Evidence map›Paper›PMID 32757791›Full record

ArticleJournal of the American Heart Association2020

Differences in Transforming Growth Factor-β1/BMP7 Signaling and Venous Fibrosis Contribute to Female Sex Differences in Arteriovenous Fistulas.

Chuanqi Cai, Sreenivasulu Kilari, Avishek K Singh, Chenglei Zhao, Michael L Simeon, Avanish Misra, Yiqing Li, Sanjay Misra

Open access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
4.0field-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

24 citing papers in PubMed, 25 citations in OpenAlex.

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  12. Fate mapping RNA-sequencing reveal Malat1 regulates Sca1Cellular and molecular life sciences : CMLS · 2023
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  15. Bindarit encapsulated nanoparticles prevent venous neointimal hyperplasia and restenosis in a murine angioplasty model.Translational research : the journal of laboratory and clinical medicine · 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

8 authors at 3 institutions in 2 countries.

Chuanqi CaiDepartment of Vascular Surgery Union Hospital Tongji Medical CollegeHuazhong University of Science and Technology Wuhan China.
Sreenivasulu KilariVascular and Interventional Radiology Translational Laboratory Department of Radiology Mayo Clinic Rochester MN.
Avishek K SinghVascular and Interventional Radiology Translational Laboratory Department of Radiology Mayo Clinic Rochester MN.
Chenglei ZhaoVascular and Interventional Radiology Translational Laboratory Department of Radiology Mayo Clinic Rochester MN.
Michael L SimeonVascular and Interventional Radiology Translational Laboratory Department of Radiology Mayo Clinic Rochester MN.
Avanish MisraVascular and Interventional Radiology Translational Laboratory Department of Radiology Mayo Clinic Rochester MN.
Yiqing LiDepartment of Vascular Surgery Union Hospital Tongji Medical CollegeHuazhong University of Science and Technology Wuhan China.
Sanjay MisraVascular and Interventional Radiology Translational Laboratory Department of Radiology Mayo Clinic Rochester MN.
Mayo Clinic · USMayo Clinic in Arizona · USUnion Hospital · CN

Funding

The Role of Hypoxia In Venous Neointimal Hyperplasia In Hemodialysis GraftsR01HL098967 · NHLBI · MAYO CLINIC ROCHESTER · PI Sanjay Misra · 2010 to 2026
$10.4M
Regulatory gene-chemokine networks in the formation of hemodialysis AVF stenosisR01DK107870 · NIDDK · MAYO CLINIC ROCHESTER · PI KUMAR, RAJIV, MISRA, SANJAY · 2017 to 2019
$716k
Regulatory gene-chemokine networks in the formation of hemodialysis AVF stenosisR56DK107870 · NIDDK · MAYO CLINIC ROCHESTER · PI KUMAR, RAJIV, MISRA, SANJAY · 2020 to 2020
$103k
NHLBI NIH HHS R01 HL098967NIDDK NIH HHS R01 DK107870NIDDK NIH HHS R56 DK107870
6 · The paper itself

Abstract

Background Women have decreased hemodialysis arteriovenous fistula (AVF) maturation and patency rates. We determined the mechanisms responsible for the sex-specific differences in AVF maturation and stenosis formation by performing whole transcriptome RNA sequencing with differential gene expression and pathway analysis, histopathological changes, and in vitro cell culture experiments from male and female smooth muscle cells. Methods and Results Mice with chronic kidney disease and AVF were used. Outflow veins were evaluated for gene expression, histomorphometric analysis, Doppler ultrasound, immunohistologic analysis, and fibrosis. Primary vascular smooth muscle cells were collected from female and male aorta vessels. In female AVFs, RNA sequencing with real-time polymerase chain reaction analysis demonstrated a significant decrease in the average gene expression of

Indexed as

Arteriovenous Shunt, SurgicalSex FactorsAnimalsApoptosisBone Morphogenetic Protein 7Cell ProliferationFemaleFibrosisGene ExpressionHyperplasiaMaleMiceMice, Inbred BALB CMuscle, Smooth, VascularNeointimaReceptors, Interleukin-17bmp7 protein, mouseBone Morphogenetic Protein 7Il17rb protein, mouseReceptors, Interleukin-17Receptor, Transforming Growth Factor-beta Type IRNATgfb1 protein, mouseTransforming Growth Factor beta1arteriovenous fistulabone morphogenetic proteinssexual diversitytransforming growth factor‐βvenous neointimal hyperplasia

Identifiers

PMID32757791
PMCPMC7660821
OpenAlexW3047576444

What OpenQuestion holds

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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.