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Intensity-based optoretinography reveals sub-clinical deficits in cone function in retinitis pigmentosa
Mina Gaffney1, Thomas B Connor2, Robert F Cooper1,2
1Joint Department of Biomedical Engineering, Marquette University and the Medical College of Wisconsin, Milwaukee, WI, United States.
Intensity based optoretinography (iORG) using adaptive optics scanning light ophthalmoscopy (AOSLO) detects early photoreceptor function deficits in retinitis pigmentosa (RP). iORG shows greater sensitivity to sub-clinical changes than traditional methods, aiding early diagnosis and therapy identification.
Area of Science:
- Ophthalmology
- Cellular Biology
- Medical Imaging
Background:
- Clinical tools for retinitis pigmentosa (RP) diagnosis often lack sensitivity, missing early photoreceptor disruption.
- Adaptive optics scanning light ophthalmoscopy (AOSLO) offers high-resolution imaging for detailed structural and functional assessment of photoreceptors.
Purpose of the Study:
- To evaluate intensity based optoretinography (iORG) via AOSLO for assessing photoreceptor structure and function in individuals with and without RP.
- To compare the sensitivity of iORG to traditional methods like macular integrity assessment (MAIA) for detecting early functional deficits.
Main Methods:
- AOSLO was used to acquire iORG in 15 healthy individuals and 7 with RP.
- Photoreceptor structure was quantified by cone nearest neighbor distance (NND) and cone outer segment length (measured via OCT-derived LRPs).
- iORG functional measures were compared with MAIA microperimeter retinal sensitivity.
Main Results:
- Individuals with RP showed increased NND and decreased outer segment length with eccentricity.
- RP participants exhibited reduced iORG amplitudes compared to controls, with greater reduction in peripheral retina.
- iORG detected earlier functional deficits than MAIA, which was more sensitive to later disease stages.
Conclusions:
- iORG is a valuable tool for detecting sub-clinical cone dysfunction across all stages of RP.
- iORG's sensitivity supports its future use in identifying cells for targeted cellular therapies in RP.
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