Evidence map›Paper›PMID 17419875›Full record

ArticleBMC medical genetics2007

Genetic mapping of a new heart rate QTL on chromosome 8 of spontaneously hypertensive rats.

Gustavo J J Silva, Alexandre C Pereira, Eduardo M Krieger, José E Krieger

Open access · goldAbstract read
In one paragraph

Article in BMC medical genetics, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

8 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
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  5. The influence of sex and estrous cycle on QTL for emotionality and ethanol consumption.Mammalian genome : official journal of the International Mammalian Genome Society · 2011
    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

4 authors at 2 institutions in 1 country.

Gustavo J J SilvaDepartment of Medicine-LIM13, Heart Institute (InCor), University of São Paulo Medical School, Av, Dr, Enéas de Carvalho Aguiar, 44, 10o andar, 05403-000, São Paulo, SP, Brazil. gjjusto@usp.br
Alexandre C Pereira
Eduardo M Krieger
José E Krieger
Universidade de São Paulo · BRHospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTachycardia is commonly observed in hypertensive patients, predominantly mediated by regulatory mechanisms integrated within the autonomic nervous system. The genetic loci and genes associated with increased heart rate in hypertension, however, have not yet been identified.

methodsAn F2 intercross of Spontaneously Hypertensive Rats (SHR) x Brown Norway (BN) linkage analysis of quantitative trait loci mapping was utilized to identify candidate genes associated with an increased heart rate in arterial hypertension.

resultsBasal heart rate in SHR was higher compared to that of normotensive BN rats (365 +/- 3 vs. 314 +/- 6 bpm, p < 0.05 for SHR and BN, respectively). A total genome scan identified one quantitative trait locus in a 6.78 cM interval on rat chromosome 8 (8q22-q24) that was responsible for elevated heart rate. This interval contained 241 genes, of which 65 are known genes.

conclusionOur data suggest that an influential genetic region located on the rat chromosome 8 contributes to the regulation of heart rate. Candidate genes that have previously been associated with tachycardia and/or hypertension were found within this QTL, strengthening our hypothesis that these genes are, potentially, associated with the increase in heart rate in a hypertension rat model.

Indexed as

Quantitative Trait LociAnimalsBlood PressureChromosome MappingChromosomes, MammalianFemaleGenetic LinkageGenetic MarkersHeart RateMalePregnancyRatsRats, Inbred BNRats, Inbred SHRGenetic Markers

Identifiers

PMID17419875
PMCPMC1865373
OpenAlexW1988554226

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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.