Monitoring Eosinophilic Esophagitis Disease Activity With Blood Eosinophil Progenitor Levels.


Journal

Journal of pediatric gastroenterology and nutrition
ISSN: 1536-4801
Titre abrégé: J Pediatr Gastroenterol Nutr
Pays: United States
ID NLM: 8211545

Informations de publication

Date de publication:
04 2020
Historique:
pubmed: 14 12 2019
medline: 22 6 2021
entrez: 14 12 2019
Statut: ppublish

Résumé

A minimally invasive biomarker to monitor disease activity is one of the greatest unmet clinical needs of the pediatric eosinophilic esophagitis (EoE) population. We aimed to determine whether circulating eosinophil progenitors (EoPs) could be used as a biomarker to identify pediatric patients with active EoE. In a prospective observational study, peripheral blood samples, symptom history, and laboratory data were collected from pediatric patients undergoing endoscopy for evaluation of EoE on dietary therapy at Cincinnati Children's Hospital. Peripheral blood EoP level was determined by flow cytometry. Thirty-four children with active (n = 16) and inactive (n = 18) EoE were included in the analysis. EoP levels in the peripheral blood were 3-fold higher in patients with active EoE than inactive EoE (P < 0.0025). Blood absolute eosinophil count did not distinguish between active and inactive EoE (P = 0.16). A cut-off EoP level ≥17 accurately detected active disease in 79% of patients with 94.4% specificity and 62.5% sensitivity (area under the curve 0.81; P < 0.0024). Antihistamine use lowered the threshold EoP level to detect active EoE. This study suggests that blood EoP levels may be used as a biomarker to detect active EoE disease in patients undergoing food trials and potentially reduce the need for repeated endoscopies. Larger prospective studies are needed to investigate the effects of antihistamines and swallowed steroids on EoP mobilization into the peripheral blood and longitudinal studies to assess the performance of the assay in individual patients over time.

Identifiants

pubmed: 31834110
doi: 10.1097/MPG.0000000000002583
pmc: PMC7772866
mid: NIHMS1656705
pii: 00005176-202004000-00020
doi:

Types de publication

Journal Article Observational Study Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

482-488

Subventions

Organisme : NIDDK NIH HHS
ID : P30 DK078392
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI130033
Pays : United States
Organisme : NIDDK NIH HHS
ID : T32 DK007727
Pays : United States

Commentaires et corrections

Type : CommentIn

Références

United European Gastroenterol J. 2017 Apr;5(3):335-358
pubmed: 28507746
Gastroenterology. 2014 Aug;147(2):324-33.e5
pubmed: 24768678
J Allergy Clin Immunol. 2012 Feb;129(2):456-63, 463.e1-3
pubmed: 22206777
Clin Gastroenterol Hepatol. 2018 Jul;16(7):1056-1063
pubmed: 29248734
Br J Pharmacol. 2001 Dec;134(7):1539-47
pubmed: 11724761
Gastroenterology. 2007 Oct;133(4):1342-63
pubmed: 17919504
Gastroenterology. 2011 Nov;141(5):1593-604
pubmed: 21835135
Am J Respir Cell Mol Biol. 1996 Nov;15(5):645-55
pubmed: 8918371
Gastroenterology. 2018 Oct;155(4):1022-1033.e10
pubmed: 30009819
Gastroenterology. 2014 Jun;146(7):1639-48
pubmed: 24534634
Ann Allergy Asthma Immunol. 2018 Aug;121(2):218-228
pubmed: 29753832
Ann Allergy Asthma Immunol. 2019 Mar;122(3):296-301
pubmed: 30578860
Clin Gastroenterol Hepatol. 2015 Jan;13(1):66-76.e3
pubmed: 24907502
Dis Esophagus. 2017 Feb 1;30(3):1-8
pubmed: 26857345
J Allergy Clin Immunol. 2011 Jul;128(1):3-20.e6; quiz 21-2
pubmed: 21477849
Gastroenterology. 2013 Dec;145(6):1289-99
pubmed: 23978633
J Allergy Clin Immunol. 2019 Mar;143(3):1221-1224.e3
pubmed: 30414854
J Allergy Clin Immunol. 2013 Feb;131(2):379-86
pubmed: 23219170
Ann Allergy Asthma Immunol. 2008 Oct;101(4):402-6
pubmed: 18939729
Curr Gastroenterol Rep. 2018 Feb 28;20(1):4
pubmed: 29492720
J Allergy Clin Immunol. 2016 Sep;138(3):915-918.e5
pubmed: 27199214
Am J Gastroenterol. 2013 May;108(5):679-92; quiz 693
pubmed: 23567357
Am J Health Syst Pharm. 2017 Jul 1;74(13):963-969
pubmed: 28645995
Ann Allergy Asthma Immunol. 2015 Sep;115(3):224-228.e1
pubmed: 26235409
PLoS One. 2015 Feb 27;10(2):e0114831
pubmed: 25723478
Clin Gastroenterol Hepatol. 2004 Jul;2(7):568-75
pubmed: 15224281

Auteurs

Anna Henderson (A)

Division of Gastroenterology, Hepatology and Nutrition.

Adam Magier (A)

Division of Allergy and Immunology.

Justin T Schwartz (JT)

Division of Allergy and Immunology.

Lisa J Martin (LJ)

Division of Human Genetics.
Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH.

Margaret H Collins (MH)

Division of Pathology and Laboratory Medicine, Cincinnati Children's Hospital Medical Center.
Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH.

Philip E Putnam (PE)

Division of Gastroenterology, Hepatology and Nutrition.
Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH.

Vincent A Mukkada (VA)

Division of Gastroenterology, Hepatology and Nutrition.
Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH.

J Pablo Abonia (JP)

Division of Allergy and Immunology.
Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH.

Marc E Rothenberg (ME)

Division of Allergy and Immunology.

Patricia C Fulkerson (PC)

Division of Allergy and Immunology.
Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH.

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