Demographic, Metabolic, and Genomic Description of Neonates With Severe Hyperbilirubinemia

Pediatrix

Status: Completed

Conditions: Jaundice; Hyperbilirubinemia

Treatments: Procedure: Gene mutation sample

Study type: Observational

Funder types: Other

Identifiers

NCT00383318

PDX 06-001

Details and patient eligibility

About

The purpose of this study is to compare the demographic, metabolic, and genomic characteristics of patients who develop severe hyperbilirubinemia to patients who never developed a significant bilirubin level.

Full description

The purpose of this study is to compare the demographic, metabolic, and genomic characteristics of patients who develop severe hyperbilirubinemia (serum bilirubin level in the "high risk zone of greater than the 95th percentile based on the Bhutani nomogram) to patients who never developed significant hyperbilirubinemia (bilirubin level in "low risk zone of less than the 40th percentile" on Bhutani nomogram and who did not require any treatment for hyperbilirubinemia). Our primary goal is to determine if common gene mutations occur at a greater frequency in patients with severe hyperbilirubinemia than in neonates without significant hyperbilirubinemia.

The gene mutations we will test for are:

• Glucose-6-phosphate Dehydrogenase Deficiency [G6PD] gene mutations
• African A- mutation (G202A;A376G)
• The common Mediterranean mutation (C563T)
• Two common Chinese mutations (G1376T and G1388A)
• UGT1A1 polymorphism. The UGT1A1 gene polymorphisms refer to those genetic defects found to be associated with Gilbert's Syndrome, including a promoter defect (T-3263G) that disrupts a transcription regulatory site, the TA repeats promoter polymorphism, and four mutations within the coding region (G211A, C686A, C1091T, and T1456G).
• Gene polymorphism for the organic anion transporting protein (OATP-2)

Enrollment: 450 estimated patients

Sex: All

Ages: Under 6 days old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

Case

• Documentation of informed consent.
• Gestational age greater than or equal to 37 weeks.
• Birth weight greater than or equal to 2000 grams.
• At least one serum bilirubin level that is greater than the 95th percentile ("high risk zone") based on the Bhutani nomogram(1), for the case population.
• Age at enrollment less than 7 days or less than or equal to 168 hours.
• No major anomalies (chromosomal abnormalities, cyanotic congenital heart disease, gastroschisis, omphalocele, diaphragmatic hernia, or other major gastrointestinal anomalies, major neurological injury or anomaly, and multiple congenital anomalies).
• Ability to follow subjects transferred to another facility for outcome data.

Control

• Documentation of informed consent.
• Gestational age greater than or equal to 37 weeks.
• Birth weight greater than or equal to 2000 grams.
• At least one estimate of serum bilirubin. Bilirubin level estimated to be less than the 40th percentile ("low risk zone") based on the Bhutani nomogram. While a serum bilirubin in the low risk zone is the preferred method for assessing the bilirubin level, many pediatricians use transcutaneous measure of bilirubin as a screening tool for identifying "low risk" patients. For this reason, we will allow controls to be identified using transcutaneous measurements and collect serum bilirubin levels only as clinically indicated.
• Age at enrollment less than 7 days or less than or equal to 168 hours.
• No major anomalies (chromosomal abnormalities, cyanotic congenital heart disease, gastroschisis, omphalocele, diaphragmatic hernia or other major gastrointestinal anomalies, major neurological injury or anomaly, and multiple congenital anomalies).
• Ability to follow subjects transferred to another facility for outcome data.

Exclusion criteria

Case and Control

• Gestational age less than 37 weeks.
• Birth weight less than 2000 grams.
• Older than 7 days of age or 168 hours.
• Any major congenital anomalies.