Evidence map›Paper›PMID 24950659›Full record

ArticleCritical care (London, England)2014

Surfactant protein A genetic variants associate with severe respiratory insufficiency in pandemic influenza A virus infection.

Estefanía Herrera-Ramos, Marta López-Rodríguez, José Juan Ruíz-Hernández, Juan Pablo Horcajada, Luis Borderías, Elisabeth Lerma, José Blanquer, María Carmen Pérez-González, María Isabel García-Laorden, Yanira Florido and 12 more

Open access · goldAbstract read
In one paragraph

Article in Critical care (London, England), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 1 pooled it
4.1field-weighted citation impact, top 6% 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

45 citing papers in PubMed, 1 synthesis or guideline pooled it, 75 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Mannose-Binding Lectin Levels in Critically Ill Children With Severe Infections.Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies · 2017
    Trial
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  5. Review
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  12. Influenza.Lancet (London, England) · 2022
    Review
  13. Article
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  15. Review
  16. Article
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  18. Article
  19. Viral Respiratory Pathogens and Lung Injury.Clinical microbiology reviews · 2021
    Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors at 7 institutions in 2 countries.

Estefanía Herrera-Ramos
Marta López-Rodríguez
José Juan Ruíz-Hernández
Juan Pablo Horcajada
Luis Borderías
Elisabeth Lerma
José Blanquer
María Carmen Pérez-González
María Isabel García-Laorden
Yanira Florido
Virginia Mas-Bosch
Milagro Montero
José María Ferrer
Luisa Sorlí
Carlos Vilaplana
Olga Rajas
Marisa Briones
Javier Aspa
Eduardo López-Granados
Jordi Solé-Violán
Felipe Rodríguez de Castro
Carlos Rodríguez-Gallego
Hospital Universitario de Gran Canaria Doctor Negrín · ESUniversidad de Las Palmas de Gran Canaria · ESHospital Clínico Universitario de Valencia · ESHospital Universitario de La Princesa · ESHospital Del Mar · ESHospital General San Jorge · ESHospital Universitario La Paz · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionInherited variability in host immune responses influences susceptibility and outcome of Influenza A virus (IAV) infection, but these factors remain largely unknown. Components of the innate immune response may be crucial in the first days of the infection. The collectins surfactant protein (SP)-A1, -A2, and -D and mannose-binding lectin (MBL) neutralize IAV infectivity, although only SP-A2 can establish an efficient neutralization of poorly glycosylated pandemic IAV strains.

methodsWe studied the role of polymorphic variants at the genes of MBL (MBL2), SP-A1 (SFTPA1), SP-A2 (SFTPA2), and SP-D (SFTPD) in 93 patients with H1N1 pandemic 2009 (H1N1pdm) infection.

resultsMultivariate analysis showed that two frequent SFTPA2 missense alleles (rs1965708-C and rs1059046-A) and the SFTPA2 haplotype 1A(0) were associated with a need for mechanical ventilation, acute respiratory failure, and acute respiratory distress syndrome. The SFTPA2 haplotype 1A(1) was a protective variant. Kaplan-Meier analysis and Cox regression also showed that diplotypes not containing the 1A(1) haplotype were associated with a significantly shorter time to ICU admission in hospitalized patients. In addition, rs1965708-C (P = 0.0007), rs1059046-A (P = 0.0007), and haplotype 1A(0) (P = 0.0004) were associated, in a dose-dependent fashion, with lower PaO2/FiO2 ratio, whereas haplotype 1A(1) was associated with a higher PaO2/FiO2 ratio (P = 0.001).

conclusionsOur data suggest an effect of genetic variants of SFTPA2 on the severity of H1N1pdm infection and could pave the way for a potential treatment with haplotype-specific (1A(1)) SP-A2 for future IAV pandemics.

Indexed as

Influenza A Virus, H1N1 SubtypeAdultBlood PressureFemaleHaplotypesHospitalizationHumansInfluenza, HumanMaleMutation, MissensePolymorphism, Single NucleotideProspective StudiesPulmonary Surfactant-Associated Protein ARetrospective StudiesSeverity of Illness IndexPulmonary Surfactant-Associated Protein ASFTPA2 protein, human

Identifiers

PMID24950659
PMCPMC4229788
OpenAlexW2033027430

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.