Evidence map›Paper›PMID 32106257›Full record

ArticlePloS one2020

Serum miR-379 expression is related to the development and progression of hypercholesterolemia in non-alcoholic fatty liver disease.

Kinya Okamoto, Masahiko Koda, Toshiaki Okamoto, Takumi Onoyama, Kenichi Miyoshi, Manabu Kishina, Tomomitsu Matono, Jun Kato, Shiho Tokunaga, Takaaki Sugihara and 10 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 2 pooled it
1.4field-weighted citation impact, top 20% 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

17 citing papers in PubMed, 2 syntheses or guidelines pooled it, 25 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Review
  6. Article
  7. Review
  8. MicroRNAs and Nonalcoholic Steatohepatitis: A Review.International journal of molecular sciences · 2023
    Review
  9. Article
  10. Article
  11. Role of miR-379 in high-fat diet-induced kidney injury and dysfunction.American journal of physiology. Renal physiology · 2022
    Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Lack ofFrontiers in cell and developmental biology · 2021
    Article
  17. The Role of microRNAs in Metabolic Syndrome-Related Oxidative Stress.International journal of molecular sciences · 2020
    Review
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

20 authors at 5 institutions in 1 country.

Kinya OkamotoSecond Department of Internal Medicine, Tottori University School of Medicine, Yonago, Tottori, Japan.ORCID 0000-0001-9087-8965
Masahiko KodaSecond Department of Internal Medicine, Tottori University School of Medicine, Yonago, Tottori, Japan.
Toshiaki OkamotoSecond Department of Internal Medicine, Tottori University School of Medicine, Yonago, Tottori, Japan.
Takumi OnoyamaSecond Department of Internal Medicine, Tottori University School of Medicine, Yonago, Tottori, Japan.
Kenichi MiyoshiSecond Department of Internal Medicine, Tottori University School of Medicine, Yonago, Tottori, Japan.
Manabu KishinaSecond Department of Internal Medicine, Tottori University School of Medicine, Yonago, Tottori, Japan.
Tomomitsu MatonoSecond Department of Internal Medicine, Tottori University School of Medicine, Yonago, Tottori, Japan.
Jun KatoSecond Department of Internal Medicine, Tottori University School of Medicine, Yonago, Tottori, Japan.
Shiho TokunagaSecond Department of Internal Medicine, Tottori University School of Medicine, Yonago, Tottori, Japan.
Takaaki SugiharaSecond Department of Internal Medicine, Tottori University School of Medicine, Yonago, Tottori, Japan.ORCID 0000-0003-0522-1884
Akira HiramatsuDepartment of Gastroenterology and Metabolism, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Hiroshima, Japan.
Hideyuki HyogoDepartment of Gastroenterology and Hepatology, JA Hiroshima General Hospital, Hatsukaichi, Hiroshima, Japan.
Hiroshi TobitaDepartment of Gastroenterology and Hepatology, Shimane University School of Medicine, Izumo, Shimane, Japan.
Shuichi SatoDepartment of Gastroenterology and Hepatology, Shimane University School of Medicine, Izumo, Shimane, Japan.
Miwa KawanakaDepartment of General Internal Medicine 2, General Medical Center, Kawasaki Medical School, Okayama, Okayama, Japan.
Yuichi HaraDepartment of Hepatology and Pancreatology, Kawasaki Medical School, Kurashiki, Okayama, Japan.
Keisuke HinoDepartment of Hepatology and Pancreatology, Kawasaki Medical School, Kurashiki, Okayama, Japan.
Kazuaki ChayamaDepartment of Gastroenterology and Metabolism, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Hiroshima, Japan.
Yoshikazu MurawakiSecond Department of Internal Medicine, Tottori University School of Medicine, Yonago, Tottori, Japan.
Hajime IsomotoSecond Department of Internal Medicine, Tottori University School of Medicine, Yonago, Tottori, Japan.
Tottori University · JPKawasaki Medical School · JPHiroshima University · JPShimane University · JPHiroshima General Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionNon-alcoholic fatty liver disease (NAFLD) has a wide spectrum, eventually leading to cirrhosis and hepatic carcinogenesis. We previously reported that a series of microRNAs (miRNAs) mapped in the 14q32.2 maternally imprinted gene region (Dlk1-Dio3 mat) are related to NAFLD development and progression in a mouse model. We examined the suitability of miR-379, a circulating Dlk1-Dio3 mat miRNA, as a human NAFLD biomarker.

methodsEighty NAFLD patients were recruited for this study. miR-379 was selected from the putative Dlk1-Dio3 mat miRNA cluster because it exhibited the greatest expression difference between NAFLD and non-alcoholic steatohepatitis in our preliminary study. Real-time PCR was used to examine the expression levels of miR-379 and miR-16 as an internal control. One patient was excluded due to low RT-PCR signal.

resultsCompared to normal controls, serum miR-379 expression was significantly up-regulated in NAFLD patients. Receiver operating characteristic curve analysis suggested that miR-379 is a suitable marker for discriminating NAFLD patients from controls, with an area under the curve value of 0.72. Serum miR-379 exhibited positive correlations with alkaline phosphatase, total cholesterol, low-density-lipoprotein cholesterol and non-high-density-lipoprotein cholesterol levels in patients with early stage NAFLD (Brunt fibrosis stage 0 to 1). The correlation between serum miR-379 and cholesterol levels was lost in early stage NAFLD patients treated with statins. Software-based predictions indicated that various energy metabolism-related genes, including insulin-like growth factor-1 (IGF-1) and IGF-1 receptor, are potential targets of miR-379.

conclusionsSerum miR-379 exhibits high potential as a biomarker for NAFLD. miR-379 appears to increase cholesterol lipotoxicity, leading to the development and progression of NAFLD, via interference with the expression of target genes, including those related to the IGF-1 signaling pathway. Our results could facilitate future research into the pathogenesis, diagnosis, and treatment of NAFLD.

Indexed as

AdultAgedBiomarkersFemaleHumansHypercholesterolemiaMaleMicroRNAsMiddle AgedNon-alcoholic Fatty Liver DiseaseUp-RegulationBiomarkersMicroRNAsMIRN379 microRNA, human

Identifiers

PMID32106257
PMCPMC7046274
OpenAlexW3007703165

What OpenQuestion holds

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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.