Evidence map›Paper›PMID 28836046›Full record

SynthesisDigestive diseases and sciences2017

Gastrointestinal Manifestations of Hereditary Hemorrhagic Telangiectasia (HHT): A Systematic Review of the Literature.

Samuel B Jackson, Nicholas P Villano, Jihane N Benhammou, Michael Lewis, Joseph R Pisegna, David Padua

Open access · greenAbstract readSystematic Review
In one paragraph

Synthesis in Digestive diseases and sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
7.7field-weighted citation impact, top 2% 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

40 citing papers in PubMed, 110 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

Samuel B JacksonDivision of Digestive Diseases, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Nicholas P VillanoDivision of Digestive Diseases, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Jihane N BenhammouDivision of Digestive Diseases, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Michael LewisDepartment of Pathology and Laboratory Medicine, Department of Human Genetics, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Joseph R PisegnaDivision of Digestive Diseases, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.ORCID 0000-0002-4343-0989
David PaduaDivision of Digestive Diseases, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA. dpadua@mednet.ucla.edu.
University of California, Los Angeles · US

Funding

Pilot and Feasibility ProgramP30DK041301 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ROZENGURT, JUAN ENRIQUE · 1990 to 2019
$18.0M
GASTROENTEROLOGYT32DK007180 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI JENSEN, DENNIS MICHAEL · 1986 to 2025
$10.0M
Gastrointestinal Hormonal Regulation of ObesityI01RX000194 · VA · VA GREATER LOS ANGELES HEALTHCARE SYSTEM · PI PISEGNA, JOSEPH R, TACHE, YVETTE FRANCE · 2012 to 2015
–
NIDDK NIH HHS P30 DK041301NIDDK NIH HHS T32 DK007180RRD VA I01 RX000194
6 · The paper itself

Abstract

Hereditary hemorrhagic telangiectasia (HHT), also called Osler-Weber-Rendu syndrome, is an autosomal dominant genetic disease that affects the vasculature of numerous organs. The prevalence of HHT is estimated to be between 1.5 and 2 persons per 10,000. While there is still much to learn about this condition, there is an increasing understanding its underlying pathophysiology, genetic basis, presentations, and management. Recognizing that the clinical manifestations of HHT can involve a number of organ systems will provide clinicians with a higher index of suspicion for the disease. This early diagnosis and genotyping can greatly reduce mortality for a patient with HHT through appropriate screening for complications. This review will focus on the gastrointestinal manifestations of HHT and how these can dictate treatment and prognosis.

Indexed as

AnimalsBiopsyEndoscopy, GastrointestinalGastrointestinal DiseasesGenetic Predisposition to DiseaseHumansMolecular Diagnostic TechniquesPhenotypePhysical ExaminationPredictive Value of TestsPrevalencePrognosisRisk FactorsTelangiectasia, Hereditary HemorrhagicTomography, X-Ray ComputedArteriovenous malformationHereditary hemorrhagic telangiectasia (HHT)Juvenile polyposis syndromeOsler–Weber–Rendu syndrome

Identifiers

PMID28836046
PMCPMC5641264
OpenAlexW2747814331

What OpenQuestion holds

Textmetadata
LicenceTDM
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.