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全血缺氧相关基因表达揭示了人类阻塞性睡眠呼吸暂停的新途径。

Whole blood hypoxia-related gene expression reveals novel pathways to obstructive sleep apnea in humans.

机构信息

Departamento de Psicobiologia, Universidade Federal de São Paulo, Brazil.

出版信息

Respir Physiol Neurobiol. 2013 Dec 1;189(3):649-54. doi: 10.1016/j.resp.2013.08.012. Epub 2013 Aug 29.

Abstract

In this study, our goal was to identify the key genes that are associated with obstructive sleep apnea (OSA). Thirty-five volunteers underwent full in-lab polysomnography and, according to the sleep apnea hypopnea index (AHI), were classified into control, mild-to-moderate OSA and severe OSA groups. Severe OSA patients were assigned to participate in a continuous positive airway pressure (CPAP) protocol for 6 months. Blood was collected and the expression of 84 genes analyzed using the RT(2) Profiler™ PCR array. Mild-to-moderate OSA patients demonstrated down-regulation of 2 genes associated with induction of apoptosis, while a total of 13 genes were identified in severe OSA patients. After controlling for body mass index, PRPF40A and PLOD3 gene expressions were strongly and independently associated with AHI scores. This research protocol highlights a number of molecular targets that might help the development of novel therapeutic strategies.

摘要

在这项研究中,我们的目标是确定与阻塞性睡眠呼吸暂停(OSA)相关的关键基因。35 名志愿者接受了全面的实验室多导睡眠图检查,并根据睡眠呼吸暂停低通气指数(AHI)将其分为对照组、轻度至中度 OSA 组和重度 OSA 组。重度 OSA 患者被安排参加为期 6 个月的持续气道正压通气(CPAP)方案。采集血液并使用 RT(2) Profiler™ PCR 阵列分析 84 个基因的表达。轻度至中度 OSA 患者表现出与细胞凋亡诱导相关的 2 个基因下调,而在重度 OSA 患者中总共鉴定出 13 个基因。在控制体重指数后,PRPF40A 和 PLOD3 基因的表达与 AHI 评分呈强烈和独立相关。该研究方案强调了一些可能有助于开发新的治疗策略的分子靶点。

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