Evidence map›Paper›PMID 37079031›Full record

ArticleJournal of neurology2023

Retinal thickness as a biomarker of cognitive impairment in manifest Huntington's disease.

Ane Murueta-Goyena, Rocío Del Pino, Marian Acera, Sara Teijeira-Portas, David Romero, Unai Ayala, Tamara Fernández-Valle, Beatriz Tijero, Iñigo Gabilondo, Juan Carlos Gómez Esteban

Open access · hybridAbstract read
In one paragraph

Article in Journal of neurology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 11% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

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  13. Visual cognition as a marker of longitudinal disease progression in Huntington's disease.International journal of clinical and health psychology : IJCHP
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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

10 authors at 4 institutions in 1 country.

Ane Murueta-Goyena *Neurodegenerative Diseases Group, Biocruces Bizkaia Health Research Institute, Barakaldo, Spain. ane.muruetagoyena@ehu.eus.ORCID http://orcid.org/0000-0002-9808-6943
Rocío Del Pino *Neurodegenerative Diseases Group, Biocruces Bizkaia Health Research Institute, Barakaldo, Spain.
Marian AceraNeurodegenerative Diseases Group, Biocruces Bizkaia Health Research Institute, Barakaldo, Spain.
Sara Teijeira-PortasNeurodegenerative Diseases Group, Biocruces Bizkaia Health Research Institute, Barakaldo, Spain.
David RomeroBiomedical Engineering Department, Faculty of Engineering, Mondragon University, Mondragon, Spain.
Unai AyalaBiomedical Engineering Department, Faculty of Engineering, Mondragon University, Mondragon, Spain.
Tamara Fernández-ValleNeurodegenerative Diseases Group, Biocruces Bizkaia Health Research Institute, Barakaldo, Spain.
Beatriz TijeroNeurodegenerative Diseases Group, Biocruces Bizkaia Health Research Institute, Barakaldo, Spain.
Iñigo GabilondoNeurodegenerative Diseases Group, Biocruces Bizkaia Health Research Institute, Barakaldo, Spain.
Juan Carlos Gómez EstebanNeurodegenerative Diseases Group, Biocruces Bizkaia Health Research Institute, Barakaldo, Spain.
BioCruces Health research Institute · ESUniversity of the Basque Country · ESMondragon Unibertsitatea · ESIkerbasque · ES

Funding

EITB Maratoia BIO17/ND/009Osasun Saila, Eusko Jaurlaritzako 2019111004
6 · The paper itself

Abstract

backgroundCognitive decline has been reported in premanifest and manifest Huntington's disease but reliable biomarkers are lacking. Inner retinal layer thickness seems to be a good biomarker of cognition in other neurodegenerative diseases.

objectiveTo explore the relationship between optical coherence tomography-derived metrics and global cognition in Huntington's Disease.

methodsThirty-six patients with Huntington's disease (16 premanifest and 20 manifest) and 36 controls matched by age, sex, smoking status, and hypertension status underwent macular volumetric and peripapillary optical coherence tomography scans. Disease duration, motor status, global cognition and CAG repeats were recorded in patients. Group differences in imaging parameters and their association with clinical outcomes were analyzed using linear mixed-effect models.

resultsPremanifest and manifest Huntington's disease patients presented thinner retinal external limiting membrane-Bruch's membrane complex, and manifest patients had thinner temporal peripapillary retinal nerve fiber layer compared to controls. In manifest Huntington's disease, macular thickness was significantly associated with MoCA scores, inner nuclear layer showing the largest regression coefficients. This relationship was consistent after adjusting for age, sex, and education and p-value correction with False Discovery Rate. None of the retinal variables were related to Unified Huntington's Disease Rating Scale score, disease duration, or disease burden. Premanifest patients did not show a significant association between OCT-derived parameters and clinical outcomes in corrected models.

conclusionsIn line with other neurodegenerative diseases, OCT is a potential biomarker of cognitive status in manifest HD. Future prospective studies are needed to evaluate OCT as a potential surrogate marker of cognitive decline in HD.

Indexed as

Cognitive DysfunctionHuntington DiseaseBiomarkersHumansRetinaTomography, Optical CoherenceBiomarkersCognitionHuntington’s diseaseOptical coherence tomographyRetina

Identifiers

PMID37079031
PMCPMC10345164
OpenAlexW4366464162

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.