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Sleep-apnoea and autonomic dysfunction: a cardiopressor and pupillometric study
G Micieli1, R Manni, C Tassorelli
1Department of Neurology, C. Mondino Foundation, University of Pavia, Italy.
Acta Neurologica Scandinavica
|May 1, 1995
Summary
Autonomic nervous system (ANS) dysfunction in obstructive sleep apnea syndrome (OSAS) is subtle, affecting both sympathetic and parasympathetic branches. Metabolic changes like hypoxia, not neurogenic causes, likely underlie this autonomic involvement in OSAS patients.
Area of Science:
- Neurology
- Sleep Medicine
- Cardiology
Background:
- Obstructive sleep apnea syndrome (OSAS) is linked to autonomic nervous system (ANS) alterations.
- The precise nature and extent of ANS involvement in OSAS remain unclear.
- Previous studies suggest isolated ANS changes in OSAS patients.
Purpose of the Study:
- To evaluate autonomic nervous functions in OSAS patients.
- To determine the sensitivity of cardiopressor and pupillometric tests in detecting ANS dysfunction in OSAS.
- To explore the relationship between ANS alterations and respiratory indices in OSAS.
Main Methods:
- Cardiopressor tests and pupillometry were used to assess autonomic functions.
- Thirteen patients diagnosed with OSAS were included in the study.
- Autonomic nervous system (ANS) function was evaluated using specific neurovegetative tests.
Main Results:
- Most OSAS patients exhibited mild ANS dysfunction, characterized by hypofunction of both sympathetic and parasympathetic branches.
- Pupillometry proved more sensitive than cardiovascular indexes in identifying neurovegetative involvement.
- Observed ANS alterations correlated with specific respiratory indices in OSAS patients.
Conclusions:
- Autonomic dysfunction in OSAS is primarily attributed to metabolic changes such as hypoxia and hypercapnia.
- The findings suggest that OSAS-related autonomic alterations are secondary to metabolic disturbances rather than primary neurogenic causes.
- Pupillometry is a valuable tool for assessing ANS involvement in obstructive sleep apnea syndrome.