Evidence map›Paper›PMID 39624674›Full record

ArticleFrontiers in neurology2024

Neuroinflammation and glycosylation-related cerebrospinal fluid proteins for predicting functional decline in amyotrophic lateral sclerosis: a proteomic study.

Kimie Nakamura, Koji Fujita, Motohisa Suzuki, Akiyoshi Kunugi, Yoshihiko Hirozane, Tomonori Kunikata, Bitoku Takahashi, Genta Narazaki, Hirofumi Kondo, Shotaro Haji and 2 more

Abstract read
In one paragraph

Article in Frontiers in neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
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

12 authors.

Kimie NakamuraNeuroscience Drug Discovery Unit, Research, Takeda Pharmaceutical Co., Ltd., Fujisawa, Japan.
Koji FujitaDepartment of Neurology, Tokushima University Graduate School of Biomedical Sciences, Tokushima, Japan.
Motohisa SuzukiNeuroscience Drug Discovery Unit, Research, Takeda Pharmaceutical Co., Ltd., Fujisawa, Japan.
Akiyoshi KunugiNeuroscience Drug Discovery Unit, Research, Takeda Pharmaceutical Co., Ltd., Fujisawa, Japan.
Yoshihiko HirozaneNeuroscience Drug Discovery Unit, Research, Takeda Pharmaceutical Co., Ltd., Fujisawa, Japan.
Tomonori KunikataRare Disease & LCM Laboratories, Group II, R&D Division, Daiichi Sankyo Co., Ltd., Tokyo, Japan.
Bitoku TakahashiRare Disease & LCM Laboratories, Group II, R&D Division, Daiichi Sankyo Co., Ltd., Tokyo, Japan.
Genta NarazakiRare Disease & LCM Laboratories, Group II, R&D Division, Daiichi Sankyo Co., Ltd., Tokyo, Japan.
Hirofumi KondoRare Disease & LCM Laboratories, Group II, R&D Division, Daiichi Sankyo Co., Ltd., Tokyo, Japan.
Shotaro HajiDepartment of Neurology, Tokushima University Graduate School of Biomedical Sciences, Tokushima, Japan.
Keisuke HiraiNeuroscience Drug Discovery Unit, Research, Takeda Pharmaceutical Co., Ltd., Fujisawa, Japan.
Yuishin IzumiDepartment of Neurology, Tokushima University Graduate School of Biomedical Sciences, Tokushima, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The rate of disease progression varies widely among patients with amyotrophic lateral sclerosis (ALS). Prognostic assessment using biomarkers is highly anticipated to improve clinical trial design. We aimed to explore the cerebrospinal fluid (CSF) for prognostic biomarkers to predict future functional decline in patients with ALS. Methods: We collected CSF samples from 64 patients with ALS and 25 disease controls. The prospective progression rate was calculated using the Revised Amyotrophic Lateral Sclerosis Functional Rating Scale (ALSFRS-R) at CSF collection and in 6 months. The ALS patients were classified into slow, intermediate, and fast progression groups. We performed comprehensive proteomic analyses of the CSF samples. Factors with significant changes between slow and fast progression groups were investigated via receiver operating characteristic curve analyses. Moreover, the correlation of the CSF factors with progression rate was evaluated by multiple regression analyses. Results: In total, 26 proteins changed significantly ( Conclusion: This study demonstrated that CSF levels of neuroinflammation and glycosylation-related proteins were significantly correlated with prospective progression rates in patients with ALS. These proteins could be useful prognostic biomarkers for ALS.

Indexed as

amyotrophic lateral sclerosisbiomarkercerebrospinal fluidglycosylationneuroinflammationprogression rate

Identifiers

PMID39624674
PMCPMC11608993

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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.