Evidence map›Paper›PMID 31175491›Full record

ReviewHeart failure reviews2019

A review of fibroblast growth factor 21 in diabetic cardiomyopathy.

Xiang Zhang, Luo Yang, Xiongfeng Xu, Fengjuan Tang, Peng Yi, Bo Qiu, Yarong Hao

Abstract readComparative StudyReview
PubMed Publisher
In one paragraph

Review in Heart failure reviews, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

26 citing papers in PubMed, 38 citations in OpenAlex.

  1. Trial
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  3. Review
  4. Article
  5. Article
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  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. Research Progress of Fibroblast Growth Factor 21 in Fibrotic Diseases.Oxidative medicine and cellular longevity · 2022
    Review
  15. Article
  16. Multi-organ FGF21-FGFR1 signaling in metabolic health and disease.Frontiers in cardiovascular medicine · 2022
    Review
  17. Review
  18. Effect of hydrogen-rich water on the lactic acid level in metformin-treated diabetic rats under hypoxia.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2021
    Article
  19. Article
  20. 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 1 country.

Xiang ZhangDepartment of Geriatrics, Renming Hospital of Wuhan University, Hubei, People's Republic of China.
Luo YangDepartment of Geriatrics, Renming Hospital of Wuhan University, Hubei, People's Republic of China.
Xiongfeng XuDepartment of Geriatrics, Renming Hospital of Wuhan University, Hubei, People's Republic of China.
Fengjuan TangDepartment of Geriatrics, Renming Hospital of Wuhan University, Hubei, People's Republic of China.
Peng YiDepartment of Geriatrics, Renming Hospital of Wuhan University, Hubei, People's Republic of China.
Bo QiuDepartment of Geriatrics, Renming Hospital of Wuhan University, Hubei, People's Republic of China.
Yarong HaoDepartment of Geriatrics, Renming Hospital of Wuhan University, Hubei, People's Republic of China. 984022801@qq.com.
Renmin Hospital of Wuhan University · CNWuhan University · CN

Funding

Natural Science Foundation of Hubei Province 2016CFB673
6 · The paper itself

Abstract

FGF21 (fibroblast growth factor 21) is a regulator of metabolism and performs an important role in glucose and lipid metabolism and the maintenance of energy balance. FGF21 is principally expressed in the liver, but it can also be found in the pancreas, skeletal muscle, and adipose tissue. It is known that levels of serum FGF21 are significantly elevated in obese, insulin-resistant patients, and those with metabolic syndrome. Elevated levels of FGF21 in serum during the early stages of various metabolic diseases are considered a compensatory response by the organism. Therefore, FGF21 is considered a hormone in response to stress and an early diagnostic marker of disease. Diabetic cardiomyopathy is a special type of cardiac complication, characterized as a chronic myocardial disorder caused by diabetes. The pathological process includes increased oxidative stress, energy metabolism in myocardial cells, an inflammatory response, and myocardial cell apoptosis. A growing body of evidence suggests that FGF21 has the potential to be an effective drug for the treatment of diabetic cardiomyopathy. Here, we review recent progress on the characteristics of FGF21 in its protective role, especially in pathological processes such as suppressing apoptosis in the myocardium, reducing inflammation in cardiomyocytes, reducing oxidative stress, and promoting fatty acid oxidation. In addition, we explore the possibility that diabetic cardiomyopathy can be delayed through the application of FGF21, providing possible therapeutic targets of the disease.

Indexed as

AnimalsApoptosisCardiotonic AgentsCardiovascular DiseasesDiabetic CardiomyopathiesEnergy MetabolismFibroblast Growth FactorsGlucoseHumansInflammationInsulin ResistanceLipid MetabolismMetabolic SyndromeMiceModels, AnimalMyocardiumCardiotonic Agentsfibroblast growth factor 21Fibroblast Growth FactorsGlucoseApoptosisCollagen depositionDiabetic cardiomyopathyFGF21 (fibroblast growth factor 21)Inflammatory responseMyocardial cell energy metabolismOxidative stress

Identifiers

PMID31175491
OpenAlexW2953822192

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.