Novel serum biomarker of Golgi protein 73 for the diagnosis of clinically significant portal hypertension in patients with compensated cirrhosis

Author:

Liu Shanghao12,Ma Jianzhong3,Chen Ping4,Liu Shirong5,Guo Ying6,Tan Mingjie7,Guo Xiaoqing6,Feng Yinong6,Wang Qinghui6,Li Wenhua6,Yang Chengchen8,Gao Bo9,Hua Yongli6,Liu Ning5,Song Haolin8,He Ruiling10,Wang Ruiying10,Gao Qi11,Liu Chuan12,Qi Xiaolong12ORCID

Affiliation:

1. Center of Portal Hypertension, Department of Radiology, Zhongda Hospital, School of Medicine Southeast University Nanjing China

2. Basic Medicine Research and Innovation Center of Ministry of Education, Zhongda Hospital Southeast University Nanjing China

3. Department of General Surgery The Third People's Hospital of Taiyuan Taiyuan China

4. Department of infectious diseases Shulan (Hangzhou) Hospital Affiliated to Zhejiang Shuren University Shulan International Medical College Hangzhou China

5. Department of Infectious Diseases Qufu People's Hospital Qufu China

6. Department of Hepatology The Third People's Hospital of Taiyuan Taiyuan China

7. Department of Gastrointestinal and Hepatology, Beijing You'An Hospital Capital Medical University Beijing China

8. College of Medicine Zhejiang University Hangzhou China

9. Medical Laboratory Qufu People's Hospital Qufu China

10. The First Clinical Medical College of Lanzhou University Lanzhou China

11. Beijing Key Laboratory of POCT for Bioemergency and Clinic (No. BZ0329); Beijing Hotgen Biotechnology Inc. Beijing China

Abstract

AbstractHepatic venous pressure gradient (HVPG) is the gold standard for evaluating clinically significant portal hypertension (CSPH). However, reliable noninvasive methods are limited. Our study aims to investigate the diagnostic value of serum Golgi protein 73 (GP73) for CSPH in patients with compensated cirrhosis. The study enrolled 262 consecutive patients with compensated cirrhosis from three centers in China from February 2021 to September 2023, who underwent both serum GP73 tests and HVPG measurements. CSPH was defined as HVPG ≥ 10 mmHg. Diagnostic accuracy was evaluated using the areas under the receiver operating characteristic curve (AUC). The prevalence of CSPH was 56.9% (n = 149). There were significant differences between the CSPH and non‐CSPH groups in the median serum GP73 level (126.8 vs. 73.1 ng/mL, p < 0.001). GP73 level showed a significant positive linear correlation with HVPG (r = 0.459, p < 0.001). The AUC for the diagnosis of CSPH using serum GP73 alone was 0.75 (95% confidence interval [CI] 0.68–0.81). Multivariate logistic regression analysis determined that the levels of GP73, platelets and international normalized ratio were independently associated with CSPH. The combination of these three markers was termed “IP73” score with an AUC value of 0.85 (95% CI 0.80–0.89) for CSPH. Using 0 as a cut‐off value, the specificity and sensitivity of IP73 score were 77.9% and 81.9%, respectively. The IP73 score offers a novel, simple and noninvasive method of assessing CSPH in patients with compensated cirrhosis. A cut‐off value of the IP73 score at 0 can distinguish patients with or without CSPH.

Publisher

Wiley

Subject

Infectious Diseases,Virology

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