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Circulating Transforming Growth Factor Beta (TGF-β) in Individuals With Marfan Syndrome

Circulating Transforming Growth Factor Beta (TGF-β) in Individuals With

Status
Withdrawn
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01361087
Enrollment
0
Registered
2011-05-26
Start date
2011-04-30
Completion date
Unknown
Last updated
2016-02-05

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

Conditions

Marfan Syndrome

Keywords

TGF-B blood levels Atenolol vs, Losartan Study, NIH, NIHLB and NMF

Brief summary

Transforming Growth Factor Beta (TGF-β) is a protein that controls proliferation, cellular differentiation, and other functions in most cells. TGF-β levels play a major role in the pathogenesis of Marfan syndrome, a disease characterized by disproportionate height, long extremities, lens dislocation in the eyes and heart complications such as mitral valve prolapse and aortic enlargement increasing the likelihood of aortic dissection. While the underlying defect in Marfan syndrome is faulty synthesis of the glycoprotein fibrillin I, normally an important component of elastic fibers it has been shown that the Marfan syndrome phenotype can be relieved by addition of a TGF-β antagonist in affected mice.

Detailed description

Transforming Growth Factor Beta (TGF-β) is a protein that controls proliferation, cellular differentiation, and other functions in most cells. TGF-β levels play a major role in the pathogenesis of Marfan syndrome, a disease characterized by disproportionate height, long extremities, lens dislocation in the eyes and heart complications such as mitral valve prolapse and aortic enlargement increasing the likelihood of aortic dissection. While the underlying defect in Marfan syndrome is faulty synthesis of the glycoprotein fibrillin I, normally an important component of elastic fibers it has been shown that the Marfan syndrome phenotype can be relieved by addition of a TGF-β antagonist in affected mice. This suggest that while the symptoms of Marfan syndrome may seem consistent with a connective tissue disorder, the mechanism is more likely related to reduced sequestration of TGF-β by fibrillin.

Interventions

OTHERBlood draw

This study includes one blood draw to measure circulating blood levels of TGF-B.

Sponsors

Johns Hopkins University
CollaboratorOTHER
Ann & Robert H Lurie Children's Hospital of Chicago
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
6 Months to 24 Years
Healthy volunteers
No

Inclusion criteria

* Individual with Marfan syndrome consented in to the Main Atenolol Vs. Losartan NIH study.

Exclusion criteria

* Subjects in the main PHN Marfan trial who have not achieved the maintenance drug dosing or who have stopped taking study drug.

Design outcomes

Primary

MeasureTime frame
To determine if circulating levels of TGF-β correlate with treatment arms: Atenolol vs. Losartan.1 year

Secondary

MeasureTime frameDescription
To determine if circulating levels of TGF-β correlate with clinical outcomes within a treatment group or independent treatment groups.1 yearThese clinical outcomes may be a change in aortic root Z-score, final aortic root dimension, final aortic root Z-score and other clinical outcomes in the main Marfan trial.

Countries

United States

Outcome results

None listed

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