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Analysis of SARS-CoV-2 reverse transcription-quantitative polymerase chain reaction cycle threshold values vis-à-vis anti-SARS-CoV-2 antibodies from a high incidence region.
Markewitz, Robert; Torge, Antje; Wandinger, Klaus-Peter; Pauli, Daniela; Dargvainiene, Justina; Franke, Andre; Bujanda, Luis; Marimón, José Maria; Banales, Jesus M; Gutierrez-Stampa, María A; Nafría, Beatriz; Junker, Ralf.
  • Markewitz R; Institute of Clinical Chemistry, University Hospital Schleswig-Holstein, Kiel, Lübeck, Germany. Electronic address: robert.markewitz@uksh.de.
  • Torge A; Institute of Clinical Chemistry, University Hospital Schleswig-Holstein, Kiel, Lübeck, Germany.
  • Wandinger KP; Institute of Clinical Chemistry, University Hospital Schleswig-Holstein, Kiel, Lübeck, Germany.
  • Pauli D; Institute of Clinical Chemistry, University Hospital Schleswig-Holstein, Kiel, Lübeck, Germany.
  • Dargvainiene J; Institute of Clinical Chemistry, University Hospital Schleswig-Holstein, Kiel, Lübeck, Germany.
  • Franke A; Institute of Clinical Molecular Biology, Christian-Albrechts-University of Kiel & University Hospital Schleswig-Holstein, Kiel, Germany.
  • Bujanda L; Department of Liver and Gastrointestinal Diseases, Biodonostia Health Research Institute - Donostia University Hospital, San Sebastián, Spain; National Institute for the Study of Liver and Gastrointestinal Diseases (CIBERehd, "Instituto de Salud Carlos III"), University of the Basque Country (UPV/EH
  • Marimón JM; Biodonostia Health Research Institute, Infectious Diseases Area, Respiratory Infection and Antimicrobial Resistance Group, Osakidetza Basque Health Service, Donostialdea Integrated Health Organisation, Microbiology Department, San Sebastián, Spain.
  • Banales JM; Department of Liver and Gastrointestinal Diseases, Biodonostia Health Research Institute - Donostia University Hospital, San Sebastián, Spain; National Institute for the Study of Liver and Gastrointestinal Diseases (CIBERehd, "Instituto de Salud Carlos III"), University of the Basque Country (UPV/EH
  • Gutierrez-Stampa MA; Osakidetza, OSI Donostialdea, Altza Primary Care; Biodonostia Health Research Institute, San Sebastián, Spain.
  • Nafría B; Clinical Biochemistry Department, Biodonostia Health Research Institute Osakidetza Basque Health Service, Donostialdea Integrated Health Organisation. San Sebastián, Spain.
  • Junker R; Institute of Clinical Chemistry, University Hospital Schleswig-Holstein, Kiel, Lübeck, Germany.
Int J Infect Dis ; 110: 114-122, 2021 Sep.
Article in English | MEDLINE | ID: covidwho-1349465
ABSTRACT

OBJECTIVES:

To examine the relationship between antibody status and cycle threshold (Ct) values, the prognostic value of the latter for COVID-19 patients, and the inter-assay comparability of SARS-CoV-2 Ct values.

METHODS:

In 347 COVID-19 inpatients, SARS-CoV-2 Ct values (via reverse transcription-quantitative polymerase chain reaction) on admission were compared between 2 assays and correlated with the antibody response (in the course of the disease), the clinical course and the time since onset of symptoms.

RESULTS:

Ct values for 2 of 3 target genes showed significant differences between the 2 assays used (P=0.012 and P<0.0001). Ct values were significantly higher for antibody positive patients (P<0.0001) and positively correlated with the amount of time since onset of symptoms (R 0.332-0.363; P<0.001). Patients with fatal outcomes showed higher viral loads than survivors (P<0.0001).

CONCLUSIONS:

Ct values depend strongly on assay used and target gene examined and should not be used as quantitative values to guide therapeutic or diagnostic decisions. The inverse association between antibody status and viral load suggests that antibodies contribute to the elimination of the virus, independent of the outcome, which is influenced by the viral load on admission and might depend more strongly on other parts of the immune response.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Observational study / Prognostic study Limits: Humans Language: English Journal: Int J Infect Dis Journal subject: Communicable Diseases Year: 2021 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Observational study / Prognostic study Limits: Humans Language: English Journal: Int J Infect Dis Journal subject: Communicable Diseases Year: 2021 Document Type: Article