Evidence map›Paper›PMID 41746132›Full record

ArticleTranslational vision science & technology2026

Exploration and Application of Multiluminance Mobility Test in Bietti Crystalline Dystrophy.

Yanni Chen, Nan Wu, Xiaohong Meng, Yanling Long, Jiayun Ren, Yu Wang, Xiao Liu, Yong Liu

Abstract read
In one paragraph

Article in Translational vision science & technology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Yanni ChenDepartment of Ophthalmology, The First Affiliated Hospital of Army Medical University (Southwest Hospital), Chongqing, China.
Nan WuXinqiao Hospital, Army Medical University, Chongqing, China.
Xiaohong MengDepartment of Ophthalmology, The First Affiliated Hospital of Army Medical University (Southwest Hospital), Chongqing, China.
Yanling LongDepartment of Ophthalmology, The First Affiliated Hospital of Army Medical University (Southwest Hospital), Chongqing, China.
Jiayun RenDepartment of Ophthalmology, The First Affiliated Hospital of Army Medical University (Southwest Hospital), Chongqing, China.
Yu WangDepartment of Ophthalmology, The First Affiliated Hospital of Army Medical University (Southwest Hospital), Chongqing, China.
Xiao LiuDepartment of Ophthalmology, The First Affiliated Hospital of Army Medical University (Southwest Hospital), Chongqing, China.
Yong LiuDepartment of Ophthalmology, The First Affiliated Hospital of Army Medical University (Southwest Hospital), Chongqing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Identifiers

PMID41746132
PMCPMC12950965

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.