Golan-Gerstl Regina, Ben Ya'acov Ami, Musseri Mirit, Goldenberg Rosi, Chammah Yehudit, Cherki Tal, Reif Shimon, Bar Gil Shitrit Ariella
Department of Pediatrics, Hebrew University Hadassah Medical Center, Jerusalem, Israel.
Digestive Diseases Institute, Eisenberg R&D Authority, Shaare Zedek Medical Center, Jerusalem, Israel.
Inflamm Bowel Dis. 2025 Apr 10;31(4):912-922. doi: 10.1093/ibd/izae290.
Although most inflammatory bowel disease (IBD) medications are considered safe during pregnancy, their impact on microRNAs (miRNAs) in breast milk is largely unknown. MiRNAs in milk, carried by milk-derived extracellular vesicles (MDEs), are transmitted to the newborn's gut to regulate genes. Aberrant miRNA expression profiles have been found in IBD within tissue, blood, and feces, but data on mother's milk are scarce.
We collected breast milk samples from 32 mothers with Crohn's disease (CD), 14 mothers with ulcerative colitis (UC), and 44 healthy controls. We analyzed miRNA expression through qualitative real-time polymerase chain reaction and Affymetrix miRNA chips. Target genes of differentially expressed miRNAs were predicted using miRATBase. Statistical analyses were conducted using GraphPad Prism software with Mann-Whitney tests.
Milk-derived extracellular vesicles from mothers with IBD showed altered miRNA profiles compared to controls. Specifically, miR-21 and miR-320 were downregulated, while Let-7a was upregulated in IBD mothers. The expression patterns varied between CD and UC, with significantly lower MiR-21 in UC and higher Let-7a in CD. Additionally, anti-tumor necrosis factor treatment during pregnancy was associated with reduced miR-21 and miR-148a levels in MDEs. Pathway analysis revealed that these miRNAs are involved in immune regulation, particularly interleukin signaling pathways.
This study highlights that miRNAs in breast milk are differentially expressed in mothers with IBD, influenced by the disease and its treatments. These findings emphasize the impact of maternal health on milk composition and potential implications for infant immune development. Understanding these findings may guide personalized treatment strategies for mothers and promote breastfeeding among mothers with IBD.
尽管大多数炎症性肠病(IBD)药物在孕期被认为是安全的,但其对母乳中微小RNA(miRNA)的影响很大程度上未知。母乳中的miRNA由母乳来源的细胞外囊泡(MDE)携带,传递至新生儿肠道以调控基因。在IBD患者的组织、血液和粪便中已发现异常的miRNA表达谱,但母乳方面的数据稀缺。
我们收集了32名克罗恩病(CD)母亲、14名溃疡性结肠炎(UC)母亲和44名健康对照者的母乳样本。我们通过定性实时聚合酶链反应和Affymetrix miRNA芯片分析miRNA表达。使用miRATBase预测差异表达miRNA的靶基因。使用GraphPad Prism软件进行曼-惠特尼检验的统计分析。
与对照组相比,IBD母亲的母乳来源细胞外囊泡显示出miRNA谱改变。具体而言,miR-21和miR-320下调,而IBD母亲中Let-7a上调。CD和UC之间的表达模式有所不同,UC中MiR-21显著更低,CD中Let-7a更高。此外,孕期接受抗肿瘤坏死因子治疗与MDE中miR-21和miR-148a水平降低相关。通路分析显示这些miRNA参与免疫调节,尤其是白细胞介素信号通路。
本研究强调母乳中的miRNA在IBD母亲中差异表达,受疾病及其治疗影响。这些发现强调了母亲健康对乳汁成分的影响以及对婴儿免疫发育的潜在影响。了解这些发现可能指导针对母亲的个性化治疗策略,并促进IBD母亲进行母乳喂养。