Longitudinal optic neuritis-unrelated visual evoked potential changes in NMO spectrum disorders

被引:42
作者
Ringelstein, Marius [1 ,2 ]
Harmel, Jens [1 ]
Zimmermann, Hanna [3 ,4 ,5 ,6 ,7 ,8 ]
Brandt, Alexander U. [3 ,4 ,5 ,6 ,7 ,8 ,9 ]
Paul, Friedemann [3 ,4 ,5 ,6 ,7 ,8 ]
Haarmann, Axel [10 ]
Buttmann, Mathias [10 ,11 ]
Huemmert, Martin W. [12 ]
Trebst, Corinna [13 ]
Schroeder, Christoph [14 ]
Ayzenberg, Ilya [14 ,15 ]
Kleiter, Ingo [14 ]
Hellwig, Kerstin [14 ]
Havla, Joachim [17 ]
Kuempfel, Tania [17 ]
Jarius, Sven [18 ]
Wildemann, Brigitte [18 ]
Rommer, Paulus [19 ]
Weber, Martin S. [20 ,21 ]
Pellkofer, Hannah [17 ,21 ]
Roepke, Luise [22 ]
Geis, Christian [22 ]
Retzlaff, Nele [23 ]
Zettl, Uwe [23 ]
Deppe, Michael [24 ]
Klotz, Luisa [16 ,24 ]
Young, Kim [25 ,26 ]
Stellmann, Jan-Patrick [25 ,26 ]
Kaste, Matthias [27 ]
Kermer, Pawel [21 ,27 ]
Marouf, Wael [28 ]
Lauda, Florian [29 ]
Tumani, Hayrettin [29 ]
Graf, Jonas [1 ]
Klistorner, Alexander [30 ]
Hartung, Hans-Peter [1 ]
Aktas, Orhan [1 ]
Albrecht, Philipp [1 ]
机构
[1] Heinrich Heine Univ Dusseldorf, Fac Med, Dept Neurol, Dusseldorf, Germany
[2] Heinrich Heine Univ Dusseldorf, LVR Klinikum, Ctr Neurol & Neuropsychiat, Dept Neurol, Dusseldorf, Germany
[3] Charite Univ Med Berlin, NeuroCure Clin Res Ctr, Berlin, Germany
[4] Charite Univ Med Berlin, Expt & Clin Res Ctr, Berlin, Germany
[5] Free Univ Berlin, Berlin, Germany
[6] Humboldt Univ, Berlin, Germany
[7] Berlin Inst Hlth, Berlin, Germany
[8] Max Delbruck Ctr Mol Med, Berlin, Germany
[9] Univ Calif Irvine, Dept Neurol, Irvine, CA 92717 USA
[10] Univ Wurzburg, Dept Neurol, Wurzburg, Germany
[11] Caritas Hosp, Dept Neurol, Bad Mergentheim, Germany
[12] Hannover Med Sch, Clin Neuroimmunol & Neurochem, Hannover, Germany
[13] Hannover Med Sch, Dept Neurol, Hannover, Germany
[14] Ruhr Univ Bochum, St Josef Hosp, Dept Neurol, Bochum, Germany
[15] Sechenov First Moscow State Med Univ, Dept Neurol, Moscow, Russia
[16] Marianne Strauss Klin, Behandlungszentrum Kempfenhausen Multiple Skleros, Berg, Germany
[17] Ludwig Maximilians Univ Munchen, Univ Hosp, Inst Clin Neuroimmunol, Munich, Germany
[18] Heidelberg Univ, Dept Neurol, Mol Neuroimmunol Grp, Heidelberg, Germany
[19] Med Univ Vienna, Dept Neurol, Vienna, Austria
[20] Univ Med Ctr Gottingen, Inst Neuropathol, Gottingen, Germany
[21] Univ Med Ctr Gottingen, Dept Neurol, Gottingen, Germany
[22] Jena Univ Hosp, Dept Neurol, Jena, Germany
[23] Univ Rostock, Dept Neurol, Neuroimmunol Sect, Rostock, Germany
[24] Univ Munster, Dept Neurol, Munster, Germany
[25] Univ Med Ctr Hamburg Eppendorf, Dept Neurol, Hamburg, Germany
[26] Univ Med Ctr Hamburg Eppendorf, Inst Neuroimmunol & MS, Hamburg, Germany
[27] Nordwest Hosp Sanderhusch, Dept Neurol, Sande, Germany
[28] Helios Hanseklinikum Stralsund, Dept Neurol, Stralsund, Germany
[29] Univ Ulm, Dept Neurol, Ulm, Germany
[30] Macquarie Univ, Fac Med & Hlth Sci, Sydney, NSW, Australia
关键词
NEUROMYELITIS-OPTICA; MULTIPLE-SCLEROSIS; CLINICAL-FEATURES; FELLOW EYES; FOLLOW-UP; PATHOLOGY; VISION;
D O I
10.1212/WNL.0000000000008684
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective To investigate if patients with neuromyelitis optica spectrum disorder (NMOSD) develop subclinical visual pathway impairment independent of acute attacks. Methods A total of 548 longitudinally assessed full-field visual evoked potentials (VEP) of 167 patients with NMOSD from 16 centers were retrospectively evaluated for changes of P100 latencies and P100-N140 amplitudes. Rates of change in latencies (RCL) and amplitudes (RCA) over time were analyzed for each individual eye using linear regression and compared using generalized estimating equation models. Results The rates of change in the absence of optic neuritis (ON) for minimal VEP intervals of >= 3 months between baseline and last follow-up were +1.951 ms/y (n = 101 eyes; SD = 6.274; p = 0.012) for the P100 latencies and -2.149 mu V/y (n = 64 eyes; SD = 5.013; p = 0.005) for the P100-N140 amplitudes. For minimal VEP intervals of >= 12 months, the RCL was +1.768 ms/y (n = 59 eyes; SD = 4.558; p = 0.024) and the RCA was -0.527 mu V/y (n = 44 eyes; SD = 2.123; p = 0.111). The history of a previous ON >6 months before baseline VEP had no influence on RCL and RCA. ONs during the observational period led to mean RCL and RCA of +11.689 ms/y (n = 16 eyes; SD = 17.593; p = 0.003) and -1.238 mu V/y (n = 11 eyes; SD = 3.708; p = 0.308), respectively. Conclusion This first longitudinal VEP study of patients with NMOSD provides evidence of progressive VEP latency delay occurring independently of acute ON. Prospective longitudinal studies are needed to corroborate these findings and help to interpret the clinical relevance.
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收藏
页码:E407 / E418
页数:12
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