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临床试验/NCT01145196
NCT01145196招募中不适用

Genotype - Phenotype Study of Patients With Plaquenil-induced Retinal Toxicity

National Eye Institute (NEI)1 个研究点 分布在 1 个国家目标入组 320 人开始时间: 2010年8月23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
320
试验地点
1
主要终点
The outcome of this study is to identify genetic mutations, starting with those in ABCA4 gene, associated with retinal toxicity in participants with a history of plaquenil use.

研究概览

简要总结

Background:

- Plaquenil (hydroxychloroquine) is an anti-inflammatory drug that is used to treat some autoimmune diseases such as lupus and rheumatoid arthritis. This drug can damage the retina by causing a condition called Plaquenil-induced retinal toxicity, which may lead to vision loss. However, most people taking Plaquenil do not develop this problem. Researchers are interested in studying whether differences in a person's genes explain why some people develop Plaquenil-induced retinal toxicity while others do not.

Objectives:

- To investigate possible correlations between certain genes or genetic mutations and Plaquenil-induced retinal toxicity.

Eligibility:

  • Individuals at least 18 years of age who have previously used Plaquenil.
  • History of systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), or Sjogren's syndrome.
  • Both individuals who have and have not developed Plaquenil-induced retinal toxicity will be eligible for this study.

Design:

  • The study requires five annual outpatient visits to the NIH Clinical Center.
  • Participants will provide a personal and family medical history, and will have a full eye examination.
  • Participants will also provide blood samples for genetic analysis, including whole exome and whole genome sequencing.
  • No treatment will be provided as part of this protocol.

详细描述

OBJECTIVE:

The objective of this study is to investigate whether there is a correlation between genetic mutations, beginning with an analysis of ABCA4, and Plaquenil(R)-induced retinal toxicity and to describe the phenotype of Plaquenil(R)-induced retinal toxicity.

STUDY POPULATION:

The study will enroll 100 patients, 18 years of age or older, found to have Plaquenil(R)-induced retinal toxicity. 200 volunteers with systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), or Sjogren's syndrome and history of Plaquenil(R) use, but without evidence of retinal toxicity, will also be recruited.

DESIGN:

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Cross Sectional

入排标准

年龄范围
18 Years 至 120 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • INCLUSION CRITERIA:
  • 1. Affected participants must be 18 years of age or older and have:
  • History of systemic lupus erythematosus (SLE), rheumatoid arthritis (RA) or Sjogren's syndrome, and
  • History of Plaquenil(R) use, and
  • Evidence of Plaquenil(R)-induced retinal toxicity, based on clinical findings.
  • 2. Unaffected volunteers must be 18 years of age or older and have:
  • History of systemic lupus erythematosus (SLE), rheumatoid arthritis (RA) or Sjogren's syndrome, and
  • History of Plaquenil(R) use, and
  • No retinal disease upon examination within the last six months.
  • 3. All participants must be able to:
  • Provide their own consent, and
  • Safely provide a blood sample.

排除标准

  • Participants with other known (genetic) retinal disease including but not limited to: Stargardt's disease and cone or cone-rod dystrophy whose diagnosis preceded their Plaquenil(R) use. Participants with no known previous genetic diagnosis but with clinical findings associated with a genetic diagnosis, such as parafoveal or macular flecks which are associated with Stargardt's disease or fundus flavimaculatus, will also be excluded.

研究组 & 干预措施

Affected

Participants affected by Plaquenil induced retinal toxicity

Unaffected

control participants without Plaquenil induced retinal toxicity

结局指标

主要结局

The outcome of this study is to identify genetic mutations, starting with those in ABCA4 gene, associated with retinal toxicity in participants with a history of plaquenil use.

时间窗: annually for five years

The outcome of this study is to identify genetic mutations, starting with those in ABCA4 gene, associated with retinal toxicity in participants with a history of plaquenil use.

次要结局

  • The secondary outcome of this study is to determine the utility of various testing metrics in evaluating the presence of retinal toxicity.(annually for five years)

研究者

申办方类型
Nih
责任方
Sponsor

研究点 (1)

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