Pharmacotherapy of hypertension

Systemic hypertension long-lasting, usually permanent increase of systolic and diastolic blood pressure

primary (essential) hypertension unknown cause; usually coincidence of more factors neural, hormonal, kidney dysfunction, ...

secondary (symptomatic) hypertension symptom (sign) of other disease

Isolated systolic hypertension increased systolic blood pressure at normal or decreased diastolic BPpseudohypertension rigid arteries in old age

white coat hypertension induced by stress at physical examination

masked hypertension - false finding of normal blood pressure during the examination; opposite of white coat hypertension

Secondary hypertension

essential hypertension 90 to 95 % of high blood pressure

prevalence: children...about 4 %, mostly secondary middle age ... 11-21 % 50-59 years old ... approximately 44 % 60-69 years old ... approximately 54 % more than 70 years old ... 64 %

(Standard guidelines, 2nd edition)

Classification of hypertension7th report of

Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure JNC 7

Classification of adults hypertensionPrevious classification of hypertension (JNC 6, WHO)

Reasons for actualisation of classification JNC 6 (1997):Completing of more new clinical studies with substantial consequences for the treatment of hypertension. Need for less complicated classification of hypertension.Need for new and clear guidelines suitable for physicians.Previous reports didnt bring expected benefits.

Classification of adults hypertension New classification of hypertension according to JNC 7Hypertenzia 3. tdia

in Europe partly remains classification of hypertension to 3 stages

ESH a ESC (European Society of Hypertension / E. S. of Cardiology) didnt adopt JNC 7 classification without comments

Risk of cardiovascular diseasesrelationship between BP and CVD (cardiovascular disease) risk is continual, consistent and not dependent on other risk factors the higher BP, the higher risk of heart failure, stroke, renal diseases each increase of systolic BP by 20 anddiastolic BP by10 mm Hg doubles the risk of CVD

Benefit of BP reductionInclinical studies was during antihypertensive therapy recorded:

35-40% incidence reduction of stroke 20-25% incidence reduction of myocardial infarctionmore than 50% share at incidence reduction of heart failure it is assumed that among patients at first stage of hypertension (140-159/90-99 mm Hg) andwith other cardiovascular risk factors, permanent reduction of BP by12 mm Hg during 10 years prevents one death from 11 treated patients (when CVS disease or organ affection, it is one from 9)

Effectivity of BP reductiondespite the fact that decreasing of BP below 140/90 mm Hg is successful among more and more patients, still their number (34%) is less than intention (50%), 30% still doesnt know about their disease

Evaluation of patientsAll of these datas influence the prognosis and therapy selection. Evaluation of patients with diagnosed hypertension has importance to:evaluate the way of living + reveal other CVS risk factors and/or associated diseases

very important is the circadian rhythm of blood pressure! physiological profound nocturnal decline, mostly around 4 a.m. ("dipping"), acts as a protection against pathological lesions of blood vessels, resp. reduces themalso hypertensive patients with significant nightime BP decrease have a more favorable prognosis ,as patients whose blood pressure at night compared to daytime values doesnt decrease (worse prognosis) according to it are patients diveded to dippers versus non-dippers improvement of diagnosis broader application of 24-hour blood pressure monitoring

Circadian rythm of BP (dippers vs. non-dippers)

We gain information about patient from :anamnesis physical examination (BP measurement, eyeground examination, BMI calculation, listening to murmurs at large arteries, detailed examination of heart, lungs, stomach, searching for enlarged kidneys, palpation of glandula thyroidea, resistency andabnormal pulsation of aorta, palpation of lower extremities to search for oedemas and pulsations, neurologic examination) laboratory examinations (ECG, urine, blood glucose, haematokrit, kallium, calcium, creatin inserum, lipid spectrum of serum)

TreatmentThe final goal of antihypertensive therapy is reduction of mortality and morbidity to CVS andrenal diseases. Primary goal is reduction of systolic BP. We wamt to reach BP less than 140/90 mm Hg (Torr), or less than 130/80 mm Hg among diabetic patients and patients with kidney diseases Needed is also increased detection!

Nonpharmacological treatmentChange of life-style:

intake of salt ... 5 6 g per day prevention of obesity dietetic modification alcohol ... 30 g per day smoking stop physical activity psychical relaxation

Pharmacologic treatment Antihypertensives

1st choice drugs: 1. diuretics 2. -blockers 3. inhibitors of ACE 4. blockers of AT1 receptors (ARB) 5. calcium channel blockers

2nd choice drugs mainly to drug combinations: 1-sympatholytics; 2-sympathomimetics; direct vasodilators; kallium channel openers; agonists of I1 receptors in CNS; other mechanisms of action

Diuretics

Diuretics increase urination

1. carboanhydrase inhibitors (acetazolamid) not used in the treatment of hypertension 2. loop diuretics (furosemide, etacrynic acid, bumetanide) strong short-lasting effect; ability to excrete to 25 % of Na+ from filtrate block active reabsorption of Na+, Cl-, K+ from ascending limb of Henles loop at treatment of hypertension is rarely used only furosemide in low dosage if simultaneously is very much reduced G filtration; they arent suitable for long-lasting application

3. thiazide diuretics (hydrochlorothiazide, chlorthalidone, clopamide) block reabsorption of Na+ and Cl- from distal tubulus effect is weaker as at loop diuretics they excrete about 5 % from Na+ filtrate most suitable diuretics for longlasting treatment of hypertension effect also in vessel wall ( volume of Na and reactivity to norepinephrine; regression of media hypertrophy) this effect is characteristic for indapamid and metipamid (increase of diuresis is negligible) also called diuretics without diuretic effect

the most is used hydrochlorothiazide daily dose 12,5 25 mg

Mechanism of Action of Thiazide Diuretics

4. K-sparing diuretics (spironolactone (aldosterone antagonist), amiloride, triamterene) at hypertension only assistant drugs to combinations to correct hypokalemia 5. other diuretics osmotic (mannitol, sorbitol) xanthine

diuretics are suitable mainly for older patients and at simultaneous chronic heart failure

ADRs of thiazide diuretics - hypokalemia, hypovolemia, hyperuricemia, metabolic ADRs (impaired glucose tolerance and dyslipidemia - mostly after high doses), erectile dysfunction

Adrenergic Receptor with Agonist

-blockersClassifications: 1. non-selective (1- aj 2-effect propranolol, metipranolol, ...); selective (1-effect metoprolol, bisoprolol, atenolol, ...); hybrid substances (beside -effect have also other effects, additional, resp. 2-mimetic effect), through which they induce vazodilation labetalol, carvedilol, nebivolol, ...) the most important classification 2. -blockers with ISA (intrinsic sympathomimetic activity pindolol, acebutolol, ...; parcial agonists) and without ISA 3. hydrophilic (atenolol, celiprolol, ...) and lipophilic -blockers (propranolol, metoprolol, carvedilol, ...) 4. classification according to generations ....... and other different classifications....

-blockers preferenced are selective and hybrid substances before nonselective dont differ very much in antihypertensive effect, selection according to adverse effect profile suitable for younger patients with sympathicoadrenal activity, hyperkinetic circulation, patients under psychical stress; patients with existent ischaemic heart disease and mainly after myocardial infarction in our country are mainly prescribed : metoprolol (Vasocardin, Egilok, Betaloc) bisoprolol (Coronal, Bisogamma, Concor) carvedilol (Dilatrend, Coryol, Talliton) nebivolol (Nebilet)

and according to tradition nonselective metipranolol (Trimepranol)

Main Effects of 1- a 2-blockade

-blockers possibilities of combinations: diuretics, Ca2+ blockers only dihydropyridines!, 1- sympatholytics, ACEI, vazodilators

ADRs: tendency to bronchoconstriction and to vasoconstriction in the periphery mainly at non-selective B metabolic ADR worsening of lipidogram; mask symptoms of hypoglycemia and can impair glucose tollerance more at non-selective B sleep disturbances, bad dreams ... depression at very high doses can worsen heart failure; if indicated at chronic heart failure, dose should be increased step by step erectile dysfunction

! selectivity of action is only relative! - at higher doses is dissapearing - even among 1-selective agents appear 2-lytic effects

they cant be combined with verapamilom a diltiazem!

treatment cant be stopped abruptly rebound effect!

stage frightIndication for Self-medication with -blockers:

Calcium Channel Blockers (CCB)Classification:

CCB Mechanism of ActionBlock influx of calcium to cell through slow L-type channels, lower its intracellular concentration what causes relaxation of smooth muscle in vessel wall, decrease of contractility, decrease of electrical irritability and conductivity

Ca2+- channel L-type

Ca2+ Channel Blockers (CCB)Different chemical structures, with different haemodynamic and clinic effects

According to chemical structure divided to:

- dihydropyridins (amlodipine, felodipine, lacidipine, nifedipine with slow release, isradipine)- phenylalkylamins (verapamil)- benzothiazepins (diltiazem)

Selectivity of CCBBlood vesselsvasodilation of arterial vasculatureHeart: decrease ofHeart rateAV conductionStrenght of contraction

Calcium channel blockers at treatment of hypertension are mostly used dihydropyridines; verapamil only at present tachycardia prototype short-acting DHP nifedipine is contraindicated! - it reduces BP too rapidly, so induces reflex activation of sympaticus with subsequent increase of BP and such a repeated BP fluctuation causes worse vessel damage as untreated hypertension instead of mortality decrease its increase! pharmacokinetic explanation: effect fluctuates for fluctuation of level in blood has low T/P (trough to peak ratio) for antihypertensive to reduce mortality and morbidity, it has to reduce BP slowly and successively, without reflex activation of sympathicus more steady level and higher T/P

FDA approves as antihypertensives only drugs, that have T/P more than 50 % this applies for the 2nd generation of dihydropyridines (isradipine, felodipine, nitrendipine) and 3rd generation of dihydropyridines (amlodipine, lacidipine, lercanidipine). Ca2+ blockers are suitable to treat hypertonic patients with DM, metabolic syndrome, at ischaemic disease of lower extremities particularly advantageous are for isolated systolic hypertension possibilities of combinations: ACEI, B (only dihydropyridines), diureticsADRs: headache, red face, perimalleolar edemas, constipation, tachycardia (dihydrop.), severe bradycardia (non-dihydropyridins), steal phenomen

nimodipine (1st generation) affinity to brain vasculature ... effectively relieves spasms of cerebral arteries used at subarachnoid bleeding lercanidipine has high T/P ratio in our country for the treatment of hypertension are prescribed mainly following dihydropyridines:

2nd generation: felodipine (Presid, Plendil), isradipine (Lomir), nitrendipine (Nitresan, Lusopress)

3rd generation: amlodipine (Amlopin, Agen, Tenox, Norvasc), lacidipine (Lacipil), lercanidipine (Lercal)

Renin-angiotensin-aldosterone system

Pharmacologic Interference to AT Cascade

Inhibitors of AC enzyme block the change of angiotensin I to angiotensin II and at the same time block inactivation of bradykinin vazodilation in both resistant and capacitance vessels accented indication: - hypertonic people with heart failure (vasodilating therapy of cardial insuficiency), also after myocardial infarction - hypertonic people with DM and different forms of diabetic nephropathy starting with mikroalbuminuria (nephroprotective effect of ACEI) excessive initial fall in BP postural hypotension or syncope; treatment should be started in bed from the lowest doses reaction of airways is often strong and irritating cough intollerance of the whole group replacement to AT1 receptor blockers

they are administered as prodrug, to effective substance are changed in liver

effect to reduce BP is in the whole group similar; they differ only in pharmacokinetic dependent from structure division to hydrophilic (blood) and lipophilic (tissue) ACEI

hydrophilic act only inside vessels and in endothelium; lipophilic also on the outer side of vessels (on adventicial angiotenzinconvertase) and in myocardial interstitium probably more effectively at regression of left ventricule hypertrophy and vessel media

typical hydrophilic ACEI: captopril (prototype substance has SH-group; nowadays used only in hypertension crisis, Tensiomin) enalapril (Enap, Ednyt), lisinopril (Dapril, Diroton) typical lipophilic ACEI: perindopril (Vidotin, Stopress, Prestarium) trandolapril (Actapril, Gopten) quinapril (Quinpres, Accupro)

ADRs: impaired renal function, hyperkalemia, hypotension, dry cough, angioneurotic edema contraindications: pregnancy!, high concentration of potassium and creatinine, stenosis of a. renalis on both sides, severe aortal stenosis, angioneurotic edema in anamnesis

Main Benefits of ACE inhibition

AT1 receptor blockers the most often replacement of ACEI in case of cough losartan (prototype; Cozaar), valsartan, kandesartan, irbesartan (Aprovel) sometimes prescribed as 1st choice, even before ACEI clinical studies indicate that they have among patients with HT and DM 2 slightly better protective effects than ACEI

Central I1 receptor agonists I1 imidazoline receptors type 1 in medulla oblongata stimulation reflectory decrease of peripheral resistency without serious hemodynamic, metabolic ADR; are metabolically neutral promising to future moxonidine (Physiotens, Moxostad, Cynt), rilmenidine (Rilmex, Tenaxum)

1-sympatholytics beside BP reduction they reduce benign prostatic hyperplasia indication mainly older man with simultaneous BPH in combination at severe resistant hypertension positively influence lipidogram strong 1st dose phenomenon! postural hypotension, syncopes prazosin (prototype; Deprazolin), doxazosin (Cardura), terazosin

1-lytic only for the treatment of BPH, without vasodilating effects tamsulosin

2-sympathomimetics

central effect stimulation of central 2 receptors through negative feedback inhibit release of norepinephrine on periphery reflex BP reduction

-metyldopa (Dopegyt), clonidine ADR: central depression sleepiness, bad dreams clonidine has significant rebound phenomenon -metyldopa is advantageous during pregnancy doesnt influence negatively blood circulation of fetus

Direct vasodilators

hydralazines specific mechanism of action is unknown; probably directly influence contractile system of vessel wall myocytes

ADR: tachycardia, palpitations, fluid retention necessary combinations dihydralazine, hydralazine suitable in pregnancy hydralazine genet. polymorphism of biotransformation at slow acetylators can develop as syndrome similar to lupus erythematodes

Kallium channel openers opening of K+ channels on the top of myocytes hyperpolarisation induction of relaxation minoxidil vazodilation in the area of arterioles retention of Na+, hirsutism, hypertrichosis used in the treatment of alopecia expensive diazoxide only short-term use at hypertension crisis induces hyperglycemia at short-term use not matters

Other antihypertensives magnesium (MgSO4) natural antagonist of calcium sodium nitroprusside simple molecule releasing NO; only i.v. at severe hypertension crisis, patient must lie, cyanide is formed; max. lenth of therapy 3 days ketanserin blocks S2 receptors for serotonin prevents effect increase of catecholamines on symp. receptors

Direct renin inhibitors (PRI) absolutely new group in many tissues is present own renin system with individual receptors (pro)renin is bind to cell surfaces; system acts pressorically and proliferatively it is activated when stimulation of AT1 receptors decreases negative feedback

this signal way apparently decreases benefit of ACEI! inhibition of the level of renin ... better control of the whole RAAS ... possible better prevention of organ damage

Aliskiren

first available peroral PRI plasmatic renin activity

indication in 2-combination aliskiren + ACEI or aliskirn + ARB dual inhibition of RAAS system product Rasilez

? - clinical results below expectations

Therapeutic algorithm of hypertension treatment (JNC 7)

Selection of pharmacotherapyResults gained in clinical studies show that BP reduction with using following antihypertensives inhibitors of angiotensin converting enzyme(ACEI), blockers of angiotensin receptors(ARB), betablockers (B), calcium channel blockers(Ca2+B) adiuretics, can reduce complications of hypertension. Base of medicament treatment of uncomplicated hypertension in the first stage should be according to JNC 7 thiazide diuretics alone, or in combination with other antihypertensives in the second stage of hypertension.

Advantages of thiazide diureticsaccording to more studies thiazide diuretics are considerably the most effective they increase antihypertensive effectivity of combined treatmentthey proved to reach BP normalisationare less expensive than other antihypertensives

Reaching BP improvement at specific patientsAmong most patients is necessary combination of 2 and more antihypertensives. Adminastration of other drug should start when monotherapy in required dose doesnt reduce BP to intended value. If the BP is by20/10 mm Hg higher than intended value, therapy should be started with combination of 2 antihypertensives.

recently is a growing trend to use combination of 2 antihypertensive drugs already in stage I hypertension

convincing evidence from relevant clinical trials

combinations perindopril-amlodipine perindopril-indapamide

Other factors influencing selection of antihypertensives Potentially prosperous effects:Tiazide diuretics slower the process of bone demineralisation at osteoporosisB can have positive influence at ventricular tachyarrhythmias andfibrilations, at migraine, short-termly at thyreotoxicosis, at essential tremor,perioperational hypertensionCa2+B can be applied at Raynaud syndrome and some arrhythmias

Other factors influencing selection of antihypertensivesPotentially negative effects: tiazide diuretics at patients withgout andhyponatremia inanamnesisB at patientswithasthma, allergic diseases of airways and with A-V blocks of 2nd and3rd stage ACEI andARB should not be given at probability of getting pregnant, are contraindicated in pregnancy, ACEI at angioneurotic oedemaaldosterone antagonists andK-sparing diuretics can cause hyperkalemia

JNC

versus European Society of Hypertension (ESH)different views (conflict ):ESH as the drug of 1st choice doesnt prefer thiazide diuretics so much, but recommends more or less equal position of all 4 groups D, B, Ca2+B, ACEI

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