Evidence map›Paper›PMID 32080334›Full record

ArticleJournal of perinatology : official journal of the California Perinatal Association2020

An omic approach to congenital diaphragmatic hernia: a pilot study of genomic, microRNA, and metabolomic profiling.

Fiammetta Piersigilli, Mansoor Syed, TuKiet T Lam, Andrea Dotta, Michela Massoud, Pamela Vernocchi, Andrea Quagliariello, Lorenza Putignani, Cinzia Auriti, Guglielmo Salvatori and 2 more

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In one paragraph

Article in Journal of perinatology : official journal of the California Perinatal Association, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 26 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

12 authors at 4 institutions in 2 countries.

Fiammetta PiersigilliDivision of Perinatal Medicine, Yale Child Health Research Center, Department of Pediatrics, Yale University School of Medicine, New Haven, CT, USA.
Mansoor SyedDivision of Perinatal Medicine, Yale Child Health Research Center, Department of Pediatrics, Yale University School of Medicine, New Haven, CT, USA.
TuKiet T LamDepartment of Molecular Biophysics & Biochemistry, Yale University, New Haven, CT, USA.
Andrea DottaDivision of Medical and Surgical Neonatology, Bambino Gesù Children's Hospital, Rome, Italy.
Michela MassoudDivision of Medical and Surgical Neonatology, Bambino Gesù Children's Hospital, Rome, Italy.
Pamela VernocchiUnit of Human Microbiome, Genetic and Rare Diseases Area, Bambino Gesù Children's Hospital, Rome, Italy.
Andrea QuagliarielloUnit of Human Microbiome, Genetic and Rare Diseases Area, Bambino Gesù Children's Hospital, Rome, Italy.
Lorenza PutignaniUnit of Human Microbiome, Genetic and Rare Diseases Area, Bambino Gesù Children's Hospital, Rome, Italy.
Cinzia AuritiDivision of Medical and Surgical Neonatology, Bambino Gesù Children's Hospital, Rome, Italy.
Guglielmo SalvatoriDivision of Medical and Surgical Neonatology, Bambino Gesù Children's Hospital, Rome, Italy.
Pietro BagolanDivision of Medical and Surgical Neonatology, Bambino Gesù Children's Hospital, Rome, Italy.
Vineet BhandariDivision of Perinatal Medicine, Yale Child Health Research Center, Department of Pediatrics, Yale University School of Medicine, New Haven, CT, USA. bhandari-vineet@cooperhealth.edu.ORCID http://orcid.org/0000-0002-4900-6636
Bambino Gesù Children's Hospital · ITYale University · USCooper University Hospital · USW. M. Keck Foundation · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe omic approach can help identify a signature that can be potentially used as biomarkers in babies with congenital diaphragmatic hernia (CDH).

objectivesTo find a specific microRNA (miR) and metabolic fingerprint of the tracheal aspirates (TA) of CDH patients. We conducted a genetic analysis from blood samples.

methodsTA samples collected in the first 48 h of life in patients with CDH, compared with age-matched controls. Metabolomics done by a mass spectroscopy-based assay. Genomics done using chromosomal microarray analysis.

resultsCDH (n = 17) and 16 control neonates enrolled. miR-16, miR-17, miR-18, miR-19b, and miR-20a had an increased expression, while miR-19a had a twofold decreased expression in CDH patients, compared with age-matched control patients. Specific metabolites separated neonates with CDH from controls. A genetic mutation found in a small subset of patients.

conclusionsSpecific patterns of metabolites and miR expression can be discerned in TA samples in infants with CDH.

Indexed as

Hernias, Diaphragmatic, CongenitalMicroRNAsGenomicsHumansInfant, NewbornLungMetabolomicsPilot ProjectsMicroRNAs

Identifiers

PMID32080334
OpenAlexW3008606776

What OpenQuestion holds

Textmetadata
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.