Regression of electrocardiographic left ventricular hypertrophy during antihypertensive therapy and reduction in sudden cardiac death -: The LIFE study

被引:165
|
作者
Wachtell, Kristian
Okin, Peter M.
Olsen, Michael H.
Dahlof, Bjorn
Devereux, Richard B.
Ibsen, Hans
Kjeldsen, Sverre E.
Lindholm, Lars H.
Nieminen, Markku S.
Thygesen, Kristian
机构
[1] Glostrup Univ Hosp, Dept Internal Med, Glostrup, Denmark
[2] Cornell Univ, Weill Med Coll, Greenberg Div Cardiol, New York, NY USA
[3] Sahlgrens Univ Hosp, Dept Internal Med, Gothenburg, Sweden
[4] Ullevaal Univ Hosp, Dept Internal Med, Oslo, Norway
[5] Umea Univ Hosp, Dept Prevent Med, S-90185 Umea, Sweden
[6] Helsinki Univ Hosp, Dept Cardiol, Helsinki, Finland
[7] Arhus Univ Hosp, Dept Internal Med, Aarhus, Denmark
关键词
death; sudden; electrocardiography; hypertension; hypertrophy; mortality;
D O I
10.1161/CIRCULATIONAHA.106.666594
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background - Sudden cardiac death ( SCD) occurs more often in patients with ECG left ventricular ( LV) hypertrophy. However, whether LV hypertrophy regression is associated with a reduced risk of SCD remains unclear. Methods and Results - The Losartan Intervention for End Point Reduction in Hypertension ( LIFE) study included 9193 patients 55 to 80 years of age with essential hypertension and ECG LV hypertrophy by gender- adjusted Cornell product ( CP) ( RaVL + SV3 [ + 6 mm in women]) . QRS duration > 2440 mm (center dot) ms) and/ or Sokolow- Lyon voltage ( SLV) ( SV1 + RV5/6 > 38 mm). During follow- up ( mean, 4.8 years), 190 patients ( 2%) experienced SCD. In time- dependent Cox analyses, absence of in- treatment LV hypertrophy was associated with a decreased risk of SCD: every 1- SD- lower in- treatment CP ( 1050 mm center dot ms) was associated with a 28% lower risk of SCD ( hazard ratio [ HR], 0.72; 95% CI, 0.66 to 0.79) and 1- SD- lower SLV ( 10.5 mm) with a 26% lower risk ( HR, 0.74; 95% CI, 0.65 to 0.84). After adjustment for time- varying systolic and diastolic blood pressures, treatment allocation, age, gender, baseline Framingham risk score, ECG strain, heart rate, urine albumin/ creatinine ratio, smoking, diabetes, congestive heart failure, coronary heart disease, atrial fibrillation, and occurrence of myocardial infarction, atrial fibrillation, heart failure, and noncardiovascular death, both in- treatment CP and SLV remained predictive of SCD: each 1- SD- lower CP was associated with a 19% lower risk of SCD ( HR, 0.81; 95% CI, 0.73 to 0.90) and 1- SD- lower SLV with an 18% lower risk ( HR, 0.82; 95% CI, 0.70 to 0.98). Absence of in- treatment LV hypertrophy by both SLV and CP was associated with a 30% lower risk of SCD ( HR, 0.70; 95% CI, 0.54 to 0.92). Conclusions - Absence of in- treatment ECG LV hypertrophy is associated with reduced risk of SCD independently of treatment modality, blood pressure reduction, prevalent coronary heart disease, and other cardiovascular risk factors in hypertensive patients with LV hypertrophy.
引用
收藏
页码:700 / 705
页数:6
相关论文
共 50 条
  • [1] Regression of ECG left ventricular hypertrophy during anti hypertensive therapy and reduction in sudden cardiac death
    Chen, Peng-Sheng
    [J]. HEART RHYTHM, 2007, 4 (11) : 1474 - 1474
  • [2] Gender Differences in Outcome During Antihypertensive Therapy in Relation to Regression of Electrocardiographic Left Ventricular Hypertrophy: The LIFE Study
    Okin, Peter M.
    Gerdts, Eva
    Hille, Darcy A.
    Kjeldsen, Sverre E.
    Edelman, Jonathan M.
    Dahlof, Bjorn
    Devereux, Richard B.
    [J]. CIRCULATION, 2009, 120 (18) : S1111 - S1111
  • [3] Gender Differences in Regression of Electrocardiographic Left Ventricular Hypertrophy During Antihypertensive Therapy
    Okin, Peter M.
    Gerdts, Eva
    Kjeldsen, Sverre E.
    Julius, Stevo
    Edelman, Jonathan M.
    Dahlof, Bjorn
    Devereux, Richard B.
    [J]. HYPERTENSION, 2008, 52 (01) : 100 - 106
  • [4] Gender Differences in the Regression of Electrocardiographic Left Ventricular Hypertrophy During Antihypertensive Therapy
    Agabiti-Rosei, Enrico
    Salvetti, Massimo
    [J]. HYPERTENSION, 2008, 52 (01) : 59 - 60
  • [5] Gender Differences in Regression of Electrocardiographic Left Ventricular Hypertrophy during Antihypertensive Therapy
    Rosenkranz, Alexander R.
    [J]. JOURNAL FUR HYPERTONIE, 2009, 13 (03): : 35 - 36
  • [6] Continued regression of electrocardiographic left ventricular hypertrophy after two years of antihypertensive therapy: The LIFE study
    Okin, PM
    Liu, JE
    Jern, S
    Julius, S
    Kjeldsen, SE
    Dahlof, B
    [J]. CIRCULATION, 2001, 104 (17) : 575 - 575
  • [7] Electrocardiographic Predictors of Sudden Cardiac Death in Patients with Left Ventricular Hypertrophy
    Panikkath, Ragesh
    Reinier, Kyndaron
    Uy-Evanado, Audrey
    Teodorescu, Carmen
    Gunson, Karen
    Jui, Jonathan
    Chugh, Sumeet S.
    [J]. ANNALS OF NONINVASIVE ELECTROCARDIOLOGY, 2013, 18 (03) : 225 - 229
  • [8] Regression of electrocardiographic left ventricular hypertrophy by both Cornell voltage-duration product and Sokolow-Lyon voltage during antihypertensive therapy is associated with decreased incidence of sudden cardiac death:: the LIFE study
    Okin, PM
    Devereux, RB
    Harris, KE
    Jern, S
    Kjeldsen, SE
    Edelman, JM
    Dahlöf, B
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2006, 47 (04) : 360A - 360A
  • [9] Regression of electrocardiographic left ventricular hypertrophy during antihypertensive treatment and the prediction of major cardiovascular events: The LIFE study
    Okin, PM
    Jern, S
    Kjeldsen, SE
    Julius, S
    Nieminen, MS
    Snapinn, S
    Harris, KE
    Aurup, P
    Edelman, JM
    Dahlof, B
    [J]. CIRCULATION, 2002, 106 (19) : 573 - 573
  • [10] Impact of diabetes mellitus on regression of electrocardiographic left ventricular hypertrophy and the prediction of outcome during antihypertensive therapy -: The Losartan Intervention for Endpoint (LIFE) Reduction in Hypertension Study
    Okin, PM
    Devereux, RB
    Gerdts, E
    Snapinn, SM
    Harris, KE
    Jern, S
    Kjeldsen, SE
    Julius, S
    Edelman, JM
    Lindholm, LH
    Dahlöf, B
    [J]. CIRCULATION, 2006, 113 (12) : 1588 - 1596