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Makhnov, N., Skov, J., Åkerström, T., Axling, F., Andernord, D., Bergenheim, M., . . . Hellman, P. (2025). Screening For Primary Aldosteronism In 1,181 Swedish Primary Care Patients With Hypertension. Frontiers in Endocrinology, 16, Article ID 1555572.
Open this publication in new window or tab >>Screening For Primary Aldosteronism In 1,181 Swedish Primary Care Patients With Hypertension
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2025 (English)In: Frontiers in Endocrinology, E-ISSN 1664-2392, Vol. 16, article id 1555572Article in journal (Refereed) Published
Abstract [en]

Objective: Primary aldosteronism (PA) is a common cause of hypertension. It entails elevated morbidity and mortality that do not sufficiently improve with conventional antihypertensive therapy. Screening for PA by plasma aldosterone–renin ratio (ARR) enables discovery and specific treatment of affected patients. By screening primary care patients with hypertension and evaluating them further according to the Endocrine Society guidelines, we aimed to assess the prevalence of PA, the factors affecting biochemical diagnostics, and the outcome of lateralization studies and of specific treatment of the discovered PA cases.

Design, patients, and methods: Prospective evaluation of screening for PA was conducted in 1,181 patients. Screening by ARR was performed under current therapy, but without mineralocorticoid receptor antagonists (MRA), under normokalemia, and confirmed by the intravenous saline suppression test, SST#1. Those with results in a defined gray zone underwent therapy adjustment and then completed SST#2. Plasma aldosterone and ARR were compared under different stages of the diagnostic process. All patients with PA were offered adrenal venous sampling, or, in certain cases, adrenocortical-specific positron emission tomography. Lateralizing cases were offered laparoscopic adrenalectomy. Patients with bilateral disease were treated with MRA. Treatment results were assessed after a minimum of 6 months.

Results: A total of 53 discovered cases of (mostly mild) PA corresponded to its prevalence of 4.5%. Initial seated ARR was higher than recumbent ARR before SST#1. At SST#2, initial ARR and final aldosterone were higher than at SST#1. Localizing studies (accepted by 45 patients) found 14 lateralized cases. Of the 11 operated cases, 4 had aldosterone-producing adenoma, and the remainder had micro- and macronodular histopathology. A total of 31 patients had bilateral PA. Both surgical and conservative treatments were well tolerated and led to improved blood pressure and higher renin, indicating risk amelioration.

Conclusions: PA is prevalent among primary care patients with hypertension and can be screened for under current antihypertensive therapy. Aldosterone-producing adenoma was rare in this cohort. The study results support active screening of primary care patients with hypertension for PA in order to offer appropriate treatment options.

Place, publisher, year, edition, pages
Frontiers Media S.A., 2025
Keywords
primary aldosteronism, screening, hypertension, outpatients, aldosterone, renin, therapeutics
National Category
Surgery Endocrinology and Diabetes
Research subject
Medical Science
Identifiers
urn:nbn:se:uu:diva-554033 (URN)10.3389/fendo.2025.1555572 (DOI)001476399600001 ()40297172 (PubMedID)2-s2.0-105003811480 (Scopus ID)
Funder
Sjukvårdsregionala forskningsrådet Mellansverige, 651241Sjukvårdsregionala forskningsrådet Mellansverige, 842171Sjukvårdsregionala forskningsrådet Mellansverige, 930708Region Värmland, 637541Region Värmland, 741191Region Värmland, 840631Region Värmland, 930327Region Värmland, 939850Region Värmland, 967684Region Värmland, 980171Region Värmland, 993231
Available from: 2025-04-05 Created: 2025-04-05 Last updated: 2025-05-09Bibliographically approved
Makhnov, N., Axling, F., Barazeghi, E., Stålberg, P., Åkerström, T. & Hellman, P. (2025). Serum microRNAs as peripheral markers of primary aldosteronism. Frontiers in Endocrinology
Open this publication in new window or tab >>Serum microRNAs as peripheral markers of primary aldosteronism
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2025 (English)In: Frontiers in Endocrinology, E-ISSN 1664-2392Article in journal (Refereed) Published
Abstract [en]

Background: Primary aldosteronism (PA) is the principal cause of secondaryhypertension; it leads to significantly elevated cardiovascular morbidity andmortality, but only a fraction of its cases ever get detected, partially due todiagnostic procedures that are difficult to perform and to interpret. Morestraightforward diagnostic methods are needed. Lateralized, or unilateral PA(uPA), is best treated by surgery. Bilateral PA (bPA) is treated medically.Aim: The aim of our study was to explore microRNA (miRNA) in peripheral bloodas markers of PA, uPA and bPA.

Methods: In groups of subjects with primary hypertension (HT, n = 11), bPA (n =12), and uPA (n = 16), peripheral serum was used for isolation of total RNA, librarypreparation, and NGS sequencing to achieve a comparative analysis of miRNAexpression. Five-fold cross-validation support vector machine learning (ML)models were employed to search for miRNA that could be used as markers ofPA and its forms.

Results: In our cohort of patients, the discovered combinations of miRNAs could,with a high level of accuracy, sensitivity, and specificity, characterize thedifference between HT and PA, as well as between a combined group of HT +bPA vs. uPA. The differentiating parameters were moderately good forcomparison of bPA vs. uPA.

Conclusion: Within our patient cohort, and using ML, the study identifieddistinctly different miRNA profiles between HT and PA, as well as between bPAand uPA. Further validation studies may lead to the emergence of a new tool forclinical diagnostics of PA.

Place, publisher, year, edition, pages
Lausanne: Frontiers Media S.A., 2025
National Category
Surgery
Research subject
Medical Science
Identifiers
urn:nbn:se:uu:diva-553580 (URN)10.3389/fendo.2025.1511096 (DOI)001457813300001 ()40182638 (PubMedID)2-s2.0-105001691132 (Scopus ID)
Available from: 2025-03-28 Created: 2025-03-28 Last updated: 2025-04-24Bibliographically approved
Organisations
Identifiers
ORCID iD: ORCID iD iconorcid.org/0009-0002-7866-677X

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