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Longitudinal Prospective Natural History Study of Retinopathy in Zellweger Spectrum Disorder

Recruiting
Conditions
Zellweger Spectrum Disorder
Registration Number
NCT06190626
Lead Sponsor
McGill University Health Centre/Research Institute of the McGill University Health Centre
Brief Summary

The goal of this observational study is to define the course of the retinal degeneration in a ZSD patient cohort.

The objective of this study is to gather information so the investigators can:

1. define the course of the retinal degeneration in a ZSD patient cohort with retinal degeneration

2. define what tests best monitor the progression of the retinal degeneration

3. generate prognostic information about vision loss in ZSD.

At each yearly visit, the participants will answer a functional vision questionnaire, have a physical evaluation, blood test, and participate in a variety of vision tests. The investigators will also collect pertinent medical history.

Participants will travel to study site. The study will provide financial support for board and travel.

Detailed Description

Participants/guardians will have a 1-hour virtual interview before the first visit to review the tests and determine which tests the participant is able to perform.

Below is a list of the vision tests used for this study:

Prior to each visit, the participant will complete the PedEyeQ or VFQ-25 questionnaire about functional vision.

At each clinic visit :

* Refraction and glasses test: this is a general vision test, as commonly conducted by an optometrist, before and after pupil dilation

* Best corrected visual acuity: the participant's vision will be tested using cards or a chart.

* Contrast sensitivity: the participant's ability to detect contrast will be tested using a chart.

* Visual field: the participant's field of vision will be tested by asking them to indicate when they see a stimulus.

* Reading test: the participant's ability to see written text will be tested using the International Reading Speed Test

* Color vision test: the participant's ability to see color will be tested using cards

* Eye exam: the participant's eyes will be examined with a lamp

* Pupil dilation: to allow the completion of some tests, the participant's pupils will be dilated using medicated eye drops

* Microperimetry: the participant's macula (central retina) will be visualized.

* Fundus photography: the participant's fundus (central retina) will be photographed in light and dark conditions

* Full field stimulus threshold test: the participant's ability to perceive light in different parts of their visual field will be tested

* Optical coherence tomography (OCT): detailed images of the participant's retina will be taken

* Fundus autofluorescence: the participant's retinal health will be assessed by imaging the natural fluorescent properties of their retinal pigment epithelium

* Chromatic pupillometry: the function of different cells in the participant's retina will be determined by measuring their response to light

* Multi-luminance mobility test (MLMT): the participant will walk through an obstacle course at varying light levels to test their functional vision in different light conditions.

* Blood collection: a blood sample will be collected and banked to measure peroxisome functions.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
30
Inclusion Criteria
  • confirmed ZSD with deleterious variants in PEX genes identified
  • confirmed or expected retinal involvement
Exclusion Criteria
  • unable to perform a minimum of one vision test
  • severe ZSD disease

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Number of participants with common patterns of retinal degeneration observed5 years

Vision test results from participants will be reviewed together to describe common patterns of retinal degeneration observed.

Number of participants with disease progression5 years

Using various tests of vision measured annually, a description of disease progression will be defined in each participant.

Secondary Outcome Measures
NameTimeMethod
Rate of progression of retinal degeneration5 years

Statistical analysis using the data from Outcome 1, will be used to generate rate of progression per year over 5 years in each individual.

Correlation of rate retinal degeneration to age and overall ZSD disease severity5 years

Statistical analysis using the data from Outcome 1, will be used to correlate rate of progression per year over 5 years to age and overall ZSD disease severity in each individual.

rate of progression of retinal degeneration5 years

Statistical analysis using the data from Outcome 1, will be used to define variance between participants in rate of progression of retinal degeneration.

Trial Locations

Locations (2)

University of Rochester Medical Center/Flaum Eye Institute

🇺🇸

Rochester, New York, United States

Frederique Arnaud

🇨🇦

Montreal, Quebec, Canada

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