Evidence map›Paper›PMID 23066327›Full record

ArticleWorld journal of gastroenterology2012

Origin of celiac disease: how old are predisposing haplotypes?

Giovanni Gasbarrini, Olga Rickards, Cristina Martínez-Labarga, Elsa Pacciani, Filiberto Chilleri, Lucrezia Laterza, Giuseppe Marangi, Franco Scaldaferri, Antonio Gasbarrini

Open access · greenAbstract readCase Reports
In one paragraph

Article in World journal of gastroenterology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

4 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Wheat-related disorders: A broad spectrum of 'evolving' diseases.United European gastroenterology journal · 2014
    Review
  3. Review
  4. 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

9 authors at 1 institution in 1 country.

Giovanni GasbarriniRicerca in Medicina Foundation NGO, Falcone and Borsellino Gallery, 40123 Bologna, Italy. agasbarrini@rm.unicatt.it
Olga Rickards
Cristina Martínez-Labarga
Elsa Pacciani
Filiberto Chilleri
Lucrezia Laterza
Giuseppe Marangi
Franco Scaldaferri
Antonio Gasbarrini
International Flame Research Foundation · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We recently presented the case of a first century AD young woman, found in the archaeological site of Cosa, showing clinical signs of malnutrition, such as short height, osteoporosis, dental enamel hypoplasia and cribra orbitalia, indirect sign of anemia, all strongly suggestive for celiac disease (CD). However, whether these findings were actually associated to CD was not shown based on genetic parameters. To investigate her human leukocyte antigen (HLA) class II polymorphism, we extracted DNA from a bone sample and a tooth and genotyped HLA using three HLA-tagging single nucleotide polymorphisms for DQ8, DQ2.2 and DQ2.5, specifically associated to CD. She displayed HLA DQ 2.5, the haplotype associated to the highest risk of CD. This is the first report showing the presence of a HLA haplotype compatible for CD in archaeological specimens.

Indexed as

Genetic Predisposition to DiseaseHaplotypesArchaeologyCeliac DiseaseDNA, MitochondrialDNA PrimersFemaleGenotypeHLA AntigensHLA-DQ AntigensHumansItalyMalabsorption SyndromesPolymorphism, GeneticRiskDNA, MitochondrialDNA PrimersHLA AntigensHLA-DQ AntigensAncient DNACeliac diseaseHuman leukocyte antigen haplotypeMalabsorptionSingle nucleotide polymorphisms

Identifiers

PMID23066327
PMCPMC3468865
OpenAlexW2119052215

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.