Correlation between T wave alternans and endomyocardial biopsy findings in patients with dilated cardiomyopathy
Markus Zabel
Authors: Heinz P Schultheiss; Christian Sticherling; Michel Noutsias; Uwe Kühl; Markus Zabel; Steffen Behrens
2:15 - 2:30

Background and Objective: Patients (pts) with dilated cardiomyopathy (DCM) frequently suffer from malignant ventricular arrhythmias. T wave alternans (TWA) testing has been proposed for risk stratification, however, the genesis of the high incidence of positive (pos) TWA in DCM pts is as yet unknown. Fibrosis and immunohistochemically proven intramyocardial inflammation in endomyocardial biopsies (EMB) are common features of DCM patients. We therefore hypothesized that TWA positivity is related to pathological EMB findings in DCM. Methods: TWA was assessed in n=103 DCM pts (LVEF: 38 +/- 16%) utilizing the Cambridge Heart exercise method. Pos TWA was defined as a TWA amplitude > 1.9 mV for > 1 min in > 1 ECG lead. Tracings were graded "indeterminate" if noise or premature ventricular beats prevented definite classification into pos or negative (neg) TWA or the heart rate threshold was not reached. Fibrosis was assessed with standardized histological techniques, and intramyocardial inflammation (CD2/CD3+ T-lymphocyte infiltrates >7.0 mm2, abundance of cell adhesion molecules/CAMs: HLA class I, HLA DR, ICAM-1) was analyzed immunohistochemically, respectively. Results: In 51/103 pts (50%), TWA was graded pos, in 41/103 pts (40%) TWA was found neg, while the remaining tests were indeterminate. Significantly increased CD2/CD3+ T-lymphocytes were found in 22/103 EMB specimens, 64/103 (62%) demonstrated CAMs abundance, and 68/103 patients (66%) showed interstitial fibrosis, respectively. TWA positivity was significantly associated with LVEF (47 +/- 13% if TWA neg, vs. 27 +/- 9% if TWA pos, vs. 42 +/- 12% if TWA indeterminate, p = 0.004). However, the TWA finding did not correlate with interstitial fibrosis (yes/no: 35/68=51% vs. 16/35=46% pos TWA, p=ns), T-lymphocytic infiltration (CD2/CD3+ infiltrates yes/no: 12/22=55% vs. 39/81=48% pos TWA, p=ns) and CAMs abundance (yes/no: 28/64=44% vs. 23/39=59% pos TWA, p=ns). Conclusions: TWA testing yields a pos finding in 50% of DCM pts. The TWA result is unrelated to histological and immunohistological EMB findings (fibrosis and intramyocardial inflammation) but particularly depends on LVEF.