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创建针对阿什肯纳兹犹太人群携带者筛查的全国性居家模式。

Creation of a National, At-home Model for Ashkenazi Jewish Carrier Screening.

作者信息

Grinzaid Karen Arnovitz, Page Patricia Zartman, Denton Jessica Johnson, Ginsberg Jessica

机构信息

Department of Human Genetics, Emory University, 5115 New Peachtree Rd., Suite 301, Atlanta, GA, 30341, USA,

出版信息

J Genet Couns. 2015 Jun;24(3):381-7. doi: 10.1007/s10897-014-9800-x. Epub 2014 Dec 12.

Abstract

Ethnicity-based carrier screening for the Ashkenazi Jewish population has been available and encouraged by advocacy and community groups since the early 1970's. Both the American College of Medical Genetics and the American Congress of Obstetricians and Gynecologists recommend carrier screening for this population (Obstetrics and Gynecology, 114(4), 950-953, 2009; Genetics in Medicine, 10(1), 55-56, 2008). While many physicians inquire about ethnic background and offer appropriate carrier screening, studies show that a gap remains in implementing recommendations (Genetic testing and molecular biomarkers, 2011). In addition, education and outreach efforts targeting Jewish communities have had limited success in reaching this at-risk population. Despite efforts by the medical and Jewish communities, many Jews of reproductive age are not aware of screening, and remain at risk for having children with preventable diseases. Reaching this population, preferably pre-conception, and facilitating access to screening is critically important. To address this need, genetic counselors at Emory University developed JScreen, a national Jewish genetic disease screening program. The program includes a national marketing and PR campaign, online education, at-home saliva-based screening, post-test genetic counseling via telephone or secure video conferencing, and referrals for face-to-face genetic counseling as needed. Our goals are to create a successful education and screening program for this population and to develop a model that could potentially be used for other at-risk populations.

摘要

自20世纪70年代初以来,针对阿什肯纳兹犹太人群体的基于种族的携带者筛查已经存在,并得到了倡导组织和社区团体的鼓励。美国医学遗传学学院和美国妇产科学院都建议对该人群进行携带者筛查(《妇产科学》,114(4),950 - 953,2009;《医学遗传学》,10(1),55 - 56,2008)。虽然许多医生会询问种族背景并提供适当的携带者筛查,但研究表明,在落实这些建议方面仍存在差距(《基因检测与分子生物标志物》,2011)。此外,针对犹太社区的教育和宣传工作在覆盖这一高危人群方面成效有限。尽管医疗界和犹太社区做出了努力,但许多育龄犹太人并不知晓筛查,仍然面临生育患可预防性疾病子女的风险。接触到这一人群,最好是在孕前,并促进他们获得筛查至关重要。为满足这一需求,埃默里大学的遗传咨询师开发了JScreen,这是一个全国性的犹太遗传病筛查项目。该项目包括全国性的营销和公关活动、在线教育、基于家庭唾液的筛查、通过电话或安全视频会议进行的检测后遗传咨询,以及根据需要转介进行面对面的遗传咨询。我们的目标是为这一人群创建一个成功的教育和筛查项目,并开发一个有可能用于其他高危人群的模式。

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