Exploratory research on developing lung cancer risk prediction model in female non-smokers
Objective: To develop a lung cancer risk prediction model for female non-smokers. Methods: Based on the Kailuan prospective dynamic cohort (2006.05-2015.12), a nested case-control study was conducted. Participants diagnosed with primary pathologically confirmed lung cancer during follow-up were identified as the case group, and others were identified as the control group. A total of 24 701 subjects were included in the study, including 86 lung cancer cases and 24 615 control population, respectively. Questionnaires, physical examinations, and laboratory tests were conducted to collect relevant information. Multivariable-adjusted logistic regressions were conducted to develop a lung cancer risk prediction model. Area Under the Curve (AUC) and Hosmer-Lemeshow tests were used to evaluate discrimination and calibration, respectively. Ten-fold cross-validation was used for internal validation. Results: Two sets of models were developed: the simple model (including age and monthly income) and the metabolic index model [including age, monthly income, fasting blood glucose (FBG), total cholesterol (TC) and high-density lipoprotein cholesterol (HDL-C)].The AUC (95%CI) [0.745 (0.719-0.771)] of the metabolic index model was higher than that of the simple prediction model [0.688 (0.660-0.716)] (P=0.004). Both the simple model (PHL=0.287) and the metabolic index model (PHL=0.134) were well-calibrated. The results of ten-fold cross-validation indicated sufficient stability, with an average AUC of 0.699 and a standard error (SD) of 0.010. Conclusion: By incorporating metabolic markers, accurate and reliable lung cancer risk prediction model for female non smokers could be developed.
| Medienart: |
E-Artikel |
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| Erscheinungsjahr: |
2020 |
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| Erschienen: |
2020 |
| Enthalten in: |
Zur Gesamtaufnahme - volume:54 |
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| Enthalten in: |
Zhonghua yu fang yi xue za zhi [Chinese journal of preventive medicine - 54(2020), 11 vom: 06. Nov., Seite 1261-1267 |
| Sprache: |
Chinesisch |
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| Beteiligte Personen: |
Lyu, Z Y [VerfasserIn] |
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| Links: |
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| Themen: |
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| Anmerkungen: |
Date Completed 06.11.2020 Date Revised 06.11.2020 published: Print Citation Status MEDLINE |
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| doi: |
10.3760/cma.j.cn112150-20200805-01093 |
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| funding: |
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| Förderinstitution / Projekttitel: |
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| PPN (Katalog-ID): |
NLM317161385 |
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| 245 | 1 | 0 | |a Exploratory research on developing lung cancer risk prediction model in female non-smokers |
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| 500 | |a Date Completed 06.11.2020 | ||
| 500 | |a Date Revised 06.11.2020 | ||
| 500 | |a published: Print | ||
| 500 | |a Citation Status MEDLINE | ||
| 520 | |a Objective: To develop a lung cancer risk prediction model for female non-smokers. Methods: Based on the Kailuan prospective dynamic cohort (2006.05-2015.12), a nested case-control study was conducted. Participants diagnosed with primary pathologically confirmed lung cancer during follow-up were identified as the case group, and others were identified as the control group. A total of 24 701 subjects were included in the study, including 86 lung cancer cases and 24 615 control population, respectively. Questionnaires, physical examinations, and laboratory tests were conducted to collect relevant information. Multivariable-adjusted logistic regressions were conducted to develop a lung cancer risk prediction model. Area Under the Curve (AUC) and Hosmer-Lemeshow tests were used to evaluate discrimination and calibration, respectively. Ten-fold cross-validation was used for internal validation. Results: Two sets of models were developed: the simple model (including age and monthly income) and the metabolic index model [including age, monthly income, fasting blood glucose (FBG), total cholesterol (TC) and high-density lipoprotein cholesterol (HDL-C)].The AUC (95%CI) [0.745 (0.719-0.771)] of the metabolic index model was higher than that of the simple prediction model [0.688 (0.660-0.716)] (P=0.004). Both the simple model (PHL=0.287) and the metabolic index model (PHL=0.134) were well-calibrated. The results of ten-fold cross-validation indicated sufficient stability, with an average AUC of 0.699 and a standard error (SD) of 0.010. Conclusion: By incorporating metabolic markers, accurate and reliable lung cancer risk prediction model for female non smokers could be developed | ||
| 650 | 4 | |a Journal Article | |
| 650 | 4 | |a Female | |
| 650 | 4 | |a Forecasting | |
| 650 | 4 | |a Lung | |
| 650 | 4 | |a Neoplasms | |
| 650 | 4 | |a Non-smokers | |
| 700 | 1 | |a Li, N |e verfasserin |4 aut | |
| 700 | 1 | |a Chen, S H |e verfasserin |4 aut | |
| 700 | 1 | |a Wang, G |e verfasserin |4 aut | |
| 700 | 1 | |a Tan, F W |e verfasserin |4 aut | |
| 700 | 1 | |a Feng, X S |e verfasserin |4 aut | |
| 700 | 1 | |a Li, X |e verfasserin |4 aut | |
| 700 | 1 | |a Wen, Y |e verfasserin |4 aut | |
| 700 | 1 | |a Yang, Z Y |e verfasserin |4 aut | |
| 700 | 1 | |a Wang, Y L |e verfasserin |4 aut | |
| 700 | 1 | |a Li, J |e verfasserin |4 aut | |
| 700 | 1 | |a Chen, H D |e verfasserin |4 aut | |
| 700 | 1 | |a Lin, C Q |e verfasserin |4 aut | |
| 700 | 1 | |a Ren, J S |e verfasserin |4 aut | |
| 700 | 1 | |a Shi, J F |e verfasserin |4 aut | |
| 700 | 1 | |a Wu, S L |e verfasserin |4 aut | |
| 700 | 1 | |a Dai, M |e verfasserin |4 aut | |
| 700 | 1 | |a He, J |e verfasserin |4 aut | |
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