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Association Study Between VDR Gene Polymorphisms and Risk and Features of MG in Han Chinese Population

Completed
Conditions
Myasthenia Gravis, Ocular
Gene Polymorphism
Interventions
Genetic: Genotype analysis for VDR rs1544410, rs2228570, rs731236, and rs7975232 polymorphisms
Registration Number
NCT05380128
Lead Sponsor
Beijing Tongren Hospital
Brief Summary

The Vitamin D receptor gene (VDR) polymorphisms are the candidate genetic variants for susceptibility to autoimmune diseases. In the present study, the investigators aimed to assess the association between VDR polymorphisms and myasthenia gravis (MG) susceptibility and disease features in Chinese Han population.The patients with MG and healthy controls were genotyped for VDR rs1544410, rs2228570, rs731236, and rs7975232 polymorphisms using the improved multiple ligase detection reaction. Information on age at onset, acetylcholine receptor antibody (AChR-Ab) and muscle-specific kinase antibody (MuSK-Ab) status, thymus status, involved muscles at onset and Osserman type at the maximum worsening during 2 years follow-up were obtained and used as the grouping basis of sub-classifications. Intergroup comparisons of allele and genotype frequencies, haplotype distributions were performed between MG group and the control group, and between each pair of MG subgroups.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
297
Inclusion Criteria
  • Clinical diagnosis of myasthenia gravis.
  • Han Chinese population.
  • Must be able to complete a 2-year follow-up visit.
Exclusion Criteria
  • Clinical data collection can not be completed.
  • Poor compliance.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Healthy controlGenotype analysis for VDR rs1544410, rs2228570, rs731236, and rs7975232 polymorphismsThe geography and ethnically matched control group consisted of 146 unrelated healthy subjects. They were genotyped for VDR rs1544410, rs2228570, rs731236, and rs7975232 polymorphisms.
MG groupGenotype analysis for VDR rs1544410, rs2228570, rs731236, and rs7975232 polymorphismsUnrelated patients with MG were included in the study. They were enrolled in the Neurology Department of Beijing Tongren Hospital, Capital Medical University and fulfilled the clinical and electromyography diagnostic criteria for acquired MG. Simply, all MG patients met the following diagnostic criteria: typical symptoms of fluctuating muscle weakness, positive result of neostigmine test, and decremental response to low-frequency repetitive nerve stimulation. Information on age at onset, AChR / MuSK Abs status (partly), thymus status, involved muscles at onset and Osserman type at the maximum worsening during 2 years follow-up were obtained and used as the grouping basis of sub-classifications. They were genotyped for VDR rs1544410, rs2228570, rs731236, and rs7975232 polymorphisms
Primary Outcome Measures
NameTimeMethod
Association between VDR gene polymorphism and MG susceptibilityup to 2 years

Codominant, dominant and recessive genetic models and haplotype analysis were applied to compare the difference between MG and control groups.

Secondary Outcome Measures
NameTimeMethod
Association of VDR gene polymorphism with MG subgroupsup to 2 years

To study the precise effect of single nucleotide polymorphisms (SNPs) in the different population, the MG patients were divided into subgroups according to essential clinical variables, including onset age (≤50 or \>50 years), thymus status (thymoma or non-thymoma, by pathology), AChR / MuSK Abs (positive or negative), onset involvement (ocular or generalized) and Osserman type at the maximum worsening (type I or IIa-IIb or III-V). The investigators analyzed the distribution of genes in each group.

Trial Locations

Locations (1)

Beijing Tongren Hospital

🇨🇳

Beijing, China

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