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Screening of Serum Exosomal miRNA as a Biomarker for Ocular Muscle Myasthenia Gravis

J

Jinan University

Status

Invitation-only

Conditions

Myasthenia Gravis

Treatments

Device: Body fluid diagnosis

Study type

Observational

Funder types

Other

Identifiers

NCT05888558
2021.11JinanU

Details and patient eligibility

About

Ocular muscle myasthenia gravis (Ocular Myasthenia Gravis, OMG) has a high incidence and is difficult to diagnose. It is very necessary to find specific diagnostic indicators for OMG. By collecting peripheral blood of OMG, systemic myasthenia gravis and healthy people, extract miRNAs derived from exosomes in the serum and perform high-throughput sequencing, then use bioinformatics analysis methods to screen specifically expressed miRNAs as biomarkers for OMG diagnosis .

Full description

Part I: (1) Collect peripheral blood samples from patients with early-onset OMG, early-onset GMG and healthy subjects of age and sex matched who have been diagnosed for the first time and have not undergone any drug treatment. There are 6 cases in each group. Extract the secretion miRNA in serum and conduct high-throughput sequencing. Analyze and compare the differential expression miRNAs between OMG, GMG and healthy control groups by edgeR. The standard of differential expression is set as | logFC |>1, p<0.05. Use miRTarBase, TargetScan, and miRDB to predict target genes for differentially expressed miRNAs. Conduct GO enrichment and KEGG signaling pathway analysis on target genes. The STRING tool is used to construct the target gene protein interaction network (PPI). According to the importance of the target gene calculated by the maximum population concentration ratio (MCC) method, the top ten genes (hub genes) are selected and analyzed.

(2) Randomly collect peripheral blood samples from patients with early-onset OMG, early-onset GMG, and age-matched healthy subjects, with 10 samples in each group. The differentially expressed miRNAs obtained during the sequencing phase were validated using real-time fluorescence quantification (RT-qPCR). Construct a receiver operating characteristic curve (ROC) curve to evaluate the diagnostic efficacy of the identified miRNA.

Enrollment

160 estimated patients

Sex

All

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Clinical manifestations: fluctuating myasthenia;

    • neostigmine test positive; ③ AChR-Ab, Musk-Ab, LRP4-Ab antibodies positive; ④repetitive nerve stimulation or single fiber EMG Positive (comply with the first one of the above diagnostic criteria and any one of the other three, and at the same time exclude ophthalmoplegia caused by other diseases, the diagnosis can be confirmed).

Exclusion criteria

①Combined with other autoimmune diseases or other inflammatory diseases; ②Patients with tumorous diseases;

  • Received targeted biologics, intravenous gamma globulin, plasma exchange therapy within three months before treatment; ④Pregnancy Status or lactation

Trial design

160 participants in 3 patient groups

Ocular myasthenia gravis group
Description:
Ocular myasthenia gravis,age between 18-50 years old
Treatment:
Device: Body fluid diagnosis
General myasthenia gravis group
Description:
General myasthenia gravis,age between 18-50 years old
Treatment:
Device: Body fluid diagnosis
Healthy control group
Description:
people who are healthy without any systemic diseases,18-50 years old
Treatment:
Device: Body fluid diagnosis

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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