Evidence map›Paper›PMID 40076577›Full record

ReviewInternational journal of molecular sciences2025

Biomarkers in Hereditary Spastic Paraplegias.

Emanuele Panza, Antonio Orlacchio

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. SPOAN Syndrome in Southern Brazil: Case Report and New Insights.Movement disorders clinical practice · 2026
    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

2 authors.

Emanuele PanzaDipartimento di Scienze Mediche e Chirurgiche, Università di Bologna, 40138 Bologna, Italy.ORCID 0000-0002-2338-1139
Antonio OrlacchioDipartimento di Medicina e Chirurgia, Università di Perugia, 06123 Perugia, Italy.ORCID 0000-0002-2602-3281

Funding

Dipartimento di Medicina e Chirurgia of the Università di Perugia Grants n. DSCH_BASE19_ORLACCHIO and RICERCABASE_2020_ORLACCHIO to A.O.Ministero della Salute Grant n. RF19.12 to A.O.Ministero dell'università e della ricerca Grant n. CN00000041 to E.Pa.Università di Perugia Grant n. RICERCA_ATENEO_ALIMENTAZIONE to A.O.
6 · The paper itself

Abstract

Hereditary spastic paraplegias (HSPs) represent a group of neurodegenerative disorders characterized by progressive spasticity and weakness in the lower limbs, with no specific treatment available for patients. At the same time, the molecular diagnosis is complicated by the high genetic heterogeneity of this group of diseases, and it can be challenging due to overlapping clinical features with other conditions. Reliable biomarkers could play a fundamental role in diagnosis, prognosis, and therapeutic interventions for HSPs. For this reason, it is necessary to increase the search for biomarkers that can be used to rapidly classify HSPs, follow the natural history of the conditions, and monitor disease correction therapies. This article provides an overview of the current understanding of biomarkers in HSPs, including genetic, biochemical, and clinical biomarkers and new cell imaging-based approaches. In this manuscript, we aim to provide an overview of the current situation in HSP biomarkers, emphasizing the limitations and the necessity of conducting more studies in this field.

Indexed as

BiomarkersSpastic Paraplegia, HereditaryArtificial IntelligenceHumansImage Processing, Computer-AssistedBiomarkersbiochemical markersclinical biomarkershereditary spastic paraplegiasimaging biomarkers

Identifiers

PMID40076577
PMCPMC11899947

What OpenQuestion holds

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LicenceCC BY
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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.