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Bone Microarchitecture Evaluation by HR-pQCT in Youngs Who Developed AN in Peri or Prepubertal Period.

Monocentric Study Evaluating Bone Microarchitecture by High Resolution Quantitative Computerized Tomography (HR-pQCT) in Young Adults and Adolescents Who Developed Anorexia Nervosa (AN) in Peri or Prepubertal Period.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02526927
Acronym
AMOS
Enrollment
34
Registered
2015-08-18
Start date
2015-11-23
Completion date
2017-11-29
Last updated
2018-02-22

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

Conditions

Anorexia Nervosa

Keywords

Anorexia Nervosa, microarchitecture, prepubertal

Brief summary

The occurrence of anorexia nervosa (AN) during childhood or adolescence rapidly induces starvation, stop of growth and impaired mineralization of bone tissue together with an interruption of pubertal development. These consequences are initially reversible following food intake return but can lead to a more irreversible status with low height, osteoporosis and high fracture risk. The onset of the disease more and more early in life, with the first stages of puberty suggest that these consequences will be even more severe as bone resistance will be damaged by more profound effects on bone growth as well. It is therefore critical to evaluate these bone metabolism alterations in order to better manage these patients. At every age and in every clinical circumstance either physiologic or pathologic, high resolution peripheral quantitative computerized tomography (HRpQCT) provides an evaluation of bone microarchitecture that is more informative than the global quantitative assessment given by conventional Dual Energy X-ray Absorptiometry) DEXA, with a better estimate of clinical fracture risk. Here, we propose to measure cortical parameters, such as cortical thickness which plays a key role in bone biomechanical strength in young adults aged between 20 and 30 years-old, who had developed AN as early as the during the first stages of puberty but no longer present, compared to age-and sex-matched healthy volunteers. Other micro-architectural parameters will also be studied. In an exploratory phase, we will evaluate these bone microarchitectural parameters together with bone biological turnover markers and markers of sexual maturation in adolescents or young adults 20 years-old or less, undernourished and currently managed for AN.

Interventions

DEVICEHR-pQCT

The Xtrem CT scanco device is a HR-pQCT used for 3D bone measurements at the tibia and the radius levels in human

DEVICEDEXA

The Lunar DEXA (Dual Energy X-ray Absorptiometry) is a third generation multi-captor DEXA device that allows short duration measurements (\< 15 min). It measures Bone Mineral Density at the spine (L1-L4) and the femoral neck

OTHERBlood samples

Sponsors

Centre Hospitalier Universitaire de Saint Etienne
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
10 Years to 30 Years
Healthy volunteers
No

Inclusion criteria

* Patients over 20 years old: * Age \> 20 and \< 30 years old * Patients managed for AN in the pediatric or endocrinology of the university hospital of St-Etienne * Patients who developed AN as early as the during the first stages of puberty defined by Tanner stage 1 to 4, with a diagnosis of AN based on DSM-IV current criteria: * Weight loss : deny of maintaining body weight over minimal normal threshold (85 % age and height matched) * Intense fear of gaining weight or becoming obese despite weight insufficiency; * Impaired perception of weight or dysmorphophobia; * Excessive role of weight or body shape in self-esteem or deny of current leanness; * Secondary amenorrhea during 3 or more menstrual cycles in young girls or primary amenorrhea * Duration of AN of at least 6 months * BMI \>85% of theoretical BMI (efficient renutrition) * Patients less than 20 years old : * Age \> 10 and \< 20 years old * Patients managed for AN in the pediatric or endocrinology of the university hospital of St-Etienne * Patients who developed AN as early as the during the first stages of puberty defined by Tanner stage 1 to 4, with a diagnosis of AN based on DSM-IV current criteria: * Weight loss : deny of maintaining body weight over minimal normal threshold (85 % age and height matched) * Intense fear of gaining weight or becoming obese despite weight insufficiency; * Impaired perception of weight or dysmorphophobia; * Excessive role of weight or body shape in self-esteem or deny of current leanness; * Secondary amenorrhea during 3 or more menstrual cycles in young girls or primary amenorrhea * Duration of AN of at least 6 months

Exclusion criteria

* Renal insufficiency * Cushing * Dysthyroidism * Inflammatory disease * Pregnancy * Lack of consent * Subject under legal protection

Design outcomes

Primary

MeasureTime frameDescription
Cortical thicknessDay 1Cortical thickness (in mm) is a composite outcome measured with HR pQCTon 3D images of distal radius and distal tibia.

Secondary

MeasureTime frameDescription
Number of patients with bone degradationDay 1Bone degradation is a composite outcome measured by cortical and architectural parameters measured with HR pQCTon 3D images of distal radius and distal tibia. The parameters are : Total volumetric bone mineral density (mg/ccm HA), Trabecular volumetric bone mineral density (mg/ccm HA), Cortical volumetric bone mineral density (mg/ccm HA), Number of bone trabeculae (1/mm), Trabecular thickness (mm) Cortical thickness (mm), Trabecular spacing (mm), Trabecular distribution (mm)
number of patients with osteoporosisDay 1Osteoporosis is measured with DEXA. DEXA measure the Bone Mineral Density (g/cm2)
Clinical and biological phenotype of AN patients 20 years-old or lessDay 1Clinical and biological phenotype of AN patients 20 years-old or less is a composite factor : Pubertal stage at disease onset, Duration of AN, Height shortening compared to optimal genetically defined height, Serum levels of FGF23, Serum levels of IGF 1, Serum levels of sexual steroids (FSH, LH, oestradiol, testosterone, SeBG, AMH, inhibin B), Serum levels of bone formation and resorption markers (cross laps, osteocalcin, total alkaline phosphatases), Serum levels of leptin, Bone mineral density measured by DXA

Countries

France

Outcome results

None listed

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