Evidence map›Paper›PMID 40285624›Full record

ArticleAnnals of neurology2025

Phosphatemia is an Independent Prognostic Factor in Amyotrophic Lateral Sclerosis.

Rosario Vasta, Emanuele Koumantakis, Antonio Canosa, Umberto Manera, Maurizio Grassano, Francesca Palumbo, Sara Cabras, Enrico Matteoni, Francesca Di Pede, Filippo De Mattei and 9 more

Abstract read
In one paragraph

Article in Annals of neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

19 authors.

Rosario VastaALS Center, Department of Neuroscience "Rita Levi Montalcini", University of Turin, Turin, Italy.ORCID 0000-0002-0393-4736
Emanuele KoumantakisDepartment of Public Health and Pediatrics, University of Turin, Turin, Italy.
Antonio CanosaALS Center, Department of Neuroscience "Rita Levi Montalcini", University of Turin, Turin, Italy.ORCID 0000-0001-5876-4079
Umberto ManeraALS Center, Department of Neuroscience "Rita Levi Montalcini", University of Turin, Turin, Italy.
Maurizio GrassanoALS Center, Department of Neuroscience "Rita Levi Montalcini", University of Turin, Turin, Italy.
Francesca PalumboALS Center, Department of Neuroscience "Rita Levi Montalcini", University of Turin, Turin, Italy.
Sara CabrasALS Center, Department of Neuroscience "Rita Levi Montalcini", University of Turin, Turin, Italy.ORCID 0000-0002-4988-2855
Enrico MatteoniALS Center, Department of Neuroscience "Rita Levi Montalcini", University of Turin, Turin, Italy.
Francesca Di PedeALS Center, Department of Neuroscience "Rita Levi Montalcini", University of Turin, Turin, Italy.
Filippo De MatteiALS Center, Department of Neuroscience "Rita Levi Montalcini", University of Turin, Turin, Italy.
Filippo VergnanoALS Center, Department of Neuroscience "Rita Levi Montalcini", University of Turin, Turin, Italy.
Jessica MandrioliDepartment of Biomedical, Metabolic and Neural Sciences, University of Modena and Reggio Emilia, Modena, Italy.
Cecilia SimoniniDepartment of Neurosciences, Azienda Ospedaliero-Universitaria Di Modena, Modena, Italy.ORCID 0000-0001-5456-2365
Ilaria MartinelliDepartment of Neurosciences, Azienda Ospedaliero-Universitaria Di Modena, Modena, Italy.ORCID 0000-0003-2566-3671
Fabiola De MarchiALS Center, Department of Neurology, Azienda Ospedaliero Universitaria Maggiore Della Carità, University of Piemonte Orientale, Novara, Italy.
Letizia MazziniALS Center, Department of Neurology, Azienda Ospedaliero Universitaria Maggiore Della Carità, University of Piemonte Orientale, Novara, Italy.
Cristina MogliaALS Center, Department of Neuroscience "Rita Levi Montalcini", University of Turin, Turin, Italy.
Andrea CalvoALS Center, Department of Neuroscience "Rita Levi Montalcini", University of Turin, Turin, Italy.ORCID 0000-0002-5122-7243
Adriano ChiòALS Center, Department of Neuroscience "Rita Levi Montalcini", University of Turin, Turin, Italy.ORCID 0000-0001-9579-5341

Funding

European Commission's Health Seventh Framework Programme 259867European Union's Horizon 2020 research and innovation programme 101137074European Union's Horizon 2020 research and innovation programme GA101017598Ministero della Salute PNRR-MAD-2022-12375731Ministero della Salute RF-2016-02362405Ministero dell'Istruzione, dell'Università e della Ricerca 2017SNW5MB
6 · The paper itself

Abstract

objectiveThe objective of this study was to evaluate the prognostic value of several muscle damage biomarkers.

methodsData from Piemonte and Valle d'Aosta Amyotrophic Lateral Sclerosis (PARALS) were considered for this study. Survival was defined as the time from diagnosis to death, tracheostomy, or the censoring date. Blood levels of potassium, creatinine, creatine kinase, phosphorus, aspartate aminotransferase (AST) and alanine aminotransferase (ALT) diagnosis were evaluated as potential prognostic biomarkers. A Cox model was developed for each biomarker and adjusted for sex, onset age, onset site, and diagnostic delay. Significant findings from PARALS were evaluated in the Pooled Resource Open-Access Amyotrophic Lateral Sclerosis Clinical Trials (PRO-ACT) database. Additionally, a joint model was constructed to evaluate the prognostic role of phosphatemia slope over time using longitudinal data from PRO-ACT.

resultsA total of 1,444 and 1,023 patients were included in the PARALS and PRO-ACT cohorts, respectively. Only creatinine (hazard ratio [HR] = 0.65, 95% confidence interval [CI] = 0.50-0.85) and phosphorus (HR = 1.14, 95% CI = 1.04-1.24) showed a significant association with survival in the PARALS cohort. These findings were further validated in the PRO-ACT cohort (creatinine HR = 0.21, 95% CI = 0.13-0.35, p < 0.0001; phosphorus HR = 2.35, 95% CI = 1.13-4.88, p = 0.02). Longitudinal data from the PRO-ACT database showed that an increase of 0.1 mmol/l per month in phosphate levels was also associated with a HR of 8.26 (95% CI = 1.07-96.6, p = 0.044).

interpretationCreatininemia was confirmed as a prognostic marker in amyotrophic lateral sclerosis (ALS). Additionally, both phosphatemia levels at diagnosis and its rate of change over time were identified as a potential prognostic marker for ALS. As with other blood biomarkers, phosphate levels are cost-effective and minimally invasive to measure, supporting their potential use in clinical trials. ANN NEUROL 2025;98:286-293.

Indexed as

Amyotrophic Lateral SclerosisHyperphosphatemiaPhosphatesAdultAgedBiomarkersCreatinineFemaleHumansMaleMiddle AgedPhosphorusPrognosisBiomarkersCreatininePhosphatesPhosphorus

Identifiers

PMID40285624
PMCPMC12278033

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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.