Evidence map›Paper›PMID 42383814›Full record

ArticleInvestigative ophthalmology & visual science2026

Unsupervised Clustering for POAG Phenotyping.

Prizka A Puspa, Uday Pratap Singh Parmar, Sayuri Sekimitsu, Mousa Moradi, Elizabeth J Rossin, David Friedman, Tobias Elze, Nazlee Zebardast

Abstract read
In one paragraph

Article 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.

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0citing papers 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

The trial behind it

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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

8 authors.

Prizka A PuspaDepartment of Ophthalmology, Massachusetts Eye and Ear, Harvard Medical School, Boston, Massachusetts, United States.
Uday Pratap Singh ParmarDepartment of Ophthalmology, Massachusetts Eye and Ear, Harvard Medical School, Boston, Massachusetts, United States.
Sayuri SekimitsuDepartment of Ophthalmology, Massachusetts Eye and Ear, Harvard Medical School, Boston, Massachusetts, United States.
Mousa MoradiDepartment of Ophthalmology, Massachusetts Eye and Ear, Harvard Medical School, Boston, Massachusetts, United States.
Elizabeth J RossinDepartment of Ophthalmology, Massachusetts Eye and Ear, Harvard Medical School, Boston, Massachusetts, United States.
David FriedmanDepartment of Ophthalmology, Massachusetts Eye and Ear, Harvard Medical School, Boston, Massachusetts, United States.
Tobias ElzeDepartment of Ophthalmology, Massachusetts Eye and Ear, Harvard Medical School, Boston, Massachusetts, United States.
Nazlee ZebardastDepartment of Ophthalmology, Massachusetts Eye and Ear, Harvard Medical School, Boston, Massachusetts, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: To identify and characterize clinically meaningful phenotypic subtypes of POAG using unsupervised clustering of multimodal clinical data. Methods: This retrospective cohort study included 4274 eyes from 4274 patients aged ≥40 years with POAG. Twenty-one clinical features encompassing visual field indices and progression slopes, retinal nerve fiber layer (RNFL) thickness, optic nerve head parameters, and IOP level and variability were analyzed. Hierarchical clustering, K-means, and fuzzy C-means algorithms were applied, with stability assessed via internal validation metrics and visual field archetypal analysis. Results: Five reproducible POAG phenotypes were identified The. k-means and fuzzy C-means performed best (Calinski-Harabasz 731.76 and 731.43; Davies-Bouldin 1.59 and 1.60), with excellent pairwise agreement between them (κ = 0.97) compared with moderate agreement with hierarchical clustering (κ ≈ 0.55), and high overall stability (mean Adjusted Rand Index, 0.98 ± 0.02). Clusters 1 and 2 represented mild, stable phenotypes (mean deviation [MD] slopes of +0.14 and +0.10 dB/year), differing primarily in IOP burden. Cluster 3 showed structural-functional dissociation-significant RNFL thinning (71.40 ± 8.14 µm) despite limited functional progression (MD slope +0.08 dB/year). Cluster 4 exhibited the most aggressive course, with rapid functional decline (MD slope of -0.98 ± 0.58 dB/year), greatest IOP variability (3.88 ± 1.82 mm Hg), and advanced structural loss (RNFL 64.44 ± 10.05 µm). Cluster 5 demonstrated advanced baseline damage (MD of -15.28 ± 4.72 dB; RNFL, 62.87 ± 9.53 µm) with relative longitudinal stability. Visual field archetypes aligned with cluster-specific severity. Conclusions: Multimodal clustering identifies distinct POAG phenotypes, supporting improved risk stratification and targeted management.

Indexed as

Glaucoma, Open-AngleOptic DiskRetinal Ganglion CellsVisual FieldsAdultAgedAlgorithmsCluster AnalysisClustering AlgorithmsDisease ProgressionFemaleHumansIntraocular PressureMaleMiddle AgedNerve Fibers

Identifiers

PMID42383814
PMCPMC13332525

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LicenceCC BY-NC-ND
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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.