Volume 77, Issue 2 pp. 184-190
Original Articles: Gastroenterology

The Spectrum of Duodenal Histologic Findings in Patients With Trisomy 21

A Multicenter Study

Erin Alexander DO

Corresponding Author

Erin Alexander DO

Division of Pediatric Gastroenterology and Hepatology, Mayo Clinic Children’s Center, Rochester, MN

Address correspondence and reprint requests to Erin Alexander, DO, Division of Pediatric Gastroenterology and Hepatology, Mayo Clinic Children’s Center, Rochester, MN 55905 (e-mail: [email protected]).Search for more papers by this author
Marisa Stahl MD, MSCS

Marisa Stahl MD, MSCS

Digestive Health Institute, Department of Pediatrics, Children’s Hospital Colorado, University of Colorado Anschutz Medical Campus, Aurora, CO

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Amy Weaver MS

Amy Weaver MS

Division of Clinical Trials and Biostatistics, Mayo Clinic, Rochester, MN

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Janaki Devara MBBS

Janaki Devara MBBS

Division of Pediatric Gastroenterology and Hepatology, Mayo Clinic Children’s Center, Rochester, MN

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Lisa M. Fahey MD

Lisa M. Fahey MD

Division of Gastroenterology, Hepatology, & Nutrition, The Children’s Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA

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Arunjot Singh MD, MPH

Arunjot Singh MD, MPH

Division of Gastroenterology, Hepatology, & Nutrition, The Children’s Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA

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Maureen M. Leonard MD, MMSc

Maureen M. Leonard MD, MMSc

Center for Celiac Research and Treatment, Division of Pediatric Gastroenterology and Nutrition, Mass General Hospital for Children, Harvard Medical School, Boston, MA

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Vanessa Weisbrod BS, CA

Vanessa Weisbrod BS, CA

Harvard Celiac Research Program, Boston Children’s Hospital, Boston, MA

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Mary Shull MD

Mary Shull MD

Digestive Health Institute, Department of Pediatrics, Children’s Hospital Colorado, University of Colorado Anschutz Medical Campus, Aurora, CO

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Jocelyn Silvester MD, PhD, FRCPC

Jocelyn Silvester MD, PhD, FRCPC

Harvard Celiac Research Program, Boston Children’s Hospital, Boston, MA

Department of Pediatrics, Harvard Medical School, Boston, MA

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Zachary Kramer BS

Zachary Kramer BS

Celiac Disease Program, Division of Gastroenterology, Hepatology, and Nutrition, Children’s National Hospital, Washington, DC

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Benny Kerzner BSc, MBBCh, FCP (SA)

Benny Kerzner BSc, MBBCh, FCP (SA)

Celiac Disease Program, Division of Gastroenterology, Hepatology, and Nutrition, Children’s National Hospital, Washington, DC

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Edwin Liu MD

Edwin Liu MD

Digestive Health Institute, Department of Pediatrics, Children’s Hospital Colorado, University of Colorado Anschutz Medical Campus, Aurora, CO

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Imad Absah MD

Imad Absah MD

Division of Pediatric Gastroenterology and Hepatology, Mayo Clinic Children’s Center, Rochester, MN

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First published: 12 May 2023
Citations: 3

M.M.L. serves as a consultant to Anokion and 9meters biopharma and performs sponsored research with Glutenostics, LLC.

Supplemental digital content is available for this article. Direct URL citations appear in the printed text, and links to the digital files are provided in the HTML text of this article on the journal’s Web site (www.jpgn.org).

E.A. and M.S. contributed equally to the article.

Abstract

Objectives:

Patients with Trisomy 21 (T21) commonly have gastrointestinal symptoms and diseases that prompt evaluation with esophagogastroduodenoscopy (EGD). Our objective is to characterize duodenal histological abnormalities in these patients when undergoing EGD. A secondary aim is to explore associations of histologic findings with different therapies.

Methods:

Patients 30 years old or younger with T21 who underwent EGD from 2000 to 2020 at 6 hospitals were included in this retrospective cohort study. Duodenal biopsies were categorized based on reported histopathology findings as normal or abnormal. Abnormal pathology reports were reviewed and categorized into villous atrophy (VA) and duodenitis without VA. The VA group was further categorized based on the presence or absence of celiac disease (CD).

Results:

We identified 836 patients with T21 who underwent EGD, 419 (50.1%) of whom had duodenal histologic abnormalities. At the time of the first (index) abnormal duodenal biopsy, 290 of 419 had VA and of those, 172 of 290 met CD diagnostic criteria, while 118 of 290 did not meet CD criteria (nonspecific VA). Among the patients with an abnormal biopsy, acid suppression at the time of the index biopsy was less common in patients with VA-CD compared to patients without VA or patients with nonspecific VA (12.2% vs 45.7% vs 44.9%).

Conclusions:

Half of the T21 patients in this cohort had abnormal duodenal biopsies including a subgroup with nonspecific VA. In this cohort, acid suppression use was more prevalent in patients with abnormalities other than CD.

Graphical Abstract

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.