Evidence map›Paper›PMID 37519217›Full record

ArticleMolecular genetics & genomic medicine2023

First-time application of droplet digital PCR for methylation testing of the 11p15.5 imprinting regions.

Elia Schlaich, Wouter H G Hubens, Thomas Eggermann

Open access · goldAbstract read
In one paragraph

Article in Molecular genetics & genomic medicine, 2023. 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
0.6field-weighted citation impact, top 23% 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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
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

3 authors at 1 institution in 1 country.

Elia SchlaichInstitute for Human Genetics and Genome Medicine, Medical Faculty, RWTH Aachen University, Aachen, Germany.
Wouter H G HubensInstitute for Stem Cell Biology, Medical Faculty, RWTH Aachen University, Aachen, Germany.
Thomas EggermannInstitute for Human Genetics and Genome Medicine, Medical Faculty, RWTH Aachen University, Aachen, Germany.ORCID 0000-0002-8419-0264
RWTH Aachen University · DE

Funding

Deutsche Forschungsgemeinschaft EG 115/13-1
6 · The paper itself

Abstract

backgroundBeckwith-Wiedemann syndrome and Silver-Russel syndrome are two imprinting disorders caused by opposite molecular alterations in 11p15.5. With the current diagnostic tests, their molecular diagnosis is challenging due to molecular heterogeneity and mosaic occurrence of the most frequent alterations. As the determination of precise (epi)genotype of patients is relevant as the basis for a personalized treatment, different approaches are needed to increase the sensitivity of diagnostic testing of imprinting disorders.

methodsWe established methylation-specific droplet digital PCR approaches (MS-ddPCR) for the two imprinting centers in 11p15.5, and analyzed patients with paternal uniparental disomy of chromosome 11p15.5 (upd(11)pat) and other imprinting defects in the region. The results were compared to those from MS-MLPA (multiplex ligation-dependent probe amplification) and MS-pyrosequencing.

resultsMS-ddPCR confirmed the molecular alterations in all patients and the results matched well with MS-MLPA. The results of MS-pyrosequencing varied between different runs, whereas MS-ddPCR results were reproducible.

conclusionWe show for the first time that MS-ddPCR is a reliable and easy applicable method for determination of MS-associated changes in imprinting disorders. It is therefore an additional tool for multimethod diagnostics of imprinting disorders suitable to improve the diagnostic yield.

Indexed as

Beckwith-Wiedemann SyndromeImprinting DisordersSilver-Russell SyndromeDNA MethylationGenomic ImprintingHumansMultiplex Polymerase Chain Reactionimprinting disordersmosaicismMS-ddPCRMS-MLPAMS-pyrosequencing

Identifiers

PMID37519217
PMCPMC10724498
OpenAlexW4385406805

What OpenQuestion holds

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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.