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Autonomic dysfunction in dementia with Lewy bodies.
P Thaisetthawatkul1, B F Boeve, E E Benarroch
1Department of Neurology, Mayo Clinic, Rochester, MN 55905, USA.
Neurology
|May 26, 2004
Summary
Autonomic dysfunction is common in dementia with Lewy bodies (DLB), with symptoms less severe than multiple system atrophy (MSA) but more severe than Parkinson disease (PD). This study assessed autonomic function in DLB patients.
Area of Science:
- Neurology
- Autonomic Neuroscience
Background:
- Dementia with Lewy bodies (DLB) is a neurodegenerative disorder characterized by cognitive decline and parkinsonism.
- Autonomic dysfunction is a recognized feature of DLB, but its severity relative to other synucleinopathies requires further elucidation.
Purpose of the Study:
- To quantitatively assess and characterize autonomic function in patients diagnosed with dementia with Lewy bodies (DLB).
- To compare the autonomic function profiles of DLB patients with those of patients with multiple system atrophy (MSA) and Parkinson disease (PD).
Main Methods:
- A comparative study involving 20 DLB patients, 20 MSA patients, and 20 PD patients, matched for age.
- Autonomic function was evaluated using the Composite Autonomic Scoring Scale (CASS) and the Thermoregulatory Sweat Test (TST).
- Statistical analyses included ANOVA, Fisher exact test, and Student t-test to compare disease characteristics and autonomic test results.
Main Results:
- Autonomic symptoms, particularly orthostatic hypotension, were prevalent in DLB patients.
- DLB patients exhibited significant impairments in sudomotor, cardiovagal, and adrenergic functions as measured by CASS.
- The overall severity of autonomic dysfunction in DLB was found to be intermediate, falling between that observed in MSA and PD.
Conclusions:
- Autonomic dysfunction is a frequent and significant clinical feature in dementia with Lewy bodies.
- The degree of autonomic impairment in DLB is less severe than in multiple system atrophy but more pronounced than in Parkinson disease.
- These findings contribute to differentiating DLB from other related neurodegenerative disorders based on autonomic function profiles.