跳至主要内容
临床试验/NCT06778239
NCT06778239招募中不适用

Natural History Study to Determine Childhood-Onset Essential Hypertension Etiology

National Human Genome Research Institute (NHGRI)2 个研究点 分布在 1 个国家目标入组 2,300 人开始时间: 2025年5月30日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
2,300
试验地点
2
主要终点
Find all genes that cause COEH.

研究概览

简要总结

Background:

Childhood-onset essential hypertension (COEH) is high blood pressure that develops in children and teens. High blood pressure is a major risk factor for heart disease. COEH is more likely to be caused by changes in genes rather than by factors like stress or diet. Researchers want to learn more about how changes in genes relate to COEH. They hope to use that information to develop better treatments for children with high blood pressure.

Objective:

This natural history study will look for genes and gene changes that may lead to COEH.

Eligibility:

People aged 2 years and older with COEH or who had COEH when they were children. Healthy relatives of those with COEH are also needed.

Design:

Participants will have one clinic visit per year for up to 10 years. All participants will have a physical exam. They will provide samples of blood and urine. At their first visit, they will have a swab (like a Q-tip) rubbed between their gums and cheeks. They may agree to having a skin biopsy; a piece of skin about the size of a pencil eraser will be removed.

Affected participants aged 2 to 17 years old will have additional tests:

  • They will have sensors placed on their skin to look at their blood vessels and see how blood is moving in their bodies.
  • They will lie or stand while a machine measures the amount of fat and muscle in their bodies.
  • They will have an ultrasound; a wand will be rubbed against their skin to take pictures of their kidneys.

Other things are optional for all participants:

  • They may have photographs taken of their bodies.
  • They may have tests of their heart function.
  • They may have different types of imaging scans....

详细描述

Study Description:

This study seeks to identify molecular processes and genetics that contribute to the development of childhood-onset essential hypertension (COEH) in a diverse cohort of children. Identification of blood pressure (BP)-regulating pathway(s) involved in COEH will allow for targeted and individualized therapy.

Objectives:

Primary Objective:

Elucidate the molecular genetic processes associated with developing COEH.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Other

入排标准

年龄范围
2 Years 至 99 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • INCLUSION CRITERIA:
  • To be eligible to participate in this study, an affected individual must meet one of the following criteria:
  • Age 2-12 years at time of enrollment with a BP of at least >95th percentile or 120/80 mm Hg verified via medical record review and a willingness to provide biological samples, undergo physical exam, provide information related to family and medical history, and undergo imaging/body measurements (e.g., renal ultrasound)
  • Age 13-17 years at time of enrollment with a BP of at least 130/80 mm Hg verified via medical record review and a willingness to provide biological samples, undergo physical exam, provide information related to family and medical history, and undergo imaging/body measurements (e.g., renal ultrasound)
  • Age 18 years or more at time of enrollment with a medical history of meeting the criteria outlined in affected individual inclusion criteria 1 or 2, depending on age at diagnosis (verified via medical record review) and a willingness to provide biological samples, undergo physical exam, and provide information related to family and medical history
  • To be eligible to participate in this study, an unaffected individual must meet all of the following criteria:
  • First-degree relative to a proband (first identified affected family member) in the study
  • Willingness to provide biological samples, undergo physical exam, and provide information related to family and medical history
  • To be eligible to participate in this study, an individual with a candidate variant (regardless of known COEH status) must meet all of the following criteria:
  • History of clinical and/or research genomic interrogation
  • Positive genomic interrogation test result for candidate variant identified in earlier stages of study or in prior studies performed by study team
  • Willingness to provide information related to family and medical history, provide access to relevant medical records, undergo physical exam, and undergo imaging/body measurements (if 2-17 years of age and evidence of COEH exists)

排除标准

  • An affected individual who meets any of the following criteria will be excluded from participation in this study:
  • BMI >95th percentile
  • Evidence that hypertension is secondary to a known condition (e.g., chronic kidney disease, aortopathy, sleep apnea, etc.)
  • Impaired decision-making capability, with or without a legally-authorized representative
  • An unaffected individual who meets any of the following criteria will be excluded from participation in this study:
  • Prior or current diagnosis of COEH
  • Second-degree or greater relationship to proband
  • Impaired decision-making capability, with or without a legally-authorized representative
  • An individual with a candidate variant (regardless of known COEH status) who meets any of the following criteria will be excluded from participation in this study:
  • No prior genomic interrogation findings available for the study team to review to confirm positive candidate variant status
  • Impaired decision-making capability, with or without a legally-authorized representative

研究组 & 干预措施

Affected

Study participants that are 2-17 years old and have COEH or participants that are 18+ years old that were diagnosed with COEH when they were children.

Unaffected

Study participants that are 2+ years old and have never been diagnosed with COEH.

结局指标

主要结局

Find all genes that cause COEH.

时间窗: 10 years

次要结局

  • Identify all of the ways that COEH affects the body.(10 years)

研究者

申办方类型
Nih
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验