Evidence map›Paper›PMID 42370641›Full record

ReviewInvestigative ophthalmology & visual science2026

Human Crystallin Variation and Cataract.

Minjun Ma, Xiaokun Zhang, Yirong Li, Yuanping Zhang, Yanbo Kong, Changlin Li, Zhengkui Cheng, Haoan Yi, Xu Zha

Abstract readReview
In one paragraph

Review in Investigative ophthalmology & visual science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Minjun MaDepartment of Ophthalmology, the Second Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, People's Republic of China.
Xiaokun ZhangFunctional Laboratory of Experimental Teaching Center, Faculty of Basic Medical Science, Kunming Medical University, Kunming, Yunnan, People's Republic of China.
Yirong LiFunctional Laboratory of Experimental Teaching Center, Faculty of Basic Medical Science, Kunming Medical University, Kunming, Yunnan, People's Republic of China.
Yuanping ZhangDepartment of Ophthalmology, the Second Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, People's Republic of China.
Yanbo KongDepartment of Ophthalmology, the Second Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, People's Republic of China.
Changlin LiDepartment of Outpatient, the Third Sanatorium for Retired Cadres of Kunming, Kunming, Yunnan, People's Republic of China.
Zhengkui ChengDepartment of Pharmacy, the Third Affiliated Hospital of Kunming Medical University, Yunnan Cancer Hospital, Peking University Cancer Hospital Yunnan, Kunming, Yunnan, People's Republic of China.
Haoan YiDepartment of Cell Biology and Medical Genetics, Faculty of Basic Medical Science, Kunming Medical University, Kunming, Yunnan, People's Republic of China.
Xu ZhaDepartment of Ophthalmology, the Second Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cataract is a leading cause of reversible childhood blindness worldwide and is largely attributable to mutations in crystallin-encoding genes of the α-, β-, and γ-crystallin families. Crystallins account for over 90% of total lens proteins and are indispensable for maintaining lens transparency and long-term proteostasis. These three crystallin families display distinct structural organizations and functional specializations: α-crystallins function as small heat shock proteins (sHSPs) with molecular chaperone activity, whereas β- and γ-crystallins serve primarily structural roles, characterized by conserved Greek-key motifs that support dense protein packing and appropriate refractive properties of the lens. Despite these differences, mutations across α-, β-, and γ-crystallins converge on common pathogenic mechanisms by perturbing protein stability, intermolecular interactions, and solubility, thereby promoting protein misfolding, aggregation, or aberrant phase behavior. Such alterations disrupt lens protein homeostasis, increase light scattering, and ultimately lead to lens opacification. Cataract-related imaging and genetic data are increasingly being analyzed using emerging computational approaches, among which artificial intelligence (AI) represents a rapidly developing direction that may further support the interpretation of disease phenotypes and molecular variants in future studies. In this review, we synthesize current knowledge on human crystallin variation, pathogenic mechanisms of crystallin gene mutations, and cataract phenotypes, and discuss how AI-assisted approaches may further refine mechanistic interpretation and molecular characterization of cataract.

Indexed as

CataractCrystallinsLens, CrystallineMutationHumansCrystallins

Identifiers

PMID42370641
PMCPMC13326903

What OpenQuestion holds

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Registered trials

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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.