Evidence map›Paper›PMID 31996409›Full record

ArticleJournal of the American Society of Nephrology : JASN2020

Prolyl Hydroxylase Domain Inhibitor Protects against Metabolic Disorders and Associated Kidney Disease in Obese Type 2 Diabetic Mice.

Mai Sugahara, Shinji Tanaka, Tetsuhiro Tanaka, Hisako Saito, Yu Ishimoto, Takeshi Wakashima, Masatoshi Ueda, Kenji Fukui, Akira Shimizu, Reiko Inagi and 3 more

Open access · greenAbstract read
In one paragraph

Article in Journal of the American Society of Nephrology : JASN, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
6.1field-weighted citation impact, top 2% 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

60 citing papers in PubMed, 105 citations in OpenAlex.

  1. How do SGLT2 inhibitors protect the kidney? A mediation analysis of the EMPA-REG OUTCOME trial.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2024
    Trial
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Intermuscular Adipose Tissue in CKD: A Window into Muscle Quality and Health?Clinical journal of the American Society of Nephrology : CJASN · 2025
    Review
  12. Observational
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. Animal models for induction of diabetes and its complications.Journal of diabetes and metabolic disorders · 2023
    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

13 authors at 3 institutions in 1 country.

Mai SugaharaDivision of Nephrology and Endocrinology.
Shinji TanakaDivision of Nephrology and Endocrinology.ORCID 0000-0003-2683-9456
Tetsuhiro TanakaDivision of Nephrology and Endocrinology, tetsu-tky@umin.ac.jp.
Hisako SaitoDivision of Nephrology and Endocrinology.
Yu IshimotoDivision of Nephrology and Endocrinology.
Takeshi WakashimaBiological and Pharmacological Laboratories, Central Pharmaceutical Research Institute, Japan Tobacco Inc., Osaka, Japan; and.
Masatoshi UedaBiological and Pharmacological Laboratories, Central Pharmaceutical Research Institute, Japan Tobacco Inc., Osaka, Japan; and.
Kenji FukuiBiological and Pharmacological Laboratories, Central Pharmaceutical Research Institute, Japan Tobacco Inc., Osaka, Japan; and.
Akira ShimizuDepartment of Analytic Human Pathology, Nippon Medical School, Tokyo, Japan.
Reiko InagiDivision of Chronic Kidney Disease Pathophysiology, and.
Toshimasa YamauchiDepartment of Diabetes and Metabolic Diseases, The University of Tokyo Graduate School of Medicine, Tokyo, Japan.
Takashi KadowakiDepartment of Diabetes and Metabolic Diseases, The University of Tokyo Graduate School of Medicine, Tokyo, Japan.
Masaomi NangakuDivision of Nephrology and Endocrinology.
Japan Tobacco (Japan) · JPThe University of Tokyo · JPNippon Medical School · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProlyl hydroxylase domain (PHD) inhibitors, which stimulate erythropoietin production through the activation of hypoxia-inducible factor (HIF), are novel therapeutic agents used for treating renal anemia. Several PHD inhibitors, including enarodustat, are currently undergoing phase 2 or phase 3 clinical trials. Because HIF regulates a broad spectrum of genes, PHD inhibitors are expected to have other effects in addition to erythropoiesis, such as protection against metabolic disorders. However, whether such beneficial effects would extend to metabolic disorder-related kidney disease is largely unknown.

methodsWe administered enarodustat or vehicle without enarodustat in feed to diabetic black and tan brachyury (BTBR)

resultsCompared with BTBR

conclusionsThese results indicate that the PHD inhibitor enarodustat has potential renoprotective effects in addition to its potential to protect against metabolic disorders.

Indexed as

AnimalsChemokine CCL2Diabetes Mellitus, ExperimentalDiabetes Mellitus, Type 2Diabetic NephropathiesDisease Models, AnimalInsulin ResistanceMetabolic DiseasesMiceMice, ObeseN-substituted GlycinesProlyl-Hydroxylase InhibitorsProlyl HydroxylasesPyridinesRandom AllocationReference ValuesChemokine CCL2enarodustatN-substituted GlycinesProlyl-Hydroxylase InhibitorsProlyl HydroxylasesPyridinesTriazolesadiponectindiabetic kidney diseasemonocyte chemoattractant protein-1prolyl hydroxylase domain inhibitors

Identifiers

PMID31996409
PMCPMC7062217
OpenAlexW3003395581

What OpenQuestion holds

Textmetadata
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.