COVID-19患者肝胆病理模式及其与炎症标志物的关系

Q4 Medicine
C. Amadi, S. Lawson, Joy I. Nyeche, Inichinbia Boniface, Wala T. Kelachi, Emmanuel M. Owamagbe, Nkeiruka J. Amadi, Azubuike Ogba, Solomon Obioha, C. J. Okafor
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引用次数: 0

摘要

背景:据报道,肝胆状况的改变与COVID-19有关,但证据有限,这与COVID-19诱导的过度炎症反应有关。因此,本研究评估了COVID-19患者的肝细胞状态及其与炎症指标的关系。方法:本研究在尼日利亚南南哈科特港的rt - pcr确诊和treatment-naïve COVID-19患者中进行。使用经过验证的数据获取模板,从存档的患者病例记录、医学回顾表、护士生命体征/用药表和中心的实验室记录中回顾性检索医疗前/手术数据。所有检索到的数据使用标准协议进行分析。结果:在396例研究中,16.7% (n=66)有肝胆病变。肝胆病变患者以重症占多数(93.3%)。重症COVID-19合并肝胆病变患者多为男性,年龄较大。胆汁特异性病理是一般肝胆病理患者和特异性轻、中、重度COVID-19患者中最常见的病理模式。在重症患者中,炎症标志物(促乳素/ c反应蛋白/ d -二聚体)与胆汁淤积特异性肝胆标志物(ALP/G-GT/TBil/CBil)呈显著正相关(p0.05)。相比之下,轻、中度COVID-19患者炎症相关标志物与所有胆汁淤积/肝细胞标志物之间无显著相关性(p < 0.05)。结论:所研究的COVID-19患者中肝胆病变多为胆汁淤积型,重症患者中与炎症标志物相关。因此,应优先进行肝胆评估,特别是在COVID-19重症患者中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Patterns of Hepatobiliary Pathologies and Their Relationship with Markers of Inflammation in COVID-19 Patients
Background: Altered hepatobiliary status has been reported in association with COVID-19 which has been linked, with limited evidence, to the exaggerated COVID-19-induced hyper-inflammatory response. Hence, the current study evaluated hepatocellular status and its association with indicators of inflammation among COVID-19 patients. Methods: This study was conducted among the RT-PCR-confirmed and treatment-naïve COVID-19 patients in Port Harcourt, South-south Nigeria. Pre-medical/surgical data were retrieved retrospectively from archived patients’ case notes, medical review charts, nurses’ vital signs/medication sheets, and laboratory records at the center using validated data acquisition templates. All retrieved data were analyzed using standard protocols. Results: Among the 396 studied, 16.7% (n=66) had hepatobiliary pathologies. The majority of those with hepatobiliary pathologies had severe COVID-19 (93.3%). Patients with severe COVID-19 and concurrent hepatobiliary pathologies were mostly males and of older age. Cholestatic-specific pathology was the most common pattern observed among the general cases with hepatobiliary pathologies and among those having specific mild, moderate, and severe COVID-19. Among those with severe COVID-19, significant positive relationships were observed between markers of inflammation (Proclacitonin/C-reactive protein/D-dimer) and cholestatic-specific hepatobiliary markers (ALP/G-GT/TBil/CBil) (p<0.05), but not with the hepatocellular-specific markers (ALT/AST) (p>0.05). In contrast, no significant relationship existed between the relevant markers of inflammation and all the cholestatic/hepatocellular markers among those with mild and moderate COVID-19 (p>0.05). Conclusion: Hepatobiliary pathologies, mostly of cholestatic patterns, are frequent among the studied COVID-19 patients which were associated with inflammatory markers among those with severe disease. Therefore, hepatobiliary evaluation should be prioritized, especially among those with severe COVID-19.
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