Related Experiment Video
Updated: Apr 10, 2026

Implementing Patch Clamp and Live Fluorescence Microscopy to Monitor Functional Properties of Freshly Isolated PKD Epithelium
Published on: September 1, 2015
Hypertension in autosomal-dominant polycystic kidney disease (ADPKD)
Laia Sans-Atxer1, Roser Torra2, Patricia Fernández-Llama3
1Hypertension Unit, Nephrology Department , Hospital del Mar, Parc de Salut Mar , Barcelona, Spain.
Insights
Hypertension management is crucial for autosomal-dominant polycystic kidney disease (ADPKD) patients, as elevated blood pressure (BP) significantly impacts cardiovascular and renal outcomes. Early diagnosis and treatment, primarily with renin-angiotensin-aldosterone system (RAAS) inhibitors, are essential for improving patient prognosis.
Area of Science:
- Nephrology
- Cardiology
- Genetics
Background:
- Cardiovascular complications are the leading cause of mortality in autosomal-dominant polycystic kidney disease (ADPKD).
- Hypertension is prevalent in ADPKD patients, often preceding renal insufficiency and contributing to target organ damage and poor renal prognosis.
- Polycystin deficiency and renin-angiotensin-aldosterone system (RAAS) stimulation are implicated in ADPKD-related hypertension pathogenesis.
Purpose of the Study:
- To highlight the critical role of hypertension management in ADPKD patients.
- To emphasize the importance of early diagnosis and appropriate treatment strategies for cardiovascular and renal complications.
- To provide guidance on blood pressure targets and therapeutic approaches in ADPKD.
Main Methods:
- Review of existing literature on hypertension in ADPKD.
- Discussion of diagnostic tools like ambulatory blood pressure monitoring.
- Analysis of therapeutic options including non-pharmacological approaches, RAAS inhibitors, and calcium channel blockers (CCBs).
Main Results:
- Elevated blood pressure is a key determinant of patient outcome in ADPKD.
- Early detection of hypertension via ambulatory BP monitoring is recommended.
- RAAS inhibitors are the primary treatment, with CCBs reserved for resistant cases.
Conclusions:
- Prompt diagnosis and management of hypertension are vital for improving CV and renal outcomes in ADPKD.
- Target blood pressure should be <140/90 mmHg for all ADPKD patients, with a stricter goal of <135/85 mmHg if microalbuminuria or left ventricular hypertrophy is present.
- RAAS inhibitors are the cornerstone of antihypertensive therapy in ADPKD.
Abstract:
Cardiovascular (CV) complications are the major cause of death in autosomal-dominant polycystic kidney disease (ADPKD) patients. Hypertension is common in these patients even before the onset of renal insufficiency. Blood pressure (BP) elevation is a key factor in patient outcome, mainly owing to the high prevalence of target organ damage together with a poor renal prognosis when BP is increased. Many factors have been implicated in the pathogenesis of hypertension, including the renin-angiotensin-aldosterone system (RAAS) stimulation. Polycystin deficiency may also contribute to hypertension because of its potential role in regulating the vascular tone. Early diagnosis and treatment of hypertension improve the CV and renal complications of this population. Ambulatory BP monitoring is recommended for prompt diagnosis of hypertension. CV risk assessment is mandatory. Even though a nonpharmacological approach should not be neglected, RAAS inhibitors are the cornerstone of hypertension treatment. Calcium channel blockers (CCBs) should be avoided unless resistant hypertension is present. The BP should be <140/90 mmHg in all ADPKD patients and a more intensive control (<135/85 mmHg) should be pursued as soon as microalbuminuria or left ventricle hypertrophy is present.
Related Concept Videos
Chronic Kidney Disease I: Introduction
Hypertension and Regulation of Blood Pressure
Hypertension II: Pathophysiology
Chronic Kidney Disease III: Interprofessional Care
Hypertension III: Clinical Manifestations and Diagnostic Studies
Chronic Kidney Disease II: Clinical Manifestations

