Evidence map›Paper›PMID 32878279›Full record

ArticleMetabolites2020

Plasma Lipid Profiling of Three Types of Drug-Induced Liver Injury in Japanese Patients: A Preliminary Study.

Kosuke Saito, Tatehiro Kagawa, Keiji Tsuji, Yuji Kumagai, Ken Sato, Shotaro Sakisaka, Naoya Sakamoto, Mitsuhiko Aiso, Shunji Hirose, Nami Mori and 13 more

Open access · goldAbstract read
In one paragraph

Article in Metabolites, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

8 citing papers in PubMed, 16 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

23 authors at 10 institutions in 1 country.

Kosuke SaitoDivision of Medical Safety Science, National Institute of Health Sciences, Kanagawa 210-9501, Japan.ORCID 0000-0002-1035-3454
Tatehiro KagawaDivision of Gastroenterology and Hepatology, Department of Internal Medicine, Tokai University School of Medicine, Isehara 259-1193, Japan.ORCID 0000-0002-5959-913X
Keiji TsujiDepartment of Gastroenterology, Hiroshima Red Cross Hospital and Atomic-Bomb Survivors Hospital, Hiroshima 730-8619, Japan.
Yuji KumagaiKitasato University School of Medicine, 1-15-1 Kitasato, Minami-ku, Sagamihara, Kanagawa 252-0374, Japan.
Ken SatoDepartment of Gastroenterology and Hepatology, Gunma University Graduate School of Medicine, Maebashi 371-8511, Japan.
Shotaro SakisakaDepartment of Gastroenterology, Fukuoka University Faculty of Medicine, Fukuoka, 814-0180, Japan.
Naoya SakamotoDepartment of Gastroenterology and Hepatology, Hokkaido University Faculty of Medicine and Graduate School of Medicine, Sapporo 060-8648, Japan.
Mitsuhiko AisoDepartment of Medicine, Teikyo University School of Medicine, Tokyo 173-8606, Japan.
Shunji HiroseDivision of Gastroenterology and Hepatology, Department of Internal Medicine, Tokai University School of Medicine, Isehara 259-1193, Japan.
Nami MoriDepartment of Gastroenterology, Hiroshima Red Cross Hospital and Atomic-Bomb Survivors Hospital, Hiroshima 730-8619, Japan.
Rieko TanakaKitasato University School of Medicine, 1-15-1 Kitasato, Minami-ku, Sagamihara, Kanagawa 252-0374, Japan.
Toshio UraokaDepartment of Gastroenterology and Hepatology, Gunma University Graduate School of Medicine, Maebashi 371-8511, Japan.
Kazuhide TakataDepartment of Gastroenterology, Fukuoka University Faculty of Medicine, Fukuoka, 814-0180, Japan.
Koji OgawaDepartment of Gastroenterology and Hepatology, Hokkaido University Faculty of Medicine and Graduate School of Medicine, Sapporo 060-8648, Japan.
Kazuhiko MoriDaiichi Sankyo Co., Ltd., Tokyo 134-8630, Japan.ORCID 0000-0003-1353-264X
Motonobu SatoAstellas Pharma Inc., Tsukuba 305-8585, Japan.
Takayoshi NishiyaDaiichi Sankyo RD Novare Co., Ltd., Tokyo 134-8630, Japan.
Kazuhiko TakamatsuAstellas Pharma Inc., Tsukuba 305-8585, Japan.
Noriaki ArakawaDivision of Medical Safety Science, National Institute of Health Sciences, Kanagawa 210-9501, Japan.
Takashi IzumiKihara Memorial Foundation, Yokohama 230-0045, Japan.
Yasuo OhnoKihara Memorial Foundation, Yokohama 230-0045, Japan.
Yoshiro SaitoDivision of Medical Safety Science, National Institute of Health Sciences, Kanagawa 210-9501, Japan.
Hajime TakikawaDepartment of Medicine, Teikyo University School of Medicine, Tokyo 173-8606, Japan.
National Institute of Health Sciences · JPAstellas Pharma (Japan) · JPDaiichi-Sankyo (Japan) · JPFukuoka University · JPGunma University · JPHiroshima Red Cross Hospital & Atomic-bomb Survivors Hospital · JPHokkaido University · JPKitasato University · JPTeikyo University · JPTokai University · JP

Funding

Japan Agency for Medical Research and Development 19mk0101045h0005, 19mk0101045s0105, 19mk0101045s0205, 19mk0101045s0305, 19mk0101045s1205, 19mk0101045s1405, 19mk0101045s1505, 19mk0101045s1605, 19mk0101045j0105, 19mk0101045j0305, 19mk0101045j0405
6 · The paper itself

Abstract

Drug-induced liver injury (DILI) is a major adverse event caused by drug treatment, which can be categorized into three types: hepatocellular, mixed, and cholestatic. Although nearly every class of drugs can cause DILI, an overall understanding of lipid profiles in DILI patients is lacking. We used lipidomics to analyze the plasma lipid profiles of patients to understand their hepatic pathophysiology and identify DILI biomarkers. We identified 463 lipids and compared their levels between the acute and recovery phases of the three types of DILI patients. Mixed and cholestatic types demonstrated specific plasma lipid alterations between the phases, but the hepatocellular type did not. Moreover, as specific indicators of mixed-type DILI, levels of several ceramides increased in the acute phase, while those of arachidonic acid-containing ether-linked phosphoglycerolipids decreased. In contrast, as specific indicators of cholestatic-type DILI, levels of palmitic acid-containing saturated or monounsaturated phosphatidylcholines increased in the acute phase, while those of arachidonic acid- or docosahexaenoic acid-containing ether-linked phosphoglycerolipids and phosphatidylinositols decreased. We also identified lipids with a relatively high capacity to discriminate the acute phase from the recovery phase and healthy subjects. These findings may help with understanding the pathophysiology of different DILI types and identify candidate biomarkers.

Indexed as

biomarkerdrug-induced liver injurylipidomicsplasma lipid profiles

Identifiers

PMID32878279
PMCPMC7569965
OpenAlexW3081996409

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.