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EDITORIAL article

Front. Endocrinol., 18 April 2023
Sec. Adrenal Endocrinology
This article is part of the Research Topic Expanding Spectrum of Primary Aldosteronism: Exploring New Grounds View all 12 articles

Editorial: Expanding spectrum of primary aldosteronism: exploring new grounds

  • 1Department of Medicine, Faculty of Medicine, Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia
  • 2Hospital Canselor Tuanku Muhriz, Jalan Yaacob Latif, Bandar Tun Razak, Kuala Lumpur, Malaysia
  • 3Department of Endocrinology, Changi General Hospital, Singapore, Singapore
  • 4Department of Medicine, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand
  • 5Department of Cardiology, National Heart Institute, Kuala Lumpur, Malaysia

Seven decades have lapsed since the first description of primary aldosteronism (PA) by Jerome W. Conn (1). Despite a significant time-lapse, PA remains an underrated cause of hypertension with devastating cardiovascular and renal complications (2, 3).

This Research Topic gathers different contributions highlighting the latest advances in the diagnosis and management of PA. In the first article by Parasiliti-Caprino et al., the accuracy of simple and adjusted aldosterone indices for assessing selectivity and lateralization of adrenal vein sampling (AVS) is evaluated. AVS is regarded as the gold standard test for PA subtyping (4). However, AVS is technically difficult and failure to cannulate both adrenal veins render the test inconclusive. The authors demonstrated the utility of aldosterone indices to determine both selectivity and lateralization. These indices could potentially be useful when only one adrenal vein is successfully cannulated, and their utility should be determined in future prospective trials.

The second article highlights the importance of accurate catheter tip placement during AVS which is critical in the interpretation of the results. Traditionally, the ratio of plasma cortisol concentration in the adrenal vein to peripheral vein defines the selectivity index (SI). However, with no standardized cut-off levels, this limits the applicability of AVS when cortisol is being utilized (5, 6). The use of free metanephrine (FMN) has been shown to be superior to cortisol in assessing SI (7, 8). This study shows that FMN is a better analyte than cortisol in confirming the correct placement of the catheter’s tip. The main limitation, however, was that no confirmatory tests were performed. Other studies have also explored the use of different analytes such as aldosterone-to-renin ratio (ARR) in combination with cortisol SI (9) and plasma metanephrines in addition to cortisol (10). While the results are promising, further research is needed to establish the utility of these markers especially in those with confirmed PA.

The diagnosis of PA requires the demonstration of an unsuppressed aldosterone level by various suppression tests (11). The oral salt loading test (OSLT) has been widely used in the diagnostic work-up, albeit its accuracy has been challenged in recent years. In the third article, Ozeki et al. present a new chemiluminescent enzyme immunoassay (CLEIA) based on a two- step sandwich method to measure 24-hour urine aldosterone excretion. The accuracy of aldosterone measurement in urine samples using various methods have also been examined previously. Liquid chromatography-tandem mass spectrometry (LC-MS/MS) was noted to have the highest accuracy (12). The lower cut-off value suggested for PA diagnosis needs to be validated in a larger clinical trial.

The fourth article focuses on the role of urinary extracellular vesicles (uEVs) sodium chloride cotransporter (NCC) in PA subtyping. In view of the invasive nature and technical difficulties of AVS, identifying a non-invasive alternative is crucial. The authors show that NCC can be potentially used to distinguish between different subtypes of PA as the expression of phosphorylated form of NCC (pNCC) in uEVs are different in various subtypes and genotypes. Previous studies have explored the use of uEVs as a biomarker in lupus nephritis and diabetic nephropathy where the presence of uEVs provide insights into the pathophysiology and aid the diagnosis and management (13, 14). The main limitations of this study include the small sample size and the lack of a validation cohort. Although the study highlights the potential of using uEVs as a non-invasive biomarker to subtype PA, further research in this field is warranted.

In the fifth article, Nguyen et al. recruited 300 patients with a recent stroke and reported the prevalence of PA amongst those with hypertension, resistant hypertension and hypertension with atrial fibrillation (AF) as 4%, 11% and 30% respectively. Previous studies have shown that patients with PA are at increased risk of stroke and AF (15, 16). This study highlights the importance of screening for PA, particularly in high-risk groups of patients. This approach will enable early detection and treatment of a potentially reversible cause of hypertension and stroke.

The sixth article by Puar et al. demonstrated that PA treatment improved subclinical left ventricular (LV) systolic function, using speckle-tracking echocardiography to assess LV global longitudinal strain (GLS). While previous studies have shown that patients with PA have impaired LV systolic function (17), this study demonstrated that surgery led to better improvement compared to medical therapy, and that reversal of renin suppression may be a key factor in improving systolic function.

The seventh article by Huang et al. investigates the relationship between vascular ageing and left ventricular concentric geometry (LVCG) in patients with newly diagnosed PA. In this study carotid intima-media thickness (cIMT) is significantly associated with left ventricular hypertrophy (LVH) whilst brachial-ankle pulse wave velocity (baPWV) is significantly associated with LVCG. While the study has some limitations, such as its retrospective and single-center design, its findings are consistent with previous research. Wang et al. (18) demonstrate a positive correlation between baPWV and left ventricular mass index in hypertensive patients. This study provides important insights into the early assessment of cardiac damage in newly diagnosed PA.

The review article by Ahmed and Hundemer provides a comprehensive literature search encompassing studies from the past two decades supporting surgical adrenalectomy as the preferred treatment option for unilateral PA compared to medical therapy. Adrenalectomy is highly successful in reversing the clinical and biochemical abnormalities, mitigating long-term risks, and offering the potential for disease cure. Several other studies also favored surgical approach with significant reductions in blood pressure, glucose, number of medications used, and cardiovascular events and mortality (2, 3, 19). This review underscores the importance of personalized treatment plans for improved patient outcomes.

Tetti et al. in their review provide an extensive overview of the current knowledge on the molecular and cellular mechanisms that contribute to the pathogenesis of PA. The authors focus on recent advances in the understanding of the disrupted cell growth mechanisms in PA through the combined application of transcriptomics, metabolomics, and epigenetics. The review is a valuable resource for clinicians as it highlights the key findings in the field, fill up the gaps in the literature and explore areas where further research is needed.

Loh and Sukor presented a review article that collates and puts into perspective current available research on the association between PA and obstructive sleep apnea (OSA). Given the high prevalence of hypertension, PA, and OSA, understanding their potential association and clinical implications is important. The authors critically analyzed the existing literature and identified several limitations in the currently available studies, which include heterogeneity in the study designs and populations, lack of uniform criteria for diagnosis and treatment of PA and OSA, and potential confounding factors such as obesity and diabetes. Although other studies have also suggested a potential link between PA and OSA (20, 21), there is a need for further research to elucidate the relationship between these two conditions.

A large majority of operated aldosterone-producing adenomas (APAs) harbour known somatic mutations, which are associated with membrane depolarisation and increased aldosterone production. However, mechanisms driving cell proliferation of these adenomas remained unknown. Abdellatif et al. summarizes the current knowledge on known regulators of adrenal growth and function. In addition, they have focused on the interplay between the hormonal and vascular interfaces which may explain the development of APAs and PA. The strength of this review lies in its comprehensive coverage of the current knowledge on the topic, drawing from various research disciplines including endocrinology, molecular genetics and vascular biology.

In conclusion, this Research Topic provides a timely overview of the latest advances in the diagnosis and treatment of PA and its associated sequelae. The articles included in this Research Topic provide valuable insights into the expanding pathophysiology of PA and the need for ongoing research to fill up the gap of this important disease entity.

Author contributions

All authors listed have made a substantial, direct, and intellectual contribution to the work and approved it for publication.

Acknowledgments

We would like to acknowledge all the editors, authors and reviewers of this Research Topic.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

1. Conn JW. The evolution of primary aldosteronism: 1954-1967. Harvey Lectures (1966) 62:257–91.

PubMed Abstract | Google Scholar

2. Sechi LA, Colussi G, Di Fabio A, Catena C. Cardiovascular and renal damage in primary aldosteronism: outcomes after treatment. Am J Hypertension (2010) 23(12):1253–60. doi: 10.1038/ajh.2010.169

CrossRef Full Text | Google Scholar

3. Rossi GP, Sechi LA, Giaccheti G, Ronconi V, Strazzullo P, Funder JW. Primary aldosteronism: cardiovascular, renal and metabolic implications. Trends Endocrinol Metab (2008) 19(3):88–90. doi: 10.1016/j.tem.2008.01.006

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Rossi GP, Sacchetto A, Chiesura-Corona M, Toni RD, Gallina M, Feltrin GP, et al. Identification of the etiology of primary aldosteronism with adrenal vein sampling in patients with equivocal computed tomography and magnetic resonance findings: results in 104 consecutive cases. J Clin Endocrinol Metab (2001) 86:1083–90. doi: 10.1210/jcem.86.3.7287

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Kline G, Leung A, So B, Chin A, Harvey A, Pasieka JL. Application of strict criteria in adrenal venous sampling increases the proportion of missed patients with unilateral disease who benefit from surgery for primary aldosteronism. J Hypertension (2018) 36(6):1407–13. doi: 10.1097/HJH.0000000000001693

CrossRef Full Text | Google Scholar

6. Rossi Gian P, Rossitto G, Amar L, Azizi M, Riester A, Reincke M, et al. Clinical outcomes of 1625 patients with primary aldosteronism subtyped with adrenal vein sampling. Hypertension (2019) 24:800–8. doi: 10.1161/HYPERTENSIONAHA.119.13463

CrossRef Full Text | Google Scholar

7. Dekkers T, Deinum J, Schultzekool LJ, Blondin D, Vonend O, Hermus AR, et al. Plasma metanephrine for assessing the selectivity of adrenal venous sampling. Hypertension (2013) 62(6):1152–7. doi: 10.1161/HYPERTENSIONAHA.113.01601

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Ceolotto G, Antonelli G, Caroccia B, Battistel M, Barbiero G, Plebani M, et al. Comparison of cortisol, androstenedione and metanephrines to assess selectivity and lateralization of adrenal vein sampling in primary aldosteronism. J Clin Med (2021) 10(20):4755. doi: 10.3390/jcm10204755

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Monticone S, Satoh F, Giacchetti G, Viola A, Morimoto R, Kudo M, et al. Effect of adrenal venous sampling on clinical outcomes in patients with primary aldosteronism: a randomized clinical trial. JAMA (2019) 322(6):1–11. doi: 10.1001/jama.2019.9814

CrossRef Full Text | Google Scholar

10. Lenders JWM, Duh Q-Y, Eisenhofer G, Gimenez-Roqueplo A-P, Grebe SKG, Murad MH, et al. Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline. J Clin Endocrinol Metab (2014) 99(6):1915–42. doi: 10.1210/jc.2014-1498

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Funder JW, Carey RM, Mantero F, Murad MH, Reincke M, Shibata H, et al. The management of primary aldosteronism: case detection, diagnosis, and treatment: an endocrine society clinical practice guideline. J Clin Endocrinol Metab (2016) 101(5):1889–916. doi: 10.1210/jc.2015-4061

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Hua K-F, Wu Y-H, Zhang S-T. Clinical diagnostic value of liquid chromatography- tandem mass spectrometry method for primary aldosteronism in patients with hypertension: a systematic review and meta-analysis. Front Endocrinol (Lausanne) (2022) 13:1032070. doi: 10.3389/fendo.2022.1032070

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Borges FT, Reis LA, Gomes CP, Moreira FT, Pereira RW. Urinary extracellular vesicles as a source of diagnostic and prognostic biomarkers in diabetic nephropathy. Front Endocrinol (2021) 12:667586. doi: 10.3389/fendo.2021.667586

CrossRef Full Text | Google Scholar

14. Yu X, Lu H, Zhou X, Huang T, Gao Y, Wu W, et al. Urinary extracellular vesicles as a potential source of biomarkers for lupus nephritis. Int J Rheumatic Dis (2020) 23(3):404–12. doi: 10.1111/1756-185X.13794

CrossRef Full Text | Google Scholar

15. Blanc J, Amar L, Azizi M, Burnier M, Chanson P, Cicala MV, et al. Diagnosis and treatment of primary aldosteronism in 2020: guidelines and recommendations from the French society of hypertension. Arch Cardiovasc Dis (2021) 114(10):645–58.

Google Scholar

16. Mulatero P, Monticone S, Bertello C, Tizzani D, Iannaccone A, Crudo V, et al. Long-term cardio- and cerebrovascular events in patients with primary aldosteronism. J Clin Endocrinol Metab (2010) 95(12):4825–33. doi: 10.1210/jc.2010-0951

CrossRef Full Text | Google Scholar

17. Chen Z-W, Huang K-C, Lee J-K, Lin L-C, Chen C-W, Chang Y-Y, et al. Aldosterone induces left ventricular subclinical systolic dysfunction: a strain imaging study. J Hypertens (2018) 36:353–60. doi: 10.1097/HJH.0000000000001534

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Wang KL, Cheng HM, Sung SH, Chuang S-Y, Li C-H, Spurgeon HA, et al. Wave reflection and arterial stiffness in the prediction of 15-year all-cause and cardiovascular mortalities: a community-based study. Hypertension (2010) 55(6):799–805. doi: 10.1161/HYPERTENSIONAHA.109.140798

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Wu J, Yan P, Chen J, Cui L, Cao J. Surgical vs. medical therapy for unilateral primary aldosteronism: a systematic review and meta-analysis. Front Endocrinol (2021) 12:693965.

Google Scholar

20. Buffolo F, Li Q, Monticone S, Heinrich DA, Mattei A, Pieroni J, et al. Primary aldosteronism and obstructive sleep apnea: a cross-sectional multi-ethnic study. Hypertension (2019) 74(6):1532–40. doi: 10.1161/HYPERTENSIONAHA.119.13833

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Dobrowolski P, Kolodziejczyk-Kruk S, Warchol-Celinska E, Kabat M, Ambroziak U, Wrobel A, et al. Primary aldosteronism is highly prevalent in patients with hypertension and moderate to severe obstructive sleep apnea. J Clin Sleep Med (2021) 17(4):629–37. doi: 10.5664/jcsm.8960

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: primary aldosteronism, aldosterone producing adenoma, adrenalectomy, Mineralocorticoid receptor (MR) antagonist, cardiovascular, adrenal venous sampling, stroke, obstructive sleep apnea

Citation: Sukor N, Puar TH, Sunthornyothin S and Kamaruddin NA (2023) Editorial: Expanding spectrum of primary aldosteronism: exploring new grounds. Front. Endocrinol. 14:1171857. doi: 10.3389/fendo.2023.1171857

Received: 22 February 2023; Accepted: 04 April 2023;
Published: 18 April 2023.

Edited and Reviewed by:

Jeff M. P. Holly, University of Bristol, United Kingdom

Copyright © 2023 Sukor, Puar, Sunthornyothin and Kamaruddin. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Norlela Sukor, drlela2020@yahoo.com

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.