Pre-hypertension: another 'pseudodisease’?
© Meier et al.; licensee BioMed Central Ltd. 2013
Received: 4 September 2013
Accepted: 4 September 2013
Published: 25 September 2013
Hypertension is one of the most important and common cardiovascular risk factors. Defining the level at which blood pressure starts causing end-organ damage is challenging, and is not easily answered. The threshold of blood pressure defining hypertension has progressively been reduced over time, from systolic >160 mmHg to >150 mmHg, then to >140 mmHg; and now even blood pressures above 130 to 120 mmHg are labeled as 'pre-hypertension’ by some expert committees. Are interest groups creating another 'pseudodisease’ or is this trend scientifically justified? A recent meta-analysis published in BMC Medicine by Huang et al. clearly indicates that pre-hypertension (120 to 140/80 to 90 mmHg) is a significant marker of increased cardiovascular risk. This raises the question as to whether we now need to lower the threshold of 'hypertension’ (as opposed to 'pre-hypertension’) to >120/80 mmHg, redefining a significant proportion of currently healthy people as 'patients’ with an established disease. These data need to be interpreted with some caution. It is controversial whether pre-hypertension is an independent risk factor or just a risk marker and even more controversial whether treatment of pre-hypertension will lower cardiovascular risk.
Please see related research: http://www.biomedcentral.com/1741-7015/11/177.
KeywordsHypertension Pre-hypertension Prevention Cardiovascular
Definitions and thresholds from various professional bodies
Systolic values (mmHg)
Diastolic values (mmHg)
European Society of Cardiology (ESC), 2013
120 to 129
80 to 84
130 to 139
85 to 89
Grade I hypertension
140 to 159
90 to 99
160 to 179
100 to 109
Isolated systolic hypertension
Joint National Committee (JNC 7), 2003
120 to 139
80 to 89
National Institute for Health and Care Excellence (NICE), 2011
Stage I hypertension
Stage II hypertension
As illustrated by these variable definitions from different committees, it is difficult to come up with a clear cut-off value to define 'good’ and 'bad’. While clinicians understandably prefer clear binary disease definitions, there is a continuous association between blood pressure and cardiovascular risk .
In a recent study published in BMC Medicine, Huang et al. challenge current guidelines which label blood pressures >140/>90 mmHg as being 'normal’ by concluding that pre-hypertension (even at lower levels of 120 to 129/80 to 84 mmHg) is a significant cardiovascular risk factor.
Huang et al. have performed a systematic review on the clinical relevance of pre-hypertension . They performed a pooled analysis of 18 prospective cohort studies including a total of 468,561 patients. Patients with pre-hypertension had a 55% increased risk for cardiovascular disease, a 50% increased risk for coronary artery disease, and a 71% increased stroke risk (RR 1.71 (95% confidence interval 1.55 to 1.89)). The authors went a step further and subdivided the pre-hypertension group into 'low-range pre-hypertension’ and 'higher-range pre-hypertension’. Even in the low-range pre-hypertension cohort, defined by blood pressures of 120 to 129/80 to 84 mmHg, the risk of cardiovascular disease was 46% higher than for individuals with normal blood pressures (RR 1.46 (1.32 to 1.62)). Therefore, according to this very large analysis, even lower-range pre-hypertension has a significant impact on morbidity and mortality.
Let us now have a closer look at some individual studies included in this meta-analysis. The Framingham Heart Study (6,859 participants who were initially free of hypertension and cardiovascular disease) showed a 2.5-fold increased risk for cardiovascular events at 10 years for women and a 1.6-fold increase for men with blood pressures between 130 to 139/85 to 89 mmHg . In line with the meta-analysis of Huang et al., the Framingham study further showed an increased risk even for those with blood pressure values of 120 to 129/80 to 84 mmHg compared with those with 'optimal’ blood pressure (<120/<80 mmHg). Another very important study in this context is the Women's Health Initiative, involving over 60,785 women in their postmenopausal phase. Pre-hypertensive women showed a 76% increased risk for cardiovascular death, a 93% increased risk for myocardial infarction and 36% increased risk for stroke . One endpoint that was not assessed in these studies was the impact of pre-hypertension on one important end organ: the kidneys. One study that did assess pre-hypertension and microalbuminuria as an early sign of kidney dysfunction showed an increased incidence compared to patients with optimal blood pressure . This finding further supports the findings of Huang et al.
The question arises based on these data, whether we should now reclassify 'pre-hypertension’ as 'hypertension’, even at the low blood pressure (BP) range, which would apply to a significant proportion of the population as newly labeled hypertensive patients? It is estimated that about 37% of people in the US, that is, more than 100 million fall within this pre-hypertension category. Whether these patients would benefit from pharmacologic therapy and if so, what the exact cost/benefit relation would be remains uncertain. Pre-hypertension is clearly associated with cardiovascular risk, but it is questionable whether a blood pressure level in this pre-hypertension range is a causal risk factor for cardiovascular events per se. We know that pre-hypertensive individuals are much more likely to progress to hypertension. In the Framingham cohort, patients with 'higher range pre-hypertension’ (130 to 139/85 to 89 mmHg) developed hypertension in 37% of cases, those with 'lower range pre-hypertension’ developed hypertension in 18% of cases and those with 'optimal blood pressure’ only in 5% of cases, over a 4-year period in patients >65 years . Of course, the long-term cardiovascular event rate is higher in those people, and this may not be related to their history of pre-hypertension. Beyond that, there are probably other 'confounding factors’. Even though most studies used multivariate adjustments to reduce confounding bias, such adjustments can only be made for available measured variables. It is likely that there are other factors which were not measured and which independently influence blood pressure and cardiovascular outcomes, such as environmental and genetic factors.
The question still remains whether active treatment of pre-hypertension will prevent progression to more advanced hypertension and future cardiovascular events. Experimental data indicate that it may actually be possible to change the natural history of pre-hypertension. In a hypertensive rat model, if antihypertensive therapy is given within the first 2 to 6 weeks of life it can prevent the development of hypertension .
In the clinical setting, these findings could not be fully confirmed. The 'TRial of Preventing Hypertension’ (TROPHY) study was a 4-year trial of 806 patients with pre-hypertension who were randomly assigned to 2 years of therapy with either candesartan or placebo (16 mg/day) . After 2 years, all patients continued therapy with placebo for another 2 years. At 2 years, the systolic and diastolic pressures were significantly lower with candesartan therapy compared to placebo. However, within 9 months of cessation of candesartan therapy, the pressures rose to values similar to those in the placebo group. Similarly, in the Medical Research Council trial in nearly 3,000 participants using thiazide diuretic or beta blockers versus placebo, the blood pressures dropped during therapy, but within 6 months after cessation, reached the levels of the placebo group .
While temporary treatment of pre-hypertension does not seem to prevent progression to hypertension, the question remains as to whether it reduces CV risk? Data on this question are conflicting. A recent meta-analysis pooling the results of trials of antihypertensive treatment in patients with cardiovascular disease but without hypertension showed a benefit. It was based on 25 randomized trials and 64,162 participants and found a 23% reduction in the risk of stroke, a 20% reduced risk of myocardial infarction, a 15% reduced risk of heart failure and a 13% reduced mortality risk . Whether this also applies to individuals without manifest cardiovascular disease is unclear.
Ambulatory blood pressure measurement (ABPM)
ABPM has become a useful tool to evaluate the true blood pressure burden and it has been shown to be a better predictor of cardiovascular events than are office blood pressure measurements. In a recent study of almost 5,000 patients from the Spanish ABPM Registry 60% of patients with office pressure of 130 to 139/85 to 89 mmHg, 42% with office pressure of 140 to 159/90 to 99 mmHg and 53% with office blood pressures of above 160/100 mmHg were actually normotensive according to the 24-h ABPM measuring criteria, that is, their mean ABPM was below 130/80 mmHg) . Clearly therefore office blood pressure measurements can be deceptive in identifying the specific stage of hypertensive cardiovascular disease. This problem was also encountered in a very recent analysis of Mahfoud et al., in patients who had renal denervation on ABPM. There was a significant reduction of 8 to 10 mm Hg systolic and 4 to 7 mm Hg diastolic, but clearly less impressive that the reduction of the office blood pressure in the same population (21 to 27 mm Hg (systolic)) and (9 to 12 mm (diastolic)) .
The data of Huang et al. clearly indicate that a blood pressure level currently defined as pre-hypertension is a significant marker of increased cardiovascular risk. However, we lack evidence that pre-hypertensive blood pressure itself is harmful and that an earlier intervention to reduce the blood pressure is beneficial in the absence of cardiovascular disease. Since pre-hypertensive individuals are at a high risk to progress to sustained hypertension, we advise periodic screening.
Pascal Meier is a cardiologist at University College London, UK, and Yale Medical School, CT, USA (http://www.drpascalmeier.com). He is editor-in-chief of the journal Open Heart and associate editor of the Cochrane Heart group (http://heart.cochrane.org/). Franz H Messerli is an expert in hypertension. He is Professor of Clinical Medicine at Columbia University College of Physicians and Surgeons, New York. Andreas Baumbach is a cardiologist at the Bristol Heart Institute. He has an interest in novel treatment options for hypertension, such as renal artery denervation. He is a co-director of the EuroPCR course, one of the major international cardiology conferences. Alexandra Lansky is a cardiologist and associate professor at Yale University School of Medicine and a renowned expert in clinical cardiovascular research. She is heading the Yale-UCL Cardiovascular Research collaborative (http://www.yale-ucl.org/index.aspx).
- Huang Y, Wang S, Cai X, Mai W, Hu Y, Tang H, Xu D: Prehypertension and incidence of cardiovascular disease: a meta-analysis. BMC Med. 2013, 11: 177-10.1186/1741-7015-11-177.View ArticlePubMedPubMed CentralGoogle Scholar
- Williams B: Hypertension and the “J-curve”. J Am Coll Cardiol. 2009, 54: 1835-1836. 10.1016/j.jacc.2009.06.043.View ArticlePubMedGoogle Scholar
- Vasan RS, Larson MG, Leip EP, Evans JC, O’Donnell CJ, Kannel WB, Levy D: Impact of high-normal blood pressure on the risk of cardiovascular disease. N Engl J Med. 2001, 345: 1291-1297. 10.1056/NEJMoa003417.View ArticlePubMedGoogle Scholar
- Hsia J, Margolis KL, Eaton CB, Wenger NK, Allison M, Wu L, LaCroix AZ, Black HR: Prehypertension and cardiovascular disease risk in the Women’s Health Initiative. Circulation. 2007, 115: 855-860. 10.1161/CIRCULATIONAHA.106.656850.View ArticlePubMedGoogle Scholar
- Zhang Y, Lee ET, Devereux RB, Yeh J, Best LG, Fabsitz RR, Howard BV: Prehypertension, diabetes, and cardiovascular disease risk in a population-based sample: the Strong Heart Study. Hypertension. 2006, 47: 410-414. 10.1161/01.HYP.0000205119.19804.08.View ArticlePubMedGoogle Scholar
- Sasamura H, Hayashi K, Ishiguro K, Nakaya H, Saruta T, Itoh H: Prevention and regression of hypertension: role of renal microvascular protection. Hypertens Res. 2009, 32: 658-664. 10.1038/hr.2009.85.View ArticlePubMedGoogle Scholar
- Julius S, Nesbitt SD, Egan BM, Weber MA, Michelson EL, Kaciroti N, Black HR, Grimm RH, Messerli FH, Oparil S, Schork MA: Trial of Preventing Hypertension (TROPHY) Study Investigators: Feasibility of treating prehypertension with an angiotensin-receptor blocker. N Engl J Med. 2006, 354: 1685-1697. 10.1056/NEJMoa060838.View ArticlePubMedGoogle Scholar
- Medical Research Council Working Party on Mild Hypertension: Course of blood pressure in mild hypertensives after withdrawal of long term antihypertensive treatment: Medical Research Council Working Party on Mild Hypertension. Br Med J (Clin Res Ed). 1986, 293: 988-992.View ArticleGoogle Scholar
- Thompson AM, Hu T, Eshelbrenner CL, Reynolds K, He J, Bazzano LA: Antihypertensive treatment and secondary prevention of cardiovascular disease events among persons without hypertension: a meta-analysis. JAMA. 2011, 305: 913-922. 10.1001/jama.2011.250.View ArticlePubMedPubMed CentralGoogle Scholar
- Banegas JR, Messerli FH, Waeber B, Rodriguez-Artalejo F, de la Sierra A, Segura J, Roca-Cusachs A, Aranda P, Ruilope LM: Discrepancies between office and ambulatory blood pressure: clinical implications. Am J Med. 2009, 122: 1136-1141. 10.1016/j.amjmed.2009.05.020.View ArticlePubMedGoogle Scholar
- Mahfoud F, Ukena C, Schmieder RE, Cremers B, Rump LC, Vonend O, Weil J, Schmidt M, Hoppe UC, Zeller T, Bauer A, Ott C, Blessing E, Sobotka PA, Krum H, Schlaich M, Esler M, Böhm M: Ambulatory blood pressure changes after renal sympathetic denervation in patients with resistant hypertension. Circulation. 2013, 128: 132-140. 10.1161/CIRCULATIONAHA.112.000949.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1741-7015/11/211/prepub
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