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Association of Baseline Luminal Narrowing With Ileal Microbial Shifts and Gene Expression Programs and Subsequent Transmural Healing in Pediatric Crohn Disease.
Ta, Allison D; Ollberding, Nicholas J; Karns, Rebekah; Haberman, Yael; Alazraki, Adina L; Hercules, David; Baldassano, Robert; Markowitz, James; Heyman, Melvin B; Kim, Sandra; Kirschner, Barbara; Shapiro, Jason M; Noe, Joshua; Oliva-Hemker, Maria; Otley, Anthony; Pfefferkorn, Marian; Kellermayer, Richard; Snapper, Scott; Rabizadeh, Shervin; Xavier, Ramnik; Dubinsky, Marla; Hyams, Jeffrey; Kugathasan, Subra; Jegga, Anil G; Dillman, Jonathan R; Denson, Lee A.
Affiliation
  • Ta AD; Cincinnati Children's Medical Hospital Center and the University of Cincinnati College of Medicine, Cincinnati, Ohio, USA.
  • Ollberding NJ; Cincinnati Children's Medical Hospital Center and the University of Cincinnati College of Medicine, Cincinnati, Ohio, USA.
  • Karns R; Cincinnati Children's Medical Hospital Center and the University of Cincinnati College of Medicine, Cincinnati, Ohio, USA.
  • Haberman Y; Cincinnati Children's Medical Hospital Center and the University of Cincinnati College of Medicine, Cincinnati, Ohio, USA.
  • Alazraki AL; Sheba Medical Center, Tel-HaShomer, affiliated with the Tel-Aviv University, Tel Aviv, Israel.
  • Hercules D; Emory University and Children's Healthcare of Atlanta, Atlanta, Georgia, USA.
  • Baldassano R; Emory University and Children's Healthcare of Atlanta, Atlanta, Georgia, USA.
  • Markowitz J; The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Heyman MB; Cohen Children's Medical Center of New York, New Hyde Park, New York, USA.
  • Kim S; University of California San Francisco, San Francisco, California, USA.
  • Kirschner B; Children's Hospital of Pittsburgh of UPMC, Pittsburgh, Pennsylvania, USA.
  • Shapiro JM; The University of Chicago, Chicago, Illinois, USA.
  • Noe J; Hasbro Children's Hospital, Providence, Rhode Island, USA.
  • Oliva-Hemker M; Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
  • Otley A; John Hopkins University, Baltimore, Maryland, USA.
  • Pfefferkorn M; IWK Health Centre, Halifax, Nova Scotia, Canada.
  • Kellermayer R; Indiana University School of Medicine, Indianapolis, Indiana, USA.
  • Snapper S; Texas Children's Hospital, Baylor College School of Medicine, Houston, Texas, USA.
  • Rabizadeh S; Children's Hospital-Boston, Boston, Massachusetts, USA.
  • Xavier R; Cedars-Sinai Medical Center, Los Angeles, California, USA.
  • Dubinsky M; Broad Institute at Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
  • Hyams J; Massachusetts General Hospital, Cambridge, Massachusetts, USA.
  • Kugathasan S; Mount Sinai Hospital, New York, New York, USA.
  • Jegga AG; Connecticut Children's Medical Center, Hartford, Connecticut, USA.
  • Dillman JR; Emory University and Children's Healthcare of Atlanta, Atlanta, Georgia, USA.
  • Denson LA; Cincinnati Children's Medical Hospital Center and the University of Cincinnati College of Medicine, Cincinnati, Ohio, USA.
Inflamm Bowel Dis ; 27(11): 1707-1718, 2021 10 20.
Article in En | MEDLINE | ID: mdl-33452801
ABSTRACT

BACKGROUND:

Transmural healing (TH) is associated with better long-term outcomes in Crohn disease (CD), whereas pretreatment ileal gene signatures encoding myeloid inflammatory responses and extracellular matrix production are associated with stricturing. We aimed to develop a predictive model for ileal TH and to identify ileal genes and microbes associated with baseline luminal narrowing (LN), a precursor to strictures. MATERIALS AND

METHODS:

Baseline small bowel imaging obtained in the RISK pediatric CD cohort study was graded for LN. Ileal gene expression was determined by RNASeq, and the ileal microbial community composition was characterized using 16S rRNA amplicon sequencing. Clinical, demographic, radiologic, and genomic variables were tested for association with baseline LN and future TH.

RESULTS:

After controlling for ileal location, baseline ileal LN (odds ratio [OR], 0.3; 95% confidence interval [CI], 0.1-0.8), increasing serum albumin (OR, 4; 95% CI, 1.3-12.3), and anti-Saccharomyces cerevisiae antibodies IgG serology (OR, 0.97; 95% CI, 0.95-1) were associated with subsequent TH. A multivariable regression model including these factors had excellent discriminant power for TH (area under the curve, 0.86; positive predictive value, 80%; negative predictive value, 87%). Patients with baseline LN exhibited increased Enterobacteriaceae and inflammatory and extracellular matrix gene signatures, coupled with reduced levels of butyrate-producing commensals and a respiratory electron transport gene signature. Taxa including Lachnospiraceae and the genus Roseburia were associated with increased respiratory and decreased inflammatory gene signatures, and Aggregatibacter and Blautia bacteria were associated with reduced extracellular matrix gene expression.

CONCLUSIONS:

Pediatric patients with CD with LN at diagnosis are less likely to achieve TH. The association between specific microbiota, wound healing gene programs, and LN may suggest future therapeutic targets.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Wound Healing / Crohn Disease / Gene Expression Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Child / Humans Language: En Journal: Inflamm Bowel Dis Journal subject: GASTROENTEROLOGIA Year: 2021 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Wound Healing / Crohn Disease / Gene Expression Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Child / Humans Language: En Journal: Inflamm Bowel Dis Journal subject: GASTROENTEROLOGIA Year: 2021 Document type: Article Affiliation country: