Related Experiment Videos

Patients with uncontrolled hypertension or concomitant hypertension and benign prostatic hyperplasia

Randall Zusman1

  • 1Massachusetts General Hospital, Boston, Massachusetts 02114, USA. Zusman.randall@MGH.harvard.edu

Clinical Cardiology
|February 26, 2004
PubMed

Insights

Doxazosin add-on therapy effectively lowers blood pressure (BP) in patients with uncontrolled hypertension. It also improves lower urinary tract symptoms in men with benign prostatic hyperplasia (BPH).

Area of Science:

  • Pharmacology
  • Cardiology
  • Urology

Background:

  • Many hypertension patients require combination therapy to reach target blood pressure (< 140/90 mmHg).
  • High-dose monotherapy may pose risks for certain patient groups.
  • Uncontrolled hypertension and benign prostatic hyperplasia (BPH) often coexist.

Purpose of the Study:

  • To evaluate the antihypertensive efficacy of doxazosin as add-on therapy.
  • To assess doxazosin's effects in patients with inadequately controlled hypertension and BPH.
  • To determine doxazosin's impact on serum lipid profiles.

Main Methods:

  • Two studies were conducted: a placebo-controlled, double-blind trial (n=70) and an open-label trial (n=491).
  • Doxazosin was administered as add-on therapy to existing antihypertensive medications.
  • Efficacy was measured by blood pressure reduction and BPH symptom scores.

Main Results:

  • Add-on doxazosin significantly lowered blood pressure (BP) in patients with uncontrolled hypertension.
  • Doxazosin improved all benign prostatic hyperplasia (BPH) symptom scores.
  • The drug positively affected serum lipid profiles and was well tolerated.

Conclusions:

  • Doxazosin as add-on therapy is effective for improving BP control in patients not at goal BP.
  • Doxazosin also improves lower urinary tract symptoms in patients with concomitant BPH.
  • This combination therapy offers a dual benefit for patients with both conditions.

Related Concept Videos

Treatment for Pulmonary Arterial Hypertension: Phosphodiesterase Inhibitors01:28

Treatment for Pulmonary Arterial Hypertension: Phosphodiesterase Inhibitors

Phosphodiesterase 5 (PDE5) inhibitors are potent enzymes that function to hydrolyze cyclic nucleotides to their corresponding 5' monophosphates. Their unique biochemical properties have been applied in treating Pulmonary Arterial Hypertension (PAH).
Among the PDE5 inhibitors, sildenafil (Revatio) stands out as a competitive and selective inhibitor. It operates by elevating cellular levels of cGMP and augmenting signaling through the cGMP-PKG pathway, promoting vasodilation. Upon oral...
Hypertension I: Introduction01:28

Hypertension I: Introduction

Hypertension is a widespread, long-term medical condition where blood pressure in the arteries remains elevated. It is characterized by systolic blood pressure readings of 130 mm Hg or above or diastolic blood pressure (DBP) readings of 80 mm Hg or higher. Unmanaged hypertension poses significant health risks, making the distinction between primary (or essential) hypertension and secondary hypertension crucial, as their management and implications vary.Primary HypertensionPrimary hypertension,...
Antihypertensive Drugs: Vasodilators01:23

Antihypertensive Drugs: Vasodilators

Vasodilators, primarily affecting the smooth muscles within arterial and venous walls, are commonly used for hypertension treatment. Medications such as minoxidil and hydralazine primarily target arteries and arterioles, while sodium nitroprusside acts on arterioles and venules. Minoxidil, functioning as a prodrug, is metabolized by hepatic sulfotransferase into its active form, minoxidil sulfate, after oral administration. This metabolite binds to the sulfonylurea receptor (SUR) component of...
Treatment for Pulmonary Arterial Hypertension: Endothelin Receptor Antagonists01:18

Treatment for Pulmonary Arterial Hypertension: Endothelin Receptor Antagonists

Endothelins (ETs) are potent vasoactive peptides critical in the human body's various physiological and pathological processes. One of the most promising therapeutic strategies for treating pulmonary arterial hypertension (PAH) involves counteracting the effects of these endothelins using a class of drugs known as endothelin receptor antagonists.
ETs are synthesized through a complex sequence of enzymatic steps, primarily involving an enzyme referred to as endothelin-converting enzyme (ECE). Of...
Treatment for Pulmonary Arterial Hypertension: Receptor Tyrosine Kinase Inhibitors and Calcium Channel Blockers01:26

Treatment for Pulmonary Arterial Hypertension: Receptor Tyrosine Kinase Inhibitors and Calcium Channel Blockers

Receptor tyrosine kinase inhibitors (TKIs) and calcium channel blockers (CCBs) are two critical categories of drugs employed in the treatment of pulmonary artery hypertension (PAH). PAH is a disease that causes high blood pressure in the pulmonary arteries, resulting in chest pain, fatigue, and shortness of breath.
TKIs, such as imatinib (Gleevec), are particularly effective in tackling the growth and mitogenic factors that become upregulated in PAH patients. These factors contribute to the...
Adrenergic Antagonists: Pharmacological Actions of &#593;-Receptor Blockers01:22

Adrenergic Antagonists: Pharmacological Actions of ɑ-Receptor Blockers

α-Adrenergic antagonists, known as α-blockers, exert their effects by inhibiting α-adrenoceptors, leading to specific physiological actions. α1-blockers and α2-blockers have distinct pharmacological actions and therapeutic applications.
α1-blockers: These drugs inhibit α1-adrenoceptors on smooth muscle cells, resulting in vasodilation. This vasodilation lowers blood pressure, making α1-blockers valuable in treating hypertension. Additionally, α1-blockers effectively address urinary obstruction...