{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,17]],"date-time":"2026-03-17T05:17:37Z","timestamp":1773724657622,"version":"3.50.1"},"reference-count":30,"publisher":"The Endocrine Society","issue":"9","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2016,9,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n               <jats:sec>\n                  <jats:title>Context:<\/jats:title>\n                  <jats:p>Androgen excess may be adrenal and\/or ovarian in origin; we hypothesized that a subgroup of patients with polycystic ovarian syndrome (PCOS) may have some degree of abnormal adrenocortical function.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Objective:<\/jats:title>\n                  <jats:p>The objective of the study was to evaluate the pituitary adrenal axis with an oral low- and high-dose dexamethasone-suppression test (Liddle's test) in women with PCOS.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Design:<\/jats:title>\n                  <jats:p>This was a case-control study.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Setting:<\/jats:title>\n                  <jats:p>The study was conducted at the National Institutes of Health Clinical Center.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Participants:<\/jats:title>\n                  <jats:p>A total of 38 women with PCOS and 20 healthy volunteers (HV) aged 16\u201329 years participated in the study.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Main Outcome Measures:<\/jats:title>\n                  <jats:p>Urinary free cortisol (UFC) and 17-hydroxysteroids (17OHS) before and after low- and high-dose dexamethasone and assessment of adrenal volume by computed tomography scan were measured.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Results:<\/jats:title>\n                  <jats:p>Twenty-four-hour urinary 17OHS and UFC were measured during day 1 to day 6 of the Liddle's test. Baseline UFC levels were not different between PCOS and HVs; on the day after the completion of high-dose dexamethasone administration (d 6), UFC was higher in the PCOS group (2.0 \u00b1 0.7 \u03bcg\/m2\u00b7d) than the HV group (1.5 \u00b1 0.5) (P = .038). On day 5, 17OHS and UFC were negatively correlated with adrenal volumes (left side, rp = \u22120.47, P = .009, and rp = \u22120.61, P &amp;lt; .001, respectively). PCOS patients above the 75th percentile for UFC and\/or 17OHS after high-dose dexamethasone (n = 15) had a significantly smaller total adrenal volume (6.9 \u00b1 1.9 cm3 vs 9.2 \u00b1 1.8 cm3, P = .003) when compared with the remaining PCOS patients (n = 22), but they did not have worse insulin resistance or hyperandrogenism.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Conclusions:<\/jats:title>\n                  <jats:p>In a subset of young women with PCOS, we detected a pattern of glucocorticoid secretion that mimicked that of patients with micronodular adrenocortical hyperplasia: they had smaller adrenal volumes and higher steroid hormone secretion after dexamethasone compared with the group of PCOS with appropriate response to dexamethasone.<\/jats:p>\n               <\/jats:sec>","DOI":"10.1210\/jc.2015-4019","type":"journal-article","created":{"date-parts":[[2016,6,23]],"date-time":"2016-06-23T21:57:34Z","timestamp":1466719054000},"page":"3353-3360","source":"Crossref","is-referenced-by-count":18,"title":["Bilateral Adrenal Hyperplasia as a Possible Mechanism for Hyperandrogenism in Women With Polycystic Ovary Syndrome"],"prefix":"10.1210","volume":"101","author":[{"given":"Evgenia","family":"Gourgari","sequence":"first","affiliation":[{"name":"Section on Endocrinology and Genetics (E.G., M.L., M.K., C.L., M.N., M.S., P.X., C.A.S.), Bethesda, Maryland 20892"},{"name":"Division of Pediatric Endocrinology (E.G.), Georgetown University Medical Center, Washington, DC 20007"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Maya","family":"Lodish","sequence":"additional","affiliation":[{"name":"Section on Endocrinology and Genetics (E.G., M.L., M.K., C.L., M.N., M.S., P.X., C.A.S.), Bethesda, Maryland 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