| Literature DB >> 32147420 |
Fabrizio Buffolo1, Silvia Monticone1, Alessio Pecori1, Jacopo Pieroni1, Isabel Losano1, Giovanni Cavaglià1, Martina Tetti1, Franco Veglio1, Paolo Mulatero2.
Abstract
Low-renin hypertension (LRH) is a frequent condition in patients with arterial hypertension, accounting for 30% of patients. Monogenic forms can cause LRH in a minority of cases. However, in the large majority of patients, LRH is caused by the combined effects of congenital and acquired factors, comprising dietary habits. Several genetic variants have been proposed as co-factors in the pathogenesis of LRH with normal-low serum aldosterone. Emerging evidences support the hypothesis that a large proportion of LRH with normal-high serum aldosterone is associated with subclinical primary aldosteronism (PA). The recent identification of aldosterone-producing cell clusters (APCCs) as the possible cause of subclinical PA, further supported the concept of a continuous spectrum of autonomous aldosterone secretion, from subclinical forms towards overt PA. In this review we describe the main aspects of LRH, focusing on molecular basis, clinical risk profile and patients' management.Entities:
Keywords: aldosterone producing adenoma; aldosterone producing cells cluster; low renin hypertension; primary aldosteronism
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Year: 2020 PMID: 32147420 DOI: 10.1016/j.beem.2020.101399
Source DB: PubMed Journal: Best Pract Res Clin Endocrinol Metab ISSN: 1521-690X Impact factor: 4.690