Literature DB >> 2537262

Inter-laboratory variation as an explanation for varying prevalence estimates of human papillomavirus infection.

J Brandsma1, R D Burk, W D Lancaster, H Pfister, M H Schiffman.   

Abstract

Human papillomavirus (HPV) infection has been strongly implicated as a cause of genital neoplasia. Although Southern blot DNA hybridization techniques are regarded as the most accurate means of identifying HPV infection, studies using this technique to measure infection have provided varying estimates of the prevalence of HPV among healthy and diseased groups. This investigation provides a possible explanation for study-to-study differences, by demonstrating inter-laboratory variability in the detection and typing of HPV by Southern blot. Four experienced laboratories tested 40 identical, masked samples of DNA extracted from presumed infected and non-infected tissues. The pairwise percentage agreement between the laboratories in judging samples as HPV-positive or negative ranged from 66 to 97%. Among samples judged to contain HPV, agreement as to type ranged from 77 to 96%. We conclude that inter-laboratory differences are an important consideration in any discussion of HPV prevalence estimates.

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Year:  1989        PMID: 2537262     DOI: 10.1002/ijc.2910430216

Source DB:  PubMed          Journal:  Int J Cancer        ISSN: 0020-7136            Impact factor:   7.396


  12 in total

1.  Comparison of ViraPap, Southern hybridization, and polymerase chain reaction methods for human papillomavirus identification in an epidemiological investigation of cervical cancer.

Authors:  E Guerrero; R W Daniel; F X Bosch; X Castellsagué; N Muñoz; M Gili; P Viladiu; C Navarro; M L Zubiri; N Ascunce
Journal:  J Clin Microbiol       Date:  1992-11       Impact factor: 5.948

Review 2.  Use of the polymerase chain reaction to study the relationship between human papillomavirus infections and cervical cancer.

Authors:  W J Melchers; H C Claas; W G Quint
Journal:  Eur J Clin Microbiol Infect Dis       Date:  1991-09       Impact factor: 3.267

3.  Evaluation of immunoassays for the detection and typing of PCR amplified human papillomavirus DNA.

Authors:  S Venturoli; M Zerbini; M La Placa; A D'Antuono; M Negosanti; G Gentilomi; G Gallinella; E Manaresi; M Musiani
Journal:  J Clin Pathol       Date:  1998-02       Impact factor: 3.411

4.  Use of AffiProbe HPV test kit for detection of human papillomavirus DNA in genital scrapes.

Authors:  M Ranki; A W Leinonen; T Jalava; P Nieminen; V R Soares; J Paavonen; A Kallio
Journal:  J Clin Microbiol       Date:  1990-09       Impact factor: 5.948

5.  Human papillomaviruses in anogenital warts in children.

Authors:  C J Lacey; P E Gibson; E C Benton
Journal:  BMJ       Date:  1990-07-28

6.  The Association of Beta-catenin Gene Mutations and Human Papillomavirus in Carcinoma of Esophagus in a High-Risk Population of India.

Authors:  Mohammad Muzaffar Mir; Javid Ahmad Dar; Nazir Ahmad Dar; A T Syed; Irfana Salam; Ghulam Nabi Lone
Journal:  Int J Health Sci (Qassim)       Date:  2007-07

7.  Comparative study of various forms of urinary diversion after radical cystectomy in muscle invasive carcinoma urinary bladder.

Authors:  Y Sherwani Afak; B S Wazir; Arif Hamid; M S Wani; Rafia Aziz
Journal:  Int J Health Sci (Qassim)       Date:  2009-01

8.  Accuracy and interlaboratory reliability of human papillomavirus DNA testing by hybrid capture.

Authors:  M H Schiffman; N B Kiviat; R D Burk; K V Shah; R W Daniel; R Lewis; J Kuypers; M M Manos; D R Scott; M E Sherman
Journal:  J Clin Microbiol       Date:  1995-03       Impact factor: 5.948

9.  Analysis of human papillomavirus types in exophytic condylomata acuminata by hybrid capture and Southern blot techniques.

Authors:  D R Brown; J T Bryan; H Cramer; K H Fife
Journal:  J Clin Microbiol       Date:  1993-10       Impact factor: 5.948

10.  Comparison of dot filter hybridization, Southern transfer hybridization, and polymerase chain reaction amplification for diagnosis of anal human papillomavirus infection.

Authors:  J M Kuypers; C W Critchlow; P E Gravitt; D A Vernon; J B Sayer; M M Manos; N B Kiviat
Journal:  J Clin Microbiol       Date:  1993-04       Impact factor: 5.948

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