Dried blood spot self-sampling at home is a feasible technique for hepatitis C RNA detection

Autor: Anders Boyd, Janke Schinkel, Marc van der Valk, Tamara Prinsenberg, Freke R Zuure, Sjoerd Rebers, Maria Prins
Přispěvatelé: Graduate School, AII - Infectious diseases, APH - Global Health, Medical Microbiology and Infection Prevention, Infectious diseases, APH - Methodology, APH - Personalized Medicine, APH - Societal Participation & Health, APH - Digital Health
Jazyk: angličtina
Rok vydání: 2020
Předmět:
RNA viruses
Physiology
medicine.medical_treatment
RNA Stability
Hepacivirus
medicine.disease_cause
Pathology and Laboratory Medicine
Gastroenterology
Biochemistry
0302 clinical medicine
Immunodeficiency Viruses
Blood plasma
Medicine and Health Sciences
030212 general & internal medicine
Saline
Multidisciplinary
Hepatitis C virus
Viral Load
Hepatitis C
Dried blood spot
Body Fluids
Nucleic acids
Separation Processes
Blood
Medical Microbiology
Viral Pathogens
Viruses
Medicine
RNA
Viral

030211 gastroenterology & hepatology
Pathogens
Anatomy
Viral load
Research Article
medicine.medical_specialty
Science
Men WHO Have Sex with Men
Research and Analysis Methods
Microbiology
Blood Plasma
Specimen Handling
03 medical and health sciences
Internal medicine
Virology
Retroviruses
medicine
Genetics
Humans
Microbial Pathogens
Flaviviruses
business.industry
Lentivirus
Organisms
RNA
Biology and Life Sciences
HIV
Elution
Hepatitis viruses
People and Places
HIV-1
Population Groupings
Gene expression
Dried Blood Spot Testing
Reagent Kits
Diagnostic

business
Viral Transmission and Infection
Self sampling
Sexuality Groupings
Zdroj: PLoS ONE
PLoS ONE, Vol 15, Iss 4, p e0231385 (2020)
PLoS ONE, 15(4):e0231385. Public Library of Science
Popis: To facilitate HCV diagnosis, we developed an HCV-RNA testing service, which involved home-sampled dried blood spots (DBS). The main objective of this study was to evaluate the feasibility of self-sampling at home. Furthermore, to optimise the processing of DBS samples for RNA detection, we evaluated two elution buffers: phosphate-buffered saline (PBS) and L6-buffer. 27 HCV-RNA and 12 HIV-1 RNA positive patients were included. Laboratory spotted DBS (LabDBS) were made by a technician from blood samples drawn at inclusion. Patients received a DBS home-sampling kit and were requested to return their self-sampled DBS (ssDBS) by mail. We compared the RNA load of PBS and L6-eluted labDBS, and of L6-eluted ssDBS, L6-eluted labDBS and plasma. LabDBS load measurements were repeated after 7-13 and 14-21 days to evaluate RNA stability. All 39 plasma samples provided quantifiable RNA loads. In 1/39 labDBS sample, RNA could not be detected (plasma HCV load: 2.98 log10 IU/ml). L6-eluted samples gave a 0.7 log10 and 0.6 log10 higher viral load for HCV and HIV-1 respectively, compared to PBS-eluted samples. Strong correlations were found between labDBS and ssDBS HCV RNA (r = 0.833; mean difference 0.3 log10 IU/mL) and HIV-1 RNA results (r = 0.857; mean difference 0.1 log10 copies/mL). Correlations between labDBS and plasma values were high for HCV (r = 0.958) and HIV-1 (r = 0.844). RNA loads in DBS remained stable over 21 days. Our study demonstrates that self-sampling dried blood spots at home is a feasible strategy for the detection of HCV and HIV-1 RNA. This could facilitate one-step diagnostics and treatment monitoring in communities with high HCV prevalence.
Databáze: OpenAIRE