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Published on: August 21, 2017
Autonomic dysfunction in people with neuromyelitis optica spectrum disorders
Luka Crnošija1, Magdalena Krbot Skorić2, Marko Andabaka3
1Referral Center for Autonomic Nervous System Disorders, Department of Neurology, University Hospital Center Zagreb, Zagreb, Croatia.
People with neuromyelitis optica spectrum disorder (NMOSD) experience significant dysautonomia, including pupillomotor and cardiovascular autonomic dysfunction, more frequently than those with multiple sclerosis (MS). This autonomic dysfunction appears distinct between NMOSD and MS patients.
Area of Science:
- Neurology
- Autonomic Neuroscience
- Clinical Research
Background:
- Dysautonomia, or autonomic nervous system dysfunction, is increasingly recognized in various neurological conditions.
- Neuromyelitis optica spectrum disorder (NMOSD) and multiple sclerosis (MS) are both inflammatory demyelinating diseases of the central nervous system, but they have distinct pathophysiology and clinical manifestations.
- Understanding the specific patterns and burden of dysautonomia in NMOSD compared to MS is crucial for comprehensive patient care and management.
Purpose of the Study:
- To compare the autonomic symptom burden using the Composite Autonomic System Score-31 (COMPASS-31) between individuals with NMOSD and individuals with MS.
- To assess the presence and characteristics of objective dysautonomia, specifically cardiovascular autonomic dysfunction (CAD), in pwNMOSD versus pwMS.
Main Methods:
- A cohort of 20 patients with NMOSD and 20 age-, sex-, and disease duration-matched patients with MS were enrolled.
- All participants completed the COMPASS-31 questionnaire to assess autonomic symptoms.
- Cardiovascular autonomic dysfunction was quantified using the adrenergic index (AI) and cardiovagal index (CI) from the Composite Autonomic Scoring Scale (CASS).
Main Results:
- Patients with NMOSD reported a higher frequency and severity in the pupillomotor domain of the COMPASS-31 compared to patients with MS (p=0.048 and p=0.006).
- Dysautonomia, including sympathetic and parasympathetic dysfunction and orthostatic hypotension, was prevalent in pwNMOSD.
- Cardiovascular autonomic dysfunction was significantly more severe in pwNMOSD than in pwMS (p=0.003), with specific autonomic parameters predicting NMOSD diagnosis.
Conclusions:
- A significant proportion of individuals with NMOSD experience clinically relevant dysautonomia.
- The pattern and burden of dysautonomia in NMOSD appear to differ from that observed in MS.
- These findings highlight the importance of evaluating autonomic function in pwNMOSD.
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