Down syndrome (DS) is the most common chromosomal disorder; with the increasing life expectancy, about 80% of DS adults reach age 65 years old. Early Alzheimer's disease (AD) is the most common cause of death within this population. DS individuals already show AD neuropathology by the age of 30, while it becomes clinically recognized in their late forties. DS subjects also exhibit olfaction defects in adulthood. To date, there is no treatment available for the cognitive or olfactory defects in DS. The development of an effective treatment targeting cognitive dysfunction in DS adolescents/adults would be warranted. GnRH, a decapeptide secreted by hypothalamic neurons is the pilot light of reproduction in all mammals. Pulsatile GnRH acts on the gonadotrophs via the GnRH receptor (GNRHR) in the pituitary gland to stimulate LH and FSH, which themselves will act on the gonads to produce gametes and steroids. However, GNRHR are also expressed in cerebral cortex, hippocampus, amygdala, habenula, olfactory structures, and adrenal gland, suggesting that GnRH may have a role beyond reproduction. Recently, GnRH has been shown to be involved in the process of ageing and lifespan control. Notably, in murine models, GnRH acts as an anti-ageing factor, independent of sex hormones. While ageing is characterized by hypothalamic inflammation and diminished neurogenesis, particularly in the hypothalamus and the hippocampus, GnRH was able to promote adult neurogenesis. The regulation of GnRH secretion is complex and involves hormonal, neuronal input, and environmental factors. Prévot et al. recently explored cognition within the Ts65Dn model and showed an age-dependent loss of the ability to recognize new objects. Also, these mice exhibit defects in olfaction. Given the role of GnRH in anti-aging mice model, pulsatile GnRH or continuous GnRH infusion (leading to desensitization of the GNRHR) were given to the Ts65Dn mice for two weeks. Amazingly, pulsatile but not continuous GnRH therapy was able to recover cognitive and olfaction defects.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
56
Drug administered by a subcutaneous pump
Drug administered by a subcutaneous pump
Centre Hospitalier Universitaire Vaudois (CHUV)
Lausanne, Canton of Vaud, Switzerland
RECRUITINGCognition
Montreal Cognitive Assessment (MoCA) total score ranges between 0 and 30 (cut-off set at 26 for the healthy population) Higher scores reflect better performance.
Time frame: Baseline to end of treatment (Week 24)
Dimensional change card sorting task (DCCS)
change in score of DCCS to assess executive functions
Time frame: baseline to end of treatment (Week 24)
Paired Associated Learning (PAL, part of the CANTAB battery)
change in score of PAL to assess learning
Time frame: baseline to end of treatment (Week 24)
Token test
change in score of Token test to assess verbal comprehension
Time frame: baseline to end of treatment (Week 24)
Corsi block tapping task
change in score to assess visuospatial memory
Time frame: baseline to end of treatment (Week 24)
Litmus non-word-repetition test
change in score of Litmus test to assess phonological abilities
Time frame: baseline to end of treatment (Week 24)
Health-related quality of life SF-12
The health-related quality of life (HRQoL) can be used to measure the effects of healthcare interventions and provide quality-improvement outcomes. The Short Form-12 (SF-12) Health Survey is widely used in measuring HRQoL. SF-12 is a reliable, valid measure in a variety of population groups; it is an equivalent substitute for the SF-36v2 for the summary scales. The response to each of the 12 items is weighted separately by the physical and mental component summary (PCS and MCS) regression coefficients and then calculated to give the SF-12 PCS and MCS scores.
Time frame: baseline to end of treatment (Week 24)
Adaptive behavior (Vineland II) - caregiver questionnaire
change in score of Vineland II (normed assessment tool that assesses adaptive behavior across the areas of communication, activities of daily living, and socialization).
Time frame: baseline to end of treatment (Week 24)
Glycemia
Glucose concentration (mmol/L) is a metabolic parameter.
Time frame: baseline to end of treatment (Week 24)
Insulinemia
Insulin concentration (nmol/L) is a metabolic parameter.
Time frame: baseline to end of treatment (Week 24)
Total cholesterol
Total cholesterol (mmol/L) is a metabolic parameter.
Time frame: baseline to end of treatment (Week 24)
High density lipoprotein (HDL)-cholesterol
HDL-cholesterol (mmol/L) is a metabolic parameter.
Time frame: baseline to end of treatment (Week 24)
Low density lipoprotein (LDL)-cholesterol
LDL-cholesterol (mmol/L) is a metabolic parameter.
Time frame: baseline to end of treatment (Week 24)
Triglycerides
Triglycerides (mmol/L) is a metabolic parameter.
Time frame: baseline to end of treatment (Week 24)
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