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一项关于阿尔茨海默病遗传风险披露简化方案的随机非劣效性试验。

A randomized noninferiority trial of condensed protocols for genetic risk disclosure of Alzheimer's disease.

作者信息

Green Robert C, Christensen Kurt D, Cupples L Adrienne, Relkin Norman R, Whitehouse Peter J, Royal Charmaine D M, Obisesan Thomas O, Cook-Deegan Robert, Linnenbringer Erin, Butson Melissa Barber, Fasaye Grace-Ann, Levinson Elana, Roberts J Scott

机构信息

Division of Genetics, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA; Partners Personalized Medicine, Boston, MA, USA.

Division of Genetics, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.

出版信息

Alzheimers Dement. 2015 Oct;11(10):1222-30. doi: 10.1016/j.jalz.2014.10.014. Epub 2014 Dec 9.

Abstract

INTRODUCTION

Conventional multisession genetic counseling is currently recommended when disclosing apolipoprotein E (APOE) genotype for the risk of Alzheimer's disease (AD) in cognitively normal individuals. The objective of this study was to evaluate the safety of brief disclosure protocols for disclosing APOE genotype for the risk of AD.

METHODS

A randomized, multicenter noninferiority trial was conducted at four sites. Participants were asymptomatic adults having a first-degree relative with AD. A standard disclosure protocol by genetic counselors (SP-GC) was compared with condensed protocols, with disclosures by genetic counselors (CP-GC) and by physicians (CP-MD). Preplanned co-primary outcomes were anxiety and depression scales 12 months after disclosure.

RESULTS

Three hundred and forty-three adults (mean age 58.3, range 33-86 years, 71% female, 23% African American) were randomly assigned to the SP-GC protocol (n = 115), CP-GC protocol (n = 116), or CP-MD protocol (n = 112). Mean postdisclosure scores on all outcomes were well below cut-offs for clinical concern across protocols. Comparing CP-GC with SP-GC, the 97.5% upper confidence limits at 12 months after disclosure on co-primary outcomes of anxiety and depression ranged from a difference of 1.2 to 2.0 in means (all P < .001 on noninferiority tests), establishing noninferiority for condensed protocols. Results were similar between European Americans and African Americans.

CONCLUSIONS

These data support the safety of condensed protocols for APOE disclosure for those free of severe anxiety or depression who are actively seeking such information.

摘要

引言

对于认知正常个体,在披露载脂蛋白E(APOE)基因型以评估阿尔茨海默病(AD)风险时,目前推荐采用传统的多阶段遗传咨询。本研究的目的是评估简短披露方案在披露APOE基因型以评估AD风险方面的安全性。

方法

在四个地点进行了一项随机、多中心非劣效性试验。参与者为有无症状的成年一级亲属患有AD。将遗传咨询师的标准披露方案(SP-GC)与精简方案进行比较,精简方案包括遗传咨询师的披露(CP-GC)和医生的披露(CP-MD)。预先计划的共同主要结局是披露后12个月的焦虑和抑郁量表。

结果

343名成年人(平均年龄58.3岁,范围33 - 86岁,71%为女性,23%为非裔美国人)被随机分配到SP-GC方案组(n = 115)、CP-GC方案组(n = 116)或CP-MD方案组(n = 112)。所有结局的披露后平均得分均远低于各方案临床关注的临界值。将CP-GC与SP-GC进行比较,披露后12个月焦虑和抑郁共同主要结局的97.5%置信上限均值差异范围为1.2至2.0(所有非劣效性检验P < .001),确定了精简方案的非劣效性。非裔美国人和欧裔美国人的结果相似。

结论

这些数据支持对于那些没有严重焦虑或抑郁且积极寻求此类信息的人,采用精简方案披露APOE的安全性。

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