Journals / Dicle Tıp Dergisi / 2010 / Cilt: 37 - Sayı: 2

Hipertansif hastalarda valsartan ve nebivololun, kan basıncı, QT dağılımı ve sol ventrikül hipertrofsi üzerine etkileri

Effects of valsartan and nebivolol on blood pressure, QT dispersion and left ventricular hypertrophy in hypertensive patients

Pages
81–88
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Both therapies were effective in reducing the LVH; Valsartan proved to be superior to Nebivolol in reducing the QT interval indexes in relation to blood pressure and LVM reduction.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Objectives: The aim of this study was to analyze the antihypertensive effect of Valsartan and Nebivolol and their effects on QT dispersion and left ventricular hypertrophy (LVH) in the treatment of naive hypertensive patients.
📊
Key Findings & Data:Methods: A prospective study with a six-month follow-up was conducted on hypertensive patients with LVH and mild/ moderate essential hypertension.
💡
Conclusion & Impact:Both therapies were effective in reducing the LVH; Valsartan proved to be superior to Nebivolol in reducing the QT interval indexes in relation to blood pressure and LVM reduction.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Objectives: The aim of this study was to analyze the antihypertensive effect of Valsartan and Nebivolol and their effects on QT dispersion and left ventricular hypertrophy (LVH) in the treatment of naive hypertensive patients. Methods: A prospective study with a six-month follow-up was conducted on hypertensive patients with LVH and mild/ moderate essential hypertension. The patients were randomly assigned to Valsartan (80 to 160 mg/day) or Nebivolol (5 to 10 mg/day) groups. The study group consisted of 108 patients, 55 in the Valsartan group and 53 in the Nebivolol group. Results: The range of mean systolic blood pressure (SBP) varied from 152±17 (baseline) to 132±17 mmHg (follow-up) in the Valsartan group (p<0.001); from 146±13 to 125±14 mmHg in the Nebivolol group (p<0.001). The decrease in mean diastolic blood pressure (DBP) was 9.5±2.5 mmHg in the Valsartan group and 12.3±5.0 mmHg in the Nebivolol group. A signifcant reduction in QT and corrected QT (Bazett&#8217;s formula) dispersion was observed in both groups, with a slightly higher reduction in the Valsartan group. Echocardiography showed a de- crease in the left ventricle mass (LVM) indices (p<0.05) in both groups with a greater reduction in the Valsartan group. Conclusion: Valsartan treatment was as effective as Nebivolol in reducing the 24 hour- SBP after a 6 month treatment. Nebivolol treatment proved to be superior to Valsartan in reducing DBP. Both therapies were effective in reducing the LVH; Valsartan proved to be superior to Nebivolol in reducing the QT interval indexes in relation to blood pressure and LVM reduction.

Özet

Amaç: Bu çalışmanın amacı valsartan ve nebivololun antihipertansif etkilerini ve bu ilaçların hipertansif hastaların tedavisinde QT dağılımı ve sol ventrikül hipertrofsi üzerine etkilerini analiz etmektir. Yöntemler: Sol ventrikül hipertrofsi (SVH) bulunan haff/orta hipertansiyonlu hastalarda 6 ay süreli takip içeren prospektif bir çalışma düzenlendi. Hastalar rastgele olarak Valsartan (80-160 mg/gün) veya Nebivolol (5-10 mg/gün) gruplarına alındı. Çalışma grubu 55’i Valsartan grubu, 53’ü Nebivolol grubunda olmak üzere toplam 108 hastadan oluşturuldu. Bulgular: Valsartan grubunda ortalama sistolik kan basıncı (SKB) 152±17 mmHg (bazal)’den 132±17 mmHg (takip)’e değişti (p<0.001). Nebivolol grubunda ise ortalama SKB, 146±13 mmHg (bazal)’den 125±14 mmHg (takip)’e değişti (p<0.001). Valsartan grubunda ortalama diyastolik kan basıncı (DBP) azalması 9.5±2.5 mmHg ve Nebivolol grubunda 12.3±5.0 mmHg idi. Her iki grupta da QT ve düzeltilmiş QT (Bazett formülü) dağılımında anlamlı azalma gözlendi ve bu azalma Valsartan grubunda haffçe daha fazla idi. Ekokardiyograf sol venrikül kitle (SVK) indekslerinde Valsartan grubunda daha fazla azalma ile birlikte her iki grupta azalmayı gösterdi (p<0.05). Sonuç: Valsartan tedavisi 24 saatlik SKB’ında 6 aylık tedavi ile Nebivolol kadar etkili bulundu. Nebivolol tedavisi DKB’ını düşürmede Valsartan tedavisine üstün bulundu. Her iki tedavi SVH’sini azaltmada etkili idi. Valsartan kan basıncı ve SVK’de azalmayla birlikte QT aralık indekslerinde azaltmada Nebivolole üstün bulundu.

🔖

Cite This Article

LATEA, L., NEGREA, Ş. L., BOLBOACA, S. D. (2010). Hipertansif hastalarda valsartan ve nebivololun, kan basıncı, QT dağılımı ve sol ventrikül hipertrofsi üzerine etkileri. Dicle Tıp Dergisi, Cilt: 37 - Sayı: 2, 81–88. https://ajindex.com/articles/349192

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (18)

  1. Kannel WB. Left ventricular hypertrophy as a risk factor in arterial hypertension. Eur Heart J 1992;13:82-8
  2. Savage DD, Garrison RJ, Kannel WB, et al. The spectrum of left ventricular hypertrophy in a general population sample: the Framingham study. Circulation 1987;75:126-33
  3. Priori SG, Schwartz PJ, Napolitano C, et al. Risk stratifcation in the long QT syndrome. N Engl J Med 2003;348:1866-74
  4. Bazett HC. An analysis of the time-relations of electrocardiograms. Heart 1920;7:353-70
  5. Oikarinen L, Nieminen MS, Viitasalo M, et al. LIFE Study Investigators. QRS duration and QT interval predict mortality in hypertensive patients with left ventricular hypertrophy. Hypertension 2004;43:1029-34
  6. Rasmussen KG, Hooten WM, Dodd ML, Ryan DA.QTc dispersion on the baseline ECG predicts arrhythmias during electroconvulsive therapy. Acta Cardiol 2007;62:345-7
  7. Yildirir A, Batur MK, Oto A. Hypertension and arrhythmia: blood pressure control and beyond. Europace 2002;4:175-82
  8. Klingbeil AU, Schneider M, Martus P, et al. A meta-analysis of the effects of treatment on left ventricular mass in essential hypertension. Am J Med 2003;115 41-6
  9. Cuspidi C, Negri F, Zanchetti A. Angiotensin II receptor blockers and cardiovascular protection: Focus on left ventricular hypertrophy regression and atrial fbrillation prevention. Vasc Health Risk Manag 2008;4: 67-73
  10. Lim PO, Nys M, Naas AA, et al. Irbesartan reduces QT dispersion in hypertensive individuals. Hypertension 1999;33:713-8
  11. Sampson UK, Pfeffer MA, McMurray JJV, et al. Predictors of stroke in high-risk patients after acute myocardial infarction: insights from the VALIANT trial. Eur Heart J 2007;28: 685-91
  12. Mangrella M, Rossi F, Fici F, Rossi F. Pharmacology of nebivolol. Pharmacol Res 1998;38:419-31
  13. Sule SS, Frishman W. Nebivolol: new therapy update. Cardiol Rev 2006;14:259-64
  14. Veverka A, Nuzum DS, Jolly JL. Nebivolol: a third-generation ß-adrenergic blocker. Ann Pharmacother 2006;40:1353-60
  15. Pessina AC. Metabolic effects and safety profle of nebivolol. J Cardiovasc Pharmacol 2001;38:S33-S35
  16. Toda N. Vasodilating ß-adrenoceptor blockers as cardiovascular therapeutics. Pharmacol Ther 2003;100:215-34
  17. Ambrosioni E, Borghi C. Tolerability of nebivolol in headtohead clinical trials versus other cardioselective β-blockers in the treatment of hypertension: a meta-analysis. High Blood Press Cardiovasc Prev 2005;12:27-35
  18. European Society of Hypertension - European Society