Evidence map›Paper›PMID 29391561›Full record

ArticleScientific reports2018

Asymmetric dimethylarginine (ADMA) is identified as a potential biomarker of insulin resistance in skeletal muscle.

Woojung Lee, Hyo Jung Lee, Han Byul Jang, Hyo-Jin Kim, Hyo-Jeong Ban, Kwang Youl Kim, Moon Suk Nam, Joo Sun Choi, Kyung-Tae Lee, Seong Beom Cho and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
3.4field-weighted citation impact, top 7% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 47 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

12 authors at 5 institutions in 1 country.

Woojung LeeCenter for Biomedical Sciences, National Institute of Health, Osong Health Technology Administration Complex, Chungcheongbuk-do, South Korea.
Hyo Jung LeeCenter for Biomedical Sciences, National Institute of Health, Osong Health Technology Administration Complex, Chungcheongbuk-do, South Korea.
Han Byul JangCenter for Biomedical Sciences, National Institute of Health, Osong Health Technology Administration Complex, Chungcheongbuk-do, South Korea.
Hyo-Jin KimCenter for Biomedical Sciences, National Institute of Health, Osong Health Technology Administration Complex, Chungcheongbuk-do, South Korea.
Hyo-Jeong BanCenter for Genome Science, National Institute of Health, Osong Health Technology Administration Complex, Chungcheongbuk-do, South Korea.
Kwang Youl KimDepartment of Clinical Pharmacology, Inha University Hospital, Incheon, South Korea.
Moon Suk NamDepartment of Internal Medicine, Inha University College of Medicine, Incheon, South Korea.
Joo Sun ChoiDepartment of Home Economics Education, College of Education, Kyungnam University, Changwon-si, Gyeongsangnam-do, South Korea.
Kyung-Tae LeeDepartment of Phamaceutical Biochemistry, College of pharmacy, Kyung Hee University, Seoul, South Korea.
Seong Beom ChoCenter for Genome Science, National Institute of Health, Osong Health Technology Administration Complex, Chungcheongbuk-do, South Korea.
Sang Ick ParkCenter for Biomedical Sciences, National Institute of Health, Osong Health Technology Administration Complex, Chungcheongbuk-do, South Korea.
Hye-Ja LeeCenter for Biomedical Sciences, National Institute of Health, Osong Health Technology Administration Complex, Chungcheongbuk-do, South Korea. hyejalee@yahoo.co.kr.
Korea National Institute of Health · KRInha University · KRInha University Hospital · KRKyung Hee University · KRKyungnam University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To unravel metabolic determinats of insulin resistance, we performed a targeted metabolomics analysis in Korean Children-Adolescent Cohort Study (KoCAS, n = 430). Sixty-seven metabolites were associated with insulin resistance in adolescents and the association also found in an adult population (KoGES, n = 2,485). Functional interactions of metabolites with gene/proteins using biological pathway with insulin resistance were not identified biological significance and regulatory effects of asymmetric dimethylarginine (ADMA). However, ADMA showed a higher association with adolescent obesity (P < 0.001) and adult diabetes (P = 0.007) and decreased after obesity intervention program. Functional studies in cellular and mouse models demonstrated that an accumulation of ADMA is associated with the regulation of obesity-induced insulin resistance in skeletal muscle. ADMA treatment inhibited dimethylarginine-dimethylaminohydrolase (DDAH) activity and mRNA expression in insulin resistance muscle cell. Moreover, the treatment led to decrease of phosphorylation of insulin receptor (IR), AKT, and GLUT4 but increase of protein-tyrosine phosphatase 1B (PTP1B). Accordingly, increased ADMA significantly inhibited glucose uptake in myotube cell. We suggest that accumulation of ADMA is associated with modulation of insulin signaling and insulin resistance. ADMA might expand the possibilities of new therapeutic target for functional and clinical implications in the control of energy and metabolic homeostasis in humans.

Indexed as

Insulin ResistanceAdolescentAdultAnimalsArginineBiomarkersCohort StudiesHumansMiceMice, Inbred C57BLMiddle AgedMuscle, SkeletalSignal TransductionArginineBiomarkersN,N-dimethylarginine

Identifiers

PMID29391561
PMCPMC5794993
OpenAlexW2806825061

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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.