Pk. Christensen et al., QTc interval length and QT dispersion as predictors of mortality in patients with non-insulin-dependent diabetes, SC J CL INV, 60(4), 2000, pp. 323-332
Citations number
28
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology","Medical Research General Topics
Journal title
SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION
Patients with non-insulin-dependent diabetes (NIDDM) are at independent ris
k of cardiovascular death. The reason is only partially understood. The aim
of our study was therefore to evaluate the impact of corrected QT interval
length (QTc) and QT dispersion (QT-disp) on mortality in a cohort of 324 C
aucasian NIDDM patients. A resting 12-lead ECG was recorded at baseline. Ma
ximum (QT-max) and minimum QT (QT-min) intervals were measured, and QT-max
was corrected for heart rate (QTc-max). QT-disp was defined as the differen
ce between QT-max and QT-min. QTc-max was 454 (376-671) ms(1/2) (median (ra
nge)) and QT-disp 61 (0-240) ms. Prolonged QTc interval (PQTc), defined as
QTc-max >440 ms(1/2), was present in 67% of the patients and prolonged QT-d
isp (PQT-disp), defined as QT-disp>50 ms, was present in 51%. During the 9-
year follow-up period, 100 patients died (52 from cardiovascular diseases).
Thirty-seven percent of the patients with PQTc died compared with 17% with
normal QTc interval (p<0.001). The Cox proportional hazard model, includin
g putative risk factors at baseline, revealed the following independent pre
dictors of all cause mortality; QTc-max (p<0.05), age (p<0.0001), albuminur
ia (p<0.01), retinopathy (p<0.01), HbA1c (p<0.05), insulin treatment (p<0.0
1), total cholesterol (p<0.01), serum creatinine (p<0.05) and presence of c
ardiac heart disease based on Minnesota coded ECG (p<0.001). Whereas QT-dis
p was not a predictor. QTc-max interval was an independent predictor of car
diovascular mortality. Our study showed a high prevalence of QTc and QT-dis
p abnormalities and indicated that QTc-max but not QT-disp is an independen
t predictor of all cause and cardiovascular mortality in NIDDM patients.