Development and Validation of Prediction Models for Subtype Diagnosis of Patients With Primary Aldosteronism
Author(s) -
Jacopo Burrello,
Alessio Burrello,
Jacopo Pieroni,
Elisa Sconfienza,
Vittorio Forestiero,
Paola Rabbia,
Christian Adolf,
Martín Reincke,
Franco Veglio,
Tracy Ann Williams,
Silvia Monticone,
Paolo Mulatero
Publication year - 2020
Publication title -
the journal of clinical endocrinology and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.206
H-Index - 353
eISSN - 1945-7197
pISSN - 0021-972X
DOI - 10.1210/clinem/dgaa379
Subject(s) - medicine , gold standard (test) , primary aldosteronism , cohort , context (archaeology) , radiology , machine learning , artificial intelligence , aldosterone , computer science , paleontology , biology
Context Primary aldosteronism (PA) comprises unilateral (lateralized [LPA]) and bilateral disease (BPA). The identification of LPA is important to recommend potentially curative adrenalectomy. Adrenal venous sampling (AVS) is considered the gold standard for PA subtyping, but the procedure is available in few referral centers. Objective To develop prediction models for subtype diagnosis of PA using patient clinical and biochemical characteristics. Design, Patients and Setting Patients referred to a tertiary hypertension unit. Diagnostic algorithms were built and tested in a training (N = 150) and in an internal validation cohort (N = 65), respectively. The models were validated in an external independent cohort (N = 118). Main outcome measure Regression analyses and supervised machine learning algorithms were used to develop and validate 2 diagnostic models and a 20-point score to classify patients with PA according to subtype diagnosis. Results Six parameters were associated with a diagnosis of LPA (aldosterone at screening and after confirmatory testing, lowest potassium value, presence/absence of nodules, nodule diameter, and computed tomography results) and were included in the diagnostic models. Machine learning algorithms displayed high accuracy at training and internal validation (79.1%-93%), whereas a 20-point score reached an area under the curve of 0.896, and a sensitivity/specificity of 91.7/79.3%. An integrated flowchart correctly addressed 96.3% of patients to surgery and would have avoided AVS in 43.7% of patients. The external validation on an independent cohort confirmed a similar diagnostic performance. Conclusions Diagnostic modelling techniques can be used for subtype diagnosis and guide surgical decision in patients with PA in centers where AVS is unavailable.
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