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嗜酸性粒细胞和肥大细胞作为儿童功能性消化不良的治疗靶点

Eosinophils and mast cells as therapeutic targets in pediatric functional dyspepsia.

作者信息

Friesen Craig A, Schurman Jennifer V, Colombo Jennifer M, Abdel-Rahman Susan M

机构信息

Craig A Friesen, Jennifer M Colombo, Division of Gastroenterology, Hepatology and Nutrition, the Children's Mercy Hospital and Clinics, Kansas City, Missouri, MO 64108, United States.

出版信息

World J Gastrointest Pharmacol Ther. 2013 Nov 6;4(4):86-96. doi: 10.4292/wjgpt.v4.i4.86.


DOI:10.4292/wjgpt.v4.i4.86
PMID:24199024
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3817289/
Abstract

There is an increasing appreciation for the importance of inflammation as a pathophysiologic entity that contributes to functional gastrointestinal disorders including functional dyspepsia (FD). Importantly, inflammation may serve as a mediator between psychologic and physiologic functions. This manuscript reviews the literature implicating two inflammatory cell types, mast cells and eosinophils, in the generation of dyspeptic symptoms and explores their potential as targets for the treatment of FD. There are a number of inciting events which may initiate an inflammatory response, and the subsequent recruitment and activation of mast cells and eosinophils. These include internal triggers such as stress and anxiety, as well as external triggers such as microbes and allergens. Previous studies suggest that there may be efficacy in utilizing medications directed at mast cells and eosinophils. Evidence exists to suggest that combining "anti-inflammatory" medications with other treatments targeting stress can improve the rate of symptom resolution in pediatric FD.

摘要

炎症作为一种病理生理实体,在包括功能性消化不良(FD)在内的功能性胃肠疾病中发挥作用,其重要性日益受到重视。重要的是,炎症可能充当心理和生理功能之间的介质。本文综述了涉及肥大细胞和嗜酸性粒细胞这两种炎症细胞类型在消化不良症状产生中的文献,并探讨了它们作为FD治疗靶点的潜力。有许多引发事件可能启动炎症反应,随后导致肥大细胞和嗜酸性粒细胞的募集和激活。这些包括内部触发因素,如压力和焦虑,以及外部触发因素,如微生物和过敏原。先前的研究表明,使用针对肥大细胞和嗜酸性粒细胞的药物可能有效。有证据表明,将“抗炎”药物与其他针对压力的治疗方法相结合,可以提高小儿FD症状缓解率。

相似文献

[1]
Eosinophils and mast cells as therapeutic targets in pediatric functional dyspepsia.

World J Gastrointest Pharmacol Ther. 2013-11-6

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[6]
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[7]
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[8]
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引用本文的文献

[1]
Rumination Syndrome in Children and Adolescents: A Mini Review.

Front Pediatr. 2021-8-19

[2]
An Update on the Assessment and Management of Pediatric Abdominal Pain.

Pediatric Health Med Ther. 2021-8-6

[3]
Update on the Role of Allergy in Pediatric Functional Abdominal Pain Disorders: A Clinical Perspective.

Nutrients. 2021-6-16

[4]
A cross-sectional study of nausea in functional abdominal pain: relation to mucosal mast cells and psychological functioning.

BMC Gastroenterol. 2020-5-11

[5]
Biliary Dyskinesia in Children and Adolescents: A Mini Review.

Front Pediatr. 2020-3-24

[6]
Diet and functional dyspepsia: Clinical correlates and therapeutic perspectives.

World J Gastroenterol. 2020-2-7

[7]
Prevalence of Non-Celiac Gluten Sensitivity in Patients with Refractory Functional Dyspepsia: a Randomized Double-blind Placebo Controlled Trial.

Sci Rep. 2020-2-12

[8]
The role of mast cells in pediatric gastrointestinal disease.

Ann Gastroenterol. 2019

[9]
Immunopathological and molecular basis of functional dyspepsia and current therapeutic approaches.

Expert Rev Clin Immunol. 2018-9-29

[10]
An observational study of headaches in children and adolescents with functional abdominal pain: Relationship to mucosal inflammation and gastrointestinal and somatic symptoms.

Medicine (Baltimore). 2018-7

本文引用的文献

[1]
Therapeutic targeting of eosinophil adhesion and accumulation in allergic conjunctivitis.

Front Pharmacol. 2012-12-26

[2]
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J Pediatr Gastroenterol Nutr. 2013-5

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J Allergy Clin Immunol. 2012-9

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ISRN Gastroenterol. 2012

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Pharmacol Ther. 2012-6-27

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Incidence of post-infectious irritable bowel syndrome and functional intestinal disorders following a water-borne viral gastroenteritis outbreak.

Am J Gastroenterol. 2012-4-24

[7]
Famotidine in the treatment of functional dyspepsia: a randomized double-blind, placebo-controlled trial.

J Egypt Public Health Assoc. 2012-4

[8]
The comparative study of the effectiveness of cimetidine, ranitidine, famotidine, and omeprazole in treatment of children with dyspepsia.

ISRN Pediatr. 2011

[9]
Novel insights in the role of peripheral corticotropin-releasing factor and mast cells in stress-induced visceral hypersensitivity.

Neurogastroenterol Motil. 2012-3

[10]
Pediatric patients with dyspepsia have chronic symptoms, anxiety, and lower quality of life as adolescents and adults.

Gastroenterology. 2012-1-5

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