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Abdul A O Naas a Department of Clinical Pharmacology and
Therapeutics, Ninewells Hospital and Medical School, Dundee DD1 9SY, b Diabetes Centre, Ninewells Hospital and Medical School, c Department of Epidemiology,
Ninewells Hospital and Medical School
Correspondence to: Professor
Struthers
Patients with non-insulin dependent diabetes mellitus have
an excess risk of dying from cardiovascular disease. One small study
suggested that a prolonged QT interval could predict cardiac death in
patients with diabetic nephropathy who have received insulin treatment.
The question now is whether the same is true in newly diagnosed
diabetes in patients who have no apparent complications. In addition,
QT dispersion, a new but related electrocardiographic variable,
predicts cardiac death in patients who have chronic heart failure,
peripheral vascular disease, or essential
hypertension.1-3 We investigated whether it also
predicted cardiac death in diabetic patients.
The study group of 182 patients with non-insulin dependent
diabetes mellitus (103 men; mean age 52.8 (SD 8.5) years) represented the Dundee cohort of the United Kingdom prospective diabetes study, which was recruited between 1982 and 1988. Patients were followed up
for a mean of 10.3 (1.7) years. The inclusion and exclusion criteria of
the study have been reported elsewhere. Patients with overt cardiac
disease at baseline were excluded. A single observer (AAON) measured QT
intervals as described previously.1-3 Cardiac death was
mostly classified at the coordinating centre in Oxford, using the codes
of the international classification of diseases, ninth revision. All
analysis was done by Cox regression analysis, with cardiac death
as the sole end point. We used forward stepwise analysis, each time
using all three QT variables along with age, systolic blood pressure,
sex, smoking, blood glucose concentration, and antihypertensive drug.
As a result, we identified age, systolic blood pressure, sex,
diuretics, and all QT variables as the potentially important variables.
Finally we fitted the regression using these four variables with each
of the three QT variables.
In those who had a cardiac death, the mean time of death after the
baseline electrocardiogram was 7.3 (3.2) years; after the 3 year
electrocardiogram it was 4.9 (2.3) years and after the 6 year
electrocardiogram 3.8 (1.0) years. The table shows that QTc max, QTc
dispersion, and QT dispersion are all highly significant and
independent predictors of cardiac death at baseline, at 3 years, and at
6 years. In multivariate analysis they outperformed all other
predictors.
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Subjects, methods, and results
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Comment |
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Our main finding was that QT dispersion, QTc dispersion, and QTc max are excellent predictors of cardiac death in patients with non-insulin dependent diabetes mellitus. QTc interval analysis has two major advantages over other possible ways of stratifying risk in patients. Firstly, measurements of QTc interval are easily obtained with a non-invasive routine test: other potential predictors of cardiac death often require extra testing with specialised equipment. Secondly, comparisons between QTc dispersion and microalbuminuria suggest that QTc dispersion is a better predictor of cardiac death.4 A QTc dispersion >78 ms at year 6 in this study had 100% sensitivity and 90% specificity, giving an odds ratio of 9.0, whereas the odds ratio for microalbuminuria was only 1.8 in a recent overview.5
The question arises why analysis of QT interval should be able to predict cardiac death. QT dispersion may be a composite term reflecting electrical inhomogeneity as a result of ischaemia, left ventricular dilatation, left ventricular hypertrophy, cardiac fibrosis, and autonomic neuropathy. Each one of these individually confers increased cardiac risk, and this may be why QT dispersion, as a composite of them, is highly predictive of cardiac death. The clinical value of analysing the QT interval may therefore be that it could be used as a screening test to select diabetic patients for more extensive cardiac investigations. Importantly, the time between measuring a pro- longed QT interval and the subsequent cardiac death is many years, which provides ample opportunity to intervene.
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Acknowledgments |
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We thank Professor Robert Turner (Oxford) and Mr Phillip Bassett (United Kingdom prospective diabetes study centre) for their assistance. We would also like to thank Lynda G Dick and Marlyn F H Foster for their help in the Ninewells Diabetes Centre with the patients from the study.
Contributors: AAON analysed all the electrocardiograms and wrote the first draft of the paper. SO performed the statistical analysis. CT, NCD, and FC helped to extract data on each patient. RWN and RTJ ran the United Kingdom prospective diabetes study in Dundee. ADS supervised the project and wrote the final draft of the paper.
Funding: NCD was supported by the British Heart Foundation.
Conflict of interest: None.
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References |
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(Accepted 16 September 1997)