Dried Blood Spot Specimens Are a Suitable Alternative Sample Type for HIV-1 Viral Load Measurement and Drug Resistance Genotyping in Patients Receiving First-Line Antiretroviral Therapy
Supporting Files
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4 2012
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File Language:
English
Details
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Alternative Title:Clin Infect Dis
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Personal Author:
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Description:Background.
Antiretroviral therapy (ART) is being administered in developing nations at unprecedented numbers following the World Health Organization’s (WHO) development of standardized first-line drug regimens. To ensure continued efficacy of these drug regimens, WHO recommends monitoring virological responses and development of human immunodeficiency virus (HIV) drug resistance (HIVDR) in HIV-infected patients in a prospective cohort. The current study compared dried fluid spot specimens with the reference standard plasma specimens as a practical tool for viral load (VL) and HIVDR genotyping in resource-limited settings.
Methods.
Dried blood spot (DBS), dried plasma spot (DPS), and plasma specimens were collected from 173 –patients receiving ART at 2 hospital sites in Abuja, Nigeria. HIV-1 VL analysis was performed using NucliSENS EasyQ HIV-1 v1.1 RUO test kits. Genotyping of the HIV-1 pol gene was performed using a broadly sensitive in-house assay.
Results.
Direct comparison of VL levels showed that DBS specimens, and not DPS specimens, gave results comparable to those of plasma specimens (P = .0619 and .0007, respectively); however, both DBS and DPS specimens had excellent correlation with plasma specimens in predicting virological failure (VL, ≥1000 copies/mL) in patients (κ = 0.78 and 0.83, respectively). Of the 18 specimens with a plasma VL ≥1000 copies/mL, HIVDR genotyping rates were 100% in DBS and 38.9% in DPS specimens, and DBS specimens identified 61 of 65 HIVDR mutations (93.8%) identified in plasma specimens.
Conclusions.
Our results indicate that DBS specimens could be used for surveys to monitor HIVDR prevention failure in resource-limited settings.
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Subjects:
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Source:Clin Infect Dis. 54(8):1187-1195
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Pubmed ID:22412066
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Pubmed Central ID:PMC11528918
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Document Type:
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Funding:
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Volume:54
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Issue:8
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Collection(s):
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Main Document Checksum:urn:sha-512:9d044c0017a4e1a632fb1a3348b8c794101a38c2b2beb5227647b62d28a74ce067f951d265682851f470e361d11fd9cb95f6b54240f04e765d673f73be56aa13
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Download URL:
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File Type:
Supporting Files
File Language:
English
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