首页> 外文期刊>Genetic Testing >Barriers To Genetic Testing Among Persons At Risk For Alpha-1 Antitrypsin Deficiency
【24h】

Barriers To Genetic Testing Among Persons At Risk For Alpha-1 Antitrypsin Deficiency

机译:Alpha-1抗胰蛋白酶缺乏症风险人群中进行基因检测的障碍

获取原文
获取原文并翻译 | 示例
           

摘要

The alpha coded testing (ACT) study offers free and confidential testing for alpha-1 antitrypsin deficiency (AATD) and includes surveys to provide data to study the psychosocial correlates of genetic testing. The purpose of the current study is to better understand reasons why some individuals complete genetic testing while others do not. Survey measures were compared between participants who requested and returned a genetic test for AATD (n = 703), and a random sample of individuals who requested a test kit, but did not return it within 3 months of their request (n = 83). Increasing decile of age (odds ratio [OR] = 0.74 [95% confidence interval = 0.60-0.82]) and fingerstick fear (OR = 0.74 [0.60-0.93]) were associated with a decreased likelihood of returning the test, while assurance of confidentiality was associated with an increased likelihood (OR = 1.26 [1.01-1.57]) of returning the genetic test. General anxiety as measured by the Beck Anxiety Inventory, family functioning as measured by the general functioning subscale of the Family Assessment Device, and stress induced by genetic testing as measured by the Impact of Events Scale did not significantly differ between responder groups (p = not significant). Results of this study help characterize factors driving genetic testing in AATD and may offer insight into population responses with other genetic tests.
机译:alpha编码测试(ACT)研究提供了针对alpha-1抗胰蛋白酶缺乏症(AATD)的免费和保密测试,并包括提供调查数据以研究基因测试的心理社会相关性的调查。本研究的目的是为了更好地理解为什么有些人完成基因检测而另一些人没有完成基因检测的原因。比较了要求和返回AATD基因测试的参与者(n = 703)与要求测试盒但在要求后三个月内未返回测试盒的个人的随机样本(n = 83)之间的调查指标。年龄的十分位数增加(赔率[OR] = 0.74 [95%置信区间= 0.60-0.82])和指尖恐惧症(OR = 0.74 [0.60-0.93])与降低返回测试的可能性相关,同时确保机密性与返回基因检测的可能性增加(OR = 1.26 [1.01-1.57])相关。由贝克焦虑量表测得的一般焦虑,由家庭评估装置的一般功能子量表测得的家庭功能以及由事件影响量表测得的基因测试所诱发的压力在应答者组之间无显着差异(p =否)。重大)。这项研究的结果有助于表征驱动AATD基因测试的因素,并可能提供其他基因测试对人群反应的洞察力。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号