Pathogenesis of Primary Aldosteronism: Impact on Clinical Outcome

Primary aldosteronism (PA) is the most common form of secondary arterial hypertension, with a prevalence of approximately 20% in patients with resistant hypertension. In the last decade, somatic pathogenic variants in KCNJ5, CACNA1D, ATP1A1 and ATP2B3 genes, which are involved in maintaining intracellular ionic homeostasis and cell membrane potential, were described in aldosterone-producing adenomas (aldosteronomas). All variants in these genes lead to the activation of calcium signaling, the major trigger for aldosterone production. Genetic causes of familial hyperaldosteronism have been expanded through the report of germline pathogenic variants in KCNJ5, CACNA1H and CLCN2 genes. Moreover, PDE2A and PDE3B variants were associated with bilateral PA and increased the spectrum of genetic etiologies of PA. Of great importance, the genetic investigation of adrenal lesions guided by the CYP11B2 staining strongly changed the landscape of somatic genetic findings of PA. Furthermore, CYP11B2 staining allowed the better characterization of the aldosterone-producing adrenal lesions in unilateral PA. Aldosterone production may occur from multiple sources, such as solitary aldosteronoma or aldosterone-producing nodule (classical histopathology) or clusters of autonomous aldosterone-producing cells without apparent neoplasia denominated aldosterone-producing micronodules (non-classical histopathology). Interestingly, KCNJ5 mutational status and classical histopathology of unilateral PA (aldosteronoma) have emerged as relevant predictors of clinical and biochemical outcome, respectively. In this review, we summarize the most recent advances in the pathogenesis of PA and discuss their impact on clinical outcome.


INTRODUCTION
Arterial hypertension (AH) represents one of the main risk factors for premature death, affecting about 10 to 40% of the world population (1,2). Primary aldosteronism (PA) is the most frequent cause of endocrine AH, with a prevalence of around 4% and 10% in hypertensive patients treated in primary and tertiary care services, respectively, reaching around 20% of patients with resistant AH (3)(4)(5)(6).
PA is characterized by autonomous production of aldosterone, independent of the renin-angiotensin system. As a consequence, sodium retention, plasma renin suppression, blood pressure (BP) elevation and K + excretion increase occur, with consequent cardiovascular damage (7). The latter is due to the fact that excess of aldosterone exerts its deleterious cardiovascular effects independent of blood pressure levels, resulting in higher cardiovascular morbidity and mortality in patients with PA when compared with patients with essential AH (8,9).
Aldosterone is a mineralocorticoid hormone, which is synthesized by the zona glomerulosa (ZG) of the adrenal cortex. Its play a major role in electrolyte regulation through sodium and water renal reabsorption (10,11). Aldosterone is synthetized from cholesterol and its biosynthesis is under the control of two principal factors: angiotensin II (Ang II) and extracellular potassium concentration (K + ) (10).
Stimulation of ZG cells by Ang II or an increase in plasma K + concentration leads to cell membrane depolarization and increase in intracellular Ca 2+ , by opening of voltage-gated Ca 2+ channels and inositol triphosphate-dependent Ca 2+ release from the endoplasmic reticulum. The increase of intracellular Ca 2+ leads to activation of a phosphorylation cascade that positively regulate aldosterone synthesis and cell proliferation, specifically by increasing the CYP11B2 gene transcription (10,12,13).
Effects of aldosterone are mediated through the mineralocorticoid receptor (MR), a hormone dependent transcription factor that is expressed in non-epithelial tissues, such as the heart and vessels, and in epithelial tissues such as the salivary glands and kidney distal tubule, where aldosterone regulates sodium/water reabsorption and potassium excretion (10).
The main causes of PA are bilateral cortical adrenal hyperplasia (idiopathic hyperaldosteronism) and aldosteronomas (14). Idiopathic hyperaldosteronism is caused by bilateral nodular hyperplasia originating from the cortical zona glomerulosa, whereas aldosteronomas are aldosterone-producing adenomas usually measuring between 1-3 cm (but can even measure less than 1 cm). Each of these accounts for about 50-60% and 40-50% of PA cases, respectively (7,14).
The two major causes of PA account for more than 95% of cases, with approximately 5% of bilateral hyperplasia occurring in a familial context. Thus, bilateral hyperplasia remains without a defined genetic etiology in most cases. Although somatic allelic variants are identified in about 90% of aldosteronomas, few advances have been made in the genetic elucidation of bilateral PA (10,15). Several genes that encode ion channels that modulate zona glomerulosa cell depolarization and aldosterone synthesis pathways have already been associated with the pathogenesis of PA (Figure 1), differing in prevalence among aldosteronomas and familial PA cohorts (12). The aim of this review is to discuss the most recent discoveries about the PA pathogenesis, as well as the clinical and prognostic impact of the genetic characterization of this very prevalent disorder, associated with a high cardiovascular morbidity.

DIAGNOSIS AND CLINICAL MANAGEMENT
According to the American Endocrine Society (The Endocrine Society), the following scenarios are indicated for PA screening in hypertensive patients: I) AH and hypokalemia (spontaneous or induced by diuretic therapy); II) AH and adrenal incidentaloma; III) Blood pressure >150x100 mmHg on three different occasions; IV) AH not controlled (≥140/90 mmHg) on three or more antihypertensive drugs (resistant AH); V) controlled AH (<140x90 mmHg) on four antihypertensive drugs (resistant AH); VI) AH associated with obstructive sleep apnea; VII) AH and family history of AH or cerebrovascular disease of the young (<40 years); VIII) AH in first-degree relatives of patients with PH (7).
PA screening should be performed with plasma aldosterone (A) and renin (R) measurements, with hypokalemia correction before the test. To avoid false negative results, diuretics and spironolactone should be withheld for at least 4 to 6 weeks before the test. Aldosterone concentration >10 ng/dL and an A/PRA ratio (plasma renin activity) ≥ 30 ng/dL/ng/mL/h or A/R ≥2.0 confer a sensitivity and specificity greater than 90% for PH diagnosis (7,16,17). It should be emphasized that A/PRA or A/R ratio should be calculated only for patients with suppressed or very low renin levels.
After laboratorial PA confirmation, patients should undergo adrenal computed tomography (CT) for etiologic characterization and exclusion of adrenal cortical carcinoma. Adrenal CT has limited accuracy (around 60-70%), especially for detection of small (<1 cm) aldosteronomas (7) or for patients with bilateral nodules (to differentiate non-functioning or cortisol producing-adenomas). Therefore, adrenal vein sampling (AVS) is indicated for the majority of patients with PA for the proper characterization of the lateralization of aldosterone production (7,16). Although AVS is the gold standard approach to define aldosterone lateralization, it should be carried out only in centers with expertise for this procedure and by a very experienced interventional radiologist. In addition, AVS should be considered only if laparoscopic surgery is a treatment option. A detailed description of PA work-up investigation is beyond the scope of this review.
Treatment of unilateral PA consists of laparoscopic adrenalectomy. The bilateral hyperplasia is treated with a mineralocorticoid antagonist (spironolactone or eplerenone). Both approaches are associated with reduced cardiovascular morbidity caused by excess of aldosterone (18,19). The reduction of cardiovascular risk after medical treatment for PA is associated with normalization of renin levels (PRA >1 ng/mL/ h) (20).

FAMILIAL HYPERALDOSTERONISM
Familial hyperaldosteronism (FH) is rare, but likely a highly underdiagnosed entity due to lack of routine screening ( Table 1). Therefore, there is a lack of prevalence data for most of pathogenic variants listed in Table 1. The first report of FH occurred in 1966 (30), with subsequent characterization of its molecular etiology (21). This autosomal dominant form of PH was caused by a chimeric gene consisting of the 11b-hydroxylase promoter (CYP11B1) and aldosterone synthase (CYP11B2) coding region, resulting from a non-homologous pairing during crossing-over. Therefore, aldosterone synthesis becomes now regulated by adrenocorticotropic hormone (ACTH) instead of Ang II (21). This presentation of familial PH was then termed  The normal resting potential of zona glomerulosa cells is hyperpolarized (highly negative membrane potential). Activation of the angiotensin receptor (AT1R) by angiotensin II or extracellular hyperkalemia results in membrane depolarization and calcium influx via activated voltage-gated calcium channels. Calcium influx activates signaling to increase expression of aldosterone synthase (CYP11B2) and ultimately aldosterone production. (B) Genetic alterations leading to cell membrane depolarization, intracellular ionic modification, and autonomous aldosterone secretion in PA. Pathogenic variants in the KCNJ5 gene (G-protein-activated inward rectifier potassium channel GIRK4) [6] promote loss of channel K + selectivity and increase permeability to Na + , leading to membrane depolarization and calcium influx via voltage-gated calcium channels. Similarly, impaired ATPase, Ca 2+ (ATP2B3) [1]; Ca v 1.3 (CACNA1D) [2]; Ca v 3.2 (CACNA1H) [3]; ATPase, Na + | K + (ATP1A1) [4], and CLC-2 (CLCN2) [5] function results in cell membrane depolarization, calcium influx and autonomous aldosterone secretion. PA, primary aldosteronism.
A diagnosis of FH 1 is highly suggestive if aldosterone suppression (<4 ng/dL) occurs after a dexamethasone suppression test (0.5 mg each 6h for 48h). However, the FH 1 diagnosis should be confirmed by the presence of the chimeric gene in a long range PCR (31). The treatment of FH 1 consists of low dose dexamethasone administration in adults (0.125-0.25mg/d) to suppress ACTH and block aldosterone synthesis (32,33). If additional blood pressure control is required, a mineralocorticoid antagonist can be added.
The molecular pathogenesis of Type 2 FH (OMIM #605635) consists of gain-of-function heterozygous germline variants in the CLCN2 gene ( Table 1). Type 2 FH is characterized by autosomal dominant inheritance, incomplete penetrance and a family history of aldosteronoma or bilateral PA (34,35). CLCN2 was mapped as a FH gene in 2018 and encodes an inwardly rectifying chloride channel (ClC-2), a member of the CLC voltage-gated Clchannels family which is expressed in the cortical zona glomerulosa (28,29).
So far, 6 missense pathogenic variants in CLCN2 have been reported in the literature associated with FH 2 ( Table 2) (48). The presence of these alleles causes an increase in Clconductance through the channel, leading to a continuous  depolarization of the plasma membrane, resulting in an increase of CYP11B2 expression and consequent stimulus for aldosterone synthesis ( Figure 1B) (28,29).
In 2008, individuals with childhood-onset PA, resistant AH, hypokalemia and bilateral macronodular adrenal hyperplasia were reported (31). In 2011, an inactivating germline variant in the KCNJ5 gene was identified in a case with a similar clinical presentation. Named FH 3 (OMIM #613677), this autosomal dominant PA subtype is caused by an impaired function of K + GIRK4 (Kir3.4) potassium channel, which is encoded by KCNJ5 gene (23).
The molecular defect in the K + GIRK4 potassium channel leads to the loss of its ionic selectivity, with a consequent increase in sodium conductance ( Figure 1B). Naturally responsible for maintaining the zona glomerulosa membrane potential, it starts to act as a channel in favor of s o d i u m i n fl u x , p r o m o t i n g c o n t i n u o u s m e m b r a n e depolarization and subsequent activation of voltagedependent Ca + channels. These increased intracellular calcium concentrations trigger CYP11B2 overexpression and aldosterone synthesis (39).
The genetic study of numerous PA cohorts and the consequent mapping of new KCNJ5 pathogenic variants allowed, over the years, to expand the phenotypic heterogeneity of this PA subtype (39-41) ( Table 2). Certain alleles between amino acids residues 151-158 of the K + GIRK4 potassium channel, more specifically p.(Gly151Arg), p.(Ile157Ser), and p.(Thr158Ala), are correlated with a more severe PA clinical presentation, with early-onset hypertension, more resistant to drug treatment and with a frequent need for bilateral adrenalectomy (24). On the other hand, some substitutions in this same region, namely p.(Gly151Glu) and p.(Tyr152Cys), result in a mild clinical presentation, with an adequate blood pressure control with aldosterone antagonists and without evidence of adrenal hyperplasia in CT evaluation (13,39). Interestingly, in vitro experiments showed that mutant KCNJ5 channels can be undermined with the use of macrolide antibiotics such as roxithromycin and clarithromycin, su ppr essing CY P11B2 expr ession and a ldosterone production (49).
Four KCNJ5 germline variants were reported in cohorts of patients with AH without a typical familial and biochemical diagnosis of PA ( Table 2) (46,47). The p.(His278Gln) variant, for example, was reported in a patient with resistant AH with normal serum K + levels, plasma renin activity and aldosterone levels. The allele was inherited from his father who had essential AH without PA (47). None of the other reported cases had a phenotype similar to FH 3 patients, with early-onset medicationresistant hypertension, hypokalemia and bilateral adrenal macronodular hyperplasia (24).
Type 4 FH (OMIM #617027), the rarest subtype of PA, is caused by gain-of-function germline variants in CACNA1H gene (autosomal dominant inheritance), which encodes calcium voltage-gated channel subunit a1 H (Ca v 3.2) (26) (Tables 1, 2). Scholl et al. identified a recurrent heterozygous variant in the CACNA1H gene in five patients with early-onset PA (26). In silico studies with the identified p.(Met1549Val) mutant demonstrated an increase in calcium influx into zona glomerulosa cells, resulting in continual stimulation of aldosterone synthesis (50). Later studies demonstrated a late and incomplete penetrance of this PA subtype (27).
In 2013, Scholl et al. sequenced the candidate CACNA1D gene in 100 unrelated individuals with early-onset PA and identified two de novo heterozygous alleles in two girls with an undescribed syndrome featuring PA, AH, seizures and neuromuscular abnormalities (OMIM #615474) (25) ( Table 2). This gene  encodes the a 1D subunit of the L-type voltage-gated Ca 2+ channel Ca v 1.3. The identified variants promote an activation of the Ca +2 channel at lower depolarization potentials, resulting in increased Ca +2 influx (25). Subsequently, two more cases were reported with de novo heterozygous CACNA1D variants, leading to a severe developmental disorder also associated with developmental delay, intellectual impairment, neurological symptoms (including seizures), and endocrine symptoms, evident as PA and/or congenital hyperinsulinemic hypoglycemia (44,45). Recently, rare heterozygous missense germline variants in the phosphodiesterase 2A (PDE2A) and 3B (PDE3B) genes were identified in 3 out of 11 patients with PA caused by bilateral hyperplasia (51). In addition, PDE2A was a marker of zona glomerulosa and aldosterone-producing hyperplastic areas and micronodules. In vitro functional studies supported the involvement of PDE2A and PDE3B in the pathogenesis of bilateral PA. PKA activity in frozen tissue was significantly higher in adrenals from patients harboring PDE2A and PDE3B variants. Interestingly, inactivating PDE2A and PDE3B variants increased SGK1 and SCNN1G/ENaCg at mRNA or protein levels (51). SGK1 (serum and glucocorticoid inducible kinase-isoform 1) belongs to a large family of serine-threonine kinases. SGK1 is expressed in numerous tissues and plays a major role in transmembrane ionic transport, being established as an important regulator of Na + transporters (52). Aldosterone is the most notorious hormonal regulator of SGK1 expression. After binding to the cytosolic mineralocorticoid receptor, aldosterone promotes the transcription of SGK1, which regulates a variety of ion transporters, such as ENaC (epithelial sodium channel). SGK1 reduces ENaC ubiquitination and degradation, as well as its cellular internalization (53). Therefore, PDE2A and PDE3B variants can induce aldosterone signaling by increasing SGK1/SCNN1G(ENag) (51). In addition, an increase in SGK1 activity also stimulates hypercoagulability, fibrosis and inflammation processes (54).
In 2013 after KCNJ5 discovery, somatic CACNA1D gain-offunction variants were reported in aldosteronomas, with a prevalence of around 10%. CACNA1D encodes the a1 subunit Ca v 1.3 of a voltage dependent L-type (long-lasting) calcium channel and its pathogenic variants affect conserved residues within the channel activation gate ( Table 3). Compared to wildtype, mutated Ca v 1.3 reaches activation in less depolarized membrane potentials, causing abnormal Ca + influx, CYP11B2 expression, and aldosterone production ( Table 4 and Figure 1B). In contrast with KCNJ5 related aldosteronomas, CACNA1D tumors are significantly smaller and more frequent in older male patients (25,56,61).
In 2013, Beuschlein et al. identified somatic variants in genes encoding ATPases, ATP1A1 and ATP2B3 in aldosteronomas (59). Missense and in-frame deletion variants in ATP1A1, which encodes Na + /K + ATPase a subunit, impair pump activity and significantly reduce affinity for potassium, resulting in inappropriate membrane depolarization ( Table 4 and Figure 1B). ATP2B3 encodes a Ca + ATPase in which lossof-function alleles (in-frame deletions) lead to a loss of physiological pump function, responsible for sodium and possibly calcium ions leaking into the cell, inducing membrane depolarization, and contributing to increased calcium concentrations. The combined prevalence of somatic variants in ATPases is around 7% and, until now, no ATPase pathogenic variants were found as germline or surrounding aldosteronoma tissue. Additionally, ATPase mutant aldosteronomas showed a high prevalence among older male patients (61,93).
As found in other adrenocortical tumors, somatic gain of function variants in CTNNB1 gene, encoding b catenin, also have been reported in around 5% of aldosteronomas (Tables 3, 4). Affected adrenals had an aberrant b catenin accumulation in the Wnt cell-differentiation pathway and overexpression of luteinizing hormone/choriogonadotropin receptor (LHCGR) and gonadotropin-releasing hormone receptor (GnRHR) (63,94,95). Patients harboring aldosteronomas with CTNNB1 variants are more frequently females (60-70%) and older individuals, with no significant differences in preoperative aldosterone levels, tumor size and frequency familial hypertension compared with those with KCNJ5 variants (64). Unfortunately, the underlying mechanism leading to CYP11B2 overexpression due to CTNNB1 mutations remains unclear. Berthon et al. (96) showed that b-catenin plays an essential role in the control of basal and Angi II-induced aldosterone secretion, by activating AT1R, CYP21 and CYP11B2 transcription (96).
The knowledge about adrenal lesions associated with PA and the detection rate of somatic variant have been significantly changed since the development of highly specific monoclonal antibodies against CYP11B1 and CYP11B2 (97). Under normal conditions, CYP11B2 was sporadically detected in the zona glomerulosa, whereas CYP11B1 was entirely detected in the zonae fasciculata-reticularis (98). In younger individuals, immunohistochemistry from normal adrenals reveals a continuous CYP11B2 expression throughout the ZG layer, but this pattern changes in adults and CYP11B2 expression becomes discontinuing in ZG (98,99). Next, Nanba et al. demonstrated that CYP11B2 immunostaining was a powerful tool for histopathological identification of adrenal lesions associated with aldosterone overproduction (100).
Fernandes Rosa et al. performed the most comprehensive study in a cohort of 474 aldosteronomas from the European Network for the Study of Adrenal Tumors, reaching a detection rate of somatic variants of 54%, although CTNNB1 sequencing was not included in this study (56). Two other studies, which included CTNNB1 sequencing, demonstrated similar findings: Wu et al. studied 219 aldosteronomas, detecting somatic variants in 58.4% of them (101), and Vilela et al. reported a discovery rate of approximately 50% (102).
Recent studies using immunohistochemistry-guided approach to determine the exact source of abnormal aldosterone production led to the identification of pathogenic somatic variants in around 90% of screened aldosteronomas (81,82,88,103). The lower prevalence of somatic variants found in aldosteronomas in previous studies using conventional approaches, not taking in account CYP11B2 expression, is explained due to the macroscopical selection of non-aldosteroneproducing adrenal lesions (81). A recent review confirmed these previous findings, showing a higher detection rate of somatic variants with CYP11B2-guided extraction (85%) when compared to the classical approach with DNA extraction from fresh frozen tissue (54%) (57). Overall, the variant-negative ratio decreased from 46% to 15%. Gene-specific detection rate also increased from 34% to 56% in KCNJ5, 8% to 10% in CACNA1D, 8% to 12% in ATP1A1 and 4% to 5% in ATP2B3 (57). Moreover, the CYP11B2-guided high throughput sequencing method has revealed a wide complexity of aldosteroneproducing lesions in patients with PA (81,82,88,103,104). In multinodular cases, tumors from the same adrenal might harbor different recurrent somatic variants, suggesting independent triggers for the somatic events (82,105). Interestingly, aldosterone production may occur from multiple sources: multiple aldosteronomas in the same adrenal gland, dominant non-producing adenoma with satellite CYP11B2 positive nondominant nodules, and clusters of autonomous aldosteroneproducing cells (APCCs) without apparent neoplasia (55,81,88,106,107).
APCCs are common in normal adrenals and accumulate with age, becoming more often detectable in morphologically normal adult adrenals (108). Somatic pathogenic variants in CACNA1D, ATP1A1 and ATP2B3 were found in 35% to 76% of the APCCs, with CACNA1D being the most mutated gene (108,109). Interestingly, the spectrum of affected gene in APCCs is different from aldosteronomas. APCCs may a key player to the understanding of the physiology and pathophysiology of aldosterone production. It has been hypothesized that aldosteronomas can derive from APCCs with autonomous aldosterone production (harboring somatic in aldosteronedriver genes) (15,99,108).
These advances in PA histopathology allowed the definition of classical and non-classical histopathological features associated with PA ( Table 5) (110). The classical histology is defined by the presence of a solitary aldosteronoma or APN. In contrast, "non-classical" histology is characterized by adrenals with multiple APNs or APMs (or multiple APMs and multiple APNs together) or aldosterone-producing diffuse hyperplasia (110,111). In summary, non-classical histology is defined by the absence of a dominant aldosterone-producing lesion (such as a solitary aldosteronoma or APN). Interestingly, the mutational spectrum is different between classical and nonclassical histology. KCNJ5 somatic variants are predominant among aldosteronomas (classical histology), whereas CACNA1D is the most frequent mutated gene in APMs (81,111).

IMPACT ON CLINICAL OUTCOME
The impact of genetic and clinical variables in outcome in PA patients have been more properly evaluated after the Primary Aldosteronism Surgical Outcome (PASO) study, which established criteria for clinical and biochemical success in unilateral PA patients after adrenalectomy (112). PASO criteria classified PA patients after adrenalectomy according to the biochemical outcome and clinical success. Complete biochemical success is defined by correction of hypokalemia when present pre-surgery and normalization of the aldosterone-to-renin ratio, and partial biochemical success as a correction of hypokalemia when present pre-surgery and a raised aldosterone-to-renin ratio, but with at least 50% decrease in baseline plasma aldosterone concentration compared to presurgical levels. Regarding blood pressure control, complete clinical success is defined as blood pressure <140x90 mmHg without anti-hypertensive medications after 6 months of follow-up, whereas partial clinical success as a reduction in the number or dose of anti-hypertensive medications when compared to pre-surgery (98).
Recently, non-classical histopathological lesions associated with aldosterone excess were found in 25% of the cases in a German cohort of unilateral PA (111). On the other side, APMs were found in only 5% (7 out of 137) of the cases in a Chinese cohort of unilateral PA (113). Therefore, additional studies from patients with different genetic backgrounds are essential to define the prevalence of classical and non-classical unilateral PA among different cohorts.
Of great importance in clinical practice, postsurgical complete biochemical success after adrenalectomy was correlated with histological features in a German cohort of unilateral PA. The rate of biochemical cure of PA was 98% in patients with the classical histopathology (solitary aldosteronoma or APN) compared with 67% in the patients with unilateral PA caused by non-classical histopathology (111). These findings suggested the presence of a baseline abnormal aldosterone production from the contralateral gland in patients with non-classical unilateral PA ( Table 5).
KCNJ5 somatic pathogenic variants have been associated with complete clinical success in cohorts of unilateral PA from Australia, West Norway, Japan and Brazil (80,102,114,115). In a Brazilian cohort of PA, complete clinical success based in PASO criteria was more frequent in patients with aldosteronomas harboring KCNJ5 pathogenic variants than in those with pathogenic variants in other driver genes (102). However, it should be emphasized that these previous studies did not conduct a genetic investigation based on CYP11B2 staining.
Interestingly, KCNJ5 pathogenic variants have been more frequently detected in aldosteronomas (classical histopathology), which is associated with a higher chance of postsurgical complete biochemical success (57). Recently, somatic KCNJ5 pathogenic variants were not associated with clinical and biochemical outcome in a small group of 38 aldosteronomas with genetic investigation guided by CYP11B2 staining. However, the influence of KCNJ5 status in the outcome of PA patients cannot be ruled out and should be further evaluated in larger cohorts of unilateral PA with genetic investigation guided by CYP11B2 staining. Furthermore, the impact of somatic KCNJ5 pathogenic variants on clinical outcome might depend on the frequency of classical histopathology among unilateral PA cases.

PERSPECTIVES
Genetics of unilateral PA has remarkably improved in the last decade. However, most cases of bilateral hyperplasia remain without genetic etiology (15). Of great importance, a new histopathological classification has been recently proposed for aldosterone-producing lesions in unilateral PA (110). Besides the impact on the comprehension of PA pathophysiology, the histopathological features have influence in the outcome after unilateral adrenalectomy. KCNJ5 mutational status and classical histopathology of unilateral PA (aldosteronoma) have emerged as relevant predictors of clinical and biochemical outcome, respectively (102,111). Further studies will be important to characterize the spectrum of classical and non-classical unilateral PA among cohorts from different genetic backgrounds.

AUTHOR CONTRIBUTIONS
LS and AG participated on acquisition, analysis and interpretation of data, and drafted the manuscript. MA designed, drafted and revising critically the manuscript. All authors contributed to the article and approved the submitted version.