Klinefelter Syndrome
Conditions
Keywords
Klinefelter syndrome, Puberty, Body composition
Brief summary
The goal of this randomized clinical trial is to study the effect of testosterone replacement therapy during puberty in boys with Klinefelter syndrome (KS, 47,XXY). The main questions to answer are how treatment with testosterone will affect body fat mass, lipid and glucose metabolism, growth and body proportions, bone mineralization as well as effects on neurocognitive development and emotional and social difficulties. Participants will be randomized to two years treatment with testosterone or placebo.
Detailed description
Klinefelter syndrome (KS, 47,XXY) is the most frequent sex chromosome disorder with a prevalence of 1:660 boys. Patients with KS are hypogonadal due to a progressive testicular destruction starting already in childhood. Consequently, the adult male with KS is characterized by small testes, signs of incomplete virilization (e.g. lack of voice deepening, sparse face and body hair, gynecomastia, low muscle mass, reduced penile length), hypergonadotropic hypogonadism, infertility and increased risk of metabolic syndrome, diabetes, cardiovascular disease, osteoporosis and psychosocial and neurodevelopmental challenges. Adults with KS have a poor health and a prevention of the major co-morbidities associated with KS and thereby an improvement in the general health would have an enormous impact on the life of a large cohort of males worldwide. Sufficient testosterone is not only important in the adult but also during puberty and adolescence for a normal virilization and to improve body composition and body proportions, as well as to maximize peak bone mass acquisition. It has therefore been internationally accepted and makes biological sense to consider testosterone replacement therapy (TRT) during puberty in KS. However, there are no evidence based recommendations, and during recent years TRT in puberty has been questioned and is no longer recommended in some countries. There is a need on an international level for evaluating the effect of this treatment. We therefore aim at evaluating the effect of 2 years TRT during early puberty in boys with KS aged 10 to 14 years in this national, multi-center, randomized, double-blind, placebo-controlled intervention study. The primary endpoint is to evaluate the effect on body fat mass. The secondary endpoints are to evaluate effects on lipid and glucose metabolism, growth and body proportions, bone mineralization as well as effects on neurocognitive development and emotional and social difficulties.
Interventions
Two years treatment with testosterone
Two years treatment with placebo
Sponsors
Study design
Intervention model description
Multi-center, national, randomized, double-blind, placebo-controlled intervention study
Eligibility
Inclusion criteria
* 47,XXY Klinefelter syndrome * Age 10-14 years at inclusion * Luteinizing Hormone \> +2 standard deviations (SD) by ultrasensitive luteinizing hormone assay * Free Testosterone\<+2 standard deviations * Signed consent from parents
Exclusion criteria
* Previous or ongoing T treatment except for TRT because of micropenis * Contraindications to testosterone treatment known hypersensitivity to testosterone or to any other constituent of the gel known or suspected prostatic cancer or breast carcinoma * Participation in any other clinical trial
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Changes in body fat mass | Baseline and 1 and two years | Evaluation of body fat percentage by whole body dual energy x-ray absorptiometry (DEXA) scan |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Pubertal development and viriliztion | Every three months for two years | Measurement of luteinizing hormone (LH) (IU/L) in serum |
| Pubertal development | At base line, and at 1 and 2 years | Measurement of the concentration of luteinizing hormone (LH) and follicle stimulating hormone (FSH) in the first, fasting, morning voiding. Measured in IU/L. |
| Anthropometry | Every three months for two years | Measurement of height (cm) |
| Bone health | At baseline and at 1 and two years | Measurement of whole body bone mineral content (BMC) evaluated by whole body DXA scan |
| Measurement of bone turnover markers | At base line, and at 1 and 2 years | Measurement of 25-OH-vitamin D in blood sample |
| Changes in growth | Base line and at 1 and 2 years | Evaluation of bone age by X-ray of left hand and evaluated using the software BoneXpert version 3 (Hørsholm, Denmark) |
| Measurement of serum concentrations of growth factors | At base line, and at 1 and 2 years | Measurement of IGF1, IGF2, IGF1BP-1-6 and acid-labile subunit (ALS)) (microg/L) |
| Muscle strength | Every three months for two years | Measurement of standing jump length (cm) |
| Pubertal development and virilization | Every three months for two years | Tanner genital (G) staging from G1 to G5. G1 is the prepubertal stage and G5 is the fully develloped stage. |
| Changes in markers of lipids | Base line and at 1 and 2 years | Measurement of cholesterol in blood sample |
| Changes in markers of metabolism | Base line and at 1 and 2 years | Measurement of adiponectin in blood sample |
| Changes in markers of inflammation | Base line and at 1 and 2 years | Measurement of CRP in blood sample |
| Neuropsychological evaluation | Baseline and after two years | The Weschler Intelligence Scale for Children - Fifth Edition (WISC-V). The result is based on a combination of seperate index scores. A higher score generally indicates stronger cognitive abilities. |
| Cryopreservation of spermatozoa | After 2 years | If the patient is able and willing he will have the possibility to deliver a semen sample for cryopreservation of potential spermatozoa |
| Epigenetic | At base line, and at 1 and 2 years | The effects on epigenetics will be evaluation by evaluating changes in DNA methylation patterns. This will be analyzed on DNA from white blood cells by applying Illumina methylation arrays. |
| Genetic effects | At base line, and at 1 and 2 years | DNA will be analyzed using a selected set of genetic polymorphisms in target genes with established or theoretic effects on hormone production and hormone receptor sensitivity. They will be analysed either by PCR genotyping or targeted sequencing (max. 200 selected genes). SNP arrays that exclusively target common variants, and not any rare variants, will be used to determine the influence of common genetic variation on the observed associations. |
| Small non-coding RNA | At base line, and at 1 and 2 years | RNA analysis of circulating, small, non-coding RNA will be performed as a biomarker for the circulating concentrations of reproductive hormones and for overweight. |
| Changes i QTc | Base line and at 1 and 2 years | Evaluation of QT Interval with electrocardiogram (ECG) |
Countries
Denmark