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Association of longer QT interval with arterial waveform and lower pulse pressure amplification: the Nagahama Study
Yasuharu Tabara1, Yoshimitsu Takahashi, Katsuhiko Kohara
1Center for Genomic Medicine, Kyoto University Graduate School of Medicine, Kyoto, Japan. tabara@genome.med.kyoto-u.ac.jp
Insights
A longer QT interval is linked to arterial waveform changes and reduced pulse pressure amplification, suggesting a connection to cardiovascular risk. Shorter QRS duration also showed a significant association with these arterial measures.
Area of Science:
- Cardiology
- Physiology
- Biomedical Engineering
Background:
- Central systolic blood pressure (cSBP) is a key cardiovascular risk indicator.
- Prolonged QT interval is associated with adverse cardiovascular outcomes.
- Investigating electrocardiogram (ECG) wave intervals' association with arterial waveform is crucial for understanding cardiovascular risk.
Purpose of the Study:
- To explore the relationship between ECG wave intervals and central systolic blood pressure (cSBP).
- To identify potential links between arterial waveform characteristics and ECG parameters in the general population.
Main Methods:
- Simultaneous measurement of brachial blood pressure and radial arterial waveform.
- Calculation of augmentation index (AIx) from radial waveform.
- Definition of cSBP as the peak pressure of the late systolic wave.
Main Results:
- A significant association was found between longer QT interval and increased AIx (r = 0.330, P < 0.001), even after heart rate adjustment (r = 0.184, P < 0.001).
- Longer corrected QT interval independently predicted increased AIx and smaller pulse pressure amplification (PPa) (β = -0.066, P < 0.001).
- Shorter QRS duration was positively associated with PPa (β = 0.056, P < 0.001).
Conclusions:
- Longer QT interval and shorter QRS duration are significantly associated with arterial waveform properties and PPa.
- These findings may help elucidate mechanisms underlying increased cardiovascular risk in individuals with prolonged QT intervals.
Background:
Central systolic blood pressure (cSBP) has been postulated to correlate closely with cardiovascular risk. Identifying factors associated with cSBP is therefore important. Prolonged QT interval is known to be associated with cardiovascular outcomes and might also be associated with the arterial waveform and cSBP. We investigated the possible associations between electrocardiogram wave interval and cSBP in general population samples.
Methods:
Brachial blood pressure and radial arterial waveform were measured simultaneously. Augmentation index (AIx) was calculated from the radial waveform as the ratio of the height of the late systolic peak to that of the first peak. cSBP was defined as the absolute pressure of the late systolic peak.
Results:
In the first panel (n = 8,085), QT interval was strongly association with AIx (r = 0.330; P < 0.001). This association remained significant even in the heart rate-adjusted analysis (r = 0.184; P < 0.001). Although subjects with a longer QT interval were older and had higher blood pressure, heart rate, and pulse wave velocity, multivariable analysis with adjustment for these covariables nevertheless identified longer corrected QT interval as an independent determinant of increased AIx and smaller pulse pressure amplification (PPa; brachial SBP minus cSBP) (β = -0.066; P < 0.001). This association was replicated in the independent second panel (n = 1,412) (β = -0.105; P < 0.001). In contrast, QRS interval was positively associated with PPa (β = 0.056; P < 0.001).
Conclusions:
Longer QT interval and short QRS duration were significantly associated with arterial waveform and PPa. Our results provide a clue to the elucidation of unidentified mechanisms of the increased cardiovascular outcome and mortality risks in subjects with longer QT interval.
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