135. IMPACT OF GENDER, RACE AND AGE OF ONSET ON THE PHENOTYPE AND COMORBIDITIES OF PEDIATRIC EOSINOPHILIC ESOPHAGITIS
Abstract Eosinophilic esophagitis (EoE) is recognized as chronic immunologic disorder of the esophagus resulting in esophageal inflammation by the accumulation of eosinophils in the epithelium. Several risk factors are thought to be associated with the development of EoE, but because of its complex...
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Veröffentlicht in: | Diseases of the esophagus 2023-08, Vol.36 (Supplement_2) |
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description | Abstract
Eosinophilic esophagitis (EoE) is recognized as chronic immunologic disorder of the esophagus resulting in esophageal inflammation by the accumulation of eosinophils in the epithelium. Several risk factors are thought to be associated with the development of EoE, but because of its complex underlying mechanisms of disease, there is little clarity in regards to the different symptoms experienced, pathological findings and associated comorbidities including atopic and allergic disorders between different gender, race and age of onset.
This study utilized a retrospective chart review on the patients seen by a multidisciplinary EoE clinic from January 2020 to December 2022. Subjects were diagnosed with EoE, and retrospectively assessed for eosinophilic counts on the initial distal and proximal esophageal biopsies, and previously specified symptoms and comorbidities. The differences of eosinophilic counts, associated symptoms and comorbidities between gender (male or female), race (White or non-White) and age of onset (≤ 6 years old is defined as early onset, or > 6 years old is defined as regular onset in this study), were statistically analyzed by t-test or Chi-Square. P |
doi_str_mv | 10.1093/dote/doad052.020 |
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Eosinophilic esophagitis (EoE) is recognized as chronic immunologic disorder of the esophagus resulting in esophageal inflammation by the accumulation of eosinophils in the epithelium. Several risk factors are thought to be associated with the development of EoE, but because of its complex underlying mechanisms of disease, there is little clarity in regards to the different symptoms experienced, pathological findings and associated comorbidities including atopic and allergic disorders between different gender, race and age of onset.
This study utilized a retrospective chart review on the patients seen by a multidisciplinary EoE clinic from January 2020 to December 2022. Subjects were diagnosed with EoE, and retrospectively assessed for eosinophilic counts on the initial distal and proximal esophageal biopsies, and previously specified symptoms and comorbidities. The differences of eosinophilic counts, associated symptoms and comorbidities between gender (male or female), race (White or non-White) and age of onset (≤ 6 years old is defined as early onset, or > 6 years old is defined as regular onset in this study), were statistically analyzed by t-test or Chi-Square. P < 0.05 is considered as significant.
Ninety patients were included in this study, of whom 72% are male (M) while 28% are female (F), and 68% are White (W) while 32% are non-White (NW). Age of onset ranges from 1 year to 17 years, with 44% being early onset while 56% being regular onset. We found females and White race were significantly more likely to report dysphagia. Non-White patients were found to have higher incidence of vomiting, asthma than White. Significant higher incidence of vomiting, and eosinophilic counts was found in early onset (EO) patients (distal: 56, proximal: 50) compared to regular onset (RO) (distal: 39, proximal: 39), while no significant difference was found between different gender and race.
Our retrospective study demonstrated that there are significant differences between different gender, race and age of onset for pediatric EoE in regard to the severity of eosinophilic inflammation, gastrointestinal symptoms and associated comorbidities. These findings could provide some guidance to clinicians in identifying proper diagnosis and developing appropriate treatment to achieve the best outcome.</description><identifier>ISSN: 1120-8694</identifier><identifier>EISSN: 1442-2050</identifier><identifier>DOI: 10.1093/dote/doad052.020</identifier><language>eng</language><publisher>Oxford University Press</publisher><ispartof>Diseases of the esophagus, 2023-08, Vol.36 (Supplement_2)</ispartof><rights>The Author(s) 2023. Published by Oxford University Press on behalf of International Society for Diseases of the Esophagus. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Mckeown, Kyle</creatorcontrib><creatorcontrib>Pritchett, Justin</creatorcontrib><creatorcontrib>Carlisle, Annette</creatorcontrib><creatorcontrib>Lieberman, Jay</creatorcontrib><creatorcontrib>Xi, Dong</creatorcontrib><title>135. IMPACT OF GENDER, RACE AND AGE OF ONSET ON THE PHENOTYPE AND COMORBIDITIES OF PEDIATRIC EOSINOPHILIC ESOPHAGITIS</title><title>Diseases of the esophagus</title><description>Abstract
Eosinophilic esophagitis (EoE) is recognized as chronic immunologic disorder of the esophagus resulting in esophageal inflammation by the accumulation of eosinophils in the epithelium. Several risk factors are thought to be associated with the development of EoE, but because of its complex underlying mechanisms of disease, there is little clarity in regards to the different symptoms experienced, pathological findings and associated comorbidities including atopic and allergic disorders between different gender, race and age of onset.
This study utilized a retrospective chart review on the patients seen by a multidisciplinary EoE clinic from January 2020 to December 2022. Subjects were diagnosed with EoE, and retrospectively assessed for eosinophilic counts on the initial distal and proximal esophageal biopsies, and previously specified symptoms and comorbidities. The differences of eosinophilic counts, associated symptoms and comorbidities between gender (male or female), race (White or non-White) and age of onset (≤ 6 years old is defined as early onset, or > 6 years old is defined as regular onset in this study), were statistically analyzed by t-test or Chi-Square. P < 0.05 is considered as significant.
Ninety patients were included in this study, of whom 72% are male (M) while 28% are female (F), and 68% are White (W) while 32% are non-White (NW). Age of onset ranges from 1 year to 17 years, with 44% being early onset while 56% being regular onset. We found females and White race were significantly more likely to report dysphagia. Non-White patients were found to have higher incidence of vomiting, asthma than White. Significant higher incidence of vomiting, and eosinophilic counts was found in early onset (EO) patients (distal: 56, proximal: 50) compared to regular onset (RO) (distal: 39, proximal: 39), while no significant difference was found between different gender and race.
Our retrospective study demonstrated that there are significant differences between different gender, race and age of onset for pediatric EoE in regard to the severity of eosinophilic inflammation, gastrointestinal symptoms and associated comorbidities. These findings could provide some guidance to clinicians in identifying proper diagnosis and developing appropriate treatment to achieve the best outcome.</description><issn>1120-8694</issn><issn>1442-2050</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNqFkM1PgzAYhxujiXN699i7Mt-2tIwjQgdNNkoAD55IV0qi0WwBd_C_t2S7e3m_8vzew4PQI4EVgZi99Icf54vpgdMVULhCCxKGNKDA4drPhEKwFnF4i-6m6ROAREysF-hEGF9htauStMV6g3NZZrJ-xnWSSpyUGU5yOd912UgPlLgtJK4KWer2vToTqd7p-lVlqlWymdlKZippa5ViqRtV6qpQ23lp_JTkHmvu0c1gvib3cOlL9LaRbVoEW52rNNkGlpAYAhMx7vrBOBMCtTGJLHU93_eRDZmj1hhnuRCcWBB9PzAX2ojPQbpf74EKwZYIzn_teJim0Q3dcfz4NuNvR6CbtXWztu6irfPafOTpHDmcjv_Tf5WhZp4</recordid><startdate>20230830</startdate><enddate>20230830</enddate><creator>Mckeown, Kyle</creator><creator>Pritchett, Justin</creator><creator>Carlisle, Annette</creator><creator>Lieberman, Jay</creator><creator>Xi, Dong</creator><general>Oxford University Press</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20230830</creationdate><title>135. IMPACT OF GENDER, RACE AND AGE OF ONSET ON THE PHENOTYPE AND COMORBIDITIES OF PEDIATRIC EOSINOPHILIC ESOPHAGITIS</title><author>Mckeown, Kyle ; Pritchett, Justin ; Carlisle, Annette ; Lieberman, Jay ; Xi, Dong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1190-a735edfaea402c917c2ed5bd7c43e2caaec56651c06ddf3e4c7511902b8b02663</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mckeown, Kyle</creatorcontrib><creatorcontrib>Pritchett, Justin</creatorcontrib><creatorcontrib>Carlisle, Annette</creatorcontrib><creatorcontrib>Lieberman, Jay</creatorcontrib><creatorcontrib>Xi, Dong</creatorcontrib><collection>CrossRef</collection><jtitle>Diseases of the esophagus</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mckeown, Kyle</au><au>Pritchett, Justin</au><au>Carlisle, Annette</au><au>Lieberman, Jay</au><au>Xi, Dong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>135. IMPACT OF GENDER, RACE AND AGE OF ONSET ON THE PHENOTYPE AND COMORBIDITIES OF PEDIATRIC EOSINOPHILIC ESOPHAGITIS</atitle><jtitle>Diseases of the esophagus</jtitle><date>2023-08-30</date><risdate>2023</risdate><volume>36</volume><issue>Supplement_2</issue><issn>1120-8694</issn><eissn>1442-2050</eissn><abstract>Abstract
Eosinophilic esophagitis (EoE) is recognized as chronic immunologic disorder of the esophagus resulting in esophageal inflammation by the accumulation of eosinophils in the epithelium. Several risk factors are thought to be associated with the development of EoE, but because of its complex underlying mechanisms of disease, there is little clarity in regards to the different symptoms experienced, pathological findings and associated comorbidities including atopic and allergic disorders between different gender, race and age of onset.
This study utilized a retrospective chart review on the patients seen by a multidisciplinary EoE clinic from January 2020 to December 2022. Subjects were diagnosed with EoE, and retrospectively assessed for eosinophilic counts on the initial distal and proximal esophageal biopsies, and previously specified symptoms and comorbidities. The differences of eosinophilic counts, associated symptoms and comorbidities between gender (male or female), race (White or non-White) and age of onset (≤ 6 years old is defined as early onset, or > 6 years old is defined as regular onset in this study), were statistically analyzed by t-test or Chi-Square. P < 0.05 is considered as significant.
Ninety patients were included in this study, of whom 72% are male (M) while 28% are female (F), and 68% are White (W) while 32% are non-White (NW). Age of onset ranges from 1 year to 17 years, with 44% being early onset while 56% being regular onset. We found females and White race were significantly more likely to report dysphagia. Non-White patients were found to have higher incidence of vomiting, asthma than White. Significant higher incidence of vomiting, and eosinophilic counts was found in early onset (EO) patients (distal: 56, proximal: 50) compared to regular onset (RO) (distal: 39, proximal: 39), while no significant difference was found between different gender and race.
Our retrospective study demonstrated that there are significant differences between different gender, race and age of onset for pediatric EoE in regard to the severity of eosinophilic inflammation, gastrointestinal symptoms and associated comorbidities. These findings could provide some guidance to clinicians in identifying proper diagnosis and developing appropriate treatment to achieve the best outcome.</abstract><pub>Oxford University Press</pub><doi>10.1093/dote/doad052.020</doi><oa>free_for_read</oa></addata></record> |
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source | Oxford University Press Journals All Titles (1996-Current) |
title | 135. IMPACT OF GENDER, RACE AND AGE OF ONSET ON THE PHENOTYPE AND COMORBIDITIES OF PEDIATRIC EOSINOPHILIC ESOPHAGITIS |
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