Evidence map›Paper›PMID 38170125›Full record

ArticleOphthalmology science

Bruch's Membrane Calcification in Pseudoxanthoma Elasticum: Comparing Histopathology and Clinical Imaging.

Sara Risseeuw, Matthew G Pilgrim, Sergio Bertazzo, Connor N Brown, Lajos Csincsik, Sarah Fearn, Richard B Thompson, Arthur A Bergen, Jacoline B Ten Brink, Elod Kortvely and 4 more

Open access · goldAbstract read
In one paragraph

Article in Ophthalmology science. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

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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 6 institutions in 4 countries.

Sara RisseeuwDepartment of Ophthalmology, University Medical Center Utrecht, Utrecht University, The Netherlands.
Matthew G PilgrimWellcome-Wolfson Institute for Experimental Medicine, School of Medicine, Dentistry and Biomedical Science, Queen's University Belfast, Belfast, Northern Ireland, United Kingdom.
Sergio BertazzoDepartment of Medical Physics and Biomedical Engineering, University College London, London, United Kingdom.
Connor N BrownWellcome-Wolfson Institute for Experimental Medicine, School of Medicine, Dentistry and Biomedical Science, Queen's University Belfast, Belfast, Northern Ireland, United Kingdom.
Lajos CsincsikWellcome-Wolfson Institute for Experimental Medicine, School of Medicine, Dentistry and Biomedical Science, Queen's University Belfast, Belfast, Northern Ireland, United Kingdom.
Sarah FearnDepartment of Materials, Imperial College London, London, United Kingdom.
Richard B ThompsonUniversity of Maryland School of Medicine, Department of Biochemistry and Molecular Biology, Baltimore, Maryland.
Arthur A BergenDepartments of Human Genetics and Ophthalmology, Amsterdam UMC, location AMC Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Jacoline B Ten BrinkDepartments of Human Genetics and Ophthalmology, Amsterdam UMC, location AMC Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Elod KortvelyRoche Pharma Research and Early Development, Roche Innovation Center Basel, Basel, Switzerland.
Wilko SpieringDepartment of Vascular Medicine, University Medical Center Utrecht, Utrecht University, The Netherlands.
Jeannette Ossewaarde-van NorelDepartment of Ophthalmology, University Medical Center Utrecht, Utrecht University, The Netherlands.
Redmer van LeeuwenDepartment of Ophthalmology, University Medical Center Utrecht, Utrecht University, The Netherlands.
Imre LengyelWellcome-Wolfson Institute for Experimental Medicine, School of Medicine, Dentistry and Biomedical Science, Queen's University Belfast, Belfast, Northern Ireland, United Kingdom.
Queen's University Belfast · GBUtrecht University · NLAmsterdam UMC Location University of Amsterdam · NLRoche (Switzerland) · CHUniversity College London · GBUniversity of Maryland, Baltimore · US

Funding

Project 4 - Mechanisms of pyrophosphate dysregulationP01AG081167 · NIA · MEDICAL COLLEGE OF WISCONSIN · PI Francesca M Marassi · 2023 to 2026
$13.0M
Imaging of Retinal Hydroxyapatite as an Early Screen for AMDR01EY030443 · NEI · UNIVERSITY OF MARYLAND BALTIMORE · PI THOMPSON, RICHARD BLAIR · 2020 to 2023
$2.1M
NEI NIH HHS R01 EY030443NIA NIH HHS P01 AG081167
6 · The paper itself

Abstract

Purpose: To investigate the histology of Bruch's membrane (BM) calcification in pseudoxanthoma elasticum (PXE) and correlate this to clinical retinal imaging. Design: Experimental study with clinicopathological correlation. Subjects and Controls: Six postmortem eyes from 4 PXE patients and 1 comparison eye from an anonymous donor without PXE. One of the eyes had a multimodal clinical image set for comparison. Methods: Calcification was labeled with OsteSense 680RD, a fluorescent dye specific for hydroxyapatite, and visualized with confocal microscopy. Scanning electron microscopy coupled with energy-dispersive x-ray spectroscopy (SEM-EDX) and time-of-flight secondary ion mass spectrometry (TOF-SIMs) were used to analyze the elemental and ionic composition of different anatomical locations. Findings on cadaver tissues were compared with clinical imaging of 1 PXE patient. Main Outcome Measures: The characteristics and topographical distribution of hydroxyapatite in BM in eyes with PXE were compared with the clinical manifestations of the disease. Results: Analyses of whole-mount and sectioned PXE eyes revealed an extensive, confluent OsteoSense labeling in the central and midperipheral BM, transitioning to a speckled labeling in the midperiphery. These areas corresponded to hyperreflective and isoreflective zones on clinical imaging. Scanning electron microscopy coupled with energy-dispersive x-ray spectroscopy and TOF-SIMs analyses identified these calcifications as hydroxyapatite in BM of PXE eyes. The confluent fluorescent appearance originates from heavily calcified fibrous structures of both the collagen and the elastic layers of BM. Calcification was also detected in an aged comparison eye, but this was markedly different from PXE eyes and presented as small snowflake-like deposits in the posterior pole. Conclusions: Pseudoxanthoma elasticum eyes show extensive hydroxyapatite deposition in the inner and outer collagenous and elastic BM layers in the macula with a gradual change toward the midperiphery, which seems to correlate with the clinical phenotype. The snowflake-like calcification in BM of an aged comparison eye differed markedly from the extensive calcification in PXE. Financial Disclosures: Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.

Indexed as

Bruch’s membraneCalcificationHydroxyapatitePseudoxanthoma elasticum

Identifiers

PMID38170125
PMCPMC10758992
OpenAlexW4387910424

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.