Progress towards non-invasive diagnosis and follow-up of celiac disease in children; a prospective multicentre study to the usefulness of plasma I-FABP
Abstract This prospective study investigates whether measurement of plasma intestinal-fatty acid binding protein (I-FABP), a sensitive marker for small intestinal epithelial damage, improves non-invasive diagnosing of celiac disease (CD), and whether I-FABP levels are useful to evaluate mucosal heal...
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Nature Portfolio
2017
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oai:doaj.org-article:76eb1bdbc1b74652987ccbd632d75edd2021-12-02T15:06:13ZProgress towards non-invasive diagnosis and follow-up of celiac disease in children; a prospective multicentre study to the usefulness of plasma I-FABP10.1038/s41598-017-07242-42045-2322https://doaj.org/article/76eb1bdbc1b74652987ccbd632d75edd2017-08-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-07242-4https://doaj.org/toc/2045-2322Abstract This prospective study investigates whether measurement of plasma intestinal-fatty acid binding protein (I-FABP), a sensitive marker for small intestinal epithelial damage, improves non-invasive diagnosing of celiac disease (CD), and whether I-FABP levels are useful to evaluate mucosal healing in patients on a gluten-free diet (GFD). Ninety children with elevated tTG-IgA titres and HLA-DQ2/DQ8 positivity were included (study group). Duodenal biopsies were taken, except in those fulfilling the ESPGHAN criteria. Plasma I-FABP levels and tTG-IgA titres were assessed sequentially during six months of follow-up. Eighty children with normal tTG-IgA titres served as control group. In 61/90 (67.8%) of the children in the study group an increased I-FABP level was found; in all these children CD diagnosis was confirmed. Interestingly, in 14/30 (46.7%) children with slightly elevated tTG-IgA titres (<10x upper limit of normal), an increased I-FABP level was found. In all these children the diagnosis of CD was confirmed histologically. After gluten elimination for six weeks I-FABP levels had decreased towards levels in the control group. Measurement of plasma I-FABP, in addition to tTG-IgA, EMA-IgA and HLAtyping, enables non-invasive diagnosing of CD in a substantial number of children, and might therefore be of value in the diagnostic approach of CD.M. P. M. AdriaanseA. MubarakR. G. RiedlF. J. W. Ten KateJ. G. M. C. DamoiseauxW. A. BuurmanR. H. J. HouwenA. C. E. VreugdenhilCeliac Disease Study GroupNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-10 (2017) |
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Medicine R Science Q M. P. M. Adriaanse A. Mubarak R. G. Riedl F. J. W. Ten Kate J. G. M. C. Damoiseaux W. A. Buurman R. H. J. Houwen A. C. E. Vreugdenhil Celiac Disease Study Group Progress towards non-invasive diagnosis and follow-up of celiac disease in children; a prospective multicentre study to the usefulness of plasma I-FABP |
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Abstract This prospective study investigates whether measurement of plasma intestinal-fatty acid binding protein (I-FABP), a sensitive marker for small intestinal epithelial damage, improves non-invasive diagnosing of celiac disease (CD), and whether I-FABP levels are useful to evaluate mucosal healing in patients on a gluten-free diet (GFD). Ninety children with elevated tTG-IgA titres and HLA-DQ2/DQ8 positivity were included (study group). Duodenal biopsies were taken, except in those fulfilling the ESPGHAN criteria. Plasma I-FABP levels and tTG-IgA titres were assessed sequentially during six months of follow-up. Eighty children with normal tTG-IgA titres served as control group. In 61/90 (67.8%) of the children in the study group an increased I-FABP level was found; in all these children CD diagnosis was confirmed. Interestingly, in 14/30 (46.7%) children with slightly elevated tTG-IgA titres (<10x upper limit of normal), an increased I-FABP level was found. In all these children the diagnosis of CD was confirmed histologically. After gluten elimination for six weeks I-FABP levels had decreased towards levels in the control group. Measurement of plasma I-FABP, in addition to tTG-IgA, EMA-IgA and HLAtyping, enables non-invasive diagnosing of CD in a substantial number of children, and might therefore be of value in the diagnostic approach of CD. |
format |
article |
author |
M. P. M. Adriaanse A. Mubarak R. G. Riedl F. J. W. Ten Kate J. G. M. C. Damoiseaux W. A. Buurman R. H. J. Houwen A. C. E. Vreugdenhil Celiac Disease Study Group |
author_facet |
M. P. M. Adriaanse A. Mubarak R. G. Riedl F. J. W. Ten Kate J. G. M. C. Damoiseaux W. A. Buurman R. H. J. Houwen A. C. E. Vreugdenhil Celiac Disease Study Group |
author_sort |
M. P. M. Adriaanse |
title |
Progress towards non-invasive diagnosis and follow-up of celiac disease in children; a prospective multicentre study to the usefulness of plasma I-FABP |
title_short |
Progress towards non-invasive diagnosis and follow-up of celiac disease in children; a prospective multicentre study to the usefulness of plasma I-FABP |
title_full |
Progress towards non-invasive diagnosis and follow-up of celiac disease in children; a prospective multicentre study to the usefulness of plasma I-FABP |
title_fullStr |
Progress towards non-invasive diagnosis and follow-up of celiac disease in children; a prospective multicentre study to the usefulness of plasma I-FABP |
title_full_unstemmed |
Progress towards non-invasive diagnosis and follow-up of celiac disease in children; a prospective multicentre study to the usefulness of plasma I-FABP |
title_sort |
progress towards non-invasive diagnosis and follow-up of celiac disease in children; a prospective multicentre study to the usefulness of plasma i-fabp |
publisher |
Nature Portfolio |
publishDate |
2017 |
url |
https://doaj.org/article/76eb1bdbc1b74652987ccbd632d75edd |
work_keys_str_mv |
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