Evidence map›Paper›PMID 31686392›Full record

ArticleJournal of molecular neuroscience : MN2020

Genetic Alterations in Patients with Two Clinical Phenotypes of Multiple Sclerosis.

Luciana Maria Feliciano, André Luiz Ventura Sávio, João Paulo de Castro Marcondes, Glenda Nicioli da Silva, Daisy Maria Fávero Salvadori

Open access · greenAbstract read
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In one paragraph

Article in Journal of molecular neuroscience : MN, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 46% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

5 authors at 4 institutions in 1 country.

Luciana Maria FelicianoFaculty of Medicine, UNESP-São Paulo State University, Botucatu, SP, Brazil.
André Luiz Ventura SávioHealth Science Dept., UNINOVE-Nove de Julho University, Bauru, SP, Brazil.
João Paulo de Castro MarcondesCESMAC-University Center, Maceió, AL, Brazil.
Glenda Nicioli da SilvaFaculty of Pharmacy, UFOP-Federal University of Ouro Preto, Ouro Preto, MG, Brazil.
Daisy Maria Fávero SalvadoriFaculty of Medicine, UNESP-São Paulo State University, Botucatu, SP, Brazil. daisy.salvadori@unesp.br.ORCID http://orcid.org/0000-0001-9323-3134
Universidade Estadual Paulista (Unesp) · BRCentro Universitário Cesmac · BRUniversidade Federal de Ouro Preto · BRUniversidade Nove de Julho · BR

Funding

CNPq (CNPq - 471312/2012-6)
6 · The paper itself

Abstract

The etiology of multiple sclerosis (MS) is still not known, but the interaction of genetic, immunological, and environmental factors seem to be involved. This study aimed to investigate genetic alterations and the vitamin D status in patients with relapsing-remitting MS (RRMS) and secondary progressive MS (SPMS). A total of 53 patients (29 RRMS; 24 SPMS) and 25 healthy subjects were recruited to evaluate the micronucleated cell (MNC) frequency and nuclear abnormalities in the buccal mucosa, gene expression profiling in mononuclear cells, and plasmatic vitamin D concentration in the blood. Results showed a higher frequency of cells with karyorrhexis (SPMS) and lower frequencies of nuclear pyknosis (RRMS and SPMS) and karyolysis (SPMS) in patients with MS. Significant increase in the frequency of MNC was detected in the buccal mucosa of RRMS and SPMS patients. HIF1A, IL13, IL18, MYC, and TNF were differentially expressed in MS patients, and APP was overexpressed in cells of RRMS compared to SPMS patients. No relationship was observed between vitamin D level and the differentially expressed genes. In conclusion, the cytogenetic alterations in the buccal mucosa can be important indicators of genetic instability and degenerative processes in patients with MS. Furthermore, our data introduced novel biomarkers associated with the molecular pathogenesis of MS.

Indexed as

Micronuclei, Chromosome-DefectivePhenotypeAdultCells, CulturedFemaleHumansHypoxia-Inducible Factor 1, alpha SubunitInterleukin-13Interleukin-18MaleMiddle AgedMouth MucosaMultiple Sclerosis, Relapsing-RemittingProto-Oncogene Proteins c-mycTumor Necrosis Factor-alphaHIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitInterleukin-13Interleukin-18Proto-Oncogene Proteins c-mycTumor Necrosis Factor-alphaBiomarkersBuccal mucosaMicronucleated cellMultiple sclerosisVitamin D

Identifiers

PMID31686392
OpenAlexW2986931446

What OpenQuestion holds

Textmetadata
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.