Evidence map›Paper›PMID 39585482›Full record

ReviewMolecular biology reports2024

Therapeutic effect of total glucosides of paeony on IgA vasculitis nephritis: progress and prospects.

Zhifeng Wang, Jiao Yang, Pengfen He, Junfeng Lan, Ting Shi, Shuangfeng Xu, Zhihui Hao, Yujiang Xi, Jian Wang, Ping He

Abstract readReview
In one paragraph

Review in Molecular biology reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
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

10 authors.

Zhifeng Wang *The First Clinical College of Yunnan University of Chinese Medicine, Kunming, Yunnan, China.
Jiao Yang *The Second Affiliated Hospital of Yunnan University of Chinese Medicine, Kunming, Yunnan, China.
Pengfen He *The First Clinical College of Yunnan University of Chinese Medicine, Kunming, Yunnan, China.
Junfeng LanThe First Clinical College of Yunnan University of Chinese Medicine, Kunming, Yunnan, China.
Ting ShiThe First Clinical College of Yunnan University of Chinese Medicine, Kunming, Yunnan, China.
Shuangfeng XuThe First Clinical College of Yunnan University of Chinese Medicine, Kunming, Yunnan, China.
Zhihui HaoThe First Clinical College of Yunnan University of Chinese Medicine, Kunming, Yunnan, China.
Yujiang XiThe First Clinical College of Yunnan University of Chinese Medicine, Kunming, Yunnan, China. 342133033@qq.com.
Jian WangThe First Clinical College of Yunnan University of Chinese Medicine, Kunming, Yunnan, China. laohaodiao@126.com.
Ping HeYunnan Provincial Hospital of Chinese Medicine, Kunming, Yunnan, China. 3109690787@qq.com.

Funding

National Natural Science Foundation of China 82160922
6 · The paper itself

Abstract

IgA vasculitis nephritis (IgAVN), a type of immune system disease characterized by the deposition of IgA in the mesangial area of the glomerulus, is most common in children. Corticosteroids and immunosuppressants agents are commonly prescribed for the clinical management of IgAVN; however, these therapies are associated with numerous adverse reactions. This necessitates the discovery of alternative, potential therapeutic agents that can offer a safer treatment option. Natural plants contain abundant total glucosides of paeony (TGP), which represent one of the most prevalent secondary metabolites found within these organisms. TGP has been proven to be a safe and desirable natural medicine, with the most central ingredient being polyphenolic. TGP, a naturally occurring and cost-effective compound, exerts its therapeutic influence on IgAVN via diverse pathways and targets, with minimal side effects. Its substantial clinical potential underscores the importance of delving deeper into its pharmacological mechanisms, which hold great promise for novel drug development. This review examines the multifaceted therapeutic mechanisms of TGP in IgAVN encompassing modulation of Wnt/β-catenin pathways and programmed cell death pathways, antioxidant and anti-inflammatory effects, and enhancement of vascular repair. Additionally, we provide an overview of recent advancements in enhancing the bioavailability of TGP and highlight crucial considerations that may inform future research endeavors.

Indexed as

GlucosidesPaeoniaAnimalsGlomerulonephritis, IGAHumansIgA VasculitisImmunoglobulin ANephritisVasculitisGlucosidesImmunoglobulin ABioavailabilityIgA vasculitis nephritisTherapeutic mechanismsTotal glucosides of paeony

Identifiers

PMID39585482
PMCPMC11588768

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.