Author: Loke, Sau Yeen; Munusamy, Prabhakaran; Koh, Geok Ling; Chan, Claire Hian Tzer; Madhukumar, Preetha; Thung, Jee Liang; Tan, Kiat Tee Benita; Ong, Kong Wee; Yong, Wei Sean; Sim, Yirong; Oey, Chung Lie; Lim, Sue Zann; Chan, Mun Yew Patrick; Ho, Teng Swan Juliana; Khoo, Boon Kheng James; Wong, Su Lin Jill; Thng, Choon Hua; Chong, Bee Kiang; Tan, Ern Yu; Tan, Veronique Kiak-Mien; Lee, Ann Siew Gek
Title: A Circulating miRNA Signature for Stratification of Breast Lesions among Women with Abnormal Screening Mammograms Cord-id: 4qsyikk5 Document date: 2019_11_26
ID: 4qsyikk5
Snippet: Although mammography is the gold standard for breast cancer screening, the high rates of false-positive mammograms remain a concern. Thus, there is an unmet clinical need for a non-invasive and reliable test to differentiate between malignant and benign breast lesions in order to avoid subjecting patients with abnormal mammograms to unnecessary follow-up diagnostic procedures. Serum samples from 116 malignant breast lesions and 64 benign breast lesions were comprehensively profiled for 2,083 mic
Document: Although mammography is the gold standard for breast cancer screening, the high rates of false-positive mammograms remain a concern. Thus, there is an unmet clinical need for a non-invasive and reliable test to differentiate between malignant and benign breast lesions in order to avoid subjecting patients with abnormal mammograms to unnecessary follow-up diagnostic procedures. Serum samples from 116 malignant breast lesions and 64 benign breast lesions were comprehensively profiled for 2,083 microRNAs (miRNAs) using next-generation sequencing. Of the 180 samples profiled, three outliers were removed based on the principal component analysis (PCA), and the remaining samples were divided into training (n = 125) and test (n = 52) sets at a 70:30 ratio for further analysis. In the training set, significantly differentially expressed miRNAs (adjusted p < 0.01) were identified after correcting for multiple testing using a false discovery rate. Subsequently, a predictive classification model using an eight-miRNA signature and a Bayesian logistic regression algorithm was developed. Based on the receiver operating characteristic (ROC) curve analysis in the test set, the model could achieve an area under the curve (AUC) of 0.9542. Together, this study demonstrates the potential use of circulating miRNAs as an adjunct test to stratify breast lesions in patients with abnormal screening mammograms.
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