Temporal evolution of nerve conduction study abnormalities in anti‐myelin‐associated glycoprotein neuropathy. Issue 3 (22nd December 2020)
- Record Type:
- Journal Article
- Title:
- Temporal evolution of nerve conduction study abnormalities in anti‐myelin‐associated glycoprotein neuropathy. Issue 3 (22nd December 2020)
- Main Title:
- Temporal evolution of nerve conduction study abnormalities in anti‐myelin‐associated glycoprotein neuropathy
- Authors:
- Bourque, Pierre R.
Masson‐Roy, Josée
Warman‐Chardon, Jodi
Massie, Rami
Melanson, Michel
Brooks, John
Breiner, Ari - Abstract:
- Abstract: Background: A distal‐predominant demyelinating symmetric pattern is most frequent in patients with neuropathy associated with anti‐myelin‐associated glycoprotein (MAG) antibodies. The literature however lacks longitudinal data to describe whether this is consistent over time. Methods: From the Ottawa Neuromuscular Center database, we identified 23 patients with both immunoglobulin M gammopathy and anti‐MAG antibodies. For median, ulnar and fibular motor conduction studies, we analyzed distal latency and amplitude, negative peak duration, terminal latency index (TLI), and conduction velocity. For median, ulnar, sural, and superficial fibular sensory conduction studies, we analyzed distal latency and amplitude. Results were compared for the earliest and the latest data sets. Results: The mean time interval between the two assessment points was 6.5 years. Median and ulnar motor nerve conduction studies did not show a significant change for any of the parameters tested. There was disproportionate prolongation of median distal motor latency and reduction in TLI, compared to the ulnar nerve. Deep fibular motor conduction studies showed a marked reduction in amplitudes over time. Sensory potentials were recordable in the upper limb in less than 50% at the first study and less than 25% on the most recent study. There was an even larger attrition of recordable sural and superficial fibular sensory potentials. Conclusions: Our results highlight the stability of median andAbstract: Background: A distal‐predominant demyelinating symmetric pattern is most frequent in patients with neuropathy associated with anti‐myelin‐associated glycoprotein (MAG) antibodies. The literature however lacks longitudinal data to describe whether this is consistent over time. Methods: From the Ottawa Neuromuscular Center database, we identified 23 patients with both immunoglobulin M gammopathy and anti‐MAG antibodies. For median, ulnar and fibular motor conduction studies, we analyzed distal latency and amplitude, negative peak duration, terminal latency index (TLI), and conduction velocity. For median, ulnar, sural, and superficial fibular sensory conduction studies, we analyzed distal latency and amplitude. Results were compared for the earliest and the latest data sets. Results: The mean time interval between the two assessment points was 6.5 years. Median and ulnar motor nerve conduction studies did not show a significant change for any of the parameters tested. There was disproportionate prolongation of median distal motor latency and reduction in TLI, compared to the ulnar nerve. Deep fibular motor conduction studies showed a marked reduction in amplitudes over time. Sensory potentials were recordable in the upper limb in less than 50% at the first study and less than 25% on the most recent study. There was an even larger attrition of recordable sural and superficial fibular sensory potentials. Conclusions: Our results highlight the stability of median and ulnar motor conduction study results over a mean observation period of 6.5 years. In contrast, lower limb motor and all sensory potentials show a marked trend toward becoming unrecordable. … (more)
- Is Part Of:
- Muscle & nerve. Volume 63:Issue 3(2021)
- Journal:
- Muscle & nerve
- Issue:
- Volume 63:Issue 3(2021)
- Issue Display:
- Volume 63, Issue 3 (2021)
- Year:
- 2021
- Volume:
- 63
- Issue:
- 3
- Issue Sort Value:
- 2021-0063-0003-0000
- Page Start:
- 401
- Page End:
- 404
- Publication Date:
- 2020-12-22
- Subjects:
- anti‐MAG neuropathy -- nerve conduction studies -- demyelinating neuropathy -- temporal evolution -- terminal latency index
Neuromuscular diseases -- Periodicals
Muscles -- Periodicals
Nerves -- Periodicals
616.74 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-4598 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/mus.27134 ↗
- Languages:
- English
- ISSNs:
- 0148-639X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5986.493000
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