Evidence map›Paper›PMID 36839892›Full record

ReviewPharmaceutics2023

The Mitochondrion: A Promising Target for Kidney Disease.

Cem Tanriover, Sidar Copur, Duygu Ucku, Ahmet B Cakir, Nuri B Hasbal, Maria Jose Soler, Mehmet Kanbay

Open access · goldAbstract readReview
In one paragraph

Review in Pharmaceutics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.6field-weighted citation impact, top 4% 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

19 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Contemporary Perspectives on Chronic Renal Disorders.Chronic diseases and translational medicine · 2025
    Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. Review
  17. Review
  18. Article
  19. 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

7 authors at 2 institutions in 2 countries.

Cem TanrioverDepartment of Medicine, Koc University School of Medicine, 34010 Istanbul, Turkey.
Sidar CopurDepartment of Medicine, Koc University School of Medicine, 34010 Istanbul, Turkey.
Duygu UckuDepartment of Medicine, Koc University School of Medicine, 34010 Istanbul, Turkey.ORCID 0000-0002-4686-8054
Ahmet B CakirDepartment of Medicine, Koc University School of Medicine, 34010 Istanbul, Turkey.ORCID 0000-0003-4699-6475
Nuri B HasbalDepartment of Medicine, Division of Nephrology, Koc University School of Medicine, 34010 Istanbul, Turkey.ORCID 0000-0002-2229-5140
Maria Jose SolerNephrology and Kidney Transplant Research Group, Vall d'Hebron Research Institute (VHIR), 08035 Barcelona, Spain.ORCID 0000-0003-3621-0766
Mehmet KanbayDepartment of Medicine, Division of Nephrology, Koc University School of Medicine, 34010 Istanbul, Turkey.ORCID 0000-0002-1297-0675
Koç University · TRVall d'Hebron Institut de Recerca · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mitochondrial dysfunction is important in the pathogenesis of various kidney diseases and the mitochondria potentially serve as therapeutic targets necessitating further investigation. Alterations in mitochondrial biogenesis, imbalance between fusion and fission processes leading to mitochondrial fragmentation, oxidative stress, release of cytochrome c and mitochondrial DNA resulting in apoptosis, mitophagy, and defects in energy metabolism are the key pathophysiological mechanisms underlying the role of mitochondrial dysfunction in kidney diseases. Currently, various strategies target the mitochondria to improve kidney function and kidney treatment. The agents used in these strategies can be classified as biogenesis activators, fission inhibitors, antioxidants, mPTP inhibitors, and agents which enhance mitophagy and cardiolipin-protective drugs. Several glucose-lowering drugs, such as glucagon-like peptide-1 receptor agonists (GLP-1-RA) and sodium glucose co-transporter-2 (SGLT-2) inhibitors are also known to have influences on these mechanisms. In this review, we delineate the role of mitochondrial dysfunction in kidney disease, the current mitochondria-targeting treatment options affecting the kidneys and the future role of mitochondria in kidney pathology.

Indexed as

acute kidney injurychronic kidney diseasemitochondrial dysfunction

Identifiers

PMID36839892
PMCPMC9960839
OpenAlexW4319599033

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.