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Confirmatory testing of primary aldosteronism with saline infusion test and LC-MS/MS. | LitMetric

Confirmatory testing of primary aldosteronism with saline infusion test and LC-MS/MS.

Eur J Endocrinol

Division of Endocrinology and Diabetes, Department of Internal Medicine I, University Hospital, University of Würzburg, Würzburg, Germany.

Published: January 2021

AI Article Synopsis

  • The study examines the effectiveness of saline infusion testing (SIT) using different methods for diagnosing primary aldosteronism (PA) compared to essential hypertension (EH).
  • The research involved analyzing 187 SIT samples using both immunoassays (IA) and liquid chromatography tandem mass spectrometry (LC-MS/MS) to establish method-specific aldosterone thresholds for PA diagnosis.
  • Results show that while both methods yield useful cut-off points for diagnosing PA, the LC-MS/MS cut-off is slightly higher, and its lower diagnostic accuracy may relate to the nature of the disease's presentation and past reliance on IA results.

Article Abstract

Objective: Saline infusion testing (SIT) for confirmation of primary aldosteronism (PA) is based on impaired aldosterone suppression in PA compared to essential hypertension (EH). In the past, aldosterone was quantified using immunoassays (IA). Liquid chromatography tandem mass spectrometry (LC-MS/MS) is increasingly used in clinical routine. We aimed at a method-specific aldosterone threshold for the diagnosis of PA during SIT and explored the diagnostic utility of steroid panel analysis.

Design: Retrospective cohort study of 187 paired SIT samples (2009-2018). Diagnosis of PA (n = 103) and EH (n = 84) was established based on clinical routine workup without using LC-MS/MS values.

Setting: Tertiary care center.

Methods: LC-MS/MS using a commercial steroid panel. Receiver operator characteristics analysis was used to determine method-specific cut-offs using a positive predictive value (PPV) of 90% as criterion.

Results: Aldosterone measured by IA was on average 31 ng/L higher than with LC-MS/MS. The cut-offs for PA confirmation were 54 ng/L for IA (sensitivity: 95%, 95% CI: 89.0-98.4; specificity: 87%, 95% CI: 77.8-93.3; area under the curve (AUC): 0.955, 95% CI: 0.924-0.986; PPV: 90%, 95% CI: 83.7-93.9) and 69 ng/L for LC-MS/MS (79%, 95% CI: 69.5-86.1; 89%, 95% CI: 80.6-95.0; 0.902, 95% CI: 0.857-0.947; 90%, 95% CI: 82.8-94.4). Other steroids did not improve SIT.

Conclusions: Aldosterone quantification with LC-MS/MS and IA yields comparable SIT-cut-offs. Lower AUC for LC-MS/MS is likely due to the spectrum of disease in PA and previous decision making based on IA results. Until data of a prospective trial with clinical endpoints are available, the suggested cut-off can be used in clinical routine.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7709890PMC
http://dx.doi.org/10.1530/EJE-20-0073DOI Listing

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