4.7 Article

11-Oxygenated Androgens Are Biomarkers of Adrenal Volume and Testicular Adrenal Rest Tumors in 21-Hydroxylase Deficiency

Journal

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
Volume 102, Issue 8, Pages 2701-2710

Publisher

ENDOCRINE SOC
DOI: 10.1210/jc.2016-3989

Keywords

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Funding

  1. National Institutes of Health [1K08DK109116, R01GM086596]
  2. Michigan Institute for Clinical and Health Research Translational Science Award [U046500]
  3. National Institutes of Health
  4. National Institutes of Health under Michigan Nutrition Obesity Center [DK089503]

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Context: Patients with 21-hydroxylase deficiency (21OHD) have long-term complications, resulting from poor disease control and/or glucocorticoid overtreatment. Lack of optimal biomarkers has made it challenging to tailor therapy and predict long-term outcomes. Objective: To identify biomarkers of disease control and long-term complications in 21OHD. Setting and Participants: Cross-sectional study of 114 patients (70 males), ages 2 to 67 years (median, 15 years), seen in a tertiary referral center. Methods: We correlated a mass-spectrometry panel of 23 steroids, obtained before first morning medication, with bone age advancement (children), adrenal volume (adults), testicular adrenal rest tumors (TART), hirsutism, menstrual disorders, and pituitary hormones. Results: Total adrenal volume correlated positively with 18 steroids, most prominently 21-deoxycortisol and four 11-oxygenated-C-19 (11oxC19) steroids: 11 beta-hydroxyandrostenedione (11OHA4), 11-ketoandrostenedione (11ketoA4), 11 beta-hydroxytestosterone (11OHT), and 11-ketotestosterone (11ketoT) (r approximate to 0.7, P < 0.0001). Nine steroids were significantly higher (P <= 0.01) in males with TART compared with those without TART, including 11OHA4 (6.8-fold), 11OHT (4.9-fold), 11ketoT (3.6-fold), 11ketoA4 (3.3-fold), and pregnenolone sulfate (PregS; 4.8-fold). PregS (28.5-fold) and 17-hydroxypregnenolone sulfate (19-fold) levels were higher (P < 0.01) in postpubertal females with menstrual disorders. In males, testosterone levels correlated positively with all 11oxC19 steroids in Tanner stages 1 and 2 (r approximate to 0.7; P, 0.001) but negatively in Tanner stage 5 (r = 20.3 and P < 0.05 for 11ketoA4 and 11ketoT). In females, testosterone level correlated positively with all four 11oxC19 steroids across all Tanner stages (r approximate to 0.8; P < 0.0001). Conclusion: 11oxC19 steroids and PregS might serve as clinically useful biomarkers of disease control and long-term complications in 21OHD.

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