Evidence map›Paper›PMID 37679868›Full record

ArticleEuropean journal of neurology2024

SerpinA1 levels in amyotrophic lateral sclerosis patients: An exploratory study.

Ilaria Martinelli, Elisabetta Zucchi, Cecilia Simonini, Giulia Gianferrari, Roberta Bedin, Chiara Biral, Andrea Ghezzi, Nicola Fini, Serena Carra, Jessica Mandrioli

Open access · hybridAbstract read
In one paragraph

Article in European journal of neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

9 citing papers in PubMed, 10 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

10 authors at 2 institutions in 1 country.

Ilaria MartinelliDepartment of Neurosciences, Azienda Ospedaliero Universitaria di Modena, Modena, Italy.ORCID 0000-0003-2566-3671
Elisabetta ZucchiDepartment of Neurosciences, Azienda Ospedaliero Universitaria di Modena, Modena, Italy.
Cecilia SimoniniDepartment of Neurosciences, Azienda Ospedaliero Universitaria di Modena, Modena, Italy.
Giulia GianferrariDepartment of Biomedical, Metabolic and Neural Sciences, University of Modena and Reggio Emilia, Modena, Italy.
Roberta BedinDepartment of Neurosciences, Azienda Ospedaliero Universitaria di Modena, Modena, Italy.
Chiara BiralDepartment of Biomedical, Metabolic and Neural Sciences, University of Modena and Reggio Emilia, Modena, Italy.
Andrea GhezziDepartment of Biomedical, Metabolic and Neural Sciences, University of Modena and Reggio Emilia, Modena, Italy.
Nicola FiniDepartment of Neurosciences, Azienda Ospedaliero Universitaria di Modena, Modena, Italy.
Serena CarraDepartment of Biomedical, Metabolic and Neural Sciences, University of Modena and Reggio Emilia, Modena, Italy.
Jessica MandrioliDepartment of Neurosciences, Azienda Ospedaliero Universitaria di Modena, Modena, Italy.
University of Modena and Reggio Emilia · ITAzienda Ospedaliero-Universitaria di Modena · IT

Funding

Agenzia di Ricerca per la Sclerosi Laterale Amiotrofica bando per la ricerca clinica 2015Agenzia Italiana del Farmaco, Ministero della Salute grant number 2016-02364678Fondazione Cassa di Risparmio di Modena Neurobiobanca di ModenaMinistero della Salute bando per la ricerca finalizzata 2016, grant number RF-2016-02361616Università Degli Studi di Modena e Reggio Emila bando FAR 2021, Progetti di ricerca Interdisciplinari Mission Oriented, NEURALS project
6 · The paper itself

Abstract

backgroundSerpinA1, a serine protease inhibitor, is involved in the modulation of microglial-mediated inflammation in neurodegenerative diseases. We explored SerpinA1 levels in cerebrospinal fluid (CSF) and serum of amyotrophic lateral sclerosis (ALS) patients to understand its potential role in the pathogenesis of the disease.

methodsSerpinA1, neurofilament light (NfL) and heavy (NfH) chain, and chitinase-3-like protein-1 (CHI3L1) were determined in CSF and serum of ALS patients (n = 110) and healthy controls (n = 10) (automated next-generation ELISA), and correlated with clinical parameters, after identifying three classes of progressors (fast, intermediate, slow). Biomarker levels were analyzed for diagnostic power and association with progression and survival.

resultsSerpinA1

conclusionsHigher SerpinA1

Indexed as

Amyotrophic Lateral SclerosisBiomarkersDisease ProgressionHumansNeurofilament ProteinsPrognosisBiomarkersNeurofilament ProteinsALSbiomarkerserpinA1

Identifiers

PMID37679868
PMCPMC11235621
OpenAlexW4386529662

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.