Díaz Marta, Quesada-López Tania, Villarroya Francesc, López-Bermejo Abel, de Zegher Francis, Ibáñez Lourdes, Casano-Sancho Paula
Endocrinology Department, Institut de Recerca Sant Joan de Déu, University of Barcelona, 08950 Barcelona, Spain.
Centro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas (CIBERDEM), Instituto de Salud Carlos III, 28029 Madrid, Spain.
Int J Mol Sci. 2025 Jul 15;26(14):6770. doi: 10.3390/ijms26146770.
Small-for-gestational-age (SGA) infants who experience a marked postnatal , mainly in weight, are at risk for developing metabolic disorders; however, the underlying mechanisms are imprecise. Exosomes and their cargo (including miRNAs) mediate intercellular communication and may contribute to altered crosstalk among tissues. We assessed the miRNA profile in cord blood-derived exosomes from 10 appropriate-for-gestational-age (AGA) and 10 SGA infants by small RNA sequencing; differentially expressed miRNAs with a fold change ≥2.4 were validated by RT-qPCR in 40 AGA and 35 SGA infants and correlated with anthropometric, body composition (DXA) and endocrine-metabolic parameters at 4 and 12 mo. miR-1-3p, miR-133a-3p and miR-206 were down-regulated, whereas miR-372-3p, miR-519d-3p and miR-1299 were up-regulated in SGA infants. The target genes of these miRNAs related to insulin, RAP1, TGF beta and neurotrophin signaling. Receiver operating characteristic analysis disclosed that these miRNAs predicted with accuracy the 0-12 mo changes in body mass index and in total and abdominal fat and lean mass. In conclusion, the exosomal miRNA profile at birth differs between AGA and SGA infants and associates with measures of growth, insulin resistance and body composition through late infancy. Further follow-up of this population will disclose whether these associations persist into childhood, puberty and adolescence.
小于胎龄(SGA)婴儿出生后体重显著增加,有发生代谢紊乱的风险;然而,其潜在机制尚不清楚。外泌体及其所载物质(包括微小RNA)介导细胞间通讯,并可能导致组织间串扰改变。我们通过小RNA测序评估了10例适于胎龄(AGA)婴儿和10例SGA婴儿脐带血来源外泌体中的微小RNA谱;在40例AGA婴儿和35例SGA婴儿中,通过RT-qPCR验证了折叠变化≥2.4的差异表达微小RNA,并将其与4个月和12个月时的人体测量、身体成分(双能X线吸收法)和内分泌代谢参数相关联。在SGA婴儿中,miR-1-3p、miR-133a-3p和miR-206下调,而miR-372-3p、miR-519d-3p和miR-1299上调。这些微小RNA的靶基因与胰岛素、RAP1、转化生长因子β和神经营养因子信号传导有关。受试者工作特征分析表明,这些微小RNA能准确预测0至12个月时体重指数、全身及腹部脂肪和瘦体重的变化。总之,AGA和SGA婴儿出生时的外泌体微小RNA谱不同,并与婴儿晚期的生长、胰岛素抵抗和身体成分指标相关。对这一人群的进一步随访将揭示这些关联是否持续至儿童期、青春期和青少年期。