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Author Notes:

E-mail address: sharron.m.close@emory.edu.

The authors wish to thank and acknowledge the boys and families of boys who participated in this study.

We also thank the Association of X and Y Chromosome Variation (AXYS) for their assistance in recruiting participants in this study.

The authors declare no conflicts of interest.

Subjects:

Research Funding:

Funded by the Pediatric Endocrine Nursing Society, the National Association of Pediatric Nurse Practitioners, Alpha Zeta Chapter of Sigma Theta Tau (S.C. while a PhD student at Columbia University School of Nursing), Yale School of Nursing National Institutes of Health (5T32NR008346-08), and the National Center for Advancing Translational Sciences, National Institutes of Health (UL1 TR000040 [Columbia University]).

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Pediatrics
  • ADOLESCENTS
  • XXY
  • XYY
  • PREVALENCE
  • DIAGNOSIS
  • CHILDREN
  • ADULTS

Phenotype and Adverse Quality of Life in Boys with Klinefelter Syndrome

Tools:

Journal Title:

Journal of Pediatric and Adolescent Gynecology

Volume:

Volume 167, Number 3

Publisher:

, Pages 650-657

Type of Work:

Article | Post-print: After Peer Review

Abstract:

Objectives: To characterize associations among psychosocial well-being, physical phenotype, and sex hormones in a sample of youth with Klinefelter syndrome (KS). We hypothesized that KS physical traits (phenotype) are associated with adverse psychosocial health measures and that testosterone levels are associated with adverse psychosocial health. Study design: Forty-three boys with KS (ages 8-18 years) participated in a cross-sectional study. Participants underwent physical examination, hormone analyses, and psychosocial health questionnaires. Results: Using an investigator-developed Klinefelter Phenotype Index Scale, the number of KS physical traits ranged from 1-13 (mean 5.1 ± 1.9). Pubertal boys presented with more KS traits compared with prepubertal boys (5.6 vs 4.2, P =.01). Boys diagnosed prenatally had a milder phenotype compared with those diagnosed postnatally. Gonadotropins were elevated without androgen deficiency in 45%. Psychosocial health scores indicated adverse quality of life (QOL) (67%), low self-esteem (38%), poor self-concept (26%), and risk for depression (16%) without a difference between pubertal groups. Linear regression showed that 22% of the variance in QOL (P =.0001) was explained by phenotype. Testosterone level was not associated with psychosocial health measures. Conclusions: Depending on the degree of phenotypic abnormality, boys with KS may be at risk for impaired QOL. Testosterone levels were not shown to influence psychosocial health. The Klinefelter Phenotype Index Scale may be a useful tool to characterize KS features in boys.

Copyright information:

© 2015 Elsevier Inc.

This is an Open Access work distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (http://creativecommons.org/licenses/by-nc-nd/4.0/).

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