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采用无麸质饮食的儿童乳糜泻血清学指标的正常化时间

Normalization Time of Celiac Serology in Children on a Gluten-free Diet.

作者信息

Gidrewicz Dominica, Trevenen Cynthia L, Lyon Martha, Butzner J Decker

机构信息

*Department of Pediatrics†Department of Pathology and Laboratory Medicine, University of Calgary, Calgary‡Department of Pathology and Laboratory Medicine, Saskatoon Health Region, Saskatoon, Canada.

出版信息

J Pediatr Gastroenterol Nutr. 2017 Mar;64(3):362-367. doi: 10.1097/MPG.0000000000001270.

Abstract

OBJECTIVES

Response to a gluten-free diet (GFD) in children with celiac disease is determined by symptom resolution and normalization of serology. We evaluated the rate of normalization of the transglutaminase (TTG) and antiendomysial (EMA) for children on a GFD after diagnosis.

METHODS

Celiac serologies were obtained over 3.5 years after starting a GFD in 228 newly diagnosed children with biopsy-proven celiac disease. Patients were classified into categories based on serology (group A, TTG ≥10 × upper limit of normal [ULN] and EMA ≥ 1:80; group B, TTG ≥10 × ULN and EMA ≤ 1:40; and group C, TTG <10 × ULN) and by severity of histologic injury at diagnosis.

RESULTS

In children with the highest serology at diagnosis (group A), 79.7% had an abnormal TTG at 12 months after diagnosis (mean TTG 12 months, 68.8 ± 7.3, normal <20 kU/L). At 2 years, an abnormal TTG persisted in 41.7%. In contrast, only 35% of children with the lowest serology at diagnosis (group C) displayed an abnormal TTG at 12 months (mean TTG 14.3 ± 1.9 kU/L). In those with the most severe mucosal injury, Marsh 3C, 74.2% and 33.2% had an abnormal TTG at 1 and 2 years.

CONCLUSIONS

Normalization of celiac serology took >1 year in approximately 75% of GFD-compliant children with the highest celiac serology or most severe mucosal injury at diagnosis. Clinicians must consider serology and histology at diagnosis to properly evaluate response to GFD.

摘要

目的

乳糜泻患儿对无麸质饮食(GFD)的反应通过症状缓解和血清学指标正常化来确定。我们评估了确诊后接受GFD治疗的儿童中转谷氨酰胺酶(TTG)和抗肌内膜抗体(EMA)的正常化率。

方法

对228名经活检证实为乳糜泻的新诊断儿童在开始GFD治疗后的3.5年内进行了乳糜泻血清学检测。根据血清学结果(A组,TTG≥10×正常上限[ULN]且EMA≥1:80;B组,TTG≥10×ULN且EMA≤1:40;C组,TTG<10×ULN)以及诊断时组织学损伤的严重程度对患者进行分类。

结果

诊断时血清学指标最高的儿童(A组)中,79.7%在诊断后12个月时TTG异常(诊断后12个月时TTG平均值为68.8±7.3,正常<20 kU/L)。到2年时,41.7%的儿童TTG仍异常。相比之下,诊断时血清学指标最低的儿童(C组)中,只有35%在12个月时TTG异常(TTG平均值为14.3±1.9 kU/L)。在黏膜损伤最严重的Marsh 3C型患儿中,74.2%和33.2%在1年和2年时TTG异常。

结论

在诊断时血清学指标最高或黏膜损伤最严重且遵循GFD的儿童中,约75%的患儿乳糜泻血清学指标正常化需要1年以上时间。临床医生在诊断时必须考虑血清学和组织学情况,以正确评估对GFD的反应。

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