Lattuada Martina, Rebora Paola, Fossati Chiara, Lazzerotti Alessandra, Paolini Lucia, Cattoni Alessandro, Panceri Roberto, Valsecchi Maria Grazia, Biondi Andrea, Zuin Giovanna
School of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.
Biostatistics and Clinical Epidemiology, Fondazione IRCCS San Gerardo dei Tintori, Monza, Italy.
Front Pediatr. 2025 Jul 17;13:1595256. doi: 10.3389/fped.2025.1595256. eCollection 2025.
Coeliac disease (CD) manifests more frequently in individuals with Down syndrome (DS) and its prevalence varies across different studies. This study aims to assess the prevalence of CD in children with DS and to describe their clinical, serological, and histological features. A secondary aim was to analyze the time needed for the normalization of anti-transglutaminase IgA (TGA-IgA) and anti-endomysium IgA (EMA-IgA) levels in DS compared to non-syndromic (NS) children.
This retrospective monocentric cohort study included patients with DS under 18 years of age, diagnosed with CD between 2005 and 2022. Each DS patient was matched for year of birth and sex with two NS celiac children. Follow-up was 6-, 12- and 24-months post-diagnosis.
The prevalence of CD in 770 children with DS was 7.5% (95% CI: 5.8%-9.6%). 57 children with CD and DS were compared with 114 CD NS matched controls (total sample size = 171). DS demonstrated less symptoms than 114 NS CD children (26% vs. 79%, < 0.001). In the CD DS group 81% had anti-TGA levels 10 times higher the upper limit of normal, compared to 72% in the control group. Among patients with CD and DS, 93% had histological damage equal to 3rd grade of Marsh-Oberhuber classification at diagnosis. The velocity of normalization of anti-TGA was higher in patients without DS ( = 0.005).
This study reinforces the higher prevalence of CD in DS, emphasizing the necessity for routine screening, even in asymptomatic individuals. Despite less symptomatic presentation, patients with DS exhibited elevated antibody levels and severe histological damage. Clinicians should expect a prolonged time for antibody normalization following gluten-free diet in DS, mirroring potential challenges in diet adherence and altered immune responses.
乳糜泻(CD)在唐氏综合征(DS)患者中更为常见,其患病率在不同研究中有所差异。本研究旨在评估DS患儿中CD的患病率,并描述其临床、血清学和组织学特征。次要目的是分析与非综合征(NS)儿童相比,DS患儿抗转谷氨酰胺酶IgA(TGA-IgA)和抗肌内膜IgA(EMA-IgA)水平恢复正常所需的时间。
这项回顾性单中心队列研究纳入了2005年至2022年间诊断为CD的18岁以下DS患者。每位DS患者按出生年份和性别与两名NS乳糜泻儿童进行匹配。随访时间为诊断后6个月、12个月和24个月。
770名DS儿童中CD的患病率为7.5%(95%CI:5.8%-9.6%)。将57名患有CD的DS儿童与114名匹配的NS CD对照儿童进行比较(总样本量=171)。DS患儿的症状少于114名NS CD儿童(26%对79%,<0.001)。在CD DS组中,81%的患儿抗TGA水平高于正常上限10倍,而对照组为72%。在患有CD的DS患者中,93%在诊断时的组织学损伤相当于Marsh-Oberhuber分类的3级。无DS患者的抗TGA恢复正常的速度更快(=0.005)。
本研究强化了DS中CD患病率较高的观点,强调了即使在无症状个体中进行常规筛查的必要性。尽管症状表现较少,但DS患者的抗体水平升高且组织学损伤严重。临床医生应预期DS患者在无麸质饮食后抗体恢复正常的时间会延长,这反映了饮食依从性和免疫反应改变方面的潜在挑战。