Evidence map›Paper›PMID 25974754›Full record

ReviewClinical pharmacology and therapeutics2015

Emerging Targets for Therapeutic Development in Diabetes and Its Complications: The RAGE Signaling Pathway.

Ems Litwinoff, C Hurtado Del Pozo, R Ramasamy, A M Schmidt

Abstract readReview
In one paragraph

Review in Clinical pharmacology and therapeutics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
–field-weighted citation impact
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

56 citing papers in PubMed.

  1. Review
  2. Review
  3. Dietary Advanced Glycation End Products and Cardiovascular-Kidney-Metabolic Complications.Clinical journal of the American Society of Nephrology : CJASN · 2026
    Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Hypolipidemic and Antithrombotic Effect of 6'-Molecules (Basel, Switzerland) · 2024
    Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Skeletal Senescence with Aging and Type 2 Diabetes.Endocrinology and metabolism (Seoul, Korea) · 2023
    Article
  16. Article
  17. Review
  18. Biochemical Markers of Bone Turnover in Older Adults With Type 1 Diabetes.The Journal of clinical endocrinology and metabolism · 2022
    Article
  19. Article
  20. 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.

Ems LitwinoffDiabetes Research Program, Division of Endocrinology, Department of Medicine, New York University School of Medicine, New York, New York, USA.
C Hurtado Del PozoDiabetes Research Program, Division of Endocrinology, Department of Medicine, New York University School of Medicine, New York, New York, USA.
R RamasamyDiabetes Research Program, Division of Endocrinology, Department of Medicine, New York University School of Medicine, New York, New York, USA.
A M SchmidtDiabetes Research Program, Division of Endocrinology, Department of Medicine, New York University School of Medicine, New York, New York, USA.

Funding

VASCULAR AND MONOCYTE DYSFUNCTION IN WOUND REPAIRP01HL060901 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI YAN, SHI FANG · 1999 to 2017
$20.2M
RAGE, Macrophages & HDL BiologyR01HL118565 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI SCHMIDT, ANN MARIE · 2013 to 2017
$2.1M
NHLBI NIH HHS P01 HL060901NHLBI NIH HHS R01 HL118565
6 · The paper itself

Abstract

Types 1 and 2 diabetes are on the rise worldwide. Although the treatment of hyperglycemia has benefited from recent advances, aggressive efforts to maintain euglycemia may be fraught with risk, especially in older subjects or in subjects vulnerable to hypoglycemic unawareness. Hence, strategies to prevent and treat the complications of hyperglycemia are essential. In this review we summarize recent updates on the biology of the receptor for advanced glycation endproducts (RAGE) in the pathogenesis of both micro- and macrovascular complications of diabetes, insights from the study of mouse models of obesity and diabetic complications, and from associative studies in human subjects. The study of the mechanisms and consequences of the interaction of the RAGE cytoplasmic domain with the formin, mDia1, in RAGE signal transduction, will be discussed. Lastly, we review the "state-of-the-art" on RAGE-directed therapeutics. Tackling RAGE/mDia1 may identify a novel class of therapeutics preventing diabetes and its complications.

Indexed as

Drug DesignMolecular Targeted TherapyAdaptor Proteins, Signal TransducingAnimalsBiomarkersBlood GlucoseDiabetes ComplicationsDiabetes Mellitus, Type 1Diabetes Mellitus, Type 2ForminsHumansHypoglycemic AgentsReceptor for Advanced Glycation End ProductsReceptors, ImmunologicSignal TransductionTreatment OutcomeAdaptor Proteins, Signal TransducingBiomarkersBlood GlucoseDIAPH1 protein, humanForminsHypoglycemic AgentsReceptor for Advanced Glycation End ProductsReceptors, Immunologic

Identifiers

PMID25974754
PMCPMC4621004

What OpenQuestion holds

Textmetadata
LicenceTDM
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.