Sensitivity and specificity of threshold tracking transcranial magnetic stimulation for diagnosis of amyotrophic lateral sclerosis: a prospective study
Summary Background Diagnosis of amyotrophic lateral sclerosis (ALS) remains problematic, with substantial diagnostic delays. We assessed the sensitivity and specificity of a threshold tracking transcranial magnetic stimulation (TMS) technique, which might allow early detection of upper motor neuron...
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description | Summary Background Diagnosis of amyotrophic lateral sclerosis (ALS) remains problematic, with substantial diagnostic delays. We assessed the sensitivity and specificity of a threshold tracking transcranial magnetic stimulation (TMS) technique, which might allow early detection of upper motor neuron dysfunction, for the diagnosis of the disorder. Methods We did a prospective study of patients referred to three neuromuscular centres in Sydney, Australia, in accordance with the Standards for Reporting of Diagnostic Accuracy. Participants had definite, probable, or possible ALS, as defined by the Awaji criteria; or pure motor disorder with clinical features of upper and lower motor neuron dysfunction in at least one body region, progressing over a 6 month follow-up period; or muscle wasting and weakness for at least 6 months. All patients underwent threshold tracking TMS at recruitment (index test), with application of the reference standard, the Awaji criteria, to differentiate patients with ALS from those with non-ALS disorders. The investigators who did the index test were masked to the results of the reference test and all other investigations. The primary outcome measures were the sensitivity and specificity of TMS in differentiating ALS from non-ALS disorders; these measures were derived from receiver operator curve analysis. Findings Between Jan 1, 2010, and March 1, 2014, we screened 333 patients; 281 met our inclusion criteria. We eventually diagnosed 209 patients with ALS and 68 with non-ALS disorders; the diagnosis of four patients was inconclusive. The threshold tracking TMS technique differentiated ALS from non-ALS disorders with a sensitivity of 73·21% (95% CI 66·66–79·08) and specificity of 80·88% (69·53–89·40) at an early stage in the disease. All patients tolerated the study well, and we did not record any adverse events from performance of the index test. Interpretation The threshold tracking TMS technique reliably distinguishes ALS from non-ALS disorders and, if these findings are replicated in larger studies, could represent a useful diagnostic investigation when combined with the Awaji criteria to prove upper motor neuron dysfunction at early stages of ALS. Funding Motor Neuron Disease Research Institute of Australia, National Health and Medical Research Council of Australia, and Pfizer. |
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We assessed the sensitivity and specificity of a threshold tracking transcranial magnetic stimulation (TMS) technique, which might allow early detection of upper motor neuron dysfunction, for the diagnosis of the disorder. Methods We did a prospective study of patients referred to three neuromuscular centres in Sydney, Australia, in accordance with the Standards for Reporting of Diagnostic Accuracy. Participants had definite, probable, or possible ALS, as defined by the Awaji criteria; or pure motor disorder with clinical features of upper and lower motor neuron dysfunction in at least one body region, progressing over a 6 month follow-up period; or muscle wasting and weakness for at least 6 months. All patients underwent threshold tracking TMS at recruitment (index test), with application of the reference standard, the Awaji criteria, to differentiate patients with ALS from those with non-ALS disorders. The investigators who did the index test were masked to the results of the reference test and all other investigations. The primary outcome measures were the sensitivity and specificity of TMS in differentiating ALS from non-ALS disorders; these measures were derived from receiver operator curve analysis. Findings Between Jan 1, 2010, and March 1, 2014, we screened 333 patients; 281 met our inclusion criteria. We eventually diagnosed 209 patients with ALS and 68 with non-ALS disorders; the diagnosis of four patients was inconclusive. The threshold tracking TMS technique differentiated ALS from non-ALS disorders with a sensitivity of 73·21% (95% CI 66·66–79·08) and specificity of 80·88% (69·53–89·40) at an early stage in the disease. All patients tolerated the study well, and we did not record any adverse events from performance of the index test. Interpretation The threshold tracking TMS technique reliably distinguishes ALS from non-ALS disorders and, if these findings are replicated in larger studies, could represent a useful diagnostic investigation when combined with the Awaji criteria to prove upper motor neuron dysfunction at early stages of ALS. Funding Motor Neuron Disease Research Institute of Australia, National Health and Medical Research Council of Australia, and Pfizer.</description><identifier>ISSN: 1474-4422</identifier><identifier>EISSN: 1474-4465</identifier><identifier>DOI: 10.1016/S1474-4422(15)00014-9</identifier><identifier>PMID: 25843898</identifier><identifier>CODEN: LANCAO</identifier><language>eng</language><publisher>England: Elsevier Limited</publisher><subject>Adult ; Aged ; Amyotrophic lateral sclerosis ; Amyotrophic Lateral Sclerosis - diagnosis ; Cerebral Cortex - physiopathology ; Councils ; Female ; Grants ; Guidelines as Topic - standards ; Humans ; Laboratories ; Male ; Middle Aged ; Neurology ; Prospective Studies ; Recruitment ; Reproducibility of Results ; ROC Curve ; Sensitivity and Specificity ; Single-Blind Method ; Transcranial Magnetic Stimulation - standards</subject><ispartof>Lancet neurology, 2015-05, Vol.14 (5), p.478-484</ispartof><rights>Elsevier Ltd</rights><rights>Copyright © 2015 Elsevier Ltd. All rights reserved.</rights><rights>Copyright Elsevier Limited May 2015</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c543t-9194a069bbedcd87f720488da0a537e26e638e89015e0f61f93614d799c9fe603</citedby><cites>FETCH-LOGICAL-c543t-9194a069bbedcd87f720488da0a537e26e638e89015e0f61f93614d799c9fe603</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/25843898$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Menon, Parvathi, PhD</creatorcontrib><creatorcontrib>Geevasinga, Nimeshan, MBBS</creatorcontrib><creatorcontrib>Yiannikas, Con, MBBS</creatorcontrib><creatorcontrib>Howells, James, PhD</creatorcontrib><creatorcontrib>Kiernan, Matthew C, Prof</creatorcontrib><creatorcontrib>Vucic, Steve, Prof</creatorcontrib><title>Sensitivity and specificity of threshold tracking transcranial magnetic stimulation for diagnosis of amyotrophic lateral sclerosis: a prospective study</title><title>Lancet neurology</title><addtitle>Lancet Neurol</addtitle><description>Summary Background Diagnosis of amyotrophic lateral sclerosis (ALS) remains problematic, with substantial diagnostic delays. We assessed the sensitivity and specificity of a threshold tracking transcranial magnetic stimulation (TMS) technique, which might allow early detection of upper motor neuron dysfunction, for the diagnosis of the disorder. Methods We did a prospective study of patients referred to three neuromuscular centres in Sydney, Australia, in accordance with the Standards for Reporting of Diagnostic Accuracy. Participants had definite, probable, or possible ALS, as defined by the Awaji criteria; or pure motor disorder with clinical features of upper and lower motor neuron dysfunction in at least one body region, progressing over a 6 month follow-up period; or muscle wasting and weakness for at least 6 months. All patients underwent threshold tracking TMS at recruitment (index test), with application of the reference standard, the Awaji criteria, to differentiate patients with ALS from those with non-ALS disorders. The investigators who did the index test were masked to the results of the reference test and all other investigations. The primary outcome measures were the sensitivity and specificity of TMS in differentiating ALS from non-ALS disorders; these measures were derived from receiver operator curve analysis. Findings Between Jan 1, 2010, and March 1, 2014, we screened 333 patients; 281 met our inclusion criteria. We eventually diagnosed 209 patients with ALS and 68 with non-ALS disorders; the diagnosis of four patients was inconclusive. The threshold tracking TMS technique differentiated ALS from non-ALS disorders with a sensitivity of 73·21% (95% CI 66·66–79·08) and specificity of 80·88% (69·53–89·40) at an early stage in the disease. All patients tolerated the study well, and we did not record any adverse events from performance of the index test. Interpretation The threshold tracking TMS technique reliably distinguishes ALS from non-ALS disorders and, if these findings are replicated in larger studies, could represent a useful diagnostic investigation when combined with the Awaji criteria to prove upper motor neuron dysfunction at early stages of ALS. Funding Motor Neuron Disease Research Institute of Australia, National Health and Medical Research Council of Australia, and Pfizer.</description><subject>Adult</subject><subject>Aged</subject><subject>Amyotrophic lateral sclerosis</subject><subject>Amyotrophic Lateral Sclerosis - diagnosis</subject><subject>Cerebral Cortex - physiopathology</subject><subject>Councils</subject><subject>Female</subject><subject>Grants</subject><subject>Guidelines as Topic - standards</subject><subject>Humans</subject><subject>Laboratories</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neurology</subject><subject>Prospective Studies</subject><subject>Recruitment</subject><subject>Reproducibility of Results</subject><subject>ROC Curve</subject><subject>Sensitivity and Specificity</subject><subject>Single-Blind Method</subject><subject>Transcranial Magnetic Stimulation - standards</subject><issn>1474-4422</issn><issn>1474-4465</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqFkctu1TAQhiMEoqXwCCBLbMoi4PuFRSVUcZMqsSisLR9n0uM2iQ-2UylPwuvinHMoEhs29tj-5p8Z_03zkuC3BBP57ppwxVvOKT0n4g3GmPDWPGpOj9dSPH6IKT1pnuV8izElXJOnzQkVmjNt9Gnz6xqmHEq4D2VBbupQ3oEPffDrOfaobBPkbRw6VJLzd2G6WYMp-7oEN6DR3UxQgke5hHEeXAlxQn1MqAv1JeaQVxU3LrGkuNtWsDKQamb2A6QVeI8c2tWoFq59QFWau-V586R3Q4YXx_2s-fHp4_fLL-3Vt89fLz9ctV5wVlpDDHdYms0GOt9p1SuKudadw04wBVSCZBq0wUQA7iXpDZOEd8oYb3qQmJ015wfd2sHPGXKxY8gehsFNEOdsiWJUM0YN-T8qFTcSS6Uq-vof9DbOaaqDrBTTwigqKyUOlK_T5wS93aUwurRYgu1qst2bbFcHLRF2b7I1Ne_VUX3ejNA9ZP1xtQIXBwDqz90HSNYPYQreDXewQP7bi83U4kOVtQgR-xKG_QbNYrol</recordid><startdate>20150501</startdate><enddate>20150501</enddate><creator>Menon, Parvathi, PhD</creator><creator>Geevasinga, Nimeshan, MBBS</creator><creator>Yiannikas, Con, MBBS</creator><creator>Howells, James, PhD</creator><creator>Kiernan, Matthew C, Prof</creator><creator>Vucic, Steve, Prof</creator><general>Elsevier Limited</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>0TZ</scope><scope>3V.</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8AO</scope><scope>8C2</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>NAPCQ</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20150501</creationdate><title>Sensitivity and specificity of threshold tracking transcranial magnetic stimulation for diagnosis of amyotrophic lateral sclerosis: a prospective study</title><author>Menon, Parvathi, PhD ; 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We assessed the sensitivity and specificity of a threshold tracking transcranial magnetic stimulation (TMS) technique, which might allow early detection of upper motor neuron dysfunction, for the diagnosis of the disorder. Methods We did a prospective study of patients referred to three neuromuscular centres in Sydney, Australia, in accordance with the Standards for Reporting of Diagnostic Accuracy. Participants had definite, probable, or possible ALS, as defined by the Awaji criteria; or pure motor disorder with clinical features of upper and lower motor neuron dysfunction in at least one body region, progressing over a 6 month follow-up period; or muscle wasting and weakness for at least 6 months. All patients underwent threshold tracking TMS at recruitment (index test), with application of the reference standard, the Awaji criteria, to differentiate patients with ALS from those with non-ALS disorders. The investigators who did the index test were masked to the results of the reference test and all other investigations. The primary outcome measures were the sensitivity and specificity of TMS in differentiating ALS from non-ALS disorders; these measures were derived from receiver operator curve analysis. Findings Between Jan 1, 2010, and March 1, 2014, we screened 333 patients; 281 met our inclusion criteria. We eventually diagnosed 209 patients with ALS and 68 with non-ALS disorders; the diagnosis of four patients was inconclusive. The threshold tracking TMS technique differentiated ALS from non-ALS disorders with a sensitivity of 73·21% (95% CI 66·66–79·08) and specificity of 80·88% (69·53–89·40) at an early stage in the disease. All patients tolerated the study well, and we did not record any adverse events from performance of the index test. Interpretation The threshold tracking TMS technique reliably distinguishes ALS from non-ALS disorders and, if these findings are replicated in larger studies, could represent a useful diagnostic investigation when combined with the Awaji criteria to prove upper motor neuron dysfunction at early stages of ALS. Funding Motor Neuron Disease Research Institute of Australia, National Health and Medical Research Council of Australia, and Pfizer.</abstract><cop>England</cop><pub>Elsevier Limited</pub><pmid>25843898</pmid><doi>10.1016/S1474-4422(15)00014-9</doi><tpages>7</tpages></addata></record> |
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subjects | Adult Aged Amyotrophic lateral sclerosis Amyotrophic Lateral Sclerosis - diagnosis Cerebral Cortex - physiopathology Councils Female Grants Guidelines as Topic - standards Humans Laboratories Male Middle Aged Neurology Prospective Studies Recruitment Reproducibility of Results ROC Curve Sensitivity and Specificity Single-Blind Method Transcranial Magnetic Stimulation - standards |
title | Sensitivity and specificity of threshold tracking transcranial magnetic stimulation for diagnosis of amyotrophic lateral sclerosis: a prospective study |
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