Evidence map›Paper›PMID 35419000›Full record

SynthesisFrontiers in immunology2022

Quantitative Comparison of the Clinical Efficacy of 6 Classes Drugs for IgA Nephropathy: A Model-Based Meta-Analysis of Drugs for Clinical Treatments.

Jiesen Yu, Jieren Luo, Haoxiang Zhu, Zichao Sui, Hongxia Liu, Lujin Li, Qingshan Zheng

Open access · goldAbstract readMeta-Analysis
In one paragraph

Synthesis in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 2 pooled it
0.3field-weighted citation impact, top 46% 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.

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

2 citing papers in PubMed, 2 syntheses or guidelines pooled it, 2 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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

7 authors at 1 institution in 1 country.

Jiesen YuCenter for Drug Clinical Research, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Jieren LuoCenter for Drug Clinical Research, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Haoxiang ZhuCenter for Drug Clinical Research, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Zichao SuiCenter for Drug Clinical Research, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Hongxia LiuCenter for Drug Clinical Research, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Lujin LiCenter for Drug Clinical Research, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Qingshan ZhengCenter for Drug Clinical Research, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Shanghai University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: There is a wide variety of drugs for the clinical treatment of immunoglobulin A (IgA) nephropathy; however, previous studies have failed to clarify the quantitative differences in the efficacy of various drugs. In this study, we aimed to quantitatively compare the clinical efficacy of 6 classes of drugs with different pharmacological mechanisms for the treatment of IgA nephropathy and to identify relevant influencing factors. Methods: Clinical trials of drugs for the treatment of IgA nephropathy were obtained from public databases. The change in daily urinary protein excretion from baseline was used as the efficacy index, and the time-effect model was established using a model-based meta-analysis method. Based on the final model, the typical efficacy was simulated, and the differences in efficacy were compared. Results: A total of 40 studies with 2288 subjects were included in this study. The results showed that the time-effect relationship of the placebo and 6 classes of drugs was consistent with the E Conclusion: This study provides the first comprehensive quantitative analysis of the differences in the efficacy of 6 classes of drugs with different pharmacological mechanisms for treating IgA nephropathy. The results of this study provide an important reference for the rational clinical use of drugs for IgA nephropathy, and also provide a reliable efficacy standard for the development of new drugs for IgA nephropathy.

Indexed as

Glomerulonephritis, IGAFemaleHumansImmunosuppressive AgentsMaleProteinuriaRenin-Angiotensin SystemTreatment OutcomeImmunosuppressive AgentscorticosteroidsIgA nephropathyimmunosuppressantsmodel-based meta-analysisN-3 fatty acidsurinary protein

Identifiers

PMID35419000
PMCPMC9000973
OpenAlexW4221068258

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.