C Dahle1, A Hagman, S Ignatova, M Ström. 1. Department of Clinical Immunology and Transfusion Medicine, Linköping University Hospital, Linköping, Sweden. charlotte.dahle@lio.se
Abstract
BACKGROUND: This study was done to evaluate the diagnostic utility of antibodies against deamidated gliadin peptides compared to traditional markers for coeliac disease. AIM: To evaluate diagnostic utility of antibodies against deamidated gliadin peptide (DGP). METHODS: Sera from 176 adults, referred for endoscopy without previous analysis of antibodies against tissue transglutaminase (tTG) or endomysium (EmA), were retrospectively analysed by ELISAs detecting IgA/IgG antibodies against DGP or a mixture of DGP and tTG, and compared with IgA-tTG and EmA. Seventy-nine individuals were diagnosed with coeliac disease. RESULTS: Receiver operating characteristic analyses verified the manufacturers' cut-off limits except for IgA/IgG-DGP/tTG. In sera without IgA deficiency, the sensitivity was higher for IgA/IgG-DGP (0.85-0.87) compared with IgA-tTg (0.76) and EmA (0.61). All tests showed high specificity (0.95-1.00). Eighteen coeliac disease-sera were negative regarding IgA-tTG, nine of which were positive for IgA/IgG-DGP. Sera from coeliac disease-patients >70 years were more often negative for IgA-tTG (50%) and IgA/IgG-DGP (36%) than younger patients (15% and 8% respectively) (P < 0.01). Three of the four IgA-deficient patients were positive in the IgA/IgG-DGP assay. CONCLUSIONS: In this study of patients unselected regarding IgA-tTg/EmA, thus unbiased in this respect, IgA/IgG-DGP identified adult coeliac disease patients negative for antibodies against endomysium and tissue transglutaminase. Serology is often negative in elderly patients with coeliac disease; a small bowel biopsy should therefore be performed generously before coeliac disease is excluded.
BACKGROUND: This study was done to evaluate the diagnostic utility of antibodies against deamidated gliadin peptides compared to traditional markers for coeliac disease. AIM: To evaluate diagnostic utility of antibodies against deamidated gliadin peptide (DGP). METHODS: Sera from 176 adults, referred for endoscopy without previous analysis of antibodies against tissue transglutaminase (tTG) or endomysium (EmA), were retrospectively analysed by ELISAs detecting IgA/IgG antibodies against DGP or a mixture of DGP and tTG, and compared with IgA-tTG and EmA. Seventy-nine individuals were diagnosed with coeliac disease. RESULTS: Receiver operating characteristic analyses verified the manufacturers' cut-off limits except for IgA/IgG-DGP/tTG. In sera without IgA deficiency, the sensitivity was higher for IgA/IgG-DGP (0.85-0.87) compared with IgA-tTg (0.76) and EmA (0.61). All tests showed high specificity (0.95-1.00). Eighteen coeliac disease-sera were negative regarding IgA-tTG, nine of which were positive for IgA/IgG-DGP. Sera from coeliac disease-patients >70 years were more often negative for IgA-tTG (50%) and IgA/IgG-DGP (36%) than younger patients (15% and 8% respectively) (P < 0.01). Three of the four IgA-deficientpatients were positive in the IgA/IgG-DGP assay. CONCLUSIONS: In this study of patients unselected regarding IgA-tTg/EmA, thus unbiased in this respect, IgA/IgG-DGP identified adult coeliac diseasepatients negative for antibodies against endomysium and tissue transglutaminase. Serology is often negative in elderly patients with coeliac disease; a small bowel biopsy should therefore be performed generously before coeliac disease is excluded.
Authors: Isabel A Hujoel; Claire L Jansson-Knodell; Philippe P Hujoel; Margaux L A Hujoel; Rok Seon Choung; Joseph A Murray; Alberto Rubio-Tapia Journal: J Clin Gastroenterol Date: 2021-04-01 Impact factor: 3.174
Authors: Ning Wang; Lennart Truedsson; Kerstin Elvin; Bengt A Andersson; Johan Rönnelid; Lucia Mincheva-Nilsson; Annica Lindkvist; Jonas F Ludvigsson; Lennart Hammarström; Charlotte Dahle Journal: PLoS One Date: 2014-04-07 Impact factor: 3.240
Authors: Johannes Wolf; Dirk Hasenclever; David Petroff; Thomas Richter; Holm H Uhlig; Martin W Laaß; Almuthe Hauer; Martin Stern; Xavier Bossuyt; Jan de Laffolie; Gunter Flemming; Danilo Villalta; Wolfgang Schlumberger; Thomas Mothes Journal: PLoS One Date: 2014-05-15 Impact factor: 3.240