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Biomarkers in EV Associated With Marrow Adiposity in Anorexia

Identification of Biomarkers in Extracellular Vesicles Associated With Marrow Adiposity and Bone Deterioration Caused by Nutritional Deficiencies

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06712485
Acronym
VE_BMAT_AN
Enrollment
30
Registered
2024-12-02
Start date
2025-05-15
Completion date
2026-07-31
Last updated
2025-05-07

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

Conditions

Anorexia Nervosa (DSM-IV Revised Criteria), Anorexia Nervosa Restricting Type

Keywords

Extracellular Vesicles, Bone Deterioration, Biomarkers, Bone Marrow Adipose Tissue, Nutritional Deficiencies

Brief summary

The aim of this observational study is to identify biomarkers in extracellular vesicles associated with medullary adiposity occurring in patients with anorexia nervosa. The main question it aims to answer is: Can this medullary adiposity be associated with the bone deterioration observed in this population? Participants will be assessed for body composition and a blood sample will be taken by non-invasive techniques.

Interventions

None listed

Sponsors

Hospital Universitario Reina Sofia de Cordoba
CollaboratorOTHER_GOV
Maimónides Biomedical Research Institute of Córdoba
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

For AN group: * Diagnosis of active AN according to DSM-5 criteria * BMI of less than 17kg/m2 * Present amenorrhoea in the 3 months prior to the start of the study. For AN-R group: * Achieved weight gain of more than 85%. * Normal menstruation in the last 3 months. For Control group: * Population of the same age and gender as the AN and AN-R groups. * If pubertal population, presenting a chronological age of ± 2 years. * Normal menstruation * Normal BMI (\>18.5 kg/m2) * No presence of previous dietary transtrons.

Exclusion criteria

* Not receiving oestrogens, contraceptives or glucocorticoids in the 3 months prior to the start of the study. * Not to suffer from chronic diseases, such as diabetes, pathologies affecting the bone system or thyroid function. * Do not take calcium or vitamin supplements.

Design outcomes

Primary

MeasureTime frameDescription
Biomarkers related to medullary adiposity1 dayBlood samples to isolate extracellular vesicles for omics studies

Secondary

MeasureTime frameDescription
Bone Mineral Density1 dayBone mineral density measured by densitometry
Body Composition1 dayFat and muscle mass measured by ultrasound

Countries

Spain

Contacts

Primary ContactMarta Camacho-Cardenosa, pHd
marta.camacho@imibic.org+34 957213814

Outcome results

None listed

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