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Should the results of TROPHY affect the JNC 7 definition of prehypertension?
1Internal Medicine and Physiology, Division of Cardiovascular Medicine, University of Michigan, 24 Frank Lloyd Wright Drive, Lobby M, 3rd Floor, Ann Arbor, MI 48106, USA. sjulius@umich.edu
Insights
Candesartan significantly reduced hypertension risk in individuals with high normal blood pressure. Researchers suggest refining "prehypertension" categories for better risk stratification.
Area of Science:
- Cardiovascular Medicine
- Clinical Pharmacology
- Hypertension Research
Background:
- The Trial of Preventing Hypertension (TROPHY) investigated interventions for individuals with high normal blood pressure.
- The Seventh Joint National Committee (JNC 7) redefined this category as 'prehypertension' (120-139 and/or 80-89 mm Hg).
Purpose of the Study:
- To evaluate the efficacy of candesartan in preventing hypertension in subjects with high normal blood pressure.
- To propose a refined classification for prehypertension based on observed outcomes.
Main Methods:
- Randomized, placebo-controlled trial involving volunteers with high normal blood pressure.
- Intervention group received candesartan (16 mg/d) for 2 years, followed by placebo for 2 years.
- Control group received placebo for 4 years.
Main Results:
- Candesartan significantly reduced the risk of developing hypertension by 66.3% at 2 years (P < 0.0001).
- The former candesartan group showed a 15.6% relative risk reduction in hypertension by study end (P < 0.007).
- Two-thirds of the placebo group developed hypertension over 4 years.
Conclusions:
- Candesartan is effective in preventing hypertension in individuals with high normal blood pressure.
- The study supports stratifying 'prehypertension' into 'high-risk prehypertension' (130-139 and/or 85-89 mm Hg) and 'high normal blood pressure' (120-129 and/or 80-84 mm Hg).
- Refined classification can better focus attention on individuals at higher risk of developing hypertension.
Abstract:
In the Trial of Preventing Hypertension (TROPHY), volunteers with "high normal blood pressure" were randomized to 4 years of placebo (n = 381) or 2 years of 16 mg/d of candesartan (n = 391) followed by 2 years of placebo. At 2 years, there was a 26.8% absolute and a 66.3% relative risk reduction (P < 0.0001) of hypertension in the candesartan group. At study end, the former candesartan group had a 9.8% absolute and a 15.6% relative risk reduction (P < 0.007) of hypertension. The treatment was well tolerated. The Seventh Joint National Committee (JNC 7) changed the nomenclature from "high normal blood pressure" to "prehypertension" and widened the range to 120 to 139 and/or 80 to 89 mm Hg. Our results support the term "prehypertension" only for the 130 to 139 and/or 85 to 89 mm Hg group; in 4 years two thirds of the placebo group developed hypertension. We suggest stratifying the JNC classification into "prehypertension" (130-139 and/or 85-89 mm Hg) and "high normal blood pressure" (120-129 and/or 80-84 mm Hg). By the present JNC definition, only one quarter of adult men have normal blood pressure. Removing the disease label from another 28% would appropriately focus attention on high-risk prehypertension.
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