Prevalence of Primary Aldosteronism Across the Stages of Hypertension Based on a New Combined Overnight Test
Autor: | Nick Voulgaris, Labrini Papanastasiou, Chara Kapsali, George P. Chrousos, Athina Markou, Sophia Vlachou, Ernestini Tyfoxylou, Eva Kassi, Evagelia Kyriazi, Alexandros Gryparis, Gregory Kaltsas, Chris Gravvanis, George Piaditis |
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Rok vydání: | 2021 |
Předmět: |
Adult
Male medicine.medical_specialty Endocrinology Diabetes and Metabolism Urinary system Clinical Biochemistry 030209 endocrinology & metabolism 030204 cardiovascular system & hematology Essential hypertension Biochemistry Gastroenterology Young Adult 03 medical and health sciences chemistry.chemical_compound Basal (phylogenetics) 0302 clinical medicine Endocrinology Primary aldosteronism Internal medicine Hyperaldosteronism Prevalence medicine Humans Mass Screening Prospective Studies Prospective cohort study Aldosterone Aged Greece Aldosterone-to-renin ratio Diagnostic Tests Routine business.industry Incidence (epidemiology) Biochemistry (medical) General Medicine Middle Aged Prognosis medicine.disease chemistry Case-Control Studies Hypertension Female business Biomarkers Follow-Up Studies |
Zdroj: | Hormone and Metabolic Research. 53:461-469 |
ISSN: | 1439-4286 0018-5043 |
Popis: | Primary aldosteronism (PA) is the most common endocrine cause of arterial hypertension. Despite the increasing incidence of hypertension worldwide, the true prevalence of PA in hypertension was only recently recognized. The objective of the work was to estimate the prevalence of PA in patients at different stages of hypertension based on a newly developed screening-diagnostic overnight test. This is a prospective study with hypertensive patients (n=265) at stage I (n=100), II (n=88), and III (n=77) of hypertension. A group of 103 patients with essential hypertension without PA was used as controls. PA diagnosis was based on a combined screening-diagnostic overnight test, the Dexamethasone-Captopril-Valsartan Test (DCVT) that evaluates aldosterone secretion after pharmaceutical blockade of angiotensin-II and adrenocorticotropic hormone. DCVT was performed in all participants independently of the basal aldosterone to renin ratio (ARR). The calculated upper normal limits for post-DCVT aldosterone levels [3 ng/dl (85 pmol/l)] and post-DCVT ARR [0.32 ng/dl/μU/ml (9 pmol/IU)] from controls, were applied together to establish PA diagnosis. Using these criteria PA was confirmed in 80 of 265 (30%) hypertensives. The prevalence of PA was: 21% (21/100) in stage I, 33% (29/88) in stage II, and 39% (30/77) in stage III. Serum K+ levels were negatively correlated and urinary K+ was positively correlated in PA patients with post-DCVT ARR (r=–0.349, p |
Databáze: | OpenAIRE |
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