Oxford Vaccine Group, University of Oxford, Oxford, Oxfordshire, UK.
Nuffield Department of Women's & Reproductive Health, University of Oxford, Oxford, Oxfordshire, UK.
Arch Dis Child. 2023 Jan;108(1):26-30. doi: 10.1136/archdischild-2022-324270. Epub 2022 Sep 28.
INGR1D (INvestigating Genetic Risk for type 1 Diabetes) was a type 1 diabetes (T1D) genetic screening study established to identify participants for a primary prevention trial (POInT, Primary Oral Insulin Trial).
The majority of participants were recruited by research midwives in antenatal clinics from 18 weeks' gestation. Using the NHS Newborn Bloodspot Screening Programme (NBSP) infrastructure, participants enrolled in INGR1D had an extra sample taken from their day 5 bloodspot card sent for T1D genetic screening. Those at an increased risk of T1D were informed of the result, given education about T1D and the opportunity to take part in POInT.
Between April 2018 and November 2020, 66% of women approached about INGR1D chose to participate. 15 660 babies were enrolled into INGR1D and 14 731 blood samples were processed. Of the processed samples, 157 (1%) had confirmed positive results, indicating an increased risk of T1D, of whom a third (n=49) enrolled into POInT (20 families were unable to participate in POInT due to COVID-19 lockdown restrictions).
The use of prospective consent to perform personalised genetic testing on samples obtained through the routine NBSP represents a novel mechanism for clinical genetic research in the UK and provides a model for further population-based genetic studies in the newborn.
INGR1D(1 型糖尿病遗传风险研究)是一项 1 型糖尿病(T1D)遗传筛查研究,旨在确定参与者参加一级预防试验(POInT,口服胰岛素初级试验)。
大多数参与者都是由孕晚期的研究助产士在产前诊所招募的。利用国民保健服务新生儿血斑筛查计划(NBSP)基础设施,INGR1D 的参与者从他们的第 5 天血斑卡中额外抽取一份样本进行 T1D 遗传筛查。那些有 T1D 高风险的人会被告知结果,并接受关于 T1D 的教育,并有机会参加 POInT。
在 2018 年 4 月至 2020 年 11 月期间,约有 66%的 INGR1D 参与者选择参与。共有 15660 名婴儿参加了 INGR1D 研究,共处理了 14731 份血样。在处理过的样本中,有 157 份(1%)结果呈阳性,表明 T1D 风险增加,其中三分之一(n=49)参加了 POInT(由于 COVID-19 封锁限制,有 20 个家庭无法参加 POInT)。
利用前瞻性同意,对通过常规 NBSP 获得的样本进行个性化基因检测,代表了英国临床基因研究的一种新机制,并为新生儿的进一步基于人群的基因研究提供了模型。