Kochańska-Dziurowicz A, Bukowska C
Laboratory of Nuclear Medicine, Institute of Occupational Medicine and Environmental Health, Sosnowiec, Poland.
J Gastroenterol. 1997 Jun;32(3):312-7. doi: 10.1007/BF02934486.
The aim of this study was to examine serum levels of beta-2-microglobulin (b-2-m) in 132 children at various stages for the evaluation of celiac disease (CD). Serum b-2-m was analyzed by a radio immunoassay (RIA) method, using a beta-2-micro RIA kit (Pharmacia, Uppsala, Sweden). The mean concentration of b-2-m in children with an established diagnosis of CD was 4.38 +/- 1.86 mg/l. In children receiving a gluten-free diet, the mean b-2-m concentration was 1.95 +/- 1.09 mg/l, and in children who received a gluten-containing diet, the concentration was 3.19 +/- 0.71 mg/l. In children with CD who were on a gluten-free diet and who presented no antibodies against EmA in class IgA serum, b-2-m concentration was within the normal range (1.86 +/- 0.55 mg/l). The concentration of b-2-m in children with secondary malabsorption syndrome was within the physiological range (1.77 +/- 0.64 mg/l). In children with IgA-EmA antibodies present in serum, the b-2-m concentration was significantly higher (3.5 +/- 1.23 mg/l; P < 0.001) than that in children with IgA-EmA in serum. We showed a linear dependence between the degree of villous atrophy in CD and concentrations of b-2-m in serum (r2 = 0.94). Determination of b-2-m concentration in sera of children with CD may be used to monitor treatment with a gluten-free diet and to differentiate secondary malabsorption syndrome from CD.
本研究旨在检测132名处于不同阶段的儿童血清中β2-微球蛋白(β2-m)水平,以评估乳糜泻(CD)。采用放射免疫分析(RIA)法,使用β2-微球蛋白RIA试剂盒(瑞典乌普萨拉法玛西亚公司)分析血清β2-m。确诊为CD的儿童中β2-m的平均浓度为4.38±1.86mg/L。接受无麸质饮食的儿童中,β2-m的平均浓度为1.95±1.09mg/L,接受含麸质饮食的儿童中,该浓度为3.19±0.71mg/L。在接受无麸质饮食且IgA血清中无抗麦醇溶蛋白抗体(EmA)的CD儿童中,β2-m浓度在正常范围内(1.86±0.55mg/L)。继发性吸收不良综合征儿童的β2-m浓度在生理范围内(1.77±0.64mg/L)。血清中存在IgA-EmA抗体的儿童,其β2-m浓度显著高于血清中存在IgA-EmA的儿童(3.5±1.23mg/L;P<0.001)。我们发现CD中绒毛萎缩程度与血清β2-m浓度之间存在线性相关性(r2=0.94)。检测CD儿童血清中β2-m浓度可用于监测无麸质饮食治疗情况,并区分继发性吸收不良综合征与CD。