Evidence map›Paper›PMID 35740238›Full record

ArticleBiomedicines2022

Association of Metabolomic Change and Treatment Response in Patients with Non-Alcoholic Fatty Liver Disease.

Kwang Seob Lee, Yongin Cho, Hongkyung Kim, Hyunkyeong Hwang, Jin Won Cho, Yong-Ho Lee, Sang-Guk Lee

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 17% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Proteomics and Metabolomics in Biomedicine.International journal of molecular sciences · 2023
    Article
  5. Article
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

7 authors at 2 institutions in 1 country.

Kwang Seob LeeDepartment of Laboratory Medicine, Yonsei University College of Medicine, Seoul 03722, Korea.ORCID 0000-0002-6286-108X
Yongin ChoDivision of Endocrinology and Metabolism, Department of Internal Medicine, Inha University School of Medicine, Incheon 22212, Korea.ORCID 0000-0002-4645-816X
Hongkyung KimDepartment of Laboratory Medicine, Yonsei University College of Medicine, Seoul 03722, Korea.ORCID 0000-0003-4185-1672
Hyunkyeong HwangDepartment of Laboratory Medicine, Yonsei University College of Medicine, Seoul 03722, Korea.
Jin Won ChoDepartment of Systems Biology, Glycosylation Network Research Center, Yonsei University, Seoul 03722, Korea.
Yong-Ho LeeDepartment of Systems Biology, Glycosylation Network Research Center, Yonsei University, Seoul 03722, Korea.ORCID 0000-0002-6219-4942
Sang-Guk LeeDepartment of Laboratory Medicine, Yonsei University College of Medicine, Seoul 03722, Korea.ORCID 0000-0003-3862-3660
Yonsei University · KRInha University · KR

Funding

National Research Foundation of Korea NRF-2016R1A5A1010764National Research Foundation of Korea NRF-2020R1F1A1051360
6 · The paper itself

Abstract

Non-alcoholic fatty liver disease (NAFLD) is the major cause of chronic liver disease, yet cost-effective and non-invasive diagnostic tools to monitor the severity of the disease are lacking. We aimed to investigate the metabolomic changes in NAFLD associated with therapeutic responses. It was conducted in 63 patients with NAFLD who received either ezetimibe plus rosuvastatin or rosuvastatin monotherapy. The treatment response was determined by MRI performed at baseline and week 24. The metabolites were measured at baseline and week 12. In the combination group, a relative decrease in xanthine was associated with a good response to liver fat decrease, while a relative increase in choline was associated with a good response to liver stiffness. In the monotherapy group, the relative decreases in triglyceride (TG) 20:5_36:2, TG 18:1_38:6, acetylcarnitine (C2), fatty acid (FA) 18:2, FA 18:1, and docosahexaenoic acid were associated with a decrease in liver fat, while hexosylceramide (d18:2/16:0) and hippuric acid were associated with a decrease in liver stiffness. Models using the metabolite changes showed an AUC of >0.75 in receiver operating curve analysis for predicting an improvement in liver fat and stiffness. This approach revealed the physiological impact of drugs, suggesting the mechanism underlying the development of this disease.

Indexed as

ezetimibemagnetic resonance elastographymagnetic resonance proton-density fat fractionmetabolomicsnon-alcoholic fatty liver diseasepredictionrosuvastatintransient elastography

Identifiers

PMID35740238
PMCPMC9220113
OpenAlexW4281490110

What Socratic holds

Textmetadata
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 Socratic graph.