Secondary nonresponsiveness to botulinum toxin A in cervical dystonia: The role of electromyogram-guided injections, botulinum toxin A antibody assay, and the extensor digitorum brevis test

We studied 20 patients with cervical dystonia who had started to respond poorly to botulinum toxin A (BTXA) injections after an initial good response. All patients had extensor digitorum brevis (EDB) tests performed in addition to BTXA immunoprecipition assay (IPA) and mouse bioassay (MBA) antibody...

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Veröffentlicht in:Movement disorders 2006-10, Vol.21 (10), p.1737-1741
Hauptverfasser: Cordivari, Carla, Misra, Vijay Peter, Vincent, Angela, Catania, Santiago, Bhatia, Kailash P., Lees, Andrew John
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container_end_page 1741
container_issue 10
container_start_page 1737
container_title Movement disorders
container_volume 21
creator Cordivari, Carla
Misra, Vijay Peter
Vincent, Angela
Catania, Santiago
Bhatia, Kailash P.
Lees, Andrew John
description We studied 20 patients with cervical dystonia who had started to respond poorly to botulinum toxin A (BTXA) injections after an initial good response. All patients had extensor digitorum brevis (EDB) tests performed in addition to BTXA immunoprecipition assay (IPA) and mouse bioassay (MBA) antibody testing. The patients were reexamined and then treated with carefully placed electromyogram (EMG)‐guided BTXA. Nine patients had a good clinical response to EMG‐guided injections and all of these patients showed an obvious decrement on the EDB test. All were BTXA blocking antibodies (Abs)–negative via IPA and MBA (apart from one patient who had low BTXA antibodies titers using IPA but no antibodies by MBA). In the other 11 patients, there was a poor clinical response to EMG‐guided BTXA injections. Seven of these 11 had small EDB decrement and BTXA antibodies using IPA, suggesting resistance to BTXA. Of the remaining four patients, two had obvious EDB decrement and low antibody titers via IPA (one of them had no antibodies via MBA), while the other two patients showed obvious decrement on the EDB test and no antibodies via IPA. This study shows that the EDB test correlates better with the clinical response than the antibody assays and that EDB decrement does not always correlate quantitatively with the BTXA antibody titers. In patients with secondary nonresponsiveness, it is recommended that an EDB test is the initial investigation of choice. In those patients where the EDB test does not demonstrate resistance to BTXA, a reexamination of the patients and carefully placed injections under EMG guidance may improve results. © 2006 Movement Disorder Society
doi_str_mv 10.1002/mds.21051
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All patients had extensor digitorum brevis (EDB) tests performed in addition to BTXA immunoprecipition assay (IPA) and mouse bioassay (MBA) antibody testing. The patients were reexamined and then treated with carefully placed electromyogram (EMG)‐guided BTXA. Nine patients had a good clinical response to EMG‐guided injections and all of these patients showed an obvious decrement on the EDB test. All were BTXA blocking antibodies (Abs)–negative via IPA and MBA (apart from one patient who had low BTXA antibodies titers using IPA but no antibodies by MBA). In the other 11 patients, there was a poor clinical response to EMG‐guided BTXA injections. Seven of these 11 had small EDB decrement and BTXA antibodies using IPA, suggesting resistance to BTXA. Of the remaining four patients, two had obvious EDB decrement and low antibody titers via IPA (one of them had no antibodies via MBA), while the other two patients showed obvious decrement on the EDB test and no antibodies via IPA. This study shows that the EDB test correlates better with the clinical response than the antibody assays and that EDB decrement does not always correlate quantitatively with the BTXA antibody titers. In patients with secondary nonresponsiveness, it is recommended that an EDB test is the initial investigation of choice. 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Disord</addtitle><description>We studied 20 patients with cervical dystonia who had started to respond poorly to botulinum toxin A (BTXA) injections after an initial good response. All patients had extensor digitorum brevis (EDB) tests performed in addition to BTXA immunoprecipition assay (IPA) and mouse bioassay (MBA) antibody testing. The patients were reexamined and then treated with carefully placed electromyogram (EMG)‐guided BTXA. Nine patients had a good clinical response to EMG‐guided injections and all of these patients showed an obvious decrement on the EDB test. All were BTXA blocking antibodies (Abs)–negative via IPA and MBA (apart from one patient who had low BTXA antibodies titers using IPA but no antibodies by MBA). In the other 11 patients, there was a poor clinical response to EMG‐guided BTXA injections. Seven of these 11 had small EDB decrement and BTXA antibodies using IPA, suggesting resistance to BTXA. Of the remaining four patients, two had obvious EDB decrement and low antibody titers via IPA (one of them had no antibodies via MBA), while the other two patients showed obvious decrement on the EDB test and no antibodies via IPA. This study shows that the EDB test correlates better with the clinical response than the antibody assays and that EDB decrement does not always correlate quantitatively with the BTXA antibody titers. In patients with secondary nonresponsiveness, it is recommended that an EDB test is the initial investigation of choice. In those patients where the EDB test does not demonstrate resistance to BTXA, a reexamination of the patients and carefully placed injections under EMG guidance may improve results. © 2006 Movement Disorder Society</description><subject>Action Potentials - drug effects</subject><subject>Antibodies, Blocking - blood</subject><subject>Biological and medical sciences</subject><subject>botulinum toxin</subject><subject>Botulinum Toxins, Type A - administration &amp; dosage</subject><subject>Botulinum Toxins, Type A - immunology</subject><subject>Diseases of striated muscles. Neuromuscular diseases</subject><subject>Drug Resistance</subject><subject>EDB text</subject><subject>Electric Stimulation</subject><subject>Electromyography - drug effects</subject><subject>EMG</subject><subject>Humans</subject><subject>Injections, Intramuscular</subject><subject>Medical sciences</subject><subject>Muscle</subject><subject>Muscle, Skeletal - innervation</subject><subject>Neurology</subject><subject>Pharmacology. 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Disord</addtitle><date>2006-10</date><risdate>2006</risdate><volume>21</volume><issue>10</issue><spage>1737</spage><epage>1741</epage><pages>1737-1741</pages><issn>0885-3185</issn><eissn>1531-8257</eissn><abstract>We studied 20 patients with cervical dystonia who had started to respond poorly to botulinum toxin A (BTXA) injections after an initial good response. All patients had extensor digitorum brevis (EDB) tests performed in addition to BTXA immunoprecipition assay (IPA) and mouse bioassay (MBA) antibody testing. The patients were reexamined and then treated with carefully placed electromyogram (EMG)‐guided BTXA. Nine patients had a good clinical response to EMG‐guided injections and all of these patients showed an obvious decrement on the EDB test. All were BTXA blocking antibodies (Abs)–negative via IPA and MBA (apart from one patient who had low BTXA antibodies titers using IPA but no antibodies by MBA). In the other 11 patients, there was a poor clinical response to EMG‐guided BTXA injections. Seven of these 11 had small EDB decrement and BTXA antibodies using IPA, suggesting resistance to BTXA. Of the remaining four patients, two had obvious EDB decrement and low antibody titers via IPA (one of them had no antibodies via MBA), while the other two patients showed obvious decrement on the EDB test and no antibodies via IPA. This study shows that the EDB test correlates better with the clinical response than the antibody assays and that EDB decrement does not always correlate quantitatively with the BTXA antibody titers. In patients with secondary nonresponsiveness, it is recommended that an EDB test is the initial investigation of choice. In those patients where the EDB test does not demonstrate resistance to BTXA, a reexamination of the patients and carefully placed injections under EMG guidance may improve results. © 2006 Movement Disorder Society</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>16874756</pmid><doi>10.1002/mds.21051</doi><tpages>5</tpages></addata></record>
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source Wiley Online Library - AutoHoldings Journals; MEDLINE
subjects Action Potentials - drug effects
Antibodies, Blocking - blood
Biological and medical sciences
botulinum toxin
Botulinum Toxins, Type A - administration & dosage
Botulinum Toxins, Type A - immunology
Diseases of striated muscles. Neuromuscular diseases
Drug Resistance
EDB text
Electric Stimulation
Electromyography - drug effects
EMG
Humans
Injections, Intramuscular
Medical sciences
Muscle
Muscle, Skeletal - innervation
Neurology
Pharmacology. Drug treatments
Retreatment
secondary nonresponders
Torticollis - drug therapy
Torticollis - immunology
title Secondary nonresponsiveness to botulinum toxin A in cervical dystonia: The role of electromyogram-guided injections, botulinum toxin A antibody assay, and the extensor digitorum brevis test
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