在X和Y变异的纵向分析中取得进展:GALAXY登记的基本原理、方法和诊断特征。

IF 1.7 4区 生物学 Q3 GENETICS & HEREDITY
Alexandra Carl, Samantha Bothwell, Karli Swenson, Ryan Bregante, Lilian Cohen, Virginia Cover, Anna Dawczyk, Gail Decker, Stephen B Gerken, David Hong, Susan Howell, Armin Raznahan, Alan D Rogol, Nicole Tartaglia, Shanlee Davis
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引用次数: 0

摘要

性染色体非整倍体(SCAs)是由非典型数量的X和/或Y染色体引起的遗传疾病家族。SCAs是最常见的染色体异常,影响约1/400活产婴儿,但往往未得到充分诊断,导致许多临床研究中受影响更严重的个体的过度代表。除了这种确定偏差之外,sca的现有工作还受到低地理和人口多样性的限制。为了解决这些限制,我们创建了X和Y变量纵向分析生成进步(GALAXY)注册表。通过优先考虑可持续性、透明度和最小化参与者负担,GALAXY Registry的总体目标是通过作为未来基于大型、异构和纵向样本的SCA研究的基础设施,改善SCA患者的健康结果。到目前为止,GALAXY已经积累了335名经过验证的SCA参与者,平均每月积累11.2名参与者(6.7 47人,XXY, 1.9 47人,XXX, 2.0 47人,XYY, 3.2 48人,XXYY, 1.8 48人,XXXY和1.3其他)。在产前确诊为SCA的人群(主要是无细胞DNA筛查)与产后诊断的人群在保险状况、入组年龄、基因检测类型和SCA诊断原因等方面存在差异。接下来的步骤包括有针对性地招募代表性不足的群体(例如,非47、XXY核型、老年人、少数群体),将病历数据提取到注册表中,进行国际扩展,并继续与SCA社区合作。作为临床研究人员和SCA社区之间的合作,GALAXY Registry是未来以患者为中心的临床研究的强大资源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Generating Advancements in Longitudinal Analysis in X and Y Variations: Rationale, Methods, and Diagnostic Characteristics for the GALAXY Registry.

Sex chromosome aneuploidies (SCAs) are a family of genetic disorders that result from an atypical number of X and/or Y chromosomes. SCAs are the most common chromosomal abnormality, affecting ~1/400 live births, yet are often underdiagnosed, leading to over-representation of more severely impacted individuals in many clinical studies. In addition to this ascertainment bias, existing work in SCAs has also been limited by low geographic and demographic diversity. To address these limitations, we have created the Generating Advancements with Longitudinal Analysis in X and Y variations (GALAXY) Registry. Through prioritizing sustainability, transparency, and minimizing participant burden, the overarching goal of the GALAXY Registry is to improve health outcomes for individuals with SCAs by serving as an infrastructure for future SCA research based on a large, heterogeneous, and longitudinal sample. To date, GALAXY has accrued 335 verified SCA participants with an average accrual of 11.2 participants/month (6.7 47,XXY, 1.9 47,XXX, 2.0 47,XYY, 3.2 48,XXYY, 1.8 48,XXXY, and 1.3 Other). Demographic data between those identified to have SCA prenatally (predominantly cell-free DNA screening) differ from those diagnosed postnatally for insurance status, age at enrollment, genetic test type, and reason for SCA diagnosis. Next steps include targeted recruitment of underrepresented groups (e.g., non-47,XXY karyotypes, older adults, minoritized individuals), extraction of medical record data into the registry, international expansion, and continued engagement with the SCA community. As a collaboration between clinician investigators and the SCA community, the GALAXY Registry is a powerful resource for future patient-centered clinical research.

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来源期刊
CiteScore
3.50
自引率
5.00%
发文量
432
审稿时长
2-4 weeks
期刊介绍: The American Journal of Medical Genetics - Part A (AJMG) gives you continuous coverage of all biological and medical aspects of genetic disorders and birth defects, as well as in-depth documentation of phenotype analysis within the current context of genotype/phenotype correlations. In addition to Part A , AJMG also publishes two other parts: Part B: Neuropsychiatric Genetics , covering experimental and clinical investigations of the genetic mechanisms underlying neurologic and psychiatric disorders. Part C: Seminars in Medical Genetics , guest-edited collections of thematic reviews of topical interest to the readership of AJMG .
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