Evidence map›Paper›PMID 34379200›Full record

ArticleJournal of neurology2022

Role of the nigrosome 1 absence as a biomarker in amyotrophic lateral sclerosis.

María Isabel Moreno-Gambín, José I Tembl, Miguel Mazón, Antonio José Cañada-Martínez, Luis Martí-Bonmatí, Teresa Sevilla, Juan F Vázquez-Costa

Open access · hybridAbstract read
In one paragraph

Article in Journal of neurology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
0.1field-weighted citation impact, top 52% 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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 4 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. 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

7 authors at 3 institutions in 1 country.

María Isabel Moreno-GambínNeurosonology Laboratory, Department of Neurology, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
José I TemblNeurosonology Laboratory, Department of Neurology, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
Miguel MazónRadiology and Biomedical Imaging Research Group (GIBI230), Hospital Universitario y Politécnico La Fe, Valencia, Spain.
Antonio José Cañada-MartínezBiostatistics Unit, Instituto de Investigación Sanitaria la Fe (IIS La Fe), Valencia, Spain.
Luis Martí-BonmatíRadiology and Biomedical Imaging Research Group (GIBI230), Hospital Universitario y Politécnico La Fe, Valencia, Spain.
Teresa SevillaALS Unit, Department of Neurology, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
Juan F Vázquez-CostaALS Unit, Department of Neurology, Hospital Universitario y Politécnico La Fe, Valencia, Spain. juan.vazquez@uv.es.ORCID http://orcid.org/0000-0002-3043-7938
Hospital Universitari i Politècnic La Fe · ESUniversitat de València · ESInstituto de Investigación Sanitaria La Fe · ES

Funding

Conselleria de Sanitat Universal i Salut Pública 2018/135Instituto de Salud Carlos III (ES) 19/01178 PIInstituto de Salud Carlos III (ES) JR19/00030 PI
6 · The paper itself

Abstract

introductionThe absence of nigrosome 1 on brain MRI and the hyperechogenicity of substantia nigra (SNh) by transcranial sonography are two useful biomarkers in the diagnosis of parkinsonisms. We aimed to evaluate the absence of nigrosome 1 in amyotrophic lateral sclerosis (ALS) and to address its meaning.

methods136 ALS patients were recruited, including 16 progressive muscular atrophy (PMA) and 22 primary lateral sclerosis (PLS) patients. The SNh area was measured planimetrically by standard protocols. The nigrosome 1 status was qualitatively assessed by two blind evaluators in susceptibility weight images of 3T MRI. Demographic and clinical data were collected and the C9ORF72 expansion was tested in all patients.

resultsNigrosome 1 was absent in 30% of ALS patients (36% of PLS, 29% of classical ALS and 19% of PMA patients). There was no relationship between radiological and clinical laterality, nor between nigrosome 1 and SNh area. Male sex (OR = 3.63 [1.51, 9.38], p = 0.005) and a higher upper motor neuron (UMN) score (OR = 1.10 [1.02, 1.2], p = 0.022) were independently associated to nigrosome 1 absence, which also was an independent marker of poor survival (HR = 1.79 [1.3, 2.8], p = 0.013).

conclusionIn ALS patients, the absence of nigrosome 1 is associated with male sex, UMN impairment and shorter survival. This suggests that constitutional factors and the degree of pyramidal involvement are related to the substantia nigra involvement in ALS. Thus, nigrosome 1 could be a marker of a multisystem degeneration, which in turn associates to poor prognosis.

Indexed as

Amyotrophic Lateral SclerosisMotor Neuron DiseaseMuscular Atrophy, SpinalBiomarkersHumansMagnetic Resonance ImagingMaleMotor NeuronsBiomarkersAmyotrophic lateral sclerosisHyperechogenicity of substantia nigraNigrosome 1Primary lateral sclerosisProgressive muscular atrophyUltrasound

Identifiers

PMID34379200
PMCPMC8857168
OpenAlexW3188683437

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.