预测 OSA 严重程度的血液学参数

Rasha Mohamed Hendy, Basma H. Hani, Salwa H. Mohammed
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摘要

阻塞性睡眠呼吸暂停综合征(OSAS)是一种常见疾病,发病率占成年人的 6% 至 13%。其特点是部分或全部上气道反复阻塞,随后出现阵发性夜间缺氧,导致间歇性睡眠唤醒和白天过度嗜睡。这项研究旨在评估全血细胞计数中的血液学参数与差值之间的关系,差值是显示全身炎症的新生物标志物,也是 OSAS 严重程度的指标。这项回顾性横断面分析包括 100 名 OSA 患者,他们分别来自 2021 年至 2022 年和 2022 年至 2023 年期间在本哈大学医院胸科就诊的患者。所有患者均接受了全面的病史采集和临床检查、心电图、胸部 X 光后正位、整夜多导睡眠图检查和全血细胞计数(含差值)。在血小板与淋巴细胞比率方面,轻度、中度和重度 OSA 患者之间的差异具有统计学意义。在中性粒细胞与淋巴细胞比率方面,轻度和重度 OSA 患者之间的差异具有统计学意义。在统计学上,OSA 严重程度与血小板水平、N/L 和 P/L 比率呈显著正相关。包括中性粒细胞与淋巴细胞比率和血小板与淋巴细胞比率在内的血液学指标可替代昂贵耗时的生化指标,用于评估 OSAS 患者的炎症和严重程度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hematological parameters as predictors of OSA severity
Obstructive sleep apnea syndrome (OSAS) is a common disease that has a prevalence of 6 to 13% of the adult population. It is characterized by recurrent obstruction partial or total upper airway and subsequent paroxysmal nocturnal hypoxia, leading to intermittent arousals from sleep and excessive daytime sleepiness. This work aimed to evaluate the relationship between the hematological parameters in CBC with differential as a new biomarker showing systemic inflammation and as an indicator of OSAS severity. This retrospective cross-sectional analysis included 100 subjects with OSA from those attending Chest departments in Benha University Hospital from 2021 to 2022 and 2022 to 2023 period. All patients were subjected to full history taking and clinical examination, electrocardiogram, chest X-ray posteroanterior view, full night of polysomnography, and complete blood count with differential. There was a statistically significant difference between mild; moderate and severe OSA patients regarding platelets to lymphocyte ratio. A statistically significant difference between mild and severe OSA regarding neutrophil to lymphocyte ratio was found. There was a statistically significant positive correlation between OSA severity and platelet level, N/L, and P/L ratio. The hematological indices including neutrophil to lymphocyte ratio and platelet to lymphocyte ratio could be alternatives to expensive time-consuming biochemical markers to evaluate the inflammation and severity in the OSAS population.
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