Evidence map›Paper›PMID 28632765›Full record

ArticlePloS one2017

CTRP3 is a novel biomarker for diabetic retinopathy and inhibits HGHL-induced VCAM-1 expression in an AMPK-dependent manner.

Zheyi Yan, Jianli Zhao, Lu Gan, Yanqing Zhang, Rui Guo, Xiaoming Cao, Wayne Bond Lau, Xin Ma, Yajing Wang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

27 citing papers in PubMed, 52 citations in OpenAlex.

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  10. Astragaloside IV Regulates Insulin Resistance and Inflammatory Response of Adipocytes via Modulating CTRP3 and PI3K/AKT Signaling.Diabetes therapy : research, treatment and education of diabetes and related disorders · 2022
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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

9 authors at 2 institutions in 2 countries.

Zheyi YanDepartment of Ophthalmology, The First Affiliated Hospital, Shanxi Medical University, Taiyuan, Shanxi, China.
Jianli ZhaoDepartment of Emergency Medicine, Thomas Jefferson University, Philadelphia, PA, United States of America.
Lu GanDepartment of Emergency Medicine, Thomas Jefferson University, Philadelphia, PA, United States of America.
Yanqing ZhangDepartment of Emergency Medicine, Thomas Jefferson University, Philadelphia, PA, United States of America.
Rui GuoDepartment of Emergency Medicine, Thomas Jefferson University, Philadelphia, PA, United States of America.
Xiaoming CaoDepartment of Orthopedics, The Second Affiliated Hospital, Shanxi Medical University, Taiyuan, Shanxi, China.
Wayne Bond LauDepartment of Emergency Medicine, Thomas Jefferson University, Philadelphia, PA, United States of America.
Xin MaDepartment of Emergency Medicine, Thomas Jefferson University, Philadelphia, PA, United States of America.
Yajing WangDepartment of Emergency Medicine, Thomas Jefferson University, Philadelphia, PA, United States of America.ORCID http://orcid.org/0000-0002-6358-6948
Thomas Jefferson University · USShanxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesDiabetic retinopathy (DR) is a severe complication of chronic diabetes. The C1q/TNF-related protein family (CTRPs) has been demonstrated to exert protective effects against obesity and atherosclerosis in animal studies. Heretofore, the association between circulating CTRPs and DR patients has been unexplored. In the current study, we attempt to define this association, as well as the effect of CTRPs upon DR pathophysiology.

designThe present investigation is a case control study that enrolled control subjects and type 2 diabetes mellitus (T2DM) patients diagnosed with DR. Serum CTRPs and sVACM-1 were determined by ELISA.

resultsSerum CTRP3 and CTRP5 levels were markedly decreased in patients with T2DM compared to controls (p<0.05) and inversely associated with T2DM. Furthermore, mutivariate regression and ROC analysis revealed CTRP3 deficiency, not CTRP5, was associated with proliferative diabetic retinopathy (PDR). Spearman's rank correlation assay demonstrated an inverse association between CTRP3 and sVCAM-1. Finally, exogenous CTRP3 administration attenuated high glucose high lipid (HGHL)-induced VCAM-1 production in an AMPK-dependent manner in cultured human retinal microvascular endothelial cells (HRMECs).

conclusionCTRP3 may serve as a novel biomarker for DR severity. CTRP3 may represent a future novel therapeutic against DR, a common ocular complication of diabetes.

Indexed as

AMP-Activated Protein KinasesBiomarkersCase-Control StudiesCells, CulturedCollagenDiabetes Mellitus, Type 2Diabetic RetinopathyEndothelium, VascularFemaleGlucoseHumansLipidsMaleMiddle AgedRetinal VesselsTumor Necrosis FactorsAMP-Activated Protein KinasesBiomarkersC1QTNF3 protein, humanC1QTNF5 protein, humanCollagenGlucoseLipidsTumor Necrosis FactorsVascular Cell Adhesion Molecule-1

Identifiers

PMID28632765
PMCPMC5478095
OpenAlexW2658538033

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Registered trials

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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.