miR-149基因rs2292832多态性与早产儿坏死性小肠结肠炎的关系

Hong Qiu, Xiaojun Wang, Yanhong Li, Renping Mao, Qin Lv
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引用次数: 0

摘要

背景:坏死性小肠结肠炎(NEC)是早产儿中一种普遍且具有挑战性的肠道疾病,缺乏与其发生一致的特异性病原体。有效预防和治疗NEC以降低死亡率仍然是当代的重大挑战。本研究旨在探讨中国汉族早产儿microRNA-149基因多态性与NEC的相关性。方法:采用逆转录-定量聚合酶链反应(RT-qPCR)检测血清miR-149的表达水平。采用聚合酶链反应检测miR-149基因rs2292832多态性。采用多因素logistic回归分析探讨rs2292832多态性与早产儿NEC危险因素的关系。结果:比较了102例诊断为NEC的早产儿和263例未诊断为NEC的早产儿的一般临床资料。在胎龄和出生体重方面观察到显著差异。然而,两组在产前类固醇使用、性别或喂养方式方面没有发现显著差异。NEC早产儿血清miR-149表达水平显著降低,且NEC组与对照组miR-149 rs2292832多态性等位基因频率存在差异。具体来说,rs2292832的T等位基因和TT基因型与NEC易感性增加相关。此外,胎龄和rs2292832多态性均显示与NEC风险显著相关,miR-149的rs2292832多态性被认为是早产儿NEC发展的最重要危险因素。结论:miR-149 rs2292832基因多态性可能对NEC易感性有潜在影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association of miR-149 gene rs2292832 polymorphism with necrotizing enterocolitis in preterm infants.

Background: Necrotizing enterocolitis (NEC) is a prevalent and challenging intestinal disease in premature infants, lacking a specific pathogen consistently associated with its occurrence. Effectively preventing and treating NEC to reduce mortality rates remains a significant contemporary challenge. The present study aimed to explore the correlation between microRNA-149 gene polymorphism and NEC in premature infants in a Chinese Han population.

Methods: The expression levels of serum miR-149 were determined using reverse transcription-quantitative polymerase chain reaction (RT-qPCR). Polymorphism detection of the miR-149 gene rs2292832 polymorphism was performed by polymerase chain reaction. Multivariate logistic regression analysis was employed to investigate the association between the rs2292832 polymorphism and risk factors for NEC in preterm infants.

Results: General clinical data were compared between 102 preterm infants diagnosed with NEC and 263 preterm infants without NEC. Significant differences were observed in gestational age and birth weight. However, no significant differences were found in antenatal steroid use, sex, or feeding patterns between the two groups. The expression level of serum miR-149 was significantly reduced in premature infants with NEC, and there were differences in the allele frequency of the miR-149 rs2292832 polymorphism between the NEC group and control group. Specifically, the T allele and TT genotype of rs2292832 were associated with an increased susceptibility to NEC. Furthermore, both gestational age and the rs2292832 polymorphism showed a significant association with NEC risk, with the rs2292832 polymorphism of miR-149 being identified as the most prominent risk factor for NEC development in preterm infants.

Conclusions: The rs2292832 gene polymorphism of miR-149 may potentially exert an influence on susceptibility to NEC.

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