Evidence map›Paper›PMID 33999292›Full record

ArticleNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology2022

Identification of a novel mutation in MEF2C gene in an atypical patient with frontotemporal lobar degeneration.

Andreia Adrião, Isabel Santana, Carolina Ribeiro, M Leonor Cancela, Natércia Conceição, Manuela Grazina

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Article in Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 34% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. 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

6 authors at 3 institutions in 1 country.

Andreia AdriãoCentre of Marine Sciences/CCMAR, University of Algarve, Faro, Portugal.
Isabel SantanaCentro Hospitalar e Universitário de Coimbra, Coimbra, Portugal.
Carolina RibeiroCNC- Center for Neuroscience and Cell Biology, University of Coimbra - Laboratory of Mitochondrial BioMedicine and Theranostics, Coimbra, Portugal.
M Leonor CancelaCentre of Marine Sciences/CCMAR, University of Algarve, Faro, Portugal.
Natércia ConceiçãoCentre of Marine Sciences/CCMAR, University of Algarve, Faro, Portugal. nconcei@ualg.pt.ORCID http://orcid.org/0000-0002-5057-0912
Manuela GrazinaFaculty of Medicine, University of Coimbra, Pólo III - Subunit I, Azinhaga de Sta. Comba Celas PT, 3000-548, Coimbra, Portugal. mgrazina.fmuc@gmail.com.
University of Algarve · PTUniversity of Coimbra · PTHospitais da Universidade de Coimbra · PT

Funding

Fundação para a Ciência e a Tecnologia PEst-C/SAU/LA0001/2013-2014Fundação para a Ciência e a Tecnologia PTDC/SAU-EPI/121811/2010Fundação para a Ciência e a Tecnologia UIDB/04326/2020 (CCMAR)
6 · The paper itself

Abstract

The MEF2C gene encodes a transcription factor known to play a crucial role in molecular pathways affecting neuronal development. MEF2C mutations were described as a genetic cause of developmental disease (MRD20), and several reports sustain its involvement in dementia-related conditions, such as Alzheimer's disease and amyotrophic lateral sclerosis. These pathologies and frontotemporal degeneration (FTLD) are thought to share common physiopathological pathways. In this exploratory study, we searched for alterations in the DNA sequence of exons and boundaries, including 5'- and 3'-untranslated regions (5'UTR, 3'UTR), of MEF2C gene in 11 patients with clinical phenotypes related with MRD20 or FTLD. We identified a heterozygous deletion of 13 nucleotides in the 5'UTR region of a 69 years old FTLD patient. This alteration was absent in 200 healthy controls, suggesting a contribution to this patient's disease phenotype. In silico analysis of the mutated sequence indicated changes in mRNA secondary structure and stability, thus potentially affecting MEF2C protein levels. Furthermore, in vitro functional analysis of this mutation revealed that the presence of this deletion abolished the transcriptional activity of the gene in human embryonic cells and rat brain neurons, probably by modifying MEF2C expression. Altogether, our results provide evidence for the involvement of MEF2C in FTLD manifesting with seizures.

Indexed as

Frontotemporal Lobar DegenerationMEF2 Transcription FactorsAgedHumansMutationMEF2C protein, humanMEF2 Transcription Factors5′ Untranslated region (5′UTR)Frontotemporal lobar degeneration (FTLD)Mental retardation autosomal dominant syndrome-20 disease (MRD20)Myocyte-specific enhancer factor 2 (MEF2C)

Identifiers

PMID33999292
OpenAlexW3162456864

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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.