Reverse circadian glucocorticoid treatment in prepubertal children with congenital adrenal hyperplasia

被引:6
|
作者
Dubinski, Ilja [1 ]
Dalla-Pozza, Susanne Bechtold [1 ]
Bidlingmaier, Martin [2 ]
Reisch, Nicole [2 ]
Schmidt, Heinrich [1 ]
机构
[1] Ludwig Maximilians Univ Munchen, Dr von Hauner Childrens Hosp, Div Pediat Endocrinol, Univ Hosp, Lindwurmstr 4, D-80337 Munich, Bavaria, Germany
[2] Ludwig Maximilians Univ Munchen, Dept Med 4, Univ Hosp, Munich, Germany
来源
关键词
17-hydroxyprogesterone; circadian rhythms of hormones; congenital adrenal hyperplasia; reverse circa-dian steroid treatment; steroid hormone metabolism; 21-HYDROXYLASE DEFICIENCY; HYDROCORTISONE; HYPOGLYCEMIA; SECRETION; CORTISOL; THERAPY;
D O I
10.1515/jpem-2021-0540
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: Children with salt-wasting congenital adrenal hyperplasia (CAH) have an impaired function of steroid synthesis pathways. They require therapy with glucocorticoid (GC) and mineralocorticoid hormones to avoid salt wasting crisis and other complications. Most commonly, children receive hydrocortisone thrice daily with the highest dose in the morning, mimicking the regular physiology. However, reverse circadian treatment (RCT) had been suggested previously. In this study, we aimed to determine the efficacy of RCT in prepubertal children with CAH by comparing the salivary 17-hydroxyprogesterone (s17-OHP) levels individually. Methods: In this retrospective study, we analyzed the records of children with classical CAH and RCT who were monitored by s17-OHP levels. The study included 23 patients. We identified nine prepubertal children with RCT schemes (three boys and six girls) and compared the s17-OHP levels in the morning, afternoon, and evening. The objective of this study was to demonstrate the non effectiveness of RCT in terms of lowering the morning s17-OHP concentration. In addition, we compared s17-OHP day profiles in six patients on RCT and non-RCT therapy (intraindividually). Results: Eight of nine children with RCT showed higher s17-OHP levels in the morning compared to the evening. In addition, none of the children showed a significant deviation of development. Three children were overweight. No adrenal crisis or pubertal development occurred. Comparison of RCT and non-RCT regimens showed no difference in 17-OHP profiles. Conclusions: Our data do not support the use of RCT schemes for GC replacement in children with CAH due to lack of benefits and unknown long-term risks.
引用
收藏
页码:1543 / 1548
页数:6
相关论文
共 50 条
  • [1] Immunophenotypic Implications of Reverse-Circadian Glucocorticoid Treatment in Congenital Adrenal Hyperplasia
    Nowotny, Hanna F.
    Choi, Hannah
    Ziegler, Selina
    Doll, Natalie
    Baeuerle, Ariane
    Welp, Ann-Christin
    Dubinski, Ilja
    Schiergens, Katharina
    Neumann, Uta
    Tschaidse, Lea
    Auer, Matthias K.
    Rothenfusser, Simon
    Schmidt, Heinrich
    Reisch, Nicole
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2025, 26 (04)
  • [2] Lost lessons of glucocorticoid potency and the treatment of children with congenital adrenal hyperplasia
    Rivkees, Scott A.
    JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, 2008, 21 (04): : 297 - 299
  • [3] Congenital adrenal hyperplasia and glucocorticoid monitoring
    Broeks, Ilse
    Otten, Barto
    Rouwe, Catrienus
    Bakker-van Waarde, Willie
    HORMONE RESEARCH, 2008, 70 : 143 - 143
  • [4] Glucocorticoid Regimens in Pre-pubertal Children with Congenital Adrenal Hyperplasia
    Apsan, Jennifer
    Thomas, Charlene
    Su, Karen
    Lekarev, Oksana
    HORMONE RESEARCH IN PAEDIATRICS, 2021, 94 (SUPPL 2): : 5 - 6
  • [5] Glucocorticoid treatment regimen and health outcomes in adults with congenital adrenal hyperplasia
    Han, T. S.
    Stimson, R. H.
    Rees, D. A.
    Krone, N.
    Willis, D. S.
    Conway, G. S.
    Arlt, W.
    Walker, B. R.
    Ross, R. J.
    CLINICAL ENDOCRINOLOGY, 2013, 78 (02) : 197 - 203
  • [6] Glucocorticoid receptors in patients with congenital adrenal hyperplasia
    Saka, N
    Güven, M
    Bas, F
    Darendeliler, F
    Bundak, R
    Günöz, H
    Sultuybek, G
    JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, 2000, 13 (08): : 1101 - 1107
  • [7] Growth Hormone Treatment in Children with Congenital Adrenal Hyperplasia
    Harbison, Madeleine D.
    Lin-Su, Karen
    New, Maria I.
    HORMONAL AND GENETIC BASIS OF SEXUAL DIFFERENTIATION DISORDERS AND HOT TOPICS IN ENDOCRINOLOGY, 2011, 707 : 107 - 107
  • [8] Congenital Adrenal Hyperplasia: Issues in Diagnosis and Treatment in Children
    Rajni Sharma
    Anju Seth
    The Indian Journal of Pediatrics, 2014, 81 : 178 - 185
  • [9] Congenital Adrenal Hyperplasia: Issues in Diagnosis and Treatment in Children
    Sharma, Rajni
    Seth, Anju
    INDIAN JOURNAL OF PEDIATRICS, 2014, 81 (02): : 178 - 185
  • [10] White matter variations in congenital adrenal hyperplasia: possible implications for glucocorticoid treatment
    Luders, Eileen
    Spencer, Debra
    Gaser, Christian
    Thankamony, Ajay
    Hughes, Ieuan A.
    Srirangalingam, Umasuthan
    Gleeson, Helena
    Kung, Karson T. F.
    Cabeen, Ryan P.
    Hines, Melissa
    Kurth, Florian
    BRAIN COMMUNICATIONS, 2024, 6 (05)