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与儿童睡眠呼吸障碍相关的血清蛋白质组学模式。

Serum proteomic patterns associated with sleep-disordered breathing in children.

作者信息

Shah Zahoor A, Jortani Saeed A, Tauman Riva, Valdes Roland, Gozal David

机构信息

Department of Pediatrics, University of Louisville, Kentucky 40202, USA.

出版信息

Pediatr Res. 2006 Mar;59(3):466-70. doi: 10.1203/01.pdr.0000198817.35627.fc.

DOI:10.1203/01.pdr.0000198817.35627.fc
PMID:16492991
Abstract

Obstructive sleep apnea (OSA) is a major public health problem affecting approximately 2% to 3% of children. However, snoring, the cardinal symptom of OSA, affects at least 5-fold more children, such that evaluation by overnight polysomnography (ONP) is required for the diagnosis. ONP is laborious, expensive, and relatively unavailable to children. Proteomic mass spectrometry coupled with bioinformatic tools provide valuable means for discovery of new biomarkers in serum for a variety of human disorders. The possibility exists that snoring children with and without OSA may exhibit different protein expression profiles in serum that could be useful in the development of novel diagnostic tools for this condition. The proteomic patterns of 20 children with OSA and of 20 children with habitual primary snoring but no evidence of OSA (HS) were evaluated using surface-enhanced laser desorption/ionization time-of-flight mass spectrometry (SELDI-TOF MS). Linear discriminative analysis identified three differentially regulated proteins with molecular masses of 5896, 3306, 6068 Da that were capable of diagnosing OSA with 93% sensitivity and 90% specificity. Thus, the proteomic signatures of sera from children with OSA differ from those of HS who do not fulfill the current criteria for treatment. Identification and sequencing of those differentially expressed proteins discovered through proteomic strategies may lead to future development of serum-based diagnostic tests for OSA in snoring children.

摘要

阻塞性睡眠呼吸暂停(OSA)是一个重大的公共卫生问题,影响着约2%至3%的儿童。然而,打鼾作为OSA的主要症状,受影响的儿童至少是前者的5倍之多,因此诊断需要通过夜间多导睡眠图(ONP)进行评估。ONP操作繁琐、费用高昂,且儿童相对难以获得。蛋白质组质谱联用生物信息学工具为发现各种人类疾病血清中的新生物标志物提供了有价值的手段。患有和未患有OSA的打鼾儿童血清中可能表现出不同的蛋白质表达谱,这可能有助于开发针对这种情况的新型诊断工具。使用表面增强激光解吸/电离飞行时间质谱(SELDI-TOF MS)评估了20名OSA儿童和20名习惯性原发性打鼾但无OSA证据(HS)儿童的蛋白质组模式。线性判别分析确定了三种分子量分别为5896、3306、6068 Da的差异调节蛋白,它们能够以93%的灵敏度和90%的特异性诊断OSA。因此,OSA儿童血清的蛋白质组特征与未满足当前治疗标准的HS儿童不同。通过蛋白质组学策略发现的那些差异表达蛋白质的鉴定和测序可能会促使未来开发针对打鼾儿童OSA的基于血清的诊断测试。

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