Literature DB >> 31730799

Effect of androgen excess and glucocorticoid exposure on metabolic risk profiles in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Luisa Paizoni1, Matthias K Auer1, Heinrich Schmidt2, Angela Hübner3, Martin Bidlingmaier1, Nicole Reisch4.   

Abstract

Data on cardiovascular morbidity in adults with congenital adrenal hyperplasia (CAH) is sparse. We therefore aimed to determine the role of androgen control and glucocorticoid therapy on metabolic health. For that purpose, we included 90 patients (N = 39 men, N = 51 women) with classic CAH due to 21-hydroxylase deficiency (N = 61 salt wasting, N = 29 simple virilizing) and an equal number of controls matched for age, sex, BMI and smoking-habits. We could show that there was no difference in intima-media-thickness between patients and controls and only one patient fulfilled all criteria of the metabolic syndrome. CAH men presented with an increased relative body fat mass in comparison to controls (25.6 % vs. 22.1 %; p = 0.011) while this was not true for CAH women. Body fat was lower in those taking hydrocortisone instead of synthetic glucocorticoids (B = -3.27; p = 0.048). While arterial hypertension was rare, 54 % of patients had an impaired systolic drop at night or were classified as non-dippers (17 %). Impaired dipping was not associated with evening glucocorticoid and fludrocortisone intake but mediated by sodium levels. Insulin resistance was more common in CAH women (B = 1.689; p = 0.036) and in those with poor androgen control (B = 0.823; p = 0.046). In summary, we could show that good cardiovascular health outcome in adult CAH patients can be achieved. Hydrocortisone is superior in terms of body composition. It is yet unclear how non-dipping will translate into cardiovascular morbidity in the long-term.
Copyright © 2019 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  21-Hydroxylase deficiency; Blood pressure; Body composition; Congenital adrenal hyperplasia; Intima media thickness; Metabolism

Mesh:

Substances:

Year:  2019        PMID: 31730799     DOI: 10.1016/j.jsbmb.2019.105540

Source DB:  PubMed          Journal:  J Steroid Biochem Mol Biol        ISSN: 0960-0760            Impact factor:   4.292


  11 in total

1.  Clinical guidelines for the diagnosis and treatment of 21-hydroxylase deficiency (2021 revision).

Authors:  Tomohiro Ishii; Kenichi Kashimada; Naoko Amano; Kei Takasawa; Akari Nakamura-Utsunomiya; Shuichi Yatsuga; Tokuo Mukai; Shinobu Ida; Mitsuhisa Isobe; Masaru Fukushi; Hiroyuki Satoh; Kaoru Yoshino; Michio Otsuki; Takuyuki Katabami; Toshihiro Tajima
Journal:  Clin Pediatr Endocrinol       Date:  2022-04-10

Review 2.  Congenital Adrenal Hyperplasia-Current Insights in Pathophysiology, Diagnostics, and Management.

Authors:  Hedi L Claahsen-van der Grinten; Phyllis W Speiser; S Faisal Ahmed; Wiebke Arlt; Richard J Auchus; Henrik Falhammar; Christa E Flück; Leonardo Guasti; Angela Huebner; Barbara B M Kortmann; Nils Krone; Deborah P Merke; Walter L Miller; Anna Nordenström; Nicole Reisch; David E Sandberg; Nike M M L Stikkelbroeck; Philippe Touraine; Agustini Utari; Stefan A Wudy; Perrin C White
Journal:  Endocr Rev       Date:  2022-01-12       Impact factor: 19.871

Review 3.  Therapy options for adrenal insufficiency and recommendations for the management of adrenal crisis.

Authors:  Hanna Nowotny; S Faisal Ahmed; Sophie Bensing; Johan G Beun; Manuela Brösamle; Irina Chifu; Hedi Claahsen van der Grinten; Maria Clemente; Henrik Falhammar; Stefanie Hahner; Eystein Husebye; Jette Kristensen; Paola Loli; Svetlana Lajic; Nicole Reisch
Journal:  Endocrine       Date:  2021-03-04       Impact factor: 3.633

Review 4.  Clinical outcomes and characteristics of P30L mutations in congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Authors:  Mirjana Kocova; Violeta Anastasovska; Henrik Falhammar
Journal:  Endocrine       Date:  2020-05-05       Impact factor: 3.633

5.  Modified-Release Hydrocortisone in Congenital Adrenal Hyperplasia.

Authors:  Deborah P Merke; Ashwini Mallappa; Wiebke Arlt; Aude Brac de la Perriere; Angelica Lindén Hirschberg; Anders Juul; John Newell-Price; Colin G Perry; Alessandro Prete; D Aled Rees; Nicole Reisch; Nike Stikkelbroeck; Philippe Touraine; Kerry Maltby; F Peter Treasure; John Porter; Richard J Ross
Journal:  J Clin Endocrinol Metab       Date:  2021-04-23       Impact factor: 5.958

6.  Long-Term Health Outcomes of Korean Adults With Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency.

Authors:  Seung Gyun Lim; Young Ah Lee; Han Na Jang; Sung Hye Kong; Chang Ho Ahn; Sang Wan Kim; Choong Ho Shin; Jung Hee Kim
Journal:  Front Endocrinol (Lausanne)       Date:  2021-10-12       Impact factor: 5.555

Review 7.  Components of Metabolic Syndrome in Youth With Classical Congenital Adrenal Hyperplasia.

Authors:  Mimi S Kim; Nicole R Fraga; Nare Minaeian; Mitchell E Geffner
Journal:  Front Endocrinol (Lausanne)       Date:  2022-03-24       Impact factor: 5.555

8.  Epidemiology and Long-Term Adverse Outcomes in Korean Patients with Congenital Adrenal Hyperplasia: A Nationwide Study.

Authors:  Jung Hee Kim; Sunkyu Choi; Young Ah Lee; Juneyoung Lee; Sin Gon Kim
Journal:  Endocrinol Metab (Seoul)       Date:  2022-02-28

9.  Molecular analysis and genotype-phenotype correlations in patients with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency from southern Poland - experience of a clinical center.

Authors:  Anna Kurzyńska; Anna Skalniak; Kim Franson; Viola Bistika; Alicja Hubalewska-Dydejczyk; Elwira Przybylik-Mazurek
Journal:  Hormones (Athens)       Date:  2022-01-26       Impact factor: 3.419

Review 10.  The Success of a Screening Program Is Largely Dependent on Close Collaboration between the Laboratory and the Clinical Follow-Up of the Patients.

Authors:  Svetlana Lajic; Leif Karlsson; Rolf H Zetterström; Henrik Falhammar; Anna Nordenström
Journal:  Int J Neonatal Screen       Date:  2020-08-26
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