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高尔基体蛋白73(GP73)对代谢功能障碍相关脂肪性肝病肝纤维化分期的诊断准确性:一项范围综述和队列研究

Diagnostic Accuracy of Golgi Protein 73 (GP73) for Liver Fibrosis Staging in Metabolic Dysfunction-Associated Steatotic Liver Disease: A Scoping Review and Cohort Study.

作者信息

Pecoraro Valentina, Nascimbeni Fabio, Cuccorese Michela, Gabrielli Filippo, Fasano Tommaso, Trenti Tommaso

机构信息

Complex Structure of Laboratory Medicine, Department of Laboratory Medicine and Pathological Anatomy, AUSL Modena, 41121 Modena, Italy.

Metabolic Medicine Unit, AOU Modena, 41124 Modena, Italy.

出版信息

Diagnostics (Basel). 2025 Feb 24;15(5):544. doi: 10.3390/diagnostics15050544.

DOI:10.3390/diagnostics15050544
PMID:40075792
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11898419/
Abstract

: Golgi protein 73 (GP73) is a transmembrane protein expressed by epithelial cells of the bile duct in the normal liver. High serum levels of GP73 have been detected in patients with acute or chronic liver diseases, MASLD, and its measurement has been suggested as a potential biomarker for liver fibrosis staging. We evaluated the utility of GP73 in the diagnosis of MASLD, MASH, and for liver fibrosis staging. : We performed a literature scoping review to map the current evidence about the accuracy of GP73 in patients with MASLD. We searched in Medline and EMBASE for English studies reporting an AUC value of GP73 in diagnosing MASLD and MASH and evaluating GP73 for fibrosis staging. A narrative synthesis of the evidence was conducted. Moreover, we performed an observational study including 84 patients with MASLD, of which 60 were biopsy-confirmed MASH, and different liver fibrosis stages, and 15 healthy controls. Serum GP73 levels were determined using a chemiluminescent assay and reported as mean and standard deviation (SD). Sensitivity (SE), specificity (SP), the area under the receiver operating characteristic (AUROC) curve, and the optimal cut-off value were calculated. Data were considered statistically significant when < 0.05. Available studies evaluating GP73 in MASLD reported the ability to discriminate MASH from simple steatosis and distinguish patients at different fibrotic stages, but the evidence is still scarce. Our experimental study showed that the serum levels of GP73 were 30 ± 12 ng/mL in MASLD and 32 ± 12 ng/mL in MASH patients and were statistically higher than those of the control group (19 ± 30 ng/mL), increasing from liver fibrosis stage F0 to F4. GP73 levels were significantly higher in patients with significant and advanced fibrosis than controls and no significant fibrosis ( > 0.05). ROC analysis demonstrated that serum GP73 had a good diagnostic potential for MASLD (AUROC 0.85; SE 90%; SP 73%), MASH (AUROC 0.75; SE 82%; SP64%), and significant fibrosis (AUROC 0.7; SE 56%; SP 79%) and was better than other biomarkers for chronic liver diseases. : Serum GP73 could support clinicians in the evaluation of patients with MASH and significant fibrosis.

摘要

高尔基体蛋白73(GP73)是一种由正常肝脏中胆管上皮细胞表达的跨膜蛋白。在急性或慢性肝病、代谢相关脂肪性肝病(MASLD)患者中检测到血清GP73水平升高,有人提出检测其水平可作为肝纤维化分期的潜在生物标志物。我们评估了GP73在MASLD、代谢相关脂肪性肝炎(MASH)诊断及肝纤维化分期中的应用价值。我们进行了一项文献综述,以梳理目前关于GP73在MASLD患者中诊断准确性的证据。我们在Medline和EMBASE中检索了英文研究,这些研究报告了GP73在诊断MASLD和MASH以及评估肝纤维化分期方面的曲线下面积(AUC)值。对证据进行了叙述性综合分析。此外,我们进行了一项观察性研究,纳入了84例MASLD患者,其中60例经活检确诊为MASH,且处于不同的肝纤维化阶段,还有15名健康对照者。使用化学发光法测定血清GP73水平,并报告为平均值和标准差(SD)。计算敏感性(SE)、特异性(SP)、受试者操作特征曲线下面积(AUROC)以及最佳截断值。当P<0.05时,数据被认为具有统计学意义。现有评估MASLD患者中GP73的研究报告了其能够区分MASH与单纯性脂肪变性,并区分不同纤维化阶段的患者,但证据仍然不足。我们的实验研究表明,MASLD患者血清GP73水平为30±12 ng/mL,MASH患者为32±12 ng/mL,均显著高于对照组(19±30 ng/mL),且从肝纤维化F0期到F4期逐渐升高。有显著和晚期纤维化的患者GP73水平显著高于对照组以及无显著纤维化的患者(P>0.05)。ROC分析表明,血清GP73对MASLD(AUROC 0.85;SE 90%;SP 73%)、MASH(AUROC 0.75;SE 82%;SP 64%)和显著纤维化(AUROC 0.7;SE 56%;SP 79%)具有良好的诊断潜力,并且优于其他慢性肝病生物标志物。血清GP73可为临床医生评估MASH和显著纤维化患者提供帮助。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a9a/11898419/b404bdef5e9c/diagnostics-15-00544-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a9a/11898419/f044d8eaa433/diagnostics-15-00544-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a9a/11898419/09f7280ae8c2/diagnostics-15-00544-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a9a/11898419/47f51d8cfe15/diagnostics-15-00544-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a9a/11898419/64e06fbc269e/diagnostics-15-00544-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a9a/11898419/b404bdef5e9c/diagnostics-15-00544-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a9a/11898419/f044d8eaa433/diagnostics-15-00544-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a9a/11898419/09f7280ae8c2/diagnostics-15-00544-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a9a/11898419/47f51d8cfe15/diagnostics-15-00544-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a9a/11898419/64e06fbc269e/diagnostics-15-00544-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a9a/11898419/b404bdef5e9c/diagnostics-15-00544-g005.jpg

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本文引用的文献

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Golgi protein 73: charting new territories in diagnosing significant fibrosis in MASLD: a prospective cross-sectional study.高尔基体蛋白73:绘制非酒精性脂肪性肝病严重纤维化诊断的新领域:一项前瞻性横断面研究
Front Endocrinol (Lausanne). 2025 Jan 13;15:1506953. doi: 10.3389/fendo.2024.1506953. eCollection 2024.
2
Golgi protein 73: the driver of inflammation in the immune and tumor microenvironment.高尔基体蛋白73:免疫和肿瘤微环境中炎症的驱动因素
Front Immunol. 2025 Jan 8;15:1508034. doi: 10.3389/fimmu.2024.1508034. eCollection 2024.
3
Metabolic dysfunction-associated steatotic liver disease: heterogeneous pathomechanisms and effectiveness of metabolism-based treatment.
代谢功能障碍相关脂肪性肝病:异质性发病机制及基于代谢的治疗效果
Lancet Diabetes Endocrinol. 2025 Feb;13(2):134-148. doi: 10.1016/S2213-8587(24)00318-8. Epub 2024 Dec 13.
4
Golgi protein 73 in liver fibrosis.肝纤维化中的高尔基蛋白 73。
Clin Chim Acta. 2025 Jan 15;565:119999. doi: 10.1016/j.cca.2024.119999. Epub 2024 Oct 12.
5
Estimation of the Eligible Population For Resmetirom Among Adults in the United States for Treatment of Non-Cirrhotic NASH with Moderate-to-Advanced Liver Fibrosis.在美国,为治疗非肝硬化性 NASH 伴中重度肝纤维化的成年人,估算有资格使用雷美替胺的人群。
Adv Ther. 2024 Nov;41(11):4172-4190. doi: 10.1007/s12325-024-02989-5. Epub 2024 Sep 18.
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Drugs. 2024 Jun;84(6):729-735. doi: 10.1007/s40265-024-02045-0. Epub 2024 May 21.
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