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Published on: September 15, 2017
Primary aldosteronism, a common entity? the myth persists
1Department of Medical Sciences, Western General Hospital, University of Edinburgh, Scotland, UK.
Journal of Human Hypertension
|March 16, 2002
Summary
Primary hyperaldosteronism is a hypertension cause, but the aldosterone-to-renin ratio test may overdiagnose it. Many identified patients have low-renin hypertension, not mineralocorticoid excess, and may not benefit from specific treatments.
Area of Science:
- Endocrinology
- Hypertension Research
- Clinical Biochemistry
Background:
- Primary hyperaldosteronism is a significant cause of hypertension.
- It is characterized by excess aldosterone production and suppressed plasma renin levels.
- Surgical cure is possible for aldosterone-secreting adenomas, but not for nodular hyperplasia.
Purpose of the Study:
- To critically examine the diagnostic utility of the aldosterone-to-renin ratio (ARR) in primary hyperaldosteronism.
- To evaluate whether an abnormal ARR reliably identifies mineralocorticoid hypertension.
- To assess the clinical implications of widespread ARR screening.
Main Methods:
- Literature review and critical analysis of existing studies on primary hyperaldosteronism and ARR testing.
- Examination of the biochemical definition of hyperaldosteronism and its relationship with renin levels.
- Assessment of the prevalence and clinical characteristics of patients identified by ARR screening.
Main Results:
- An abnormal ARR is often a marker of the low-renin state rather than definitive mineralocorticoid hypertension.
- Many patients identified by ARR screening have low-renin hypertension, which is not amenable to specific therapies.
- True primary hyperaldosteronism (Conn's syndrome) is less common than suggested by ARR screening.
Conclusions:
- The aldosterone-to-renin ratio test may not be a sufficiently specific or cost-effective screening tool for primary hyperaldosteronism.
- Widespread use of ARR testing may lead to overdiagnosis of mineralocorticoid hypertension and unnecessary investigations.
- Further controlled trials are needed to validate claims regarding spironolactone sensitivity in patients with abnormal ARR results.
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