Evidence map›Paper›PMID 30646802›Full record

ArticleJournal of the American Heart Association2019

Risk Factors Associated With Altered Circulating Micro RNA -125b and Their Influences on Uremic Vascular Calcification Among Patients With End-Stage Renal Disease.

Chia-Ter Chao, Tzu-Hang Yuan, Hsiang-Yuan Yeh, Hsuan-Yu Chen, Jenq-Wen Huang, Huei-Wen Chen

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Journal of the American Heart Association, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
2.2field-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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

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  10. Vascular frailty, a proposal for new frailty type: A narrative review.The Kaohsiung journal of medical sciences · 2023
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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

6 authors at 4 institutions in 1 country.

Chia-Ter Chao1 Department of Medicine National Taiwan University Hospital BeiHu Branch Taipei Taiwan.
Tzu-Hang Yuan4 Graduate Institute of Toxicology National Taiwan University Taipei Taiwan.
Hsiang-Yuan Yeh5 School of Big Data Management Soochow University Taipei Taiwan.
Hsuan-Yu Chen6 Institute of Statistical Science Academia Sinica Taipei Taiwan.
Jenq-Wen Huang2 Nephrology Division Department of Internal Medicine National Taiwan University Hospital Taipei Taiwan.
Huei-Wen Chen4 Graduate Institute of Toxicology National Taiwan University Taipei Taiwan.
Institute of Statistical Science, Academia Sinica · TWNational Taiwan University Hospital · TWNational Taiwan University · TWSoochow University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background Micro RNA -125b (miR-125b) has been shown to regulate vascular calcification ( VC ), and serum miR-125b levels are a potential biomarker for estimating the risk of uremic VC status. However, it is unknown whether clinical features, including chronic kidney disease-mineral bone disorder molecules, affect serum miR-125b levels. Methods and Results Patients receiving chronic dialysis for ≥3 months were recruited from different institutes. Serum miR-125b and chronic kidney disease-mineral bone disorder effectors, including intact parathyroid hormone, 25- OH -D, fibroblast growth factor-23, osteoprotegerin, and fetuin-A, were quantified. We used multivariate regression analyses to identify factors associated with low serum miR-125b levels and an area under receiver operating characteristic curve curve to derive optimal cutoffs for factors exhibiting close associations. Further regression analyses evaluated the influence of miR-125b on VC risk. Among 223 patients receiving chronic dialysis (mean age, 67.3 years; mean years of dialysis, 5.2), 54 (24.2%) had high serum miR-125b levels. Osteoprotegerin ( P=0.013), fibroblast growth factor-23 ( P=0.006), and fetuin-A ( P=0.036) were linearly associated with serum miR-125b levels. High osteoprotegerin levels independently correlated with high serum miR-125 levels. Adding serum miR-125b levels and serum osteoprotegerin levels (≥400 pg/mL) into models estimating the risk of uremic VC increased the area under receiver operating characteristic curve values (for models without miR-125b/osteoprotegerin, with miR-125b, and both: 0.74, 0.79, and 0.81, respectively). Conclusions Serum osteoprotegerin levels ≥400 pg/mL and serum miR-125b levels synergistically increased the accuracy of estimating VC risk among patients receiving chronic dialysis. Taking miR-125b and osteoprotegerin levels into consideration when estimating VC risk may be recommended.

Indexed as

AgedBiomarkersEnzyme-Linked Immunosorbent AssayFemaleFollow-Up StudiesHumansKidney Failure, ChronicMaleMicroRNAsOsteoprotegerinProspective StudiesRadiographyRadioimmunoassayRenal DialysisRisk FactorsUremiaBiomarkersMicroRNAsMIRN125 microRNA, humanOsteoprotegerinbiomarkerchronic kidney diseaseend‐stage renal diseasefibroblast growth factor‐23microRNA‐125bosteoprotegerinvascular calcification

Identifiers

PMID30646802
PMCPMC6497364
OpenAlexW2909788535

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.