Evidence map›Paper›PMID 25342047›Full record

ReviewAmerican journal of physiology. Gastrointestinal and liver physiology2014

Animal models of gastrointestinal and liver diseases. Animal models of infant short bowel syndrome: translational relevance and challenges.

Per T Sangild, Denise M Ney, David L Sigalet, Andreas Vegge, Douglas Burrin

Open access · greenAbstract readReview
In one paragraph

Review in American journal of physiology. Gastrointestinal and liver physiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 3 pooled it
4.9field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

39 citing papers in PubMed, 3 syntheses or guidelines pooled it, 63 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Review
  5. Article
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  8. Review
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  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. A Model of Short Bowel Syndrome in Rodents in a Long-Term Experiment.Bulletin of experimental biology and medicine · 2022
    Article
  18. Review
  19. Starvation and Its Effects on the Gut.Advances in nutrition (Bethesda, Md.) · 2021
    Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 4 institutions in 3 countries.

Per T SangildDepartment of Nutrition, Exercise and Sports, Faculty of Science, University of Copenhagen, Frederiksberg, Denmark; Department of Paediatrics and Adolescent Medicine, Rigshospitalet, Copenhagen, Denmark; psa@life.ku.dk.
Denise M NeyDepartment of Nutritional Sciences, University of Wisconsin-Madison, Madison, Wisconsin;
David L SigaletSidra Medical and Research Center, Doha, Qatar;
Andreas VeggeDepartment of Nutrition, Exercise and Sports, Faculty of Science, University of Copenhagen, Frederiksberg, Denmark; Diabetes Pharmacology, Novo Nordisk, Måløv, Denmark; and.
Douglas BurrinUSDA-ARS Children's Nutrition Research Center, Baylor College of Medicine, Houston, Texas.
University of Copenhagen · DKChildren's Nutrition Research Center at Baylor College of Medicine · USSidra Medical and Research Center · QAUniversity of Wisconsin–Madison · US

Funding

Tissue Analysis & Molecular Imaging CoreP30DK056338 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI James Versalovic · 2001 to 2026
$28.3M
Regulation of Hepatic Metabolic Function by Parenteral NutritionR01DK094616 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI BURRIN, DOUGLAS G · 2013 to 2022
$2.3M
TOTAL PARENTERAL NUTRITION AND SOMATOMEDIN RESPONSESR01DK042835 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI NEY, DENISE M · 1995 to 2009
$1.8M
Nutritional and Hormonal Mechanisms of Intestinal AdaptationR56DK042835 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI NEY, DENISE M · 2011 to 2011
$57k
TOTAL PARENTERAL NUTRITION AND SOMATOMEDIN RESPONSESR29DK042835 · NIDDK · UNIVERSITY OF WISCONSIN MADISON · PI NEY, DENISE M · 1990 to 1994
–
NIDDK NIH HHS DK-042835NIDDK NIH HHS DK-094616NIDDK NIH HHS P30 DK-56338
6 · The paper itself

Abstract

Intestinal failure (IF), due to short bowel syndrome (SBS), results from surgical resection of a major portion of the intestine, leading to reduced nutrient absorption and need for parenteral nutrition (PN). The incidence is highest in infants and relates to preterm birth, necrotizing enterocolitis, atresia, gastroschisis, volvulus, and aganglionosis. Patient outcomes have improved, but there is a need to develop new therapies for SBS and to understand intestinal adaptation after different diseases, resection types, and nutritional and pharmacological interventions. Animal studies are needed to carefully evaluate the cellular mechanisms, safety, and translational relevance of new procedures. Distal intestinal resection, without a functioning colon, results in the most severe complications and adaptation may depend on the age at resection (preterm, term, young, adult). Clinically relevant therapies have recently been suggested from studies in preterm and term PN-dependent SBS piglets, with or without a functional colon. Studies in rats and mice have specifically addressed the fundamental physiological processes underlying adaptation at the cellular level, such as regulation of mucosal proliferation, apoptosis, transport, and digestive enzyme expression, and easily allow exogenous or genetic manipulation of growth factors and their receptors (e.g., glucagon-like peptide 2, growth hormone, insulin-like growth factor 1, epidermal growth factor, keratinocyte growth factor). The greater size of rats, and especially young pigs, is an advantage for testing surgical procedures and nutritional interventions (e.g., PN, milk diets, long-/short-chain lipids, pre- and probiotics). Conversely, newborn pigs (preterm or term) and weanling rats provide better insights into the developmental aspects of treatment for SBS in infants owing to their immature intestines. The review shows that a balance among practical, economical, experimental, and ethical constraints will determine the choice of SBS model for each clinical or basic research question.

Indexed as

Disease Models, AnimalParenteral Nutrition, TotalAnimalsHumansInfantMiceRatsShort Bowel Syndromeglucagon-like peptide 2intestinemousenewbornparenteral and enteral nutritionpigratresection

Identifiers

PMID25342047
PMCPMC4269678
OpenAlexW2334193991

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.