Evidence map›Paper›PMID 42238820›Full record

ArticleFrontiers in genetics2026

Episignature-based modelled first-tier diagnostic approach in the Dutch Caribbean: advancing equal care through epigenetic classification.

Liselot van der Laan, Amanda Luijckx, Shirley Lo-A-Njoe, Ginette M Ecury-Goossen, Farah A Falix, Sonja Faries, Meindert E Manshande, Patricia A E A C Philippi, Evelyn M van der Plas, Hans D Veenhuis and 6 more

Abstract read
In one paragraph

Article in Frontiers in genetics, 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

16 authors.

Liselot van der LaanDepartment of Human Genetics, Amsterdam UMC, Amsterdam, Netherlands.
Amanda LuijckxDepartment of Human Genetics, Amsterdam UMC, Amsterdam, Netherlands.
Shirley Lo-A-NjoeDepartment of Pediatrics, Curaçao Medical Center (CMC), Willemstad, Curaçao.
Ginette M Ecury-GoossenDepartment of Pediatrics, Dr. Horacio E. Oduber Hospital, Oranjestad, Aruba.
Farah A FalixDepartment of Pediatrics, Dr. Horacio E. Oduber Hospital, Oranjestad, Aruba.
Sonja FariesDepartment of Pediatrics, Dr. Horacio E. Oduber Hospital, Oranjestad, Aruba.
Meindert E ManshandeDepartment of Pediatrics, Dr. Horacio E. Oduber Hospital, Oranjestad, Aruba.
Patricia A E A C PhilippiDepartment of Pediatrics, Dr. Horacio E. Oduber Hospital, Oranjestad, Aruba.
Evelyn M van der PlasDepartment of Pediatrics, Dr. Horacio E. Oduber Hospital, Oranjestad, Aruba.
Hans D VeenhuisDepartment of Pediatrics, Dr. Horacio E. Oduber Hospital, Oranjestad, Aruba.
Louise Rafael-CroesDepartment of Pediatrics, Dr. Horacio E. Oduber Hospital, Oranjestad, Aruba.
Marcel M A M MannensDepartment of Human Genetics, Amsterdam UMC, Amsterdam, Netherlands.
Bekim SadikovicVerspeeten Clinical Genome Centre, London Health Sciences Centre, London, ON, Canada.
Peter HennemanDepartment of Human Genetics, Amsterdam UMC, Amsterdam, Netherlands.
Mariëlle AldersDepartment of Human Genetics, Amsterdam UMC, Amsterdam, Netherlands.
Mieke M van HaelstDepartment of Human Genetics, Amsterdam UMC, Amsterdam, Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Access to advanced genetic testing in the Dutch Caribbean is limited due to financial and logistical constraints. As a result, many patients with rare disorders remain undiagnosed or receive uncertain results, leading to unequal genetic care. DNA methylation profiles, or episignatures, provide sensitive and specific biomarkers. The clinically validated EpiSign™ assay offers a cost-effective and rapid diagnostic approach. Methods: In this study, we evaluated EpiSign™ as a modelled first-tier screening approach within a proposed diagnostic workflow in a resource-limited setting and assessed its diagnostic yield and clinical utility in 19 patients from the Dutch Caribbean. Peripheral blood DNA was analyzed using the EPIC array, and methylation profiles were classified via a support vector machine algorithm against the EpiSign™ Knowledge Database. All patients underwent ID-WES and/or CGH-array analysis as part of the diagnostic workup. Positive EpiSign™ findings were subsequently confirmed by these molecular analyses. Results: EpiSign™ helped provide a clinical diagnosis for six cases, including Fragile X syndrome, Intellectual Developmental Disorder X-linked 93 (MRX93), ReNU syndrome, and Kleefstra syndrome 1, all confirmed by subsequent analyses. Several patients harbored variants of uncertain significance in genes not yet associated with known episignatures. Discussion: These results demonstrate that EpiSign™ provides actionable diagnostic insights as a first-tier diagnostic tool, particularly when combined with genomic analyses in the absence of parental samples. Its dynamic database allows reanalysis as new episignatures are identified, increasing its potential clinical utility in resource-limited settings.

Indexed as

Dutch Caribbeanepisignaturesequal healthcaregenetic serviceshealthcare challengesrare disorders

Identifiers

PMID42238820
PMCPMC13229482

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.