Hypertension in Adults: Part 1. Prevalence, types, causes and effects
Introduction
Arterial hypertension is a common and preventable cardiovascular risk factor, leading to about 1.7 million deaths/year worldwide.
Prevalence
The incidence and prevalence of hypertension depends upon the racial composition of population and criteria used to define hypertension (see Table 1). The prevalence of hypertension in the USA ranges from 4% in 18-29 years olds to 65% in those aged 80 years and over. Prevalence of hypertension in South Sudan is unknown but a review of studies in sub-Saharan Africa1 showed it was higher in urban than rural areas and, like other races, increased with age. In most studies reviewed:
- Less than 40% of people with blood pressure above the defined normal range had been detected
- Of people with previously diagnosed hypertension, less than 30% were on drug treatment.
Table 1. Classification of BP levels (according to The British Hypertension Society)
Category |
Systolic BP (mm Hg) |
Diastolic BP (mm Hg) |
Optimal |
< 120 |
< 80 |
Normal |
< 130 |
< 85 |
High Normal |
130 - 139 |
85 - 89 |
Grade 1 (mild) |
140 - 159 |
90 - 99 |
Grade 2 (moderate) |
160 - 179 |
100 - 109 |
Grade 3 (severe) |
> 180 |
> 110 |
Hypertension occurs more frequently in ‘black’ compared to ‘white’ populations and is associated with:
- A higher incidence of cerebrovascular and renal complications
- A greater tendency to develop left ventricular hypertrophy
- Enhanced sodium retention with a higher incidence of salt-sensitive hypertension, expanded plasma volume and A higher prevalence of low plasma renin activity.
- Reduced sodium-potassium ATPase activity with a tendency towards increased intracellular sodium and calcium concentrations
- Greater frequency of proteinuria.
Types of hypertension
There are two types:
- Primary or essential hypertension (97-98%) has no clear underlying cause but appears to be the result of an interplay of complex genetic and environmental factors.
- Secondary hypertension (2-3%) is caused by a specific underlying mechanism usually involving kidneys or endocrine system.
Mechanisms in primary hypertension
Several patho-physiological mechanisms contribute to the development of primary hypertension. The factors include:
- Genetics
- High salt intake
- Low physical activity
- Obesity
- Insulin resistance
- Renin – angiotension system
- Sympathetic nervous system
- Intrauterine nutrition and low birth weight
Causes of secondary hypertension
These are unusual but are important because the cause may be curable:
- Endocrine
causes:
- Cushing’s syndrome
- Conn’s syndrome
- Phaeochromocytoma
- Hyper / Hypothyroidism
- Acromegaly
- Hyperparathyroidism
- Exogenous hormones, e.g. contraceptive pills, glucocorticoids.
- Renal
causes:
- Glomerulonephritis
- Diabetic nephropathy
- Polycystic kidney disease
- Renal artery stenosis.
- Other
causes:
- Coarctation of the aorta
- Pregnancy associated hypertension
- Alcohol
- Acute stress.
Effects of Hypertension
Damage to organs (end organ damage) appears in two main forms:
- Obstruction to arterial blood flow: atherosclerosis causing cerebral infarction (“stroke”), coronary and peripheral arterial disease.
- Rupture of arteries: e.g. cerebral haemorrhage (“stroke”) and aortic dissection.
Organ damage can also result from drugs used for treatment of hypertension. Other common complications of hypertension include:
- Atrial fibrillation
- Left ventricular hypertrophy and failure
- Kidney damage leading to failure
- Retinopathy.
- Black race
- Youth
- Male gender
- Persistent diastolic BP > 115 mm Hg
- Smoking
- Diabetes Mellitus
- Hypercholesterolaemia
- Obesity
- Excess alcohol intake
- Evidence of end organ damage.
Risk Factors for a poor prognosis in hypertension
- Black race
- Youth
- Male gender
- Persistent diastolic BP > 115 mm Hg
- Smoking
- Diabetes Mellitus
- Hypercholesterolaemia
- Obesity
- Excess alcohol intake
- Evidence of end organ damage.
References
1. Addo J, Smeeth L & Lean DA 2007 Hypertension in Sub-Saharan Africa: A Systematic Review
Hypertension. 2007;50:1012.
http://hyper.ahajournals.org/cgi/content/abstract/50/6/1012 )
With thanks to Dr David Tibbutt for editing this article.