Evidence map›Paper›PMID 33518522›Full record

ArticleBMJ open2021

Sex differences in vectorcardiogram of African-Americans with and without cardiovascular disease: a cross-sectional study in the Jackson Heart Study cohort.

James D Pollard, Kazi T Haq, Katherine J Lutz, Nichole M Rogovoy, Kevin A Paternostro, Elsayed Z Soliman, Joseph Maher, Joao Ac Lima, Solomon Musani, Larisa G Tereshchenko

Open access · goldAbstract read
In one paragraph

Article in BMJ open, 2021. 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
0.9field-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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
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

10 authors at 4 institutions in 1 country.

James D Pollard *University of Mississippi Medical Center, Jackson, Mississippi, USA.
Kazi T Haq *Department of Medicine, Cardiovascular Division, Oregon Health & Science University School of Medicine, Portland, Oregon, USA.
Katherine J LutzDepartment of Medicine, Cardiovascular Division, Oregon Health & Science University School of Medicine, Portland, Oregon, USA.
Nichole M RogovoyDepartment of Medicine, Cardiovascular Division, Oregon Health & Science University School of Medicine, Portland, Oregon, USA.
Kevin A PaternostroDepartment of Medicine, Cardiovascular Division, Oregon Health & Science University School of Medicine, Portland, Oregon, USA.
Elsayed Z SolimanEpidemiological Cardiology Research Center, Division of Public Health Sciences and Department of Medicine, Cardiology Section, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
Joseph MaherUniversity of Mississippi Medical Center, Jackson, Mississippi, USA.
Joao Ac LimaDepartment of Medicine, Cardiovascular Division, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Solomon MusaniUniversity of Mississippi Medical Center, Jackson, Mississippi, USA.
Larisa G TereshchenkoDepartment of Medicine, Cardiovascular Division, Oregon Health & Science University School of Medicine, Portland, Oregon, USA tereshch@ohsu.edu.ORCID 0000-0002-6976-1313
Oregon Health & Science University · USJackson Memorial Hospital · USJohns Hopkins University · USWake Forest University · US

Funding

Novel ECG Measures and Risk of Sudden Cardiac DeathR01HL118277 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI TERESHCHENKO, LARISA GENNADIEVNA · 2013 to 2016
$1.5M
Novel ECG measures and risk of sudden cardiac deathR56HL118277 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI TERESHCHENKO, LARISA GENNADIEVNA · 2018 to 2018
$396k
NHLBI NIH HHS HHSN268201800010INHLBI NIH HHS HHSN268201800011CNHLBI NIH HHS HHSN268201800011INHLBI NIH HHS HHSN268201800012CNHLBI NIH HHS HHSN268201800012INHLBI NIH HHS HHSN268201800014CNHLBI NIH HHS HHSN268201800014INHLBI NIH HHS HHSN268201800015INHLBI NIH HHS R01 HL118277NHLBI NIH HHS R56 HL118277NIMHD NIH HHS HHSN268201800013I
6 · The paper itself

Abstract

objectivesWe hypothesised that (1) the prevalent cardiovascular disease (CVD) is associated with global electrical heterogeneity (GEH) after adjustment for demographic, anthropometric, socioeconomic and traditional cardiovascular risk factors, (2) there are sex differences in GEH and (3) sex modifies an association of prevalent CVD with GEH.

designCross-sectional, cohort study.

settingProspective African-American The Jackson Heart Study (JHS) with a nested family cohort in 2000-2004 enrolled residents of the Jackson, Mississippi metropolitan area.

participantsParticipants from the JHS with analysable ECGs recorded in 2009-2013 (n=3679; 62±12 y; 36% men; 863 family units). QRS, T and spatial ventricular gradient (SVG) vectors' magnitude and direction, spatial QRS-T angle and sum absolute QRST integral (SAI QRST) were measured. OUTCOME: Prevalent CVD was defined as the history of (1) coronary heart disease defined as diagnosed/silent myocardial infarction, or (2) revascularisation procedure defined as prior coronary/peripheral arterial revascularisation, or (3) carotid angioplasty/carotid endarterectomy, or (4) stroke.

resultsIn adjusted mixed linear models, women had a smaller spatial QRS-T angle (-12.2 (95% CI -19.4 to -5.1)°; p=0.001) and SAI QRST (-29.8 (-39.3 to -20.3) mV*ms; p<0.0001) than men, but larger SVG azimuth (+16.2(10.5-21.9)°; p<0.0001), with a significant random effect between families (+20.8 (8.2-33.5)°; p=0.001). SAI QRST was larger in women with CVD as compared with CVD-free women or men (+15.1 (3.8-26.4) mV*ms; p=0.009). Men with CVD had a smaller T area (by 5.1 (95% CI 1.2 to 9.0) mV*ms) and T peak magnitude (by 44 (95%CI 16 to 71) µV) than CVD-free men. T vectors pointed more posteriorly in women as compared with men (peak T azimuth + 17.2(8.9-25.6)°; p<0.0001), with larger sex differences in T azimuth in some families by +26.3(7.4-45.3)°; p=0.006.

conclusionsThere are sex differences in the electrical signature of CVD in African-American men and women. There is a significant effect of unmeasured genetic and environmental factors on cardiac repolarisation.

Indexed as

Cardiovascular DiseasesBlack or African AmericanCohort StudiesCross-Sectional StudiesFemaleHumansLongitudinal StudiesMaleMississippiProspective StudiesRisk FactorsSex Characteristicsadult cardiologycardiac epidemiologycoronary heart diseasepacing & electrophysiology

Identifiers

PMID33518522
PMCPMC7852937
OpenAlexW3126153125

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.