Evidence map›Paper›PMID 33599110›Full record

ArticleJournal of cellular and molecular medicine2021

FGF21 promotes ischaemic angiogenesis and endothelial progenitor cells function under diabetic conditions in an AMPK/NAD+-dependent manner.

Qiaoxia Dai, Xia Fan, Xue Meng, Shiyue Sun, Yue Su, Xiao Ling, Xiangjuan Chen, Kai Wang, Xiaozhen Dai, Chi Zhang and 10 more

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed, 27 citations in OpenAlex.

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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

20 authors at 5 institutions in 1 country.

Qiaoxia DaiChinese-American Research Institute for Diabetic Complications, Department of Pharmacy, Wenzhou Medical University, Wenzhou, China.
Xia FanChinese-American Research Institute for Diabetic Complications, Department of Pharmacy, Wenzhou Medical University, Wenzhou, China.
Xue MengChinese-American Research Institute for Diabetic Complications, Department of Pharmacy, Wenzhou Medical University, Wenzhou, China.
Shiyue SunChinese-American Research Institute for Diabetic Complications, Department of Pharmacy, Wenzhou Medical University, Wenzhou, China.
Yue SuThe Second School of Medicine, Wenzhou Medical University, Wenzhou, China.
Xiao LingDepartment of Pharmacy, The People's Hospital of YuHuan, Taizhou, China.
Xiangjuan ChenDepartment of Obstetrics and Gynecology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Kai WangThe First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Xiaozhen DaiSchool of Biomedicine, Chengdu Medical College, Chengdu, China.ORCID 0000-0002-2315-6871
Chi ZhangRuian Center of Chinese-American Research Institute for Diabetic Complications, the Third Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.ORCID 0000-0002-3717-7665
Sun DaInstitute of Life Sciences, Wenzhou University, Wenzhou, China.ORCID 0000-0001-7747-9951
Guigui ZhangChinese-American Research Institute for Diabetic Complications, Department of Pharmacy, Wenzhou Medical University, Wenzhou, China.
Chunjie GuChinese-American Research Institute for Diabetic Complications, Department of Pharmacy, Wenzhou Medical University, Wenzhou, China.
Hui ChenChinese-American Research Institute for Diabetic Complications, Department of Pharmacy, Wenzhou Medical University, Wenzhou, China.
Junhong HeChinese-American Research Institute for Diabetic Complications, Department of Pharmacy, Wenzhou Medical University, Wenzhou, China.
Haiqi HuDepartment of Pharmacy, Jinhua Municipal Central Hospital, Jinhua, China.
Lechu YuRuian Center of Chinese-American Research Institute for Diabetic Complications, the Third Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Xiaohong PanChinese-American Research Institute for Diabetic Complications, Department of Pharmacy, Wenzhou Medical University, Wenzhou, China.
Yi TanChinese-American Research Institute for Diabetic Complications, Department of Pharmacy, Wenzhou Medical University, Wenzhou, China.
Xiaoqing YanChinese-American Research Institute for Diabetic Complications, Department of Pharmacy, Wenzhou Medical University, Wenzhou, China.ORCID 0000-0001-9113-5274
Wenzhou Medical University · CNChengdu Medical College · CNJinhua Central Hospital · CNWenzhou University · CNYuxian People's Hospital · CN

Funding

Key Science and Technology Development Plan from Wenzhou City Y20160082Medicine Health Science and Technology Plan of Zhejiang Province 2017KY106Medicine Health Science and Technology Plan of Zhejiang Province 2018KY769National Key R&D Program of China 2017YFA0506000National Natural Science Foundation of China 51901160National Natural Science Foundation of China 81670767National Natural Science Foundation of China 81700732National Natural Science Foundation of China 81770305National Natural Science Foundation of China 81873466Natural Science Foundation of Zhejiang Province LY16H020010Natural Science Foundation of Zhejiang Province Q19E010021Opening Project of Zhejiang Provincial Top Key Discipline of Pharmaceutical Sciences YKFJ002Research Development Fund of Wenzhou Medical University QTJ15014
6 · The paper itself

Abstract

Diabetic vascular complications are closely associated with long-term vascular dysfunction and poor neovascularization. Endothelial progenitor cells (EPCs) play pivotal roles in maintaining vascular homeostasis and triggering angiogenesis, and EPC dysfunction contributes to defective angiogenesis and resultant diabetic vascular complications. Fibroblast growth factor 21 (FGF21) has received substantial attention as a potential therapeutic agent for diabetes via regulating glucose and lipid metabolism. However, the effects of FGF21 on diabetic vascular complications remain unclear. In the present study, the in vivo results showed that FGF21 efficiently improved blood perfusion and ischaemic angiogenesis in both type 1 and type 2 diabetic mice, and these effects were accompanied by enhanced EPC mobilization and infiltration into ischaemic muscle tissues and increases in plasma stromal cell-derived factor-1 concentration. The in vitro results revealed that FGF21 directly prevented EPC damage induced by high glucose, and the mechanistic studies demonstrated that nicotinamide adenine dinucleotide (NAD

Indexed as

Neovascularization, PhysiologicAMP-Activated Protein KinasesAnimalsBiomarkersDiabetes Mellitus, ExperimentalEndothelial Progenitor CellsFibroblast Growth FactorsGlucoseHindlimbHumansHyperglycemiaImmunophenotypingIschemiaMaleMiceModels, BiologicalAMP-Activated Protein KinasesBiomarkersfibroblast growth factor 21Fibroblast Growth FactorsGlucoseNADAMPKdiabetesendothelial progenitor cellsfibroblast growth factor 21NAD+

Identifiers

PMID33599110
PMCPMC7957202
OpenAlexW3130650015

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.