Salivary Profiles of 11-oxygenated Androgens Follow a Diurnal Rhythm in Patients With Congenital Adrenal Hyperplasia

被引:8
|
作者
Nowotny, Hanna Franziska [1 ]
Auer, Matthias K. [1 ]
Lottspeich, Christian [1 ]
Schmidt, Heinrich [2 ]
Dubinski, Ilja [2 ]
Bidlingmaier, Martin [1 ]
Adaway, Jo [3 ]
Hawley, James [3 ]
Keevil, Brian [3 ]
Reisch, Nicole [1 ]
机构
[1] LMU Munchen, Klinikum Univ Munchen, Med Klin & Poliklin 4, D-80336 Munich, Germany
[2] LMU Munchen, Dr von Haunersches Childrens Hosp, Dept Pediat Endocrinol, Klinikum Univ Munchen, D-80336 Munich, Germany
[3] Manchester Univ Fdn NHS Trust, Manchester Acad Hlth Sci Ctr, Dept Clin Biochem, Manchester M23 9LT, Lancs, England
来源
关键词
congenital adrenal hyperplasia; saliva; diurnal rhythm; 11-ketotestosterone; 11-oxygenated androgens; STEROIDS; ANDROSTENEDIONE; 17-HYDROXYPROGESTERONE; PROGESTERONE; THERAPY; PLASMA; ADULT;
D O I
10.1210/clinem/dgab446
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context: Several studies have highlighted the importance of the 11-oxygenated 19-carbon (11oxC19) adrenal-derived steroids as potential biomarkers for monitoring patients with 21-hydroxylase deficiency (21OHD). Objective: To analyze circadian rhythmicity of 11oxC19 steroids in saliva profiles and evaluate their relevance as potential monitoring parameters in 21OHD. Design, Setting, and Participants: Cross-sectional single-center study including 59 patients with classic 21OHD (men=30; women=29) and 49 body mass index- and age-matched controls (men=19; women=30). Outcome Measures: Salivary concentrations of the following steroids were analyzed by liquid chromatography-tandem mass spectrometry: 17-hydroxyprogesterone (17OHP), androstenedione (A4), testosterone (T), 11 beta-hydroxyandrostenedione (11OHA4), and 11-ketotestosterone (11KT). Results: Similar to the previously described rhythmicity of 17OHP, 11-OHA4 and 11KT concentrations followed a distinct diurnal rhythm in both patients and controls with highest concentrations in the early morning and declining throughout the day (11OHA4: mean reduction of hormone concentrations between timepoint 1 and 5 (Delta(mean)) in male patients=66%; male controls Delta(mean)=83%; female patients Delta(mean)=47%; female controls Delta(mean)=86%; 11KT: male patients Delta(mean)=57%; male controls Delta(mean)=63%; female patients Delta(mean)=50%; female controls Delta(mean)=76%). Significant correlations between the area under the curve for 17OHP and 11KT (r(male)(p)=0.773(<0.0001); r(female)(p)=0.737(<0.0001)), and 11OHA4 (r(male)(p)=0.633(0.0002); r(female)(p)=0.564(0.0014)) were observed in patients but not present or reduced in controls. Conclusions: Adrenal 11oxC19 androgens are secreted following a diurnal pattern. This should be considered when evaluating their utility for monitoring treatment control.
引用
收藏
页码:E4509 / E4519
页数:11
相关论文
共 50 条
  • [41] CHARACTERIZATION OF ZONA GLOMERULOSA FUNCTION IN PATIENTS WITH CLASSIC AND NONCLASSIC FORMS OF CONGENITAL ADRENAL-HYPERPLASIA DUE TO 11-BETA-HYDROXYLASE DEFICIENCY
    CASTROMAGANA, M
    ANGULO, M
    CANAS, JA
    MAZUR, B
    SARRANTONIO, M
    VITOLLO, P
    PALEKAR, A
    FUENTES, B
    LEE, A
    [J]. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, 1995, 8 (01): : 19 - 25
  • [42] Two novel mutations in CYP11B1 and modeling the consequent alterations of the translated protein in classic congenital adrenal hyperplasia patients
    Mohammad Reza Abbaszadegan
    Soolmaz Hassani
    Rahim Vakili
    Mohammad Reza Saberi
    Alireza Baradaran-Heravi
    Azadeh A’rabi
    Mahin Hashemipour
    Maryam Razzaghi-Azar
    Omeed Moaven
    Ali Baratian
    Mitra Ahadian
    Fatemeh Keify
    Nathalie Meurice
    [J]. Endocrine, 2013, 44 : 212 - 219
  • [43] Phenotypic, metabolic, and molecular genetic characterization of six patients with congenital adrenal hyperplasia caused by novel mutations in the CYP11B1 gene
    Huy-Hoang Nguyen
    Eiden-Plach, Antje
    Hannemann, Frank
    Malunowicz, Ewa M.
    Hartmann, Michaela F.
    Wudy, Stefan A.
    Bernhardt, Rita
    [J]. JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2016, 155 : 126 - 134
  • [44] Erratum to: Two novel mutations in CYP11B1 and modeling the consequent alterations of the translated protein in classic congenital adrenal hyperplasia patients
    Mohammad Reza Abbaszadegan
    Soolmaz Hassani
    Rahim Vakili
    Mohammad Reza Saberi
    Alireza Baradaran-Heravi
    Azadeh A’rabi
    Mahin Hashemipour
    Maryam Razzaghi-Azar
    Omeed Moaven
    Ali Baratian
    Mitra Ahadian
    Fatemeh Keify
    Nathalie Meurice
    [J]. Endocrine, 2013, 44 : 271 - 271
  • [45] Long term follow up of adult male patients with classic congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency: outcome in 23 affected male patients
    de la Perriere, Aude Brac
    Tardy, Veronique
    Bretones, Patricia
    Plotton, Ingrid
    David, Michel
    Morel, Yves
    Chatelain, Pierre
    Pugeat, Michel
    [J]. HORMONE RESEARCH, 2009, 72 : 68 - 68
  • [46] Long-term follow-up of female patients with congenital adrenal hyperplasia from 21-hydroxylase deficiency, with special emphasis on the results of vaginoplasty
    Krege, S
    Walz, KH
    Hauffa, BP
    Körner, II
    Rübben, H
    [J]. BJU INTERNATIONAL, 2000, 86 (03) : 253 - 258
  • [47] A Rare Cause of Congenital Adrenal Hyperplasia: Clinical and Genetic Findings and Follow-up Characteristics of Six Patients with 17-Hydroxylase Deficiency Including Two Novel Mutations
    Kardelen, Asli Derya
    Toksoy, Guvon
    Bas, Firdevs
    Abali, Zehra Yavas
    Gencay, Genco
    Poyrazoglu, Sukran
    Bundak, Ruveyde
    Altunoglu, Umut
    Avci, Sahin
    Najafli, Adam
    Uyguner, Oya
    Karaman, Birsen
    Basaran, Seher
    Darendeliler, Feyza
    [J]. JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, 2018, 10 (03) : 206 - 215
  • [48] Long-term follow-up of female patients with congenital adrenal hyperplasia from 21-hydroxylase deficiency, with special emphasis on the results of vaginoplasty - Editorial comment
    Gearhart, JP
    [J]. BJU INTERNATIONAL, 2000, 86 (03) : 258 - 259
  • [49] Two novel mutations in CYP11B1 and modeling the consequent alterations of the translated protein in classic congenital adrenal hyperplasia patients (vol 44, pg 212, 2013)
    Abbaszadegan, Mohammad Reza
    Hassani, Soolmaz
    Vakili, Rahim
    Saberi, Mohammad Reza
    Baradaran-Heravi, Alireza
    A'rabi, Azadeh
    Hashemipour, Mahin
    Razzaghi-Azar, Maryam
    Moaven, Omeed
    Baratian, Ali
    Ahadian, Mitra
    Keify, Fatemeh
    Meurice, Nathalie
    [J]. ENDOCRINE, 2013, 44 (01) : 271 - 271
  • [50] Serum 21-deoxycortisol, 17-hydroxyprogesterone, and 11-deoxycortisol in classic congenital adrenal hyperplasia:: Clinical and hormonal correlations and identification of patients with 11β-hydroxylase deficiency among a large group with alleged 21-hydroxylase deficiency
    Tonetto-Fernandes, Vania
    Lemos-Marini, Sofia H. V.
    Kuperman, Hilton
    Ribeiro-Neto, Luciane M.
    Verreschi, Ieda T. N.
    Kater, Claudio E.
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2006, 91 (06): : 2179 - 2184