Pregled bibliografske jedinice broj: 1044371
Longitudinal assessment of autonomic nervous system in patients with first demyelinating event suggestive of multiple sclerosis
Longitudinal assessment of autonomic nervous system in patients with first demyelinating event suggestive of multiple sclerosis // European journal of neurology, 26 (2019), 11; 1377-1383 doi:10.1111/ene.13989 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 1044371 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Longitudinal assessment of autonomic nervous system
in patients with first demyelinating event suggestive
of multiple sclerosis
Autori
Habek, Mario ; Crnošija, Luka ; Gabelić, Tereza ; Barun, Barbara ; Adamec, Ivan ; Junaković, Anamari ; Ruška, Berislav ; Pavičić, Tin ; Krbot Skorić, Magdalena
Izvornik
European journal of neurology (1351-5101) 26
(2019), 11;
1377-1383
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
Composite Autonomic Scoring Scale ; Croatian version of the Composite Autonomic System Score-31 ; autonomic nervous system ; magnetic resonance imaging ; multiple sclerosis
Sažetak
BACKGROUND AND PURPOSE: As a high proportion of people with clinically isolated syndrome (pwCIS) exhibit sympathetic adrenergic and sudomotor dysfunction, the aim of this study was to investigate the evolution of autonomic nervous system (ANS) abnormalities in pwCIS over a 2-year follow-up. METHODS: This was a prospective cohort study in which 121 pwCIS were enrolled and followed for 2 years. After 2-year follow-up, data were available for 84 pwCIS. ANS symptoms were evaluated with the Composite Autonomic System Score-31 (COMPASS-31) and results of the ANS tests were expressed using the Composite Autonomic Scoring Scale (CASS) at baseline and visit at month 24. Symptomatic dysautonomia was defined if the patient had a COMPASS-31 value above the median of the whole cohort at baseline evaluation (COMPASS- 31 > 6.79) and CASS score >0. RESULTS: Complete CASS data at baseline and month 24 were available for 62 patients ; in 24 (38.7%) patients there was worsening, in 16 (25.8%) there was improvement and in 22 (35.5%) there was no change in CASS score. In 90% of pwCIS (72 of 80) there was no change in parasympathetic nervous system tests, whereas 47.3% (35 of 74) had either worsening or improvement in sympathetic adrenergic and 28.6% (20 of 70) had either worsening or improvement in sudomotor function. A multivariable regression model identified the total number of T2 lesions as an independent predictor for worsening of symptomatic dysautonomia. No predictors for worsening or improving of CASS score were identified. CONCLUSION: A substantial proportion of pwCIS experienced worsening of ANS abnormalities during the 2- year follow-up and magnetic resonance imaging parameters seemed to predict these abnormalities.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Projekti:
UIP-2013-11-2622 - Evocirani potencijali moždanog debla i testiranje autonomnog živčanog sustava kao metode procijene progresije bolesti u bolesnika s klinički izoliranim sindromom (BACIS) (Habek, Mario, HRZZ - 2013-11) ( CroRIS)
Ustanove:
Fakultet elektrotehnike i računarstva, Zagreb,
Medicinski fakultet, Zagreb,
Klinički bolnički centar Zagreb
Profili:
MAGDALENA KRBOT SKORIĆ
(autor)
Tereza Gabelić
(autor)
Mario Habek
(autor)
Berislav Ruška
(autor)
Anamari Junaković
(autor)
Ivan Adamec
(autor)
Barbara Barun
(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