Evidence map›Paper›PMID 31888179›Full record

ReviewInternational journal of molecular sciences2019

Complement and Complement Targeting Therapies in Glomerular Diseases.

Sofia Andrighetto, Jeremy Leventhal, Gianluigi Zaza, Paolo Cravedi

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

16 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Observational
  7. Article
  8. Functional variant rs12614 inFrontiers in immunology · 2022
    Article
  9. Observational
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. 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

4 authors at 2 institutions in 2 countries.

Sofia AndrighettoDepartment of Medicine, Division of Nephrology, Icahn School of Medicine at Mount Sinai, 1 Levy Place, New York, NY 10029, USA.
Jeremy LeventhalDepartment of Medicine, Division of Nephrology, Icahn School of Medicine at Mount Sinai, 1 Levy Place, New York, NY 10029, USA.
Gianluigi ZazaRenal Unit, Department of Medicine, University/Hospital of Verona, 37126 Verona, Italy.ORCID 0000-0002-6004-6196
Paolo CravediDepartment of Medicine, Division of Nephrology, Icahn School of Medicine at Mount Sinai, 1 Levy Place, New York, NY 10029, USA.ORCID 0000-0001-7837-0923
Icahn School of Medicine at Mount Sinai · USUniversity of Verona · IT

Funding

Mechanisms of complement-mediated podocyte injury in FSGSR01DK119431 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CRAVEDI, PAOLO · 2019 to 2021
$763k
NIDDK NIH HHS R01 DK119431
6 · The paper itself

Abstract

The complement cascade is part of the innate immune system whose actions protect hosts from pathogens. Recent research shows complement involvement in a wide spectrum of renal disease pathogenesis including antibody-related glomerulopathies and non-antibody-mediated kidney diseases, such as C3 glomerular disease, atypical hemolytic uremic syndrome, and focal segmental glomerulosclerosis. A pivotal role in renal pathogenesis makes targeting complement activation an attractive therapeutic strategy. Over the last decade, a growing number of anti-complement agents have been developed; some are approved for clinical use and many others are in the pipeline. Herein, we review the pathways of complement activation and regulation, illustrate its role instigating or amplifying glomerular injury, and discuss the most promising novel complement-targeting therapies.

Indexed as

Molecular Targeted TherapyAnimalsAntibodiesComplement ActivationComplement System ProteinsHumansKidney DiseasesKidney GlomerulusAntibodiesComplement System Proteinsalternative complement pathwayC3 glomerulopathycomplementcomplement-targeting therapiesfocal segmental glomerulosclerosishemolytic uremic syndrome

Identifiers

PMID31888179
PMCPMC6940904
OpenAlexW2996356524

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.