Incidence of Pediatric Celiac Disease Varies by Region

被引:22
|
作者
Stahl, Marisa [1 ]
Li, Qian [2 ]
Lynch, Kristian [3 ]
Koletzko, Sibylle [4 ,5 ]
Mehta, Pooja [1 ]
Gragert, Loren [6 ]
Norris, Jill M. [7 ]
Aronsson, Carin Andren
Lindfors, Katri [8 ]
Kurppa, Kalle [8 ,9 ]
Ilonen, Jorma [10 ]
Krischer, Jeffrey [3 ]
Alkolkar, Beena [11 ,12 ,13 ]
Ziegler, Anette-G [14 ,15 ]
Toppari, Jorma [16 ]
Rewers, Marian J. [17 ]
Agardh, Daniel
Hagopian, William
Liu, Edwin [1 ]
TEDDY Study Grp
机构
[1] Univ Colorado Anschutz Med Campus, Digest Hlth Inst, Sch Med, Dept Pediat, Aurora, CO 80045 USA
[2] St Jude Childrens Res Hosp, Dept Biostat, Memphis, TN USA
[3] Univ S Florida, Hlth Informat Inst, Morsani Coll Med, Tampa, FL USA
[4] LMU Klinikum, Dept Pediat, Dr Von Hauner Kinderspital, Munich, Germany
[5] Univ Warmia & Mazury, Dept Pediat Gastroenterol & Nutr, Sch Med, Coll Med, Olsztyn, Poland
[6] Tulane Univ, Pathol & Lab Med, Sch Med, New Orleans, LA USA
[7] Univ Colorado Anschutz Med Campus, Colorado Sch Publ Hlth, Dept Epidemiol, Aurora, CO USA
[8] Tampere Univ, Celiac Dis Res Ctr, Tampere, Finland
[9] Tampere Univ Hosp, Diabet & Celiac Dis, Tampere, Finland
[10] Tampere Univ, Fac Med & Hlth Technol, Tampere Ctr Child Adolescent & Maternal Hlth Res, Tampere, WA, Finland
[11] Univ Turku, Inst Biomed, Immunogenet Lab, Turku, Finland
[12] Turku Univ Hosp, Dept Pediat, Turku, Finland
[13] NIDDKD, Bethesda, MD USA
[14] Forschergrp Diabet e V, Munich, Germany
[15] Helmholtz Zentrum, Inst Diabet Res, Munich, Germany
[16] Univ Turku, Inst Biomed, Ctr Integrat Physiol & Pharmacol, Turku, Finland
[17] Univ Colorado Anschutz Med Campus, Barbara Davis Ctr Diabet, Sch Med, Aurora, CO USA
来源
AMERICAN JOURNAL OF GASTROENTEROLOGY | 2023年 / 118卷 / 03期
关键词
ENVIRONMENTAL DETERMINANTS; INCREASING INCIDENCE; RISK; AUTOIMMUNITY; POPULATION; GLUTEN; FEATURES;
D O I
10.14309/ajg.0000000000002056
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
INTRODUCTION: The Environmental Determinants of Diabetes in the Young study follows an HLA risk selected birth cohort for celiac disease (CD) development using a uniform protocol. Children under investigation come from 6 different regions within Europe and the United States. Our aim was to identify regional differences in CD autoimmunity and CD cumulative incidence for children born between 2004 and 2010.METHODS: Children (n = 6,628) with DQ2.5 and/or DQ8.1 were enrolled prospectively from birth in Georgia, Washington, Colorado, Finland, Germany, and Sweden. Children underwent periodic study screening for tissue transglutaminase antibodies and then CD evaluation per clinical care. Population-specific estimates were calculated by weighting the study-specific cumulative incidence with the population-specific haplogenotype frequencies obtained from large stem cell registries from each site.RESULTS: Individual haplogenotype risks for CD autoimmunity and CD varied by region and affected the cumulative incidence within that region. The CD incidence by age 10 years was highest in Swedish children at 3%. Within the United States, the incidence by age 10 years in Colorado was 2.4%. In the model adjusted for HLA, sex, and family history, Colorado children had a 2.5-fold higher risk of CD compared to Washington. Likewise, Swedish children had a 1.4-fold and 1.8-fold higher risk of CD compared with those in Finland and Germany, respectively.DISCUSSION: There is high regional variability in cumulative incidence of CD, which suggests differential environmental, genetic, and epigenetic influences even within the United States. The overall high incidence warrants a low threshold for screening and further research on region-specific CD triggers.
引用
收藏
页码:539 / 545
页数:7
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