Department of Hepatobiliary Surgery, Affiliated Hospital of Chengde Medical University, Chengde, Hebei Province, China.
Department of Pediatrics, Affiliated Hospital of Chengde Medical University, Chengde, Hebei Province, China.
PLoS One. 2022 Dec 30;17(12):e0279591. doi: 10.1371/journal.pone.0279591. eCollection 2022.
To evaluate the clinical value of Aldo-keto reductase family 1 member B10 (AKR1B10) in the diagnosis and prognosis of hepatocellular carcinoma (HCC).
A search of the PubMed, China Biology Medicine, Cochrane, and Embase databases was performed to conduct meta-analyses to evaluate the accuracy of AKR1B10 in diagnosing HCC and to assess the impact on prognosis of patients after curative resection of HCC.
A total of 12 different cohorts from 11 studies including 2747 HCC patients and 2053 controls showed that the pooled specificity and the pooled sensitivity of AKR1B10 for the diagnosis of HCC were 0.78 (95% CI: 0.69-0.85) and 0.85 (95% CI: 0.77-0.90), respectively. The pooled sensitivity and specificity of serum AKR1B10 for the diagnosis of HCC were 0.80 (95% CI: 0.70-0.86) and 0.87 (95% CI: 0.77-0.93), respectively. The pooled sensitivity and specificity of AKR1B10 in malignant tumor tissue for the diagnosis of HCC were 0.78 (95% CI: 0.61-0.89) and 0.82 (95% CI: 0.69-0.90), respectively. The pooled sensitivity and specificity of AKR1B10 to distinguish HCC from benign liver disease were 0.71 (95% CI: 0.62-0.78) and 0.84 (95% CI: 0.77-0.89), respectively. The sensitivity and specificity of AKR1B10 combined with alpha fetoprotein (AFP) in the diagnosis of HCC were 0.84 (95% CI: 0.79-0.88) and 0.88 (95% CI: 0.73-0.95), respectively. The pooled sensitivity and specificity of AKR1B10 in malignant tumor tissue for the diagnosis of early-stage HCC were 0.85 (95% CI: 0.62-0.95) and 0.88 (95% CI: 0.81-0.93), respectively. A meta-analysis of five studies including 798 patients demonstrated that high AKR1B10 expression in liver malignant tumor was associated with better overall survival in patients with HCC after hepatectomy (HR = 0.54, 95% CI: 0.41-0.72, p < 0.001).
AKR1B10 exhibits a great clinical value in the diagnosis of HCC, especially for early-stage HCC, with excellent diagnostic accuracy. Furthermore, AKR1B10 expression can predict the prognosis of HCC patients after hepatic resection.
评估醛酮还原酶家族 1 成员 B10(AKR1B10)在肝细胞癌(HCC)诊断和预后中的临床价值。
检索PubMed、中国生物医学文献数据库、Cochrane 和 Embase 数据库,进行荟萃分析,评估 AKR1B10 诊断 HCC 的准确性,并评估其对 HCC 患者根治性切除术后预后的影响。
共纳入来自 11 项研究的 12 个不同队列,包括 2747 例 HCC 患者和 2053 例对照,结果显示 AKR1B10 对 HCC 的诊断的合并特异性和合并敏感度分别为 0.78(95%CI:0.69-0.85)和 0.85(95%CI:0.77-0.90)。血清 AKR1B10 对 HCC 的诊断的合并敏感度和特异性分别为 0.80(95%CI:0.70-0.86)和 0.87(95%CI:0.77-0.93)。AKR1B10 在恶性肿瘤组织中对 HCC 的诊断的合并敏感度和特异性分别为 0.78(95%CI:0.61-0.89)和 0.82(95%CI:0.69-0.90)。AKR1B10 对 HCC 与良性肝病的鉴别诊断的合并敏感度和特异性分别为 0.71(95%CI:0.62-0.78)和 0.84(95%CI:0.77-0.89)。AKR1B10 联合甲胎蛋白(AFP)对 HCC 的诊断的合并敏感度和特异性分别为 0.84(95%CI:0.79-0.88)和 0.88(95%CI:0.73-0.95)。AKR1B10 在恶性肿瘤组织中对早期 HCC 的诊断的合并敏感度和特异性分别为 0.85(95%CI:0.62-0.95)和 0.88(95%CI:0.81-0.93)。对 5 项研究共 798 例患者的荟萃分析显示,肝癌组织中 AKR1B10 的高表达与 HCC 患者肝切除术后的总体生存率改善相关(HR=0.54,95%CI:0.41-0.72,p<0.001)。
AKR1B10 在 HCC 的诊断中具有重要的临床价值,特别是对早期 HCC,具有良好的诊断准确性。此外,AKR1B10 的表达可以预测 HCC 患者肝切除术后的预后。