Evidence map›Paper›PMID 30334187›Full record

ArticleMolecular neurobiology2019

SNAP25 Gene Polymorphisms Protect Against Parkinson's Disease and Modulate Disease Severity in Patients.

Cristina Agliardi, Franca Rosa Guerini, Milena Zanzottera, Giulio Riboldazzi, Roberta Zangaglia, Andrea Sturchio, Carlo Casali, Cherubino Di Lorenzo, Brigida Minafra, Raffaello Nemni and 1 more

Abstract read
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In one paragraph

Article in Molecular neurobiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

9 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
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  7. Association Analyses ofNeuropsychiatric disease and treatment · 2021
    Article
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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

11 authors at 5 institutions in 1 country.

Cristina AgliardiIRCCS Fondazione Don Carlo Gnocchi, Milano, Italy. cagliardi@dongnocchi.it.ORCID http://orcid.org/0000-0003-2022-3386
Franca Rosa GueriniIRCCS Fondazione Don Carlo Gnocchi, Milano, Italy.
Milena ZanzotteraIRCCS Fondazione Don Carlo Gnocchi, Milano, Italy.
Giulio RiboldazziCenter for Parkinson's Disease and Movement Disorders, Ospedale di Circolo e Fondazione Macchi, Varese, Italy.
Roberta ZangagliaParkinson's disease and Movement Disorders Unit, IRCCS National Neurological Institute C. Mondino, Pavia, Italy.
Andrea SturchioNeurology Unit-Varese, Insubria University Varese, Varese, Italy.
Carlo CasaliDepartment of Medical-Surgical Sciences and Biotechnologies, University of Rome, Rome, Italy.
Cherubino Di LorenzoIRCCS Fondazione Don Carlo Gnocchi, Milano, Italy.
Brigida MinafraParkinson's disease and Movement Disorders Unit, IRCCS National Neurological Institute C. Mondino, Pavia, Italy.
Raffaello NemniIRCCS Fondazione Don Carlo Gnocchi, Milano, Italy.
Mario ClericiIRCCS Fondazione Don Carlo Gnocchi, Milano, Italy.
Don Carlo Gnocchi Foundation · ITUniversity of Milan · ITOspedale di Circolo e Fondazione Macchi · ITUniversità Campus Bio-Medico · ITUniversity of Insubria · IT

Funding

Italian Ministry of Health RC2015
6 · The paper itself

Abstract

Parkinson's disease (PD) is a α-synucleinopathy in which intracellular aggregates of α-synuclein (α-syn) result in neurodegeneration and in the impairment of the soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) complex-mediated release of neurotransmitters. SNAP25 is a SNARE complex component: its concentration is increased in the cerebrospinal fluid of PD patients and this is related to the severity of cognitive and motor symptoms. Five SNAP25 single-nucleotide polymorphisms (SNPs) that modulate gene expression and were described to play a role in neurologic conditions (rs363050, rs363039, rs363043, rs3746544, and rs1051312) were analyzed in a cohort of 412 sporadic Italian PD patients and 1103 healthy controls (HC) in order to identify possible correlation with the disease. The SNAP25 rs1051312 C allele and CC genotype confer protection against PD onset, in particular in males (p = 0.003, OR(95%CI) = 0.67(0.51-0.88)) (p

Indexed as

Genetic Predisposition to DiseaseNeuroprotectionSeverity of Illness IndexAgedAllelesCase-Control StudiesFemaleHaplotypesHumansLinkage DisequilibriumMaleParkinson DiseasePolymorphism, Single NucleotideSynaptosomal-Associated Protein 25SNAP25 protein, humanSynaptosomal-Associated Protein 25GeneticsParkinson’s diseasePDPolymorphismSNAP25SNP

Identifiers

PMID30334187
OpenAlexW2896080446

What OpenQuestion holds

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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.