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Agrin and LRP4 antibodies as new biomarkers of myasthenia gravis

  • Min Yan
    ,
  • Guang Lin Xing
    ,
  • Wen Cheng Xiong
    ,
  • Lin Mei(corresponding author)
*Corresponding author for this work
  • Case Western Reserve University
    ,
  • Nanchang University
    ,
  • Department of Veterans Affairs
Scholary Output:
Contribution to journal
Review article
Peer-review

Abstract

Myasthenia gravis (MG) is a common disorder that affects the neuromuscular junction. It is caused by antibodies against acetylcholine receptor and muscle-specific tyrosine kinase; however, some MG patients do not have antibodies against either of the proteins. Recent studies have revealed antibodies against agrin and its receptor LRP4—both critical for neuromuscular junction formation and maintenance—in MG patients from various populations. Results from experimental autoimmune MG animal models indicate that anti-LRP4 antibodies are causal to MG. Clinical studies have begun to reveal the significance of the new biomarkers. With their identification, MG appears to be a complex disease entity that can be classified into different subtypes with different etiology, each with unique symptoms. Future systematic studies of large cohorts of well-diagnosed MG patients are needed to determine whether each subtype of patients would respond to different therapeutic strategies. Results should contribute to the goal of precision medicine for MG patients. Anti-agrin and anti-LRP4 antibodies are also detectable in some patients with amyotrophic lateral sclerosis or Lou Gehrig's disease; however, whether they are a cause or response to the disorder remains unclear.

Publication Information

Output type

Scholary Output:
Contribution to journal
Review article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 126-135 (10 pages)

Journal (Volume, Issue Number)

Annals of the New York Academy of Sciences (Volume 1413, Issue 1)

Publication milestones

  • Published - 2018

Publication status

Published - 2018

ISSN

0077-8923

Publication IDs

  • Scopus: 85041073423

Publication metrics

Metrics

SciVal
FWCI
1.58
SciVal
Author count
4
SciVal
citations
15
SciVal
Paper percentile
88
Scopus
citations
Fractional count
2
Fractional count
0.50
Fractional count
2
Fractional count
0.50
Fractional count
2
Fractional count
1

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Captures
64
Mentions
2
Citation count
36

Funding Details

The work in the authors’ labs was supported in part by grants from the National Institutes of Health (NS082007, NS090083, and AG051510), the Muscular Dystrophy Association, and Veterans Affairs (BX001020A).
FundersFunding numbers
NIH
NS082007, NS090083, AG051510
VA
BX001020A
MDA
-