Skip to content

Turner Syndrome Minipuberty Study

Turner Syndrome Minipuberty Study A Prospective, Descriptive Cohortstudy

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04189406
Acronym
Minipuberty
Enrollment
30
Registered
2019-12-06
Start date
2020-02-01
Completion date
2024-12-01
Last updated
2023-11-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gonadal Dysgenesis, Infertility, Female, Ovarian Diseases, Premature Menopause, Premature Ovarian Failure, Sex Chromosome Disorders, Turner Syndrome

Keywords

Minipuberty, Turner Syndrome, Infertility, Premature Ovarian Failure

Brief summary

Rationale: Due to accelerated germ cell loss, infertility is a major problem in girls with Turner syndrome (TS). Therefore, cryopreservation of ovarian tissue or oocytes before exhaustion of the ovarian reserve may preserve fertility in patients with TS. However, in the majority of females with TS , the ovarian reserve is exhausted before the age of menarche. Early markers indicating and predicting the ovarian reserve are necessary. During mid-childhood the hypothalamic-pituitary-gonadal (HPG) axis is quiescent and gonadotropins are usually unmeasurable. Nonetheless, this axis is active during infancy. Therefore, gonadotropins are measurable with peak values at 3 months of age and with lower (but still measurable) values at 9 months of age, in a period called the minipuberty. The aim of this study is to find markers of ovarian capacity, during the minipuberty, in order to predict ovarian reserve in the future. Objective: The hormonal range of LH, FSH, AMH, inhibin B, testosterone and estradiol in girls with TS during the minipuberty and the relation of the hormone serum levels with the karyotype. Study design: A prospective, cohort study with a duration of 3 years. Study population: Girls with a pre- or perinatal diagnosis TS who are born in a medical centre in the Netherlands during the duration of the study Main study parameters/endpoints: Serum levels of FSH, LH, AMH, inhibin B, testosterone and estradiol at the age of 3 and 9 months.

Detailed description

Nature and extent of the burden and risks associated with participation, benefit and group relatedness: The subjects will have twice an extra venapunction for collection of 3.5mL blood during their infancy, which is not stated in the guidelines for TS. There is very little risk for adverse events associated with this blood sample collection, however it is an extra procedure. The outcome parameters will not be helpful for individual study participants, however they are likely to help clinicians and researchers in understanding how the ovarian function operates develops in girls with TS. Furthermore, these markers could be used to estimate the ovarian reserve and the urgency of fertility preservation in young females with TS. This information could help clinicians, patients and their parents in decision making.

Interventions

A blood sample of 3.5 mL (0.2 mL serum for FSH and LH, 0.15 mL serum for E2, 0.15 mL serum for T, 0.15 mL serum for AMH and 0.25 mL serum for Inhibin B) will be collected of all girls with TS at 3 months and 9 months of age. For the girls with TS, this will be collected with an extra venapuncture during a regular outpatient visit within the usual care.

Sponsors

Radboud University Medical Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
1 Months to 3 Months
Healthy volunteers
Yes

Inclusion criteria

In order to be eligible to participate in the TS group of this study, a subject must meet all of the following criteria: * A diagnosis of TS before the age of three months; * Girls with a diagnosis of classic TS or other variants (i.e. 45,X, 45,X/46XiXq, 45,X/46,XY, 45,X/46,XX, 45,X/47,XXX, 45,X/46,X,r(X), 46,XiXq, other); * Whose parents have agreed to participate in the study through a signed written informed consent form. In order to be eligible to participate in the control group of this study, a subject must meet all of the following criteria: * No diagnosis of TS or any other diagnosis that might affect the HPG axis; * Girls that will have a blood collection within their usual care at 3 months and at 9 months of age. * Whose parents have agreed to participate in the study through a signed informed consent form.

Exclusion criteria

A potential subject who meets any of the following criteria will be excluded from participation in this study: * Any other diagnosis besides TS that might affect the HPG axis; * Ovarian surgery in the medical history; * Critical illness; * The use of medication affecting the HPG axis (e.g. estrogen suppletion therapy)

Design outcomes

Primary

MeasureTime frameDescription
Defining the inhibin B range during minipuberty in girls with TS at 3 months of age and at 9 months of age1 year after venapunctureinhibin B will be collected with a venapuncture and analysed with the GEN II ELISEA of Beckman Coulter.
Defining the LH range in blood during minipuberty in girls with TS at 3 months of age and at 9 months of age1 year after venapunctureLH (luteinizing hormone) will be collected with a venapuncture and analysed with the Elecsys method on the Cobas E801system of Roche.
Defining the FSH range during minipuberty in girls with TS at 3 months of age and at 9 months of age1 year after venapunctureFSH (follicle stimulating hormone) will be collected with a venapuncture and analysed with the Elecsys method on the Cobas E801system of Roche.
Defining the AMH range during minipuberty in girls with TS at 3 months of age and at 9 months of age1 year after venapunctureAMH (Anti-Müllerian hormone) will be collected with a venapuncture and analysed on the Access of Beckman Coulter.
Defining the estradiol range during minipuberty in girls with TS at 3 months of age and at 9 months of age1 year after venapunctureestradiol will be collected with a venapuncture and analysed with the LCMSMS analysis method.
Defining the testosterone range during minipuberty in girls with TS at 3 months of age and at 9 months of age1 yeartestosterone will be collected with a venapuncture and analysed with the LCMSMS analysis method.

Secondary

MeasureTime frameDescription
Patient's karyotype vs LH1 year after venapunctureThe association between patient's karyotype and LH level at 3 months of age and 9 months of age
Patient's karyotype vs FSH1 year after venapunctureThe association between patient's karyotype and FSH level at 3 months of age and 9 months of age
Patient's karyotype vs AMH1 year after venapunctureThe association between patient's karyotype and AMH level at 3 months of age and 9 months of age
Patient's karyotype vs estradiol1 year after venapunctureThe association between patient's karyotype and estradiol level at 3 months of age and 9 months of age
Patient's karyotype vs testosterone1 year after venapunctureThe association between patient's karyotype and testosterone level at 3 months of age and 9 months of age
Patient's karyotype vs inhibin B1 year after venapunctureThe association between patient's karyotype and inhibin B level at 3 months of age and 9 months of age

Countries

Denmark, Germany, Netherlands, Poland, Sweden

Contacts

Primary ContactSanne vd Coelen, MD
sanne.vandercoelen@radboudumc.nl+31243098078
Backup ContactJanielle vd Velden, MD, PhD
Janielle.vanderVelden@radboudumc.nl+24 3614430

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026