From Klinefelter Syndrome to High Grade Aneuploidies: Expanding the Gene-dosage Effect of Supernumerary X Chromosomes

Author:

Spaziani Matteo1ORCID,Carlomagno Francesco1ORCID,Tarantino Chiara1ORCID,Angelini Francesco1,Paparella Roberto2ORCID,Tarani Luigi2ORCID,Putotto Carolina2,Badagliacca Roberto3,Pozza Carlotta1ORCID,Isidori Andrea M14ORCID,Gianfrilli Daniele1ORCID

Affiliation:

1. Section of Medical Pathophysiology and Endocrinology, Department of Experimental Medicine, Sapienza University of Rome , 00161 Rome , Italy

2. Department of Maternal Infantile and Urological Sciences, Sapienza University of Rome , 00161 Rome , Italy

3. Department of Clinical, Anaesthesiologic and Cardiological Sciences, Sapienza University of Rome , 00161 Rome , Italy

4. Endocrine and Andrological Regional Rare Disease Center (Endo-ERN accredited), Policlinico Umberto I , 00161, Rome , Italy

Abstract

Abstract Objective High-grade aneuploidies of X and Y sex chromosomes (HGAs) are exceedingly rare and complex conditions. We aimed to investigate the effect of supernumerary X chromosomes (extra-Xs) on the clinical, hormonal, metabolic, and echocardiographic features of patients with HGAs. Design and Methods In a cross-sectional study, we compared 23 subjects with HGAs and 46 age-matched subjects with 47,XXY Klinefelter syndrome (KS), according to the number of extra-Xs: two (47,XXY and 48,XXYY), three (48,XXXY and 49,XXXYY), or four supernumerary Xs (49,XXXXY). A second cohort consisting of 46 pubertal stage-matched KS subjects was employed for validation. Clinical, hormonal, metabolic and ultrasonographic parameters were collected and analyzed. Results The increase in the number of extra-Xs was associated with a progressive adverse effect on height, pubertal development, testicular volume and function, adrenal steroidogenesis, and thyroid function. A progressive linear increase in ACTH and a decrease in cortisol/ACTH ratios were found. Weight and body mass index, Sertoli cell function, lipid profile, and glucose tolerance post-oral glucose tolerance test were all worse in the HGA cohort compared to KS. Cardiac evaluation revealed a linear association with reduced left and right end-diastolic diameters and reduced ejection fraction. Conclusion The increase in the number of extra-Xs is associated with a “dose-dependent” progressive impairment in steroid producing glands, thyroid function, cardiac structure, and performance.

Funder

European Union–NextGenerationEU

Italian Ministry of University and Research

Sapienza University of Rome

Publisher

The Endocrine Society

Subject

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

Reference42 articles.

1. Sex chromosome tetrasomy and pentasomy;Linden;Pediatrics,1995

2. Uniparental origin of sex chromosome polysomies;Lorda-Sanchez;Hum Hered,1992

3. A child with 49 chromosomes;Fraccaro;Lancet,1960

4. An XXXYY sex-chromosome anomaly. Report of a mentally deficient male;Bray;JAMA,1963

5. A 49, XXXYY male;Salamanca-Gomez;Am J Med Genet,1981

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