论文部分内容阅读
AIM:To investigate whether celiac disease(CD)patients with tissue-transglutaminase antibody(tTGA)≥100 U/mL are different from patients with lower tTGA levels.METHODS:Biopsy-proven(MarshⅢ)pediatric CD patients(n=116)were prospectively included between March 2009 and October 2012.The biopsies were evaluated by a single pathologist who was blinded to all of the patients’clinical data.The patients were distributed into 2 groups according to their tTGA level,which was measured using enzyme-linked immunoassay:tTGA≥100 U/mL and Ttga<100 U/mL.The patients’characteristics,symptoms,human leukocyte antigen(HLA)genotype and degree of histological involvement were compared between the 2 groups.RESULTS:A total of 34(29.3%)children had tTGA values<100 U/mL and 82(70.7%)tTGA levels of≥100 U/mL.Patients with high tTGA levels had lower average body weight-for-height standard deviation scores(SDS)than did patients with tTGA<100 U/mL(-0.20±1.19 SDS vs 0.23±1.03 SDS,P=0.025).In the low tTGA group,gastrointestinal symptoms were more common(97.1%vs 75.6%,P=0.006).More specifically,abdominal pain(76.5%vs 51.2%;P=0.012)and nausea(17.6%vs 3.7%,P=0.018)were more frequent among patients with low tTGA.In contrast,patients with solely extraintestinal manifestations were only present in the high tTGA group(18.3%,P=0.005).These patients more commonly presented with aphthous stomatitis(15.9%vs 0.0%,P=0.010)and anemia(32.9%vs 11.8%,P=0.019).In addition,when evaluating the number of CD-associated HLA-DQ heterodimers(HLA-DQ2.5,HLA-DQ2.2 and HLA-DQ8),patients with low tTGA levels more commonly had only1 disease-associated heterodimer(61.8%vs 31.7%,P=0.005),while patients with high tTGA more commonly had multiple heterodimers.Finally,patients with tTGA≥100 U/mL more often had a MarshⅢc lesion(73.2%vs 20.6%,P≤0.001)while in patients with low tTGA patchy lesions were more common(42.4%vs6.8%,P≤0.001).CONCLUSION:Patients with tTGA≥100 U/mL show several signs of more advanced disease.They also carry a larger number of CD associated HLA-DQ heterodimers.
AIM: To investigate whether celiac disease (CD) patients with tissue-transglutaminase antibody (tTGA) ≧ 100 U / mL are different from patients with lower tTGA levels. METHODS: Biopsy-proven (MarshIII) pediatric CD patients prospectively included between March 2009 and October 2012.The biopsies were evaluated by a single pathologist who was blinded to all of the patients’clinical data.The patients were distributed into 2 groups according to their tTGA level, which was measured using enzyme-linked immunoassay : tTGA ≧ 100 U / mL and Ttga <100 U / mL. The patients’characteristics, symptoms, human leukocyte antigen (HLA) genotype and degree of histological involvement were compared between the 2 groups .RESULTS: A total of 34 (29.3% ) tATGA levels of> 100 U / mL. Patients with high tTGA levels had lower average body weight-for-height standard deviation scores (SDS) than did patients with tTGA <100 U / mL (-0.20 ± 1.19 SDS vs 0.23 ± 1.03 SDS, P = 0.025) .In the low tTGA g More specifically, abdominal pain (76.5% vs 51.2%; P = 0.012) and nausea (17.6% vs 3.7%, P = 0.018) were more frequent among patients with low tTGA.In contrast, patients with solely extraintestinal manifestations were only present in the high tTGA group (18.3%, P = 0.005) .These patients more generally presented with aphthous stomatitis (15.9% vs 0.0%, P = 0.010 ) and anessment (32.9% vs 11.8%, P = 0.019) .In addition, when evaluating the number of CD-associated HLA-DQ heterodimers (HLA-DQ2.5, HLA-DQ2.2 and HLA- DQ8), patients with Low tTGA levels more often had only 1 disease-associated heterodimer (61.8% vs 31.7%, P = 0.005), while patients with high tTGA more often had multiple heterodimers. F inally, patients with tTGA ≥ 100 U / mL more often had a MarshⅢc lesion (73.2% vs 20.6%, P≤0.001) while in patients with low tTGA patchy lesions were more common (42.4% vs 6.8%, P≤0.001) .CONCLUSION: Patients with tTGA ≥100 U / mL show several signs of more advanced disease. They also carry a largernumber of CD associated HLA-DQ heterodimers.