Abstract | OBJECTIVE: METHODS: We measured NT-proBNP and other cardiovascular risk factors at randomization and after 13 months of therapy in a subset of 357 PROGRESS participants. RESULTS: Baseline systolic and pulse pressures were higher in individuals with elevated baseline NT-proBNP levels. In comparison with placebo, active treatment reduced the blood pressure and NT-proBNP levels, and increased renin levels. Reduction of NT-proBNP levels by active treatment was most evident in individuals with baseline NT-proBNP levels in the highest quarter (> 26 pmol/l), with a median reduction of 16 pmol/l (interquartile range 0-51 pmol/l, P = 0.004), corresponding to a median decrease of 39% (interquartile range 0-69%). Active treatment reduced blood pressure similarly for individuals in each of the four quarters of baseline NT-proBNP. Active therapy had no effect on plasma lipid, C-reactive protein, homocysteine, or soluble vascular cell adhesion molecule 1 levels. CONCLUSION: We conclude that plasma NT-proBNP level, in addition to predicting cardiovascular risk, may provide a measure of risk reduction by blood pressure-lowering therapy.
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Authors | Duncan J Campbell, Mark Woodward, John P Chalmers, Samuel A Colman, Alicia J Jenkins, Bruce E Kemp, Bruce C Neal, Anushka Patel, Stephen W MacMahon |
Journal | Journal of hypertension
(J Hypertens)
Vol. 25
Issue 3
Pg. 699-705
(Mar 2007)
ISSN: 0263-6352 [Print] Netherlands |
PMID | 17278987
(Publication Type: Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antihypertensive Agents
- Biomarkers
- Peptide Fragments
- pro-brain natriuretic peptide (1-76)
- Natriuretic Peptide, Brain
- Perindopril
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Topics |
- Aged
- Antihypertensive Agents
(pharmacology)
- Biomarkers
- Blood Pressure
(drug effects)
- Cardiovascular Diseases
(prevention & control)
- Cerebrovascular Disorders
(complications, prevention & control)
- Female
- Humans
- Male
- Middle Aged
- Natriuretic Peptide, Brain
(blood, drug effects)
- Peptide Fragments
(blood, drug effects)
- Perindopril
(pharmacology)
- Risk Factors
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