Evidence map›Paper›PMID 34282172›Full record

ArticleScientific reports2021

Circulating miRNA is a useful diagnostic biomarker for nonalcoholic steatohepatitis in nonalcoholic fatty liver disease.

Tae Hyung Kim, Yoonseok Lee, Young-Sun Lee, Jeong-An Gim, Eunjung Ko, Sun Young Yim, Young Kul Jung, SeongHee Kang, Moon Young Kim, Hayeon Kim and 7 more

Abstract readValidation Study
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

50 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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  19. Serum miR‑29 is increased in mice with early liver fibrosis.Experimental and therapeutic medicine · 2024
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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

17 authors.

Tae Hyung Kim *Department of Internal Medicine, Division of Gastroenterology and Hepatology, Guro Hospital, Korea University College of Medicine, Korea University Medical Center, 97, Guro-Dong Gil, Guro-Dong, Guro-Ku, Seoul, 08308, Republic of Korea.
Yoonseok Lee *Department of Internal Medicine, Division of Gastroenterology and Hepatology, Guro Hospital, Korea University College of Medicine, Korea University Medical Center, 97, Guro-Dong Gil, Guro-Dong, Guro-Ku, Seoul, 08308, Republic of Korea.
Young-Sun LeeDepartment of Internal Medicine, Division of Gastroenterology and Hepatology, Guro Hospital, Korea University College of Medicine, Korea University Medical Center, 97, Guro-Dong Gil, Guro-Dong, Guro-Ku, Seoul, 08308, Republic of Korea. lys810@korea.ac.kr.
Jeong-An GimMedical Science Research Center, Korea University Medical Center, Anam-dong 5-ga, Seongbuk-gu, Seoul, 02841, Republic of Korea. vitastar@korea.ac.kr.
Eunjung KoDepartment of Internal Medicine, Division of Gastroenterology and Hepatology, Guro Hospital, Korea University College of Medicine, Korea University Medical Center, 97, Guro-Dong Gil, Guro-Dong, Guro-Ku, Seoul, 08308, Republic of Korea.
Sun Young YimDepartment of Internal Medicine, Division of Gastroenterology and Hepatology, Guro Hospital, Korea University College of Medicine, Korea University Medical Center, 97, Guro-Dong Gil, Guro-Dong, Guro-Ku, Seoul, 08308, Republic of Korea.
Young Kul JungDepartment of Internal Medicine, Division of Gastroenterology and Hepatology, Guro Hospital, Korea University College of Medicine, Korea University Medical Center, 97, Guro-Dong Gil, Guro-Dong, Guro-Ku, Seoul, 08308, Republic of Korea.
SeongHee KangDepartment of Internal Medicine, Wonju Severance Christian Hospital, Wonju, Republic of Korea.
Moon Young KimDepartment of Internal Medicine, Wonju Severance Christian Hospital, Wonju, Republic of Korea.
Hayeon KimDepartment of Pathology, Korea University Medical Center, Seoul, Republic of Korea.
Baek-Hui KimDepartment of Pathology, Korea University Medical Center, Seoul, Republic of Korea.
Ji Hoon KimDepartment of Internal Medicine, Division of Gastroenterology and Hepatology, Guro Hospital, Korea University College of Medicine, Korea University Medical Center, 97, Guro-Dong Gil, Guro-Dong, Guro-Ku, Seoul, 08308, Republic of Korea.
Yeon Seok SeoDepartment of Internal Medicine, Division of Gastroenterology and Hepatology, Guro Hospital, Korea University College of Medicine, Korea University Medical Center, 97, Guro-Dong Gil, Guro-Dong, Guro-Ku, Seoul, 08308, Republic of Korea.
Hyung Joon YimDepartment of Internal Medicine, Division of Gastroenterology and Hepatology, Guro Hospital, Korea University College of Medicine, Korea University Medical Center, 97, Guro-Dong Gil, Guro-Dong, Guro-Ku, Seoul, 08308, Republic of Korea.
Jong Eun YeonDepartment of Internal Medicine, Division of Gastroenterology and Hepatology, Guro Hospital, Korea University College of Medicine, Korea University Medical Center, 97, Guro-Dong Gil, Guro-Dong, Guro-Ku, Seoul, 08308, Republic of Korea.
Soon Ho UmDepartment of Internal Medicine, Division of Gastroenterology and Hepatology, Guro Hospital, Korea University College of Medicine, Korea University Medical Center, 97, Guro-Dong Gil, Guro-Dong, Guro-Ku, Seoul, 08308, Republic of Korea.
Kwan Soo ByunDepartment of Internal Medicine, Division of Gastroenterology and Hepatology, Guro Hospital, Korea University College of Medicine, Korea University Medical Center, 97, Guro-Dong Gil, Guro-Dong, Guro-Ku, Seoul, 08308, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nonalcoholic steatohepatitis (NASH) is considered as a progressive form of nonalcoholic fatty liver disease (NAFLD). To distinguish NASH from nonalcoholic fatty liver (NAFL), we evaluated the diagnostic value of circulating miRNAs. Small RNA sequencing was performed on 12 NAFL patients and 12 NASH patients, and the miRNA expression was compared. After selecting miRNAs for the diagnosis of NASH, we analyzed the diagnostic accuracy of each miRNA and the combination of miRNAs. External validation was performed using quantitative reverse transcription PCR. Among the 2,588 miRNAs, 26 miRNAs significantly increased in the NASH group than in the NAFL group. Among the 26 elevated miRNAs in the NASH group, 8 miRNAs were selected, and in silico analysis was performed. Only four miRNAs (miR-21-5p, miR-151a-3p, miR-192-5p, and miR-4449) showed significant area under the receiver operating characteristic curve (AUC) values for NASH diagnosis. The combination of the four miRNAs showed satisfactory diagnostic accuracy for NASH (AUC 0.875; 95% CI 0.676-0.973). External validation revealed similar diagnostic accuracy for NASH (AUC 0.874; 95% CI 0.724-0.960). NASH represents significantly distinct miRNA expression profile compared with NAFL. The combination of serum circulating miRNAs can be used as a novel biomarker for the NASH diagnosis in NAFLD.

Indexed as

AdultBiomarkersCirculating MicroRNADiagnosis, DifferentialFatty LiverFemaleHumansMaleMicroRNAsMiddle AgedNon-alcoholic Fatty Liver DiseasePredictive Value of TestsSensitivity and SpecificityBiomarkersCirculating MicroRNAMicroRNAs

Identifiers

PMID34282172
PMCPMC8289842

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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.