Identification of Genetic Variants That Contribute to Keloid Formation in Families and Isolated Cases.
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 7,000
- 试验地点
- 2
- 主要终点
- Identification of genetic elements
研究概览
简要总结
Keloids have a strong genetic component. The goal of this study is to identify genes and regulatory elements on chromosomes that are the cause for keloids or contribute to keloid scarring.
详细描述
Keloids are scars that keep growing beyond the border of the original wound. They typically persist for several years, expand for an extensive period of time and are sometimes called benign tumors. Keloids often have a lumpy surface and are often tender, itchy or inflamed around the growing border.
Keloids in most keloid patients do not run in the family. In the inheritable form of keloids it is possible that there is one major gene mutation that puts family members at risk for developing keloids. There may be other variations in the DNA (DNA makes up the chromosomes) that determine whether keloids become large and aggressive or stay small and without many symptoms.
For this study we will:
- Send out study participation kits and consent by phone
- Collect a saliva sample from eligible individuals
- Obtain information regarding the keloids
- Document keloids with photos
- If keloid patients undergo keloid surgery we ask to obtain some scar tissue that would otherwise be discarded
- Isolate DNA from the saliva sample
- Perform genetic analyses of the DNA with the most up-to-date methods available to identify genetic variations
- Study in the laboratory why the genetic variations cause keloids
研究设计
- 研究类型
- Observational
- 观察模型
- Case Control
- 时间视角
- Prospective
入排标准
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •unaffected individuals only if part of a participating keloid family
排除标准
- •no keloids;
- •unaffected individuals only as part of a participating keloid family
研究组 & 干预措施
affected
individuals with keloids
unaffected
unrelated unaffected controls or unaffected family members
结局指标
主要结局
Identification of genetic elements
时间窗: at time of identification
The goal is to identify relevant genes or genetic elements that cause the disease or contribute to the disease progression and severity.
次要结局
未报告次要终点
研究者
Ernst Reichenberger
Associate Professor
UConn Health
