GNAS-AUTAX: Determination of Circulating Autotaxin in Patients With GNAS or PTH Abnormalities

Sponsor

Hospices Civils de Lyon (Other)

Overall Status

Recruiting

CT.gov ID

NCT04671719

Collaborator

(none)

110

Enrollment

Locations

Anticipated Duration (Months)

36.7

Patients Per Site

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

PTH secretion defects (grouped under the name hypoparathyroidism) are due to abnormalities in the PTH gene, abnormalities in the development of the parathyroid glands which synthesize PTH or abnormalities of the calcium sening receptor whose role is to adapt PTH level to ambient calcium level.

In contrast, primary hyperparathyroidism in children is also exceptional; expressed by hypercalcemia, with a renal and bon risk.

Pseudo-hypoparathyroidism, now known under the term inactivating PTH / PTHrP Signaling Disorder or iPPSD, are rare pathologies characterized by resistance to the action of PTH sometimes associated with other symptoms, in particular chondrodysplasia. They are linked to a defect in the action of a factor in the signaling pathway of G protein-coupled receptors that activate the production of cyclic AMP (cAMP). IPPSDs are most often due to a molecular defect in the GNAS gene, subject to parental imprint.

Fibrous dysplasia / McCune-Albright syndrome is a rare disease caused by somatic "gain-of-function" mutations in the GNAS gene located on chromosome 20q13 leading to activation of the protein Gαs and inappropriate production of intracellular cyclic adenosine monophosphate (cAMP). The clinical phenotype is determined by the location and extent of the tissues affected by this mutation.

Autotaxin (ATX) is a protein secreted by different tissues including the liver, fatty tissue, and bone. Today, ATX is described as the major source of LPA in the bloodstream. LPA interacts with one of its receptors on the surface of the cell membrane. Depending on the receptor engaged, one or more Gα subunits (G12 / 13, GQ, Gi / o or Gs) will activate multiple cell signaling pathways.

In bone, ATX is expressed by osteoclasts and osteoblasts. Recent laboratory data have shown that PTH stimulates ATX expression in osteoblasts in a dose-dependent manner.

The objective of this study is to provide clinical proof of concept that the PTH / Gαs / ATX pathway is truly significant in physiology and pathology, by studying the full spectrum of PTH and GNAS pathologies. If this proof of concept is obtained, therapeutic applications will probably be possible in the long term.

Condition or Disease	Intervention/Treatment	Phase
Fibrous Dysplasia Albright Syndrome Adult Children Hypoparathyroidism Hyperparathyroidism Pseudo Hypoparathyroidism	Biological: blood sample

Study Design

Study Type:

Observational

Anticipated Enrollment :

110 participants

Observational Model:

Case-Control

Time Perspective:

Prospective

Official Title:

Autotaxin in Patients With GNAS/PTH Abnormalities

Actual Study Start Date :

Mar 10, 2021

Anticipated Primary Completion Date :

Mar 10, 2024

Anticipated Study Completion Date :

Mar 10, 2024

Outcome Measures

Primary Outcome Measures

Concentration of circulating autotaxin [At inclusion]
Concentration of circulating autotaxin measured in patient serum by ELISA assay

Eligibility Criteria

Criteria

Ages Eligible for Study:

10 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Pediatric patients :

Children from 10 to 18 years old
Patients with Fibrous dysplasia / McCune-Albright syndrome,hypoparathyroïdism, hyperparathyroïdism, or iPPSD, from References Centers for rare diseases (Calcium and phosphate metabolism, constitutional bone diseases) followed at hôpital Femme Mère Enfant (Bron) or at hôpital Bicêtre Paris Saclay (Paris).
Patients and parent / holder of parental authority who have been informed of the study and do not object to participate

• Adults:

Patients > 18 years old
Patients with Fibrous dysplasia / McCune-Albright syndrome, followed in reference center for constitutional bone diseases at hôpital Edouard Herriot (Lyon)
Patients who have been informed of the study and do not object to participate

Exclusion Criteria:

Children < 8 kg
Patient with hepatic disease
Patients under tutorship or curatorship
Pregnant and / or breastfeeding woman
Patient deprived of liberty
Patient in emergency situation who can not agree to participate

Contacts and Locations

Locations

	Site	City	Country	Postal Code
1	Centre de compétence des maladies rares de l'insulino-sécrétion et de l'insulino-sensibilité	Bron	France	69500
2	Centre de référence Dysplasie Fibreuse des os Service rhumatologie et pathologie osseuse Hôpital Edouard Herriot, Lyon	Lyon	France	69003
3	Centre de Référence des Maladies Rares du Métabolisme du Calcium et du Phosphate Service d'Endocrinologie et Diabète de l'Enfant Hôpital Bicêtre Paris Saclay	Paris	France	94270