Volume 45, Issue 4 e16241
ORIGINAL ARTICLE

Identification of Clinically Significant Portal Hypertension in cACLD Individuals With Spleen Stiffness Measurement

Xiaofeng Zhang

Xiaofeng Zhang

Hepatology Unit, Department of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China

Department of Hepatology, Zengcheng Branch, Nanfang Hospital, Southern Medical University, Guangzhou, China

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Ling Zhou

Ling Zhou

Hepatology Unit, Department of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China

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Weihao Liang

Weihao Liang

Hepatology Unit, Department of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China

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Xiao Cheng

Xiao Cheng

Hepatology Unit, Department of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China

Department of Hepatology, Zengcheng Branch, Nanfang Hospital, Southern Medical University, Guangzhou, China

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Qinjun He

Qinjun He

Hepatology Unit, Department of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China

Department of Hepatology, Zengcheng Branch, Nanfang Hospital, Southern Medical University, Guangzhou, China

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Hui Li

Hui Li

Hepatology Unit, Department of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China

Department of Hepatology, Zengcheng Branch, Nanfang Hospital, Southern Medical University, Guangzhou, China

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Wenfan Luo

Wenfan Luo

Hepatology Unit, Department of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China

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Jing Huang

Jing Huang

Hepatology Unit, Department of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China

Department of Hepatology, Zengcheng Branch, Nanfang Hospital, Southern Medical University, Guangzhou, China

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Junying Li

Junying Li

Hepatology Unit, Department of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China

Department of Hepatology, Zengcheng Branch, Nanfang Hospital, Southern Medical University, Guangzhou, China

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Weibin Wang

Weibin Wang

Hepatology Unit, Department of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China

Department of Hepatology, Zengcheng Branch, Nanfang Hospital, Southern Medical University, Guangzhou, China

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Minghan Tu

Minghan Tu

Hepatology Unit, Department of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China

Department of Hepatology, Zengcheng Branch, Nanfang Hospital, Southern Medical University, Guangzhou, China

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Haiyu Wang

Haiyu Wang

Hepatology Unit, Department of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China

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Pengcheng Ou

Pengcheng Ou

Hepatology Unit, Department of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China

Department of Infectious Diseases, Shenzhen People's Hospital, The First Affiliated Hospital of Southern University of Science and Technology, Shenzhen, China

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Biao Wen

Biao Wen

Department of Gastroenterology, The First Affiliated Hospital of Chengdu Medical College, Chengdu, China

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Lushan Xiao

Lushan Xiao

Hepatology Unit, Department of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China

Department of Hepatology, Zengcheng Branch, Nanfang Hospital, Southern Medical University, Guangzhou, China

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Damei Zhou

Damei Zhou

Hepatology Unit, Department of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China

Department of Hepatology, Zengcheng Branch, Nanfang Hospital, Southern Medical University, Guangzhou, China

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Vincent Wai-Sun Wong

Vincent Wai-Sun Wong

Department of Medicine and Therapeutics, Chinese University of Hong Kong, Hong Kong, China

State Key Laboratory of Digestive Disease, Chinese University of Hong Kong, Hong Kong, China

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Jinjun Chen

Corresponding Author

Jinjun Chen

Hepatology Unit, Department of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China

Department of Hepatology, Zengcheng Branch, Nanfang Hospital, Southern Medical University, Guangzhou, China

State Key Laboratory of Organ Failure Research, Ministry of Education, China

Key Laboratory of Infectious Diseases Research in South China, Ministry of Education, China

Guangdong Provincial Key Laboratory for Prevention and Control of Major Liver Diseases, China

Correspondence:

Jinjun Chen ([email protected])

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First published: 19 March 2025

Handling Editor: Luca Valenti

Funding: This study was supported by the National Science and Technology Major Project (2022YFC2304800 and 2018ZX10723203); National Natural Science Foundation of China (82070650, 82370614, 82300698, and 82000544). Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program (2017BT01S131). Clinical Research Program of Nanfang Hospital. Southern Medical University (2020CR026); and Clinical Research Startup Program of Southern Medical University by High-level University Construction Funding of Guangdong Provincial Department of Education (LC2019ZD006).

Xiaofeng Zhang, Ling Zhou, Weihao Liang, and Xiao Cheng contributed equally to this study.

ABSTRACT

Background and Aims

The Baveno VII consensus recommends spleen stiffness measurement (SSM) for the detection of clinically significant portal hypertension (CSPH) in patients with compensated advanced chronic liver disease (cACLD). We aimed to evaluate the performance of SSM-based algorithms.

Methods

Consecutive cACLD individuals who underwent hepatic venous pressure gradient measurement, liver stiffness measurement (LSM), and SSM measured with the dedicated 100-Hz probe by vibration-controlled transient elastography were prospectively enrolled.

Results

From July 2021 to August 2024, a total of 395 patients were screened, and 185 cACLD cases were enrolled, of which 101 patients had CSPH. An SSM > 50 kPa demonstrated a positive predictive value (PPV) of 98.0% and a specificity of 98.8% for ruling in CSPH, correctly identifying 47.5% (48/101) of CSPH cases. Sensitivity analysis revealed that in 60 patients with aetiology removal or suppression, SSM > 50 kPa achieved both a PPV and specificity of 100%. Among the 125 patients with ongoing aetiologies, the PPV and specificity were 96.4% and 98.3%, respectively. Across HBV (with or without viral suppression) and non-HBV subgroups, the PPV and specificity consistently exceeded 90%. In decision curve analysis, SSM > 50 kPa provided the highest net benefit compared with other elastography-based algorithms when threshold probabilities exceeded 0.8.

Conclusions

We prospectively validated that SSM > 50 kPa, measured using the spleen-dedicated probe, is sufficient for identifying CSPH in individuals with cACLD.

Trial Registration

NCT04820166

Conflicts of Interest

The authors declare no conflicts of interest.

Data Availability Statement

The cleared data are available upon reasonable requirements and with approval from Prof. Jinjun Chen.

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