Gastroentérologie Pédiatrique, Hôpital des Enfants, Bordeaux, France.
J Pediatr Gastroenterol Nutr. 2011 Jun;52(6):729-33. doi: 10.1097/MPG.0b013e31820a724d.
The aim of this study was to evaluate the value of HLA-DQ2/DQ8 allelic genotyping combined with serologic testing for the diagnosis of celiac disease (CD).
One hundred seventy children, who underwent jejunal biopsy for digestive symptoms or malnutrition, were tested for HLA-DQ2/DQ8 and serologic markers (tTG and/or anti-endomysial antibodies). Children were classified in 2 groups, according to jejunal histology: group 1, when partial or total villous atrophy was associated with an increased intraepithelial lymphocytosis suggesting CD, and group 2, when these histological criteria were absent.
Eight children were excluded from the study because their intestinal histology was not informative; 82 children were classified in group 1 and 80 in group 2. Eighty-one of 82 children in group 1 were positive for HLA and serologic testing. The other child had negative HLA and serologic testing but marked villous atrophy, and further investigation showed an allergic disease. Among the 80 children in group 2, 53 were negative for both HLA and serologic testing, 22 were positive for HLA but negative for serologic testing, 2 were negative for HLA and positive for serologic testing, and 3 patients were positive for both HLA and serologic testing. The last 3 children were shown to have an autoimmune background and had probably a latent form of CD. The association of HLA-DQ2/DQ8 and serologic markers had a sensitivity of 98.8%, a specificity of 96.2%, a positive likelihood ratio of 26.3, and a negative likelihood ratio of 0.013.
The association of positive HLA-DQ2/DQ8 and serologic testing has a high predictive value for CD. We suggest that symptomatic children with high titers of immunoglobulin (Ig)A tTG could be diagnosed as patients with CD without performing jejunal biopsy. In other children, HLA-DQ2/DQ8 could be useful to exclude the diagnosis of CD if negative. In cases of low IgA tTG titers or in patients with IgA deficiency, intestinal biopsy remains mandatory.
本研究旨在评估 HLA-DQ2/DQ8 等位基因分型联合血清学检测对乳糜泻(CD)诊断的价值。
170 名因消化症状或营养不良而行空肠活检的患儿,进行 HLA-DQ2/DQ8 和血清学标志物(tTG 和/或抗肌内膜抗体)检测。根据空肠组织学,患儿分为 2 组:组 1,部分或全部绒毛萎缩伴有上皮内淋巴细胞增多,提示 CD;组 2,这些组织学标准不存在。
8 名患儿因肠组织学无信息而被排除研究;82 名患儿归入组 1,80 名患儿归入组 2。组 1 中 82 名患儿中有 81 名 HLA 和血清学检测均阳性。另 1 名患儿 HLA 和血清学检测均阴性,但绒毛萎缩明显,进一步检查发现为过敏性疾病。组 2 中 80 名患儿,53 名 HLA 和血清学检测均阴性,22 名 HLA 阳性但血清学检测阴性,2 名 HLA 阴性但血清学检测阳性,3 名患儿 HLA 和血清学检测均阳性。最后 3 名患儿有自身免疫背景,可能患有潜在的 CD。HLA-DQ2/DQ8 与血清学标志物联合检测的敏感性为 98.8%,特异性为 96.2%,阳性似然比为 26.3,阴性似然比为 0.013。
HLA-DQ2/DQ8 与血清学检测联合具有较高的 CD 预测价值。我们建议,高 IgA tTG 滴度的有症状患儿可不经空肠活检诊断为 CD 患者。在其他患儿中,如果 HLA-DQ2/DQ8 阴性,有助于排除 CD 诊断。在 IgA tTG 滴度低或 IgA 缺乏的情况下,仍需进行肠道活检。