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Study Description

The Neonatal Microbiome and Necrotizing enterocolitis (NEC) study is a multi-centered case control study testing the hypothesis that NEC is a direct or indirect consequence of the enteric biomass, its products, or both. Very low birth weight infants (VLBW; birth weight ≤ 1500 grams) admitted to the neonatal intensive care unit are prospectively followed over the first 5 week or until they reach 36 weeks gestation, whichever occurs later. VLBW infants with a lethal clinical condition are excluded. Over the course of the study period, prospective samples are obtained on all infants, and include all stools, and weekly blood samples, palm and oral swabs. Clinical data is collected over the course of the entire hospitalization. Cases are identified based on Bell's staging for NEC, requiring Bell's stage II (abdominal clinical signs and radiographic evidence of pneumatosis, portal venous gas or pneumoperitoneum). Controls are identified from the pool of prospectively enrolled subjects, matching for gestational age, birth weight, post-natal age and birth date.

The microbial components of stool and its products before and at the onset of NEC, are then compared between cases and controls.

The Aims of this proposal are to (1) conduct a case cohort study in which we compare clinical data and biological specimens from cases and well-matched controls; (2) determine if the kind and density of intestinal biomass, its gene content, and transcriptional activity are associated with, and potential determinants of, NEC; and (3) determine if host risk alleles for intestinal inflammation play a role in the development of NEC.

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Publicly Available Data
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Study Inclusion/Exclusion Criteria

For all participants:

Inclusion criteria:

  • birth weights are ≤ 1500 grams

Exclusion criteria:

  • severe medical problems evident at birth, such that survival is unlikely

NEC cases are defined using Bell's staging for NEC criteria (Walsh, M.C. et al. Pediatr Clin North Am, 1986. 33(1): p. 179-201, PMID: 3081865). Only cases with Bell's Stage II or greater are included. These criteria include:

Gastrointestinal Signs Radiographic Findings
Stage I Abdominal distention
Gastric residuals/emesis
Bloody stools
Intestinal Dilation
Ilius
Stage II Plus abdominal tenderness
+/- cellulitis
Pneumotosis intestinalis
Portal venous air
Stage III Plus marked distention/tenderness
Peritonitis
Pneumoperitoneum

Controls are matched for gestational age at birth and birth weight, date of birth, and postnatal age.

Molecular Data
TypeSourcePlatformNumber of Oligos/SNPsSNP Batch IdComment
16S rRNA Sequencing Roche 454 GS FLX Titanium N/A N/A
Whole Genome Sequencing Illumina MiSeq N/A N/A
Selected Publications
Diseases/Traits Related to Study (MeSH terms)
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Study Attribution
  • Principal Investigators
    • Phillip Tarr, MD. Washington University in St. Louis, St. Louis, MO, USA.
  • Co-Investigators
    • Vincent Magrini. Washington University in St. Louis, St. Louis, MO, USA.
    • Rakesh Nagarajan. Washington University in St. Louis, St. Louis, MO, USA.
    • William Shannon. Washington University in St. Louis, St. Louis, MO, USA.
    • Erica Sodegren Weinstock. Washington University in St. Louis, St. Louis, MO, USA.
    • David Wang. Washington University in St. Louis, St. Louis, MO, USA.
    • Barabara Warner. Washington University in St. Louis, St. Louis, MO, USA.
    • George Weinstock. Washington University in St. Louis, St. Louis, MO, USA.
  • Institute
    • National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
  • Funding Sources
    • 1UH2AI083265-01. National Institutes of Health, Bethesda, MD, USA.