Evidence map›Paper›PMID 34683186›Full record

ArticleJournal of personalized medicine2021

Influence of Polymorphism on the

Esdras E B Pereira, Darlen C de Carvalho, Luciana P C Leitão, Juliana C G Rodrigues, Antônio A C Modesto, Evitom C de Sousa, Sidney E B Dos Santos, Marianne R Fernandes, Ney P C Dos Santos

Abstract read
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In one paragraph

Article in Journal of personalized medicine, 2021. 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
–field-weighted citation impact
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.

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

9 authors.

Esdras E B PereiraLaboratory of Human and Medical Genetics, Institute of Biological Science, Federal University of Pará, Belém 66077-830, Pará, Brazil.ORCID 0000-0003-4830-4233
Darlen C de CarvalhoOncology Research Center, Federal University of Pará, Belém 66073-005, Pará, Brazil.
Luciana P C LeitãoOncology Research Center, Federal University of Pará, Belém 66073-005, Pará, Brazil.ORCID 0000-0002-1635-7288
Juliana C G RodriguesOncology Research Center, Federal University of Pará, Belém 66073-005, Pará, Brazil.ORCID 0000-0003-1665-3535
Antônio A C ModestoLaboratory of Human and Medical Genetics, Institute of Biological Science, Federal University of Pará, Belém 66077-830, Pará, Brazil.ORCID 0000-0003-1854-0358
Evitom C de SousaResistance Exercise and Health Laboratory, State University of Pará, Belém 66095-049, Pará, Brazil.ORCID 0000-0002-4002-239X
Sidney E B Dos SantosLaboratory of Human and Medical Genetics, Institute of Biological Science, Federal University of Pará, Belém 66077-830, Pará, Brazil.
Marianne R FernandesOncology Research Center, Federal University of Pará, Belém 66073-005, Pará, Brazil.ORCID 0000-0002-1396-3442
Ney P C Dos SantosLaboratory of Human and Medical Genetics, Institute of Biological Science, Federal University of Pará, Belém 66077-830, Pará, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSarcopenia is a disease characterized by progressive reduction in muscle mass and strength or function. Although it is known that sarcopenia may be associated with environmental factors, studies suggest the identification of genes related to skeletal muscle maintenance that explain the susceptibility to the disease.

objectiveTo analyze the influence of

methodsThis is a case-control study, which included 219 elderly people, 74 elderly people with sarcopenia, and 145 without sarcopenia. Samples were analyzed for

resultsIt was observed that the

conclusionThe INDEL polymorphism of the

Indexed as

genetic biomarkersNFkB1sarcopeniaskeletal muscle

Identifiers

PMID34683186
PMCPMC8537608

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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.