中国胰腺癌患者血浆溶血磷脂酸浓度测定的临床评价

IF 0.2 Q4 GASTROENTEROLOGY & HEPATOLOGY
Gong Yongling, Wang Shaokai, C. Tao, Chen Jinfei, Wang Shukui, Cao Xiufeng, Lv Guangmei, Lim Pin
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引用次数: 0

摘要

目的:观察胰腺癌患者血浆溶血磷脂酸(LPA)浓度的变化,评价其临床诊断价值。方法:采用LPA检测试剂盒检测50例胰腺癌患者、32例胰腺良性病变患者及36例健康体检者血浆LPA浓度,并测定CA19-9、AFP、CEA等相关指标。分析结果并与病理改变的相关性。结果:胰腺癌患者LPA浓度(4.10±2.03µmol/L)显著高于良性病变患者(3.28±1.26µmol/L)和健康对照组(2.27±1.02µmol/L) (p < 0.05)。胰腺癌患者血浆LPA浓度与血清CA19-9水平相关(r = 0.9070)。LPA诊断胰腺癌的敏感性为89.6%,特异性为79。CA19-9的敏感性为91.8%,特异性为84.8%。经统计学分析,血浆LPA浓度与血清CA19-9活性无显著差异。而血浆LPA的改变与肿瘤大小、病理分型、病理分期、包膜细胞浸润、周围淋巴结及特定组织病理特征有显著相关性。结论:LPA可为临床医生提供胰腺癌诊断、转移及预后的附加指标,是一种有前景的胰腺癌生物标志物。我们的研究结果表明LPA可能是治疗胰腺癌的潜在靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical evaluation on the determination of plasma lysophosphatidic acid concentration in Chinese human pancreatic cancer
Aims: Observing the alteration of plasma Lysophosphatidic acid (LPA) concentration in patients with pancreatic cancer and evaluating its clinical potential for diagnosis. Methods: We examined the plasma LPA concentrations by using a LPA assay kit and related parameters of CA19­9, AFP and CEA were measured in 50 patients with pancreatic cancer, 32 patients with benign pancreatic lesions and 36 healthy check­ up volunteers. Findings were analyzed and correlation with pathological changes. Results: The LPA concentration was significantly higher in pancreatic cancer patients (4.10±2.03 µmol/L) than in patients with benign lesions (3.28±1.26µmol/L) and healthy controls (2.27±1.02 µmol/L) (p < 0.05). Plasma LPA concentration correlated with serum CA19­9 level (r = 0.9070) in patients with pancreatic cancer. For diagnosis of pancreatic cancer, the sensitivity of LPA was 89.6% and the specificity 79. 4%, while the sensitivity of CA19­9 was 91.8% and specificity 84.8%. Statistical analysis showed no difference between the plasma LPA concentration and serum CA19­9 activity. However, alteration of plasma LPA has shown significant correlations with the tumor size, pathological classification, pathological stage, infiltration of capsule cells, surrounding lymph nodes and specific histopathological features. Conclusion: LPA might provide clinical physicians with aditional indicator of diagnosis, metastasis and prognosis, making it a promising biomarker for pancreatic cancer. Our findings suggested that LPA would be a potential target for treatment of pancreatic cancers.
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