Electrocardiographic ST-T Area Assessed by a Computerized Quantitative Method and Its Relation to Cardiovascular Events: The J-HOP Study.


Journal

American journal of hypertension
ISSN: 1941-7225
Titre abrégé: Am J Hypertens
Pays: United States
ID NLM: 8803676

Informations de publication

Date de publication:
12 02 2019
Historique:
received: 26 09 2018
accepted: 06 12 2018
pubmed: 12 12 2018
medline: 12 5 2020
entrez: 12 12 2018
Statut: ppublish

Résumé

Although many studies have reported that the presence of minor or major ST-T change of electrocardiography (ECG) was associated with a risk of cardiovascular events, it is not clear whether there is a difference in the prognostic power depending on the summation of ST-T area (ST-Tarea) assessed by a quantitative method. Electrocardiograms were performed in 834 clinical patients with one or more cardiovascular risks. ST-Tarea was assessed as the area enclosed by the baseline from the end of the QRS complex to the end of the ST-T segment using a computerized quantitative method. We used the lower magnitude of ST-Tarea in the V5 or V6 lead for the analysis. After a mean follow-up 8.4 ± 2.9 years (7,001 person-years), there were 92 cardiovascular events. With adjustment for covariates, the results from Cox proportional hazards models (Model 1) suggested that the lowest quartile of ST-Tarea was associated with a higher risk for cardiovascular outcome compared with the remaining quartile groups (hazard ratio, 2.08; 95% confidence interval, 1.36-3.16, P < 0.01). Even when adding the ECG left ventricular hypertrophy by Cornell voltage (Model 2) and Cornell product (Model 3) to Model 1, the significance remained (both P < 0.01). When we used ST-Tarea as a continuous variable substitute for the lowest quartile of ST-Tarea, these associations were similar in all models (all P < 0.01). The lower summations of ST-T area assessed by a computerized quantitative method were associated with increased risk of cardiovascular disease incidence in a clinical population.

Sections du résumé

BACKGROUND
Although many studies have reported that the presence of minor or major ST-T change of electrocardiography (ECG) was associated with a risk of cardiovascular events, it is not clear whether there is a difference in the prognostic power depending on the summation of ST-T area (ST-Tarea) assessed by a quantitative method.
METHODS
Electrocardiograms were performed in 834 clinical patients with one or more cardiovascular risks. ST-Tarea was assessed as the area enclosed by the baseline from the end of the QRS complex to the end of the ST-T segment using a computerized quantitative method. We used the lower magnitude of ST-Tarea in the V5 or V6 lead for the analysis.
RESULTS
After a mean follow-up 8.4 ± 2.9 years (7,001 person-years), there were 92 cardiovascular events. With adjustment for covariates, the results from Cox proportional hazards models (Model 1) suggested that the lowest quartile of ST-Tarea was associated with a higher risk for cardiovascular outcome compared with the remaining quartile groups (hazard ratio, 2.08; 95% confidence interval, 1.36-3.16, P < 0.01). Even when adding the ECG left ventricular hypertrophy by Cornell voltage (Model 2) and Cornell product (Model 3) to Model 1, the significance remained (both P < 0.01). When we used ST-Tarea as a continuous variable substitute for the lowest quartile of ST-Tarea, these associations were similar in all models (all P < 0.01).
CONCLUSION
The lower summations of ST-T area assessed by a computerized quantitative method were associated with increased risk of cardiovascular disease incidence in a clinical population.

Identifiants

pubmed: 30535252
pii: 5236603
doi: 10.1093/ajh/hpy180
doi:

Types de publication

Journal Article Multicenter Study Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

282-288

Auteurs

Satoshi Hoshide (S)

Department of Medicine, Division of Cardiovascular Medicine, School of Medicine, Jichi Medical University, Tochigi, Japan.

Tomoyuki Kabutoya (T)

Department of Medicine, Division of Cardiovascular Medicine, School of Medicine, Jichi Medical University, Tochigi, Japan.

Tatsuya Yoneyama (T)

R&D Head Office, Fukuda Denshi Co., Ltd., Tokyo, Japan.

Kyohei Fukatani (K)

Academic Promotion Section, Fukuda Denshi Co., Ltd., Tokyo, Japan.

Kazuomi Kario (K)

Department of Medicine, Division of Cardiovascular Medicine, School of Medicine, Jichi Medical University, Tochigi, Japan.

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