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  1. Home
  2. Genetic And Clinical Determinants Of Neonatal Jaundice And Growth Patterns In The Qingdao Birth Cohort: A Genome-wide Association Study.
  1. Home
  2. Genetic And Clinical Determinants Of Neonatal Jaundice And Growth Patterns In The Qingdao Birth Cohort: A Genome-wide Association Study.

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Genetic and clinical determinants of neonatal jaundice and growth patterns in the Qingdao birth cohort: A genome-wide

Xu Chen1,2, Peina Du3,4, Shuo Li5

  • 1Department of Physiology, Shandong Provincial Key Laboratory of Pathogenesis and Prevention of Neurological Disorders and State Key Disciplines: Physiology, School of Basic Medicine, Qingdao University, Qingdao, China.

Plos One
|January 16, 2026

View abstract on PubMed

Summary
This summary is machine-generated.

This study identified genetic factors influencing newborn growth and jaundice in East Asian infants. Novel mutations in ATP7 and UGT1A genes were linked to birth weight and jaundice, aiding early health assessments.

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Area of Science:

  • Genetics and Genomics
  • Neonatal Health
  • Human Growth and Development

Background:

  • Neonatal jaundice and early growth are key health indicators.
  • Genetic and clinical factors influence these traits.
  • Limited evidence exists for East Asian newborns.

Purpose of the Study:

  • Investigate genetic determinants of Healthy Newborn Growth Indicators (HNGI) in East Asian infants.
  • Focus on neonatal jaundice (JAU), jaundice resolution (JAUR), birth weight (BW), and early growth metrics.
  • Identify novel genetic variants and pathways influencing newborn health.

Main Methods:

  • Genome-wide association study (GWAS) on a Qingdao cohort.
  • Analysis of single-nucleotide polymorphisms (SNPs) and missense mutations.
  • Functional enrichment analysis and assessment of clinical risk factors using Biobank Japan (BBJ) data.
  • Main Results:

    • Identified 778 SNPs in 120 genes associated with HNGI, including 7 novel missense mutations.
    • Confirmed rs4148323 in UGT1A for JAU and discovered novel mutations for JAU and JAUR.
    • Found a novel missense mutation rs148399850 in ATP7 associated with BW, suggesting its role in birth weight regulation.
    • Highlighted 18 genes in 14 metabolic pathways crucial for growth and development.
    • Demonstrated significant influence of clinical factors on HNGI.

    Conclusions:

    • Provides critical data for expanding molecular marker databases for prenatal screening.
    • Offers potential for early warnings for neonatal jaundice.
    • Guides strategies for promoting healthy newborn growth.