Fibroblast Line Evaluation for COL5A eXpression and Thoracic Aortic Aneurysms: in Vitro Characterization of Cutaneous Fibroblasts in Adult Patients

NCT ID: NCT07282717

Last Updated: 2026-02-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

20 participants

Study Classification

OBSERVATIONAL

Study Start Date

2026-01-13

Study Completion Date

2028-12-31

Brief Summary

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This study examines adults with COL5A gene mutations to understand why some develop aortic aneurysms while others do not. Participants provide a small skin biopsy, and researchers analyze fibroblasts to evaluate collagen production, extracellular matrix organization, and connective-tissue signaling pathways. The goal is to identify biological differences that may explain variable vascular risk and support future personalized monitoring and treatment strategies.

Detailed Description

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Individuals with mutations in the collagent type V, alpha (COL5A) gene show variable clinical outcomes. While some develop aortic aneurysms, others with the same mutation remain free of cardiovascular complications. The mechanisms driving this variability are not fully understood.

This study aims to investigate biological differences at the cellular level by analyzing fibroblasts derived from a small skin biopsy. Fibroblasts play a key role in the production and organization of type V collagen and the extracellular matrix.

Researchers will:

Grow fibroblasts from participants' skin samples.

Assess cell growth, migration, and extracellular matrix formation.

Measure the quantity and type of collagen produced.

Evaluate molecules involved in collagen breakdown and repair.

The study compares individuals with COL5A mutations who have documented aortic aneurysms to those with the same mutation but no vascular involvement. Analyses will also consider differences among family members who share the same genetic variant.

By characterizing fibroblast behavior, the study seeks to clarify why some individuals develop aortic disease while others remain unaffected. Findings may help identify cellular features associated with increased or reduced vascular risk and guide future strategies for monitoring, prevention, and personalized care in patients with COL5A mutations.

Conditions

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Mutations Affecting the COL5A Gene Aneurysm Aortic

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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Young patients with COL5A mutation and TAAD

Young patients (aged 18-50 years) with COL5A mutation and aortic manifestations

No interventions assigned to this group

Young patients with COL5A mutation without TAAD

Young patients (aged 18-50 years) with COL5A mutation in the absence of aortic manifestations

No interventions assigned to this group

Adult patients with COL5A with TAAD

Adult patients (aged over 50 years) with COL5A mutation and aortic manifestations

No interventions assigned to this group

Adult patients with COL5A mutation without TAAD

Adult patients (aged over 50 years) with COL5A mutation in the absence of aortic manifestations

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Subjects aged 18 and above
* Mutation in COL5A
* Signed informed consent

Exclusion Criteria

* Corticosteroid or Steroids or Fluorochinolones treatment within six months before enrollment
* Subjects on chronic immunosuppressive therapies such as oral steroids, but also on chronic topical steroids in the area of investigation
* Subject on anticoagulant therapy
* History of coagulation factor defects/alterations (data found in anamnesis and medical records)
* A history of keloid formation (data found in anamnesis and medical records)
* Anesthetic drug allergy (data found in anamnesis and medical records)
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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IRCCS Policlinico S. Donato

OTHER

Sponsor Role lead

Responsible Party

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Alessandro Pini

Director

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Cardiovascular Genetic Centre IRCCS Policlinico San Donato

San Donato Milanese, Italy, Italy

Site Status

Countries

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Italy

Central Contacts

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Alessandro Pini Alessandro Giorgio Pini,MD, Medical degree

Role: CONTACT

+39 0252774705

Nathasha Samali Udugmpolage

Role: CONTACT

+39 0252774705

Facility Contacts

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Nathasha Samali UDUGAMPOLAGE

Role: primary

(+39) 02 52774705

References

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Phan QM, Fine GM, Salz L, Herrera GG, Wildman B, Driskell IM, Driskell RR. Lef1 expression in fibroblasts maintains developmental potential in adult skin to regenerate wounds. Elife. 2020 Sep 29;9:e60066. doi: 10.7554/eLife.60066.

Reference Type RESULT
PMID: 32990218 (View on PubMed)

Lu P, Takai K, Weaver VM, Werb Z. Extracellular matrix degradation and remodeling in development and disease. Cold Spring Harb Perspect Biol. 2011 Dec 1;3(12):a005058. doi: 10.1101/cshperspect.a005058.

Reference Type RESULT
PMID: 21917992 (View on PubMed)

Plikus MV, Wang X, Sinha S, Forte E, Thompson SM, Herzog EL, Driskell RR, Rosenthal N, Biernaskie J, Horsley V. Fibroblasts: Origins, definitions, and functions in health and disease. Cell. 2021 Jul 22;184(15):3852-3872. doi: 10.1016/j.cell.2021.06.024.

Reference Type RESULT
PMID: 34297930 (View on PubMed)

Other Identifiers

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FLEX5 project

Identifier Type: -

Identifier Source: org_study_id

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