Evidence map›Paper›PMID 26385028›Full record

ArticleAmerican heart journal2015

Genetic mutations in African patients with atrial fibrillation: Rationale and design of the Study of Genetics of Atrial Fibrillation in an African Population (SIGNAL).

Gerald S Bloomfield, Tecla M Temu, Constantine O Akwanalo, Peng-Sheng Chen, Wilfred Emonyi, Susan R Heckbert, Myra M Koech, Imran Manji, Changyu Shen, Matteo Vatta and 4 more

Open access · greenAbstract readMulticenter Study
In one paragraph

Article in American heart journal, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 24% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

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  4. Review
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

14 authors at 8 institutions in 2 countries.

Gerald S BloomfieldDepartment of Medicine, Duke University, Durham, NC; Duke Clinical Research Institute and Duke Global Health Institute, Duke University, Durham, NC. Electronic address: gerald.bloomfield@duke.edu.
Tecla M TemuDepartment of Epidemiology, Brown University School of Public Health, Providence, RI.
Constantine O AkwanaloDivision of Medicine, Moi Teaching and Referral Hospital, Eldoret, Kenya; AMPATH Partnership, Eldoret, Kenya.
Peng-Sheng ChenKrannert Institute of Cardiology, Indiana University, Indianapolis, IN; Department of Medicine, Indiana University, Indianapolis, IN.
Wilfred EmonyiDivision of Medicine, Moi Teaching and Referral Hospital, Eldoret, Kenya; AMPATH Partnership, Eldoret, Kenya.
Susan R HeckbertDepartment of Epidemiology, University of Washington, Seattle, WA.
Myra M KoechDivision of Medicine, Moi Teaching and Referral Hospital, Eldoret, Kenya.
Imran ManjiDivision of Medicine, Moi Teaching and Referral Hospital, Eldoret, Kenya; AMPATH Partnership, Eldoret, Kenya.
Changyu ShenDepartment of Biostatistics, Indiana University School of Medicine, Richard M. Fairbanks School of Public Health, Indiana University, Indianapolis, IN.
Matteo VattaDepartment of Medicine, Indiana University, Indianapolis, IN; Department of Medical and Molecular Genetics, Indiana University, Indianapolis, IN.
Eric J VelazquezDepartment of Medicine, Duke University, Durham, NC; Duke Clinical Research Institute and Duke Global Health Institute, Duke University, Durham, NC.
Jennifer WesselDepartment of Medicine, Indiana University, Indianapolis, IN.
Sylvester KimaiyoDivision of Medicine, Moi Teaching and Referral Hospital, Eldoret, Kenya; AMPATH Partnership, Eldoret, Kenya; Department of Medicine, School of Medicine, College of Health Sciences, Moi University, Eldoret, Kenya.
Thomas S InuiAMPATH Partnership, Eldoret, Kenya; Department of Medicine, Indiana University, Indianapolis, IN; Department of Medicine, School of Medicine, College of Health Sciences, Moi University, Eldoret, Kenya.
Moi University · KEIndiana University – Purdue University Indianapolis · USAMPATH · KEBrown University · USClinical Research Institute · USDuke University · USIndiana University School of MedicineUniversity of Washington · US

Funding

Quality Assurance and Quality Control Project Management: Improving Submissions and Study Conduct in the Human Subjects Research Prior Approval ProcessUL1TR002529 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI MOE, SHARON M, WIEHE, SARAH ELIZABETH · 2018 to 2022
$27.2M
Indiana Clinical and Translational Sciences InstituteUL1TR001108 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI DENNE, SCOTT C., SHEKHAR, ANANTHA · 2013 to 2017
$23.3M
WAVE DYNAMICS IN NORMAL AND DISEASED RABBIT HEARTSP01HL078931 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WEISS, JAMES · 2005 to 2015
$20.7M
Thoracic Veins and Sustained Atrial FibrillationR01HL071140 · NHLBI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI CHEN, PENG-SHENG · 2002 to 2014
$4.7M
Risk Factors for Atherosclerosis among Patients with Heart Failure in KenyaK01TW008407 · FIC · DUKE UNIVERSITY · PI BLOOMFIELD, GERALD SAMUEL · 2011 to 2014
$490k
Interactive Vagal Stimulation and Atrial FibrillationR21HL106554 · NHLBI · INDIANA UNIVERSITY INDIANAPOLIS · PI LIN, SHIEN-FONG · 2011 to 2012
$424k
Sympathetic Nerve Activity Recorded From the Skin and Cardiac ArrhythmiasR41HL124741 · NHLBI · ARRHYTHMOTECH, LLC · PI EVERETT, THOMAS H · 2014 to 2014
$213k
FIC NIH HHS K01 TW008407FIC NIH HHS K01TW008407NCATS NIH HHS UL1 TR001108NHLBI NIH HHS HHSN268200900031CNHLBI NIH HHS P01 HL078931NHLBI NIH HHS P01 HL78931NHLBI NIH HHS R01 HL071140NHLBI NIH HHS R01 HL71140NHLBI NIH HHS R21 HL106554NHLBI NIH HHS R41 HL124741NHLBI NIH HHS R41HL124741PHS HHS HHSN268200900031C
6 · The paper itself

Abstract

backgroundThere is an urgent need to understand genetic associations with atrial fibrillation in ethnically diverse populations. There are no such data from sub-Saharan Africa, despite the fact that atrial fibrillation is one of the fastest growing diseases. Moreover, patients with valvular heart disease are underrepresented in studies of the genetics of atrial fibrillation.

methodsWe designed a case-control study of patients with and without a history of atrial fibrillation in Kenya. Cases with atrial fibrillation included those with and without valvular heart disease. Patients underwent clinical phenotyping and will have laboratory analysis and genetic testing of >240 candidate genes associated with cardiovascular diseases. A 12-month follow-up assessment will determine the groups' morbidity and mortality. The primary analyses will describe genetic and phenotypic associations with atrial fibrillation.

resultsWe recruited 298 participants: 72 (24%) with nonvalvular atrial fibrillation, 78 (26%) with valvular atrial fibrillation, and 148 (50%) controls without atrial fibrillation. The mean age of cases and controls were 53 and 48 years, respectively. Most (69%) participants were female. Controls more often had hypertension (45%) than did those with valvular atrial fibrillation (27%). Diabetes and current tobacco smoking were uncommon. A history of stroke was present in 25% of cases and in 5% of controls.

conclusionThis is the first study determining genetic associations in valvular and nonvalvular atrial fibrillation in sub-Saharan Africa with a control population. The results advance knowledge about atrial fibrillation and will enhance international efforts to decrease atrial fibrillation-related morbidity.

Indexed as

MutationAtrial FibrillationDNADNA Mutational AnalysisEchocardiographyElectrocardiographyFemaleFollow-Up StudiesGenetic Association StudiesHumansKenyaMaleMiddle AgedMorbidityPopulation SurveillanceRetrospective StudiesDNA

Identifiers

PMID26385028
PMCPMC4575772
OpenAlexW2107920410

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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.