Pregled bibliografske jedinice broj: 1225306
Sudomotor dysfunction in people with neuromyelitis optica spectrum disorders
Sudomotor dysfunction in people with neuromyelitis optica spectrum disorders // European journal of neurology, 29 (2022), 9; 2772-2780 doi:10.1111/ene.15413 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 1225306 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Sudomotor dysfunction in people with neuromyelitis
optica spectrum disorders
Autori
Habek, Mario ; Andabaka, Marko ; Fanciulli, Alessandra ; Brecl Jakob, Gregor ; Drulović, Jelena ; Leys, Fabian ; Di Pauli, Franziska ; Hegen, Harald ; Auer, Michael ; Pekmezović, Tatjana ; Mesaroš, Šarlota ; Jovičević, Vanja ; Junaković, Anamari ; Wenning, Gregor K. ; Deisenhammer, Florian ; Gabelić, Tereza ; Barun, Barbara ; Adamec, Ivan ; Krbot Skorić, Magdalena
Izvornik
European journal of neurology (1351-5101) 29
(2022), 9;
2772-2780
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
multiple sclerosis ; neuromyelitis optica spectrum disorders ; sudomotor function
Sažetak
Background and purpose: The aim was to determine the extent of sudomotor dysfunction in people with neuromyelitis optica spectrum disorder (pwNMOSD) and to compare findings with a historical cohort of people with relapsing-remitting multiple sclerosis (pwRRMS). Methods: Forty-eight pwNMOSD were enrolled from four clinical centers. All participants completed the Composite Autonomic Symptom Score 31 to screen for symptoms of sudomotor dysfunction. Sudomotor function was assessed using the quantitative sudomotor axon reflex test. The results were compared with a historical cohort of 35 pwRRMS matched for age, sex and disease duration. Results: Symptoms of sudomotor dysfunction, defined by a score in the Composite Autonomic Symptom Score 31 secretomotor domain >0, were present in 26 (54%) of pwNMOSD. The quantitative sudomotor axon reflex test confirmed a sudomotor dysfunction in 25 (52.1%) of pwNMOSD ; in 14 of them (29.2%) sudomotor dysfunction was moderate or severe. No difference was observed between pwNMOSD and pwRRMS in any of the studied parameters. However, symptomatic sudomotor dysfunction was more frequent in pwNMOSD (n = 8, 22.9%) compared to pwRRMS (n = 1, 3% ; p = 0.028). In a multivariable logistic regression analysis, statistically significant predictors for symptomatic sudomotor failure were age and diagnosis of neuromyelitis optica spectrum disorder. Conclusions: Sudomotor dysfunction is common in pwNMOSD and more often symptomatic compared to pwRRMS.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
Fakultet elektrotehnike i računarstva, Zagreb,
Medicinski fakultet, Zagreb,
Klinički bolnički centar Zagreb
Profili:
MAGDALENA KRBOT SKORIĆ
(autor)
Tereza Gabelić
(autor)
Mario Habek
(autor)
Ivan Adamec
(autor)
Barbara Barun
(autor)
Anamari Junaković
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE