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Empirical Classification of T-Wave Inversion Patterns as Lower-risk or Higher-risk in Black Adults: A Wall-Based Prevalence and Outcomes Analysis from the Jackson Heart Study.

Created on 26 Sep 2026

Authors

José Nunes de Alencar

Published in

Cardiology. Pages 1. Sep 25, 2026. Epub Sep 25, 2026.

Abstract

Background T-wave inversion (TWI) in Black adults is interpreted through criteria derived from White populations or competitive athletes, never tested with outcomes data in non-athletic community adults. Objective To classify TWI patterns as lower-risk or higher-risk using lead-specific outcomes thresholds, and derive a race-specific reference from a healthy subcohort. Methods We analyzed 3,514 Black adults from the Jackson Heart Study Exam 1 (2000-2004). A wall-based system classified higher-risk TWI as Tnet <-100 µV in lateral, anterior, or inferior leads; benign patterns were isolated V1 and isolated lead III. A healthy subcohort (N=668) free of hypertension, diabetes, obesity, CKD, coronary disease, heart failure, and left ventricular hypertrophy (LVH) ECG criteria served as reference. Logistic regression assessed cardiometabolic associations; Cox models assessed incident outcomes over median 11.8-year follow-up. Results Higher-risk TWI was present in 262 (7.5%; healthy: 3.0%); lower-risk patterns in 685 (19.5%). Higher-risk TWI independently predicted Hard coronary heart disease (CHD), with an adjusted hazard ratio of 2.47 (95% CI 1.51-4.04), and was associated with hypertension (OR 1.98) and ECG-LVH (OR 3.98). Benign V1 showed inverse associations with diabetes (OR 0.48) and LVH (OR 0.36), with 1 Hard CHD event during follow-up; the higher-risk effect was homogeneous across health strata (P-interaction=0.455). The classic V1-V2-V3 juvenile pattern occurred in 1 of 3,514; V3 inversion carried Hard CHD HR 3.49. Conclusion Anterior T-wave inversion in V2, V3, or V4 in non-athletic Black community-dwelling adults is not necessarily a benign signal and should not be assumed to represent a persistent juvenile variant. These data provide the first outcomes-anchored ECG reference for this population.

PMID:
42789464
Bibliographic data and abstract were imported from PubMed on 26 Sep 2026.

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