File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1136/bmjdrc-2020-001950
- Scopus: eid_2-s2.0-85105250877
- PMID: 34117050
- WOS: WOS:000661556800001
Supplementary
- Citations:
- Appears in Collections:
Article: Development of a predictive risk model for all-cause mortality in patients with diabetes in Hong Kong
Title | Development of a predictive risk model for all-cause mortality in patients with diabetes in Hong Kong |
---|---|
Authors | |
Keywords | epidemiology risk factors |
Issue Date | 2021 |
Citation | BMJ Open Diabetes Research and Care, 2021, v. 9, n. 1, article no. e001950 How to Cite? |
Abstract | Introduction Patients with diabetes mellitus are risk of premature death. In this study, we developed a machine learning-driven predictive risk model for all-cause mortality among patients with type 2 diabetes mellitus using multiparametric approach with data from different domains. Research design and methods This study used territory-wide data of patients with type 2 diabetes attending public hospitals or their associated ambulatory/outpatient facilities in Hong Kong between January 1, 2009 and December 31, 2009. The primary outcome is all-cause mortality. The association of risk variables and all-cause mortality was assessed using Cox proportional hazards models. Machine and deep learning approaches were used to improve overall survival prediction and were evaluated with fivefold cross validation method. Results A total of 273 678 patients (mean age: 65.4±12.7 years, male: 48.2%, median follow-up: 142 (IQR=106-142) months) were included, with 91 155 deaths occurring on follow-up (33.3%; annualized mortality rate: 3.4%/year; 2.7 million patient-years). Multivariate Cox regression found the following significant predictors of all-cause mortality: age, male gender, baseline comorbidities, anemia, mean values of neutrophil-to-lymphocyte ratio, high-density lipoprotein-cholesterol, total cholesterol, triglyceride, HbA1c and fasting blood glucose (FBG), measures of variability of both HbA1c and FBG. The above parameters were incorporated into a score-based predictive risk model that had a c-statistic of 0.73 (95% CI 0.66 to 0.77), which was improved to 0.86 (0.81 to 0.90) and 0.87 (0.84 to 0.91) using random survival forests and deep survival learning models, respectively. Conclusions A multiparametric model incorporating variables from different domains predicted all-cause mortality accurately in type 2 diabetes mellitus. The predictive and modeling capabilities of machine/deep learning survival analysis achieved more accurate predictions. |
Persistent Identifier | http://hdl.handle.net/10722/330700 |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lee, Sharen | - |
dc.contributor.author | Zhou, Jiandong | - |
dc.contributor.author | Leung, Keith Sai Kit | - |
dc.contributor.author | Wu, William Ka Kei | - |
dc.contributor.author | Wong, Wing Tak | - |
dc.contributor.author | Liu, Tong | - |
dc.contributor.author | Wong, Ian Chi Kei | - |
dc.contributor.author | Jeevaratnam, Kamalan | - |
dc.contributor.author | Zhang, Qingpeng | - |
dc.contributor.author | Tse, Gary | - |
dc.date.accessioned | 2023-09-05T12:13:23Z | - |
dc.date.available | 2023-09-05T12:13:23Z | - |
dc.date.issued | 2021 | - |
dc.identifier.citation | BMJ Open Diabetes Research and Care, 2021, v. 9, n. 1, article no. e001950 | - |
dc.identifier.uri | http://hdl.handle.net/10722/330700 | - |
dc.description.abstract | Introduction Patients with diabetes mellitus are risk of premature death. In this study, we developed a machine learning-driven predictive risk model for all-cause mortality among patients with type 2 diabetes mellitus using multiparametric approach with data from different domains. Research design and methods This study used territory-wide data of patients with type 2 diabetes attending public hospitals or their associated ambulatory/outpatient facilities in Hong Kong between January 1, 2009 and December 31, 2009. The primary outcome is all-cause mortality. The association of risk variables and all-cause mortality was assessed using Cox proportional hazards models. Machine and deep learning approaches were used to improve overall survival prediction and were evaluated with fivefold cross validation method. Results A total of 273 678 patients (mean age: 65.4±12.7 years, male: 48.2%, median follow-up: 142 (IQR=106-142) months) were included, with 91 155 deaths occurring on follow-up (33.3%; annualized mortality rate: 3.4%/year; 2.7 million patient-years). Multivariate Cox regression found the following significant predictors of all-cause mortality: age, male gender, baseline comorbidities, anemia, mean values of neutrophil-to-lymphocyte ratio, high-density lipoprotein-cholesterol, total cholesterol, triglyceride, HbA1c and fasting blood glucose (FBG), measures of variability of both HbA1c and FBG. The above parameters were incorporated into a score-based predictive risk model that had a c-statistic of 0.73 (95% CI 0.66 to 0.77), which was improved to 0.86 (0.81 to 0.90) and 0.87 (0.84 to 0.91) using random survival forests and deep survival learning models, respectively. Conclusions A multiparametric model incorporating variables from different domains predicted all-cause mortality accurately in type 2 diabetes mellitus. The predictive and modeling capabilities of machine/deep learning survival analysis achieved more accurate predictions. | - |
dc.language | eng | - |
dc.relation.ispartof | BMJ Open Diabetes Research and Care | - |
dc.subject | epidemiology | - |
dc.subject | risk factors | - |
dc.title | Development of a predictive risk model for all-cause mortality in patients with diabetes in Hong Kong | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1136/bmjdrc-2020-001950 | - |
dc.identifier.pmid | 34117050 | - |
dc.identifier.scopus | eid_2-s2.0-85105250877 | - |
dc.identifier.volume | 9 | - |
dc.identifier.issue | 1 | - |
dc.identifier.spage | article no. e001950 | - |
dc.identifier.epage | article no. e001950 | - |
dc.identifier.eissn | 2052-4897 | - |
dc.identifier.isi | WOS:000661556800001 | - |