Newborn Sequencing Screening in China

The Application of Targeted Sequencing in the Screening of Neonatal Diseases

The project will carry out the genetic testing of 10000 neonates. The aim of the project is to assess the application of targeted sequencing technology in the screening of neonatal diseases.

Study Overview

• Status: Not yet recruiting
• Conditions: Newborns
• Intervention / Treatment: Genetic: NGS

Detailed Description

Neonatal screening (NBS) is the last step of birth defects prevention. Currently, biochemical and mass spectrometry are commonly used for NBS, but there are limited diseases and certain false positive/negative. High-throughput sequencing (NGS) has been widely used in prenatal diagnosis, tumor-targeted biomarkers detection and pathogen detection. Although the application of NGS in new screening has a broad prospect and many countries around the world have begun to explore it, there are still challenges in the selection of screening diseases, gene clinical phenotypes, genetic counseling and clinical pathway.

Since 2019, our team began to explore the appllication of NGS technologies in the clinical application of tertiary prevention, combined with Clinva, HGMD, OMIM database, on the basis of screening specific disease-causing genes and mutation sites as the target, A NGS panel for Newborns in China (NeoExome) was designed, covering 542 single-gene diseases with 601 genes. The rationality and validity of the NGS panel was preliminarily verified in 3423 neonatal blood samples collected from 5 new screening centers in China.

In order to further optimize the gene screening spectrum of neonatal diseases in the Chinese population, evaluate the efficacy of targeted sequencing technology in the screening and diagnosis of neonatal diseases, standardize the clinical pathway, and lay a foundation for the formulation of China's new screening NGS guidelines, the investigators further optimized the targeted sequencing package (NeoexOME-V2) on the basis of the first phase. 491 genes covering 485 single-gene genetic diseases were designed to launch the "Budding Action". The project plans to collect 10000 samples nationwide and carry out the multi-center clinical research on the application of targeted sequencing technology in the screening of neonatal diseases.

• Study Type: Observational
• Enrollment (Anticipated): 10000

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 1 day to 4 weeks (CHILD)
• Accepts Healthy Volunteers: N/A
• Genders Eligible for Study: All

• Sampling Method: Non-Probability Sample

Study Population

All newborns are our targeted population.

Description

Inclusion Criteria:

• -- Subjects: all newborns (from birth to 28 days);
• -- After fully understanding the program, the guardian signs the informed consent and agrees to participate in the program.

Exclusion Criteria:

• Other similar clinical research projects are under way for the examined neonates;
• Neonates have received transfusion of allogeneic blood products;
• Newborns whose guardians explicitly refuse to participate in the program after receiving the mission.

Elimination criteria

• Samples that are not properly collected or stored for testing;
• Samples with non-standard data records;
• Samples without clinical follow-up results;
• The project recalls newborns who are required to withdraw by their guardians during the follow-up.

Study Plan

How is the study designed?

Number of groups / cohorts

1

Cohorts and Interventions

Group / Cohort	Intervention / Treatment
National multicenter screening; NGS was performed based on conventional NBS. The relationship between NGS detected gene variation and disease occurrence was studied through follow-up.	Genetic: NGS; In the Nation multicenter screening cohort, NGS testing was performed on the basis of conventional NBS to study the relationship between gene variation and disease occurrence;

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Disease incidence among NGS positive participants	Newborn was followed up for 3 years after birth, and the follow-up results were compared to evaluate and study the relationship between gene variation and disease occurrence	3 years

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
The consistency of test results of NGS and conventional NBS	Conventional NBS was used as the standard to study the application potential of targeted sequencing technology in neonatal screening and evaluate its consistency	1 year

Collaborators and Investigators

• Sponsor: Shanghai Children's Hospital
• Collaborators: Children's Hospital of Chongqing Medical University; Northwest Women's and Children's Hospital, Xi'an, Shaanxi; Xuzhou maternal and Child Health Care Hospital; Zunyi Maternal and Child Health Care Hospital; Inner Mongolia Maternal and Child Health Care Hospital; Huzhou Maternity and Child Health Care Hospital

Study record dates

Study Major Dates

• Study Start (ANTICIPATED): August 5, 2022
• Primary Completion (ANTICIPATED): August 31, 2025
• Study Completion (ANTICIPATED): December 31, 2025

Study Registration Dates

• First Submitted: July 19, 2022
• First Submitted That Met QC Criteria: July 25, 2022
• First Posted (ACTUAL): July 27, 2022

Study Record Updates

• Last Update Posted (ACTUAL): July 27, 2022
• Last Update Submitted That Met QC Criteria: July 25, 2022
• Last Verified: July 1, 2022

More Information

Terms related to this study

• Other Study ID Numbers: shercru-20220003

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: UNDECIDED

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No