Evidence map›Paper›PMID 27547430›Full record

ArticleOpen heart

Genomic ancestry as a predictor of haemodynamic profile in heart failure.

Sabrina Bernardez-Pereira, Luciana Gioli-Pereira, Fabiana G Marcondes-Braga, Paulo Caleb Junior Lima Santos, Joceli Mabel Rocha Spina, Andréa Roseli Vançan Russo Horimoto, Hadassa Campos Santos, Fernando Bacal, Fábio Fernandes, Alfredo Jose Mansur and 4 more

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Article in Open heart. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–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

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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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

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4 · The record

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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

14 authors.

Sabrina Bernardez-PereiraFluminense Federal University, Niteroi, Rio de Janeiro, Brazil; Heart Institute, University of São Paulo Medical School, Sao Paulo, Brazil.
Luciana Gioli-PereiraHeart Institute, University of São Paulo Medical School , Sao Paulo , Brazil.
Fabiana G Marcondes-BragaHeart Institute, University of São Paulo Medical School , Sao Paulo , Brazil.
Paulo Caleb Junior Lima SantosHeart Institute, University of São Paulo Medical School , Sao Paulo , Brazil.
Joceli Mabel Rocha SpinaHeart Institute, University of São Paulo Medical School , Sao Paulo , Brazil.
Andréa Roseli Vançan Russo HorimotoHeart Institute, University of São Paulo Medical School , Sao Paulo , Brazil.
Hadassa Campos SantosHeart Institute, University of São Paulo Medical School , Sao Paulo , Brazil.
Fernando BacalHeart Institute, University of São Paulo Medical School , Sao Paulo , Brazil.
Fábio FernandesHeart Institute, University of São Paulo Medical School , Sao Paulo , Brazil.
Alfredo Jose MansurHeart Institute, University of São Paulo Medical School , Sao Paulo , Brazil.
Ricardo PietrobonUniversity of California , San Francisco, California , USA.
José Eduardo KriegerHeart Institute, University of São Paulo Medical School , Sao Paulo , Brazil.
Evandro Tinoco MesquitaFluminense Federal University , Niteroi, Rio de Janeiro , Brazil.
Alexandre Costa PereiraHeart Institute, University of São Paulo Medical School , Sao Paulo , Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe aim of this study is to assess the association between genetic ancestry, self-declared race and haemodynamic parameters in patients with chronic heart failure (HF).

methodsObservational, cross-sectional study. Eligible participants were aged between 18 and 80 years; ejection fraction was ≤50%. Patients underwent genetic analysis of ancestry informative markers, echocardiography and impedance cardiography (ICG). Race was determined by self-classification into two groups: white and non-white. Genomic ancestry was estimated using a panel of 101 348 polymorphic markers and three continental reference populations (European, African and Native American).

resultsOur study included 362 patients with HF between August 2012 and August 2014. 123 patients with HF declared themselves as white and 234 patients declared themselves as non-white. No statistically significant differences were found regarding the ICG parameters according to self-declared race. The Amerindian ancestry was positively correlated with systolic time ratio (r=0.109, p<0.05). The thoracic fluid content index (r=0.124. p<0.05), E wave peak (r=0.127. p<0.05) and E/e' ratio (r=0.197. p<0.01) were correlated positively with African ancestry. In multiple linear regression, African ancestry remained associated with the E/e' ratio, even after adjustment to risk factors.

conclusionsThe African genetic ancestry was associated with worse parameters of diastolic function; the Amerindian ancestry correlated with a worse pattern of ventricular contractility, while self-declared colour was not helpful to infer haemodynamic profiles in HF. TRIALS REGISTRATION NUMBER: NTC02043431.

Indexed as

HEART FAILURE

Identifiers

PMID27547430
PMCPMC4975862

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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.