Evidence map›Paper›PMID 42030304›Full record

ArticlePloS one2026

Optical coherence tomography angiography parameters in Marfan syndrome: Genetic determinants and associations with cardiovascular manifestations.

Klaudia Kéki-Kovács, Roland Stengl, Bence Ágg, András Végh, Erika Maka, Mária Bausz, Csaba Bödör, Cristina M Șulea, Máté Csonka, Kálmán Benke and 3 more

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Article in PloS one, 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

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

13 authors.

Klaudia Kéki-KovácsDepartment of Ophthalmology, Semmelweis University, Budapest, Hungary.ORCID https://orcid.org/0000-0002-1801-2347
Roland StenglHeart and Vascular Center, Semmelweis University, Budapest, Hungary.
Bence ÁggHeart and Vascular Center, Semmelweis University, Budapest, Hungary.ORCID https://orcid.org/0000-0002-6492-0426
András VéghDepartment of Ophthalmology, Semmelweis University, Budapest, Hungary.ORCID https://orcid.org/0000-0001-6281-3363
Erika MakaDepartment of Ophthalmology, Semmelweis University, Budapest, Hungary.
Mária BauszDepartment of Ophthalmology, Semmelweis University, Budapest, Hungary.
Csaba BödörDepartment of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.
Cristina M ȘuleaHeart and Vascular Center, Semmelweis University, Budapest, Hungary.
Máté CsonkaHeart and Vascular Center, Semmelweis University, Budapest, Hungary.
Kálmán BenkeHeart and Vascular Center, Semmelweis University, Budapest, Hungary.
Miklós PólosHeart and Vascular Center, Semmelweis University, Budapest, Hungary.
Zoltán SzabolcsHeart and Vascular Center, Semmelweis University, Budapest, Hungary.
Zoltán Zsolt NagyDepartment of Ophthalmology, Semmelweis University, Budapest, Hungary.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In addition to aortic manifestations, Marfan syndrome can affect retinal vessels. Our aim was to evaluate retinal circulation, and its correlation with genotype and cardiovascular manifestation identifying predictors of aortic involvement (dilation and/or dissection). In the retrospective, cross-sectional study, 39 Marfan syndrome patients with optical coherence tomography angiography records were included. Retinal thickness, superficial and deep vessel density in total retina, fovea, parafovea, perifovea, area and perimeter of foveal avascular zone, fractal dimension were measured. Two groups were created by mutation type: haploinsufficient, dominant negative. Latter were divided into two subgroups according to whether mutation resulted in cysteine elimination. Subjects were assigned into cardiovascular risk based on previous aortic surgery. Retina of haploinsufficient patients was thinner in total, foveal, parafoveal, perifoveal areas compared to dominant negative subjects (p ≤ 0.047). Retinal thickness of haploinsufficient individuals was thinner in total, parafoveal areas compared to dominant negative without (LSD p = 0.038, Bonferroni p = 0.027, respectively) and with cysteine elimination variants (LSD p = 0.032, Bonferroni p = 0.002, respectively). In fovea and perifovea, retinal thickness was decreased in haploinsufficient patients in comparison to dominant negative with cysteine elimination group (Bonferroni p ≤ 0.029). Total, parafoveal, perifoveal superficial and total, parafoveal deep vessel density of subjects who underwent aortic surgery were lower compared to non-operated patients (p ≤ 0.043). To the best of our knowledge, our study is the first to describe a relationship between genotype and optical coherence tomography angiography parameters in Marfan syndrome. These findings along with correlations between genetics and cardiovascular manifestations reported previously, suggest that these parameters may be indirect predictors of increased cardiovascular risk. Here we demonstrated associations between these parameters and aortic involvement.

Indexed as

Cardiovascular DiseasesMarfan SyndromeRetinal VesselsTomography, Optical CoherenceAdultCross-Sectional StudiesFemaleFluorescein AngiographyHaploinsufficiencyHumansMaleMiddle AgedMutationRetrospective Studies

Identifiers

PMID42030304
PMCPMC13108799

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