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Comprehensive Autopsy Program for Individuals with Multiple Sclerosis
Published on: July 19, 2019
Polyneuropathies and chronic inflammatory demyelinating polyradiculoneuropathy in multiple sclerosis
Narupat Suanprasert1, Bruce V Taylor2, Christopher J Klein3
1Peripheral Neuropathy Research Laboratory, Department of Neurology, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA; Department of Neurology, Prasat Neurological Institute, 312 Ratchawithi Rd, Khwaeng Thung Phaya Thai, Khet Ratchathewi, Bangkok 10400, Thailand.
Polyneuropathies in multiple sclerosis (MS) patients are often underdiagnosed but contribute to disability. Recognizing treatable forms like chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is crucial for better patient outcomes.
Area of Science:
- Neurology
- Immunology
- Clinical Medicine
Background:
- Polyneuropathies frequently coexist with multiple sclerosis (MS), potentially exacerbating disability.
- These co-occurring conditions are often underdiagnosed, hindering timely and appropriate patient management.
Purpose of the Study:
- To identify the prevalence and types of polyneuropathies in patients with MS.
- To compare the clinical and electrophysiological characteristics of MS with chronic inflammatory demyelinating polyradiculoneuropathy (MS-CIDP) against MS with other non-inflammatory polyneuropathies.
Main Methods:
- A retrospective chart review was conducted on patients diagnosed with both MS and polyneuropathy at the Mayo Clinic.
- Serum samples from MS-CIDP patients were analyzed for IgG autoantibodies targeting neurofascin-155.
Main Results:
- 133 cases of MS with co-occurring polyneuropathy were identified between 1980-2013.
- Inflammatory neuropathies, including CIDP, were observed in 28 cases, while 15 had inherited neuropathies and 32 had diabetic sensorimotor polyneuropathy.
- MS-CIDP cases exhibited distinct features, such as absent ankle reflexes, earlier neuropathy onset, greater impairment, and specific electrophysiological findings, with a subset showing IgG4 autoantibodies to neurofascin-155.
Conclusions:
- Polyneuropathies significantly contribute to the neurological disability experienced by MS patients.
- The diagnosis of polyneuropathy in MS patients is challenging and likely underreported, emphasizing the need for increased recognition, especially for treatable conditions like CIDP.
- The increased incidence of inflammatory neuropathy, particularly CIDP, in MS suggests a potential shared autoimmune pathogenesis, further supported by the presence of neurofascin-155 autoantibodies.
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