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Interpretation of Abnormal Dexamethasone Suppression Test is Enhanced With Use of Synchronous Free Cortisol Assessment.
Genere, Natalia; Kaur, Ravinder Jeet; Athimulam, Shobana; Thomas, Melinda A; Nippoldt, Todd; Van Norman, Molly; Singh, Ravinder; Grebe, Stefan; Bancos, Irina.
Afiliação
  • Genere N; Division of Endocrinology, Metabolism, and Lipid Research, Washington University School of Medicine; Saint Louis, MO 63130, USA.
  • Kaur RJ; Division of Endocrinology, Diabetes, Metabolism and Nutrition, Mayo Clinic, Rochester, MN 55905, USA.
  • Athimulam S; Division of Endocrinology, Diabetes, Metabolism and Nutrition, Mayo Clinic, Rochester, MN 55905, USA.
  • Thomas MA; Division of Endocrinology, Diabetes, Metabolism and Nutrition, Mayo Clinic, Rochester, MN 55905, USA.
  • Nippoldt T; Department of Medicine, Division of Endocrinology, Diabetes, Bone and Mineral Disorders, Henry Ford Health System, Detroit, MI 48202, USA.
  • Van Norman M; Division of Endocrinology, Diabetes, Metabolism and Nutrition, Mayo Clinic, Rochester, MN 55905, USA.
  • Singh R; Division of Endocrinology, Diabetes, Metabolism and Nutrition, Mayo Clinic, Rochester, MN 55905, USA.
  • Grebe S; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN 55905, USA.
  • Bancos I; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN 55905, USA.
J Clin Endocrinol Metab ; 107(3): e1221-e1230, 2022 02 17.
Article em En | MEDLINE | ID: mdl-34648626
ABSTRACT
CONTEXT Interpretation of dexamethasone suppression test (DST) may be influenced by dexamethasone absorption and metabolism and by the altered cortisol binding.

OBJECTIVE:

We aimed to determine the normal ranges of free cortisol during DST in participants without adrenal disorders and to identify the population of patients where post-DST free cortisol measurements add value to the diagnostic workup. DESIGN AND

SETTING:

Cross-sectional study conducted in a tertiary medical center.

PARTICIPANTS:

Adult volunteers without adrenal disorders (n = 168; 47 women on oral contraceptive therapy [OCP], 66 women not on OCP, 55 men) and patients undergoing evaluation for hypercortisolism (n = 196; 16 women on OCP). MEASUREMENTS Post-DST dexamethasone and free cortisol (mass spectrometry) and total cortisol (immunoassay). MAIN OUTCOME

MEASURES:

Reference range for post-DST free cortisol, diagnostic accuracy of post-DST total cortisol.

RESULTS:

Adequate dexamethasone concentrations (≥0.1 mcg/dL) were seen in 97.6% volunteers and 96.3% patients. Only 25.5% of women volunteers on OCP had abnormal post-DST total cortisol (>1.8 mcg/dL). In volunteers, the upper post-DST free cortisol range was 48 ng/dL in men and women not on OCP, and 79 ng/dL in women on OCP. When compared with post-DST free cortisol, diagnostic accuracy of post-DST total cortisol was 87.3% (95% CI, 81.7-91.7); all false-positive results occurred in patients with post-DST cortisol between 1.8 and 5 mcg/dL. OCP use was the only factor associated with false-positive results (21.1% vs 4.9%, P = 0.02).

CONCLUSIONS:

Post-DST free cortisol measurements are valuable in patients with optimal dexamethasone concentrations and post-DST total cortisol between 1.8 and 5 mcg/dL.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Dexametasona / Hidrocortisona / Síndrome de Cushing Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Dexametasona / Hidrocortisona / Síndrome de Cushing Idioma: En Ano de publicação: 2022 Tipo de documento: Article