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Reductions in albuminuria and in electrocardiographic left ventricular hypertrophy independently improve prognosis in hypertension: the LIFE study

Olsen, M. H. (author)
Wachtell, K. (author)
Ibsen, H. (author)
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Lindholm, Lars H (author)
Umeå universitet,Allmänmedicin
Dahlöf, Björn, 1953 (author)
Gothenburg University,Göteborgs universitet,Institutionen för medicin, avdelningen för akut och kardiovaskulär medicin,Institute of Medicine, Department of Emergeny and Cardiovascular Medicine
Devereux, R. B. (author)
Kjeldsen, S. E. (author)
Oikarinen, L. (author)
Okin, P. M. (author)
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 (creator_code:org_t)
Ovid Technologies (Wolters Kluwer Health), 2006
2006
English.
In: J Hypertens. - : Ovid Technologies (Wolters Kluwer Health). - 0263-6352. ; 24:4, s. 775-81
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • BACKGROUND: In the Losartan Intervention For Endpoint reduction in hypertension (LIFE) study, reduced urine albumin/creatinine ratio (UACR) as well as regression of left ventricular hypertrophy have been associated with lower incidence of cardiovascular events. We wanted to investigate whether these prognostic improvements were independent. METHODS: In 6679 hypertensive patients included in the LIFE study, we measured UACR, left ventricular hypertrophy by electrocardiography, serum cholesterol, plasma glucose and blood pressure after 2 weeks of placebo treatment and again after 1 year of anti-hypertensive treatment with either an atenolol- or a losartan-based regimen. During this first year of treatment, 77 patients encountered a non-fatal stroke or myocardial infarction and were excluded to avoid bias. During the next 3-4 years, 610 composite endpoints [cardiovascular death (n = 228), fatal or non-fatal myocardial infarction or stroke] were recorded. RESULTS: In Cox regression analyses, the composite endpoint was after adjustment for treatment allocation predicted by baseline logUACR [hazard ratio (HR) = 1.16 per 10-fold increase, P < 0.05], 1-year logUACR (HR = 1.29 per 10-fold increase), baseline Sokolow-Lyon voltage (HR = 1.01 per mm, both P < 0.001) and 1-year Cornell product (HR = 1.01 per 100 mm x ms, P < 0.01). Cardiovascular death was predicted by 1-year logUACR (HR = 1.59, P < 0.001), baseline Sokolow-Lyon voltage (HR = 1.01, P = 0.06) and 1-year Cornell product (HR = 1.02, P < 0.001). Both were predicted independent of age, Framingham risk score, current smoking, history of cardiovascular disease and diabetes. Gender, serum cholesterol, plasma glucose and blood pressure did not enter the models. CONCLUSIONS: Baseline UACR and Sokolow-Lyon voltage, as well as in-treatment UACR and Cornell product, added to the risk prediction independent of traditional risk factors, indicating that albuminuria and left ventricular hypertrophy reflect different aspects of cardiovascular damage and are modifiable cardiovascular risk factors.

Keyword

Aged
Albuminuria/metabolism/*prevention & control
Antihypertensive Agents/therapeutic use
Atenolol/therapeutic use
Blood Glucose/metabolism
Blood Pressure/drug effects
Cholesterol/blood
Creatinine/urine
Electrocardiography/statistics & numerical data
Female
Follow-Up Studies
Humans
Hypertension/*drug therapy/metabolism/physiopathology
Hypertrophy
control
Losartan/therapeutic use
Male
Middle Aged
Prognosis
Proportional Hazards Models
Survival Analysis
Treatment Outcome
Aged

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