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Williams Syndrome Strength, Hormones, Activity & Adiposity, DNA Programming, Eating Study

Williams Syndrome SHAAPE STUDY [Strength, Hormones, Activity & Adiposity, DNA Programming, Eating Study]

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03758651
Acronym
SHAAPE
Enrollment
144
Registered
2018-11-29
Start date
2018-10-01
Completion date
2023-09-14
Last updated
2023-10-19

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

Conditions

Lipedema, Williams Syndrome

Keywords

Williams Syndrome, Lipedema, Body Composition, Glucose, Bone Density

Brief summary

Williams syndrome (WS) is a rare microdeletion genetic disorder that has a broad phenotype including many endocrine and metabolic abnormalities. Dr. Pober and colleagues at MGH have reported the following findings in adults with WS: abnormal body composition (excess body fat accumulation with a lipedema phenotype), decreased bone mineral density, abnormal glucose tolerance, and reduced lean mass. Despite the high prevalence and potential effect of metabolic abnormalities on the health of persons with WS, their full phenotypic range, potential causal factors (either genetic and/or hormonal) along with their impact on other aspects of health (such as risk of falls and fractures or interaction with emotional behavioral concerns) remain incompletely characterized. The purpose of the current study in a large cohort of subjects with WS is to: collect further information to characterize the timing of onset and distribution of body fat; better characterize hormonal status of WS subjects; and screen for genetic variation using single-nucleotide-polymorphism (SNP) analysis that could elucidate genetic contributors to the lipedema phenotype as well as the other observed metabolic and bone abnormalities.

Interventions

None listed

Sponsors

Williams Syndrome Association
CollaboratorUNKNOWN
Massachusetts General Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

For those participating in-person at Massachusetts General Hospital: Inclusion Criteria 1. Male or Female age 18-70 years old 2. Diagnosis of Williams syndrome (WS), established by experienced clinician, parent report, or confirmed by genetic testing such as FISH (fluorescent in situ hybridization) or chromosomal microarray (WS only) 3. Availability of a parent or guardian to review details of the study with their family member with WS and participate in the consent process (all WS regardless of age) 4. Availability of a parent or guardian to provide selected medical information (WS only)

Exclusion criteria

1. History of weight loss surgery or liposuction 2. Positive urine pregnancy test (females only) 3. Obesity or abnormal fat distribution due to a known secondary cause (except WS) such as Cushing syndrome, HIV-infection, etc.

Design outcomes

Primary

MeasureTime frameDescription
Bone Mineral Density - Lumbar Spinebaseline only
Whole Body DEXA (dual energy x-ray absorptiometry) scanbaseline onlyTo assess body proportions of fat, bone, and muscle

Secondary

MeasureTime frame
Serum Total Testosteronebaseline only
Bone Mineral Density - Hipbaseline only
Fasting blood sugar and Oral glucose tolerance test (OGTT)baseline only
Serum Estrogenbaseline only
Resting energy expenditurebaseline only

Countries

United States

Outcome results

None listed

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