Evidence map›Paper›PMID 41062763›Full record

ArticlePediatric cardiology2026

Clinical and Experimental Studies of Structural Valve Degeneration of Bovine Jugular Vein Valves: Mitigation with Polyoxazoline Modification.

Morgan K Moroi, Yaagnik Kosuri, Sameer K Singh, Yingfei Xue, Andrey Zakharchenko, Cary Karcher, Alexis Martinez, Krushang Patel, Alexey Abramov, Chrystalle Katte Carreon and 3 more

Abstract read
In one paragraph

Article in Pediatric cardiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Morgan K Moroi *Departments of Surgery and Biomedical Engineering, Columbia University Irving Medical Center, 630 W 168Th Street 17.413, New York, NY, USA.
Yaagnik Kosuri *Departments of Surgery and Biomedical Engineering, Columbia University Irving Medical Center, 630 W 168Th Street 17.413, New York, NY, USA.
Sameer K SinghDepartments of Surgery and Biomedical Engineering, Columbia University Irving Medical Center, 630 W 168Th Street 17.413, New York, NY, USA.
Yingfei XueDepartments of Surgery and Biomedical Engineering, Columbia University Irving Medical Center, 630 W 168Th Street 17.413, New York, NY, USA.
Andrey ZakharchenkoDivision of Cardiology, Department of Pediatrics, Pediatric Heart Valve Center, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Cary KarcherDepartments of Surgery and Biomedical Engineering, Columbia University Irving Medical Center, 630 W 168Th Street 17.413, New York, NY, USA.
Alexis MartinezDivision of Cardiology, Department of Pediatrics, Pediatric Heart Valve Center, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Krushang PatelDepartments of Surgery and Biomedical Engineering, Columbia University Irving Medical Center, 630 W 168Th Street 17.413, New York, NY, USA.
Alexey AbramovDepartments of Surgery and Biomedical Engineering, Columbia University Irving Medical Center, 630 W 168Th Street 17.413, New York, NY, USA.
Chrystalle Katte CarreonDepartments of Cardiology, Pathology, and Cardiac Surgery, The Cardiac Registry, Boston Children's Hospital, Boston, MA, USA.
Stephen P SandersDepartments of Cardiology, Pathology, and Cardiac Surgery, The Cardiac Registry, Boston Children's Hospital, Boston, MA, USA.
Robert J LevyDivision of Cardiology, Department of Pediatrics, Pediatric Heart Valve Center, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Giovanni FerrariDepartments of Surgery and Biomedical Engineering, Columbia University Irving Medical Center, 630 W 168Th Street 17.413, New York, NY, USA. gf2375@cumc.columbia.edu.

Funding

POSTDOCTORAL TRAINING IN CARDIOVASCULAR DISEASET32HL007854 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Marwah Abdalla, Michael Argenziano · 1996 to 2026
$14.7M
POSTDOCTORAL TRAINING IN ARTERIOSCLEROSIS RESEARCHT32HL007343 · NHLBI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI HENRY N GINSBERG, Muredach P Reilly · 1985 to 2026
$12.7M
Oxidation-mediated structural degeneration of bioprosthetic heart valvesR01HL143008 · NHLBI · CHILDREN'S HOSP OF PHILADELPHIA · PI FERRARI, GIOVANNI, LEVY, ROBERT J · 2018 to 2021
$3.2M
Revision to Mechanisms of accelerated calcification and structural degeneration of implantable biomaterials in pediatric cardiac surgeryR01HL163085 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Giovanni Ferrari · 2023 to 2026
$2.7M
NHLBI NIH HHS L40 HL175843NHLBI NIH HHS R01 HL143008NHLBI NIH HHS R01 HL163085NHLBI NIH HHS T32 HL007343NHLBI NIH HHS T32 HL007854NIH HHS R01 HL143008NIH HHS R01 HL163085NIH HHS T32 HL007343NIH HHS T32 HL007854
6 · The paper itself

Abstract

Bovine jugular vein (BJV) valves are widely used in congenital heart surgery but are limited in durability due to structural valve degeneration (SVD). Here, we examine mechanisms of BJV prosthesis failure and test BJV modification with poly-2-methyl-2-oxazoline (POZ), a polymer shown to inhibit protein and advanced glycation end-product (AGE) absorption. Clinical BJV valve explants (Melody valve, N = 13) underwent Von Kossa staining and immunohistochemistry (IHC) for AGE, carboxymethyllysine (CML), and serum albumin (SA). Collagen structure was analyzed using second-harmonic generation (SHG) imaging. Unmodified and POZ-modified BJV valved conduits underwent 5-week in vitro glycation incubation. Effective orifice area (EOA) and mean pressure gradient (MPG) were recorded weekly using a heart pulse duplicator system. Following incubation, leaflet thickness, IHC, and SHG analyses were performed. In vivo 28-day subcutaneous BJV leaflet implantations were performed in juvenile rats for IHC. Clinical BJV explants demonstrated AGE, CML, and SA infiltration. In vitro glycation induced leaflet thickening (control, 0.03 ± 0.01 vs non-modified, 0.23 ± 0.07 mm, p < 0.001), CML and SA infiltration, and collagen disruption (alignment coefficient: control, 0.76 ± 0.03 vs non-modified, 0.50 ± 0.19, p < 0.01). POZ-modified leaflets remained similar in thickness to unglycated controls. POZ modification reduced CML and SA accumulation and mitigated collagen malalignment. BJV conduits did not reveal clinically significant changes in MPG or EOA. In vivo studies verified POZ modification protected against microcalcification as well as AGE, CML, and SA deposition. BJV valves are subject to SVD-related mechanisms of AGE accumulation, serum protein infiltration, and collagen misalignment. POZ modification mitigates BJV leaflet thickening, AGE and protein infiltration, and collagen disruption.

Indexed as

BioprosthesisHeart Valve ProsthesisJugular VeinsOxazolesProsthesis FailureVenous ValvesAnimalsCattleGlycation End Products, AdvancedHumansRatsGlycation End Products, AdvancedOxazolesBovine jugular veinMelody valvePolyoxazolineStructural valve degenerationValve durability

Identifiers

PMID41062763
PMCPMC12714419

What OpenQuestion holds

Textmetadata
LicenceTDM
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.