超越新生儿筛查:反向级联检测在家族性疾病检测中的作用。

IF 5.5 2区 医学 Q1 MEDICAL LABORATORY TECHNOLOGY
Amy Gaviglio, Kostantinos Petritis, Veronica Tagi, Alessandra Vasco, Alessia Mauri, Gianvincenzo Zuccotti, Elvira Verduci, Cristina Cereda, Simona Ferraro
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引用次数: 0

摘要

在过去的60年里,预防性公共健康筛查方案从一开始就不断发展,现在包括新生儿筛查(NBS),旨在确定出生后的婴儿是否患有一些罕见的、先天性的、遗传性的疾病。通过NBS检测到的大多数疾病都是常染色体隐性遗传病或表现为x连锁遗传,这意味着患有这些疾病的个体的家庭成员患该病或专性杂合子的风险更高。例如,筛查组中的x连锁肾上腺脑白质营养不良(X-ALD)通过随后的测试来识别受影响的新生儿和无症状的亲属。因此,通过应用反向级联测试(RCS),国家统计局成为全家庭预防的门户。在本文中,我们研究了RCS可能适用的场景。因此,我们确定了一系列评估NBS疾病是否受益于RCS的标准:(1)常染色体隐性遗传或x连锁遗传;(2)高带菌率,(3)易表达性,(4)轻度或晚发型;(5)与诊断延迟和最近加入筛查小组的关系。一种疾病要受益于RCS,通常需要满足不止一个标准。我们已经确定了一系列疾病,并强调了RCS的潜在益处:X-ALD、囊性纤维化、镰状细胞病、脊髓性肌萎缩症和庞贝病。在NBS中还有其他情况,产妇疾病状况(3-甲基丁基辅酶a羧化酶缺乏症和肉碱摄取缺乏症)或产妇营养状况(维生素B12缺乏症)可能导致NBS筛查结果呈阳性。当产妇营养缺乏是NBS阳性的潜在原因时,这表明新生儿患有非遗传性疾病,可能需要治疗,因为某些继发性缺陷可能导致新生儿神经损伤和正常生长迟缓。对于这些病例,建议采用RCS,因为母亲的状况可能使她面临未来不良事件(即心血管和肌肉骨骼疾病、肝脏受累和神经退行性变)的风险。本文讨论的RCS- nbs战略提供了一套标准,可以根据这些标准评估疾病对RCS的潜在需求。实施这一战略需要考虑几个因素,包括教育需求、伦理问题、检测的采用、扩大筛查和咨询的后勤和成本,以及是否有适当的专家进行持续管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Beyond newborn screening: the role of reverse cascade testing in familial disease detection.

Over the past 60 years, preventative public health screening programs have evolved since their inception and now include newborn screening (NBS) aimed at identifying infants after birth for a number of rare, congenital, inherited diseases. Most of the conditions detected through NBS are autosomal recessive disorders or exhibit X-linked inheritance, meaning that family members of individuals with these conditions have a higher risk for being either affected or obligate heterozygotes. For example, the X-linked adrenoleukodystrophy (X-ALD) in the screening panel identifies affected newborns and asymptomatic relatives through subsequent testing. Thus, NBS becomes a gateway to family-wide prevention, through the application of reverse cascade testing (RCS). In this paper we examined the scenarios where RCS may be appropriate. Accordingly, we have identified a list of criteria assessing whether a NBS disease would benefit from RCS: (1) autosomal recessive or X-linked inheritance; (2) high carrier rates, (3) variable expressivity, (4) mild or late-onset forms; and (5) association with diagnostic delays and recent addition to the screening panel. More than one criterion usually needs to be met for a disease to benefit from RCS. We have identified a list of diseases and highlighted the potential benefits of RCS: X-ALD, Cystic Fibrosis, Sickle Cell Disease, Spinal Muscular Atrophy and Pompe disease. There are additional scenarios within NBS where disease maternal conditions (3-methylcrotonyl-CoA carboxylase deficiency and carnitine uptake deficiency) or nutritional maternal conditions (vitamin B12 deficiency) may cause a screen-positive NBS result. Whenever a maternal nutritional deficiency is a potential reason for a positive NBS, this is indicative of a non-inherited condition that may require treatment in the newborn owing to possible neurological damage and delay in normal growth in newborns with certain secondary deficiencies. For these cases RCS is recommended, as the mother's status may put her at risk for future adverse events (i.e. cardiovascular and musculoskeletal disorders, hepatic involvement, and neurodegeneration). The RCS-NBS strategy discussed in this paper offers a set of criteria against which diseases can be assessed for the potential need for RCS. Implementation of this strategy requires several considerations including educational needs, ethical issues, uptake of testing, logistics and costs for this expanded screening and counseling, and availability of appropriate specialists for ongoing management.

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来源期刊
CiteScore
20.00
自引率
0.00%
发文量
25
审稿时长
>12 weeks
期刊介绍: Critical Reviews in Clinical Laboratory Sciences publishes comprehensive and high quality review articles in all areas of clinical laboratory science, including clinical biochemistry, hematology, microbiology, pathology, transfusion medicine, genetics, immunology and molecular diagnostics. The reviews critically evaluate the status of current issues in the selected areas, with a focus on clinical laboratory diagnostics and latest advances. The adjective “critical” implies a balanced synthesis of results and conclusions that are frequently contradictory and controversial.
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