Development and validation of a nomogram predictive model for colorectal adenoma with low-grade intraepithelial neoplasia using routine laboratory tests: A single-center case-control study in China

被引:0
作者
Wang, Huaguang [1 ]
Liu, Xinjuan [2 ]
Long, Jiang [3 ]
Huang, Jincan [4 ]
Lyu, Shaocheng [4 ]
Zhao, Xin [4 ]
Zhao, Baocheng [5 ]
He, Qiang [4 ,6 ]
An, Zhuoling [1 ,6 ]
Hao, Jianyu [2 ,6 ]
机构
[1] Capital Med Univ, Beijing Chao Yang Hosp, Dept Pharm, Beijing 100020, Peoples R China
[2] Capital Med Univ, Beijing Chao Yang Hosp, Dept Gastroenterol, Beijing 100020, Peoples R China
[3] Beijing Univ Chinese Med, Dongzhimen Hosp, Beijing Minimally Invas Oncol Med Ctr Tradit Chine, Beijing 101121, Peoples R China
[4] Capital Med Univ, Beijing Chao Yang Hosp, Dept Hepatobiliary Surg, Beijing 100020, Peoples R China
[5] Capital Med Univ, Beijing Chao Yang Hosp, Dept Gen Surg, Beijing 100020, Peoples R China
[6] 8 Gongren Tiyuchang Nanlu, Beijing 100020, Peoples R China
关键词
Predictive model; Nomogram; Colorectal adenoma; Laboratory tests; Risk factor; DECISION CURVE ANALYSIS; METABOLIC SYNDROME; CANCER INCIDENCE; RISK; COLONOSCOPY; MORTALITY; MONOCYTES; MACROPHAGES; PREVENTION; DISEASES;
D O I
10.1016/j.heliyon.2023.e20996
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Colorectal cancer (CRC) is the third most common cancer in the world and has a high mortality rate. Colorectal adenoma (CRA) is precancerous lesions of CRC. The purpose of the present study was to construct a nomogram predictive model for CRA with low-grade intra-epithelial neoplasia (LGIN) in order to identify high-risk individuals, facilitating early diagnosis and treatment, and ultimately reducing the incidence of CRC. Methods: We conducted a single-center case-control study. Based on the results of colonoscopy and pathology, 320 participants were divided into the CRA group and the control group, the demographic and laboratory test data were collected. A development cohort (n = 223) was used for identifying the risk factors for CRA with LGIN and to develop a predictive model, followed by an internal validation. An independent validation cohort (n = 97) was used for external validation. Receiver operating characteristic curve, calibration plot and decision curve analysis were used to evaluate discrimination ability, accuracy and clinical practicability of the model. Results: Four predictors, namely sex, age, albumin and monocyte count, were included in the predictive model. In the development cohort, internal validation and external validation cohort, the area under the curve (AUC) of this risk predictive model were 0.946 (95%CI: 0.919-0.973), 0.909 (95 % CI: 0.869-0.940) and 0.928 (95%CI: 0.876-0.980), respectively, which demonstrated the model had a good discrimination ability. The calibration plots showed a good agreement and the decision curve analysis (DCA) suggested the predictive model had a high clinical net benefit. Conclusion: The nomogram model exhibited good performance in predicting CRA with LGIN, which can aid in the early detection of high-risk patients, improve early treatment, and ultimately reduce the incidence of CRC.
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页数:10
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