TY - JOUR
T1 - Metabolic subtyping of adrenal tumors
T2 - Prospective multi-center cohort study in korea
AU - Ku, Eu Jeong
AU - Lee, Chaelin
AU - Shim, Jaeyoon
AU - Lee, Sihoon
AU - Kim, Kyoung Ah
AU - Kim, Sang Wan
AU - Rhee, Yumie
AU - Kim, Hyo Jeong
AU - Lim, Jung Soo
AU - Chung, Choon Hee
AU - Chun, Sung Wan
AU - Yoo, Soon Jib
AU - Ryu, Ohk Hyun
AU - Cho, Ho Chan
AU - Ram Hong, A.
AU - Ahn, Chang Ho
AU - Kim, Jung Hee
AU - Choi, Man Ho
N1 - Publisher Copyright:
© 2021 Korean Endocrine Society. All rights reserved.
PY - 2021/10
Y1 - 2021/10
N2 - Background: Conventional diagnostic approaches for adrenal tumors require multi-step processes, including imaging studies and dynamic hormone tests. Therefore, this study aimed to discriminate adrenal tumors from a single blood sample based on the combination of liquid chromatography-mass spectrometry (LC-MS) and machine learning algorithms in serum profiling of adrenal steroids. Methods: The LC-MS-based steroid profiling was applied to serum samples obtained from patients with nonfunctioning adenoma (NFA, n=73), Cushing's syndrome (CS, n=30), and primary aldosteronism (PA, n=40) in a prospective multicenter study of adrenal disease. The decision tree (DT), random forest (RF), and extreme gradient boost (XGBoost) were performed to categorize the subtypes of adrenal tumors. Results: The CS group showed higher serum levels of 11-deoxycortisol than the NFA group, and increased levels of tetrahydrocortisone (THE), 20α-dihydrocortisol, and 6β-hydroxycortisol were found in the PA group. However, the CS group showed lower levels of dehydroepiandrosterone (DHEA) and its sulfate derivative (DHEA-S) than both the NFA and PA groups. Patients with PA expressed higher serum 18-hydroxycortisol and DHEA but lower THE than NFA patients. The balanced accuracies of DT, RF, and XGBoost for classifying each type were 78%, 96%, and 97%, respectively. In receiver operating characteristics (ROC) analysis for CS, XGBoost, and RF showed a significantly greater diagnostic power than the DT. However, in ROC analysis for PA, only RF exhibited better diagnostic performance than DT. Conclusion: The combination of LC-MS-based steroid profiling with machine learning algorithms could be a promising one-step diagnostic approach for the classification of adrenal tumor subtypes.
AB - Background: Conventional diagnostic approaches for adrenal tumors require multi-step processes, including imaging studies and dynamic hormone tests. Therefore, this study aimed to discriminate adrenal tumors from a single blood sample based on the combination of liquid chromatography-mass spectrometry (LC-MS) and machine learning algorithms in serum profiling of adrenal steroids. Methods: The LC-MS-based steroid profiling was applied to serum samples obtained from patients with nonfunctioning adenoma (NFA, n=73), Cushing's syndrome (CS, n=30), and primary aldosteronism (PA, n=40) in a prospective multicenter study of adrenal disease. The decision tree (DT), random forest (RF), and extreme gradient boost (XGBoost) were performed to categorize the subtypes of adrenal tumors. Results: The CS group showed higher serum levels of 11-deoxycortisol than the NFA group, and increased levels of tetrahydrocortisone (THE), 20α-dihydrocortisol, and 6β-hydroxycortisol were found in the PA group. However, the CS group showed lower levels of dehydroepiandrosterone (DHEA) and its sulfate derivative (DHEA-S) than both the NFA and PA groups. Patients with PA expressed higher serum 18-hydroxycortisol and DHEA but lower THE than NFA patients. The balanced accuracies of DT, RF, and XGBoost for classifying each type were 78%, 96%, and 97%, respectively. In receiver operating characteristics (ROC) analysis for CS, XGBoost, and RF showed a significantly greater diagnostic power than the DT. However, in ROC analysis for PA, only RF exhibited better diagnostic performance than DT. Conclusion: The combination of LC-MS-based steroid profiling with machine learning algorithms could be a promising one-step diagnostic approach for the classification of adrenal tumor subtypes.
KW - Adrenal neoplasms
KW - Cushing syndrome
KW - Primary hyperaldosteronism
KW - Steroid metabolism
KW - Supervised machine learning
UR - http://www.scopus.com/inward/record.url?scp=85119262523&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85119262523&partnerID=8YFLogxK
U2 - 10.3803/EnM.2021.1149
DO - 10.3803/EnM.2021.1149
M3 - Article
C2 - 34674508
AN - SCOPUS:85119262523
SN - 2093-596X
VL - 36
SP - 1131
EP - 1141
JO - Endocrinology and Metabolism
JF - Endocrinology and Metabolism
IS - 5
ER -