Evidence map›Paper›PMID 12651880›Full record

ReviewGut2003

Chronic pancreatitis and cystic fibrosis.

H Witt

Open access · bronzeAbstract readReview
In one paragraph

Review in Gut, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
6.0field-weighted citation impact, top 3% 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

20 citing papers in PubMed, 84 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. CFTR and Gastrointestinal Cancers: An Update.Journal of personalized medicine · 2022
    Review
  6. Review
  7. The histopathology of SPINK1-associated chronic pancreatitis.Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.] · 2020
    Article
  8. Review
  9. Article
  10. Article
  11. Anti-fibrotic effects of phenolic compounds on pancreatic stellate cells.BMC complementary and alternative medicine · 2015
    Article
  12. Genetics of acute and chronic pancreatitis: An update.World journal of gastrointestinal pathophysiology · 2014
    Review
  13. Review
  14. Review
  15. Pancreatic exocrine insufficiency in LXRbeta-/- mice is associated with a reduction in aquaporin-1 expression.Proceedings of the National Academy of Sciences of the United States of America · 2008
    Article
  16. Genetic aspects of tropical calcific pancreatitis.Reviews in endocrine & metabolic disorders · 2008
    Review
  17. Hereditary chronic pancreatitis.Orphanet journal of rare diseases · 2007
    Review
  18. Chronic pancreatitis.Indian journal of pediatrics · 2006
    Review
  19. Recurrent pancreatitis: not just alcohol, gallstones and scorpion venom.Journal of the Royal Society of Medicine · 2004
    Article
  20. Genotype-phenotype correlation in 9 patients with tropical pancreatitis and identified gene mutations.Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology
    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

1 author at 1 institution in 1 country.

H WittKinderklinik, Charité-Campus Virchow-Klinikum, Humboldt-Universität, Berlin, Germany. heiko.witt@charite.de
Charité - Universitätsmedizin Berlin · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent discoveries of trypsinogen and trypsin inhibitor mutations in patients with chronic pancreatitis (CP) support the hypothesis that an inappropriate activation of pancreatic zymogens to active enzymes within the pancreatic parenchyma starts the inflammatory process. Current data suggest that CP may be inherited dominant, recessive, or complex as a result of mutations in the above mentioned or yet unidentified genes. Evaluation of patients with CP should include genetic testing. Cystic fibrosis (CF) is an autosomal recessive inherited disorder caused by mutations in the CF transmembrane conductance regulator (CFTR) gene and is characterised by pancreatic insufficiency and chronic bronchopulmonary infection. The progression and severity of pulmonary disease differs considerably between people with identical CFTR mutations and does not seem to correlate with the type or class of the CFTR mutation. The identification of further disease modifying genetic factors will increase the pathophysiological understanding and may help to identify new therapeutic targets.

Indexed as

Chronic DiseaseCystic FibrosisGenetic Predisposition to DiseaseHumansMaleModels, GeneticMutationPancreatitisPancreatitis, AlcoholicVas Deferens

Identifiers

PMID12651880
PMCPMC1867753
OpenAlexW2159228736

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.