Evidence map›Paper›PMID 31318908›Full record

Observational studyPloS one2019

Improvement in detecting cytomegalovirus drug resistance mutations in solid organ transplant recipients with suspected resistance using next generation sequencing.

Rubén López-Aladid, Alba Guiu, Maria Mar Mosquera, Francisco López-Medrano, Frederic Cofán, Laura Linares, Julián Torre-Cisneros, Elisa Vidal, Asunción Moreno, Jose María Aguado and 18 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

18 citing papers in PubMed, 35 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

28 authors at 14 institutions in 2 countries.

Rubén López-AladidDepartment of Clinical Microbiology, Hospital Clinic, Universidad de Barcelona, Institute for Global Health, (ISGlobal), Barcelona, Spain.
Alba GuiuDepartment of Clinical Microbiology, Hospital Clinic, Universidad de Barcelona, Institute for Global Health, (ISGlobal), Barcelona, Spain.
Maria Mar MosqueraDepartment of Clinical Microbiology, Hospital Clinic, Universidad de Barcelona, Institute for Global Health, (ISGlobal), Barcelona, Spain.
Francisco López-MedranoUnit of Infectious Diseases, Instituto de Investigación Hospital 12 Octubre (i + 12) University Hospital 12 de Octubre, Universidad Complutense, Madrid, Spain.
Frederic CofánDepartment of Nephrology and Renal Transplant, Hospital Clinic, Universidad de Barcelona, Barcelona, Spain.
Laura LinaresDepartment of Infectious Diseases, Hospital Clinic, Institut d'Investigacions Biomediques August Pi I Sunyer (IDIBAPS), Universidad de Barcelona, Barcelona, Spain.
Julián Torre-CisnerosClinical Unit of Infectious Diseases, Hospital Universitario Reina Sofia-IMIBIC-UCO, Córdoba, Spain.
Elisa VidalClinical Unit of Infectious Diseases, Hospital Universitario Reina Sofia-IMIBIC-UCO, Córdoba, Spain.
Asunción MorenoDepartment of Infectious Diseases, Hospital Clinic, Institut d'Investigacions Biomediques August Pi I Sunyer (IDIBAPS), Universidad de Barcelona, Barcelona, Spain.
Jose María AguadoUnit of Infectious Diseases, Instituto de Investigación Hospital 12 Octubre (i + 12) University Hospital 12 de Octubre, Universidad Complutense, Madrid, Spain.
Elisa CorderoDepartment of Infectious Diseases, Instituto de Biomedicina de Sevilla (IBIS), University Hospital Virgen del Rocío, Sevilla, Spain.
Cecilia Martin-GandulDepartment of Infectious Diseases, Instituto de Biomedicina de Sevilla (IBIS), University Hospital Virgen del Rocío, Sevilla, Spain.
Jordi CarrataláDepartment of Infectious Diseases, Bellvitge University Hospital, IDIBELL, Barcelona, Spain.
Nuria SabéDepartment of Infectious Diseases, Bellvitge University Hospital, IDIBELL, Barcelona, Spain.
Jordi NiubóDepartment of Clinical Microbiology, Bellvitge University Hospital, IDIBELL, Barcelona, Spain.
Carlos CerveraDepartment of Medicine, Division of Infectious Diseases, University of Alberta, Edmonton, Canada.ORCID 0000-0002-0161-1749
Alicia CapónDepartment of Clinical Microbiology, Hospital Clinic, Universidad de Barcelona, Institute for Global Health, (ISGlobal), Barcelona, Spain.
Anna CervillaDepartment of Clinical Microbiology, Hospital Clinic, Universidad de Barcelona, Institute for Global Health, (ISGlobal), Barcelona, Spain.
Marta SantosDepartment of Clinical Microbiology, Hospital Clinic, Universidad de Barcelona, Institute for Global Health, (ISGlobal), Barcelona, Spain.ORCID 0000-0001-5270-4454
Marta BodroDepartment of Infectious Diseases, Hospital Clinic, Institut d'Investigacions Biomediques August Pi I Sunyer (IDIBAPS), Universidad de Barcelona, Barcelona, Spain.
Patricia MuñozDepartment of Clinical Microbiology and Infectious Diseases, Hospital General Universitario Gregorio Marañón, Instituto de Investigación Sanitario Gregorio Marañón, Madrid, Spain.
Maria Carmen FariñasUnit of Infectious Diseases, University Hospital Marqués de Valdecilla, Universidad de Cantabria, Santander, Spain.
Andrés AntónMicrobiology Service, Hospital Vall d'Hebron, Barcelona, Spain.
Maitane AranzamendiMicrobiology Service, Hospital Universitario de Cruces, Bilbao, Spain.
Miguel MontejoDepartment of Infectious Diseases, Hospital Universitario de Cruces, Bilbao, Spain.
Pilar Pérez-RomeroNational Center for Microbiology, Instituto de Salud Carlos III, Majadahonda, Madrid, Spain.
Oscar LenDepartment of Infectious Diseases, Hospital Universitari Vall d'Hebrón, Uniiversidad Autónoma de Barcelona, Barcelona, Spain.
Maria Ángeles MarcosDepartment of Clinical Microbiology, Hospital Clinic, Universidad de Barcelona, Institute for Global Health, (ISGlobal), Barcelona, Spain.ORCID 0000-0001-8250-3311
Barcelona Institute for Global Health · ESBellvitge University Hospital · ESConsorci Institut D'Investigacions Biomediques August Pi I Sunyer · ESHospital de Cruces · ESInstituto de Biomedicina de Sevilla · ESInstituto Maimónides de Investigación Biomédica de Córdoba · ESResearch Institute Hospital 12 de Octubre · ESHospital General Universitario Gregorio Marañón · ESInstituto de Salud Carlos III · ESUniversidad de Cantabria · ESUniversitat Autònoma de Barcelona · ESUniversitat de Barcelona · ESUniversity of Alberta · CAVall d'Hebron Hospital Universitari · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objetivesThe aim of this study was to identify CMV drug resistance mutations (DRM) in solid organ transplant (SOT) recipients with suspected resistance comparing next-generation sequencing (NGS) with Sanger sequencing and assessing risk factors and the clinical impact of resistance.

methodsUsing Sanger sequencing as the reference method, we prospectively assessed the ability of NGS to detect CMV DRM in the UL97 and UL54 genes in a nationwide observational study from September 2013 to August 2016.

resultsAmong 44 patients recruited, 14 DRM were detected by Sanger in 12 patients (27%) and 20 DRM were detected by NGS, in 16 (36%). NGS confirmed all the DRM detected by Sanger. The additional six mutations detected by NGS were present in <20% of the sequenced population, being located in the UL97 gene and conferring high-level resistance to ganciclovir. The presence of DRM by NGS was associated with lung transplantation (p = 0.050), the administration of prophylaxis (p = 0.039), a higher mean time between transplantation and suspicion of resistance (p = 0.038) and longer antiviral treatment duration before suspicion (p = 0.024). However, the latter was the only factor independently associated with the presence of DRM by NGS in the multivariate analysis (OR 2.24, 95% CI 1.03 to 4.87).

conclusionsNGS showed a higher yield than Sanger sequencing for detecting CMV resistance mutations in SOT recipients. The presence of DRM detected by NGS was independently associated with longer antiviral treatment.

Indexed as

Transplant RecipientsCytomegalovirusDrug Resistance, ViralFemaleGenes, ViralHigh-Throughput Nucleotide SequencingHumansMaleMiddle AgedMutation

Identifiers

PMID31318908
PMCPMC6638921
OpenAlexW2963435216

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.