Evidence map›Paper›PMID 29462546›Full record

ReviewThe Korean journal of internal medicine2018

Role of the renin-angiotensin system in hepatic fibrosis and portal hypertension.

Kwang Yong Shim, Young Woo Eom, Moon Young Kim, Seong Hee Kang, Soon Koo Baik

Registry-linked trialOpen access · goldAbstract readReview
In one paragraph

Review in The Korean journal of internal medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04901169 (Angiotensin II in Liver Transplantation), which is not on this map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
6.1field-weighted citation impact, top 2% of its field
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.

NCT04901169 phase2 / phase3active not recruitingnot on this mapstarted 2022, after this paper: background citation

Angiotensin II in Liver Transplantation (AngLT-1): A Pilot Randomized Controlled Trial

TypeinterventionalSponsorUniversity of California, San FranciscoRan2022 to 2027Enrolled50ConditionsLiver Transplant, Complications, VasoplegiaArmsAngiotensin II, Saline
3 · Its place in the literature

Who cites it

39 citing papers in PubMed, 86 citations in OpenAlex.

  1. Unifying and unique roles of non-coding RNA biomarkers in liver and heart fibrosis.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2026
    Review
  2. Article
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  4. Review
  5. Article
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  11. Vitamin D improves hepatic alterations inSaudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2023
    Article
  12. Article
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  14. Review
  15. Review
  16. Article
  17. In focus in HCB.Histochemistry and cell biology · 2022
    Article
  18. Review
  19. Review
  20. Review
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

5 authors at 1 institution in 1 country.

Kwang Yong ShimDepartment of Internal Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea.
Young Woo EomCell Therapy and Tissue Engineering Center, Yonsei University Wonju College of Medicine, Wonju, Korea.
Moon Young KimDepartment of Internal Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea.
Seong Hee KangDepartment of Internal Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea.
Soon Koo BaikDepartment of Internal Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea.
Yonsei University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The renin-angiotensin system (RAS) is an important regulator of cirrhosis and portal hypertension. As hepatic fibrosis progresses, levels of the RAS components angiotensin (Ang) II, Ang-(1-7), angiotensin-converting enzyme (ACE), and Ang II type 1 receptor (AT1R) are increased. The primary effector Ang II regulates vasoconstriction, sodium homoeostasis, fibrosis, cell proliferation, and inflammation in various diseases, including liver cirrhosis, through the ACE/Ang II/AT1R axis in the classical RAS. The ACE2/Ang-(1-7)/Mas receptor and ACE2/Ang-(1-9)/AT2R axes make up the alternative RAS and promote vasodilation, antigrowth, proapoptotic, and anti-inflammatory effects; thus, countering the effects of the classical RAS axis to reduce hepatic fibrogenesis and portal hypertension. Patients with portal hypertension have been treated with RAS antagonists such as ACE inhibitors, Ang receptor blockers, and aldosterone antagonists, with very promising hemodynamic results. In this review, we examine the RAS, its roles in hepatic fibrosis and portal hypertension, and current therapeutic approaches based on the use of RAS antagonists in patients with portal hypertension.

Indexed as

Hypertension, PortalLiver CirrhosisRenin-Angiotensin SystemAngiotensin-Converting Enzyme InhibitorsAngiotensin IIHumansPeptide FragmentsAngiotensin-Converting Enzyme InhibitorsAngiotensin IIPeptide FragmentsAngiotensinsHepatic fibrosisHypertension, portalReceptors, angiotensinRenin-angiotensin system

Identifiers

PMID29462546
PMCPMC5943664
OpenAlexW2788671266

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

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.