Evidence map›Paper›PMID 40175492›Full record

ArticleScientific reports2025

Therapeutic effects of lomerizine on vasculopathy in Fabry disease.

Jong Bin Choi, Hyo-Sang Do, Dong-Won Seol, Hee-Young Yang, Taek-Min Kim, Youkyeong Gloria Byun, Jae-Min Park, Heounjeong Go, Jungjoo Park, Won-Suk Chung and 4 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Fabry Disease: A Focus on the Role of Oxidative Stress.Antioxidants (Basel, Switzerland) · 2026
    Review
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.

Jong Bin Choi *Department of Biological Sciences, KAIST, Daejeon, Republic of Korea.
Hyo-Sang Do *Asan Institute for Life Sciences, Asan Medical Center, University of Ulsan College of Medicine, Seoul, 05505, Republic of Korea.
Dong-Won Seol *Laboratory Animal Center, Daegu-Gyeongbuk Medical Innovation Foundation (DGMIF), Daegu, Republic of Korea.
Hee-Young YangLaboratory Animal Center, Daegu-Gyeongbuk Medical Innovation Foundation (DGMIF), Daegu, Republic of Korea.
Taek-Min KimGraduate School of Medical Science and Engineering, KAIST, Daejeon, Republic of Korea.
Youkyeong Gloria ByunDepartment of Biological Sciences, KAIST, Daejeon, Republic of Korea.
Jae-Min ParkLaboratory Animal Center, Daegu-Gyeongbuk Medical Innovation Foundation (DGMIF), Daegu, Republic of Korea.
Heounjeong GoDepartment of Pathology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, 05505, Republic of Korea.
Jungjoo ParkDepartment of Biological Sciences, KAIST, Daejeon, Republic of Korea.
Won-Suk ChungDepartment of Biological Sciences, KAIST, Daejeon, Republic of Korea.
Jae Myoung SuhGraduate School of Medical Science and Engineering, KAIST, Daejeon, Republic of Korea.
Beom Hee LeeDepartment of Pediatrics, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, 05505, Republic of Korea. bhlee@amc.seoul.kr.
Gabbine WeeLaboratory Animal Center, Daegu-Gyeongbuk Medical Innovation Foundation (DGMIF), Daegu, Republic of Korea. gabbine@kmedihub.re.kr.
Yong-Mahn HanDepartment of Biological Sciences, KAIST, Daejeon, Republic of Korea. ymhan@kaist.ac.kr.

Funding

The Korean Fund for Regenerative Medicine (KFRM) 21A0402L1-12
6 · The paper itself

Abstract

Fabry disease (FD) is a lysosomal storage disorder in which α-galactosidase (GLA) deficiency leads to a build-up of globo-triaosylceramide (Gb3) in various cell types. Gb3 accumulation leads to the abnormalities of microvascular function associated with FD. Previously, we discovered significant abnormalities in vascular endothelial cells (VECs) derived from FD-induced pluripotent stem cells. We then used a cell-based system to screen a group of clinical compounds for candidates capable of rescuing those abnormalities. Lomerizine was one of the most promising candidates because it alleviated a variety of FD-associated phenotypes both in vitro and in vivo. Lomerizine reduced mitochondria Ca

Indexed as

Fabry DiseasePiperazinesVascular Diseasesalpha-GalactosidaseAnimalsCalciumDisease Models, AnimalEndothelial CellsHumansMaleMiceMitochondriaReactive Oxygen Speciesalpha-GalactosidaseCalciumlomerizinePiperazinesReactive Oxygen SpeciesDrug screeningFabry diseaseiPSCsLomerizineVascular endothelial cells

Identifiers

PMID40175492
PMCPMC11965366

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.