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RecruitingNCT06440148Updated Jun 3, 2024

Relationship Between Circulating Sclerostin and Bone Lesions in Patients With Mastocytosis

An observational study in Mastocytosis and Bones, sponsored by Medical University of Lublin. Recruiting at 1 site in Poland. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-06-03.

Sponsored by Medical University of Lublin · Observational

From the registry’s dates

  • Started Sep 2019; still recruiting 7 years 1 month later.
Study type
Observational
Model
Case-control
Time perspective
Retrospective
Enrollment
50
Ages
18 Years and older
Sex
All
01

Study summary

Mastocytosis is very rare and highly heterogeneous group of disorders, characterized by the accumulation of clonal mast cells which can infiltrate several organs and tissues.

Bones are the most frequent localization of systemic mastocytosis. The aim of our research was to explain the potential role of sclerostin in the pathogenesis of bone disease in mastocytosis.

Read the detailed description

Mastocytosis is a heterogeneous group of disorders, characterized by the accumulation of clonal mast cells which can infiltrate several organs, such as the skin, bone marrow or liver. The skeleton is the most frequent localization of systemic mastocytosis (SM). Bone involvement occurs in approximately 70% of SM patients. Pathogenesis of mastocytosis bone disease is poorly understood.

The aim of our research is to explain the potential role of sclerostin, a recently discovered bone tissue protein, in the pathogenesis of bone changes in patients with mastocytosis.

The study group consists of adult patients with mastocytosis divided according to their clinical variants of disease (aggressive systemic mastocytosis - ASM, systemic mastocytosis with an associated hematological neoplasms SM-AHN, smouldering systemic mastocytosis - SSM, indolent systemic mastocytosis - ISM and cutaneous mastocytosis - CM; and group of healthy volunteers.

The concentration of sclerostin, bioactive sclerostin and expression of the SOST gene in human plasma and HMC-1.2 human mast cell culture supernatants is assessed. The Real-Time PCR method is used to evaluate the expression of sclerostin at the mRNA level, while the concentration of the sclerostin protein and its bioactive form is assessed using the enzyme immunoassay ELISA method. The obtained results are correlated with selected demographic, clinical, laboratory and radiological findings. Low-dose CT scan is used to assess bone changes.

These preliminary results could serve that sclerostin may be a new therapeutic target in patients with mastocytosis.

02

Conditions studied

  • Mastocytosis
  • Bones

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Keywords

  • Bones
  • Mastocytosis
  • Osteolysis
  • Osteosclerosis
  • Sclerostin
03

In context

Mastocytosis

75 studies on the registry are indexed under Mastocytosis; 16 are open to participants now.

This study's planned enrollment of 50 is below the median of 200 across 31 observational studies indexed under Mastocytosis.

Browse Mastocytosis studies →

Lead sponsor

Medical University of Lublin is the lead sponsor of 60 studies on the registry; 10 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

The study group consists of adult patients diagnosed with mastocytosis, divides according to the clinical variants: aggressive systemic mastocytosis (ASM), systemic mastocytosis with associated hematological neoplasm (SM-AHN), indolent systemic mastocytosis (ISM), smoldering systemic mastocytosis (SSM) and cutaneous mastocytosis (CM).

The diagnosis of mastocytosis should be established based on biopsy of the affected organ (bone marrow trephine biopsy, skin affected by the disease), following the 2022 WHO classification. The control group comprised 30 healthy volunteers matched with the study group in terms of age and gender.

Inclusion criteria

  • Age > 18 years
  • Mastocytosis defined according to WHO criteria
  • Known KIT mutation status

Exclusion criteria

Exclusion Criteria:

  • History of organ transplant
  • Inability to give informed consent
  • Pregnancy, Breastfeeding
  • Vulnerable Patient, defined as: patient with another uncontrolled severe disease; patient under juridical protection
05

Study design

Observational model
Case-control
Time perspective
Retrospective
Enrollment
50 participants (estimated)
Patient registry
No
Biospecimen retention
Samples with dna

Interventions

  • BiologicalSCLEROSTIN

    Pathogenesis of mastocytosis bone disease

06

What researchers measure

Primary outcomes

  1. plasma sclerostin measurements (in pmol/l) SOST gene expression by Real-Time PCR dimensions of osteolytic lesions on low-dose computed tomography (in mm) dimensions of osteosclerotic lesions on low-dose computed tomography (in mm)

    The Primary Outcome Measures concern: * the measurements of plasma levels of sclerostin and its bioactive form in patients with mastocytosis and healthy volunteers * the measurements of levels of sclerostin and its bioactive form in HMC-1.2 human mast cells unstimulated and stimutaled with Il-6

    Time frame: 1 year

  2. dimensions of osteolytic lesions (in mm)

    The Primary Outcome Measures concern: - the measurements of the dimensions of osteolytic bone lesions on low-dose computed tomography in patients with mastocytosis

    Time frame: 1 year

  3. dimensions of osteosclerotic lesions (in mm)

    The Primary Outcome Measures concern: - the measurements of the dimensions of osteosclerotic bone lesions on low-dose computed tomography in patients with mastocytosis

    Time frame: 1 year

07

Study locations

1 of 1 sites recruiting
  • Department of Hematooncology and Bone Marrow Transplantation
    Lublin, Lubelskie 20-081, Poland
    Recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 3, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06440148
Lead sponsor
Medical University of Lublin
Responsible party
Aneta Szudy Szczyrek (Doctor of Medicine, Medical University of Lublin) — Principal investigator
First posted
Jun 3, 2024
Start date
Sep 1, 2019
Primary completion
May 1, 2024
Completion
Dec 31, 2026 (estimated)
Last update
Jun 3, 2024

Study contacts

Aneta Szudy-Szczyrek, MD., PhD.
Contact
aneta.szudy-szczyrek@umlub.pl
+48815345468
Aneta A Szudy-Szczyrek, MD., PhD.
principal investigator · Medical University of Lublin

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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