Peripheral Silent Period In Cervical and Generalized Dystonia
Dicle Tıp Dergisi / Dicle Med J (2021) 48 (1) : 205-211
Original Article / Özgün Araştırma
Peripheral Silent Period In Cervical and Generalized Dystonia
Melih Tutuncu
1,
Hikmat Abbaszade
1,
Aysegul Gunduz
1,
Meral E. Kiziltan
1
1 Department of Neurology, Cerrahpasa Medical Faculty, Istanbul University-Cerrahpasa, Istanbul, Turkey
Received: 14.02.2021; Revised: 01.03.2021; Accepted: 01.03.2021
Abstract
Objective: Dystonia is a movement disorder described by continuous or alternating muscle contractions causing unusual
postures or insistent motions. Abnormal sensorimotor integration and abnormalities in inhibitory pathways are thought
to have a role in pathogenesis. This paper aims to research the state of inhibitory pathways in the spinal cord in dystonia
through documenting a silent period (SP) through cutaneous stimulation (CuSP) or mixed nerve stimulation (MnSP).
Methods: 23 patients with dystonia were included in the study. Also, 19 healthy subjects were included in the study as a
control group. Ages were similar between two groups. (p=0.092). CuSP and MnSP are recorded through abductor pollicis
brevis and median nerve at the wrist respectively.
Results: Onset latency, time, and suppression index of CuSP were equivalent between two groups. Moreover, the
initiation and terminate latencies of MnSP, also duration, were similar between these two groups. I2 suppression index
was lower in generalized dystonia patients compared to patients with cervical dystonia (100.0 vs 86.7±21.4%; F=4.252,
0.035).
Conclusions: The most striking result to emerge from the data is that there was lower suppression during CuSP in
generalized dystonia patients. Our results suggest that spinal inhibitory circuits are less active if only there is clinical
involvement of the relevant segment.
Keyword: Dystonia, Cutaneous silent period, mixed nerve silent period
DOI: 10.5798/dicletip.888781
Correspondence / Yazışma Adresi: Melih Tutuncu, Department of Neurology, Cerrahpasa Medical Faculty, Istanbul University-Cerrahpasa, Istanbul,
Turke e-mail:
205
Tutuncu M., Abbaszade H., Gundu A., KiziltaM.E.
Servikal ve Jeneralize Distonide Periferik Sessiz Periyot
Öz
Amaç: Distoni, sürekli veya aralıklı kas kasılmalarının anormal duruşlara veya tekrarlayan hareketlere neden olduğu
istemsiz bir hareket bozukluğudur. Distoni sadece bir motor sistem hastalığı değildir. Patofizyolojisinde, anormal
sensorimotor entegrasyon yaygın olarak kabul edilmektedir. Diğer bir patofizyolojik açıklama, inhibitör yolaklardaki
anormalliklerdir. Bu çalışmanın amacı, kutanöz stimülasyonu (CuSP) veya miks sinir stimülasyonunu (MnSP) takiben
sessiz period (SP) kaydederek distonide, omurilikteki inhibitör yolakların durumunu araştırmaktır.
Yöntemler: Çalışmaya 23 distonili hasta dahil edildi. Ayrıca kontrol grubu olarak 19 sağlıklı denek mevcuttu. Yaş gruplar
arasında benzerdi. (p = 0.092). CuSP ve MnSP, sırasıyla abdüktör pollicis brevis ve median sinir aracılığıyla kaydedildi.
Bulgular: CuSP'nin başlangıç latansı, süresi ve supresyon indeksi ile ilgili olarak, distoni hastaları ile sağlıklı bireyler
arasında fark yoktu. MnSP'nin başlangıç ve bitiş latansları ayrıca süreleri, hastalar ve sağlıklı bireyler arasında farklı
değildi. Segmental ve jeneralize distonili hastaların karşılaştırılması, jeneralize distoni hastalarında I2 supresyon
indeksinin düşük olduğunu gösterdi (100.0'a karşı 86.7 ± 21.4%; F = 4.252, 0.035).
Tartışma: Jeneralize distonili hastalarda CuSP sırasında daha az supresyon görülürken, servikal distonili hastalarda
sağlıklı deneklere benzerdi. Sonuçlarımız, spinal inhibitör devrelerin, sadece ilgili segmentin klinik tutulumu varsa daha
az aktif olduğunu.
Anahtar kelimeler: Distoni, kutanöz sessiz dönem, Mikst sinir sessiz dönemi.
INTRODUCTION
Dystonia is a condition that is resistant to most
medical treatments, which may affect almost all
body parts due to various etiologies. It is a
hyperkinetic movement disorder described by
continuous or alternating muscle contractions
causing unusual posture1. The contractions
have similar features: abnormal twisting or
repetitive
movements.
An
involuntary
movement that involves muscle often triggers
dystonia. Also, contractions may develop in the
muscles that should not participate in the
activity during voluntary movement (overflow
phenomenon)2.
The cutaneous silent phase (CuSP) is a powerful
inhibition of EMG activity, due to exposure of
the cutaneous nerve fibers in the fingers to
relatively great intensity, painful electrical
stimuli3. The electromyographic silent period
generated by electrical stimulation of larger
fibers is a mixed nerve silent period (MNSP).
The electrophysiological principles and
adaptive function of the CuSP, which is thought
to be a spinal reflex consisting of afferent arc Adelta fibers, and efferent arc consisting of alpha
motor neurons, have not been clarified yet. The
CuSP is thought to represent the inhibitory part
of the complex defensive reflex. It works with
excitatory cutaneous withdrawal reflexes,
which are used to pull the extremity from the
painful stimulus4.
Various movement disorders such as dystonia
and tremor have been studied in spinal cord
injuries
such
as
syringomyelia
and
5,6
intramedullary masses . To date, various
electrophysiological studies have been
conducted in dystonia. Blink reflex (BR), BR
recovery cycle; startle reflexes showed the
hyperexcitability of the relevant circuits. The
transcranial magnetic stimulation study
showed that intracortical facilitation decreased
during sensory manipulation. Dystonia is not
just a motor system disease. Although the
nociceptive pathways are normal, the activity of
the somatosensory pathways has also been
shown to increase. Besides, it was observed that
the activity increased during the movement
dystonia. This paper aims to evaluate the
condition of nociceptive pathways in dystonia
through MNSP and CuSP7,8.
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Dicle Tıp Dergisi / Dicle Med J (2021) 48 (1) : 205-211
SUBJECTS AND METHOD
Subjects
23 patients (12 female, 11 male); 10 patients
with cervical dystonia, and 13 patients with
generalized dystonia were included in the
study. Also, 19 healthy subjects (11 female, 8
male; p=0.711) were included in the study as a
control group. There were no similarities in
terms of age. (41.4±12.1 vs 36.2±5.2 years,
p=0.092).
We excluded all patients with diseases that
prevent electrophysiological examinations or
create contraindications for examinations and
had any other neurological disease that may
affect electrophysiological examinations.
The study was approved by İstanbul UniversityCerrahpaşa ethical committee at 21 May 2021
with decision number A-06 and the patients
signed informed consent.
METHOD
Electrophysiological recordings were done
using Neuropack Sigma MEB-5500 (Nihon
Kohden, Tokyo, Japan) EMG device and silversilver chloride surface electrodes. Individuals
were in a comfortable chair, which support the
arm. The elbow joint was maintained at a 90⁰
angle (...truncated)