Principal component analysis of the T wave and prediction of cardiovascular mortality in American Indians: the Strong Heart Study. Academic Article uri icon

Overview

abstract

  • BACKGROUND: Increased QT interval dispersion (QTd) is a proposed ECG marker of vulnerability to ventricular arrhythmias and of cardiovascular (CV) mortality. However, principal component analysis (PCA) of the T-wave vector loop may more accurately represent repolarization abnormalities than QTd. METHODS AND RESULTS: Predictive values of QTd and PCA were assessed in 1839 American Indian participants in the first Strong Heart Study examination. T-wave loop morphology was quantified by the ratio of the second to first eigenvalues of the T-wave vector by PCA (PCA ratio); QTd was quantified as the difference between maximum and minimum QT intervals. After 3.7+/-0.9 years mean follow-up, there were 55 CV deaths. In univariate analyses, an increased PCA ratio predicted CV mortality in women (chi2=7.8, P=0.0053) and men (chi2=9.5, P=0.0021). In contrast, increased QTd was a significant predictor of CV mortality in women (chi2=30.6, P<0.0001) but not in men (chi2=2.0, P=NS). In multivariate Cox analyses controlling for risk factors and rate-corrected QT interval, the PCA ratio remained a significant predictor of CV mortality in women (chi2=4.0 P=0.043) and men (chi2=6.4, P=0.011); QTd was a significant predictor in women only (chi2=11.0, P=0.0009). PCA ratios >90th percentile (32% in women and 24.6% in men) identified women with a 3.68-fold increased risk of CV mortality (95% CI, 1.54 to 8.83) and men with a 2.77-fold increased risk (95% CI, 1.18 to 6.49). CONCLUSIONS: Abnormalities of repolarization measured by PCA of the T-wave loop predict CV death in men and women, supporting use of PCA for quantifying repolarization abnormalities.

publication date

  • February 12, 2002

Research

keywords

  • Cardiovascular Diseases
  • Electrocardiography
  • Indians, North American
  • Principal Component Analysis

Identity

Scopus Document Identifier

  • 0037065917

Digital Object Identifier (DOI)

  • 10.1161/hc0602.103585

PubMed ID

  • 11839627

Additional Document Info

volume

  • 105

issue

  • 6