Anthropometry in Klinefelter Syndrome - Multifactorial Influences Due to CAG Length, Testosterone Treatment and Possibly Intrauterine Hypogonadism

Author:

Chang Simon1,Skakkebæk Anne1,Trolle Christian1,Bojesen Anders2,Hertz Jens Michael3,Cohen Arieh4,Hougaard David Michael4,Wallentin Mikkel56,Pedersen Anders Degn78,Østergaard John Rosendahl9,Gravholt Claus Højbjerg110

Affiliation:

1. Department of Endocrinology and Internal Medicine (MEA) (S.C., A.S., C.T., C.H.G.), Section of Neonatal Screening and Hormones

2. Department of Clinical Genetics (A.B.), Vejle Hospital, Sygehus Lillebaelt, 7100 Vejle, Denmark

3. Department of Clinical Genetics (J.M.H.), Odense University Hospital, 5000 Odense, Denmark

4. Department of Clinical Biochemistry (A.C., D.M.H.), Immunology and Genetics, Statens Serum Institute, 8000 Aarhus C, Denmark

5. Center of Functionally Integrative Neuroscience (M.W.), Centre for Rare Diseases, 8000 Aarhus C, Denmark

6. Center for Semiotics (M.W.), Aarhus University Hospital, 8000 Aarhus C, Denmark

7. Department of Psychology and Behavioral Sciences (A.D.P.), 8000 Aarhus C, Denmark

8. Vejleford Rehabilitation Center (A.D.P.), 7140 Stouby, Denmark

9. Department of Pediatrics (J.R.Ø.), 8000 Aarhus C, Denmark

10. Department of Molecular Medicine (C.H.G.), Aarhus University Hospital, 8200 Aarhus N, Denmark

Abstract

Context: Klinefelter syndrome, 47, XXY (KS), is underdiagnosed partly due to few clinical signs complicating identification of affected individuals. Certain phenotypic traits are common in KS. However, not all aspects of the KS phenotype are well described. Objective: To describe anthropometry and body composition in KS and relate findings to biochemistry and X-chromosome related genetic markers. Design, Setting and Participants: Seventy three KS males referred to our clinic and 73 age-matched controls underwent comprehensive measurements of anthropometry and body composition in a cross-sectional, case-controlled study. Furthermore, genetic analysis for parental origin of the supernumerary X-chromosome, skewed X-chromosome inactivation and androgen receptor (AR) CAG repeat length was done. Main Outcome Measure: Anthropometry and body composition in KS and the effect of genotype hereon. Results: KS males were taller (absolute difference: 5.1 cm, P < .001) with longer legs (5.7 cm, P < .001) compared with controls. Furthermore, 2D:4D was increased in KS males (relative effect size: Cohen's d = 0.40), reflecting reduced fetal testosterone exposure. Also, bi-iliac width (0.41), waist (0.52), and hip circumference (0.47) (P < .02 for all), as well as total fat mass (0.74), abdominal fat mass (0.67), and total body fat percentage (0.84) was increased in KS males (P < .001 for all), while bitesticular volume was reduced (4.6). AR CAG repeat length was comparable in KS and controls, and among KS CAG correlated to arm length (P = .04), arm span (P = .01), and leg length (P = .04). Effects of parental origin of the supernumerary X-chromosome and skewed X-chromosome inactivation were negligible. Conclusions: Anthropometry and body composition in KS is specific and dysmorphic and affected by AR CAG repeat length and decreased exposure to testosterone already during fetal life.

Publisher

The Endocrine Society

Subject

Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference40 articles.

1. Prenatal and postnatal prevalence of Klinefelter syndrome: a national registry study;Bojesen;J Clin Endocrinol Metab,2003

2. Klinefelter syndrome in clinical practice;Bojesen;Nat Clin Pract Urol,2007

3. Clinical and social characteristics of Korean men with Klinefelter syndrome;Bak;Int J Urol,2012

4. Syndrome characterized by gynecomastia, aspermatogenesis without A-Leydigism, and increased excretion of follicle-stimulating hormone;Klinefelter;J Clin Endocrinol. Metab,1942

5. Clinical and diagnostic features of patients with suspected Klinefelter syndrome;Kamischke;J Androl,2003

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