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在州政策不断演变的情况下进行新生儿干血斑检索的可行性 (2009-2010):一项儿童肿瘤学组的研究。

Feasibility of neonatal dried blood spot retrieval amid evolving state policies (2009-2010): a Children's Oncology Group study.

机构信息

Division of Pediatric Epidemiology and Clinical Research, Department of Pediatrics, University of Minnesota, Minneapolis, 55455, USA.

出版信息

Paediatr Perinat Epidemiol. 2011 Nov;25(6):549-58. doi: 10.1111/j.1365-3016.2011.01228.x. Epub 2011 Aug 10.

Abstract

Dried blood spots (DBS) are collected uniformly from US newborns to test for metabolic and other disorders. Because evidence exists for prenatal origins of some diseases, DBS may provide unique prenatal exposure records. Some states retain residual DBS and permit their use in aetiological studies. The primary study aim was to assess the feasibility of obtaining residual DBS from state newborn screening programmes for paediatric and adolescent cancer patients nationwide with parental/subject consent/assent. Families of leukaemia and lymphoma patients aged ≤21 years diagnosed from 1998 to 2007 at randomly selected Children's Oncology Group institutions across the US were questioned (n = 947). Parents/guardians and patients aged ≥18 years were asked to release DBS to investigators in spring 2009. DBS were then requested from states. Overall, 299 families (32%) released DBS. Consenting/assenting patients were born in 39 US states and 46 DBS were obtained from five states; 124 DBS were unobtainable because patients were born prior to dates of state retention. State policies are rapidly evolving and there is ongoing discussion regarding DBS storage and secondary research uses. Currently, population-based DBS studies can be conducted in a limited number of states; fortunately, many have large populations to provide reasonably sized paediatric subject groups.

摘要

干血斑(DBS)从美国新生儿中均匀采集,用于检测代谢和其他疾病。由于一些疾病存在产前起源的证据,因此 DBS 可能提供独特的产前暴露记录。一些州保留残余的 DBS,并允许在病因研究中使用。主要研究目的是评估在获得全国儿科和青少年癌症患者的剩余 DBS 的可行性,这些患者是在父母/受试者同意/同意的情况下从全国随机选择的儿童肿瘤学组机构诊断出的 1998 年至 2007 年期间的白血病和淋巴瘤患者(n=947)。询问了年龄≤21 岁的白血病和淋巴瘤患者的家属(n=947)。18 岁及以上的父母/监护人被要求在 2009 年春季将 DBS 释放给研究人员。然后从各州请求 DBS。总体而言,有 299 个家庭(32%)释放了 DBS。同意/同意的患者出生在美国 39 个州,从 5 个州获得了 46 个 DBS;由于患者出生在州保留日期之前,因此有 124 个 DBS 无法获得。州政策正在迅速演变,并且正在讨论 DBS 存储和二次研究用途。目前,基于人群的 DBS 研究可以在有限数量的州进行;幸运的是,许多州都有大量人口,可以为相当规模的儿科受试者群体提供服务。

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