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Published on: September 1, 2015
Hyperaldosteronism and cardiovascular risk in patients with autosomal dominant polycystic kidney disease
Silvia Lai1, Luigi Petramala, Daniela Mastroluca
1Department of Clinical Medicine, Sapienza University of Rome, Rome Department of Internal Medicine and Medical Specialities, Sapienza University of Rome, Rome Cobellis Clinic, Tirreno SRL, Vallo della lucania, Sapri, Salerno Department of Radiological, Oncological and Pathological Sciences, Sapienza University of Rome, Rome Department of Clinical and Experimental Sciences, University of Brescia, Brescia Department of Obstetrical-Gynecological Sciences and Urologic Sciences, Sapienza University of Rome, Rome, Italy.
Insights
Primary aldosteronism (PA) is common in autosomal dominant polycystic kidney disease (ADPKD) patients, linked to increased cardiovascular risk markers. Screening for PA in ADPKD patients is recommended to identify those at higher risk.
Area of Science:
- Nephrology
- Endocrinology
- Cardiology
Background:
- Hypertension is a common comorbidity in autosomal dominant polycystic kidney disease (ADPKD), often preceding renal failure.
- The underlying mechanisms linking hypertension and ADPKD, particularly the role of hyperaldosteronism, require further elucidation.
- Hyperaldosteronism may contribute to insulin resistance, endothelial dysfunction, and cardiorenal disease progression in ADPKD.
Purpose of the Study:
- To determine the prevalence of primary aldosteronism (PA) in patients with ADPKD.
- To identify surrogate biomarkers of cardiovascular risk associated with PA in ADPKD patients.
- To investigate the association between PA and markers of atherosclerosis and metabolic dysfunction in ADPKD.
Main Methods:
- Enrolled 27 hypertensive ADPKD patients with eGFR ≥ 60 mL/min.
- Evaluated the renin-angiotensin-aldosterone system (RAAS), inflammatory markers, homocysteine (Hcy), HOMA-IR, mineral metabolism, and microalbuminuria.
- Assessed surrogate markers of atherosclerosis including cIMT, ABI, FMD, RRI, LVMI, and utilized 3 Tesla MRI.
Main Results:
- Primary aldosteronism (PA) was present in 33% of the studied ADPKD patients.
- PA group showed significantly higher LVMI, HOMA-IR, and Hcy levels compared to the non-PA group.
- The PA group exhibited lower FMD, lower 25-hydroxyvitamin D levels, and a higher prevalence of the non-dipper pattern on ABPM.
Conclusions:
- A significant prevalence of PA exists in ADPKD patients, even at early stages of the disease.
- PA in ADPKD is associated with adverse cardiovascular risk markers, including increased left ventricular mass index, insulin resistance, homocysteine, and endothelial dysfunction.
- Screening for PA is recommended in all ADPKD patients to identify individuals with potentially higher cardiovascular risk due to inappropriate aldosterone secretion.
Abstract:
Hypertension is commonly associated with autosomal dominant polycystic kidney disease (ADPKD), often discovered before the onset of renal failure, albeit the pathogenetic mechanisms are not well elucidated. Hyperaldosteronism in ADPKD may contribute to the development of insulin resistance and endothelial dysfunction, and progression of cardiorenal disease. The aim of study was to evaluate the prevalence of primary aldosteronism (PA) in ADPKD patients and identify some surrogate biomarkers of cardiovascular risk.We have enrolled 27 hypertensive ADPKD patients with estimated glomerular filtration rate (eGFR) ≥ 60 mL/min, evaluating the renin-angiotensin-aldosterone system (RAAS), inflammatory indexes, nutritional status, homocysteine (Hcy), homeostasis model assessment-insulin resistance (HOMA-IR), mineral metabolism, microalbuminuria, and surrogate markers of atherosclerosis [carotid intima media thickness (cIMT), ankle/brachial index (ABI), flow mediated dilation (FMD), renal resistive index (RRI) and left ventricular mass index (LVMI)]. Furthermore, we have carried out the morpho-functional magnetic resonance imaging (MRI) with high-field 3 T Magnetom Avanto.We have divided patients into group A, with normal plasma aldosterone concentration (PAC) and group B with PA, present in 9 (33%) of overall ADPKD patients. Respect to group A, group B showed a significant higher mean value of LVMI, HOMA-IR and Hcy (P = 0.001, P = 0.004, P = 0.018; respectively), and a lower value of FMD and 25-hydroxyvitamin D (25-OH-VitD) (P = 0.037, P = 0.019; respectively) with a higher prevalence of non-dipper pattern at Ambulatory Blood Pressure Monitoring (ABPM) (65% vs 40%, P < 0.05) at an early stage of the disease.In this study, we showed a high prevalence of PA in ADPKD patients, associated to higher LVMI, HOMA-IR, Hcy, lower FMD, and 25-OH-VitD, considered as surrogate markers of atherosclerosis, compared to ADPKD patients with normal PAC values. Our results indicate a higher overall cardiovascular risk in ADPKD patients with inappropriate aldosterone secretion, and a screening for PA in all patients with ADPKD is recommended.
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