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Article: Development and Validation of Mortality Prediction Models among Frail Participants in the UK Biobank Study
| Title | Development and Validation of Mortality Prediction Models among Frail Participants in the UK Biobank Study |
|---|---|
| Authors | |
| Keywords | Biomarker Physical measurement Survey data |
| Issue Date | 2-May-2025 |
| Publisher | Oxford University Press |
| Citation | The Journals of Gerontology, Series A: Biological Sciences and Medical Sciences, 2025, v. 80, n. 7 How to Cite? |
| Abstract | Background Identifying effective risk assessment strategies and prediction models for frail populations is crucial for precise mortality risk identification and improved patient management. This study aimed to evaluate whether prediction models incorporating survey data combined with biomarkers, physical measurements, or both could enhance mortality risk prediction in frail individuals than survey-only models. Methods 15 754 frail participants aged 40–72 from the UK Biobank were included. We used Cox models to assess all-cause mortality risk and Light Gradient Boosting Machines for variable selection by sex. Performance was evaluated through discrimination, calibration, and reclassification. Results In the survey-only models, we selected 24 predictors for males and 19 for females; age and number of treatments were the top predictors for both sexes. In the biomarker models, we selected 15 predictors for males and 24 for females. In the physical measurement models, we retained 24 predictors for males and 23 for females. The base models showed good discrimination: C-statistic was 0.73 (95% CI, 0.72–0.75) for males and 0.74 (95% CI, 0.72–0.76) for females in development, and 0.70 (95% CI, 0.65–0.75) for males and 0.78 (95% CI, 0.73–0.83) for females in validation. Although incorporating additional predictors led to some improvement in model performance, the overall enhancement was not substantial. Conclusions Survey-based models predicted mortality in frail individuals effectively, with only minor improvements from adding biomarkers or physical measurements. These findings highlighted the value of surveys in forecasting outcomes and informed personalized management strategies to improve health for the frail. |
| Persistent Identifier | http://hdl.handle.net/10722/362681 |
| ISSN | 2023 Impact Factor: 4.3 2023 SCImago Journal Rankings: 1.285 |
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Wu, Chenkai | - |
| dc.contributor.author | Wang, Yanxin | - |
| dc.contributor.author | Tang, Junhan | - |
| dc.contributor.author | Xu, Jianhong | - |
| dc.contributor.author | Mak, Jonathan K L | - |
| dc.contributor.author | Xue, Qian-Li | - |
| dc.date.accessioned | 2025-09-26T00:36:56Z | - |
| dc.date.available | 2025-09-26T00:36:56Z | - |
| dc.date.issued | 2025-05-02 | - |
| dc.identifier.citation | The Journals of Gerontology, Series A: Biological Sciences and Medical Sciences, 2025, v. 80, n. 7 | - |
| dc.identifier.issn | 1079-5006 | - |
| dc.identifier.uri | http://hdl.handle.net/10722/362681 | - |
| dc.description.abstract | <p>Background</p><p>Identifying effective risk assessment strategies and prediction models for frail populations is crucial for precise mortality risk identification and improved patient management. This study aimed to evaluate whether prediction models incorporating survey data combined with biomarkers, physical measurements, or both could enhance mortality risk prediction in frail individuals than survey-only models.</p><p>Methods</p><p>15 754 frail participants aged 40–72 from the UK Biobank were included. We used Cox models to assess all-cause mortality risk and Light Gradient Boosting Machines for variable selection by sex. Performance was evaluated through discrimination, calibration, and reclassification.</p><p>Results</p><p>In the survey-only models, we selected 24 predictors for males and 19 for females; age and number of treatments were the top predictors for both sexes. In the biomarker models, we selected 15 predictors for males and 24 for females. In the physical measurement models, we retained 24 predictors for males and 23 for females. The base models showed good discrimination: <em>C</em>-statistic was 0.73 (95% CI, 0.72–0.75) for males and 0.74 (95% CI, 0.72–0.76) for females in development, and 0.70 (95% CI, 0.65–0.75) for males and 0.78 (95% CI, 0.73–0.83) for females in validation. Although incorporating additional predictors led to some improvement in model performance, the overall enhancement was not substantial.</p><p>Conclusions</p><p>Survey-based models predicted mortality in frail individuals effectively, with only minor improvements from adding biomarkers or physical measurements. These findings highlighted the value of surveys in forecasting outcomes and informed personalized management strategies to improve health for the frail.</p> | - |
| dc.language | eng | - |
| dc.publisher | Oxford University Press | - |
| dc.relation.ispartof | The Journals of Gerontology, Series A: Biological Sciences and Medical Sciences | - |
| dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
| dc.subject | Biomarker | - |
| dc.subject | Physical measurement | - |
| dc.subject | Survey data | - |
| dc.title | Development and Validation of Mortality Prediction Models among Frail Participants in the UK Biobank Study | - |
| dc.type | Article | - |
| dc.identifier.doi | 10.1093/gerona/glaf096 | - |
| dc.identifier.scopus | eid_2-s2.0-105008807686 | - |
| dc.identifier.volume | 80 | - |
| dc.identifier.issue | 7 | - |
| dc.identifier.eissn | 1758-535X | - |
| dc.identifier.issnl | 1079-5006 | - |
