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Postganglionic sudomotor denervation in patients with multiple system atrophy
Vincenzo Provitera1, Maria Nolano2, Giuseppe Caporaso2
1From the Neurology Division (V.P., M.N., G.C., A.S., B.L.), "Salvatore Maugeri" Foundation, Medical Center of Telese Terme (BN); the Department of Neurosciences and Reproductive and Odontostomatologic Sciences (F.M., R.I., A.D.R., G.D.M., L.S.), University "Federico II" of Naples, Italy; the Department of Neurology (M.M.S.), University of Minnesota, Minneapolis; and the Center for Neurodegenerative Diseases (M.T.P.), University of Salerno, Italy. vincenzo.provitera@fsm.it.
Multiple system atrophy (MSA) involves postganglionic autonomic nerves, evidenced by reduced sudomotor innervation in skin biopsies. This nerve impairment contributes to dysautonomic disorders in MSA patients.
Area of Science:
- Neurology
- Autonomic Neuroscience
- Pathology
Background:
- Multiple system atrophy (MSA) is a neurodegenerative disorder characterized by autonomic dysfunction.
- The precise mechanisms underlying dysautonomia in MSA, particularly the involvement of peripheral autonomic nerves, require further elucidation.
Purpose of the Study:
- To investigate postganglionic autonomic nervous system involvement in multiple system atrophy (MSA).
- To quantify sudomotor innervation in skin biopsies of MSA patients and compare it with healthy controls.
Main Methods:
- Skin biopsies were obtained from the thigh, leg, and fingertip of 29 MSA patients and 29 healthy controls.
- Sudomotor innervation was assessed using immunofluorescence and morphometric analysis of nerve density.
- Autonomic symptoms were evaluated using the SCOPA-AUT questionnaire and sudomotor function by the silastic imprint test.
Main Results:
- Sudomotor nerve density was significantly lower in MSA patients compared to controls across all examined skin sites (fingertip, thigh, and leg).
- Measurements of nerve density showed good correlation with unbiased stereologic methods.
- A trend towards lower sudomotor function and higher dysautonomic complaints was observed in MSA patients.
Conclusions:
- The findings support the hypothesis of postganglionic autonomic impairment in MSA.
- This peripheral nerve involvement, alongside central degeneration, likely contributes to the development of dysautonomic disorders in MSA.
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