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Effects of telmisartan, ramipril, and their combination on left ventricular hypertrophy in individuals at high vascular risk in the Ongoing Telmisartan Alone and in Combination With Ramipril Global End Point Trial and the Telmisartan Randomized Assessment Study in ACE Intolerant Subjects With Cardiovascular Disease.
Verdecchia, Paolo; Sleight, Peter; Mancia, Giuseppe; Fagard, Robert; Trimarco, Bruno; Schmieder, Roland E; Kim, Jae-Hyung; Jennings, Garry; Jansky, Petr; Chen, Jyh-Hong; Liu, Lisheng; Gao, Peggy; Probstfield, Jeffrey; Teo, Koon; Yusuf, Salim.
Afiliação
  • Verdecchia P; McMaster University, Population Health Research Institute, 237 Barton St E, Hamilton, ON L8L2X2 Canada. verdec@tin.it
Circulation ; 120(14): 1380-9, 2009 Oct 06.
Article em En | MEDLINE | ID: mdl-19770395
ABSTRACT

BACKGROUND:

Angiotensin-converting enzyme (ACE) inhibitors and angiotensin receptor blockers reduce left ventricular hypertrophy (LVH). The effect of these drugs on LVH in high-risk patients without heart failure is unknown. METHODS AND

RESULTS:

In the Ongoing Telmisartan Alone and in Combination With Ramipril Global End Point Trial (ONTARGET), patients at high vascular risk and tolerant of ACE inhibitors were randomly assigned to ramipril, telmisartan, or their combination (n=23 165). In the Telmisartan Randomized Assessment Study in ACE Intolerant Subjects With Cardiovascular Disease (TRANSCEND), patients intolerant of ACE inhibitors were randomized to telmisartan or placebo (n=5343). Prevalence of LVH at entry in TRANSCEND was 12.7%. It was reduced by telmisartan (10.5% and 9.9% after 2 and 5 years) compared with placebo (12.7% and 12.8% after 2 and 5 years) (overall odds ratio, 0.79; 95% confidence interval [CI], 0.68 to 0.91; P=0.0017). New-onset LVH occurred less frequently with telmisartan compared with placebo (overall odds ratio, 0.63; 95% CI, 0.51 to 0.79; P=0.0001). LVH regression was similar in the 2 groups. In ONTARGET, prevalence of LVH at entry was 12.4%. At follow-up, it occurred slightly less frequently with telmisartan (odds ratio, 0.92; 95% CI, 0.83 to 1.01; P=0.07) and the combination (odds ratio, 0.93; 95% CI, 0.84 to 1.02; P=0.12) than with ramipril, but differences between the groups were not significant. New-onset LVH was associated with a higher risk of primary outcome during follow-up (hazard ratio, 1.77; 95% CI, 1.50 to 2.07).

CONCLUSIONS:

In patients at high vascular risk, telmisartan is more effective than placebo in reducing LVH. New-onset LVH is reduced by 37%. The effect of combination of the 2 drugs on LVH is similar to that of ramipril alone.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Benzimidazóis / Benzoatos / Inibidores da Enzima Conversora de Angiotensina / Doenças Cardiovasculares / Ramipril / Hipertrofia Ventricular Esquerda / Anti-Hipertensivos Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Prevalence_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male Idioma: En Ano de publicação: 2009 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Benzimidazóis / Benzoatos / Inibidores da Enzima Conversora de Angiotensina / Doenças Cardiovasculares / Ramipril / Hipertrofia Ventricular Esquerda / Anti-Hipertensivos Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Prevalence_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male Idioma: En Ano de publicação: 2009 Tipo de documento: Article