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DOI 10.7314/apjcp.2015.16.14.5843

Медицинская библиотека · Asian Pacific journal of cancer prevention : APJCP · 2015

Value of PAX1 Methylation Analysis by MS-HRM in the Triage of Atypical Squamous Cells of Undetermined Significance.

Li Shi-Rong, Wang Zhen-Ming, Wang Yu-Hui, Wang Xi-Bo, Zhao Jian-Qiang, Xue Hai-Bin, Jiang Fu-Guo

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND

Detection of cervical high grade lesions in patients with atypical squamous cells of undetermined significance (ASCUS) is still a challenge. Our study tested the efficacy of the paired boxed gene 1 (PAX1) methylation analysis by methylation-sensitive high-resolution melting (MS-HRM) in the detection of high grade lesions in ASCUS and compared performance with the hybrid capture 2 (HC2) human papillomavirus (HPV) test.

MATERIALS AND

METHODS

A total of 463 consecutive ASCUS women from primary screening were selected. Their cervical scrapings were collected and assessed by PAX1 methylation analysis (MS-HRM) and high-risk HPV-DNA test (HC2). All patients with ASCUS were admitted to colposcopy and cervical biopsies. The Chi- square test was used to test the differences of PAX1 methylation or HPV infection between groups.

RESULTS

The specificity, sensitivity, and accuracy for detecting CIN2 + lesions were: 95.6%, 82.4%, and 94.6%, respectively, for the PAX1 MS-HRM test; and 59.7%, 64.7%, and 60.0% for the HC2 HPV test.

CONCLUSIONS

The PAX1 methylation analysis by MS-HRM demonstrated a better performance than the high-risk HPV-DNA test for the detection of high grade lesions (CIN2 +) in ASCUS cases. This approach could screen out the majority of low grade cases of ASCUS, and thus reduce the referral rate to colposcopy.

Для цитирования: Li Shi-Rong, Wang Zhen-Ming, Wang Yu-Hui, Wang Xi-Bo, Zhao Jian-Qiang, Xue Hai-Bin, Jiang Fu-Guo. Value of PAX1 Methylation Analysis by MS-HRM in the Triage of Atypical Squamous Cells of Undetermined Significance.. Asian Pacific journal of cancer prevention : APJCP. 2015. DOI: 10.7314/apjcp.2015.16.14.5843.

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