Performance Evaluation of Manual and Automated (MagNA Pure) Nucleic Acid Isolation in HPV Detection and Genotyping Using Roche Linear Array HPV Test

Nucleic acids of human papillomavirus (HPV) isolated by manual extraction method (AmpliLute) and automated MagNA pure system were compared and evaluated with cytohistological findings in 253 women. The concordance level between AmpliLute and MagNA was very good 93.3% (𝜅=0.864, 𝑃<.0001). Overall H...

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Main Authors: Aikaterini Chranioti, Evangelia Aga, Niki Margari, Christine Kottaridi, Asimakis Pappas, Ioannis Panayiotides, Petros Karakitsos
Format: Article
Language:English
Published: Hindawi Limited 2011-01-01
Series:Infectious Diseases in Obstetrics and Gynecology
Online Access:http://dx.doi.org/10.1155/2011/931281
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spelling doaj-1dd4bc067b094f8aa12180a66ad58c602020-11-24T22:38:49ZengHindawi LimitedInfectious Diseases in Obstetrics and Gynecology1064-74491098-09972011-01-01201110.1155/2011/931281931281Performance Evaluation of Manual and Automated (MagNA Pure) Nucleic Acid Isolation in HPV Detection and Genotyping Using Roche Linear Array HPV TestAikaterini Chranioti0Evangelia Aga1Niki Margari2Christine Kottaridi3Asimakis Pappas4Ioannis Panayiotides5Petros Karakitsos6Department of Diagnostic Cytopathology, University General Hospital “Attikon”, Rimini 1, Chaidari, 12462 Athens, GreeceDepartment of Diagnostic Cytopathology, University General Hospital “Attikon”, Rimini 1, Chaidari, 12462 Athens, GreeceDepartment of Diagnostic Cytopathology, University General Hospital “Attikon”, Rimini 1, Chaidari, 12462 Athens, GreeceDepartment of Diagnostic Cytopathology, University General Hospital “Attikon”, Rimini 1, Chaidari, 12462 Athens, Greece3rd Department of Obstetrics and Gynecology, University General Hospital “Attikon”, Rimini 1, Chaidari, 12462 Athens, Greece2nd Department of Pathology, University General Hospital “Attikon”, Rimini 1, Chaidari, 12462 Athens, GreeceDepartment of Diagnostic Cytopathology, University General Hospital “Attikon”, Rimini 1, Chaidari, 12462 Athens, GreeceNucleic acids of human papillomavirus (HPV) isolated by manual extraction method (AmpliLute) and automated MagNA pure system were compared and evaluated with cytohistological findings in 253 women. The concordance level between AmpliLute and MagNA was very good 93.3% (𝜅=0.864, 𝑃<.0001). Overall HPVpositivity detected by AmpliLute was 57.3% (30.4% as single and 27% as multiple infections) in contrast to MagNA 54.5% (32% and 23%, resp.). Discrepant results observed in 25 cases: 11 MagNA(−)/AmpliLute(+), 10 of which had positive histology; 5 MagNA(+)/AmpliLute(−) with negative histology; 8 MagNA(+)/AmpliLute(+): in 7 of which AmpliLute detected extra HPV genotypes and 1 MagNA(invalid)/AmpliLute(+) with positive histology. Both methods performed well when compared against cytological (area under curve (AUC) of AmpliLute 0.712 versus 0.672 of MagNA) and histological diagnoses (AUC of AmpliLute 0.935 versus 0.877 of MagNA), with AmpliLute showing a slightly predominance over MagNA. However, higher sensitivities, specificities, and positive/negative predictive values were obtained by AmpliLute.http://dx.doi.org/10.1155/2011/931281
collection DOAJ
language English
format Article
sources DOAJ
author Aikaterini Chranioti
Evangelia Aga
Niki Margari
Christine Kottaridi
Asimakis Pappas
Ioannis Panayiotides
Petros Karakitsos
spellingShingle Aikaterini Chranioti
Evangelia Aga
Niki Margari
Christine Kottaridi
Asimakis Pappas
Ioannis Panayiotides
Petros Karakitsos
Performance Evaluation of Manual and Automated (MagNA Pure) Nucleic Acid Isolation in HPV Detection and Genotyping Using Roche Linear Array HPV Test
Infectious Diseases in Obstetrics and Gynecology
author_facet Aikaterini Chranioti
Evangelia Aga
Niki Margari
Christine Kottaridi
Asimakis Pappas
Ioannis Panayiotides
Petros Karakitsos
author_sort Aikaterini Chranioti
title Performance Evaluation of Manual and Automated (MagNA Pure) Nucleic Acid Isolation in HPV Detection and Genotyping Using Roche Linear Array HPV Test
title_short Performance Evaluation of Manual and Automated (MagNA Pure) Nucleic Acid Isolation in HPV Detection and Genotyping Using Roche Linear Array HPV Test
title_full Performance Evaluation of Manual and Automated (MagNA Pure) Nucleic Acid Isolation in HPV Detection and Genotyping Using Roche Linear Array HPV Test
title_fullStr Performance Evaluation of Manual and Automated (MagNA Pure) Nucleic Acid Isolation in HPV Detection and Genotyping Using Roche Linear Array HPV Test
title_full_unstemmed Performance Evaluation of Manual and Automated (MagNA Pure) Nucleic Acid Isolation in HPV Detection and Genotyping Using Roche Linear Array HPV Test
title_sort performance evaluation of manual and automated (magna pure) nucleic acid isolation in hpv detection and genotyping using roche linear array hpv test
publisher Hindawi Limited
series Infectious Diseases in Obstetrics and Gynecology
issn 1064-7449
1098-0997
publishDate 2011-01-01
description Nucleic acids of human papillomavirus (HPV) isolated by manual extraction method (AmpliLute) and automated MagNA pure system were compared and evaluated with cytohistological findings in 253 women. The concordance level between AmpliLute and MagNA was very good 93.3% (𝜅=0.864, 𝑃<.0001). Overall HPVpositivity detected by AmpliLute was 57.3% (30.4% as single and 27% as multiple infections) in contrast to MagNA 54.5% (32% and 23%, resp.). Discrepant results observed in 25 cases: 11 MagNA(−)/AmpliLute(+), 10 of which had positive histology; 5 MagNA(+)/AmpliLute(−) with negative histology; 8 MagNA(+)/AmpliLute(+): in 7 of which AmpliLute detected extra HPV genotypes and 1 MagNA(invalid)/AmpliLute(+) with positive histology. Both methods performed well when compared against cytological (area under curve (AUC) of AmpliLute 0.712 versus 0.672 of MagNA) and histological diagnoses (AUC of AmpliLute 0.935 versus 0.877 of MagNA), with AmpliLute showing a slightly predominance over MagNA. However, higher sensitivities, specificities, and positive/negative predictive values were obtained by AmpliLute.
url http://dx.doi.org/10.1155/2011/931281
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