Journal List > Korean Circ J > v.50(6) > 1144908

Cheung, Or, Fei, and Tsoi: A 2020 Vision of Hypertension

Abstract

Hypertension is a common chronic disease affecting a large section of the general population. Hypertension is highly prevalent in the elderly because blood pressure (BP) rises with age. The risk of developing hypertension increases with predisposing genes, intrauterine growth retardation, prematurity and childhood obesity. BP is easier to control in the young. Non-pharmacological treatment through lifestyle changes, such as weight control and leisure-time physical activity, is more likely to be successful in young people. Hypertension in older adults is more difficult to control, requiring the use of more than one antihypertensive drug. Adverse effects and compliance become problematic. Much research is now directed at novel ways of controlling BP such as denervation. The change in definition of hypertension in the American guideline highlights the need to identify and manage hypertension early, at a stage when it is potentially reversible.

INTRODUCTION

Hypertension is a common chronic disease affecting a large section of the general population. In the US, about 33.2% of the general population is hypertensive.1) There are 244.5 million adults with hypertension in China.2) The prevalence of hypertension in other parts of Asia is also considerable.3) In South Korea, the prevalence is approximately 30% in adults.4) In this review, the progression of hypertension from an elevation in blood pressure (BP) to stage 1 and 2 hypertension is discussed, highlighting the role that plays in this process. This offers an opportunity for prevention of hypertension before it develops.

A 2020 VISION OF HYPERTENSION

The epidemiology of hypertension has been carefully documented in the Hong Kong Cardiovascular Prevalence Study.5)6)7) In this population study of healthy people randomly chosen, the prevalence of hypertension was below 2% in young subjects aged 25–34, but the prevalence increased to around 50% in those 65–75 years of age.8) Premenopausal women have much lower BP than men but the BP rises sharply with age such that after the menopause, the sex difference in BP is no longer apparent. Studies in the US also show this sex difference in the trajectory in BP.9)
As hypertension is often asymptomatic, many people with are unaware of it and even if they have been told that their BP is elevated, many stop taking medications and miss follow-up appointments. This gives rise to the so-called ‘rule of halves’—half of the people with hypertension are unaware of it, and among those diagnosed, only half take treatment and among those treated, only half of them have good BP control.10) There are many reasons for the poor control rate. Not checking the BP in apparently healthy people is one of the most important. Therefore, every adult should have his or her BP periodically checked. If the BP is elevated, then rechecking the BP at intervals should be arranged.
Another reason for the poor control of BP is the ineffectiveness of current antihypertensive medications; most patients require more than one drug class to achieve target.11) This may reflect the multiple pathways involved in BP control. Coupled with the ineffectiveness is the presence of side-effects, which may affect compliance. Measures to improve compliance cited in guidelines include combination pills and once-daily formulations.12) More novel ways of treating hypertension are being explored, such as renal denervation,13) splanchnic denervation,14) ROX coupler,15) vaccine16), and antisense DNA.17) These expensive treatments, not without risks, have the merit of bypassing the need for compliance to take daily medications.
Prevention is better than cure. As BP rises with age, this means that prevention should be started early rather than in old age when hypertension is already common. How early is early? At the last count, there are over 100 genes involved in BP control.18) There are so many genes contributing to hypertension that counselling and prenatal diagnosis are not practised. After all, hypertension is not a life-threatening disease that justifies contraception or abortion. Intrauterine growth retardation increases the risk of the metabolic syndrome and hypertension in later life.19) Better antenatal care and postnatal care of pre-term infants20) may prevent cardiovascular diseases including hypertension.
Our own work suggests that childhood obesity is an important determinant of BP in childhood and adolescence.21) In the United States National Health and Nutrition Examination Survey (NHANES), there is a strong relationship between body mass index (or waist circumference) and BP in children (Figure 1).22) Unlike in adults, this relationship is not confounded by antihypertensive medications, smoking and alcohol intake.
Figure 1

Relationship between SBP and body mass index in children in US NHANES 2011–2012. Children aged 8–11, 12–15, and 16–19 years are represented by circles, triangles and squares respectively. The regression lines are shown as solid, dashed and dotted lines respectively.

NHANES = National Health and Nutrition Examination Survey; SBP = systolic blood pressure.
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Clearly, here is the window of opportunity for the prevention of hypertension before BP starts to rise. BP control rates are much higher in the young than in the elderly,23) so it should be much easier to achieve BP target in the young. Moreover, a large proportion of young hypertensives may respond to lifestyle measures and not require pharmacological treatment.24)
Data from South Korea,25) as well as the USA,26) suggest that prehypertension, or what is now known as stage 1 hypertension, in young adults is already associated with an increase in cardiovascular and mortality risk. We have recently analysed 20-year follow-up data in US NHANES. Compared to young adults with normal BP (<120/80 mmHg), an elevated BP is already associated with increased mortality (Figure 2).27) The current American College of Cardiology/American Heart Association guideline on the prevention, detection, evaluation and management of high BP is therefore timely in defining stage 1 hypertension to include people with a systolic BP of 130–139 mmHg or a diastolic BP of 80–89 mmHg.28) The guideline is based on the findings of Systolic Blood Pressure Intervention Trial.29) We have performed a network meta-analysis on the relationship between outcome and achieved BP in large randomised trials of antihypertensive drugs, and confirmed that an achieved BP of <130/80 mmHg is associated with the best outcome.30)
Figure 2

Kaplan-Meier plot showing the survival curves of US NHANES participants with different levels of BP at baseline. Participants were categorized as normal BP (SBP <120 mmHg and DBP <80 mmHg); elevated BP (SBP 120–129 mmHg and DBP <80 mmHg); stage 1 HT (SBP 130–139 mmHg or DBP 80–89 mmHg); or stage 2 HT (SBP ≥140 mmHg or DBP ≥90 mmHg). Note the curves for elevated BP and stage 1 HT are superimposable and therefore shown as one curve.

BP = blood pressure; DBP = diastolic blood pressure; HT = hypertension; NHANES = National Health and Nutrition Examination Survey; SBP = systolic blood pressure.
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In changing the definition of hypertension, the US hypertension guideline makes many people in the general population hypertensive. This may be undesirable in countries that are still struggling to treat stage 2 hypertension, but in countries that have a good health system, it is the next big target to identify people in the community at risk of progression to stage 2 hypertension and cardiovascular events. The characteristics of people with ‘stage 1 hypertension’ are interesting; most of them are male and obese (Table 1).31) Fortunately, as mentioned above, hypertension at this early stage is easy to control and weight loss is less difficult in young people.
Table 1

Characteristics of adult participants with stage I hypertension in NHANES 2015–2016

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NHANES survey cycle 2015–2016
Without anti-HT drug prescription With anti-HT drug prescription
No. 558 396
Age (years) 46.35±0.83 57.89±0.85
20–39 36.62 (31.67–41.78) 11.27 (8.29–15.14)
40–59 44.22 (37.66–50.92) 39.74 (32.47–47.48)
≥60 19.17 (14.61–24.43) 49.00 (41.73–56.31)
Female 44.03 (40.04–48.08) 48.59 (40.89–56.36)
SBP (mmHg) 128.98±0.41 131.78±0.40
DBP (mmHg) 77.04±0.73 72.60±0.93
BMI (kg/m2) 30.16±0.32 31.58±0.42
Waist circumference (cm) 102.39±0.82 106.57±1.25
Abdominal obesity US cut-offs* 62.76 (54.64–70.38) 73.78 (66.82–79.72)
Abdominal obesity IDF cut-offs 79.70 (75.75–83.27) 89.60 (83.50–93.61)
Medical history
History of CVD 2.31 (1.48–3.42) 14.45 (8.92–22.57)
Diabetes mellitus 2.46 (1.31–4.18) 3.67 (2.06–6.44)
Cigarette smoking 16.82 (12.07–22.52) 18.30 (12.99–25.15)
Data are shown as mean±standard error or percentage (95% CI).
BMI = body mass index; CI = confidence interval; CVD = cardiovascular disease; DBP = diastolic blood pressure; HT = hypertension; IDF = International Diabetes Federation; NHANES = National Health and Nutrition Examination Survey; SBP = systolic blood pressure.
*Abdominal obesity is defined as ≥102 cm and ≥88 cm for male and female, respectively; Abdominal obesity is defined as ≥94 cm and ≥80 cm for male and female, respectively.
Obesity is a problem that afflicts many parts of the world.32) It is a huge problem in the US, but it is also a problem among the poor in developing countries. In most Asian countries, US-style fast food may not be the main cause of obesity. Instead, changing from a rural to an urban environment with less physical activity (PA), from physically demanding jobs to office jobs, may be an important underlying factor. We compared leisure-time PA (LTPA) with occupational PA recently, and found that while people who had no PA have the highest mortality rate, adequate LTPA was associated with half the risk of death (Figure 3).33)
Figure 3

Kaplan-Meier plot showing the survival curves of each PA group for US NHANES participants aged 18 to 64 years old at baseline. Participants were categorized into groups by their weekly amount of LTPA, OPA, and the tPA. Values for PA are in minutes/week. The groups with LTPA ≥150 minutes/week had higher survival when compared with the group with no PA (all p<0.001).

LTPA = leisure-time physical activity; NHANES = National Health and Nutrition Examination Survey; OPA = occupational physical activity; PA = physical activity; tPA = total physical activity.
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In many parts of Asia, rice is part of the staple diet. While it is inherently low in fat, when boiled, it has a high glycaemic index.34) Indeed, the blood glucose profile after eating a bowl of rice is like that of an oral glucose test.35) Before the days of cars, machines and computers, the glucose would be utilised; in modern times, the excess calories are stored as fat.
Hypertension is part of the metabolic syndrome36) and in a large proportion of people with hypertension, obesity is an important underlying cause. Reduction in body weight is the most effective nonpharmacological way of reducing BP (Table 2).28)37) Bariatric surgery can reduce body weight dramatically and the reduction in BP is also equally impressive.38) Less drastic ways of reducing body weight, such as orlistat,39) glucagon-like peptide-1 receptor agonist40) and sodium-glucose cotransporter-2 (SGLT2) inhibitor,41) can also reduce BP. By inhibiting the reabsorption of glucose in the proximal convoluted tubules, SGLT2 inhibitors cause a net loss of up to 300 calories a day. This is weight loss without dieting and without exercise! In addition, there is cardiovascular risk reduction,42) even in non-diabetics. It would not be surprising if this drug class would earn an indication for use in people with hypertension, who are often obese and have other cardiovascular risk factors.
Table 2

Effect of lifestyle modification on SBP

kcj-50-469-i002
Modification Approximate SBP reduction
Weight reduction 5–20 mmHg/10 kg weight loss
DASH diet 8–14 mmHg
Low sodium diet 2–8 mmHg
Physical activity 4–9 mmHg
Moderate alcohol consumption 2–4 mmHg
Adapted from The Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure (JNC 7) produced by the National Heart Lung and Blood Institute, US (http://www.nhlbi.nih.gov/guidelines/hypertension/jnc7full.pdf).37)
DASH = dietary approaches to stop hypertension; SBP = systolic blood pressure.

CONCLUSION

In 2020, detecting and adequately treating hypertension remains an important goal. Cardiovascular risk assessment and promoting a healthy lifestyle in the young are likely to forestall hypertension and future cardiovascular disease. Preventing or reversing hypertension is no longer an impossible dream.

Notes

Conflict of Interest: The authors have no financial conflicts of interest.

Author Contributions:

  • Conceptualization: Cheung BMY.

  • Data curation: Or B, Tsoi MF.

  • Formal analysis: Or B, Tsoi MF.

  • Visualization: Or B, Tsoi MF.

  • Writing - original draft: Cheung BMY.

  • Writing - review & editing: Cheung BMY, Or B, Fei Y, Tsoi MF.

References

1. Centers for Disease Control and Prevention. Hypertension [Internet]. Atlanta (GA): Centers for Disease Control and Prevention;2018. cited 2020 Feb 18. Available from: https://www.cdc.gov/nchs/fastats/hypertension.htm.
2. Wang Z, Chen Z, Zhang L, et al. Status of hypertension in China: results from the China hypertension survey, 2012–2015. Circulation. 2018; 137:2344–2356. PMID: 29449338.
3. Cheung BM, Ong KL. The challenge of managing hypertension. In : Finkel ML, editor. Public Health in the 21st Century. Vol. 1. Santa Barbara (CA): Praeger Publishing;2011. p. 117–128.
4. Kim HC, Ihm SH, Kim GH, et al. 2018 Korean Society of Hypertension guidelines for the management of hypertension: part I-epidemiology of hypertension. Clin Hypertens. 2019; 25:16. PMID: 31388451.
crossref
5. Cheung BM, Wat NM, Man YB, et al. Relationship between the metabolic syndrome and the development of hypertension in the Hong Kong cardiovascular risk factor prevalence study-2 (CRISPS2). Am J Hypertens. 2008; 21:17–22. PMID: 18091739.
crossref
6. Cheung BM, Wat NM, Tam S, et al. Components of the metabolic syndrome predictive of its development: a 6-year longitudinal study in Hong Kong Chinese. Clin Endocrinol (Oxf). 2008; 68:730–737. PMID: 17980012.
crossref
7. Cheung BM, Wat NM, Tso AW, et al. Association between raised blood pressure and dysglycemia in Hong Kong Chinese. Diabetes Care. 2008; 31:1889–1891. PMID: 18556342.
crossref
8. Janus ED. Epidemiology of cardiovascular risk factors in Hong Kong. Clin Exp Pharmacol Physiol. 1997; 24:987–988. PMID: 9406673.
crossref
9. Ong KL, Tso AW, Lam KS, Cheung BM. Gender difference in blood pressure control and cardiovascular risk factors in Americans with diagnosed hypertension. Hypertension. 2008; 51:1142–1148. PMID: 18259031.
crossref
10. Wilber JA, Barrow JG. Hypertension--a community problem. Am J Med. 1972; 52:653–663. PMID: 5027555.
crossref
11. Kotseva K, Wood D, De Bacquer D, et al. EUROASPIRE IV: a European Society of Cardiology survey on the lifestyle, risk factor and therapeutic management of coronary patients from 24 European countries. Eur J Prev Cardiol. 2016; 23:636–648. PMID: 25687109.
12. Williams B, Mancia G, Spiering W, et al. 2018 ESC/ESH guidelines for the management of arterial hypertension. Eur Heart J. 2018; 39:3021–3104. PMID: 30165516.
13. Bhatt DL, Kandzari DE, O'Neill WW, et al. A controlled trial of renal denervation for resistant hypertension. N Engl J Med. 2014; 370:1393–1401. PMID: 24678939.
crossref
14. Zhen Z, Liao SY, Zhu ZY, et al. Catheter-based splanchnic denervation for treatment of hypertensive cardiomyopathy. Hypertension. 2019; 74:47–55. PMID: 31132949.
crossref
15. Lobo MD, Ott C, Sobotka PA, et al. Central iliac arteriovenous anastomosis for uncontrolled hypertension: one-year results from the ROX CONTROL HTN trial. Hypertension. 2017; 70:1099–1105. PMID: 29061728.
16. Nakagami H, Morishita R. Recent advances in therapeutic vaccines to treat hypertension. Hypertension. 2018; 72:1031–1036. PMID: 30354822.
crossref
17. Phillips MI. Gene therapy for hypertension: the preclinical data. Hypertension. 2001; 38:543–548. PMID: 11566928.
18. Warren HR, Evangelou E, Cabrera CP, et al. Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk. Nat Genet. 2017; 49:403–415. PMID: 28135244.
19. Calkins K, Devaskar SU. Fetal origins of adult disease. Curr Probl Pediatr Adolesc Health Care. 2011; 41:158–176. PMID: 21684471.
crossref
20. Parkinson JR, Hyde MJ, Gale C, Santhakumaran S, Modi N. Preterm birth and the metabolic syndrome in adult life: a systematic review and meta-analysis. Pediatrics. 2013; 131:e1240–63. PMID: 23509172.
crossref
21. Cheung BM. Hypertension: a weighty problem in children. Postgrad Med J. 2017; 93:647. PMID: 28823997.
crossref
22. Cheung AJ, Cheung BMY. Association of increased systolic blood pressure in children with obesity and the metabolic syndrome. J Hum Hypertens. 2015; 29(Suppl1):S15.
23. Ong KL, Cheung BM, Man YB, Lau CP, Lam KS. Prevalence, awareness, treatment, and control of hypertension among United States adults 1999–2004. Hypertension. 2007; 49:69–75. PMID: 17159087.
crossref
24. Muntner P, Carey RM, Gidding S, et al. Potential U.S. population impact of the 2017 ACC/AHA high blood pressure guideline. J Am Coll Cardiol. 2018; 71:109–118. PMID: 29146532.
crossref
25. Son JS, Choi S, Kim K, et al. Association of blood pressure classification in Korean young adults according to the 2017 American College of Cardiology/American Heart Association guidelines with subsequent cardiovascular disease events. JAMA. 2018; 320:1783–1792. PMID: 30398603.
crossref
26. Yano Y, Reis JP, Colangelo LA, et al. Association of blood pressure classification in young adults using the 2017 American College of Cardiology/American Heart Association blood pressure guideline with cardiovascular events later in life. JAMA. 2018; 320:1774–1782. PMID: 30398601.
crossref
27. Or B, Tsoi MF, Cheung TT, Cheung BM. Decreased survival in young adults with stage 1 and 2 hypertension in the National Health and Nutrition Examination Survey III. Hong Kong Med J. 2020; 26(Suppl 1):14.
28. Whelton PK, Carey RM, Aronow WS, et al. 2017 ACC/AHA/AAPA/ABC/ACPM/AGS/APhA/ASH/ASPC/NMA/PCNA guideline for the prevention, detection, evaluation, and management of high blood pressure in adults: executive summary: a report of the American College of Cardiology/American Heart Association task force on clinical practice guidelines. Hypertension. 2018; 71:1269–1324. PMID: 29133354.
crossref
29. SPRINT Research Group, Wright JT Jr, Williamson JD, et al. A randomized trial of intensive versus standard blood-pressure control. N Engl J Med. 2015; 373:2103–2116. PMID: 26551272.
crossref
30. Fei Y, Tsoi MF, Cheung BM. Determining the optimal systolic blood pressure for hypertensive patients: a network meta-analysis. Can J Cardiol. 2018; 34:1581–1589. PMID: 30414702.
crossref
31. Tsoi MF, Fei Y, Cheung TT, Cheung BM. Characteristics of Americans with stage-1 hypertension: United States National Health Nutrition and Examination Survey 2011–2016. Hong Kong Med J. 2018; 24(Suppl 1):54.
32. Ng M, Fleming T, Robinson M, et al. Global, regional, and national prevalence of overweight and obesity in children and adults during 1980–2013: a systematic analysis for the Global Burden of Disease Study 2013. Lancet. 2014; 384:766–781. PMID: 24880830.
33. Or B, Tsoi MF, Cheung TT, Cheung BM. Leisure time, occupational aerobic physical activity, and mortality risk in adults of United States: National Health and Nutrition Examination Survey 2007–2016. Hong Kong Med J. 2020; 26(Suppl 1):13.
34. Ludwig DS. The glycemic index: physiological mechanisms relating to obesity, diabetes, and cardiovascular disease. JAMA. 2002; 287:2414–2423. PMID: 11988062.
35. Chan HM, Brand-Miller JC, Holt SH, Wilson D, Rozman M, Petocz P. The glycaemic index values of Vietnamese foods. Eur J Clin Nutr. 2001; 55:1076–1083. PMID: 11781674.
crossref
36. Cheung BM. The cardiovascular continuum in Asia--a new paradigm for the metabolic syndrome. J Cardiovasc Pharmacol. 2005; 46:125–129. PMID: 16044022.
crossref
37. National Heart, Lung, and Blood Institute (US). The Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure. Bethesda (MD): National Heart, Lung, and Blood Institute;2004.
38. Vest AR, Heneghan HM, Agarwal S, Schauer PR, Young JB. Bariatric surgery and cardiovascular outcomes: a systematic review. Heart. 2012; 98:1763–1777. PMID: 23077152.
crossref
39. Sharma AM, Golay A. Effect of orlistat-induced weight loss on blood pressure and heart rate in obese patients with hypertension. J Hypertens. 2002; 20:1873–1878. PMID: 12195131.
crossref
40. Wang B, Zhong J, Lin H, et al. Blood pressure-lowering effects of GLP-1 receptor agonists exenatide and liraglutide: a meta-analysis of clinical trials. Diabetes Obes Metab. 2013; 15:737–749. PMID: 23433305.
crossref
41. Georgianos PI, Agarwal R. Ambulatory blood pressure reduction with SGLT-2 inhibitors: dose-response meta-analysis and comparative evaluation with low-dose hydrochlorothiazide. Diabetes Care. 2019; 42:693–700. PMID: 30894383.
crossref
42. Fei Y, Tsoi MF, Cheung BMY. Cardiovascular outcomes in trials of new antidiabetic drug classes: a network meta-analysis. Cardiovasc Diabetol. 2019; 18:112. PMID: 31462224.
crossref
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