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      Long-term health and treatment outcomes in adult coeliac disease patients diagnosed by screening in childhood

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          Abstract

          Background

          The diagnostic yield of coeliac disease could be improved by screening in at-risk groups, but long-term benefits of this approach are obscure.

          Objective

          To investigate health, quality of life and dietary adherence in adult coeliac patients diagnosed in childhood by screening.

          Methods

          After thorough evaluation of medical history, follow-up questionnaires were sent to 559 adults with a childhood coeliac disease diagnosis. The results were compared between screen-detected and clinically-detected patients, and also between originally asymptomatic and symptomatic screen-detected patients.

          Results

          In total, 236 (42%) patients completed the questionnaires a median of 18.5 years after childhood diagnosis. Screen-detected patients ( n = 48) had coeliac disease in the family and type 1 diabetes more often, and were less often smokers and members of coeliac societies compared to clinically-detected patients, whereas the groups did not differ in current self-experienced health or health concerns, quality of life or dietary adherence. Screen-detected, originally asymptomatic patients had more anxiety than those presenting with symptoms, whereas the subgroups were comparable in other current characteristics.

          Conclusion

          Comparable long-term outcomes between screen-detected and clinically-detected patients support risk-group screening for coeliac disease. However, asymptomatic patients may require special attention.

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          Most cited references27

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          Celiac disease revealed in 3% of Swedish 12-year-olds born during an epidemic.

          Sweden experienced a marked epidemic of celiac disease between 1984 and 1996 in children younger than 2 years of age, partly explained by changes in infant feeding. The objective of this study was to determine the prevalence of celiac disease in 12-year-olds born during the epidemic (1993), including both symptomatic and screening detected cases. All sixth-grade children in participating schools were invited (n = 10,041). Symptomatic and, therefore, previously diagnosed celiac disease cases were ascertained through the National Swedish Childhood Celiac Disease Register and/or medical records. All serum samples were analyzed for antihuman tissue transglutaminase (tTG)-IgA (Celikey), and serum-IgA, and some for tTG-IgG and endomysial antibodies. A small intestinal biopsy was recommended for all children with suspected undiagnosed celiac disease. Participation was accepted by 7567 families (75%). Previously diagnosed celiac disease was found in 67 children; 8.9/1000 (95% confidence interval [CI] 6.7-11). In another 192 children, a small intestinal biopsy was recommended and was performed in 180. Celiac disease was verified in 145 children, 20/1000 (95% CI 17-23). The total prevalence was 29/1000 (95% CI 25-33). The celiac disease prevalence of 29/1000 (3%)-with two thirds of cases undiagnosed before screening-is 3-fold higher than the usually suggested prevalence of 1%. When these 12-year-olds were infants, the prevailing feeding practice was to introduce gluten abruptly, often without ongoing breast-feeding, which might have contributed to this unexpectedly high prevalence.
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            The US Preventive Services Task Force 2017 Draft Recommendation Statement on Screening for Prostate Cancer

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              Duration of exposure to gluten and risk for autoimmune disorders in patients with celiac disease

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                Author and article information

                Journal
                United European Gastroenterol J
                United European Gastroenterol J
                UEG
                spueg
                United European Gastroenterology Journal
                SAGE Publications (Sage UK: London, England )
                2050-6406
                2050-6414
                17 May 2018
                August 2018
                : 6
                : 7
                : 1022-1031
                Affiliations
                [1 ]Center for Child Health Research, University of Tampere and Tampere University Hospital, Tampere, Finland
                [2 ]Department of Pediatrics, Hospital District of South Ostrobothnia, Seinäjoki, Finland
                [3 ]Institute for Mother and Child Health Bucharest, University of Medicine and Pharmacy ‘Carol Davila’, Bucharest, Romania
                [4 ]Department of Pediatrics, Hospital District of Kanta-Häme, Hämeenlinna, Finland
                [5 ]Faculty of Social Sciences, University of Tampere, Tampere, Finland
                [6 ]Department of Internal Medicine, Tampere University Hospital, Tampere, Finland
                [7 ]Celiac Disease Research Center, University of Tampere, Tampere, Finland
                Author notes
                [*]Kalle Kurppa, MD, Center for Child Health Research, University of Tampere and Tampere University Hospital, Lääkärinkatu 1, FI-33014 Tampere, Finland. Email: kalle.kurppa@ 123456uta.fi
                Article
                PMC6137595 PMC6137595 6137595 10.1177_2050640618778386
                10.1177/2050640618778386
                6137595
                30228890
                8f9b6c87-ab7e-43c9-8a3d-0eb691f5f74c
                © Author(s) 2018
                History
                : 7 March 2018
                : 29 April 2018
                Funding
                Funded by: Yrjö Jahnssonin Säätiö, FundRef https://doi.org/10.13039/100010114;
                Funded by: Mary and Georg C. Ehrnrooth Foundation, FundRef ;
                Funded by: Competitive State Research Financing of the Expert Area of Tampere University Hospital, FundRef ;
                Funded by: Foundation for Pediatric Research, FundRef ;
                Funded by: Suomen Lääketieteen Säätiö, FundRef https://doi.org/10.13039/100008723;
                Funded by: Maud Kuistilan Muistosäätiö, FundRef https://doi.org/10.13039/100010129;
                Funded by: Maire Rossi Foundation, FundRef ;
                Categories
                Original Articles

                screening,quality of life,long-term follow-up,gluten-free diet,Children,diagnosis

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