Evidence map›Paper›PMID 22438897›Full record

SynthesisPloS one2012

The role of host genetics in susceptibility to influenza: a systematic review.

Peter Horby, Nhu Y Nguyen, Sarah J Dunstan, J Kenneth Baillie

Open access · goldAbstract readSystematic Review
In one paragraph

Synthesis in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed, 2 pooled it
10.3field-weighted citation impact, top 1% 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

58 citing papers in PubMed, 2 syntheses or guidelines pooled it, 116 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  4. Review
  5. Article
  6. Article
  7. Review
  8. Coronavirus infection and ABO blood grouping: Correlation or coincidence?Journal of family medicine and primary care · 2023
    Article
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  12. N-Glycomics of Human Erythrocytes.International journal of molecular sciences · 2021
    Article
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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

4 authors at 2 institutions in 2 countries.

Peter HorbyOxford University Clinical Research Unit-Wellcome Trust Major Overseas Programme, Hanoi, Vietnam. peter.horby@gmail.com
Nhu Y Nguyen
Sarah J Dunstan
J Kenneth Baillie
Oxford University Clinical Research Unit · VNUniversity of Edinburgh · GB

Funding

Wellcome Trust 077078/Z/05/ZWellcome Trust 081613/Z/06/ZWellcome Trust 089276
6 · The paper itself

Abstract

backgroundThe World Health Organization has identified studies of the role of host genetics on susceptibility to severe influenza as a priority. A systematic review was conducted to summarize the current state of evidence on the role of host genetics in susceptibility to influenza (PROSPERO registration number: CRD42011001380). METHODS AND

findingsPubMed, Web of Science, the Cochrane Library, and OpenSIGLE were searched using a pre-defined strategy for all entries up to the date of the search. Two reviewers independently screened the title and abstract of 1,371 unique articles, and 72 full text publications were selected for inclusion. Mouse models clearly demonstrate that host genetics plays a critical role in susceptibility to a range of human and avian influenza viruses. The Mx genes encoding interferon inducible proteins are the best studied but their relevance to susceptibility in humans is unknown. Although the MxA gene should be considered a candidate gene for further study in humans, over 100 other candidate genes have been proposed. There are however no data associating any of these candidate genes to susceptibility in humans, with the only published study in humans being under-powered. One genealogy study presents moderate evidence of a heritable component to the risk of influenza-associated death, and while the marked familial aggregation of H5N1 cases is suggestive of host genetic factors, this remains unproven.

conclusionThe fundamental question "Is susceptibility to severe influenza in humans heritable?" remains unanswered. Not because of a lack of genotyping or analytic tools, nor because of insufficient severe influenza cases, but because of the absence of a coordinated effort to define and assemble cohorts of cases. The recent pandemic and the ongoing epizootic of H5N1 both represent rapidly closing windows of opportunity to increase understanding of the pathogenesis of severe influenza through multi-national host genetic studies.

Indexed as

Genetic Predisposition to DiseaseABO Blood-Group SystemAnimalsBirdsDisease Models, AnimalFamilyGTP-Binding ProteinsHLA AntigensHost-Pathogen InteractionsHumansInfluenza, HumanInfluenza in BirdsMiceMice, Inbred StrainsMyxovirus Resistance ProteinsSpecies SpecificityABO Blood-Group SystemGTP-Binding ProteinsHLA AntigensMX1 protein, humanMx1 protein, mouseMyxovirus Resistance Proteins

Identifiers

PMID22438897
PMCPMC3305291
OpenAlexW2119603672

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.