Department of Neonatology, Weifang People's Hospital, Weifang, Shandong, China (mainland).
Department of Gastroenterology, Weifang People's Hospital, Weifang, Shandong, China (mainland).
Med Sci Monit. 2021 May 31;27:e930015. doi: 10.12659/MSM.930015.
BACKGROUND High-mobility group box 1 (HMGB1) plays a crucial role in a variety of diseases, including neonatal necrotizing enterocolitis (NEC). The purpose of this study was to investigate the association of HMGB1 gene single-nucleotide polymorphisms (SNPs) with susceptibility and survival prognosis in Chinese Han neonates with NEC. MATERIAL AND METHODS The HMGB1 gene rs1360485, rs1045411, and rs2249825 site SNPs were genotyped in all participants. The mRNA expression of serum HMGB1 was examined using quantitative reverse transcription-polymerase chain reaction. The correlation of the HMGB1 rs1360485 SNP with NEC neonatal survival prognosis was evaluated by univariate analysis and logistic multivariate regression analysis. RESULTS The TC and CC genotype and C allele distribution frequencies of the rs1360485 SNP were lower in the NEC group, and the differences were statistically significant (all P<0.05). Individuals carrying the TC and CC genotype or C allele had a low risk of being affected by NEC. However, the genotype and allele distributions of rs1045411 and rs2249825 were not significantly different between the patient and control groups (P>0.05). NEC neonates with HMGB1 gene rs1360485 site mutations had lower mRNA levels of serum HMGB1 than those with rs1360485 site wild-type, and the rs1360485 genotypes TC and CC could independently predict better survival outcomes in NEC neonates. CONCLUSIONS This study demonstrated that the rs1360485 SNP of the HMGB1 gene is associated with susceptibility of NEC in neonates, and the rs1360485 genotypes TC and CC may affect HMGB1 expression and are associated with the survival prognosis of neonates with NEC.
高迁移率族蛋白 B1(HMGB1)在多种疾病中发挥着关键作用,包括新生儿坏死性小肠结肠炎(NEC)。本研究旨在探讨 HMGB1 基因单核苷酸多态性(SNP)与中国汉族新生儿 NEC 易感性和生存预后的关系。
对所有参与者进行 HMGB1 基因 rs1360485、rs1045411 和 rs2249825 位点 SNP 分型。采用定量逆转录-聚合酶链反应检测血清 HMGB1 的 mRNA 表达。采用单因素分析和 logistic 多因素回归分析评估 HMGB1 rs1360485 单核苷酸多态性与 NEC 新生儿生存预后的相关性。
rs1360485 单核苷酸多态性的 TC 和 CC 基因型和 C 等位基因分布频率在 NEC 组中较低,差异具有统计学意义(均 P<0.05)。携带 TC 和 CC 基因型或 C 等位基因的个体患 NEC 的风险较低。然而,rs1045411 和 rs2249825 的基因型和等位基因分布在患者和对照组之间无显著差异(P>0.05)。HMGB1 基因 rs1360485 位点突变的 NEC 新生儿血清 HMGB1 的 mRNA 水平低于 rs1360485 野生型,rs1360485 基因型 TC 和 CC 可独立预测 NEC 新生儿的生存结局更好。
本研究表明,HMGB1 基因 rs1360485 单核苷酸多态性与新生儿 NEC 的易感性相关,rs1360485 基因型 TC 和 CC 可能影响 HMGB1 表达,并与 NEC 新生儿的生存预后相关。