Evidence map›Paper›PMID 31088717›Full record

ArticlePancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.]2019

Genetic variants in acute, acute recurrent and chronic pancreatitis affect the progression of disease in children.

Maisam Abu-El-Haija, C Alexander Valencia, Lindsey Hornung, Nour Youssef, Tyler Thompson, Nathaniel W Barasa, Xinjian Wang, Lee A Denson

Open access · greenAbstract read
In one paragraph

Article in Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.], 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 2 pooled it
4.4field-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

18 citing papers in PubMed, 2 syntheses or guidelines pooled it, 37 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Misfolding PRSS1 variant p.Ala61Val in a case of suspected intrauterine pancreatitis.Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.] · 2025
    Article
  6. Turkish Society of Gastroenterology: Pancreas Working Group, Acute Pancreatitis Committee Consensus Report.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2024
    Review
  7. The Role of Pancreatitis Risk Genes in Endocrine Insufficiency Development After Acute Pancreatitis in Children.Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association · 2024
    Observational
  8. Novel chymotrypsin C (CTRC) variants from real-world genetic testing of pediatric chronic pancreatitis cases.Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.] · 2024
    Article
  9. Acute pancreatitis is associated with gut dysbiosis in children.Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver · 2024
    Observational
  10. Clinical and Genetic Description of Hereditary Chronic Pancreatitis in Pakistani Children.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2023
    Article
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  13. Article
  14. Review
  15. Article
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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

8 authors at 2 institutions in 1 country.

Maisam Abu-El-HaijaCincinnati Children's Hospital Medical Center, Gastroenterology, Hepatology & Nutrition, 3333 Burnet Ave, Cincinnati, OH, 45229, USA; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, USA. Electronic address: Maisam.Haija@cchmc.org.
C Alexander ValenciaCincinnati Children's Hospital Medical Center, USA. Electronic address: alexander.valencia@perkinelmer.com.
Lindsey HornungCincinnati Children's Hospital Medical Center, Biostatistics and Epidemiology, 3333 Burnet Ave, Cincinnati, OH, 45229, USA. Electronic address: Lindsey.hornung@cchmc.org.
Nour YoussefCincinnati Children's Hospital, Clinical Rotation, LAU, School of Medicine, Lebanon. Electronic address: ny31@aub.edu.lb.
Tyler ThompsonCincinnati Children's Hospital Medical Center, Gastroenterology, Hepatology & Nutrition, 3333 Burnet Ave, Cincinnati, OH, 45229, USA. Electronic address: Tyler.Thompson@cchmc.org.
Nathaniel W BarasaDivision of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA; Laboratory Genetics and Genomics, 3333 Burnet Ave, Cincinnati, OH, 45229, USA. Electronic address: Nathaniel.barasa@cchmc.org.
Xinjian WangDivision of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA; Laboratory Genetics and Genomics, 3333 Burnet Ave, Cincinnati, OH, 45229, USA. Electronic address: Xinjian.Wang@cchmc.org.
Lee A DensonCincinnati Children's Hospital Medical Center, Gastroenterology, Hepatology & Nutrition, 3333 Burnet Ave, Cincinnati, OH, 45229, USA; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, USA. Electronic address: Lee.denson@cchmc.org.
Cincinnati Children's Hospital Medical Center · USUniversity of Cincinnati Medical Center · US

Funding

Stem Cell/Organoid and Genome Editing CoreP30DK078392 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI Theresa Alenghat · 2007 to 2026
$24.4M
Year 9 Administrative Supplement to INSPPIRE 2U01DK108334 · NIDDK · UNIVERSITY OF IOWA · PI MARK E. LOWE, Aliye Uc · 2015 to 2026
$10.5M
Predicting Severity and Improving the Outcomes of Pediatric PancreatitisK23DK118190 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI ABU-EL-HAIJA, MAISAM · 2018 to 2022
$947k
PancreasCHIP - A diagnostic tool for Inheritable Pancreatic DiseaseR43DK105640 · NIDDK · P2D, INC. · PI ABU-EL-HAIJA, MAISAM, ZEMLAN, FRANK · 2015 to 2015
$266k
NIDDK NIH HHS K23 DK118190NIDDK NIH HHS P30 DK078392NIDDK NIH HHS R43 DK105640NIDDK NIH HHS U01 DK108334
6 · The paper itself

Abstract

BACKGROUND/

objectivesAcute pancreatitis (AP) is emerging in pediatrics. A subset of children with AP progresses to acute recurrent pancreatitis (ARP) and chronic pancreatitis (CP). The role of extensive gene testing in the progression has not been investigated previously. We have followed children enrolled in the registry and at our center for progression to ARP and CP after the first attack.

methodsThis study utilizes an extensive gene sequencing panel as a platform to evaluate the role of genetics in first attack AP, and the progression over time, from first attack to ARP and CP in children.

resultsGenes, with corresponding variants were involved in the 3 groups studied: AP, ARP and CP. We have shown that the presence of gene variants from the eight tested genes is enriched in the CP group compared to the AP and ARP groups. The presence of more than one gene was associated with CP (p = 0.01). SPINK1 mutation(s) was significantly associated with faster progression to ARP, (p = 0.04). Having a variant from CFTR, SPINK1 or PRSS1, was associated with the faster progression from AP to CP over time (p < 0.05).

conclusionsThis study shows that genetics have a significant role in progression to ARP and CP from the first attack of pancreatitis.

Indexed as

Acute DiseaseAdolescentChildChild, PreschoolCohort StudiesCystic Fibrosis Transmembrane Conductance RegulatorDisease ProgressionFemaleGenetic TestingGenetic VariationHumansMalePancreatitisPancreatitis, ChronicProspective StudiesRecurrenceCFTR protein, humanCystic Fibrosis Transmembrane Conductance RegulatorPRSS1 protein, humanSPINK1 protein, humanTrypsinTrypsin Inhibitor, Kazal PancreaticExtensive genetic testingPediatric pancreatitis

Identifiers

PMID31088717
PMCPMC6589390
OpenAlexW2944770419

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.