Literature DB >> 24302749

Increased psychiatric morbidity in men with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Henrik Falhammar1, Agnieszka Butwicka, Mikael Landén, Paul Lichtenstein, Agneta Nordenskjöld, Anna Nordenström, Louise Frisén.   

Abstract

CONTEXT: Reports on psychiatric morbidity in males with congenital adrenal hyperplasia (CAH) are lacking.
OBJECTIVE: The aim was to study psychiatric disorders in CAH males. DESIGN, SETTING, AND PARTICIPANTS: We studied males with CAH (21-hydroxylase deficiency, n = 253; CYP21A2 mutations known, n = 185), and compared them with controls (n = 25 300). Data were derived through linkage of national population-based registers. We assessed the subgroups of CYP21A2 genotype separately (null, I2splice, I172N, P30L, and NC), as well as outcomes before and after the introduction of national neonatal screening in 1986. MAIN OUTCOME MEASURES: Psychiatric disorders including attempted and completed suicide (suicidality) were reviewed.
RESULTS: Psychiatric disorders (suicidality not included), suicidality, and alcohol misuse were increased in CAH males compared with controls (odds ratios, 1.5, 2.3, and 1.9; 95% confidence intervals, 1.1-2.2, 1.1-5.0, and 1.0-3.5, respectively). In the null genotype group, no increased rates were seen; in the I2splice group, psychiatric disorders, personality disorders, and alcohol misuse were increased; in the I172N group, suicide attempt and drug misuse were increased; and in the P30L and NC groups, psychotic disorders were increased. In CAH males born before the neonatal screening, the rates of psychiatric disorders and suicidality were increased, but only psychotic disorders increased in those born afterward. There was no increased risk for any neurodevelopmental disorder.
CONCLUSIONS: CAH males have an increased psychiatric morbidity. Psychiatric morbidity was not raised in the most severe genotype group. Late diagnosis of CAH may explain some of the findings. Those born before the introduction of neonatal screening were more affected, which may be explained by the higher age.

Entities:  

Mesh:

Substances:

Year:  2013        PMID: 24302749     DOI: 10.1210/jc.2013-3707

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  29 in total

1.  How Early Hormones Shape Gender Development.

Authors:  Sheri A Berenbaum; Adriene M Beltz
Journal:  Curr Opin Behav Sci       Date:  2016-02

2.  Complement component 4 variations may influence psychopathology risk in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Authors:  Qizong Lao; Marcia Des Jardin; Rahul Jayakrishnan; Monique Ernst; Deborah P Merke
Journal:  Hum Genet       Date:  2018-11-21       Impact factor: 4.132

Review 3.  Clinical perspectives in congenital adrenal hyperplasia due to 11β-hydroxylase deficiency.

Authors:  Krupali Bulsari; Henrik Falhammar
Journal:  Endocrine       Date:  2016-12-07       Impact factor: 3.633

Review 4.  Nonclassic congenital adrenal hyperplasia due to 21-hydroxylase deficiency: clinical presentation, diagnosis, treatment, and outcome.

Authors:  Henrik Falhammar; Anna Nordenström
Journal:  Endocrine       Date:  2015-06-17       Impact factor: 3.633

5.  Gender Dsyphoria and Psychiatric Disorders in Children and Adolescents with Congenital Adrenal Hyperplasia.

Authors:  H Doktur; C Tanidir; H Güneş; T Aytemiz; G Durcan; H Önal; E Kutlu
Journal:  Acta Endocrinol (Buchar)       Date:  2021 Jul-Sep       Impact factor: 0.877

6.  Behavioral Health Diagnoses in Youth with Differences of Sex Development or Congenital Adrenal Hyperplasia Compared with Controls: A PEDSnet Study.

Authors:  Rachel Sewell; Cindy L Buchanan; Shanlee Davis; Dimitri A Christakis; Amanda Dempsey; Anna Furniss; Anne E Kazak; Anna J Kerlek; Brianna Magnusen; Nathan M Pajor; Laura Pyle; Louise C Pyle; Hanieh Razzaghi; Beth I Schwartz; Maria G Vogiatzi; Natalie J Nokoff
Journal:  J Pediatr       Date:  2021-08-27       Impact factor: 4.406

Review 7.  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

8.  Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline.

Authors:  Phyllis W Speiser; Wiebke Arlt; Richard J Auchus; Laurence S Baskin; Gerard S Conway; Deborah P Merke; Heino F L Meyer-Bahlburg; Walter L Miller; M Hassan Murad; Sharon E Oberfield; Perrin C White
Journal:  J Clin Endocrinol Metab       Date:  2018-11-01       Impact factor: 5.958

Review 9.  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

10.  Steroid 21-hydroxylase gene variants and late-life depression.

Authors:  Marie-Laure Ancelin; Joanna Norton; Karen Ritchie; Isabelle Chaudieu; Joanne Ryan
Journal:  BMC Res Notes       Date:  2021-05-25
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.