2019
DOI: 10.1053/j.ackd.2019.03.018
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Dr. Conn Lives on: Insights Into Screening and Genetics of Primary Aldosteronism

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Cited by 4 publications
(4 citation statements)
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“…40 Even among academic centers, <10% of patients with resistant hypertension are screened for primary aldosteronism, and early diagnosis remains uncommon. 41,42 Beyond patients with true resistant hypertension, it is also reasonable to evaluate secondary causes in young hypertensive individuals, patients with accelerated or abrupt-onset hypertension, and in patients with signs, symptoms or laboratory findings indicating a discrete etiology. The presence of hypertension-mediated organ damage or severe comorbidities will intensify the need for BP lowering.…”
Section: Lack Of Progress In Hypertension Controlmentioning
confidence: 99%
See 1 more Smart Citation
“…40 Even among academic centers, <10% of patients with resistant hypertension are screened for primary aldosteronism, and early diagnosis remains uncommon. 41,42 Beyond patients with true resistant hypertension, it is also reasonable to evaluate secondary causes in young hypertensive individuals, patients with accelerated or abrupt-onset hypertension, and in patients with signs, symptoms or laboratory findings indicating a discrete etiology. The presence of hypertension-mediated organ damage or severe comorbidities will intensify the need for BP lowering.…”
Section: Lack Of Progress In Hypertension Controlmentioning
confidence: 99%
“…The prevalence of primary aldosteronism in patients with resistant hypertension is above 20% but largely unrecognized 40 . Even among academic centers, <10% of patients with resistant hypertension are screened for primary aldosteronism, and early diagnosis remains uncommon 41,42 …”
Section: Multidisciplinary Evaluation and Treatment Decision‐makingmentioning
confidence: 99%
“…Most of the mutations identified activate intracellular pathways leading to increased intracellular calcium and trigger increased aldosterone production. Identifying these gene mutations can have potential implications for diagnosis and treatment but to date remain a research tool that is not yet clinically applied [25 ▪▪ ,26 ▪ ].…”
Section: Primary Aldosteronismmentioning
confidence: 99%
“…Існування різновидів родинного гіперальдостеронізму з відомими генетичними мутаціями дало унікальну можливість вивчити незалежно від артеріального тиску ефекти надлишку альдостерону. Дослідження членів цих родин дозволило виявити осіб з підтвердженим біохімічним способом ПГА до початку АГ, а отже, й оцінити ефекти надлишку альдостерону незалежно від рівня артеріального тиску [29,30].…”
Section: рисунок 3 механізми за допомогою яких надлишок альдостерону спричиняє розвиток фібриляції передсердь і серцевої недостатностіunclassified