Evidence map›Paper›PMID 33167591›Full record

ArticleInternational journal of molecular sciences2020

Amyotrophic Lateral Sclerosis Is Accompanied by Protein Derangements in the Olfactory Bulb-Tract Axis.

Mercedes Lachén-Montes, Naroa Mendizuri, Karina Ausin, Pol Andrés-Benito, Isidro Ferrer, Joaquín Fernández-Irigoyen, Enrique Santamaría

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-weighted citation impact, top 21% 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

12 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Olfactory status in neurodegeneration with brain iron accumulation disorders.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2024
    Article
  6. Article
  7. Article
  8. Sensory Involvement in Amyotrophic Lateral Sclerosis.International journal of molecular sciences · 2022
    Review
  9. Review
  10. Article
  11. Article
  12. 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 2 institutions in 1 country.

Mercedes Lachén-MontesClinical Neuroproteomics Unit, Navarrabiomed, Complejo Hospitalario de Navarra (CHN), Universidad Pública de Navarra (UPNA), Irunlarrea 3, 31008 Pamplona, Spain.
Naroa MendizuriClinical Neuroproteomics Unit, Navarrabiomed, Complejo Hospitalario de Navarra (CHN), Universidad Pública de Navarra (UPNA), Irunlarrea 3, 31008 Pamplona, Spain.
Karina AusinProteored-ISCIII, Proteomics Platform, Navarrabiomed, Complejo Hospitalario de Navarra (CHN), Universidad Pública de Navarra (UPNA), Irunlarrea 3, 31008 Pamplona, Spain.ORCID 0000-0003-4914-9466
Pol Andrés-BenitoBellvitge Biomedical Research Institute (IDIBELL), 08908 Hospitalet de Llobregat, Spain.ORCID 0000-0003-3000-0338
Isidro FerrerBellvitge Biomedical Research Institute (IDIBELL), 08908 Hospitalet de Llobregat, Spain.ORCID 0000-0001-9888-8754
Joaquín Fernández-IrigoyenClinical Neuroproteomics Unit, Navarrabiomed, Complejo Hospitalario de Navarra (CHN), Universidad Pública de Navarra (UPNA), Irunlarrea 3, 31008 Pamplona, Spain.ORCID 0000-0001-5072-4099
Enrique SantamaríaClinical Neuroproteomics Unit, Navarrabiomed, Complejo Hospitalario de Navarra (CHN), Universidad Pública de Navarra (UPNA), Irunlarrea 3, 31008 Pamplona, Spain.ORCID 0000-0001-8046-8102
Universidad Publica de Navarra · ESInstituto de Salud Carlos III · ES

Funding

Department of Economic and Business Development from Government of Navarra 0011-1411-2020-000028Ministry of Economy and Competiveness, Institute of Health Carlos III (ISCIII) FISPI17/000809Spanish Ministry of Science Innovation and Universities PID2019-110356RB-I00
6 · The paper itself

Abstract

Amyotrophic lateral sclerosis (ALS) is a fatal disease characterized by progressive muscle paralysis due to the degeneration of upper and lower motor neurons. Recent studies point out an involvement of the non-motor axis during disease progression. Despite smell impairment being considered a potential non-motor finding in ALS, the pathobiochemistry at the olfactory level remains unknown. Here, we applied an olfactory quantitative proteotyping approach to analyze the magnitude of the olfactory bulb (OB) proteostatic imbalance in ALS subjects (

Indexed as

AgedAmyotrophic Lateral SclerosisDisease ProgressionDNA-Binding ProteinsFemaleFrontotemporal Lobar DegenerationGlial Fibrillary Acidic ProteinHumansInclusion BodiesMaleMiddle AgedMotor NeuronsOlfaction DisordersOlfactory BulbProteomeProteomicsDNA-Binding ProteinsGFAP protein, humanGlial Fibrillary Acidic ProteinProteomeTARDBP protein, humanAmyotrophic lateral sclerosisolfactory bulbolfactory tractproteomicssignalingTDP-43 proteinopathy

Identifiers

PMID33167591
PMCPMC7664257
OpenAlexW3097955897

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.