Evidence mapPaperPMID 38617564Full record

ArticleiScience2024

Unveiling the pathophysiology of restless legs syndrome through transcriptome analysis.

Maria P Mogavero, Michele Salemi, Giuseppe Lanza, Antonio Rinaldi, Giovanna Marchese, Maria Ravo, Maria Grazia Salluzzo, Amedeo Antoci, Lourdes M DelRosso, Oliviero Bruni and 2 more

Open access · goldAbstract read
In one paragraph

Article in iScience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
10.4field-weighted citation impact, top 1% 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

19 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. The evolving treatment landscape of restless legs syndrome.Therapeutic advances in neurological disorders · 2026
    Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Evidence of Involvement of the Calcitonin Gene-Related Peptide in Restless Legs Syndrome.Movement disorders : official journal of the Movement Disorder Society · 2025
    Article
  13. Article
  14. Review
  15. Article
  16. Association between inflammatory cytokines and disease severity in restless legs syndrome.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2024
    Article
  17. Review
  18. Article
  19. 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

12 authors at 6 institutions in 2 countries.

Maria P MogaveroVita-Salute San Raffaele University, 20132 Milan, Italy.
Michele SalemiOasi Research Institute-IRCCS, 94018 Troina, Italy.
Giuseppe LanzaOasi Research Institute-IRCCS, 94018 Troina, Italy.
Antonio RinaldiGenomix4Life Srl, 84081 Baronissi, Italy.
Giovanna MarcheseGenomix4Life Srl, 84081 Baronissi, Italy.
Maria RavoGenomix4Life Srl, 84081 Baronissi, Italy.
Maria Grazia SalluzzoOasi Research Institute-IRCCS, 94018 Troina, Italy.
Amedeo AntociOasi Research Institute-IRCCS, 94018 Troina, Italy.
Lourdes M DelRossoUniversity of California San Francisco-Fresno, Fresno, CA 93721, USA.
Oliviero BruniSapienza University of Rome, Developmental and Social Psychology, 00185 Rome, Italy.
Luigi Ferini-StrambiVita-Salute San Raffaele University, 20132 Milan, Italy.
Raffaele FerriOasi Research Institute-IRCCS, 94018 Troina, Italy.
Oasi Maria SS · ITCenter for Genomic Science · ITVita-Salute San Raffaele University · ITSapienza University of Rome · ITUniversity of California, San Francisco · USUniversity of Catania · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to analyze signaling pathways associated with differentially expressed messenger RNAs in people with restless legs syndrome (RLS). Seventeen RLS patients and 18 controls were enrolled. Coding RNA expression profiling of 12,857 gene transcripts by next-generation sequencing was performed. Enrichment analysis by pathfindR tool was carried-out, with p-adjusted ≤0.001 and fold-change ≥2.5. Nine main different network groups were significantly dysregulated in RLS: infections, inflammation, immunology, neurodegeneration, cancer, neurotransmission and biological, blood and metabolic mechanisms. Genetic predisposition plays a key role in RLS and evidence indicates its inflammatory nature; the high involvement of mainly neurotropic viruses and the TORCH complex might trigger inflammatory/immune reactions in genetically predisposed subjects and activate a series of biological pathways-especially IL-17, receptor potential channels, nuclear factor kappa-light-chain-enhancer of activated B cells, NOD-like receptor, mitogen-activated protein kinase, p53, mitophagy, and ferroptosis-involved in neurotransmitter mechanisms, synaptic plasticity, axon guidance, neurodegeneration, carcinogenesis, and metabolism.

Indexed as

BioinformaticsNeurologyTranscriptomics

Identifiers

PMID38617564
PMCPMC11015462
OpenAlexW4393198100

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.