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Determination of Genetic Susceptibility in Severe Recurrences of Ocular Toxoplasmosis

Not Applicable
Terminated
Conditions
Toxoplasmosis Infection
Genotype II
Ocular Toxoplasmosis With Recurrences
Interventions
Biological: seropositive for Toxoplasma gondii
Registration Number
NCT02863588
Lead Sponsor
University Hospital, Strasbourg, France
Brief Summary

Ocular toxoplasmosis (OT) is a major cause of visual impairment worldwide. OT is responsible for 30 to 50% of posterior uveitis. It is characterized by dormant infections that may reactivate without known reasons, causing severe irreversible visual loss. The overall recurrence rate of OT in Europe is greater than 80% for patients and may range from one episode to 11 episodes (1% of OT) in the most extreme cases. Current treatments do not reduce the risk of recurrences and the risk of toxoplasmosis recurrence cannot be predicted in these immunocompetent patients. These clinical and biological expression changes might be related to an individual genetic susceptibility of each patient. The advanced analysis of the entire genome now possible to consider the project.

Detailed Description

Not available

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
16
Inclusion Criteria
  • seropositive for Toxoplasma gondii (for patient and parents)
  • Infection with genotype II (for patient and parents)
  • ocular toxoplasmosis recurrences >5 (patients only)
Exclusion Criteria
  • Parents seronegative for T. gondii infection
  • Infection with others genotypes than type II

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
seropositive for Toxoplasma gondiiseropositive for Toxoplasma gondii-
Primary Outcome Measures
NameTimeMethod
Highlighting of genetic mutations associated with the susceptibility to Toxoplasma gondii.severe eye recurrences. Mutation analysis will be done by exome sequencing of the subjects included in this studyThis analysis will be performed on a blood sample taken in patients included in the inclusion visit
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University Hospital, Strasbourg, france

🇫🇷

Strasbourg, France

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