Increased disorderliness and amplified basal and pulsatile aldosterone secretion in patients with primary aldosteronism

H. M. Siragy, Johannes D Veldhuis, S. Pincus, J. D. Veldhuis

Research output: Contribution to journalArticle

81 Citations (Scopus)

Abstract

To investigate the pathophysiology of altered aldosterone secretion in patients with primary aldosteronism, the pulsatile mode of in vivo aldosterone and cortisol release was examined by quantitative deconvolution analysis in 5 normal subjects (controls) and 10 patients with aldosterone- producing adenomas (APA) under conditions of sodium (150 meq/day) balance. Episodic release of aldosterone and cortisol was assessed by sampling blood at 10-min intervals for 24 h. A waveform-independent deconvolution algorithm was used to calculate endogenous aldosterone and cortisol secretion rates on a sample by sample basis in each subject. There were no differences in the number of aldosterone or cortisol secretory bursts per day or their mean interpulse intervals between normal subjects and patients with primary aldosteronism. A 24-h rhythmicity in serum aldosterone concentrations was maintained in APA patients. Patients with primary aldosteronism had significantly higher (P < 0.01) aldosterone mean secretory rates, mean mass of aldosterone secreted per burst, maximal aldosterone secretion rates attained within each burst, and mean basal (nadir) aldosterone secretion rates. A recently introduced regularity statistic, approximate entropy (ApEn), was used to test for orderliness (small ApEn) vs. randomness (large ApEn) in the aldosterone time series. ApEn was significantly larger for the APA patients (1.433 ± 0.148) than for normal subjects (0.306 ± 0.098; P < 0.001), with complete group segmentation yielding 100% sensitivity and specificity. In contrast, a scale-invariant form of this measure, normalized ApEn, showed no significant distinction between tumoral and normal aldosterone release patterns. These ApEn findings taken together are consistent with the deconvolution results from an entirely distinct perspective, reinforcing an amplitude difference, but no frequency difference, between normal subjects and APA patients. Unexpectedly, patients with APA had significantly lower mean cortisol secretory rates, reduced cortisol secretory burst mass, and attenuated maximal cortisol secretory rates than normal subjects (P < 0.01). Plasma cortisol and aldosterone concentrations in patients remained positively correlated over short time lags. In summary, the present findings demonstrate that in normal subjects and patients with APA, both aldosterone and cortisol are secreted in a burst- like mode. The presence of substantial basal aldosterone release and increased irregularity of serial aldosterone concentrations distinguishes APA from normal subjects. Moreover, the increased plasma aldosterone concentrations in primary aldosteronism are largely due to an increase in the mass of aldosterone secreted per burst, increased interpeak (basal) aldosterone release, and a higher maximal aldosterone secretory rate (amplitude) achieved per burst. Consequently, we conclude that the proximate pathophysiological derangements of aldosterone secretion in primary aldosteronism are the enhancement of tonic aldosterone secretion with increased irregularity of serial plasma mineralocorticoid measures and failure of normal amplitude modulation of aldosterone release episodes. These findings were specific, because the frequency of aldosterone hormone secretory bursts, their concordance with cortisol, and 24-h plasma aldosterone rhythmicity remained physiological in APA.

Original languageEnglish (US)
Pages (from-to)28-33
Number of pages6
JournalJournal of Clinical Endocrinology and Metabolism
Volume80
Issue number1
StatePublished - 1995
Externally publishedYes

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Hyperaldosteronism
Aldosterone
Hydrocortisone
Adenoma
Entropy
Secretory Rate
Deconvolution
Plasmas
Periodicity

ASJC Scopus subject areas

  • Biochemistry
  • Endocrinology, Diabetes and Metabolism

Cite this

Increased disorderliness and amplified basal and pulsatile aldosterone secretion in patients with primary aldosteronism. / Siragy, H. M.; Veldhuis, Johannes D; Pincus, S.; Veldhuis, J. D.

In: Journal of Clinical Endocrinology and Metabolism, Vol. 80, No. 1, 1995, p. 28-33.

Research output: Contribution to journalArticle

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