Cited by 38Cytomegalovirus and herpesvirus researchHerpesvirus Infections and TreatmentsViral-associated cancers and disorders

The DOI matches its Crossref record; 21 of the 21 references it cites were found in a registry or an index.

Clinical Significance of Low Cytomegalovirus DNA Levels in Human Plasma

Open access
Waggoner, Jesse, Ho, Dora Y., Libiran, Paolo, Pinsky, Benjamin A.·2012·Journal of Clinical Microbiology

Abstract

The clinical significance of the detection of low copy numbers of cytomegalovirus (CMV) DNA in immune-suppressed patients remains unclear. In this study, we compared the artus CMV Rotor-Gene PCR, utilizing an automated nucleic acid extraction and assay setup (the artus CMV protocol), with the COBAS Amplicor CMV Monitor test (our reference protocol). We then analyzed the results of all CMV PCR tests ordered following the implementation of the artus CMV protocol at our institution and followed 91 adult patients with positive test results. The artus CMV protocol had a linear range extending from 2.0 to 7.0 log(10) copies/ml and had a lower limit of 95% detection of 57 copies/ml. With archived plasma samples, this protocol demonstrated 100% sensitivity and 94% specificity for the detection of CMV DNA. Following implementation of the artus CMV protocol, 320 of 1,403 (22.8%) plasma samples tested positive (compared with 323/3,579 [9.0%] samples in the preceding 6 months), and 227 (16.2%) samples had copy numbers of <400/ml. Ninety-one adult patients had at least one positive test. The data were analyzed using a threshold of 200 copies/ml, and in 22 episodes, the viral load increased from <200 copies/ml to ≥ 200 copies/ml on sequential tests. In 21 of these 22 episodes, either the viral load continued to increase or antiviral treatment was initiated in response to the repeat value. In summary, we evaluate the performance characteristics of a protocol utilizing the artus CMV PCR and identify clinically meaningful changes in CMV DNA copy numbers even when they are initially detected at a low level.

Overview

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Crossref · 10.1128/jcm.06800-11

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21 of 21 references verified0 citation errors · 0 not checkable

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Research works printed but not linked: 2

  1. Argene, Inc. 2012. CMV R-gene product information. Argene, Inc., Shirley, NY.
  2. College of American Pathologists. 2011. VLS-A, viral load participant summary. Surveys and Anatomic Pathology Education Programs, Northfield, IL.

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Metadata

Authors
Waggoner, J., Ho, D. Y., Libiran, P., & Pinsky, B. A.
Affiliations
Stanford Medicine (US)
Venue
Journal of Clinical Microbiology
Published
2012-07
Volume
50
Issue
7
Pages
2378-2383
ISSN
  • 0095-1137 (ISSN-L)
  • 1098-660X
OpenAlex
W2007125953
Cited by
38
References
21
Citations by year
2025: 1 · 2024: 3 · 2023: 3 · 2022: 1 · 2021: 2 · 2020: 1 · 2019: 4 · 2018: 2 · 2017: 2 · 2016: 5 · 2015: 3 · 2014: 4 · 2013: 4 · 2012: 3
FWCI
3.34
Type
journal article
Language
en
Open access
Locations
  • Journal of Clinical Microbiology (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Epidemiology › Cytomegalovirus and herpesvirus research
  • Health Sciences › Medicine › Infectious Diseases › Herpesvirus Infections and Treatments
  • Health Sciences › Medicine › Oncology › Viral-associated cancers and disorders
Keywords
cytomegalovirus, low viral load, immunocompromised patients, viral load threshold, antiviral treatment initiation
MeSH terms
Adult, Aged, Automation, Cytomegalovirus Infections, Cytomegalovirus, DNA, Viral, Female, Humans, Male, Middle Aged, Plasma, Sensitivity and Specificity, Virology, Immunocompromised Host, Viral Load, Molecular Diagnostic Techniques

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