Home Projects Publications Presentations Repositories Photo Gallery Career
  • Turning The Pages Online
  • MyMorph
  • Medical Article Records GROUNDTRUTH (MARG)
  • MD on Tap
  • AnatQuest
Links to Feeds:
PublicationsRSS  RSS
CEB NewsRSS  RSS

Last updated: August 11, 2008

Staff Bibliography

Back to previousBack to previous  Print this Print this  E-mail this E-mail this

Document Abstract

Jeronimo J, Wentzensen N, Long R, Schiffman M, Dunn ST, Allen RA, Walker JL, Gold MA, Zuna RE, Sherman ME, Wacholder S, Wang SS.

Evaluation of Linear Array Human Papillomavirus Genotyping Using Automatic Optical Imaging Software.

JOURNAL OF CLINICAL MICROBIOLOGY. . August 2008;46(8):2759-65.

Variations in biological behavior suggest that each carcinogenic human papillomavirus (HPV) type should be considered individually in etiologic studies. HPV genotyping assays might have clinical applications if they are approved for use by the FDA. A widely used genotyping assay is the Roche Linear Array HPV genotyping test (LA). We used LA to genotype the HPV isolates from cervical specimens from women with the full spectrum of cervical disease: cervical cancer, cervical intraepithelial neoplasia (CIN), and HPV infections. To explore the feasibility and value of the automated reading of the LA results, we custom-designed novel, optical imaging software that provides optical density measurements of LA bands. We compared unmagnified visual examination with the automated measurements. The two measurements were highly associated. By either method, the threshold between a negative and a positive result was fairly sharp, with a clear bimodal distribution. Visually, most positive results were judged to be strong or medium, with fewer equivocal results categorized as weak (9.5% of positive samples), very weak (6.5% of positive samples), or extremely weak (7.7% of positive samples). The automated measurements of the intensities were significantly associated with the strength of the visual categories (P < 0.001). At the extremes of the automated signal intensities (< or = 20 units or > or = 120 units), the bands were almost always categorized visually as negative and positive, respectively. In the equivocal zone (20 to 119 units), specimens were more increasingly likely to be judged to be visually positive as the number of other, definite infections on the same strip increased (P for trend < 0.001). Multiple, concurrent infections comprise > or = 25% of HPV infections; thus, any systematic visual tendency that influences their evaluation when the result is equivocal should be minimized. Therefore, automated reading is probably worth development if easy-to-calibrate hardware and software can be optimized.



More about this article:

Full Text (PDF) | View Citation

 

National Institutes of Health (NIH)National Institutes of Health (NIH)
9000 Rockville Pike
Bethesda, Maryland 20892

U.S. Dept. of Health and Human ServicesU.S. Dept. of Health
and Human Services

USA.gov Website