Evidence map›Paper›PMID 31560377›Full record

ArticleInflammatory bowel diseases2020

The Unique Disease Course of Children with Very Early onset-Inflammatory Bowel Disease.

Judith R Kelsen, Maire A Conrad, Noor Dawany, Trusha Patel, Rawan Shraim, Audrey Merz, Kelly Maurer, Kathleen E Sullivan, Marcella Devoto

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Inflammatory bowel diseases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

30 citing papers in PubMed, 65 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

9 authors at 1 institution in 2 countries.

Judith R KelsenDivision of Gastroenterology, Hepatology, and Nutrition, The Children's Hospital of Philadelphia.
Maire A ConradDivision of Gastroenterology, Hepatology, and Nutrition, The Children's Hospital of Philadelphia.
Noor DawanyDepartment of Biomedical and Health Informatics, The Children's Hospital of Philadelphia.
Trusha PatelDivision of Gastroenterology, Hepatology, and Nutrition, The Children's Hospital of Philadelphia.
Rawan ShraimDivision of Gastroenterology, Hepatology, and Nutrition, The Children's Hospital of Philadelphia.
Audrey MerzDivision of Gastroenterology, Hepatology, and Nutrition, The Children's Hospital of Philadelphia.
Kelly MaurerDivision of Immunology and Allergy, The Children's Hospital of Philadelphia.
Kathleen E SullivanDepartment of Pediatrics, Perelman School of Medicine, University of Pennsylvania.
Marcella DevotoDepartment of Pediatrics, Perelman School of Medicine, University of Pennsylvania.
Children's Hospital of Philadelphia · US

Funding

Integration of genomics and transcriptomics to investigate biological pathways in very early onset IBDR01DK127044 · NIDDK · CHILDREN'S HOSP OF PHILADELPHIA · PI KELSEN, JUDITH RACHEL · 2021 to 2025
$3.4M
Identifying Genomic and Microbial Contributions in Early Childhood-Inflammatory Bowel DiseaseK23DK119585 · NIDDK · CHILDREN'S HOSP OF PHILADELPHIA · PI CONRAD, MAIRE ABRAHAM · 2019 to 2023
$927k
Very Early-onset inflammatory bowel diseaseK23DK100461 · NIDDK · CHILDREN'S HOSP OF PHILADELPHIA · PI KELSEN, JUDITH RACHEL · 2014 to 2018
$893k
An integrative approach to understanding the genetic basis of very early onset inflammatory bowel diseaseR01DK111843 · NIDDK · CHILDREN'S HOSP OF PHILADELPHIA · PI KELSEN, JUDITH RACHEL · 2018 to 2020
$772k
NIDDK NIH HHS K23 DK100461NIDDK NIH HHS K23 DK119585NIDDK NIH HHS R01 DK111843NIDDK NIH HHS R01 DK127044
6 · The paper itself

Abstract

backgroundInsight into the pathogenesis of very early onset-inflammatory bowel disease (VEO-IBD) has expanded through the identification of causative monogenic defects detected in a subset of patients. However, the clinical course of this population remains uncertain. The study objective is to determine whether VEO-IBD is associated with more severe disease, defined as increased surgical intervention and growth failure, than older pediatric IBD. Secondary outcomes included therapeutic response and hospitalizations.

methodsSubjects with IBD diagnosed younger than 6 years old (VEO-IBD) were compared with children diagnosed 6 to 10 (intermediate-onset) and older than 10 years of age (older-onset IBD). Metadata obtained from the medical record included age of onset, disease phenotype and location, surgeries, medical therapy, and comorbid conditions. Length of follow-up was at least 1 year from diagnosis.

resultsThere were 229, 221, and 521 subjects with VEO, intermediate-onset, and older-onset IBD, respectively. Very early onset-inflammatory bowel disease subjects underwent more diverting ileostomies (P < 0.001) and colectomies (P < 0.001) than the older children. There was less improvement in weight- and height-for-age Z scores during the follow-up period in subjects with VEO-IBD. Additionally, subjects with VEO-IBD had higher rates of medication failure at 1 year and were more frequently readmitted to the hospital. Targeted therapy was successfully used almost exclusively in VEO-IBD.

conclusionPatients with VEO-IBD can have a more severe disease course with increased surgical interventions and poor growth as compared with older-onset IBD patients. Further, VEO-IBD patients are more likely to be refractory to conventional therapies. Strategies using targeted therapy in these children can improve outcome and, in some cases, be curative.

Indexed as

AdolescentChildChild, PreschoolFemaleHumansInflammatory Bowel DiseasesMalePhenotypePhiladelphiaRetrospective StudiesSeverity of Illness IndexTreatment Failuredisease coursegrowth failurevery early onset-inflammatory bowel disease

Identifiers

PMID31560377
PMCPMC7216772
OpenAlexW2975725016

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.