expanded Disability Status Scale 1.5) compared to 6 healthy controls (n = 12 eyes, age 14.3 ± .95). The intraclass correlation coefficient for repeated trials was 0.85. Adjusting for age, saccadic latency was 60 milliseconds (ms) longer for cases than controls (95% confidence interval = 26.4, 93.8; P = .0005). For antisaccadic latency, we observed a similar trend of 60 ms longer for cases than controls (P = .06).
Conclusion:
Eye-tracking is a short noninvasive examination, and high intertest repeatability supports use of eye-tracking technology in pediatric multiple sclerosis. Longer saccadic latencies were seen in children with multiple sclerosis despite short disease duration and low Expanded Disability Status Scale scores. |
doi_str_mv | 10.1177/0883073818807787 |
format | Article |
fullrecord | <record><control><sourceid>proquest_hal_p</sourceid><recordid>TN_cdi_hal_primary_oai_HAL_hal_04736182v1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sage_id>10.1177_0883073818807787</sage_id><sourcerecordid>2179230599</sourcerecordid><originalsourceid>FETCH-LOGICAL-c413t-4702f80a8d2dcfdf2980ea4c193bbc8d70242c431ea389d57a4b0f42907b9083</originalsourceid><addsrcrecordid>eNp1kE1Lw0AQhhdRbP24e5Ic9RCd_Wh39ihaP6BFob0vm81GVzZJzSaF_nsTqj0IngbmfeaFeQi5oHBDqZS3gMhBcqSIICXKAzKmEjBFhvyQjIc4HfIROYnxEwBwouCYjDiIKRdTOSaLZZfZ4CtvTUiWxlqTe5vMti5Z1BtXuqpNHrax6Crb-rpKfJW8udybtumpRRdavw4uWdrgmjr6eEaOChOiO_-Zp2T1OFvdP6fz16eX-7t5agXlbSoksALBYM5yW-QFUwjOCEsVzzKLeR8LZgWnznBU-UQakUEhmAKZKUB-Sq53tR8m6HXjS9NsdW28fr6b62EHQvIpRbahPXu1Y9dN_dW52OrSR-tCMJWru6gZlYpxmCjVo7BDbf9MbFyx76agB9_6r-_-5PKnvctKl-8PfgX3QLoDonl3-rPumqoX83_hN2a0hls</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2179230599</pqid></control><display><type>article</type><title>Subclinical Saccadic Eye Movement Dysfunction in Pediatric Multiple Sclerosis</title><source>MEDLINE</source><source>SAGE Complete A-Z List</source><creator>Yousef, Andrew ; Devereux, Michael ; Gourraud, Pierre-Antoine ; Jonzzon, Soren ; Suleiman, Leena ; Waubant, Emmanuelle ; Green, Ari ; Graves, Jennifer S.</creator><creatorcontrib>Yousef, Andrew ; Devereux, Michael ; Gourraud, Pierre-Antoine ; Jonzzon, Soren ; Suleiman, Leena ; Waubant, Emmanuelle ; Green, Ari ; Graves, Jennifer S.</creatorcontrib><description>Background:
Efferent visual dysfunction in children could lead to impaired quality of life at home and school. Eye-tracking can detect subtle efferent dysfunction missed on bedside examination but has not been validated in the pediatric multiple sclerosis population.
Objective:
We sought to determine the feasibility of eye-tracking in children and associations with multiple sclerosis.
Methods:
Participants meeting criteria for pediatric multiple sclerosis without acute efferent vision abnormalities and healthy controls were recruited. Multiple sclerosis participants underwent a clinical assessment and saccade and antisaccade testing paradigms. Intraclass correlation coefficients were generated for intertest repeatability. Adjusting for age and intereye correlations, generalized estimating equations compared latencies with case status, Expanded Disability Status Scale and Symbol Digit Modalities Test (SDMT) scores.
Results:
We eye-tracked 15 children with multiple sclerosis (n = 30 eyes, mean age 15.6 ± 2.1, mean disease duration 3.9 years, median Expanded Disability Status Scale 1.5) compared to 6 healthy controls (n = 12 eyes, age 14.3 ± .95). The intraclass correlation coefficient for repeated trials was 0.85. Adjusting for age, saccadic latency was 60 milliseconds (ms) longer for cases than controls (95% confidence interval = 26.4, 93.8; P = .0005). For antisaccadic latency, we observed a similar trend of 60 ms longer for cases than controls (P = .06).
Conclusion:
Eye-tracking is a short noninvasive examination, and high intertest repeatability supports use of eye-tracking technology in pediatric multiple sclerosis. Longer saccadic latencies were seen in children with multiple sclerosis despite short disease duration and low Expanded Disability Status Scale scores.</description><identifier>ISSN: 0883-0738</identifier><identifier>EISSN: 1708-8283</identifier><identifier>DOI: 10.1177/0883073818807787</identifier><identifier>PMID: 30463467</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Adolescent ; Cohort Studies ; Disability Evaluation ; Eye Movement Measurements ; Feasibility Studies ; Female ; Humans ; Life Sciences ; Male ; Multiple Sclerosis ; Multiple Sclerosis - complications ; Multiple Sclerosis - diagnosis ; Multiple Sclerosis - physiopathology ; Ocular Motility Disorders ; Ocular Motility Disorders - complications ; Ocular Motility Disorders - diagnosis ; Ocular Motility Disorders - physiopathology ; Pilot Projects ; Proof of Concept Study ; Reproducibility of Results ; Saccades ; Saccades - physiology</subject><ispartof>Journal of child neurology, 2019-01, Vol.34 (1), p.38-43</ispartof><rights>The Author(s) 2018</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c413t-4702f80a8d2dcfdf2980ea4c193bbc8d70242c431ea389d57a4b0f42907b9083</citedby><cites>FETCH-LOGICAL-c413t-4702f80a8d2dcfdf2980ea4c193bbc8d70242c431ea389d57a4b0f42907b9083</cites><orcidid>0000-0003-1131-9554</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/0883073818807787$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/0883073818807787$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>230,314,780,784,885,21818,27923,27924,43620,43621</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30463467$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-04736182$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Yousef, Andrew</creatorcontrib><creatorcontrib>Devereux, Michael</creatorcontrib><creatorcontrib>Gourraud, Pierre-Antoine</creatorcontrib><creatorcontrib>Jonzzon, Soren</creatorcontrib><creatorcontrib>Suleiman, Leena</creatorcontrib><creatorcontrib>Waubant, Emmanuelle</creatorcontrib><creatorcontrib>Green, Ari</creatorcontrib><creatorcontrib>Graves, Jennifer S.</creatorcontrib><title>Subclinical Saccadic Eye Movement Dysfunction in Pediatric Multiple Sclerosis</title><title>Journal of child neurology</title><addtitle>J Child Neurol</addtitle><description>Background:
Efferent visual dysfunction in children could lead to impaired quality of life at home and school. Eye-tracking can detect subtle efferent dysfunction missed on bedside examination but has not been validated in the pediatric multiple sclerosis population.
Objective:
We sought to determine the feasibility of eye-tracking in children and associations with multiple sclerosis.
Methods:
Participants meeting criteria for pediatric multiple sclerosis without acute efferent vision abnormalities and healthy controls were recruited. Multiple sclerosis participants underwent a clinical assessment and saccade and antisaccade testing paradigms. Intraclass correlation coefficients were generated for intertest repeatability. Adjusting for age and intereye correlations, generalized estimating equations compared latencies with case status, Expanded Disability Status Scale and Symbol Digit Modalities Test (SDMT) scores.
Results:
We eye-tracked 15 children with multiple sclerosis (n = 30 eyes, mean age 15.6 ± 2.1, mean disease duration 3.9 years, median Expanded Disability Status Scale 1.5) compared to 6 healthy controls (n = 12 eyes, age 14.3 ± .95). The intraclass correlation coefficient for repeated trials was 0.85. Adjusting for age, saccadic latency was 60 milliseconds (ms) longer for cases than controls (95% confidence interval = 26.4, 93.8; P = .0005). For antisaccadic latency, we observed a similar trend of 60 ms longer for cases than controls (P = .06).
Conclusion:
Eye-tracking is a short noninvasive examination, and high intertest repeatability supports use of eye-tracking technology in pediatric multiple sclerosis. Longer saccadic latencies were seen in children with multiple sclerosis despite short disease duration and low Expanded Disability Status Scale scores.</description><subject>Adolescent</subject><subject>Cohort Studies</subject><subject>Disability Evaluation</subject><subject>Eye Movement Measurements</subject><subject>Feasibility Studies</subject><subject>Female</subject><subject>Humans</subject><subject>Life Sciences</subject><subject>Male</subject><subject>Multiple Sclerosis</subject><subject>Multiple Sclerosis - complications</subject><subject>Multiple Sclerosis - diagnosis</subject><subject>Multiple Sclerosis - physiopathology</subject><subject>Ocular Motility Disorders</subject><subject>Ocular Motility Disorders - complications</subject><subject>Ocular Motility Disorders - diagnosis</subject><subject>Ocular Motility Disorders - physiopathology</subject><subject>Pilot Projects</subject><subject>Proof of Concept Study</subject><subject>Reproducibility of Results</subject><subject>Saccades</subject><subject>Saccades - physiology</subject><issn>0883-0738</issn><issn>1708-8283</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kE1Lw0AQhhdRbP24e5Ic9RCd_Wh39ihaP6BFob0vm81GVzZJzSaF_nsTqj0IngbmfeaFeQi5oHBDqZS3gMhBcqSIICXKAzKmEjBFhvyQjIc4HfIROYnxEwBwouCYjDiIKRdTOSaLZZfZ4CtvTUiWxlqTe5vMti5Z1BtXuqpNHrax6Crb-rpKfJW8udybtumpRRdavw4uWdrgmjr6eEaOChOiO_-Zp2T1OFvdP6fz16eX-7t5agXlbSoksALBYM5yW-QFUwjOCEsVzzKLeR8LZgWnznBU-UQakUEhmAKZKUB-Sq53tR8m6HXjS9NsdW28fr6b62EHQvIpRbahPXu1Y9dN_dW52OrSR-tCMJWru6gZlYpxmCjVo7BDbf9MbFyx76agB9_6r-_-5PKnvctKl-8PfgX3QLoDonl3-rPumqoX83_hN2a0hls</recordid><startdate>20190101</startdate><enddate>20190101</enddate><creator>Yousef, Andrew</creator><creator>Devereux, Michael</creator><creator>Gourraud, Pierre-Antoine</creator><creator>Jonzzon, Soren</creator><creator>Suleiman, Leena</creator><creator>Waubant, Emmanuelle</creator><creator>Green, Ari</creator><creator>Graves, Jennifer S.</creator><general>SAGE Publications</general><general>SAGE Publications (UK and US)</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>7X8</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0003-1131-9554</orcidid></search><sort><creationdate>20190101</creationdate><title>Subclinical Saccadic Eye Movement Dysfunction in Pediatric Multiple Sclerosis</title><author>Yousef, Andrew ; Devereux, Michael ; Gourraud, Pierre-Antoine ; Jonzzon, Soren ; Suleiman, Leena ; Waubant, Emmanuelle ; Green, Ari ; Graves, Jennifer S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c413t-4702f80a8d2dcfdf2980ea4c193bbc8d70242c431ea389d57a4b0f42907b9083</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adolescent</topic><topic>Cohort Studies</topic><topic>Disability Evaluation</topic><topic>Eye Movement Measurements</topic><topic>Feasibility Studies</topic><topic>Female</topic><topic>Humans</topic><topic>Life Sciences</topic><topic>Male</topic><topic>Multiple Sclerosis</topic><topic>Multiple Sclerosis - complications</topic><topic>Multiple Sclerosis - diagnosis</topic><topic>Multiple Sclerosis - physiopathology</topic><topic>Ocular Motility Disorders</topic><topic>Ocular Motility Disorders - complications</topic><topic>Ocular Motility Disorders - diagnosis</topic><topic>Ocular Motility Disorders - physiopathology</topic><topic>Pilot Projects</topic><topic>Proof of Concept Study</topic><topic>Reproducibility of Results</topic><topic>Saccades</topic><topic>Saccades - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yousef, Andrew</creatorcontrib><creatorcontrib>Devereux, Michael</creatorcontrib><creatorcontrib>Gourraud, Pierre-Antoine</creatorcontrib><creatorcontrib>Jonzzon, Soren</creatorcontrib><creatorcontrib>Suleiman, Leena</creatorcontrib><creatorcontrib>Waubant, Emmanuelle</creatorcontrib><creatorcontrib>Green, Ari</creatorcontrib><creatorcontrib>Graves, Jennifer S.</creatorcontrib><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>Hyper Article en Ligne (HAL)</collection><jtitle>Journal of child neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yousef, Andrew</au><au>Devereux, Michael</au><au>Gourraud, Pierre-Antoine</au><au>Jonzzon, Soren</au><au>Suleiman, Leena</au><au>Waubant, Emmanuelle</au><au>Green, Ari</au><au>Graves, Jennifer S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Subclinical Saccadic Eye Movement Dysfunction in Pediatric Multiple Sclerosis</atitle><jtitle>Journal of child neurology</jtitle><addtitle>J Child Neurol</addtitle><date>2019-01-01</date><risdate>2019</risdate><volume>34</volume><issue>1</issue><spage>38</spage><epage>43</epage><pages>38-43</pages><issn>0883-0738</issn><eissn>1708-8283</eissn><abstract>Background:
Efferent visual dysfunction in children could lead to impaired quality of life at home and school. Eye-tracking can detect subtle efferent dysfunction missed on bedside examination but has not been validated in the pediatric multiple sclerosis population.
Objective:
We sought to determine the feasibility of eye-tracking in children and associations with multiple sclerosis.
Methods:
Participants meeting criteria for pediatric multiple sclerosis without acute efferent vision abnormalities and healthy controls were recruited. Multiple sclerosis participants underwent a clinical assessment and saccade and antisaccade testing paradigms. Intraclass correlation coefficients were generated for intertest repeatability. Adjusting for age and intereye correlations, generalized estimating equations compared latencies with case status, Expanded Disability Status Scale and Symbol Digit Modalities Test (SDMT) scores.
Results:
We eye-tracked 15 children with multiple sclerosis (n = 30 eyes, mean age 15.6 ± 2.1, mean disease duration 3.9 years, median Expanded Disability Status Scale 1.5) compared to 6 healthy controls (n = 12 eyes, age 14.3 ± .95). The intraclass correlation coefficient for repeated trials was 0.85. Adjusting for age, saccadic latency was 60 milliseconds (ms) longer for cases than controls (95% confidence interval = 26.4, 93.8; P = .0005). For antisaccadic latency, we observed a similar trend of 60 ms longer for cases than controls (P = .06).
Conclusion:
Eye-tracking is a short noninvasive examination, and high intertest repeatability supports use of eye-tracking technology in pediatric multiple sclerosis. Longer saccadic latencies were seen in children with multiple sclerosis despite short disease duration and low Expanded Disability Status Scale scores.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>30463467</pmid><doi>10.1177/0883073818807787</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0003-1131-9554</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Cohort Studies Disability Evaluation Eye Movement Measurements Feasibility Studies Female Humans Life Sciences Male Multiple Sclerosis Multiple Sclerosis - complications Multiple Sclerosis - diagnosis Multiple Sclerosis - physiopathology Ocular Motility Disorders Ocular Motility Disorders - complications Ocular Motility Disorders - diagnosis Ocular Motility Disorders - physiopathology Pilot Projects Proof of Concept Study Reproducibility of Results Saccades Saccades - physiology |
title | Subclinical Saccadic Eye Movement Dysfunction in Pediatric Multiple Sclerosis |
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