控制衰减参数与 miR-192-5p 结合对非酒精性脂肪肝急性胰腺炎患者的临床预测价值。

Yang Hu, Liang Zhu, Ronglai Cao
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引用次数: 0

摘要

简介:对照衰减参数(CAP)可检测非酒精性脂肪肝(NAFLD)。我们之前的研究发现,miR-192-5p 可筛查非酒精性脂肪肝患者的急性胰腺炎(AP)。本研究的重点是 CAP 和 miR-192-5p 在急性 AP 非酒精性脂肪肝中的作用。根据 CAP 值将 AP 患者分为 NAFLD/AP 患者和非 NAFLD/AP 患者。CAP通过肝脏瞬态弹性成像测量。血清 miR-192-5p 通过反转录定量聚合酶链反应(RT-qPCR)测定。对非酒精性脂肪肝的发病风险因素进行了逻辑回归分析。结果非酒精性脂肪肝在 AP 组比对照组更常见(35.00% 对 8.75%)。非酒精性脂肪肝 AP 患者的 CAP 值高于非酒精性脂肪肝患者,而 miR-192-5p 在非酒精性脂肪肝 AP 患者中明显较低。此外,患有非酒精性脂肪肝的 AP 患者更有可能出现呼吸衰竭、全身炎症反应综合征(SIRS)和胰腺坏死,住院时间更长,并会加剧中度至重度 AP 的发生率。miR-192-5p和TG都是AP患者发生非酒精性脂肪肝的潜在危险因素。此外,随着 AP 严重程度的增加,CAP 值逐渐升高,而 miR-192-5p 则逐渐降低。最后,CAP 联合 miR-192-5p 预测中重度 AP 的灵敏度和特异度分别为 82.61% 和 82.43%。我们的研究可为 AP 的疾病进展和治疗提供更多参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical predictive value of Control attenuation parameters in combination with miR-192-5p in patients with acute pancreatitis in nonalcoholic fatty liver disease.
INTRODUCTION Control attenuation parameters (CAP) can detect nonalcoholic fatty liver disease (NAFLD). Our previous study found that miR-192-5p could screen for acute pancreatitis (AP) in NAFLD patients. This study focused on the role of CAP and miR-192-5p in NAFLD of acute AP. MATERIAL AND METHODS AP patients and controls were enrolled. Classification of AP patients into NAFLD/AP patients and non-NAFLD/AP was made based on the CAP value. CAP was measured by liver transient elastography. Serum miR-192-5p was measured by reverse transcription-quantitative polymerase chain reaction (RT-qPCR). Logistic regression analysis was conducted to examine the risk factors for the development of NAFLD. Receiver operating characteristic (ROC) was assessed for the predictive value of AP severity. RESULTS NAFLD was more common in the AP group than in the controls (35.00% vs. 8.75%). The CAP value was higher in AP patients with NAFLD than in non-NAFLD, whereas miR-192-5p was significantly lower in AP patients with NAFLD. Additionally, AP patients with NALFD are more likely to experience respiratory failure, systemic inflammatory response syndrome (SIRS), and pancreatic necrosis with longer hospitalisation and exacerbate the incidence of moderate to severe AP. Both miR-192-5p and TG are potential risk factors for the development of NAFLD in patients with AP. Furthermore, the CAP value gradually increased with increasing AP severity, while miR-192-5p gradually decreased. Finally, the sensitivity and specificity of CAP combined with miR-192-5p for the prediction of moderate to severe AP were scored as 82.61% and 82.43%, respectively. CONCLUSIONS NAFLD exacerbated the progression of AP, and CAP combined with miR-192-5p could predict the severity of AP. Our study may provide more reference for AP disease progression and treatment.
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