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Research Article| Volume 250, ISSUE 1-2, P133-139, December 01, 2006

Ipsilateral silent period: A marker of callosal conduction abnormality in early relapsing–remitting multiple sclerosis?

      Abstract

      Objective

      The corpus callosum (CC) is commonly affected in multiple sclerosis (MS). The ipsilateral silent period (iSP) is a putative electrophysiological marker of callosal demyelination. The purpose of this study was to re-assess, under recently established optimised protocol conditions [Jung P., Ziemann U. Differences of the ipsilateral silent period in small hand muscles. Muscle Nerve in press.], its diagnostic sensitivity in MS, about which conflicting results were reported in previous studies.

      Methods

      ISP measurements (onset, duration, and depth) were obtained in the abductor pollicis brevis (APB) muscle of either hand in 49 patients with early relapsing–remitting MS (RRMS) (mean EDSS, 1.3). Standard central motor conduction times to the APB (CMCTAPB) and tibial anterior muscles (CMCTTA), and magnetic resonance images (MRI) were also obtained.

      Results

      ISP measurements showed a similar diagnostic sensitivity (28.6%) as CMCTAPB (24.5%), while diagnostic sensitivities of CMCTTA (69.4%) and MRI of the CC (78.6%) were much higher. Prolongation of iSP duration was the most sensitive single iSP measure. ISP prolongation occurred more frequently when CMCTAPB to the same hand was also prolonged (40.0% vs. 8.4%, p<0.0001). The correlation between iSP duration and CMCTAPB was significant (Pearson's r=0.24, p<0.02), suggesting that iSP duration can be contaminated by demyelination of the contralateral corticospinal tract. ISP duration did not correlate with MRI abnormalities of the CC.

      Conclusions

      ISP measures are neither a sensitive nor a specific marker of callosal conduction abnormality in early RRMS.

      Keywords

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      References

        • Jung P.
        • Ziemann U.
        Differences of the ipsilateral silent period in small hand muscles.
        Muscle Nerve. 2006; 34: 431-436
        • Dietemann J.L.
        • Beigelman C.
        • Rumbach L.
        • Vouge M.
        • Tajahmady T.
        • Faubert C.
        • et al.
        Multiple sclerosis and corpus callosum atrophy: relationship of MRI findings to clinical data.
        Neuroradiology. 1988; 30: 478-480
        • Gean-Marton A.D.
        • Vezina L.G.
        • Marton K.I.
        • Stimac G.K.
        • Peyster R.G.
        • Taveras J.M.
        • et al.
        Abnormal corpus callosum: a sensitive and specific indicator of multiple sclerosis.
        Radiology. 1991; 180: 215-221
        • Simon J.H.
        • Holtas S.L.
        • Schiffer R.B.
        • Rudick R.A.
        • Herndon R.M.
        • Kido D.K.
        • et al.
        Corpus callosum and subcallosal-periventricular lesions in multiple sclerosis: detection with MR.
        Radiology. 1986; 160: 363-367
        • Evangelou N.
        • Esiri M.M.
        • Smith S.
        • Palace J.
        • Matthews P.M.
        Quantitative pathological evidence for axonal loss in normal appearing white matter in multiple sclerosis.
        Ann Neurol. 2000; 47: 391-395
        • Chard D.T.
        • Griffin C.M.
        • Parker G.J.
        • Kapoor R.
        • Thompson A.J.
        • Miller D.H.
        Brain atrophy in clinically early relapsing–remitting multiple sclerosis.
        Brain. 2002; 125: 327-337
        • De Stefano N.
        • Narayanan S.
        • Francis G.S.
        • Arnaoutelis R.
        • Tartaglia M.C.
        • Antel J.P.
        • et al.
        Evidence of axonal damage in the early stages of multiple sclerosis and its relevance to disability.
        Arch Neurol. 2001; 58: 65-70
        • Pelletier J.
        • Suchet L.
        • Witjas T.
        • Habib M.
        • Guttmann C.R.
        • Salamon G.
        • et al.
        A longitudinal study of callosal atrophy and interhemispheric dysfunction in relapsing–remitting multiple sclerosis.
        Arch Neurol. 2001; 58: 105-111
        • Barkhof F.J.
        • Elton M.
        • Lindeboom J.
        • Tas M.W.
        • Schmidt W.F.
        • Hommes O.R.
        • et al.
        Functional correlates of callosal atrophy in relapsing–remitting multiple sclerosis patients. A preliminary MRI study.
        J Neurol. 1998; 245: 153-158
        • Lindeboom J.
        • ter Horst R.
        Interhemispheric disconnection effects in multiple sclerosis.
        J Neurol Neurosurg Psychiatry. 1988; 51: 1445-1447
        • Pelletier J.
        • Habib M.
        • Lyon-Caen O.
        • Salamon G.
        • Poncet M.
        • Khalil R.
        Functional and magnetic resonance imaging correlates of callosal involvement in multiple sclerosis.
        Arch Neurol. 1993; 50: 1077-1082
        • Boroojerdi B.
        • Hungs M.
        • Mull M.
        • Topper R.
        • Noth J.
        Interhemispheric inhibition in patients with multiple sclerosis.
        Electroencephalogr Clin Neurophysiol. 1998; 109: 230-237
        • Höppner J.
        • Kunesch E.
        • Buchmann J.
        • Hess A.
        • Grossmann A.
        • Benecke R.
        Demyelination and axonal degeneration in corpus callosum assessed by analysis of transcallosally mediated inhibition in multiple sclerosis.
        Clin Neurophysiol. 1999; 110: 748-756
        • Schmierer K.
        • Niehaus L.
        • Röricht S.
        • Meyer B.U.
        Conduction deficits of callosal fibres in early multiple sclerosis.
        J Neurol Neurosurg Psychiatry. 2000; 68: 633-638
        • Schmierer K.
        • Irlbacher K.
        • Grosse P.
        • Roricht S.
        • Meyer B.U.
        Correlates of disability in multiple sclerosis detected by transcranial magnetic stimulation.
        Neurology. 2002; 59: 1218-1224
        • Wassermann E.M.
        • Fuhr P.
        • Cohen L.G.
        • Hallett M.
        Effects of transcranial magnetic stimulation on ipsilateral muscles.
        Neurology. 1991; 41: 1795-1799
        • Meyer B.U.
        • Röricht S.
        • Gräfin von Einsiedel H.
        • Kruggel F.
        • Weindl A.
        Inhibitory and excitatory interhemispheric transfers between motor cortical areas in normal humans and patients with abnormalities of the corpus callosum.
        Brain. 1995; 118: 429-440
        • Meyer B.-U.
        • Röricht S.
        • Woiciechowsky C.
        Topography of fibers in the human corpus callosum mediating interhemispheric inhibition between the motor cortices.
        Ann Neurol. 1998; 43: 360-369
        • Hess C.W.
        • Mills K.R.
        • Murray N.M.
        • Schriefer T.N.
        Magnetic brain stimulation: central motor conduction studies in multiple sclerosis.
        Ann Neurol. 1987; 22: 744-752
        • Jones S.M.
        • Streletz L.J.
        • Raab V.E.
        • Knobler R.L.
        • Lublin F.D.
        Lower extremity motor evoked potentials in multiple sclerosis.
        Arch Neurol. 1991; 48: 944-948
        • Mayr N.
        • Baumgartner C.
        • Zeitlhofer J.
        • Deecke L.
        The sensitivity of transcranial cortical magnetic stimulation in detecting pyramidal tract lesions in clinically definite multiple sclerosis.
        Neurology. 1991; 41: 566-569
        • Ravnborg M.
        • Liguori R.
        • Christiansen P.
        • Larsson H.
        • Sorensen P.S.
        The diagnostic reliability of magnetically evoked motor potentials in multiple sclerosis.
        Neurology. 1992; 42: 1296-1301
        • McDonald W.I.
        • Compston A.
        • Edan G.
        • Goodkin D.
        • Hartung H.P.
        • Lublin F.D.
        • et al.
        Recommended diagnostic criteria for multiple sclerosis: guidelines from the International Panel on the diagnosis of multiple sclerosis.
        Ann Neurol. 2001; 50: 121-127
        • Rieckmann P.
        • Toyka K.V.
        Escalating immunotherapy of multiple sclerosis. New aspects and practical application.
        J Neurol. 2004; 251: 1329-1339
        • Kurtzke J.F.
        Rating neurologic impairment in multiple sclerosis: an expanded disability status scale (EDSS).
        Neurology. 1983; 33: 1444-1452
        • Wassermann E.M.
        • Pascual-Leone A.
        • Hallett M.
        Cortical motor representation of the ipsilateral hand and arm.
        Exp Brain Res. 1994; 100: 121-132
        • Rossini P.M.
        • Berardelli A.
        • Deuschl G.
        • Hallett M.
        • Maertens de Noordhout A.M.
        • Paulus W.
        • et al.
        Applications of magnetic cortical stimulation.
        Electroencephalogr Clin Neurophysiol, Suppl. 1999; 52: 171-185
        • Witelson S.F.
        Hand and sex differences in the isthmus and genu of the human corpus callosum. A postmortem morphological study.
        Brain. 1989; 112: 799-835
        • Ranjeva J.P.
        • Audoin B.
        • Au Duong M.V.
        • Ibarrola D.
        • Confort-Gouny S.
        • Malikova I.
        • et al.
        Local tissue damage assessed with statistical mapping analysis of brain magnetization transfer ratio: relationship with functional status of patients in the earliest stage of multiple sclerosis.
        AJNR Am J Neuroradiol. 2005; 26: 119-127
        • Pagani E.
        • Rocca M.A.
        • Gallo A.
        • Rovaris M.
        • Martinelli V.
        • Comi G.
        • et al.
        Regional brain atrophy evolves differently in patients with multiple sclerosis according to clinical phenotype.
        AJNR Am J Neuroradiol. 2005; 26: 341-346
        • Garvey M.A.
        • Ziemann U.
        • Becker D.A.
        • Barker C.A.
        • Bartko J.J.
        New graphical method to measure silent periods evoked by transcranial magnetic stimulation.
        Clin Neurophysiol. 2001; 112: 1451-1460
        • Claus D.
        Central motor conduction: method and normal results.
        Muscle Nerve. 1990; 13: 1125-1132
        • O'Connor P.
        • Marchetti P.
        • Lee L.
        • Perera M.
        Evoked potential abnormality scores are a useful measure of disease burden in relapsing–remitting multiple sclerosis.
        Ann Neurol. 1998; 44: 404-407
        • Fuhr P.
        • Borggrefe-Chappuis A.
        • Schindler C.
        • Kappos L.
        Visual and motor evoked potentials in the course of multiple sclerosis.
        Brain. 2001; 124: 2162-2168
        • Miller D.H.
        • Grossman R.I.
        • Reingold S.C.
        • McFarland H.F.
        The role of magnetic resonance techniques in understanding and managing multiple sclerosis.
        Brain. 1998; 121: 3-24
        • Wahl M.
        • Lauterbach-Soon B.
        • Hattingen E.
        • Ogrezeanu G.
        • Lanfermann H.
        • Ziemann U.
        Determining the topography of interhemispheric fibres in the human corpus callosum (CC) between the primary motor cortices with a combined fMRI/DTI-fibretracking prodecure [Abstract].
        Klin Neurophysiol. 2006; 37: 96-97
        • Gould H.J.D.
        • Cusick C.G.
        • Pons T.P.
        • Kaas J.H.
        The relationship of corpus callosum connections to electrical stimulation maps of motor, supplementary motor, and the frontal eye fields in owl monkeys.
        J Comp Neurol. 1986; 247: 297-325
        • Rouiller E.M.
        • Babalian A.
        • Kazennikov O.
        • Moret V.
        • Yu X.H.
        • Wiesendanger M.
        Transcallosal connections of the distal forelimb representations of the primary and supplementary motor cortical areas in macaque monkeys.
        Exp Brain Res. 1994; 102: 227-243
        • Aboitiz F.
        • Scheibel A.B.
        • Fisher R.S.
        • Zaidel E.
        Fiber composition of the human corpus callosum.
        Brain Res. 1992; 598: 143-153
        • Röricht S.
        • Meyer B.-U.
        • Woichiechowsky C.
        • Lehmann R.
        Callosal and corticospinal tract function in patients with hydrocephalus: a morphometric and transcranial magnetic stimulation study.
        J Neurol. 1998; 245: 280-288
        • Wolters A.
        • Classen J.
        • Kunesch E.
        • Grossmann A.
        • Benecke R.
        Measurements of transcallosally mediated cortical inhibition for differentiating parkinsonian syndromes.
        Mov Disord. 2004; 19: 518-528