Evidence map›Paper›PMID 30054559›Full record

ArticleScientific reports2018

Sputum Detection of Predisposing Genetic Mutations in Women with Pulmonary Nontuberculous Mycobacterial Disease.

Julie V Philley, Kate L Hertweck, Anbarasu Kannan, Barbara A Brown-Elliott, Richard J Wallace, Anna Kurdowska, Harrison Ndetan, Karan P Singh, Edmund J Miller, David E Griffith and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
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

11 authors at 3 institutions in 1 country.

Julie V PhilleyDepartment of Medicine, The University of Texas Health Science Center at Tyler, Tyler, Texas, USA.
Kate L HertweckDepartment of Biology, The University of Texas at Tyler, Tyler, Texas, USA.
Anbarasu KannanDepartment of Cellular and Molecular Biology, The University of Texas Health Science Center at Tyler, Tyler, Texas, USA.
Barbara A Brown-ElliottDepartment of The Mycobacteria/Nocardia Research Laboratory Department of Microbiology, The University of Texas Health Science Center at Tyler, Tyler, Texas, USA.
Richard J WallaceDepartment of The Mycobacteria/Nocardia Research Laboratory Department of Microbiology, The University of Texas Health Science Center at Tyler, Tyler, Texas, USA.
Anna KurdowskaDepartment of Cellular and Molecular Biology, The University of Texas Health Science Center at Tyler, Tyler, Texas, USA.
Harrison NdetanDepartment of Epidemiology and Biostatistics, The University of Texas Health Science Center at Tyler, Tyler, Texas, USA.
Karan P SinghDepartment of Epidemiology and Biostatistics, The University of Texas Health Science Center at Tyler, Tyler, Texas, USA.
Edmund J MillerDepartment of The Center for Heart and Lung Research, The Feinstein Institute for Medical Research, Manhasset, New York, USA.
David E GriffithDepartment of Medicine, The University of Texas Health Science Center at Tyler, Tyler, Texas, USA.
Santanu DasguptaDepartment of Cellular and Molecular Biology, The University of Texas Health Science Center at Tyler, Tyler, Texas, USA. santanu.dasgupta@uthct.edu.ORCID 0000-0002-1499-0039
The University of Texas Health Science Center at Tyler · USFeinstein Institute for Medical Research · USThe University of Texas at Tyler · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nontuberculous mycobacterial lung disease (NTM), including Mycobacterium avium complex (MAC), is a growing health problem in North America and worldwide. Little is known about the molecular alterations occurring in the tissue microenvironment during NTM pathogenesis. Utilizing next generation sequencing, we sequenced sputum and matched lymphocyte DNA in 15 MAC patients for a panel of 19 genes known to harbor cancer susceptibility associated mutations. Thirteen of 15 NTM subjects had a diagnosis of breast cancer (BCa) before or after NTM infection. Thirty three percent (4/12) of these NTM-BCa cases exhibited at least 3 somatic mutations in sputa compared to matched lymphocytes. Twenty four somatic mutations were detected with at least one mutation in ATM, ERBB2, BARD1, BRCA1, BRCA2, AR, TP53, PALB2, CASP8, BRIP1, NBN and TGFB1 genes. All four NTM-BCa patients harboring somatic mutations also exhibited 15 germ line BRCA1 and BRCA2 mutations. The two NTM subjects without BCa exhibited twenty somatic mutations spanning BRCA1, BRCA1, BARD1, BRIP1, CHEK2, ERBB2, TP53, ATM, PALB2, TGFB1 and 3 germ line mutations in BRCA1 and BRCA2 genes. A single copy loss of STK11 and AR gene was noted in NTM-BCa subjects. Periodic screening of sputa may aid to develop risk assessment biomarkers for neoplastic diseases in NTM patients.

Indexed as

Genetic Predisposition to DiseaseAgedBRCA1 ProteinBRCA2 ProteinBreast NeoplasmsChromosomes, HumanDNA Copy Number VariationsFemaleGenome, HumanHumansMiddle AgedMutationMycobacterium Infections, NontuberculousSputumBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, human

Identifiers

PMID30054559
PMCPMC6063893
OpenAlexW2884095533

What OpenQuestion holds

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LicenceCC BY
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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.