Back to Search Start Over

Ambulatory blood pressure and drug treatment for orthostatic hypotension as predictors of mortality in patients with multiple system atrophy.

Authors :
Pavy-Le Traon A
Foubert-Samier A
Ory-Magne F
Fabbri M
Senard JM
Meissner WG
Rascol O
Amar J
Source :
European journal of neurology [Eur J Neurol] 2022 Apr; Vol. 29 (4), pp. 1025-1034. Date of Electronic Publication: 2022 Jan 27.
Publication Year :
2022

Abstract

Objectives: Multiple system atrophy (MSA) is a rare fatal neurodegenerative disease characterized by parkinsonism, cerebellar ataxia and autonomic failure. This study was aimed at investigating possible associations between mortality, 24-h blood pressure (BP) level and variability, and drug treatments for orthostatic hypotension (OH) in MSA patients.<br />Methods: A total of 129 patients followed at the French Reference Center for MSA who underwent routine 24-h ambulatory BP monitoring were included. Unified MSA Rating Scale (UMSARS) scores, drug treatments and the occurrence and cause of death were recorded.<br />Results: Seventy patients died during follow-up (2.9 ± 1.8 years), mainly from terminal illness, pulmonary or sudden death. Multivariate Cox regression analysis, after adjustment for gender, disease duration and severity (UMSARS I+II score), showed that increased daytime systolic BP variability, OH severity and OH drug treatment were independently correlated with mortality. OH treatment was associated with the risk of cardiac causes and/or sudden death (p = 0.01). In a fully adjusted model, male gender [(female vs. male) hazard ratio (HR) 0.56, 95% CI 0.34-0.94, p = 0.03], UMSARS I+II score (HR 1.04, 95% CI 1.02-1.06, p < 0.01), systolic BP daytime variability (HR 3.66, 95% CI 1.46-9.17, p < 0.01) and OH treatment (HR: 2.13, 95% CI 1.15-3.94, p = 0.02) predicted mortality.<br />Conclusions: Increased daytime BP variability and OH treatment were predictive of mortality in patients with MSA, independently from disease severity. Further studies are required to assess if these associations are explained by more severe autonomic dysfunction or if OH treatment exposes per se to a specific risk in this population.<br /> (© 2021 European Academy of Neurology.)

Details

Language :
English
ISSN :
1468-1331
Volume :
29
Issue :
4
Database :
MEDLINE
Journal :
European journal of neurology
Publication Type :
Academic Journal
Accession number :
34971021
Full Text :
https://doi.org/10.1111/ene.15232