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Updated: Jun 11, 2025

Invasive Hemodynamic Characterization of the Portal-hypertensive Syndrome in Cirrhotic Rats
Published on: August 1, 2018
Porto-Sinusoidal Vascular Disease: A New Nomenclature Different from Idiopathic Non-Cirrhotic Portal Hypertension
Jie Liu1, Qian Zhang2, Yao Liu2
1Department of Hepatology, Tianjin Second People's Hospital, Tianjin 300192, China.
Insights
Porto-sinusoidal vascular disease (PSVD) criteria aid early diagnosis. While PSVD patients may show higher liver stiffness, idiopathic non-cirrhotic portal hypertension (INCPH) patients face worse liver-related complications and survival outcomes.
Area of Science:
- Hepatology
- Vascular Biology
- Diagnostic Criteria Development
Background:
- Porto-sinusoidal vascular disease (PSVD) is a novel concept evolving from idiopathic non-cirrhotic portal hypertension (INCPH).
- Comparing diagnostic criteria for PSVD and INCPH is crucial for understanding disease characteristics and prognosis.
Purpose of the Study:
- To compare clinical, biochemical, histological features, and prognosis between PSVD and INCPH diagnostic criteria.
- To evaluate the utility of novel PSVD criteria in patient diagnosis and management.
Main Methods:
- Retrospective analysis of 65 patients with liver biopsies.
- Review of clinical, pathological, and prognosis data based on PSVD and INCPH criteria.
Main Results:
- 31 out of 65 PSVD patients also met INCPH criteria.
- PSVD patients exhibited higher liver stiffness (LSM) than INCPH patients (p=0.039).
- INCPH patients showed a significantly higher cumulative incidence of liver-related complications (86.95%) compared to PSVD patients (35.71%, p<0.001).
Conclusions:
- Novel PSVD criteria enable earlier diagnosis.
- Elevated LSM in PSVD patients may indicate co-existing liver diseases.
- Prognosis and survival in PSVD are linked to portal hypertension severity.
Background And Aims:
Porto-sinusoidal vascular disease (PSVD) as a novel clinical conception was modified on the basis of idiopathic non-cirrhotic portal hypertension (INCPH). This study aimed to compare the clinical, biochemical histological features and prognosis between the diagnostic criteria for PSVD and that of INCPH.
Methods:
A total of 65 patients who underwent liver biopsies were analyzed retrospectively. The clinical, pathological and prognosis date were reviewed and screened according to the latest diagnostic criteria of PSVD and INCPH.
Results:
A total of 65 patients were diagnosed with PSVD, of which 31 (47.69%) also fulfilled INCPH criteria. Specific histological and specific clinical portal hypertension (PH) signs were found in 34 (52.31%) and 30 (46.15%) of the patients, respectively. PSVD patients showed higher LSM levels (11.45 (6.38, 18.08) vs. 7.90 (6.70, 13.00), p = 0.039) than the INCPH patients. INCPH patients had a higher cumulative incidence of liver-related complications than the PSVD patients (86.95% vs. 35.71%, log-rank p < 0.001).
Conclusion:
Novel PSVD criteria facilitate early diagnosis. PSVD patients with other liver diseases may have higher LSM values. Disease progression and survival outcomes are correlated with PH in PSVD patients.
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