Literature DB >> 33961029

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

Hedi L Claahsen-van der Grinten1, Phyllis W Speiser2, S Faisal Ahmed3, Wiebke Arlt4,5, Richard J Auchus6, Henrik Falhammar7,8, Christa E Flück9, Leonardo Guasti10, Angela Huebner11, Barbara B M Kortmann12, Nils Krone13,14, Deborah P Merke15, Walter L Miller16, Anna Nordenström17,18, Nicole Reisch19, David E Sandberg20, Nike M M L Stikkelbroeck21, Philippe Touraine22, Agustini Utari23, Stefan A Wudy24, Perrin C White25.   

Abstract

Congenital adrenal hyperplasia (CAH) is a group of autosomal recessive disorders affecting cortisol biosynthesis. Reduced activity of an enzyme required for cortisol production leads to chronic overstimulation of the adrenal cortex and accumulation of precursors proximal to the blocked enzymatic step. The most common form of CAH is caused by steroid 21-hydroxylase deficiency due to mutations in CYP21A2. Since the last publication summarizing CAH in Endocrine Reviews in 2000, there have been numerous new developments. These include more detailed understanding of steroidogenic pathways, refinements in neonatal screening, improved diagnostic measurements utilizing chromatography and mass spectrometry coupled with steroid profiling, and improved genotyping methods. Clinical trials of alternative medications and modes of delivery have been recently completed or are under way. Genetic and cell-based treatments are being explored. A large body of data concerning long-term outcomes in patients affected by CAH, including psychosexual well-being, has been enhanced by the establishment of disease registries. This review provides the reader with current insights in CAH with special attention to these new developments.
© The Author(s) 2021. Published by Oxford University Press on behalf of the Endocrine Society. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  zzm321990 CYP21A2zzm321990 ; 21-hydroxylase deficiency; Steroid biosynthesis; aldosterone; cortisol; glucocorticoid; mineralocorticoid

Mesh:

Substances:

Year:  2022        PMID: 33961029      PMCID: PMC8755999          DOI: 10.1210/endrev/bnab016

Source DB:  PubMed          Journal:  Endocr Rev        ISSN: 0163-769X            Impact factor:   19.871


  721 in total

1.  Prenatal glucocorticoid exposure leads to offspring hyperglycaemia in the rat: studies with the 11 beta-hydroxysteroid dehydrogenase inhibitor carbenoxolone.

Authors:  R S Lindsay; R M Lindsay; B J Waddell; J R Seckl
Journal:  Diabetologia       Date:  1996-11       Impact factor: 10.122

2.  The Role of Patient Advocacy and the Declining Rate of Clitoroplasty in 46,XX Patients With Congenital Adrenal Hyperplasia.

Authors:  Morgan B Schoer; Phillip Nam Nguyen; Diane F Merritt; Victoria G Wesevich; Abby S Hollander
Journal:  Clin Pediatr (Phila)       Date:  2018-09-27       Impact factor: 1.168

3.  The potential role for corticosterone in the induction of cleft palate in mice after treatment with a selective NK-1 receptor antagonist, casopitant (GW679769B).

Authors:  Mary K Ziejewski; Howard M Solomon; Dinesh Stanislaus; Robert L Clark; Tacey E White; April R Apostoli
Journal:  Birth Defects Res B Dev Reprod Toxicol       Date:  2011-11-29

4.  Ethics, genetics and public policies in Uruguay: newborn and infant screening as a paradigm.

Authors:  Mariela Larrandaburu; Ursula Matte; Ana Noble; Zully Olivera; Maria Teresa V Sanseverino; Luis Nacul; Lavinia Schuler-Faccini
Journal:  J Community Genet       Date:  2015-05-29

5.  Restoration of adrenal steroidogenesis by adenovirus-mediated transfer of human cytochromeP450 21-hydroxylase into the adrenal gland of21-hydroxylase-deficient mice.

Authors:  T Tajima; T Okada; X M Ma; W Ramsey; S Bornstein; G Aguilera
Journal:  Gene Ther       Date:  1999-11       Impact factor: 5.250

6.  The pathophysiology and genetics of congenital lipoid adrenal hyperplasia.

Authors:  H S Bose; T Sugawara; J F Strauss; W L Miller
Journal:  N Engl J Med       Date:  1996-12-19       Impact factor: 91.245

7.  Use of PET/CT with cosyntropin stimulation to identify and localize adrenal rest tissue following adrenalectomy in a woman with congenital adrenal hyperplasia.

Authors:  Melissa K Crocker; Stephanie Barak; Corina M Millo; Stephanie A Beall; Mahtab Niyyati; Richard Chang; Nilo A Avila; Carol Van Ryzin; James Segars; Martha Quezado; Deborah P Merke
Journal:  J Clin Endocrinol Metab       Date:  2012-08-17       Impact factor: 5.958

8.  Cortisol response to operative stress with anesthesia in healthy children.

Authors:  Lisa K Taylor; Richard J Auchus; Laurence S Baskin; Walter L Miller
Journal:  J Clin Endocrinol Metab       Date:  2013-07-16       Impact factor: 5.958

Review 9.  Biochemical and genetic diagnosis of 21-hydroxylase deficiency.

Authors:  Henrik Falhammar; Anna Wedell; Anna Nordenström
Journal:  Endocrine       Date:  2015-09-04       Impact factor: 3.633

10.  First-Trimester Prenatal Dexamethasone Treatment Is Associated With Alterations in Brain Structure at Adult Age.

Authors:  Annelies Van't Westeinde; Leif Karlsson; Anna Nordenström; Nelly Padilla; Svetlana Lajic
Journal:  J Clin Endocrinol Metab       Date:  2020-08-01       Impact factor: 6.134

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  30 in total

1.  Normal bone health in young adults with 21-hydroxylase enzyme deficiency undergoing glucocorticoid replacement therapy.

Authors:  Juliano Henrique Borges; Daniel Minutti de Oliveira; Sofia Helena Valente de Lemos-Marini; Bruno Geloneze; Gil Guerra-Júnior; Ezequiel Moreira Gonçalves
Journal:  Osteoporos Int       Date:  2021-08-18       Impact factor: 4.507

2.  Face-sparing Congenital Generalized Lipodystrophy Type 1 Associated With Nonclassical Congenital Adrenal Hyperplasia.

Authors:  Sara Costa; Lurdes Sampaio; Ana Berta Sousa; Chao Xing; Anil K Agarwal; Abhimanyu Garg
Journal:  J Clin Endocrinol Metab       Date:  2022-08-18       Impact factor: 6.134

3.  Clinical analysis of the etiological spectrum of bilateral adrenal lesions: A large retrospective, single-center study.

Authors:  Fangfang Yan; Jinyang Zeng; Yulong Chen; Yu Cheng; Yu Pei; Li Zang; Kang Chen; Weijun Gu; Jin Du; Qinghua Guo; Xianling Wang; Jianming Ba; Zhaohui Lyu; Jingtao Dou; Guoqing Yang; Yiming Mu
Journal:  Endocrine       Date:  2022-05-23       Impact factor: 3.925

4.  Gender Differences in Caring for Children with Genetic or Rare Diseases: A Mixed-Methods Study.

Authors:  Shao-Yin Chu; Chin-Chen Wen; Chun-Ying Weng
Journal:  Children (Basel)       Date:  2022-04-27

5.  Prevalence of CAH-X Syndrome in Italian Patients with Congenital Adrenal Hyperplasia (CAH) Due to 21-Hydroxylase Deficiency.

Authors:  Rosa Maria Paragliola; Alessia Perrucci; Laura Foca; Andrea Urbani; Paola Concolino
Journal:  J Clin Med       Date:  2022-07-01       Impact factor: 4.964

6.  Congenital adrenal hyperplasia in patients with adrenal tumors: a population-based case-control study.

Authors:  F Sahlander; J Patrova; B Mannheimer; J D Lindh; H Falhammar
Journal:  J Endocrinol Invest       Date:  2022-10-21       Impact factor: 5.467

Review 7.  Emerging treatment for congenital adrenal hyperplasia.

Authors:  Perrin C White
Journal:  Curr Opin Endocrinol Diabetes Obes       Date:  2022-06-01       Impact factor: 3.626

Review 8.  Target Diseases for Neonatal Screening in Germany.

Authors:  Ute Spiekerkoetter; Heiko Krude
Journal:  Dtsch Arztebl Int       Date:  2022-04-29       Impact factor: 8.251

Review 9.  Molecular Diagnosis of Steroid 21-Hydroxylase Deficiency: A Practical Approach.

Authors:  María Arriba; Begoña Ezquieta
Journal:  Front Endocrinol (Lausanne)       Date:  2022-03-29       Impact factor: 5.555

Review 10.  Management challenges and therapeutic advances in congenital adrenal hyperplasia.

Authors:  Ashwini Mallappa; Deborah P Merke
Journal:  Nat Rev Endocrinol       Date:  2022-04-11       Impact factor: 47.564

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