Evidence map›Paper›PMID 42479159›Full record

ArticleGraefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie2026

Association between AREDS/2 supplementation and structural and functional progression in macular telangiectasia type 2.

Kensington Hatcher, Thomas Aaberg, Muna Bitar, David Sarraf

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In one paragraph

Article in Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie, 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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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

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No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Kensington HatcherNeurotech Pharmaceuticals, 900 Highland Corporate Drive, Cumberland, RI, 02864, USA. k.hatcher@neurotechusa.com.ORCID http://orcid.org/0009-0009-0657-7162
Thomas AabergNeurotech Pharmaceuticals, 900 Highland Corporate Drive, Cumberland, RI, 02864, USA.ORCID http://orcid.org/0000-0003-4160-2844
Muna BitarNeurotech Pharmaceuticals, 900 Highland Corporate Drive, Cumberland, RI, 02864, USA.ORCID http://orcid.org/0009-0003-0397-8688
David SarrafStein Eye Institute, University of California Los Angeles, Los Angeles, CA, USA.ORCID http://orcid.org/0000-0003-4018-2702

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo evaluate whether oral Age-Related Eye Disease Study (AREDS/2) supplementation is associated with structural or functional disease progression over 24 months in patients with Macular Telangiectasia Type 2 (MacTel).

methodsThis post hoc analysis included 208 participants enrolled in two 24-month Phase 3 clinical trials of revakinagene taroretcel-lwey for MacTel (sham, n = 98; treated, n = 110). Consistent AREDS/2 exposure was defined by documented intake at baseline and month 24. The primary outcome was 24-month change in ellipsoid zone (EZ) area loss. Secondary outcomes included changes in reading speed, best-corrected visual acuity (BCVA), and aggregate retinal sensitivity. Non-randomized exposure was adjusted using a doubly robust framework combining inverse probability of treatment weighting (IPTW) and multivariable survey-weighted linear regression.

resultsIn the sham cohort, AREDS/2 supplementation was not associated with statistically significant differences in 24-month EZ area loss (P = 0.258). In the treated cohort, an initial association with greater EZ area loss among AREDS/2 users (P = 0.032) became non-significant after full multivariable adjustment for age, sex, and diabetes status (P = 0.577). Secondary functional metrics showed no significant differences between groups across either cohort.

conclusionsAREDS/2 supplementation was not associated with meaningful differences in structural or functional MacTel progression over a 24-month period. These findings do not provide evidence that routine AREDS/2 supplementation slows EZ area loss or preserves visual function in this population.

Indexed as

AREDSEllipsoid ZoneFunctional VisionMacular Telangiectasia Type 2

Identifiers

PMID42479159

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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.