Evidence map›Paper›PMID 41209046›Full record

ArticleInternational journal of women's health2025

High Grade Squamous Intraepithelial Lesion (HSIL) Positive Disease Risk Nomogram Model: A Single Centre Retrospective Analysis.

Qiu-Zhen Wu, Mao-Hua Lin, Jian-Rui Zheng, Xiu-Qing Weng, Li-Li Zheng, Ying-Yu Mao

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Article in International journal of women's health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Qiu-Zhen WuDepartment of Pathology, Mindong Hospital Affiliated to Fujian Medical University, Fuan, 355000, People's Republic of China.
Mao-Hua LinDepartment of Pathology, Mindong Hospital Affiliated to Fujian Medical University, Fuan, 355000, People's Republic of China.
Jian-Rui ZhengDepartment of Pathology, Mindong Hospital Affiliated to Fujian Medical University, Fuan, 355000, People's Republic of China.
Xiu-Qing WengDepartment of Pathology, Mindong Hospital Affiliated to Fujian Medical University, Fuan, 355000, People's Republic of China.
Li-Li Zheng *Department of Gynecology, Mindong Hospital Affiliated to Fujian Medical University, Fuan, 355000, People's Republic of China.
Ying-Yu Mao *Department of Pathology, Mindong Hospital Affiliated to Fujian Medical University, Fuan, 355000, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: To develop and validate a nomogram for predicting high-grade squamous intraepithelial lesions or worse (HSIL+), incorporating results from ThinPrep cytologic test (TCT) and Aptima HPV E6/E7 mRNA (AHPV) testing. Patients and Methods: This diagnostic study consecutively enrolled 3,202 patients referred for colposcopy due to abnormal cervical screening results. All participants underwent colposcopy with biopsy (targeted and/or endocervical) to obtain a definitive histopathological result, which served as the reference standard. The cohort was randomly split into training (70%) and validation (30%) sets. A binary logistic regression model was developed, and a nomogram was constructed. Model performance was evaluated using receiver operating characteristic (ROC) curves, calibration plots, and decision curve analysis (DCA). Results: The final multivariate model was defined by the equation: Logit(P) = -4.014 + 1.677 × OHR + 2.917 × HPV16 + 1.938 × HPV18/45 + 2.343 × HPV(16+18/45) + 0.326 × ASC-US + 1.676 × ASC-H + 1.161 × LSIL + 1.593 × AGC + 4.939 × ≥HSIL. A nomogram was developed using the R rms package. The model demonstrated excellent discrimination in internal validation, with areas under the ROC curves (AUCs) of 0.843 (95% CI: 0.824-0.863) in the training set and 0.833 (95% CI: 0.813-0.873) in the validation set, along with good calibration. DCA confirmed its clinical utility across a risk threshold of 2%-50%. Conclusion: The developed logistic-nomogram provides an accurate and practical tool for predicting HSIL+, potentially aiding in individualized clinical management.

Indexed as

AHPVcervical cancer screeningHSIL+nomogramTCT

Identifiers

PMID41209046
PMCPMC12595985

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