Pilot Study of Rapid Whole Genome Sequencing of Severely Ill Patients in Pediatric Intensive Care in Belgium

NCT ID: NCT05337462

Last Updated: 2022-04-26

Basic Information

• Recruitment Status: UNKNOWN
• Total Enrollment: 30 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2021-02-08
• Study Completion Date: 2022-12-31

Brief Summary

Prospective, multi-site, non-randomized (single arm) study to evaluate the feasibility, the yield and clinical utility of trio WGS in 30 critically ill patients in neonatology intensive care units (NICU) and pediatric intensive care units (PICU) in Belgium. Results are expected to be returned within 7 days after receipt of blood samples in the laboratory. Primary outcome will be evaluated after clinical interpretation, whereas secondary outcome will be evaluated from the clinical utility survey to be completed by clinical geneticists.

Detailed Description

This is a prospective, multi-site, non-randomized (single arm) study to evaluate the feasibility, the yield and clinical utility of trio WGS in critically ill patients in neonatology intensive care units (NICU) and pediatric intensive care units (PICU) in Belgium. Each proband responding to our eligibility criteria will receive a trio WGS.

Blood samples from enrolled probands and their parents will be collected and shipped to the Laboratoire de Génétique Humaine, University of Liège, Liège, Belgium, which is a research facility. Blood samples will be lysed using the Illumina Lysis Kit. Lysis product will be used for library preparation with Illumina DNA PCR-Free Prep, Tagmentation library preparation kit and IDT® for Illumina® DNA/RNA Unique Dual Indexes Set A, Tagmentation. Pooled libraries will be sequenced on a NovaSeq 6000. Sequencing data will be automatically transferred to Cloud Space (BaseSpace Sequence Hub) were primary bioinformatic analysis will be performed upon completion of sequencing and data transfer. Annotated variant calling files for SNVs and CNVs will be analyzed with Moon (Invitae) and in-house bioinformatic analysis solutions. Clinical interpretation will be performed by the principal investigator.

WGS results were communicated to pediatrician. The clinical utility survey was filled by clinical geneticists at least a month after the return of sequencing results.

Conditions

Rare Diseases

Study Design

• Observational Model Type: CASE_ONLY
• Study Time Perspective: PROSPECTIVE

Eligibility Criteria

Inclusion Criteria

• at least two major malformations involving two different systems
• A specific malformation highly suggestive of a genetic etiology, including but not limited to any of the following abnormalities:

• Choanal atresia,
• Coloboma,
• Hirschsprung's disease,
• Meconium ileus (except in case of prematurity),
• Agenesis of the corpus callosum or Lissencephaly
• An abnormal laboratory test suggesting a genetic disease or a complex metabolic phenotype, including but not limited to any of the following:

• Conventional abnormal neonatal screening
• Conjugated hyperbilirubinemia not due to total parental nutrition (TPN) cholestasis
• Hyperammonemia
• Lactic acidosis not due to poor perfusion
• Refractory or severe hypoglycaemia
• An abnormal response to standard treatment for a major underlying condition

• Significant hypotonia
• Persistent seizures
• Infant with high-risk stratification on assessment of a Brief Resolved Unexplained Event (BRUE) with any of the following features :

• Recurrent events without respiratory infection
• Recurrent seizures observed
• Unexplained cardiopulmonary resuscitation (CPR) required
• Significantly abnormal biochemical status, including but not limited to electrolytes, bicarbonate or lactic acid, venous blood gases, glucose, or other tests suggestive of an inborn error of metabolism
• Significantly abnormal electrocardiogram (ECG), including but not limited to possible channelopathies, arrhythmias, cardiomyopathies, myocarditis, or structural heart disease
• Positive family history of:

• Arrhythmia
• BRUE at the brother
• Developmental delay / mental retardation
• Inborn error of metabolism or genetic disease without genetic diagnosis
• Long QT Syndrome (LQTS)
• Sudden unexplained death (including unexplained car accident or drowning) in first- or second-degree relatives before age 35, and especially as an infant.

Exclusion Criteria

• An infection with a normal response to treatment
• A confirmed genetic diagnosis explaining the disease
• Hypoxic ischemic encephalopathy (HIE) with a clear precipitating event
• Isolated prematurity
• Isolated transient tachypnea of the newborn (TTN)
• Isolated unconjugated hyperbilirubinemia
• Non-viable neonates
• Entity of multifactorial cause or unknown genetic cause, including but not limited to any of the following: Sequence of amniotic bands, Isolated Pierre Robin sequence, Spina bifida

• Minimum Eligible Age: 1 Day
• Maximum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Centre Hospitalier Universitaire de Liege

OTHER

Sponsor Role: lead

Responsible Party

AIME LUMAKA

Doctor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

AIME LUMAKA, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Centre Hospitalier Universitaire de Liege

Locations

Centre Hospitalier Régional de la Citadelle

Liège, , Belgium

Site Status: RECRUITING

CHC Mont-Légia

Liège, , Belgium

Site Status: RECRUITING

Countries

Belgium

Central Contacts

AIME LUMAKA, MD, PhD

Role: CONTACT

aime.lumaka@uliege.be

+3243664720

VINCENT BOURS, MD, PhD

Role: CONTACT

vbours@uliege.be

+3243668144

Facility Contacts

Vincent Rigo, MD, PhD

Role: primary

vincent.rigo@chuliege.be

+3243674585

Serpil Alkan, MD

Role: backup

serpil.alkan@chuliege.be

André Mulder, MD

Role: primary

ANDRE.MULDER@CHC.BE

Other Identifiers

2020/143

Identifier Type: -

Identifier Source: org_study_id