Evidence map›Paper›PMID 42503905›Full record

ReviewZhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology2026

[Novel targets and drugs for the treatment of portal hypertension in liver cirrhosis].

C P Zhu, W F Xie

Abstract readReviewEnglish Abstract
In one paragraph

Review in Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

C P ZhuDepartment of Gastroenterology, the Second Affiliated Hospital of Naval Medical University (Shanghai Changzheng Hospital), Shanghai 200003, China.
W F XieDepartment of Gastroenterology, the Second Affiliated Hospital of Naval Medical University (Shanghai Changzheng Hospital), Shanghai 200003, China.

Funding

National Key Research and Development Program of China 2023YFC2507500
6 · The paper itself

Abstract

Portal hypertension in liver cirrhosis is a key factor driving decompensation and mortality, and pharmacological therapy has been the cornerstone of treatment. Although traditional medications, mainly non-selective β-receptor blockers, have played an important role in preventing decompensated events such as variceal bleeding, there still exist difficulties such as low response rates and high side effects, which complicate meeting the treatment requirements. In recent years, with the deepening understanding of the disease, drug intervention is shifting from simply reducing portal blood flow direction to strategies that remodel the hepatic microenvironment and target the gut-hepatic axis. This article systematically summarizes novel intervention strategies that target hepatic microenvironment remodeling, such as hepatic sinusoidal endothelial cell dysfunction, procoagulant states, and hepatocyte phenotypic transformation. Simultaneously, it focuses on reviewing the research progress on gut microbiota regulation and targeting portal vein therapy based on the "mid-blood flow" theory.

Indexed as

Hypertension, PortalLiver CirrhosisHumans

Identifiers

PMID42503905
PMCPMC13416782

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.