Evidence map›Paper›PMID 42275159›Full record

ArticleJCI insight2026

Fatty acid amide hydrolase inhibition for treatment of amyotrophic lateral sclerosis.

Daisuke Ito, Madoka Iida, Yohei Iguchi, Atsushi Hashizume, Shinichiro Yamada, Yoshiyuki Kishimoto, Shota Komori, Kazuki Obara, Shuto Nishisaki, Satoshi Yokoi and 13 more

Abstract read
In one paragraph

Article in JCI insight, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Daisuke ItoDepartment of Neurology.
Madoka IidaDepartment of Neurology.
Yohei IguchiDepartment of Neurology.
Atsushi HashizumeDepartment of Clinical Research Education.
Shinichiro YamadaDepartment of Neurology.
Yoshiyuki KishimotoDepartment of Neurology.
Shota KomoriDepartment of Neurology.
Kazuki ObaraDepartment of Neurology.
Shuto NishisakiDepartment of Pathophysiological Laboratory Sciences.
Satoshi YokoiDepartment of Neurology.
Teppei ShimamuraDivision of Systems Biology.
Yuto TakemotoPublic Health Informatics Unit, Department of Integrated Health Sciences, and.
Masahiro NakatochiPublic Health Informatics Unit, Department of Integrated Health Sciences, and.
Tomohiro AkashiDivision of Systems Biology.
Kunihiko HinoharaDepartment of Immunology, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan.
Hyeon-Cheol Lee-OkadaDepartment of Biochemistry, Juntendo University Graduate School of Medicine, Bunkyo-ku, Tokyo, Japan.
Yohei OkadaDepartment of Neural iPSC Research Institute for Medical Science of Aging, Aichi Medical University, Nagakute, Aichi, Japan.
Junichi NiwaDepartment of Neurology and.
Gen SobueAichi Medical University School of Medicine, Nagakute, Aichi, Japan.
Shinji TanakaSohyaku, Innovative Research Division, Mitsubishi Tanabe Pharma Corporation, Yokohama, Japan.
Ken TakashinaSohyaku, Innovative Research Division, Mitsubishi Tanabe Pharma Corporation, Yokohama, Japan.
Takehiko YokomizoDepartment of Biochemistry, Juntendo University Graduate School of Medicine, Bunkyo-ku, Tokyo, Japan.
Masahisa KatsunoDepartment of Neurology.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease caused by the selective loss of upper and lower motor neurons. There is a considerable variability in the disease progression of sporadic ALS, but the molecular basis for phenotypic heterogeneity remains largely unknown. Patients with ALS often manifest systemic metabolic abnormalities such as glucose intolerance and hypermetabolic state. We conducted reverse translational research to explore therapeutic targets in ALS based on the systemic metabolic alterations in patients and identified several metabolites associated with the disease progression, including metabolites involved in the expanded endocannabinoid system (ECS). In particular, the levels of N-acyl taurines (NATs) were correlated with the longitudinal change in the revised ALS functional rating scale and survival. Experiments with ALS cellular models and induced pluripotent stem (iPS) cells derived from patients with ALS and SOD1G93A transgenic mice revealed that PF-04457845, a fatty acid amide hydrolase inhibitor, upregulated the expanded ECS, particularly the levels of NATs and ameliorated motor neuron degeneration through the regulation of microglial environment, synapse plasticity, and neuronal development. These results collectively indicate that dysregulation of NATs is associated with ALS progression and PF-04457845 may represent a potential disease-modifying therapy for ALS.

Indexed as

AmidohydrolasesAmyotrophic Lateral SclerosisAnimalsDisease Models, AnimalDisease ProgressionEndocannabinoidsFatty Acid Amide HydrolasesFemaleHumansInduced Pluripotent Stem CellsMaleMiceMice, TransgenicMotor NeuronsSuperoxide Dismutase-1AmidohydrolasesEndocannabinoidsFatty Acid Amide HydrolasesSuperoxide Dismutase-1ALSBiomarkersDrug therapyMetabolismNeuroscience

Identifiers

PMID42275159
PMCPMC13463617

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.