Symptoms and Mucosal Changes Stable During Rapid Increase of Pediatric Celiac Disease in Norway
ABSTRACT Objectives: We aimed to study whether the incidence of pediatric celiac disease (CD) in South‐Eastern Norway changed from 2000 to 2010. We also examined whether there was a change in symptoms and histopathological morphology in the duodenal biopsies during the same period. Methods: In 3 hos...
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Veröffentlicht in: | Journal of pediatric gastroenterology and nutrition 2017-04, Vol.64 (4), p.586-591 |
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creator | Beitnes, Ann‐Christin R. Vikskjold, Florin B. Jóhannesdóttir, Gróa B. Perminow, Gøri Olbjørn, Christine Andersen, Solveig N. Bentsen, Beint S. Rugtveit, Jarle Størdal, Ketil |
description | ABSTRACT
Objectives:
We aimed to study whether the incidence of pediatric celiac disease (CD) in South‐Eastern Norway changed from 2000 to 2010. We also examined whether there was a change in symptoms and histopathological morphology in the duodenal biopsies during the same period.
Methods:
In 3 hospitals in South‐Eastern Norway, records from pediatric patients (0–14.9 years) diagnosed with CD during two 3‐year periods (2000–2002 and 2008–2010) were reviewed. Only cases with a duodenal biopsy diagnosis of CD classified as Marsh grade 2 and 3a−c were included. Frequencies of symptoms, anthropometric data, and laboratory results were compared, in addition to re‐examinations of histological sections from one of the hospitals.
Results:
A total of 400 cases were diagnosed with a female to male ratio of 1.5:1. The incidence rate for 2000 to 2002 was 15.9 cases per 100,000 person‐years (95% confidence interval 12.8–19.4), compared with 45.5 cases per 100,000 person‐years during 2008 to 2010 (95% confidence interval 40.5–50.9), P < 0.001. The relative frequencies of symptoms and the distribution of histopathological changes were similar in the 2 periods, whereas weight z scores and hemoglobin levels were significantly lower in the first period.
Conclusions:
We found a 3‐fold increase in the incidence rate for CD in the Norwegian pediatric population during the decade 2000 to 2010. Slightly higher weight and hemoglobin levels at diagnosis in the latter period may be due to improved CD awareness. Unaltered relative frequencies of symptoms and histopathological changes in the gut, however, suggest a true increase of CD in Norwegian children. |
doi_str_mv | 10.1097/MPG.0000000000001307 |
format | Article |
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Objectives:
We aimed to study whether the incidence of pediatric celiac disease (CD) in South‐Eastern Norway changed from 2000 to 2010. We also examined whether there was a change in symptoms and histopathological morphology in the duodenal biopsies during the same period.
Methods:
In 3 hospitals in South‐Eastern Norway, records from pediatric patients (0–14.9 years) diagnosed with CD during two 3‐year periods (2000–2002 and 2008–2010) were reviewed. Only cases with a duodenal biopsy diagnosis of CD classified as Marsh grade 2 and 3a−c were included. Frequencies of symptoms, anthropometric data, and laboratory results were compared, in addition to re‐examinations of histological sections from one of the hospitals.
Results:
A total of 400 cases were diagnosed with a female to male ratio of 1.5:1. The incidence rate for 2000 to 2002 was 15.9 cases per 100,000 person‐years (95% confidence interval 12.8–19.4), compared with 45.5 cases per 100,000 person‐years during 2008 to 2010 (95% confidence interval 40.5–50.9), P < 0.001. The relative frequencies of symptoms and the distribution of histopathological changes were similar in the 2 periods, whereas weight z scores and hemoglobin levels were significantly lower in the first period.
Conclusions:
We found a 3‐fold increase in the incidence rate for CD in the Norwegian pediatric population during the decade 2000 to 2010. Slightly higher weight and hemoglobin levels at diagnosis in the latter period may be due to improved CD awareness. Unaltered relative frequencies of symptoms and histopathological changes in the gut, however, suggest a true increase of CD in Norwegian children.</description><identifier>ISSN: 0277-2116</identifier><identifier>EISSN: 1536-4801</identifier><identifier>DOI: 10.1097/MPG.0000000000001307</identifier><identifier>PMID: 27299421</identifier><language>eng</language><publisher>United States: by European Society for Pediatric Gastroenterology, Hepatology, and Nutrition and North American Society for Pediatric Gastroenterology</publisher><subject>Adolescent ; Biopsy ; celiac disease ; Celiac Disease - diagnosis ; Celiac Disease - epidemiology ; Celiac Disease - pathology ; Child ; Child, Preschool ; Duodenum - pathology ; epidemiology ; Female ; histopathology ; Humans ; Incidence ; Infant ; Infant, Newborn ; Intestinal Mucosa - pathology ; Male ; Norway - epidemiology ; Retrospective Studies ; symptoms</subject><ispartof>Journal of pediatric gastroenterology and nutrition, 2017-04, Vol.64 (4), p.586-591</ispartof><rights>2017 by European Society for European Society for Pediatric Gastroenterology, Hepatology, and Nutrition and North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition</rights><rights>2017 by European Society for Pediatric Gastroenterology, Hepatology, and Nutrition and North American Society for Pediatric Gastroenterology</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4107-7690444427806cb07e50c61af8add904d05ad8d53ee32d2d08261fe9e031be5b3</citedby><cites>FETCH-LOGICAL-c4107-7690444427806cb07e50c61af8add904d05ad8d53ee32d2d08261fe9e031be5b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1097%2FMPG.0000000000001307$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1097%2FMPG.0000000000001307$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27299421$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Beitnes, Ann‐Christin R.</creatorcontrib><creatorcontrib>Vikskjold, Florin B.</creatorcontrib><creatorcontrib>Jóhannesdóttir, Gróa B.</creatorcontrib><creatorcontrib>Perminow, Gøri</creatorcontrib><creatorcontrib>Olbjørn, Christine</creatorcontrib><creatorcontrib>Andersen, Solveig N.</creatorcontrib><creatorcontrib>Bentsen, Beint S.</creatorcontrib><creatorcontrib>Rugtveit, Jarle</creatorcontrib><creatorcontrib>Størdal, Ketil</creatorcontrib><title>Symptoms and Mucosal Changes Stable During Rapid Increase of Pediatric Celiac Disease in Norway</title><title>Journal of pediatric gastroenterology and nutrition</title><addtitle>J Pediatr Gastroenterol Nutr</addtitle><description>ABSTRACT
Objectives:
We aimed to study whether the incidence of pediatric celiac disease (CD) in South‐Eastern Norway changed from 2000 to 2010. We also examined whether there was a change in symptoms and histopathological morphology in the duodenal biopsies during the same period.
Methods:
In 3 hospitals in South‐Eastern Norway, records from pediatric patients (0–14.9 years) diagnosed with CD during two 3‐year periods (2000–2002 and 2008–2010) were reviewed. Only cases with a duodenal biopsy diagnosis of CD classified as Marsh grade 2 and 3a−c were included. Frequencies of symptoms, anthropometric data, and laboratory results were compared, in addition to re‐examinations of histological sections from one of the hospitals.
Results:
A total of 400 cases were diagnosed with a female to male ratio of 1.5:1. The incidence rate for 2000 to 2002 was 15.9 cases per 100,000 person‐years (95% confidence interval 12.8–19.4), compared with 45.5 cases per 100,000 person‐years during 2008 to 2010 (95% confidence interval 40.5–50.9), P < 0.001. The relative frequencies of symptoms and the distribution of histopathological changes were similar in the 2 periods, whereas weight z scores and hemoglobin levels were significantly lower in the first period.
Conclusions:
We found a 3‐fold increase in the incidence rate for CD in the Norwegian pediatric population during the decade 2000 to 2010. Slightly higher weight and hemoglobin levels at diagnosis in the latter period may be due to improved CD awareness. Unaltered relative frequencies of symptoms and histopathological changes in the gut, however, suggest a true increase of CD in Norwegian children.</description><subject>Adolescent</subject><subject>Biopsy</subject><subject>celiac disease</subject><subject>Celiac Disease - diagnosis</subject><subject>Celiac Disease - epidemiology</subject><subject>Celiac Disease - pathology</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Duodenum - pathology</subject><subject>epidemiology</subject><subject>Female</subject><subject>histopathology</subject><subject>Humans</subject><subject>Incidence</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Intestinal Mucosa - pathology</subject><subject>Male</subject><subject>Norway - epidemiology</subject><subject>Retrospective Studies</subject><subject>symptoms</subject><issn>0277-2116</issn><issn>1536-4801</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkM1P3DAQxa2qCLbAf1BVPvYSGNtJnBx6aJfyJT5WQM-WY09Yt06y2IlW-98T2KVCXGAuc3i_92b0CPnK4IBBKQ8vZycH8GqYAPmJTFgm8iQtgH0mE-BSJpyxfId8ifHvCMk0g22ywyUvy5SzCVG3q2bRd02kurX0cjBd1J5O57q9x0hve115pEdDcO09vdELZ-lZawLqiLSr6Qyt031whk7RO23okYvPmmvpVReWerVHtmrtI-5v9i75c_z7bnqaXFyfnE1_XiQmZSATmZeQjsNlAbmpQGIGJme6LrS1o2Qh07awmUAU3HILBc9ZjSWCYBVmldgl39e5i9A9DBh71bho0HvdYjdExUZDXkqW8hFN16gJXYwBa7UIrtFhpRiop2rVWK16W-1o-7a5MFQN2v-mly5HoFgDy873GOI_PywxqDlq38_fy_6xsTqPqw_9o85nV-LXMUAumHgElC2VTw</recordid><startdate>201704</startdate><enddate>201704</enddate><creator>Beitnes, Ann‐Christin R.</creator><creator>Vikskjold, Florin B.</creator><creator>Jóhannesdóttir, Gróa B.</creator><creator>Perminow, Gøri</creator><creator>Olbjørn, Christine</creator><creator>Andersen, Solveig N.</creator><creator>Bentsen, Beint S.</creator><creator>Rugtveit, Jarle</creator><creator>Størdal, Ketil</creator><general>by European Society for Pediatric Gastroenterology, Hepatology, and Nutrition and North American Society for Pediatric Gastroenterology</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201704</creationdate><title>Symptoms and Mucosal Changes Stable During Rapid Increase of Pediatric Celiac Disease in Norway</title><author>Beitnes, Ann‐Christin R. ; Vikskjold, Florin B. ; Jóhannesdóttir, Gróa B. ; Perminow, Gøri ; Olbjørn, Christine ; Andersen, Solveig N. ; Bentsen, Beint S. ; Rugtveit, Jarle ; Størdal, Ketil</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4107-7690444427806cb07e50c61af8add904d05ad8d53ee32d2d08261fe9e031be5b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adolescent</topic><topic>Biopsy</topic><topic>celiac disease</topic><topic>Celiac Disease - diagnosis</topic><topic>Celiac Disease - epidemiology</topic><topic>Celiac Disease - pathology</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Duodenum - pathology</topic><topic>epidemiology</topic><topic>Female</topic><topic>histopathology</topic><topic>Humans</topic><topic>Incidence</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Intestinal Mucosa - pathology</topic><topic>Male</topic><topic>Norway - epidemiology</topic><topic>Retrospective Studies</topic><topic>symptoms</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Beitnes, Ann‐Christin R.</creatorcontrib><creatorcontrib>Vikskjold, Florin B.</creatorcontrib><creatorcontrib>Jóhannesdóttir, Gróa B.</creatorcontrib><creatorcontrib>Perminow, Gøri</creatorcontrib><creatorcontrib>Olbjørn, Christine</creatorcontrib><creatorcontrib>Andersen, Solveig N.</creatorcontrib><creatorcontrib>Bentsen, Beint S.</creatorcontrib><creatorcontrib>Rugtveit, Jarle</creatorcontrib><creatorcontrib>Størdal, Ketil</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of pediatric gastroenterology and nutrition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Beitnes, Ann‐Christin R.</au><au>Vikskjold, Florin B.</au><au>Jóhannesdóttir, Gróa B.</au><au>Perminow, Gøri</au><au>Olbjørn, Christine</au><au>Andersen, Solveig N.</au><au>Bentsen, Beint S.</au><au>Rugtveit, Jarle</au><au>Størdal, Ketil</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Symptoms and Mucosal Changes Stable During Rapid Increase of Pediatric Celiac Disease in Norway</atitle><jtitle>Journal of pediatric gastroenterology and nutrition</jtitle><addtitle>J Pediatr Gastroenterol Nutr</addtitle><date>2017-04</date><risdate>2017</risdate><volume>64</volume><issue>4</issue><spage>586</spage><epage>591</epage><pages>586-591</pages><issn>0277-2116</issn><eissn>1536-4801</eissn><abstract>ABSTRACT
Objectives:
We aimed to study whether the incidence of pediatric celiac disease (CD) in South‐Eastern Norway changed from 2000 to 2010. We also examined whether there was a change in symptoms and histopathological morphology in the duodenal biopsies during the same period.
Methods:
In 3 hospitals in South‐Eastern Norway, records from pediatric patients (0–14.9 years) diagnosed with CD during two 3‐year periods (2000–2002 and 2008–2010) were reviewed. Only cases with a duodenal biopsy diagnosis of CD classified as Marsh grade 2 and 3a−c were included. Frequencies of symptoms, anthropometric data, and laboratory results were compared, in addition to re‐examinations of histological sections from one of the hospitals.
Results:
A total of 400 cases were diagnosed with a female to male ratio of 1.5:1. The incidence rate for 2000 to 2002 was 15.9 cases per 100,000 person‐years (95% confidence interval 12.8–19.4), compared with 45.5 cases per 100,000 person‐years during 2008 to 2010 (95% confidence interval 40.5–50.9), P < 0.001. The relative frequencies of symptoms and the distribution of histopathological changes were similar in the 2 periods, whereas weight z scores and hemoglobin levels were significantly lower in the first period.
Conclusions:
We found a 3‐fold increase in the incidence rate for CD in the Norwegian pediatric population during the decade 2000 to 2010. Slightly higher weight and hemoglobin levels at diagnosis in the latter period may be due to improved CD awareness. Unaltered relative frequencies of symptoms and histopathological changes in the gut, however, suggest a true increase of CD in Norwegian children.</abstract><cop>United States</cop><pub>by European Society for Pediatric Gastroenterology, Hepatology, and Nutrition and North American Society for Pediatric Gastroenterology</pub><pmid>27299421</pmid><doi>10.1097/MPG.0000000000001307</doi><tpages>6</tpages></addata></record> |
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subjects | Adolescent Biopsy celiac disease Celiac Disease - diagnosis Celiac Disease - epidemiology Celiac Disease - pathology Child Child, Preschool Duodenum - pathology epidemiology Female histopathology Humans Incidence Infant Infant, Newborn Intestinal Mucosa - pathology Male Norway - epidemiology Retrospective Studies symptoms |
title | Symptoms and Mucosal Changes Stable During Rapid Increase of Pediatric Celiac Disease in Norway |
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