Evidence map›Paper›PMID 35128793›Full record

ArticleEuropean journal of neurology2022

Serum asymmetric dimethylarginine level correlates with the progression and prognosis of amyotrophic lateral sclerosis.

Kensuke Ikenaka, Yasuhiro Maeda, Yuji Hotta, Seiichi Nagano, Shinichiro Yamada, Daisuke Ito, Ryota Torii, Keita Kakuda, Harutsugu Tatebe, Naoki Atsuta and 8 more

Open access · hybridAbstract read
In one paragraph

Article in European journal of neurology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 26% 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, 7 citations in OpenAlex.

  1. Trial
  2. The Emerging Role of the DDAH Proteins in Psychiatric Disorders.Biological psychiatry global open science · 2025
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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

18 authors at 6 institutions in 1 country.

Kensuke IkenakaDepartment of Neurology, Osaka University Graduate School of Medicine, Suita, Japan.ORCID 0000-0002-5559-1966
Yasuhiro MaedaCenter for Joint Research Facilities Support, Fujita Health University, Toyoake, Japan.
Yuji HottaDepartment of Hospital Pharmacy, Nagoya City University Graduate School of Pharmaceutical Sciences, Nagoya, Japan.
Seiichi NaganoDepartment of Neurology, Osaka University Graduate School of Medicine, Suita, Japan.
Shinichiro YamadaDepartment of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Daisuke ItoDepartment of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Ryota ToriiDepartment of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Keita KakudaDepartment of Neurology, Osaka University Graduate School of Medicine, Suita, Japan.
Harutsugu TatebeT & T Brothers Corporation, Chiba, Japan.
Naoki AtsutaDepartment of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Cesar AguirreDepartment of Neurology, Osaka University Graduate School of Medicine, Suita, Japan.
Yasuyoshi KimuraDepartment of Neurology, Osaka University Graduate School of Medicine, Suita, Japan.
Kousuke BabaDepartment of Neurology, Osaka University Graduate School of Medicine, Suita, Japan.
Takahiko TokudaT & T Brothers Corporation, Chiba, Japan.
Masahisa KatsunoDepartment of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.ORCID 0000-0001-9453-9311
Kazunori KimuraDepartment of Hospital Pharmacy, Nagoya City University Graduate School of Pharmaceutical Sciences, Nagoya, Japan.
Gen SobueResearch Division of Dementia and Neurodegenerative Disease, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Hideki MochizukiDepartment of Neurology, Osaka University Graduate School of Medicine, Suita, Japan.
The University of Osaka · JPNagoya University · JPAichi Medical University · JPNagoya City University · JPTDK (Japan) · JPFujita Health University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeThe aim was to investigate the association between serum asymmetric dimethylarginine (ADMA) levels and the progression and prognosis of amyotrophic lateral sclerosis (ALS), and to compare cerebrospinal fluid (CSF) and serum ADMA levels with other biomarkers of ALS.

methodsSerum ADMA levels of sporadic ALS patients (n = 68), disease control patients (n = 54) and healthy controls (n = 20) were measured using liquid chromatography tandem mass spectrometry. Correlations of the ADMA level and other markers (nitric oxide and neurofilament light chain levels) were analyzed. Changes in the ALS Functional Rating Scale Revised (ALSFRS-R) score from the onset of disease (ALSFRS-R pre-slope) was used to assess disease progression. Survival was evaluated using the Cox proportional hazards model and Kaplan-Meier analysis.

resultsThe serum ADMA level was substantially higher in patients with ALS than in healthy controls and disease controls. Serum ADMA level correlated with CSF ADMA level (r = 0.591, p < 0.0001) and was independently associated with the ALSFRS-R pre-slope (r = 0.505, p < 0.0001). Patients with higher serum ADMA levels had less favorable prognoses. CSF ADMA level significantly correlated with CSF neurofilament light chain level (r = 0.456, p = 0.0002) but not with nitric oxide level (r = 0.194, p = 0.219).

conclusionSerum ADMA level is an independent biomarker of ALS disease progression and prognosis and reflects the degree of motor neuron degeneration.

Indexed as

Amyotrophic Lateral SclerosisArginineBiomarkersDisease ProgressionHumansNitric OxidePrognosisArginineBiomarkersNitric OxideN,N-dimethylarginineamyotrophic lateral sclerosisbiomarkerdimethylarginine

Identifiers

PMID35128793
PMCPMC9305138
OpenAlexW4226188551

What OpenQuestion holds

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LicenceCC BY-NC-ND
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 OpenQuestion graph.