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Exploration and Application of Multiluminance Mobility Test in Bietti Crystalline Dystrophy
Yanni Chen1,2, Nan Wu3, Xiaohong Meng1,2,4
1Department of Ophthalmology, The First Affiliated Hospital of Army Medical University (Southwest Hospital), Chongqing, China.
Purpose:
This study evaluated the multiluminance mobility test (MLMT) as a functional vision assessment tool for Bietti crystalline dystrophy (BCD) and explored its relationship with structural and visual function parameters.
Methods:
A retrospective study of 34 BCD patients (67 eyes) incorporated 2 additional low light levels (0.1 and 0.5 lux) into the MLMT. Visual function assessments included best-corrected visual acuity, visual field (VF), and microperimetry (MP). Macular structure was evaluated via spectral-domain optical coherence tomography. MLMT performance was correlated with these parameters using Spearman's rank correlation tests.
Results:
Despite severe global photoreceptor dysfunction, a notable proportion of participants (38.8%) passed the MLMT at 1 lux or less, with 23.9% reaching the lowest luminance (0.1 lux). MLMT lux scores correlated significantly with best-corrected visual acuity (ρ = -0.5322; P = 0.0012), mean defect of VF (ρ = -0.5919; P = 0.0005), and mean macular sensitivity of MP (MS-MP; ρ = 0.7175; P < 0.0001). Subgroup analysis revealed that subjects with preserved foveal ellipsoid zone had significantly higher MLMT lux scores and better MS-MP (both P < 0.05) than those with ellipsoid zone atrophy. Although visual function parameters were markedly impaired in certain patients, their MLMT performance remained relatively favorable.
Conclusions:
The standardized MLMT has a limited range for assessing advanced BCD. Preservation of central macular structure, rather than visual acuity alone, appears to be critical for mobility performance in BCD patients. Disease-specific adaptations of functional end points are needed for BCD clinical trials.
Translational Relevance:
To assess functional vision for BCD, the MLMT requires adaptation, and clinical trials should incorporate macular structural parameters.
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