Modulation of the QT interval duration in hypertension with antihypertensive treatment

被引:27
作者
Klimas, Jan [1 ]
Kruzliak, Peter [2 ,3 ]
Rabkin, Simon W. [4 ]
机构
[1] Comenius Univ, Fac Pharm, Dept Pharmacol & Toxicol, Bratislava, Slovakia
[2] St Annes Univ Hosp, Int Clin Res Ctr, Dept Cardiovasc Dis, Brno 65691, Czech Republic
[3] Masaryk Univ, Brno 65691, Czech Republic
[4] Univ British Columbia, Dept Med, Div Cardiol, Vancouver, BC, Canada
关键词
antihypertensive treatment; arterial hypertension; electrocardiography; left ventricular hypertrophy; QT interval duration; LEFT-VENTRICULAR HYPERTROPHY; CONVERTING-ENZYME-INHIBITION; TORSADE-DE-POINTES; SYMPATHETIC-NERVOUS-SYSTEM; SUDDEN CARDIAC DEATH; CALCIUM-CHANNEL BLOCKADE; RENIN-ANGIOTENSIN SYSTEM; HEART-RATE-VARIABILITY; ACQUIRED LONG QT; BLOOD-PRESSURE;
D O I
10.1038/hr.2015.30
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
The duration of the QT interval as measured by 12-lead electrocardiography is a measure of myocardial repolarization and is widely used to describe cardiac abnormalities, to determine the presence of cardiac toxicity and to evaluate drug safety. In hypertension, the QT interval is a predictor of the risk of both coronary events and cardiovascular death, after adjusting for the effects of additional risk factors. The mechanism of QT interval prolongation is multifactorial and includes cardiomyocyte hypertrophy and increased left ventricular mass, with accompanying changes in left ventricular transmural dispersion of repolarization, as well as changes in the tone of the autonomic nervous system of some patients with hypertension and mechano-electrical feedback, although this mechanism is less likely. Antihypertensive drugs vary in their effect on QT interval duration. The mechanisms underlying their effect depend on changes in left ventricular mass and autonomic nervous system tone, as well as changes in the activity of cardiac ion channels. Although blood pressure reduction is the primary goal of antihypertensive drug therapy and although the choice of antihypertensive drug treatment regimens varies among different individuals, the data regarding the disparate effects of antihypertensive drugs on the duration of the QT interval warrant consideration when implementing long-term pharmacotherapy for hypertension.
引用
收藏
页码:447 / 454
页数:8
相关论文
共 138 条
[1]   Cellular and ionic mechanism for drug-induced long QT syndrome and effectiveness of verapamil [J].
Aiba, T ;
Shimizu, W ;
Inagaki, M ;
Noda, T ;
Miyoshi, S ;
Ding, WG ;
Zankov, DP ;
Toyoda, F ;
Matsuura, H ;
Horie, M ;
Sunagawa, K .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2005, 45 (02) :300-307
[2]   Continuous administration of nicorandil decreases QT dispersion during the chronic phase of acute myocardial infarction [J].
Akagi, Tadasu ;
Sarazawa, Katsuhiro ;
Inai, Yoshihito ;
Kitagawa, Motoaki ;
Takahashi, Nobuki ;
Hamanaka, Ichiro ;
Yamazaki, Taketoshi ;
Takebe, Masato ;
Hama, Norio ;
Hiraoka, Yuji ;
Ueda, Kinzo ;
Nakazawa, Kiyoshi ;
Matsumoto, Naoki .
INTERNATIONAL HEART JOURNAL, 2006, 47 (03) :351-361
[3]   Renin-angiotensin system and sympathetic nervous system in cardiac pressure-overload hypertrophy [J].
Akers, WS ;
Cross, A ;
Speth, R ;
Dwoskin, LP ;
Cassis, LA .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2000, 279 (06) :H2797-H2806
[4]   Associations of Hemodynamic Load and Ventricular Repolarization in Patients With Newly Diagnosed Essential Hypertension: A Long- Term Follow- Up Study [J].
Antonakis, Velissaris ;
Tsioufis, Costas ;
Tsiachris, Dimitris ;
Andrikou, Ioannis ;
Fantaki, Maria ;
Dagres, Nikos ;
Vrachnis, Nikos ;
Stefanadis, Christodoulos .
JOURNAL OF CLINICAL HYPERTENSION, 2014, 16 (03) :219-224
[5]   Ionic, molecular, and cellular bases of QT-interval prolongation and torsade de pointes [J].
Antzelevitch, Charles .
EUROPACE, 2007, 9 :4-15
[6]   Electrical and structural remodeling of the failing ventricle [J].
Armoundas, AA ;
Wu, R ;
Juang, G ;
Marbán, E ;
Tomaselli, GF .
PHARMACOLOGY & THERAPEUTICS, 2001, 92 (2-3) :213-230
[7]   Dihydropyridine action on voltage-dependent potassium channels expressed in Xenopus oocytes [J].
Avdonin, V ;
Shibata, EF ;
Hoshi, T .
JOURNAL OF GENERAL PHYSIOLOGY, 1997, 109 (02) :169-180
[8]   Significance at late ventricular potentials in myotonic dystrophy [J].
Babuty, D ;
Fauchier, L ;
Tena-Carbi, D ;
Poret, P ;
Leche, J ;
Raynoud, M ;
Fauchier, JP ;
Cosnay, P .
AMERICAN JOURNAL OF CARDIOLOGY, 1999, 84 (09) :1099-+
[9]   Converting enzyme inhibition normalizes QT interval in spontaneously hypertensive rats [J].
Baillard, C ;
Mansier, P ;
Ennezat, PV ;
Mangin, L ;
Medigue, C ;
Swynghedauw, B ;
Chevalier, B .
HYPERTENSION, 2000, 36 (03) :350-354
[10]   Electrogram prolongation and nifedipine-suppressible ventricular arrhythmias in mice following targeted disruption of KCNE1 [J].
Balasubramaniam, R ;
Grace, AA ;
Saumarez, RC ;
Vandenberg, JI ;
Huang, CLH .
JOURNAL OF PHYSIOLOGY-LONDON, 2003, 552 (02) :535-546