Twenty-four-hour blood pressure profile in idiopathic REM sleep behavior disorder

Author:

Terzaghi Michele12ORCID,Pilati Laura13,Ghiotto Natascia4,Arnaldi Dario56ORCID,Versino Maurizio78,Rustioni Valter12,Rustioni Gianluca2,Sartori Ivana9,Manni Raffaele1

Affiliation:

1. Unit of Sleep Medicine and Epilepsy, IRCCS Mondino Foundation, Pavia, Italy

2. Department of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy

3. Department of Biomedicine and Clinical Neuroscience, University of Palermo, Palermo, Italy

4. Interinstitutional Center of Neurological Medicine, IRCCS Mondino Foundation, Pavia, Italy

5. Clinical Neurology, DINOGMI, University of Genoa, Genoa, Italy

6. IRCCS Ospedale Policlinico San Martino, Genoa, Italy

7. Neurology and Stroke Unit, ASST Sette laghi Ospedale di Circolo, Varese, Italy

8. DMC University of Insubria, Varese, Italy

9. C. Munari Center of Epilepsy Surgery, Niguarda Hospital, Milan, Italy

Abstract

Abstract Study Objectives To determine whether autonomic dysfunction in idiopathic REM sleep behavior disorder (iRBD) affects circadian blood pressure (BP) profile. Methods Twenty-one iRBD (mean age 68.8 ± 6.4, mean age at onset 62.2 ± 9.3), 21 drug-free de novo Parkinson’s disease (PD) and 21 control participants (HCs), comparable for age and sex, underwent 24-h ambulatory BP monitoring. A prospective follow-up study was performed to evaluate the occurrence of neurodegenerative disorders in the iRBD cohort. Results In the iRBD group, nighttime systolic BP (SBP) was higher (124.0 ± 20.0, p = .026), nocturnal BP decrease lower (4.0 ± 8.7% for SBP and 8.7 ± 8.0% for diastolic BP [DBP], p = .001), and nondipping status more frequent (71.4% for SBP and 52.4% for DBP; p = .001 and p = .01, respectively) than in the HCs. Reverse dipping of SBP was found in 23.8% (p = .048) of the iRBD participants. Nondipping status was not associated with differences in gender, age, disease duration, age at disease onset, UPDRS score, presence of antihypertensive therapy, or polysomnographic measures. Patients with PD showed daytime and nighttime BP profiles comparable to those observed in iRBD. A subgroup analysis considering only the participants without antihypertensive therapy (12 iRBD, 12 PD) showed results superimposable on those of the whole iRBD and PD groups. Longitudinal follow-up (mean 5.1 ± 1.9 years) showed no differences in BP profile at baseline between converters (n = 6) and nonconverters. Conclusions Twenty-four-hour BP control was impaired in iRBD. This impairment, similar to patterns observed in de novo PD, consisted of reduced amplitude of nocturnal dipping and increased frequency of nondipping status. These findings could have implications for cardiovascular morbidity and mortality in iRBD.

Publisher

Oxford University Press (OUP)

Subject

Physiology (medical),Clinical Neurology

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