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1.
Scand J Gastroenterol ; 36(9): 955-8, 2001 Sep.
Article in English | MEDLINE | ID: mdl-11521986

ABSTRACT

BACKGROUND: Since transglutaminase was shown to be the antigen of endomysial antibodies (EMA), it has become possible to screen for coeliac disease (CD) with an enzyme-linked immunosorbent assay (ELISA) for transglutaminase antibodies (TTA). However, it is possible that sera used to show that TTA are found in CD were obtained from patients diagnosed because they were positive for EMA. So, a comparison between EMA and TTA has not been possible so far. METHODS: EMA and TTA were tested in sera from 52 controls and 56 untreated CD patients, who had not undergone serological testing. Samples were tested for TTA with an ELISA kit. Based on the ROC analysis of a pilot study, results were considered as either positive, borderline, or negative. EMA were analysed by indirect immunofluorescence on monkey oesophagus. RESULTS: Forty-nine CD patients were positive for TTA, six borderline, one negative. Forty-four controls were negative, seven borderline, one positive. If we consider borderline results to be positive, sensitivity is 98.2% and specificity 84.6%. EMA were positive in 53 CD patients; the controls were all negative. Performing TTA in all cases and EMA only in the few TTA borderline cases (12.0%) would have a sensitivity of 94.6% and a specificity of 98.1%. CONCLUSIONS: This study is the first to compare TTA with EMA. Due to 100% specificity and high sensitivity, EMA seems to be the most accurate coeliac antibody. Conversely, TTA offer advantages in terms of sensitivity and simplicity. A satisfactory strategy is to use TTA first and then EMA to confirm the borderline results.


Subject(s)
Celiac Disease/immunology , GTP-Binding Proteins/immunology , Muscles/immunology , Transglutaminases/immunology , Adult , Celiac Disease/blood , Celiac Disease/diagnosis , Enzyme-Linked Immunosorbent Assay , Female , Humans , Male , Protein Glutamine gamma Glutamyltransferase 2 , Sensitivity and Specificity
2.
Scand J Clin Lab Invest ; 57(3): 271-3, 1997 May.
Article in English | MEDLINE | ID: mdl-9238763

ABSTRACT

We report hyperamylasemia due to macroamylasemia in a 33-year-old-woman with gluten enteropathy. Macroamylasemia was demonstrated by precipitation of 97% of amylase activity with PEG 6000. It was associated with increased serum IgA, with elevated values of specific IgA antibodies against alpha-gliadin and with a high titre of IgA anti-endomysium antibodies. Macroamylasemia disappeared after 2 months of a strict gluten-free diet. These data suggest that the increased IgA concentration in adult gluten enteropathy led to increased macroamylase formation.


Subject(s)
Amylases/blood , Celiac Disease/blood , Celiac Disease/enzymology , Adult , Amylases/urine , Celiac Disease/immunology , Female , Gliadin/immunology , Humans , Macromolecular Substances
3.
Int J Biol Markers ; 6(2): 115-21, 1991.
Article in English | MEDLINE | ID: mdl-1890315

ABSTRACT

CA 125 and CA 15.3 antigens were determined by enzyme immunoassay in 78 patients with ovarian cancer for a total of 540 determinations. The antigens were also investigated in sera from 100 women with other gynaecological diseases, 82 lung cancer patients and in 39 pleural fluids of varying origin. CA 15.3 reference values were evaluated in 91 healthy women (cut-off: 25 U/ml). CA 15.3 sensitivity at diagnosis (60%) and for detecting relapse (44%) was lower than that of CA 125 (90% and 64.7%, respectively). However, CA 15.3 does not increase with aspecific mesothelial cell reaction and thus it is more specific than CA 125. Combined use of the markers during follow-up improves early detection of relapse (at least one of the two was positive in 79% of cases). Therefore both CA 15.3 and CA 125 should be routinely determined for the detection and monitoring of ovarian cancer.


Subject(s)
Antigens, Tumor-Associated, Carbohydrate/blood , Ovarian Neoplasms/blood , Ascites , Female , Follow-Up Studies , Humans , Neoplasms/blood , Ovarian Neoplasms/diagnosis , Prognosis , Recurrence , Survival Rate
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