Evidence map›Paper›PMID 30333828›Full record

ArticleFrontiers in immunology2018

Genetic Association of Pulmonary Surfactant Protein Genes, SFTPA1, SFTPA2, SFTPB, SFTPC, and SFTPD With Cystic Fibrosis.

Zhenwu Lin, Nithyananda Thorenoor, Rongling Wu, Susan L DiAngelo, Meixia Ye, Neal J Thomas, Xiaojie Liao, Tony R Lin, Stuart Warren, Joanna Floros

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

35 citing papers in PubMed, 47 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

10 authors at 4 institutions in 2 countries.

Zhenwu LinDepartment of Radiology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, United States.
Nithyananda ThorenoorDepartment of Pediatrics, Center for Host Defense, Inflammation, and Lung Disease (CHILD) Research, Pennsylvania State University, Hershey, PA, United States.
Rongling WuPublic Health Science, College of Medicine, Pennsylvania State University, Hershey, PA, United States.
Susan L DiAngeloDepartment of Pediatrics, Center for Host Defense, Inflammation, and Lung Disease (CHILD) Research, Pennsylvania State University, Hershey, PA, United States.
Meixia YePublic Health Science, College of Medicine, Pennsylvania State University, Hershey, PA, United States.
Neal J ThomasDepartment of Pediatrics, Center for Host Defense, Inflammation, and Lung Disease (CHILD) Research, Pennsylvania State University, Hershey, PA, United States.
Xiaojie LiaoDepartment of Pediatrics, Center for Host Defense, Inflammation, and Lung Disease (CHILD) Research, Pennsylvania State University, Hershey, PA, United States.
Tony R LinDepartment of Pediatrics, Center for Host Defense, Inflammation, and Lung Disease (CHILD) Research, Pennsylvania State University, Hershey, PA, United States.
Stuart WarrenDepartment of Pediatrics, Center for Host Defense, Inflammation, and Lung Disease (CHILD) Research, Pennsylvania State University, Hershey, PA, United States.
Joanna FlorosDepartment of Pediatrics, Center for Host Defense, Inflammation, and Lung Disease (CHILD) Research, Pennsylvania State University, Hershey, PA, United States.
Pennsylvania State University · USBeijing Forestry University · CNPenn State Milton S. Hershey Medical Center · USUniversity of Pennsylvania · US

Funding

The Role of surfactant protein genetic variants in cyst*R01HL068947 · NHLBI · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI FLOROS, JOANNA · 2001 to 2005
$1.7M
NHLBI NIH HHS R01 HL068947
6 · The paper itself

Abstract

Surfactant proteins (SP) are involved in surfactant function and innate immunity in the human lung. Both lung function and innate immunity are altered in CF, and altered SP levels and genetic association are observed in Cystic Fibrosis (CF). We hypothesized that single nucleotide polymorphisms (SNPs) within the SP genes associate with CF or severity subgroups, either through single SNP or via SNP-SNP interactions between two SNPs of a given gene (intragenic) and/or between two genes (intergenic). We genotyped a total of 17 SP SNPs from 72 case-trio pedigree (SFTPA1 (5), SFTPA2 (4), SFTPB (4), SFTPC (2), and SFTPD (2)), and identified SP SNP associations by applying quantitative genetic principles. The results showed (a) Two SNPs, SFTPB rs7316 (

Indexed as

Polymorphism, Single NucleotideAdultChildChild, PreschoolCystic FibrosisFemaleHumansMalePulmonary Surfactant-Associated Protein APulmonary Surfactant-Associated Protein CPulmonary Surfactant-Associated Protein APulmonary Surfactant-Associated Protein CSFTPA1 protein, humanSFTPA2 protein, humanSFTPC protein, humancystic fibrosisSP-ASP-BSP-CSP-Dsurfactant protein

Identifiers

PMID30333828
PMCPMC6175982
OpenAlexW2895641600

What OpenQuestion holds

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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.