Impact of Elastin Mediated Vascular Stiffness on End Organs
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 159
- 试验地点
- 2
- 主要终点
- By testing both WS and SVAS and WS gene region variation subgroups, we can investigate both the effect of elastin insufficiency mediated vascular disease on end organ function and look for a synergistic effect of the larger gene deletion on elas...
研究概览
简要总结
Background:
People with Williams Syndrome (WS) and supravalvular aortic stenosis (SVAS) have less elasticity in their blood vessels. This is called blood vessel stiffness. Blood vessels may have focal narrowings called stenoses or may just be globally more narrow.
Objectives:
Researchers want to see how blood vessel differences in people with Williams Syndrome and supravalvular aortic stenosis affect organs in the body including the heart, gut, kidneys, and brain.
Eligibility:
People ages 3-85 who have WS or SVAS
Healthy volunteers ages 3-85
Design:
- Participants will have yearly visits for up to 10 years. All participants will be offered the same tests.
- Participants will give consent for the study team to review their medical records. If the participant is a child or an adult with WS, a parent or guardian will give the consent.
- Participants will visit the NIH where they will have a physical exam and medical history. Based on their health history, participants will undergo a series of imaging tests and measures of blood vessel function over the course of 2-4 days. Tests of cognitive abilites will also be performed. Blood will be drawn and an IV may be placed for specific tests.
详细描述
Elasticity in the aorta buffers the body from damage due to pulsatile blood flow. Data from humans and mice show that with increasing age, vessels lose elasticity and become stiff. Vascular stiffness is associated with progressive cognitive impairment and dementia in aging adults, but little is known about the effects of early-onset/congenital vascular stiffness. Similarly, elastin-mediated arteriopathy in the form of stenosis has the potential to impact additional end organs such as the heart, lungs, gut, skeletal muscle and kidney causing feeding and exercise intolerance, as well hypertension. This study evaluates the impact of elastin arteriopathy and vascular stiffness on end organs.
Following consent, the investigators will work with the subjects and their caregivers to determine which tests are most appropriate for the patient based on their age/capabilities and preferences and may include:
- testing of cognitive and neurobehavioral abilities as well as measures of general health and well being
- undergo non-invasive measurements of vascular stiffness
- undergo brain imaging by MRI
- undergo echocardiogram
- undergo ECG
- undergo 24-hour ambulatory electrocardiogram monitor
- undergo ultrasound imaging and flow studies of various vascular beds and tissues
- undergo CT angiogram of relevant vessels
- undergo non-invasive tissue oxygenation and endothelial functional assessment with near infrared spectroscopy (NIRS) of the limbs and/or head/brain (fNIRS)
- perform a 6 minute walk test
- perform pulmonary function tests
- receive an eye exam and Optical coherence tomography (OCT)
- give blood/urine for relevant laboratories
- evaluate biomechanical properties of skin
- evaluate baseline fitness information using a fitness tracker
- complete medica photography evaluating relevant features of the condition
- receive a dental examination and dental photography
Visits may be conducted in person at the Clinical Center, by telehealth, or with a combination of in person and telehealth, at the discretion of the study team. All telehealth activities will be performed according to HRPP Policy 303 and only testing that can be performed at home (e.g. clinical consultations, neurobehavioral testing, fitness tracking, ambulatory ecg monitoring, and photography) will be selected. The other tests require the individual to be on site at the CC.
Consequently, some participants may have certain consultations at home and other testing on site to limit time in the CC
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 3 Years 至 85 Years（Child, Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •We will recruit individuals with people with WS, SVAS or other WS region variation conditions (cases) and demographically similar control (unaffected) participants.
- •Children or adults with WS must:
- •be between the ages of 3 and 85
- •have a presumed or confirmed diagnosis of WS (genetic testing is not performed in this research study).
- •have a parent/guardian available to provide consent and assist in answering medical questions
- •not be pregnant
- •Children or adults with SVAS must:
- •be between the ages of 3 and 85
- •have clinical features suggestive of SVAS or an SVAS-like condition OR have no clinical features of SVAS or an SVAS-like condition but have genetic testing results that imply affected status (SVAS has decreased penetrance). No genetic testing will be done as part of this protocol.
- •have a parent/guardian available to provide consent and assist in answering medical questions if they are a minor (not applicable to adults)
- •Children or adults with WS region gene changes:
- •be between the ages of 3 and 85
- •have clinical or research genetic testing that reports gene variation in a non-ELN gene in the WS region.
- •have a parent/guardian available to provide consent and assist in answering medical questions if they are a minor or if they have cognitive impairment that would impede their ability to consent on their own behalf.
- •Children or adults participating in the study as part of control group must:
- •be between the ages of 3 and 85
- •not have clinical features or genetic profile suggestive of WS, SVAS or an SVAS-like condition. No genetic testing will be performed in this research study.
- •have a parent/guardian available to provide consent and assist in answering medical questions if they are a minor (not applicable to adults)
排除标准
- 未提供
研究组 & 干预措施
Case
Subjects with WS/SVAS/WS gene region variation
Controls
Healthy volunteers
结局指标
主要结局
By testing both WS and SVAS and WS gene region variation subgroups, we can investigate both the effect of elastin insufficiency mediated vascular disease on end organ function and look for a synergistic effect of the larger gene deletion on elas...
时间窗: ongoing
Pilot studies aimed at identifying differences between the WS/SVAS/WS gene region variation population and controls.
次要结局
未报告次要终点