98 线粒体功能障碍与新生儿重症监护室疼痛/压力早产儿神经发育结果之间的相互关系

IF 2.1 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Tingting Zhao, Xiaolin Chang, Subrata Biswas, Jeremy Balsbaugh, Jennifer Liddle, Ming-hui Chen, Adam Matson, Xiaomei Cong
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引用次数: 0

摘要

目的/目标:生命早期的痛苦/压力会影响婴儿的神经发育结果。线粒体功能障碍可能是婴儿压力和神经发育之间的接口。本研究旨在调查早产儿的疼痛/压力、线粒体功能障碍相关蛋白质和神经行为反应之间的关联。方法/研究对象:该研究对 2017 年 9 月至 2022 年 7 月期间在康涅狄格州哈特福德和法明顿的两家附属新生儿监护病房注册的 33 名早产儿进行了前瞻性队列研究。记录了新生儿重症监护室期间的日常疼痛/压力体验。在月龄后 36-38 周(PMA),使用新生儿重症监护室网络神经行为量表(NNNS)和颊拭子进行基于质谱的蛋白质组学分析,评估神经行为结果。采用拉索统计方法研究蛋白质丰度与婴儿 NNNS 总分之间的关系。还进行了多元线性回归和基因本体(GO)富集分析,以研究临床特征和神经发育结果如何与蛋白质水平和潜在的分子通路相关联。结果/预期结果:在新生儿重症监护室住院期间,早产儿胎膜早破(PPROM)与神经行为结果呈负相关。蛋白质功能(包括瘦素受体结合活性、谷胱甘肽二硫氧化还原酶活性、对氧化应激的反应、脂质代谢、磷酸盐和质子跨膜转运体活性)与神经行为结果呈负相关。相反,细胞骨架调节、上皮屏障和保护功能则与神经发育结果呈正相关。此外,还发现线粒体功能障碍相关蛋白(SPRR2A、PAIP1、S100A3、MT-CO2、PiC、GLRX、PHB2、BNIPL-2、ABLIM1、UNC45A、Keratins、MUC1 和 CYB5B)与神经行为结果相关。讨论/意义:观察发现线粒体功能障碍相关蛋白与婴儿早期疼痛/压力和神经发育结果有关。口腔蛋白质可用于预测潜在的神经行为结果。此外,在新生儿重症监护室住院期间,应为早产儿提供个性化的皮肤完整性保护。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
98 The Crosstalk between Mitochondrial Dysfunction and Neurodevelopmental Outcomes in Preterm Infants with Pain/Stress in the NICU

OBJECTIVES/GOALS: Early life pain/stress impacts infants’ neurodevelopmental outcomes. Mitochondrial dysfunction may interface between infants’ stress and neurodevelopment. The study aims to investigate the associations between pain/stress, proteins associated with mitochondrial dysfunction, and neurobehavioral responses in preterm infants. METHODS/STUDY POPULATION: A prospective cohort study was conducted with 33 preterm infants enrolled between September 2017 and July 2022 at two affiliated NICUs in Hartford and Farmington, CT. Daily pain/stress experienced during NICU was documented. At 36-38 weeks post-menstrual age (PMA), neurobehavioral outcomes were evaluated using the NICU Network Neurobehavioral Scale (NNNS) and buccal swabs for Mass spectrometry-based proteomics analysis. Lasso statistical methods were conducted to study the association between protein abundance and infants’ NNNS summary scores. Multiple linear regression and Gene Ontology (GO) enrichment analyses were performed to examine how clinical characteristics and neurodevelopmental outcomes may be associated with protein levels and underlying molecular pathways. RESULTS/ANTICIPATED RESULTS: During NICU hospitalization, preterm premature rupture of membrane (PPROM) was negatively associated with neurobehavioral outcomes. The protein functions, including leptin receptor binding activity, glutathione disulfide oxidoreductase activity, and response to oxidative stress, lipid metabolism, phosphate, and proton transmembrane transporter activity, were negatively associated with neurobehavioral outcomes. In contrast, cytoskeletal regulation, epithelial barrier, and protection function were found to be positively associated with neurodevelopmental outcomes. In addition, mitochondrial dysfunction-related proteins (SPRR2A, PAIP1, S100A3, MT-CO2, PiC, GLRX, PHB2, and BNIPL-2, ABLIM1, UNC45A, Keratins, MUC1, and CYB5B) were found to be associated with neurobehavioral outcomes. DISCUSSION/SIGNIFICANCE: Mitochondrial dysfunction-related proteins were observed to be associated with early life pain/stress and neurodevelopmental outcomes in infants. Buccal proteins could be used to predict potential neurobehavioral outcomes. In addition, individualized skin integrity protection should be provided to preterm infants during their NICU stay.

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来源期刊
Journal of Clinical and Translational Science
Journal of Clinical and Translational Science MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
2.80
自引率
26.90%
发文量
437
审稿时长
18 weeks
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