TESTO: Testosterone Effects on Short-Term Outcomes in Infants With XXY
Trial Snapshot
- Phase
- Phase 4
- Status
- Completed
- Enrollment
- 72
- Locations
- 1
- Primary Endpoint
- Change in Composite Motor Score on Alberta Infant Motor Scale
Study Overview
Brief Summary
This research study in infant males with Klinefelter syndrome (47,XXY) will learn more about the effect of testosterone on early health and development. The study is a total of three visits over 6 months with assessments of motor skills, body composition (muscle and fat), and hormone levels. This is a randomized, placebo-controlled study but all infants will receive testosterone treatment during the study period. The investigators will learn how testosterone treatment in infancy effects short term outcome measures on health and development.
Detailed Description
XXY (also known as Klinefelter syndrome) is the most common chromosomal abnormality in males, affecting 1/600 boys. The extra X chromosome leads to insufficient development of the testicles and subsequent testosterone deficiency. Males with XXY also have a high risk for developmental delays, learning disabilities, and cardiovascular disease. An essential question is how much of this risk is because of testosterone deficiency and could therefore be reduced by testosterone supplementation, particularly during critical periods of development.
In typical male development, there is a surge of testosterone in the first few months of life, commonly known as the "mini-puberty period of infancy." This testosterone surge may be critical for neurodevelopmental and cardiometabolic programming throughout life. Recently there has been increased off-label use of testosterone in infants with XXY, however neither the short or long term safety or efficacy have been evaluated. This study aims to quantify the short term effects of testosterone treatment in infants with XXY on neurodevelopment, growth, body composition, testicular function, and safety parameters. This is a double blind randomized placebo controlled trial of testosterone injections 25 mg every 4 weeks for 3 doses in boys with XXY enrolled between 1 and 3 months of age. Outcomes including body fat percentage, scaled motor developmental scores, growth velocity, testicular hormone concentrations, specific metabolites, and safety parameters will be assessed 12 weeks into the study. The groups will then cross-over (all subjects will receive testosterone during the study period) and the outcomes will be reassessed 24 weeks into the study. The secondary questions the investigators will answer with this cross-over is 1) whether benefits in the treatment group at 12 weeks are sustained at 24 weeks, and 2) whether the same benefits are seen if treated after the mini-puberty period.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Crossover
- Primary Purpose
- Treatment
- Masking
- Double (Care Provider, Investigator)
Eligibility Criteria
- Ages
- 31 Days to 90 Days (Child)
- Sex
- Male
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Male infants with 47,XXY karyotype identified prenatally who are 4-12 weeks old (31 to 90 days of age). 47,XXY must be from a diagnostic test such as Chorionic Villus Sampling (CVS), amniocentesis, or post-natal blood/tissue. Non-invasive prenatal screening results alone will not be accepted.
Exclusion Criteria
- •>20 percent mosaicism for a normal cell line
- •Gestational age at birth <36 weeks
- •Birth weight <2.5th percentile or >97.5 percentile for age (small or large for gestational age)
- •History of thrombosis in self or a first degree relative
- •Exposure to androgen therapy outside the study protocol
- •Use of medications known to affect body composition, such as growth hormone or insulin
- •Known allergy to the testosterone cypionate solution components including benzyl benzoate, benzyl alcohol, or cottonseed oil
Arms & Interventions
Visit 1 Drug, Visit 2 Placebo
Subjects in this group will be randomized to receive Testosterone Cypionate 200 Milligram/Milliliter Injectable Solution every 4 weeks x 3 doses, beginning at visit 1, and Placebo Injectable Saline beginning at visit 2.
Intervention: Testosterone Cypionate 200 Milligram/Milliliter Injectable Solution (Drug)
Visit 1 Drug, Visit 2 Placebo
Subjects in this group will be randomized to receive Testosterone Cypionate 200 Milligram/Milliliter Injectable Solution every 4 weeks x 3 doses, beginning at visit 1, and Placebo Injectable Saline beginning at visit 2.
Intervention: Placebo injectable saline (Drug)
Visit 1 Placebo, Visit 2 Drug
Subjects in this group will be randomized to receive Placebo Injectable Saline beginning at visit 1, and Testosterone Cypionate 200 Milligram/Milliliter Injectable Solution every 4 weeks x 3 doses beginning at visit 2.
Intervention: Testosterone Cypionate 200 Milligram/Milliliter Injectable Solution (Drug)
Visit 1 Placebo, Visit 2 Drug
Subjects in this group will be randomized to receive Placebo Injectable Saline beginning at visit 1, and Testosterone Cypionate 200 Milligram/Milliliter Injectable Solution every 4 weeks x 3 doses beginning at visit 2.
Intervention: Placebo injectable saline (Drug)
Outcomes
Primary Outcomes
Change in Composite Motor Score on Alberta Infant Motor Scale
Time Frame: 3 months
Motor development will be assessed using the standardized Alberta Infant Motor Scale
Change in Body Fat Percentage
Time Frame: Baseline and 3 months
Body fat percentage will be measured using air displacement plethysmography (PEA POD) at the beginning and end of the study period
Change in C14:1 Long Chain Acylcarnitines (LCAC) through targeted metabolomics
Time Frame: Baseline and 3 months
Plasma will be processed and stored until batch analysis using electrospray tandem mass spectroscopy per standard protocols to quantify acylcarnitines (short, medium, and long-chain) and Branched-Chain Amino Acids (BCAA--leucine/isoleucine and valine) at baseline and 12 weeks.
Secondary Outcomes
- Change in insulin(6 months)
- Change in serum leptin(6 months)
- Change in lipids(6 months)
- Change in weight(6 months)
- Change in height(6 months)
- Change in weight-for-length(6 months)
- Change in waist circumference(6 months)
- Change in serum Luteinizing Hormone (LH)(6 months)
- Change in serum Follicle Stimulating Hormone (FSH)(6 months)
- Change in Inhibin B (INHB)(6 months)
- Change in Fine Motor Scores(6 months)
- Change in Anti-Mullerian Hormone (AMH)(6 months)
- Change in Total Testosterone (Total T)(6 months)
- Change in Gross Motor Scores on the Alberta Infant Motor Scales(6 months)
- Change in Adaptive Functioning(6 months)
- Change in Serum BCAA, other LCAC(6 months)
- Change in Gross Motor Scores on the Peabody Developmental Motor Scales 2(6 months)
- Change in Cognitive and Language Composite Scores on the Bayley III(6 months)
- Change in Pathway analysis(3 months)
- Change in Number and Type of Adverse Events(6 months)
