Evidence map›Paper›PMID 38289919›Full record

ArticlePloS one2024

Characterizing differences in retinal and choroidal microvasculature and structure in individuals with Huntington's Disease compared to healthy controls: A cross-sectional prospective study.

Suzanna Joseph, Cason B Robbins, Alice Haystead, Angela Hemesath, Ariana Allen, Anita Kundu, Justin P Ma, Burton L Scott, Kathryn P L Moore, Rupesh Agrawal and 4 more

Open access · goldAbstract 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. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.3field-weighted citation impact, top 23% of its field
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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Article
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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

14 authors at 2 institutions in 2 countries.

Suzanna JosephDepartment of Ophthalmology, Duke University School of Medicine, Durham, NC, United States of America.ORCID 0000-0002-4495-7221
Cason B RobbinsDepartment of Ophthalmology, Duke University School of Medicine, Durham, NC, United States of America.ORCID 0000-0001-7909-510X
Alice HaysteadiMIND Research Group, Durham, NC, United States of America.
Angela HemesathDepartment of Ophthalmology, Duke University School of Medicine, Durham, NC, United States of America.ORCID 0000-0003-0003-158X
Ariana AllenDepartment of Ophthalmology, Duke University School of Medicine, Durham, NC, United States of America.
Anita KunduDepartment of Ophthalmology, Duke University School of Medicine, Durham, NC, United States of America.
Justin P MaiMIND Research Group, Durham, NC, United States of America.
Burton L ScottDepartment of Neurology, Duke University School of Medicine, Durham, NC, United States of America.
Kathryn P L MooreDepartment of Neurology, Duke University School of Medicine, Durham, NC, United States of America.
Rupesh AgrawalNational Healthcare Group Eye Institute, Tan Tock Seng Hospital, Singapore, Singapore.
Vithiya GunasanNational Healthcare Group Eye Institute, Tan Tock Seng Hospital, Singapore, Singapore.
Sandra S StinnettDepartment of Ophthalmology, Duke University School of Medicine, Durham, NC, United States of America.
Dilraj S GrewalDepartment of Ophthalmology, Duke University School of Medicine, Durham, NC, United States of America.
Sharon FekratDepartment of Ophthalmology, Duke University School of Medicine, Durham, NC, United States of America.ORCID 0000-0003-4403-5996
Duke University · USNanyang Technological University · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo characterize retinal and choroidal microvascular and structural changes in patients who are gene positive for mutant huntingtin protein (mHtt) with symptoms of Huntington's Disease (HD).

methodsThis study is a cross-sectional comparison of patients who are gene positive for mHtt and exhibit symptoms of HD, either motor manifest or prodromal (HD group), and cognitively normal individuals without a family history of HD (control group). HD patients were diagnosed by Duke movement disorder neurologists based on the Unified Huntington's Disease Rating Scale (UHDRS). Fovea and optic nerve centered OCT and OCTA images were captured using Zeiss Cirrus HD-5000 with AngioPlex. Outcome metrics included central subfield thickness (CST), peripapillary retinal nerve fiber layer (pRNFL) thickness, ganglion cell-inner plexiform layer (GCIPL) thickness, and choroidal vascularity index (CVI) on OCT, and foveal avascular zone (FAZ) area, vessel density (VD), perfusion density (PD), capillary perfusion density (CPD), and capillary flux index (CFI) on OCTA. Generalized estimating equation (GEE) models were used to account for inter-eye correlation.

resultsForty-four eyes of 23 patients in the HD group and 77 eyes of 39 patients in the control group were analyzed. Average GCIPL thickness and FAZ area were decreased in the HD group compared to controls (p = 0.001, p < 0.001). No other imaging metrics were significantly different between groups.

conclusionsPatients in the HD group had decreased GCIPL thickness and smaller FAZ area, highlighting the potential use of retinal biomarkers in detecting neurodegenerative changes in HD.

Indexed as

Huntington DiseaseCross-Sectional StudiesFluorescein AngiographyHumansMicrovesselsProspective StudiesRetinal Ganglion CellsRetinal VesselsTomography, Optical Coherence

Identifiers

PMID38289919
PMCPMC10826956
OpenAlexW4391343208

What OpenQuestion holds

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LicenceCC BY
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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.