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Metabolic Phenotyping in vEDS

Metabolic Phenotyping in Individuals With Vascular Ehlers-Danlos Syndrome (vEDS)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07516496
Acronym
MPEDS
Enrollment
15
Registered
2026-04-08
Start date
2026-03-05
Completion date
2031-04-04
Last updated
2026-04-08

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

Conditions

Vascular EDS (vEDS), Vascular Ehlers Danlos Syndrome, Vascular Ehlers-Danlos Syndrome

Keywords

vascular Ehlers Danlos syndrome, insulin resistance, partial lipodystrophy

Brief summary

This research study will investigate whether people with vascular Ehlers-Danlos syndrome (vEDS), a rare inherited condition, have problems with the way their body stores and uses fat (adipose tissue). vEDS is caused by changes in a gene called COL3A1, which makes a protein important for the structure of many tissues. While vEDS is best known for making blood vessels fragile, there is some early evidence that it may also affect fat tissue and increase the risk of problems such as insulin resistance (where the body does not respond properly to insulin) and diabetes. Fat tissue is important for keeping the body healthy. It stores extra energy, but it also sends signals to other organs. If fat tissue cannot expand or work properly, fat can build up in the liver or muscles instead, leading to high blood sugar, high cholesterol, and greater risk of diabetes and heart disease. In this study, we will invite 12-17 adults with genetically confirmed vEDS to take part, along with a group of age-, sex-, and weight-matched controls without vEDS. Participants will attend a research visit at Addenbrooke's Hospital, Cambridge. They will have measurements of body fat distribution (using a DEXA scan), a liver scan, blood tests, and a standard oral glucose tolerance test (drinking a sugary drink with blood samples before and after). Some participants may also choose to provide a small fat biopsy under local anaesthetic to allow more detailed analysis of tissue structure. The main aim is to see whether people with vEDS show changes in fat distribution and insulin sensitivity compared to those without vEDS.

Interventions

There is no intervention

Sponsors

Cambridge University Hospitals NHS Foundation Trust
Lead SponsorOTHER
University of Cambridge
CollaboratorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

* Age over 18 years * Confirmed pathogenic or likely pathogenic COL3A1 mutation with vascular Ehlers-Danlos syndrome * Capacity to provide informed consent

Exclusion criteria

for those with vEDS: * Current corticosteroid use * Pregnancy or lactation * Acute illness at the time of assessment

Design outcomes

Primary

MeasureTime frameDescription
OGTT-derived free fatty acid suppression test in vEDS vs matched controls3 yearsTo compare adipose-tissue insulin sensitivity, quantified by the oral glucose tolerance test (OGTT)-derived free fatty acid (FFA) suppression index, between adults with genetically confirmed vascular Ehlers-Danlos syndrome (vEDS) and age-, sex-, and BMI-matched controls.

Secondary

MeasureTime frameDescription
To describe body-fat distribution (using DEXA trunk and leg fat; trunk:leg ratio) and compare profiles between groups.3 yearsTo describe body-fat distribution (using DEXA trunk and leg fat; trunk:leg ratio) and compare profiles between groups.
To examine relationships between adipose-tissue insulin sensitivity (OGTT)-derived free fatty acid (FFA) suppression index and biomarkers, including leptin, adiponectin, leptin/adiponectin ratio, hs-CRP, and standard lipids/biochemistry.3 yearsTo examine relationships between adipose-tissue insulin sensitivity (OGTT)-derived free fatty acid (FFA) suppression index and biomarkers, including leptin, adiponectin, leptin/adiponectin ratio, hs-CRP, and standard lipids/biochemistry.

Countries

United Kingdom

Contacts

CONTACTAgnieszka Jakubowska, MBBS
aj776@cam.ac.uk+447487602584

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 9, 2026