Proton-pump Inhibitor Response Prediction Using Esophageal microRNAs in Children With Eosinophilic Esophagitis

被引:17
|
作者
Canas, Jose Antonio [1 ,2 ]
Tabares, Ana [3 ]
Barbero, Claudia [1 ]
Garcia-Sanchez, Daniel [1 ]
Sastre, Beatriz [1 ,2 ]
Rodrigo-Munoz, Jose Manuel [1 ,2 ]
Mahillo-Fernandez, Ignacio [4 ]
Rayo, Ana [5 ]
Borrell, Belen [5 ]
Cilleruelo, Ma Luz [6 ]
Roman, Enriqueta [6 ]
Fernandez-Fernandez, Sonia [5 ]
Gutierrez-Junquera, Carolina [6 ]
del Pozo, Victoria [1 ,2 ]
机构
[1] IIS Fdn Jimenez Diaz, Dept Immunol, Ave Reyes Catolicos 2, Madrid 28040, Spain
[2] Hosp San Rafael, CIBER Enfermedades Resp CIBERES, Madrid, Spain
[3] Hosp San Rafael, Pediat Gastroenterol Unit, Dept Pediat, Madrid, Spain
[4] IIS Fdn Jimenez Diaz, Epidemiol & Biostat Unit, Madrid, Spain
[5] Hosp Univ Severo Ochoa, Pediat Gastroenterol Unit, Madrid, Spain
[6] Hosp Univ Puerta Hierro Majadahonda, Dept Pediat, Pediat Gastroenterol Unit, Madrid, Spain
关键词
eosinophilic esophagitis; esophagus; microRNA; proton-pump inhibitor; responsiveness; DISEASE; RECOMMENDATIONS; PREVALENCE; EXPRESSION; DIAGNOSIS; RNA;
D O I
10.1097/MPG.0000000000002957
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objectives: Eosinophilic esophagitis (EoE) is a chronic esophageal disease characterized by eosinophilic inflammation. Proton-pump inhibitors (PPI) induce disease remission but no predictive factors of PPI-responsiveness have been identified yet. So, a biomarker must be found to differentiate between responders (PPI-R) and nonresponder patients (PPI-NR) to PPI. Aims were to identify any molecular biomarker that could predict PPI responsiveness and to study molecular remission after PPI therapy. Methods: This prospective study enrolled 39 controls and 43 pediatric children with EoE from 2 hospitals, and they were treated with esomeprazole for 8 to 12 weeks. After therapy, patients were classified as either PPI-R or PPI-NR. Biopsies were collected and RNA, microRNAs, and proteins were isolated from them, measuring levels by qPCR and Western blot (WB). Also, miRNAs were evaluated in serum. Results: We found several esophageal miRNAs with different expression values between PPI-R and PPI-NR children, which can be used to discriminate them (area under curve = 0.90). No useful serum miRNAs were, however, identified. Also, these miRNAs were dysregulated in responder patients before and after PPI therapy. Moreover, we corroborated in this child population, that PPI-R displayed a significant decrease in eotaxin-3, IL-5, IL-13, periostin, and major basic protein (P < 0.05) and a significant increase in filaggrin levels after PPI treatment (P < 0.01). Conclusions: Esophageal miRNA levels found are able to discriminate between both PPI-R and PPI-NR at baseline, and before and after treatment in PPI-R, so they could be used as biomarkers. Furthermore, we observed clinical and esophageal molecular restoration in PPI-R patients after PPI therapy.
引用
收藏
页码:755 / 763
页数:9
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