Sympathetic outflow to skin predicts central autonomic dysfunction in multiple system atrophy.

Central autonomic dysfunction Multiple system atrophy Reflex latency Skin blood flow Skin sympathetic nerve activity

Journal

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
ISSN: 1590-3478
Titre abrégé: Neurol Sci
Pays: Italy
ID NLM: 100959175

Informations de publication

Date de publication:
Aug 2020
Historique:
received: 19 09 2019
accepted: 13 03 2020
pubmed: 22 3 2020
medline: 15 5 2021
entrez: 22 3 2020
Statut: ppublish

Résumé

To find out the physiological method for evaluating the severity of central autonomic dysfunction, we performed detailed evaluation of cutaneous vasomotor neural function in a comparatively large sample of multiple system atrophy (MSA). We evaluated cutaneous vasomotor neural function in 24 MSA patients. Skin sympathetic nerve activity (SSNA) and sympathetic skin response (SSR) and skin blood flow (skin vasomotor reflex [SVR]) were recorded at rest, as well as reflex changes after electrical stimulation. The parameters investigated were SSNA frequency at rest, reflex latency and amplitude of SSNA reflex bursts, absolute decrease and percent reduction of SVR, recovery time, and spontaneous SVR and SSR frequency. There were negative correlations between resting SSNA and disease duration or the SCOPA-AUT score, but these were not significant. SSNA reflex latency displayed significant positive correlations with disease duration and SCOPA-AUT score (p < 0.001 and p < 0.01, respectively). In all five patients who underwent the same examination twice, SSNA reflex latency was significantly longer at the second examination than at the first examination (p < 0.005). A significant positive correlation was identified between recovery time of skin blood flow and SCOPA-AUT score or reflex latency (p < 0.05). Significant correlations were not observed between SCOPA-AUT score or disease duration and other parameters. These results suggest that some MSA patients with a comparatively short duration of disease potentially have impaired thermoregulatory function. Measurement of sympathetic outflow to the skin is potentially a useful tool for predicting the severity of central autonomic dysfunction in MSA.

Sections du résumé

BACKGROUND BACKGROUND
To find out the physiological method for evaluating the severity of central autonomic dysfunction, we performed detailed evaluation of cutaneous vasomotor neural function in a comparatively large sample of multiple system atrophy (MSA).
METHODS METHODS
We evaluated cutaneous vasomotor neural function in 24 MSA patients. Skin sympathetic nerve activity (SSNA) and sympathetic skin response (SSR) and skin blood flow (skin vasomotor reflex [SVR]) were recorded at rest, as well as reflex changes after electrical stimulation. The parameters investigated were SSNA frequency at rest, reflex latency and amplitude of SSNA reflex bursts, absolute decrease and percent reduction of SVR, recovery time, and spontaneous SVR and SSR frequency.
RESULTS RESULTS
There were negative correlations between resting SSNA and disease duration or the SCOPA-AUT score, but these were not significant. SSNA reflex latency displayed significant positive correlations with disease duration and SCOPA-AUT score (p < 0.001 and p < 0.01, respectively). In all five patients who underwent the same examination twice, SSNA reflex latency was significantly longer at the second examination than at the first examination (p < 0.005). A significant positive correlation was identified between recovery time of skin blood flow and SCOPA-AUT score or reflex latency (p < 0.05). Significant correlations were not observed between SCOPA-AUT score or disease duration and other parameters.
CONCLUSIONS CONCLUSIONS
These results suggest that some MSA patients with a comparatively short duration of disease potentially have impaired thermoregulatory function. Measurement of sympathetic outflow to the skin is potentially a useful tool for predicting the severity of central autonomic dysfunction in MSA.

Identifiants

pubmed: 32198655
doi: 10.1007/s10072-020-04340-6
pii: 10.1007/s10072-020-04340-6
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2241-2248

Subventions

Organisme : Health Promotion Administration, Ministry of Health and Welfare (TW)
ID : JSPS KAKENHI Grant Number JP18K07495

Auteurs

Kazumasa Shindo (K)

Department of Neurology, University of Yamanashi, 1110 Shimokatou, Chuo City, Yamanashi, 409-3898, Japan. kshindo@yamanashi.ac.jp.

Toko Fukao (T)

Department of Neurology, University of Yamanashi, 1110 Shimokatou, Chuo City, Yamanashi, 409-3898, Japan.

Naofumi Kurita (N)

Department of Neurology, University of Yamanashi, 1110 Shimokatou, Chuo City, Yamanashi, 409-3898, Japan.

Akane Satake (A)

Department of Neurology, University of Yamanashi, 1110 Shimokatou, Chuo City, Yamanashi, 409-3898, Japan.

Mai Tsuchiya (M)

Department of Neurology, University of Yamanashi, 1110 Shimokatou, Chuo City, Yamanashi, 409-3898, Japan.

Yuta Ichinose (Y)

Department of Neurology, University of Yamanashi, 1110 Shimokatou, Chuo City, Yamanashi, 409-3898, Japan.

Takanori Hata (T)

Department of Neurology, University of Yamanashi, 1110 Shimokatou, Chuo City, Yamanashi, 409-3898, Japan.

Kishin Koh (K)

Department of Neurology, University of Yamanashi, 1110 Shimokatou, Chuo City, Yamanashi, 409-3898, Japan.

Takamura Nagasaka (T)

Department of Neurology, University of Yamanashi, 1110 Shimokatou, Chuo City, Yamanashi, 409-3898, Japan.

Yoshihisa Takiyama (Y)

Department of Neurology, University of Yamanashi, 1110 Shimokatou, Chuo City, Yamanashi, 409-3898, Japan.

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Classifications MeSH