Unitat de Recerca en Pediatria, Hospital Universitari Sant Joan de Reus, Nutrició i Desenvolupament Humà, IISPV, Universitat Rovira i Virgili, 43204 Reus, Spain.
Complejo Asistencial de Zamora, 49022 Zamora, Spain.
Nutrients. 2023 Mar 3;15(5):1267. doi: 10.3390/nu15051267.
The worldwide prevalence of asymptomatic coeliac disease (CD) is increasing, which is in part due to the routine screening of children with risk factors. Both symptomatic and asymptomatic patients with CD are at risk of long-term complications. The objective of this study was to compare the clinical characteristics of asymptomatic and symptomatic children at the time of CD diagnosis. A case-control study was conducted using data from a cohort of 4838 CD patients recruited from 73 centers across Spain between 2011 and 2017. A total of 468 asymptomatic patients (cases) were selected and matched by age and sex with 468 symptomatic patients (controls). Clinical data, including any reported symptoms, as well as serologic, genetic, and histopathologic data were collected. No significant differences were found between the two groups in most clinical variables, nor in the degree of intestinal lesion. However, the asymptomatic patients were taller (height z-score -0.12 (1.06) vs. -0.45 (1.19), < 0.001) and were less likely to have anti transglutaminase IgA antibodies ≥ 10 times the upper normal limit (66.2% vs. 758.4%, = 0.002). Among the 37.1% of asymptomatic patients who were not screened for CD due to the absence of risk factors, only 34% were truly asymptomatic, while the remaining 66% reported non-specific CD-related symptoms. Therefore, expanding CD screening to any child who undergoes a blood test could reduce the burden of care for some children, as many of those considered asymptomatic reported non-specific CD-related symptoms.
全球无症状乳糜泻 (CD) 的患病率正在上升,这在一定程度上是由于对有风险因素的儿童进行常规筛查。有症状和无症状的 CD 患者都有发生长期并发症的风险。本研究的目的是比较无症状和有症状 CD 患者在诊断时的临床特征。使用 2011 年至 2017 年在西班牙 73 个中心招募的 4838 例 CD 患者队列的数据进行了病例对照研究。共选择了 468 例无症状患者(病例),并按年龄和性别与 468 例有症状患者(对照)进行匹配。收集了临床数据,包括任何报告的症状,以及血清学、遗传学和组织病理学数据。在大多数临床变量和肠损伤程度方面,两组之间没有发现显著差异。然而,无症状患者更高(身高 z 分数 -0.12(1.06)vs. -0.45(1.19),<0.001),并且不太可能存在抗转谷氨酰胺酶 IgA 抗体≥10 倍正常上限(66.2%vs.758.4%,=0.002)。在因无风险因素而未进行 CD 筛查的 37.1%无症状患者中,只有 34%是真正无症状的,而其余 66%报告了非特异性 CD 相关症状。因此,将 CD 筛查扩展到任何接受血液检查的儿童,可能会减轻一些儿童的护理负担,因为许多被认为无症状的儿童报告了非特异性 CD 相关症状。