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=== Multiple Sklerose und Trigeminusreflexe ===
=== Multiple sclerosis and trigeminal reflexes ===
Wir müssen eine zusätzliche Prämisse über die axonale Demyelinisierung bei Multipler Sklerose machen. Aus einer Studie von Joanna Kamińska andt al.<ref>Joanna Kamińska, Olga M Koper, Kinga Piechal, Halina Kemona . [https://pubmed.ncbi.nlm.nih.gov/28665284/ Multiple sclerosis - etiology and diagnostic potential].Postepy Hig Med Dosw. 2017 Jun 30;71(0):551-563.doi: 10.5604/01.3001.0010.3836.
We must make a further premise concerning axonal demilienization in multiple sclerosis. From a study by Joanna Kamińska et al.<ref>Joanna Kamińska, Olga M Koper, Kinga Piechal, Halina Kemona . [https://pubmed.ncbi.nlm.nih.gov/28665284/ Multiple sclerosis - etiology and diagnostic potential].Postepy Hig Med Dosw. 2017 Jun 30;71(0):551-563.doi: 10.5604/01.3001.0010.3836.
</ref>Es scheint, dass Multiple Sklerose (MS) eine chronisch entzündliche und demyelinisierende Erkrankung autoimmunen Ursprungs ist. Zu den Hauptagenten, die für die Entwicklung von MS verantwortlich sind, gehören exogene, umweltbedingte und genetische Faktoren. MS ist gekennzeichnet durch eine multifokale und zeitlich verteilte Schädigung des zentralen Nervensystems (ZNS), die zu einer axonalen Schädigung führt. Unter den klinischen Verläufen der MS können wir schubförmig verlaufende Multiple Sklerose (RRMS), sekundär progrediente Multiple Sklerose (MSPS), primär progrediente Multiple Sklerose (PPMS) und schubförmig progrediente Multiple Sklerose (PRMS) unterscheiden. Abhängig von der Schwere der Anzeichen und Symptome kann MS entweder als benigne MS oder bösartige MS beschrieben werden. Die Diagnose von MS basiert auf den diagnostischen Kriterien von McDonald's, die die klinische Manifestation mit den charakteristischen Läsionen verknüpfen, die durch Magnetresonanztomographie (MRT), Analyse der Zerebrospinalflüssigkeit (CSF) und visuell evozierte Potenziale nachgewiesen werden.  
</ref> it appears that multiple sclerosis (MS) is a chronic inflammatory and demyelinating disease of autoimmune origin. The main agents responsible for the development of MS include exogenous, environmental and genetic factors. MS is characterized by multifocal and temporally scattered damage of the central nervous system (CNS) leading to axonal damage. Among the clinical courses of MS we can distinguish relapsing-remitting multiple sclerosis (RRMS), secondary progressive multiple sclerosis (SPSM), primary progressive multiple sclerosis (PPMS) and relapsing progressive multiple sclerosis (RPMS). Depending on the severity of the signs and symptoms, MS can be described as benign MS or malignant MS. Diagnosis of MS is based on McDonald's diagnostic criteria, which link clinical manifestation with characteristic lesions demonstrated by magnetic resonance imaging (MRI), cerebrospinal fluid (CSF) analysis, and visual evoked potentials.  


Es ist festzuhalten, dass trotz der enormen Fortschritte bei MS und der Verfügbarkeit unterschiedlicher diagnostischer Methoden diese Erkrankung noch immer eine diagnostische Herausforderung darstellt. Dies kann daran liegen, dass MS einen anderen klinischen Verlauf hat und ein einzelner Test fehlt, der die entsprechende diagnostische Sensitivität und Spezifität für eine schnelle und genaue Diagnose hätte.
It should be emphasized that despite the enormous progress in MS and the availability of different diagnostic methods, this disease still represents a diagnostic challenge. It may result from the fact that MS has a different clinical course and a single test is missing, which would be of appropriate diagnostic sensitivity and specificity for rapid and accurate diagnosis.


  <blockquote>Gerade in Bezug auf diese letzte Beobachtung müssen wir auf eine weitere wichtige Information hinweisen, die sich aus einer Studie von S. K. Yates und W. F. Brown ergibt<ref>S K Yates, W F Brown. The human jaw jerk: electrophysiologic methods to measure the latency, normal values, and changes in multiple sclerosis.Neurology. 1981 May;31(5):632-4.doi: 10.1212/wnl.31.5.632.
  <blockquote>Precisely in reference to this last observation we must point out another significant data that emerged from a study by S K Yates and W F Brown<ref>S K Yates, W F Brown. The human jaw jerk: electrophysiologic methods to measure the latency, normal values, and changes in multiple sclerosis.Neurology. 1981 May;31(5):632-4.doi: 10.1212/wnl.31.5.632.
</ref>in der wir lesen, dass der Kaumasseterreflex bei allen Kontrollpersonen vorhanden ist, aber bei Sklerosepatienten im Allgemeinen fehlt. definiertes Vielfaches (SM). Bei einigen MS-Patienten war die Latenz verlängert. Anomalien des Kieferreflexes sind jedoch weniger häufig als Blinzelreflexreaktionen auf eine supraorbitale Nervenstimulation. Es gab jedoch Patienten, bei denen die Blinzelreflexe normal, aber die Kieferzuckungsreaktionen anormal waren. Die letztere Beobachtung legt nahe, dass der Kieferreflex manchmal nützlich sein kann, um Läsionen des Hirnstamms bei MS zu erkennen.</blockquote>Aber an dieser Stelle wird der Zweifel in dem Sinne wahr: Was sollen wir von den Anomalien der Trigeminusreflexe halten, die in unseren Mary Poppins hervorgehoben werden? Könnten wir einer Form von „Multiple Sklerose“ gegenüberstehen? Wie unterscheiden wir den Ort jeglicher Abwicklung, zentral oder peripher im Trigeminus-Nervensystem?
</ref> in which we read that the jaw jerk of the masseter is present in all control subjects but commonly absent in patients with sclerosis. multiple defined (SM). In some MS patients, the latency was prolonged. Abnormalities in jaw jerk, however, are less common than blink reflex responses to supraorbital nerve stimulation. However, there have been patients in whom the reflex blinks were normal but the jaw jerk responses were abnormal. The latest observation suggests that jaw jerk may occasionally be useful in detecting brain stem injury in MS.</blockquote>But at this point the doubt becomes reality in the sense: what should we think of the anomalies of the trigeminal reflexes highlighted in our Mary Poppins? Could we be facing a form of 'Multiple Sclerosis? How do we distinguish the location of any demienization, Central or Peripheral in the trigeminal nervous system?
<center>
<center>
<gallery widths="350" heights="200" perrow="4" slideshow""="">
<gallery widths="350" heights="200" perrow="4" slideshow""="">
File:Spasmo emimasticatorio JJ.jpg|Abbildung 6: Elektrophysiologisch nachgewiesener Kieferruck im rechten (obere Spuren) und linken (untere Spuren) Masseter
File:Spasmo emimasticatorio JJ.jpg|'''Figure 6:''' Jaw jerk detected electrophysiologically on the right (upper traces) and left (lower traces) masseters
File:Spasmo emimasticatorio SP.jpg|Abbildung 7: Elektrophysiologisch detektierte mechanische Schweigeperiode im rechten (obere überlappende Spuren) und linken (untere überlappende Spuren) Masseter
File:Spasmo emimasticatorio SP.jpg|'''Figure 7:''' Period of mechanical silence detected electrophysiologically on the right (upper overlapping traces) and left (lower overlapping traces) masseters
</gallery>
</gallery>
</center>
</center>

Latest revision as of 11:44, 1 May 2023

Multiple sclerosis and trigeminal reflexes

We must make a further premise concerning axonal demilienization in multiple sclerosis. From a study by Joanna Kamińska et al.[1] it appears that multiple sclerosis (MS) is a chronic inflammatory and demyelinating disease of autoimmune origin. The main agents responsible for the development of MS include exogenous, environmental and genetic factors. MS is characterized by multifocal and temporally scattered damage of the central nervous system (CNS) leading to axonal damage. Among the clinical courses of MS we can distinguish relapsing-remitting multiple sclerosis (RRMS), secondary progressive multiple sclerosis (SPSM), primary progressive multiple sclerosis (PPMS) and relapsing progressive multiple sclerosis (RPMS). Depending on the severity of the signs and symptoms, MS can be described as benign MS or malignant MS. Diagnosis of MS is based on McDonald's diagnostic criteria, which link clinical manifestation with characteristic lesions demonstrated by magnetic resonance imaging (MRI), cerebrospinal fluid (CSF) analysis, and visual evoked potentials.

It should be emphasized that despite the enormous progress in MS and the availability of different diagnostic methods, this disease still represents a diagnostic challenge. It may result from the fact that MS has a different clinical course and a single test is missing, which would be of appropriate diagnostic sensitivity and specificity for rapid and accurate diagnosis.

Precisely in reference to this last observation we must point out another significant data that emerged from a study by S K Yates and W F Brown[2] in which we read that the jaw jerk of the masseter is present in all control subjects but commonly absent in patients with sclerosis. multiple defined (SM). In some MS patients, the latency was prolonged. Abnormalities in jaw jerk, however, are less common than blink reflex responses to supraorbital nerve stimulation. However, there have been patients in whom the reflex blinks were normal but the jaw jerk responses were abnormal. The latest observation suggests that jaw jerk may occasionally be useful in detecting brain stem injury in MS.

But at this point the doubt becomes reality in the sense: what should we think of the anomalies of the trigeminal reflexes highlighted in our Mary Poppins? Could we be facing a form of 'Multiple Sclerosis? How do we distinguish the location of any demienization, Central or Peripheral in the trigeminal nervous system?

  1. Joanna Kamińska, Olga M Koper, Kinga Piechal, Halina Kemona . Multiple sclerosis - etiology and diagnostic potential.Postepy Hig Med Dosw. 2017 Jun 30;71(0):551-563.doi: 10.5604/01.3001.0010.3836.
  2. S K Yates, W F Brown. The human jaw jerk: electrophysiologic methods to measure the latency, normal values, and changes in multiple sclerosis.Neurology. 1981 May;31(5):632-4.doi: 10.1212/wnl.31.5.632.