Evidence map›Paper›PMID 31842275›Full record

ArticleNutrients2019

Exploring the Benefit of 2-Methylbutyric Acid in Patients Undergoing Hemodialysis Using a Cardiovascular Proteomics Approach.

Ping-Hsun Wu, Yi-Wen Chiu, Hsin-Bai Zou, Cheng-Chih Hsu, Su-Chu Lee, Yi-Ting Lin, Yi-Chun Tsai, Mei-Chuan Kuo, Shang-Jyh Hwang

Open access · goldAbstract readEvaluation Study
In one paragraph

Article in Nutrients, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

12 citing papers in PubMed, 18 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

9 authors at 3 institutions in 2 countries.

Ping-Hsun WuGraduate Institute of Clinical Medicine, College of Medicines, Kaohsiung Medical University, Kaohsiung 80708, Taiwan.ORCID 0000-0003-1021-8161
Yi-Wen ChiuDivision of Nephrology, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung 80708, Taiwan.
Hsin-Bai ZouDepartment of Chemistry, National Taiwan University, Taipei 10617, Taiwan.
Cheng-Chih HsuDepartment of Chemistry, National Taiwan University, Taipei 10617, Taiwan.ORCID 0000-0002-2892-5326
Su-Chu LeeDivision of Nephrology, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung 80708, Taiwan.ORCID 0000-0002-8587-7324
Yi-Ting LinGraduate Institute of Clinical Medicine, College of Medicines, Kaohsiung Medical University, Kaohsiung 80708, Taiwan.
Yi-Chun TsaiFaculty of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung 80708, Taiwan.ORCID 0000-0003-4923-3342
Mei-Chuan KuoFaculty of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung 80708, Taiwan.
Shang-Jyh HwangFaculty of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung 80708, Taiwan.
Kaohsiung Medical University · TWNational Taiwan University · TWUppsala University · SE

Funding

Kaohsiung Medical University KMUH106-6T03Kaohsiung Medical University KMUH106-6T07Kaohsiung Medical University KMU-Q108024Kaohsiung Medical University KMU-Q108027Kaohsiung Medical University Chung-Ho Memorial Hospital KMUH105-5R15Kaohsiung Medical University Chung-Ho Memorial Hospital KMUH106-6R17Kaohsiung Medical University Chung-Ho Memorial Hospital KMUH107-7R16Kaohsiung Medical University Chung-Ho Memorial Hospital KMUH107-7R78Ministry of Science and Technology, Taiwan MOST 105-2628-B-037-005-MY2Ministry of Science and Technology, Taiwan MOST 106-2113-M-002 -013-MY2Ministry of Science and Technology, Taiwan MOST 107-2314-B-037-098-MY3Ministry of Science and Technology, Taiwan MOST 107-2314-B-037-104
6 · The paper itself

Abstract

Short-chain fatty acids (SCFAs) can reduce pro-inflammatory parameters and oxidative stress, providing potential cardiovascular (CV) benefits. Although some evidence links SCFAs with host metabolic health via several biological mechanisms, the role of SCFA on CV disease in patients with kidney disease remains unclear. Herein, we investigate the association between a SCFA, 2-methylbutyric acid, and target CV proteomics to explore the potential pathophysiology of SCFA-related CV benefit in patients with kidney disease. Circulating 2-methylbutyric acid was quantified by high-performance liquid chromatography and 181 CV proteins by a proximity extension assay in 163 patients undergoing hemodialysis (HD). The associations between 2-methylbutyric acid and CV proteins were evaluated using linear regression analysis with age and gender, and multiple testing adjustment. The selected CV protein in the discovery phase was further confirmed in multivariable-adjusted models and evaluated by continuous scale association. The mean value of circulating 2-methylbutyric acid was 0.22 ± 0.02 µM, which was negatively associated with bone morphogenetic protein 6 (BMP-6) according to the false discovery rate (FDR) multiple testing adjustment method. The 2-methylbutyric acid level remained negatively associated with BMP-6 (β coefficient -1.00, 95% confidence interval -1.45 to -0.55,

Indexed as

Renal DialysisAdultAgedBone Morphogenetic Protein 6ButyratesCardiovascular DiseasesCardiovascular SystemFemaleHumansMaleMiddle AgedProteomicsRenal Insufficiency, Chronic2-methylbutanoic acidBMP6 protein, humanBone Morphogenetic Protein 6Butyrates2-methylbutyric acidbone morphogenetic protein 6end-stage renal diseasehemodialysisshort-chain fatty acidstarget proteomics

Identifiers

PMID31842275
PMCPMC6950398
OpenAlexW2995711111

What OpenQuestion holds

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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.