4.3 Article

Variability of Aldosterone Measurements During Adrenal Venous Sampling for Primary Aldosteronism

Journal

AMERICAN JOURNAL OF HYPERTENSION
Volume 34, Issue 1, Pages 34-45

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/ajh/hpaa151

Keywords

adrenal venous sampling; aldosterone; blood pressure; hypertension; primary aldosteronism

Funding

  1. National Institutes of Health [R01 DK115392, R01 DK16618, R01 HL153004, 2T32 HL007609-32]

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The study investigated patients with primary aldosteronism who underwent adrenal venous sampling (AVS) and found significant variability in aldosterone concentrations during the procedure. A single measurement of venous aldosterone lacks precision and reproducibility in primary aldosteronism.
BACKGROUND Variability of aldosterone concentrations has been described in patients with primary aldosteronism. METHODS We performed a retrospective cohort study of 340 patients with primary aldosteronism who underwent adrenal venous sampling (AVS) at a tertiary referral center, 116 of whom also had a peripheral venous aldosterone measured hours before the procedure. AVS was performed by the same interventional radiologist using bilateral, simultaneous sampling, under unstimulated and then stimulated conditions, and each sample was obtained in triplicate. Main outcome measures were: (i) change in day of AVS venous aldosterone from pre-AVS to intra-AVS and (ii) variability of triplicate adrenal venous aldosterone concentrations during AVS. RESULTS Within an average duration of 131 minutes, 81% of patients had a decline in circulating aldosterone concentrations (relative decrease of 51% and median decrease of 7.0 ng/dl). More than a quarter (26%) of all patients had an inferior vena cava aldosterone of <= 5 ng/dl at AVS initiation. The mean coefficient of variation of triplicate adrenal aldosterone concentrations was 30% and 39%, in the left and right veins, respectively (corresponding to a percentage difference of 57% and 73%), resulting in lateralization discordance in up to 17% of patients if the lateralization index were calculated using only one unstimulated aldosterone-to-cortisol ratio rather than the average of triplicate measures. CONCLUSIONS Circulating aldosterone levels can reach nadirs conventionally considered incompatible with the primary aldosteronism diagnosis, and adrenal venous aldosterone concentrations exhibit acute variability that can confound AVS interpretation. A single venous aldosterone measurement lacks precision and reproducibility in primary aldosteronism. [GRAPHICS] .

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