Evidence map›Paper›PMID 24307101›Full record

ReviewMolecular and cellular biochemistry2014

Conundrum of pathogenesis of diabetic cardiomyopathy: role of vascular endothelial dysfunction, reactive oxygen species, and mitochondria.

Mandip Joshi, Sainath R Kotha, Smitha Malireddy, Vaithinathan Selvaraju, Abhay R Satoskar, Alexender Palesty, David W McFadden, Narasimham L Parinandi, Nilanjana Maulik

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular and cellular biochemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
4.9field-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

42 citing papers in PubMed, 71 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. [Fucoxanthin regulates Nrf2/Keap1 signaling to alleviate myocardial hypertrophy in diabetic rats].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2022
    Article
  8. Review
  9. Review
  10. Plin5, a New Target in Diabetic Cardiomyopathy.Oxidative medicine and cellular longevity · 2022
    Review
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. The Exosome: a New Player in Diabetic Cardiomyopathy.Journal of cardiovascular translational research · 2019
    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

9 authors at 4 institutions in 1 country.

Mandip JoshiDepartment of Surgery, University of Connecticut Health Center, Farmington Avenue, Farmington, CT, 06032, USA.
Sainath R Kotha
Smitha Malireddy
Vaithinathan Selvaraju
Abhay R Satoskar
Alexender Palesty
David W McFadden
Narasimham L Parinandi
Nilanjana Maulik
UConn Health · USLung Institute · USThe Ohio State University · USSt Mary's Hospital · US

Funding

Ventricular Remodeling in the Adapted HeartR01HL069910 · NHLBI · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI MAULIK, NILANJANA · 2003 to 2012
$3.4M
PRECONDITIONING IN OPEN HEART SURGERYR01HL056803 · NHLBI · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI MAULIK, NILANJANA · 2000 to 2011
$3.1M
PRECONDITIONING IN OPEN HEART SURGERYR29HL056803 · NHLBI · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI MAULIK, NILANJANA · 1998 to 1999
–
NHLBI NIH HHS HL-56803NHLBI NIH HHS HL-69910
6 · The paper itself

Abstract

Diabetic cardiomyopathy and heart failure have been recognized as the leading causes of mortality among diabetics. Diabetic cardiomyopathy has been characterized primarily by the manifestation of left ventricular dysfunction that is independent of coronary artery disease and hypertension among the patients affected by diabetes mellitus. A complex array of contributing factors including the hypertrophy of left ventricle, alterations of metabolism, microvascular pathology, insulin resistance, fibrosis, apoptotic cell death, and oxidative stress have been implicated in the pathogenesis of diabetic cardiomyopathy. Nevertheless, the exact mechanisms underlying the pathogenesis of diabetic cardiomyopathy are yet to be established. The critical involvement of multifarious factors including the vascular endothelial dysfunction, microangiopathy, reactive oxygen species (ROS), oxidative stress, mitochondrial dysfunction has been identified in the mechanism of pathogenesis of diabetic cardiomyopathy. Although it is difficult to establish how each factor contributes to disease, the involvement of ROS and mitochondrial dysfunction are emerging as front-runners in the mechanism of pathogenesis of diabetic cardiomyopathy. This review highlights the role of vascular endothelial dysfunction, ROS, oxidative stress, and mitochondriopathy in the pathogenesis of diabetic cardiomyopathy. Furthermore, the review emphasizes that the puzzle has to be solved to firmly establish the mitochondrial and/or ROS mechanism(s) by identifying their most critical molecular players involved at both spatial and temporal levels in diabetic cardiomyopathy as targets for specific and effective pharmacological/therapeutic interventions.

Indexed as

Diabetic CardiomyopathiesEndothelium, VascularHumansMitochondria, HeartReactive Oxygen SpeciesReactive Oxygen Species

Identifiers

PMID24307101
OpenAlexW2147941189

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.