Literature DB >> 30637954

The incidence of anxiety symptoms in boys with 47,XXY (Klinefelter syndrome) and the possible impact of timing of diagnosis and hormonal replacement therapy.

Carole Samango-Sprouse1,2,3,4, Patricia Lasutschinkow4, Sherida Powell1, Teresa Sadeghin4, Andrea Gropman1,2.   

Abstract

47,XXY (Klinefelter syndrome) is the most common X and Y chromosomal variation (1:660 males). The incidence of anxiety disorders and the impact of hormonal replacement therapy (HRT) is not well understood. Child Behavior Checklist and Screen for Childhood Anxiety Related Emotional Disorders were completed by parents of 80 boys with 47,XXY. Forty received HRT prior to 10 years of age while 40 did not. HRT (22.5%) received early hormonal treatment prior to 18 months. About 32.5% received hormone booster treatment between 5 and 10 years. The remaining 42.5% received both. There were fewer reported social (p = .015), thought (p = .012), and affective problems (p = .048) in treated boys when compared to untreated. Boys with both treatments demonstrated fewer symptoms on anxious/depressed scale (p = .001) compared to those with early treatment only. Within the treated group, prenatally diagnosed showed fewer indications of anxiety problems (p = .02) than their postnatal counterparts. This comparative, cross-sectional study expands previous findings on the possible positive effect of HRT in boys with 47,XXY. Anxiety disorders appear to be a penetrant aspect of the 47,XXY phenotype. Further investigation is warranted to explore the relationship between biological treatment and individual responses to HRT to develop more personalized and precise medicine.
© 2019 Wiley Periodicals, Inc.

Entities:  

Keywords:  47,XXY; Klinefelter syndrome; X and Y chromosomal variations; anxiety disorders; hormonal replacement therapy; sex chromosome abnormalities and aneuploidies

Mesh:

Year:  2019        PMID: 30637954     DOI: 10.1002/ajmg.a.61038

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  5 in total

Review 1.  Minipuberty in Klinefelter syndrome: Current status and future directions.

Authors:  Lise Aksglaede; Shanlee M Davis; Judith L Ross; Anders Juul
Journal:  Am J Med Genet C Semin Med Genet       Date:  2020-06-01       Impact factor: 3.908

2.  Prenatal phenotype of 47, XXY (Klinefelter syndrome).

Authors:  Kate Swanson; Juliet C Bishop; Huda B Al-Kouatly; Mona Makhamreh; Thomas Felton; Neeta L Vora; Teresa N Sparks; Angie C Jelin
Journal:  Prenat Diagn       Date:  2021-12-07       Impact factor: 3.242

Review 3.  Update On The Clinical Perspectives And Care Of The Child With 47,XXY (Klinefelter Syndrome).

Authors:  Carole A Samango-Sprouse; Debra R Counts; Selena L Tran; Patricia C Lasutschinkow; Grace F Porter; Andrea L Gropman
Journal:  Appl Clin Genet       Date:  2019-10-23

4.  Noninvasive prenatal testing for assessing foetal sex chromosome aneuploidy: a retrospective study of 45,773 cases.

Authors:  Xinran Lu; Chaohong Wang; Yuxiu Sun; Junxiang Tang; Keting Tong; Jiansheng Zhu
Journal:  Mol Cytogenet       Date:  2021-01-06       Impact factor: 2.009

5.  DNA methylation and behavioral dysfunction in males with 47,XXY and 49,XXXXY: a pilot study.

Authors:  Richard S Lee; Sophia Q Song; Henri M Garrison-Desany; Jenny L Carey; Patricia Lasutschinkow; Andrew Zabel; Joseph Bressler; Andrea Gropman; Carole Samango-Sprouse
Journal:  Clin Epigenetics       Date:  2021-07-01       Impact factor: 6.551

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.