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临床试验/NCT03802708
NCT03802708已完成不适用

Fetal Alcohol Spectrum Disorder-Is This a Ciliopathy?

University of Alberta2 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2018年9月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
12
试验地点
2
主要终点
Nitric Oxide metabolites in urine

研究概览

简要总结

Urine sample and exhaled Nitric Oxide will analyzed and compared between children diagnosed with Fetal Alcohol Spectrum Disorder and healthy control.

Pilot study- 5 children in each group

详细描述

Background: The term "fetal alcohol spectrum disorder" (FASD) describes a broad spectrum of neurodevelopmental presentations resulting from alcohol exposure in utero. The prevalence has been estimated at 1 in 100 people, and estimated to be more than 330 000 affected individuals in Canada. The Canadian Diagnostic Guidelines describe the physical and neurodevelopmental effects resulting from prenatal alcohol exposure. These include distinct facial features, microcephaly and neurodevelopmental deficits.

Ethanol toxicity is researched in association to the concentration, duration, and timing of ethanol exposure and the possible pathways leading to phenotypic translation to teratogenesis. Studies of FASD in animal models are beginning to implicate a number of susceptibility genes that are involved in various molecular pathways on gene-ethanol interactions. Some of which are reportedly involved in ethanol teratogenesis as a part of their roles in DNA damage control, Central Nervous System axis formation, cellular survival as well as proliferation and growth.

A mutation in one particular gene, neuronal nitric oxide synthase (nNOS)) is known to worsen alcohol induced neuronal death both in vivo and in vitro, and expression of the nNOS gene protects neurons against alcohol toxicity Nitric Oxide (NO) is synthesized by the enzyme nitric oxide synthase (NOS through) L-arginine There are three NOS isoforms: neuronal NOS (nNOS, NOS-1), inducible NOS (iNOS, NOS-2), and endothelial NOS (eNOS, NOS-3) .NO is associated with modulation of neurotransmission and memory formation along with other vital activities. In the presence of O2, radicals form that can lead to toxicity. They may be disruptive to cell signaling processes and result in pathological conditions.

Data suggest that ethanol alters NOS expression and activity in the brain There are known effects of ethanol on production of NO, NOS activities, and interactions of NO with alcohol metabolism enzymes.

Dose and length of ethanol exposure are the main factors determining ethanol effects on NO production, NOS activity or NOS expression.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Basic Science
盲法
None

盲法说明

this is N/A

入排标准

年龄范围
5 Years 至 16 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Children ages 5-16
  • Diagnosis of FASD

排除标准

  • Sinopulmonary anomaly
  • Cardiac anomaly
  • Previously known Genetic condition
  • Previously known Metabolic condition
  • Polypharmacy

结局指标

主要结局

Nitric Oxide metabolites in urine

时间窗: At time of enrollment

metabolomic analysis

次要结局

  • nitric oxide concentration(At time of enrollment)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Helly Goez

Principal Investigator

University of Alberta

研究点 (2)

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