Evaluation of genital sites and sampling techniques for detection of human papillomavirus DNA in men

被引:197
作者
Weaver, BA
Feng, QH
Holmes, KK
Kiviat, N
Lee, SK
Meyer, C
Stern, M
Koutsky, LA
机构
[1] Univ Washington, Harborview Med Ctr, Dept Med, Ctr AIDS & STD Res, Seattle, WA 98104 USA
[2] Univ Washington, HPV Res Lab, Seattle, WA 98104 USA
[3] Univ Washington, Dept Pathol, HPV Res Grp, Seattle, WA 98104 USA
[4] Univ Washington, Dept Biostat, HPV Res Grp, Seattle, WA 98104 USA
[5] Univ Washington, Hall Hlth Primary Care Ctr, Seattle, WA 98104 USA
[6] Univ Washington, Dept Epidemiol, HPV Res Grp, Seattle, WA 98104 USA
关键词
D O I
10.1086/381395
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
To evaluate methods for detection of genital human papillomavirus (HPV) DNA in men, samples were obtained from 3 consecutive groups of 10 men attending a sexually transmitted disease clinic by use of (1) a saline-wetted Dacron swab alone, (2) a saline-wetted cytobrush, or (3) emery paper (600A-grit Wetordry Tri-M-ite; 3M) abrasion followed by a saline-wetted Dacron swab. By use of a polymerase chain reaction-based assay, 45% of emery-paper samples were found to be positive for beta-globin, compared with 23% of swab-alone and 0% of cytobrush samples. Subsequently, emery paper and saline-wetted Dacron swabs were used to obtain penile shaft, glans, foreskin, and scrotum samples from 318 male university students. Urine samples were also obtained. Of 1323 samples tested, 1288 (97%) were found to be positive for beta-globin. HPV DNA was detected in samples from 104 men (33%): 24% from the penile shaft, 16% from the glans, 28% from the foreskin, 17% from the scrotum, and 6% in urine. The HPV prevalence was similar for circumcised and uncircumcised men. Testing multiple sites increased the number of men for whom HPV DNA was detected.
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页码:677 / 685
页数:9
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