Szaflarska-Poplawska Anna, Odrowaz-Sypniewska Grazyna
Department of Pediatrics, Allergology and Gastroenterology Head: M. Czerwionka-Szaflarska M.D., Ph.D., Professor.
Department of Laboratory Medicine Head: G. Odrowaz-Sypniewska Ph.D., Assoc. Professor.
EJIFCC. 2004 Dec 28;15(4):117-122. eCollection 2004 Dec.
Identification of tissue transglutaminase (tTG) as a major target antigen of IgA anti-endomysial antibodies and detection of auto-antibodies against tTG in the serum pointed out a new direction in the serologic diagnosis of coeliac disease. Clinical utility of determination of anti-tTGIgA antibodies, with recombinant human tTG used as antigen, was evaluated for the diagnosis of coeliac disease and monitoring the adherence to the diet in children and adolescents.
The study was performed in 169 patients aged 2-24 years, including 42 children (26 girls, 16 boys, mean age 8.01 ± 5.69, range 2-18) with newly diagnosed coeliac disease (CD) (group I), 60 patients (39 females, 21 males, mean age 15.68 ± 4.74, range 5-24) with CD recognized at least 3 years before entering the study, non-compliants with gluten-free diet (group II) and 67 children (34 girls, 33 boys, mean age 6,28± 4.48, range 2-16) suspected of malabsorption, in whom diagnosis of CD had been excluded.
Serum samples were taken from all patients and tested for total IgA, anti-endomysial IgA (IgAEmA) or IgG autoantibodies (IgGEmA), only in cases with IgA deficiency, by indirect immunofluorescence method and anti-tTGIgA antibodies by ELISA.
[Table: see text] Strong significant associations between anti-tTGIgA present in the serum and IgAEmA (Kendall τ 0.7748, p<0.0001) and good correlation between the levels of anti-tTGIgA and IgAEmA (r=0,488, p=0.001) were found in group I. We have not shown the relationship between the presence of both types of antibodies in patients of group II (Kendall τ 0.2102, p=0.0937). However, a good significant correlation between the levels of these parameters was observed (r=0,813, p<0,0001). Anti-tTGIgA concentration was nificantly higher in patients of group I compared to group II (38.35 U/ml v. 23.13 U/ml, p=0,0356). The sensitivity of anti- tTGIgA test in group I was 88.1%, in group II - 91.7% while specificity reached 97%.
Determination of anti-tTGIgA shows high sensitivity (88.1%) and specificity (97%) for the detection of coeliac disease. This test can be used alternatively with the immunofluorescent IgAEmA in diagnosis of coeliac disease, and also as a marker of compliance with gluten-free diet. However, both IgAEmA and anti-tTGIgA tests do not reach 100% sensitivity and specificity for diagnosis and nitoring of celiac disease. Therefore small intestinal biopsy is still recommended as a ? gold standard?.
组织转谷氨酰胺酶(tTG)被鉴定为IgA抗肌内膜抗体的主要靶抗原,并且血清中抗tTG自身抗体的检测为乳糜泻的血清学诊断指出了一个新方向。评估了以重组人tTG作为抗原测定抗tTG IgA抗体在儿童和青少年乳糜泻诊断及监测饮食依从性方面的临床实用性。
该研究纳入了169例年龄在2至24岁的患者,其中包括42例新诊断为乳糜泻(CD)的儿童(26名女孩,16名男孩,平均年龄8.01±5.69岁,范围2至18岁)(I组),60例在进入研究前至少3年就已确诊CD、未遵循无麸质饮食的患者(39名女性,21名男性,平均年龄15.68±4.74岁,范围5至24岁)(II组),以及67例疑似吸收不良、但已排除CD诊断的儿童(34名女孩,33名男孩,平均年龄6.28±4.48岁,范围2至16岁)。
采集所有患者的血清样本,检测总IgA、抗肌内膜IgA(IgAEmA)或IgG自身抗体(IgGEmA)(仅在IgA缺乏的病例中检测),采用间接免疫荧光法检测,采用ELISA法检测抗tTG IgA抗体。
[表格:见正文]I组中血清中抗tTG IgA与IgAEmA之间存在强显著相关性(肯德尔τ系数0.7748,p<0.0001),抗tTG IgA水平与IgAEmA水平之间存在良好相关性(r = 0.488,p = 0.001)。我们未发现II组患者中两种抗体的存在之间存在相关性(肯德尔τ系数0.2102,p = 0.0937)。然而,观察到这些参数水平之间存在良好的显著相关性(r = 0.813,p<0.0001)。I组患者的抗tTG IgA浓度显著高于II组(38.35 U/ml对23.13 U/ml,p = 0.0356)。I组中抗tTG IgA检测的敏感性为88.1%,II组中为91.7%,而特异性达到97%。
抗tTG IgA测定对乳糜泻检测具有高敏感性(88.1%)和特异性(97%)。该检测可替代免疫荧光IgAEmA用于乳糜泻诊断,也可作为无麸质饮食依从性的标志物。然而,IgAEmA和抗tTG IgA检测在乳糜泻诊断和监测中的敏感性和特异性均未达到100%。因此,仍建议小肠活检作为“金标准”。