Primary aldosteronism (PA) has become increasingly recognised as a frequent and
clinically important cause of resistant hypertension. In the past, the importance of
PA was marginalised, but the newest research indicates that it may be present in a
significant number of patients with persistently uncontrolled hypertension, despite
the use of multiple antihypertensive drugs. The main reason for treatment
resistance is aldosterone excess. It leads to volume expansion, vascular remodelling,
endothelial dysfunction, and direct organ damage, which limit the effectiveness of
standard antihypertensive therapies. Diagnostic evaluation in patients with
resistant hypertension is challenging. One main reason is the interference from
medications during hormonal testing, along with variations in aldosterone-renin
ratio (ARR) results. The limitations of confirmatory procedures and the common
occurrence of normokalemic disease must also be considered during diagnosis.
Relying only on ARR and strict diagnostic guidelines can slow the diagnosis of
primary aldosteronism (PA). This leads to a longer exposure to excess aldosterone,
which raises the chances of heart, kidney, and metabolic problems. Treatment
options include mineralocorticoid receptor antagonists or adrenalectomy. These
treatments help control blood pressure and lower overall cardiovascular risk.
Furthermore, adrenalectomy can completely cure some cases. This review brings
together current evidence on the prevalence, underlying causes, diagnostic
challenges, and treatment implications of primary aldosteronism in patients with
resistant hypertension. The key point is the need for individualised and clinically
focused diagnostic approaches that combine biochemical data with clinical
evaluation and suitable imaging.
Keywords: primary aldosteronism, resistant hypertension, aldosterone–renin ratio;
secondary hypertension; mineralocorticoid receptor antagonists
