Evidence map›Paper›PMID 39514529›Full record

ArticlePloS one2024

Angioarchitectural alterations in the retina and choroid in frontotemporal dementia.

Ariana Allen, Cason B Robbins, Suzanna Joseph, Angela Hemesat, Anita Kundu, Justin P Ma, Alice Haystead, Lauren Winslow, Rupesh Agrawal, Kim G Johnson and 4 more

Erratum issuedAbstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. [Neurodegeneration and retinal changes-A literature overview].Zeitschrift fur Gerontologie und Geriatrie · 2025
    Review
  3. Review
  4. Review
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Ariana AlleniMIND Study Group, Duke University School of Medicine, Durham, NC, United States of America.ORCID 0000-0001-7320-2381
Cason B RobbinsiMIND Study Group, Duke University School of Medicine, Durham, NC, United States of America.ORCID 0000-0001-7909-510X
Suzanna JosephiMIND Study Group, Duke University School of Medicine, Durham, NC, United States of America.
Angela HemesatiMIND Study Group, Duke University School of Medicine, Durham, NC, United States of America.
Anita KunduiMIND Study Group, Duke University School of Medicine, Durham, NC, United States of America.
Justin P MaiMIND Study Group, Duke University School of Medicine, Durham, NC, United States of America.
Alice HaysteadiMIND Study Group, Duke University School of Medicine, Durham, NC, United States of America.
Lauren WinslowiMIND Study Group, Duke University School of Medicine, Durham, NC, United States of America.
Rupesh AgrawalNational Healthcare Group Eye Institute, Tan TOCK SENG Hospital, Singapore, Singapore.
Kim G JohnsoniMIND Study Group, Duke University School of Medicine, Durham, NC, United States of America.
Andrea C BozokiDepartment of Neurology, University of North Carolina School of Medicine, Chapel Hill, NC, United States of America.
Sandra S StinnettiMIND Study Group, Duke University School of Medicine, Durham, NC, United States of America.
Dilraj S GrewaliMIND Study Group, Duke University School of Medicine, Durham, NC, United States of America.
Sharon FekratiMIND Study Group, Duke University School of Medicine, Durham, NC, United States of America.ORCID 0000-0003-4403-5996

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveFrontotemporal dementia (FTD) is a progressive neurodegenerative disorder that affects the frontal and temporal lobes of the brain, leading to cognitive decline and personality changes. The objective of this cross-sectional study was to characterize angioarchitectural changes in the retina and choroid of individuals with FTD compared to cognitively normal controls using optical coherence tomography (OCT) and OCT angiography (OCTA).

methodsCross-sectional comparison of patients with FTD and controls with normal cognition. All participants underwent Mini-Mental State Examination (MMSE) at the time of imaging. Outcome measures included OCT parameters: retinal nerve fiber layer (RNFL) thickness, ganglion cell layer-inner plexiform layer (GC-IPL) thickness, central subfield thickness (CST), subfoveal choroidal thickness (SFCT), choroidal vascularity index (CVI); and OCTA superficial capillary plexus parameters: foveal avascular zone (FAZ) area, 3x3mm and 6x6mm macular perfusion density (PD) and vessel density (VD), 4.5x4.5mm peripapillary capillary perfusion density (CPD) and capillary flux index (CFI). Generalized estimating equation analysis was used to account for the inclusion of 2 eyes from the same participant.

results29 eyes of 19 patients with FTD and 85 eyes of 48 controls were analyzed. In FTD, 3x3mm macular PD (p = 0.02) and VD (p = 0.02) and CFI (p = 0.01) were reduced compared to controls. There was no difference in average 4.5x4.5mm CPD, RNFL thickness, GC-IPL thickness, CST, SFCT, CVI, FAZ, or 6x6mm VD or PD between FTD and controls (all p > 0.05); however, there was a trend toward lower macular 6x6mm PD and VD in patients with FTD.

conclusionDecline of peripapillary and macular OCT and OCTA parameters merit further investigation as potential biomarkers for FTD detection. Noninvasive retinal and choroidal imaging may hold promise for earlier detection, and future longitudinal studies will clarify their role in monitoring of FTD.

Indexed as

ChoroidFrontotemporal DementiaRetinaTomography, Optical CoherenceAgedCase-Control StudiesCross-Sectional StudiesFemaleHumansMaleMiddle AgedRetinal Vessels

Identifiers

PMID39514529
PMCPMC11548753

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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.