Evidence map›Paper›PMID 34906158›Full record

ArticleMalaria journal2021

The association between acute fatty liver disease and nitric oxide during malaria in pregnancy.

Mamoru Niikura, Toshiyuki Fukutomi, Shoichiro Mineo, Jiro Mitobe, Fumie Kobayashi

Open access · goldAbstract read
In one paragraph

Article in Malaria journal, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 44% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Perilipin1 inhibitsMicrobiology spectrum · 2024
    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

5 authors at 3 institutions in 1 country.

Mamoru NiikuraDepartment of Infectious Diseases, Kyorin University School of Medicine, 6-20-2 Shinkawa, Mitaka, Tokyo, 181-8611, Japan. mniikura@ks.kyorin-u.ac.jp.ORCID http://orcid.org/0000-0002-1647-2745
Toshiyuki FukutomiDepartment of Pharmacology and Toxicology, Kyorin University School of Medicine, Tokyo, Japan.
Shoichiro MineoDepartment of Molecular Pathology, Tokyo Medical University, Tokyo, 160-8402, Japan.
Jiro MitobeDepartment of Infectious Diseases, Kyorin University School of Medicine, 6-20-2 Shinkawa, Mitaka, Tokyo, 181-8611, Japan.
Fumie KobayashiDepartment of Environmental Science, School of Life and Environmental Science, Azabu University, Kanagawa, 252-5201, Japan.
Kyorin University · JPAzabu University · JPTokyo Medical University · JP

Funding

Japan Society for the Promotion of Science 18K07093Japan Society for the Promotion of Science 21K06997
6 · The paper itself

Abstract

backgroundLiver disease is a common feature of malaria in pregnancy, but its pathogenesis remains unclear.

methodsTo understand the pathogenesis of liver disease during malaria in pregnancy, comparative proteomic analysis of the liver in a mouse model of malaria in pregnancy was performed.

resultsDecreased levels of mitochondrial and peroxisomal proteins were observed in the livers of pregnant mice infected with the lethal rodent malaria parasite Plasmodium berghei strain NK65. By contrast, increased levels of perilipin-2, amyloid A-1, and interferon (IFN)-γ signalling pathway-related proteins were observed in the livers of infected pregnant mice, suggesting that IFN-γ signalling may contribute to the development of liver disease during malaria in pregnancy. IFN-γ signalling is a potential trigger of inducible nitric oxide synthase (iNOS) expression. Liver disease associated with microvesicular fatty infiltration and elevated liver enzymes in pregnant wild-type mice infected with malaria parasites was improved by iNOS deficiency.

conclusionsIn this study, a causative role of iNOS in liver disease associated with microvesicular fatty infiltration during malaria in pregnancy was demonstrated. These findings provide important insight for understanding the role of iNOS-mediated metabolic responses and the pathogenesis of high-risk liver diseases in pregnancy, such as acute fatty liver.

Indexed as

Acute DiseaseAnimalsDisease Models, AnimalFatty LiverFemaleMalariaMaleMiceMice, Inbred C57BLNitric OxidePlasmodium bergheiPregnancyPregnancy Complications, ParasiticNitric OxideFatty liveriNOSLiver diseaseMalariaPregnancyProteome

Identifiers

PMID34906158
PMCPMC8670279
OpenAlexW4200370909

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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 OpenQuestion graph.