Evidence map›Paper›PMID 35408886›Full record

ReviewInternational journal of molecular sciences2022

New Insights into the Treatment of Glomerular Diseases: When Mechanisms Become Vivid.

Da-Wei Lin, Cheng-Chih Chang, Yung-Chien Hsu, Chun-Liang Lin

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 8% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Cyclophosphamide ameliorates membranous nephropathy by upregulating miR-223 expression, promoting M2 macrophage polarization and inhibiting inflammation.Technology and health care : official journal of the European Society for Engineering and Medicine · 2024
    Article
  12. Review
  13. Review
  14. 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

4 authors at 3 institutions in 1 country.

Da-Wei LinDepartment of Internal Medicine, St. Martin De Porres Hospital, Chiayi 60069, Taiwan.ORCID 0000-0003-1209-6743
Cheng-Chih ChangDepartment of Surgery, Chang Gung Memorial Hospital, Chiayi 613016, Taiwan.
Yung-Chien HsuDepartment of Nephrology, Chang Gung Memorial Hospital, Chiayi 613016, Taiwan.
Chun-Liang LinDepartment of Nephrology, Chang Gung Memorial Hospital, Chiayi 613016, Taiwan.ORCID 0000-0002-5710-8405
Chiayi Chang Gung Memorial Hospital · TWChang Gung Memorial Hospital · TWSt. Martin de Porres Hospital · TW

Funding

Chang Gung Memorial Hospital at Chiayi, Taiwan CMRPG6F0381-3
6 · The paper itself

Abstract

Treatment for glomerular diseases has been extrapolated from the experience of other autoimmune disorders while the underlying pathogenic mechanisms were still not well understood. As the classification of glomerular diseases was based on patterns of juries instead of mechanisms, treatments were typically the art of try and error. With the advancement of molecular biology, the role of the immune agent in glomerular diseases is becoming more evident. The four-hit theory based on the discovery of gd-IgA1 gives a more transparent outline of the pathogenesis of IgA nephropathy (IgAN), and dysregulation of Treg plays a crucial role in the pathogenesis of minimal change disease (MCD). An epoch-making breakthrough is the discovery of PLA2R antibodies in the primary membranous nephropathy (pMN). This is the first biomarker applied for precision medicine in kidney disease. Understanding the immune system's role in glomerular diseases allows the use of various immunosuppressants or other novel treatments, such as complement inhibitors, to treat glomerular diseases more reasonable. In this era of advocating personalized medicine, it is inevitable to develop precision medicine with mechanism-based novel biomarkers and novel therapies in kidney disease.

Indexed as

Glomerulonephritis, IGAGlomerulonephritis, MembranousBiomarkersHumansImmunoglobulin ABiomarkersImmunoglobulin AIgA nephropathyimmunosuppressantmembranous nephropathyminimal change diseaseprecision medicine

Identifiers

PMID35408886
PMCPMC8998908
OpenAlexW4221082524

What Socratic 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 Socratic graph.