Development and internal validation of machine learning algorithms for end-stage renal disease risk prediction model of people with type 2 diabetes mellitus and diabetic kidney disease
Diabetic kidney disease (DKD) is the most common cause of end-stage renal disease (ESRD) and is associated with increased morbidity and mortality in patients with diabetes. Identification of risk factors involved in the progression of DKD to ESRD is expected to result in early detection and appropri...
Uložené v:
| Vydané v: | Renal failure Ročník 44; číslo 1; s. 562 - 570 |
|---|---|
| Hlavní autori: | , , , , , , , , , , , , , , , , |
| Médium: | Journal Article |
| Jazyk: | English |
| Vydavateľské údaje: |
England
Taylor & Francis
01.12.2022
Taylor & Francis Ltd Taylor & Francis Group |
| Predmet: | |
| ISSN: | 0886-022X, 1525-6049, 1525-6049 |
| On-line prístup: | Získať plný text |
| Tagy: |
Pridať tag
Žiadne tagy, Buďte prvý, kto otaguje tento záznam!
|
| Abstract | Diabetic kidney disease (DKD) is the most common cause of end-stage renal disease (ESRD) and is associated with increased morbidity and mortality in patients with diabetes. Identification of risk factors involved in the progression of DKD to ESRD is expected to result in early detection and appropriate intervention and improve prognosis. Therefore, this study aimed to establish a risk prediction model for ESRD resulting from DKD in patients with type 2 diabetes mellitus (T2DM).
Between January 2008 and July 2019, a total of 390 Chinese patients with T2DM and DKD confirmed by percutaneous renal biopsy were enrolled and followed up for at least 1 year. Four machine learning algorithms (gradient boosting machine, support vector machine, logistic regression, and random forest (RF)) were used to identify the critical clinical and pathological features and to build a risk prediction model for ESRD.
There were 158 renal outcome events (ESRD) (40.51%) during the 3-year median follow up. The RF algorithm showed the best performance at predicting progression to ESRD, showing the highest AUC (0.90) and ACC (82.65%). The RF algorithm identified five major factors: Cystatin-C, serum albumin (sAlb), hemoglobin (Hb), 24-hour urine urinary total protein, and estimated glomerular filtration rate. A nomogram according to the aforementioned five predictive factors was constructed to predict the incidence of ESRD.
Machine learning algorithms can efficiently predict the incident ESRD in DKD participants. Compared with the previous models, the importance of sAlb and Hb were highlighted in the current model.
Highlights
What is already known? Identification of risk factors for the progression of DKD to ESRD is expected to improve the prognosis by early detection and appropriate intervention.
What this study has found? Machine learning algorithms were used to construct a risk prediction model of ESRD in patients with T2DM and DKD. The major predictive factors were found to be CysC, sAlb, Hb, eGFR, and UTP.
What are the implications of the study? In contrast with the treatment of participants with early-phase T2DM with or without mild kidney damage, major emphasis should be placed on indicators of kidney function, nutrition, anemia, and proteinuria for participants with T2DM and advanced DKD to delay ESRD, rather than age, sex, and control of hypertension and glycemia. |
|---|---|
| AbstractList | AimsDiabetic kidney disease (DKD) is the most common cause of end-stage renal disease (ESRD) and is associated with increased morbidity and mortality in patients with diabetes. Identification of risk factors involved in the progression of DKD to ESRD is expected to result in early detection and appropriate intervention and improve prognosis. Therefore, this study aimed to establish a risk prediction model for ESRD resulting from DKD in patients with type 2 diabetes mellitus (T2DM).MethodsBetween January 2008 and July 2019, a total of 390 Chinese patients with T2DM and DKD confirmed by percutaneous renal biopsy were enrolled and followed up for at least 1 year. Four machine learning algorithms (gradient boosting machine, support vector machine, logistic regression, and random forest (RF)) were used to identify the critical clinical and pathological features and to build a risk prediction model for ESRD.ResultsThere were 158 renal outcome events (ESRD) (40.51%) during the 3-year median follow up. The RF algorithm showed the best performance at predicting progression to ESRD, showing the highest AUC (0.90) and ACC (82.65%). The RF algorithm identified five major factors: Cystatin-C, serum albumin (sAlb), hemoglobin (Hb), 24-hour urine urinary total protein, and estimated glomerular filtration rate. A nomogram according to the aforementioned five predictive factors was constructed to predict the incidence of ESRD.ConclusionMachine learning algorithms can efficiently predict the incident ESRD in DKD participants. Compared with the previous models, the importance of sAlb and Hb were highlighted in the current model.HighlightsWhat is already known? Identification of risk factors for the progression of DKD to ESRD is expected to improve the prognosis by early detection and appropriate intervention.What this study has found? Machine learning algorithms were used to construct a risk prediction model of ESRD in patients with T2DM and DKD. The major predictive factors were found to be CysC, sAlb, Hb, eGFR, and UTP.What are the implications of the study? In contrast with the treatment of participants with early-phase T2DM with or without mild kidney damage, major emphasis should be placed on indicators of kidney function, nutrition, anemia, and proteinuria for participants with T2DM and advanced DKD to delay ESRD, rather than age, sex, and control of hypertension and glycemia. Diabetic kidney disease (DKD) is the most common cause of end-stage renal disease (ESRD) and is associated with increased morbidity and mortality in patients with diabetes. Identification of risk factors involved in the progression of DKD to ESRD is expected to result in early detection and appropriate intervention and improve prognosis. Therefore, this study aimed to establish a risk prediction model for ESRD resulting from DKD in patients with type 2 diabetes mellitus (T2DM). Between January 2008 and July 2019, a total of 390 Chinese patients with T2DM and DKD confirmed by percutaneous renal biopsy were enrolled and followed up for at least 1 year. Four machine learning algorithms (gradient boosting machine, support vector machine, logistic regression, and random forest (RF)) were used to identify the critical clinical and pathological features and to build a risk prediction model for ESRD. There were 158 renal outcome events (ESRD) (40.51%) during the 3-year median follow up. The RF algorithm showed the best performance at predicting progression to ESRD, showing the highest AUC (0.90) and ACC (82.65%). The RF algorithm identified five major factors: Cystatin-C, serum albumin (sAlb), hemoglobin (Hb), 24-hour urine urinary total protein, and estimated glomerular filtration rate. A nomogram according to the aforementioned five predictive factors was constructed to predict the incidence of ESRD. Machine learning algorithms can efficiently predict the incident ESRD in DKD participants. Compared with the previous models, the importance of sAlb and Hb were highlighted in the current model.Highlights Identification of risk factors for the progression of DKD to ESRD is expected to improve the prognosis by early detection and appropriate intervention. Machine learning algorithms were used to construct a risk prediction model of ESRD in patients with T2DM and DKD. The major predictive factors were found to be CysC, sAlb, Hb, eGFR, and UTP. In contrast with the treatment of participants with early-phase T2DM with or without mild kidney damage, major emphasis should be placed on indicators of kidney function, nutrition, anemia, and proteinuria for participants with T2DM and advanced DKD to delay ESRD, rather than age, sex, and control of hypertension and glycemia. Diabetic kidney disease (DKD) is the most common cause of end-stage renal disease (ESRD) and is associated with increased morbidity and mortality in patients with diabetes. Identification of risk factors involved in the progression of DKD to ESRD is expected to result in early detection and appropriate intervention and improve prognosis. Therefore, this study aimed to establish a risk prediction model for ESRD resulting from DKD in patients with type 2 diabetes mellitus (T2DM). Between January 2008 and July 2019, a total of 390 Chinese patients with T2DM and DKD confirmed by percutaneous renal biopsy were enrolled and followed up for at least 1 year. Four machine learning algorithms (gradient boosting machine, support vector machine, logistic regression, and random forest (RF)) were used to identify the critical clinical and pathological features and to build a risk prediction model for ESRD. There were 158 renal outcome events (ESRD) (40.51%) during the 3-year median follow up. The RF algorithm showed the best performance at predicting progression to ESRD, showing the highest AUC (0.90) and ACC (82.65%). The RF algorithm identified five major factors: Cystatin-C, serum albumin (sAlb), hemoglobin (Hb), 24-hour urine urinary total protein, and estimated glomerular filtration rate. A nomogram according to the aforementioned five predictive factors was constructed to predict the incidence of ESRD. Machine learning algorithms can efficiently predict the incident ESRD in DKD participants. Compared with the previous models, the importance of sAlb and Hb were highlighted in the current model. Highlights What is already known? Identification of risk factors for the progression of DKD to ESRD is expected to improve the prognosis by early detection and appropriate intervention. What this study has found? Machine learning algorithms were used to construct a risk prediction model of ESRD in patients with T2DM and DKD. The major predictive factors were found to be CysC, sAlb, Hb, eGFR, and UTP. What are the implications of the study? In contrast with the treatment of participants with early-phase T2DM with or without mild kidney damage, major emphasis should be placed on indicators of kidney function, nutrition, anemia, and proteinuria for participants with T2DM and advanced DKD to delay ESRD, rather than age, sex, and control of hypertension and glycemia. Aims Diabetic kidney disease (DKD) is the most common cause of end-stage renal disease (ESRD) and is associated with increased morbidity and mortality in patients with diabetes. Identification of risk factors involved in the progression of DKD to ESRD is expected to result in early detection and appropriate intervention and improve prognosis. Therefore, this study aimed to establish a risk prediction model for ESRD resulting from DKD in patients with type 2 diabetes mellitus (T2DM).Methods Between January 2008 and July 2019, a total of 390 Chinese patients with T2DM and DKD confirmed by percutaneous renal biopsy were enrolled and followed up for at least 1 year. Four machine learning algorithms (gradient boosting machine, support vector machine, logistic regression, and random forest (RF)) were used to identify the critical clinical and pathological features and to build a risk prediction model for ESRD.Results There were 158 renal outcome events (ESRD) (40.51%) during the 3-year median follow up. The RF algorithm showed the best performance at predicting progression to ESRD, showing the highest AUC (0.90) and ACC (82.65%). The RF algorithm identified five major factors: Cystatin-C, serum albumin (sAlb), hemoglobin (Hb), 24-hour urine urinary total protein, and estimated glomerular filtration rate. A nomogram according to the aforementioned five predictive factors was constructed to predict the incidence of ESRD.Conclusion Machine learning algorithms can efficiently predict the incident ESRD in DKD participants. Compared with the previous models, the importance of sAlb and Hb were highlighted in the current model.HighlightsWhat is already known? Identification of risk factors for the progression of DKD to ESRD is expected to improve the prognosis by early detection and appropriate intervention.What this study has found? Machine learning algorithms were used to construct a risk prediction model of ESRD in patients with T2DM and DKD. The major predictive factors were found to be CysC, sAlb, Hb, eGFR, and UTP.What are the implications of the study? In contrast with the treatment of participants with early-phase T2DM with or without mild kidney damage, major emphasis should be placed on indicators of kidney function, nutrition, anemia, and proteinuria for participants with T2DM and advanced DKD to delay ESRD, rather than age, sex, and control of hypertension and glycemia. Diabetic kidney disease (DKD) is the most common cause of end-stage renal disease (ESRD) and is associated with increased morbidity and mortality in patients with diabetes. Identification of risk factors involved in the progression of DKD to ESRD is expected to result in early detection and appropriate intervention and improve prognosis. Therefore, this study aimed to establish a risk prediction model for ESRD resulting from DKD in patients with type 2 diabetes mellitus (T2DM).AIMSDiabetic kidney disease (DKD) is the most common cause of end-stage renal disease (ESRD) and is associated with increased morbidity and mortality in patients with diabetes. Identification of risk factors involved in the progression of DKD to ESRD is expected to result in early detection and appropriate intervention and improve prognosis. Therefore, this study aimed to establish a risk prediction model for ESRD resulting from DKD in patients with type 2 diabetes mellitus (T2DM).Between January 2008 and July 2019, a total of 390 Chinese patients with T2DM and DKD confirmed by percutaneous renal biopsy were enrolled and followed up for at least 1 year. Four machine learning algorithms (gradient boosting machine, support vector machine, logistic regression, and random forest (RF)) were used to identify the critical clinical and pathological features and to build a risk prediction model for ESRD.METHODSBetween January 2008 and July 2019, a total of 390 Chinese patients with T2DM and DKD confirmed by percutaneous renal biopsy were enrolled and followed up for at least 1 year. Four machine learning algorithms (gradient boosting machine, support vector machine, logistic regression, and random forest (RF)) were used to identify the critical clinical and pathological features and to build a risk prediction model for ESRD.There were 158 renal outcome events (ESRD) (40.51%) during the 3-year median follow up. The RF algorithm showed the best performance at predicting progression to ESRD, showing the highest AUC (0.90) and ACC (82.65%). The RF algorithm identified five major factors: Cystatin-C, serum albumin (sAlb), hemoglobin (Hb), 24-hour urine urinary total protein, and estimated glomerular filtration rate. A nomogram according to the aforementioned five predictive factors was constructed to predict the incidence of ESRD.RESULTSThere were 158 renal outcome events (ESRD) (40.51%) during the 3-year median follow up. The RF algorithm showed the best performance at predicting progression to ESRD, showing the highest AUC (0.90) and ACC (82.65%). The RF algorithm identified five major factors: Cystatin-C, serum albumin (sAlb), hemoglobin (Hb), 24-hour urine urinary total protein, and estimated glomerular filtration rate. A nomogram according to the aforementioned five predictive factors was constructed to predict the incidence of ESRD.Machine learning algorithms can efficiently predict the incident ESRD in DKD participants. Compared with the previous models, the importance of sAlb and Hb were highlighted in the current model.HighlightsWhat is already known? Identification of risk factors for the progression of DKD to ESRD is expected to improve the prognosis by early detection and appropriate intervention.What this study has found? Machine learning algorithms were used to construct a risk prediction model of ESRD in patients with T2DM and DKD. The major predictive factors were found to be CysC, sAlb, Hb, eGFR, and UTP.What are the implications of the study? In contrast with the treatment of participants with early-phase T2DM with or without mild kidney damage, major emphasis should be placed on indicators of kidney function, nutrition, anemia, and proteinuria for participants with T2DM and advanced DKD to delay ESRD, rather than age, sex, and control of hypertension and glycemia.CONCLUSIONMachine learning algorithms can efficiently predict the incident ESRD in DKD participants. Compared with the previous models, the importance of sAlb and Hb were highlighted in the current model.HighlightsWhat is already known? Identification of risk factors for the progression of DKD to ESRD is expected to improve the prognosis by early detection and appropriate intervention.What this study has found? Machine learning algorithms were used to construct a risk prediction model of ESRD in patients with T2DM and DKD. The major predictive factors were found to be CysC, sAlb, Hb, eGFR, and UTP.What are the implications of the study? In contrast with the treatment of participants with early-phase T2DM with or without mild kidney damage, major emphasis should be placed on indicators of kidney function, nutrition, anemia, and proteinuria for participants with T2DM and advanced DKD to delay ESRD, rather than age, sex, and control of hypertension and glycemia. |
| Author | Li, Lin Tong, Nanwei Zou, Yutong Wang, Yiting Wang, Tingli Zhao, Lijun Wu, Yucheng Zhang, Junlin Zhao, Yuancheng Xu, Huan Chai, Zhonglin Ren, Honghong Wang, Jiali Cooper, Mark E. Zhang, Rui Qin, Chunmei Liu, Fang |
| Author_xml | – sequence: 1 givenname: Yutong surname: Zou fullname: Zou, Yutong organization: Laboratory of Diabetic Kidney Disease, Centre of Diabetes and Metabolism Research, West China Hospital of Sichuan University – sequence: 2 givenname: Lijun orcidid: 0000-0001-7750-1864 surname: Zhao fullname: Zhao, Lijun organization: Laboratory of Diabetic Kidney Disease, Centre of Diabetes and Metabolism Research, West China Hospital of Sichuan University – sequence: 3 givenname: Junlin surname: Zhang fullname: Zhang, Junlin organization: Laboratory of Diabetic Kidney Disease, Centre of Diabetes and Metabolism Research, West China Hospital of Sichuan University – sequence: 4 givenname: Yiting surname: Wang fullname: Wang, Yiting organization: Laboratory of Diabetic Kidney Disease, Centre of Diabetes and Metabolism Research, West China Hospital of Sichuan University – sequence: 5 givenname: Yucheng surname: Wu fullname: Wu, Yucheng organization: Laboratory of Diabetic Kidney Disease, Centre of Diabetes and Metabolism Research, West China Hospital of Sichuan University – sequence: 6 givenname: Honghong surname: Ren fullname: Ren, Honghong organization: Laboratory of Diabetic Kidney Disease, Centre of Diabetes and Metabolism Research, West China Hospital of Sichuan University – sequence: 7 givenname: Tingli surname: Wang fullname: Wang, Tingli organization: Laboratory of Diabetic Kidney Disease, Centre of Diabetes and Metabolism Research, West China Hospital of Sichuan University – sequence: 8 givenname: Rui surname: Zhang fullname: Zhang, Rui organization: Laboratory of Diabetic Kidney Disease, Centre of Diabetes and Metabolism Research, West China Hospital of Sichuan University – sequence: 9 givenname: Jiali surname: Wang fullname: Wang, Jiali organization: Laboratory of Diabetic Kidney Disease, Centre of Diabetes and Metabolism Research, West China Hospital of Sichuan University – sequence: 10 givenname: Yuancheng surname: Zhao fullname: Zhao, Yuancheng organization: Laboratory of Diabetic Kidney Disease, Centre of Diabetes and Metabolism Research, West China Hospital of Sichuan University – sequence: 11 givenname: Chunmei surname: Qin fullname: Qin, Chunmei organization: Laboratory of Diabetic Kidney Disease, Centre of Diabetes and Metabolism Research, West China Hospital of Sichuan University – sequence: 12 givenname: Huan surname: Xu fullname: Xu, Huan organization: Division of Pathology, West China Hospital of Sichuan University – sequence: 13 givenname: Lin surname: Li fullname: Li, Lin organization: Division of Pathology, West China Hospital of Sichuan University – sequence: 14 givenname: Zhonglin surname: Chai fullname: Chai, Zhonglin organization: Department of Diabetes, Central Clinical School, Monash University – sequence: 15 givenname: Mark E. surname: Cooper fullname: Cooper, Mark E. organization: Department of Diabetes, Central Clinical School, Monash University – sequence: 16 givenname: Nanwei surname: Tong fullname: Tong, Nanwei organization: Division of Endocrinology, West China Hospital of Sichuan University – sequence: 17 givenname: Fang orcidid: 0000-0003-1121-3004 surname: Liu fullname: Liu, Fang organization: Laboratory of Diabetic Kidney Disease, Centre of Diabetes and Metabolism Research, West China Hospital of Sichuan University |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/35373711$$D View this record in MEDLINE/PubMed |
| BookMark | eNqFkstu1DAUhiNURC_wCCBLbNhMcez4EiGhonKrVIkNSOysM_HJ1K1jBzvTat6Mx8OZaSvaBWwcxfn-T8fOf1jthRiwql7W9Limmr6lWkvK2M9jVtayCEkFf1Id1IKJhaRNu1cdzMxihvarw5wvKa2FVuxZtc8FV1zV9UH1-yNeo4_jgGEiECxxYcIUwJNr8M7C5GIgsScDdBcuIPEIKbiwIuBXMbnpYsikj4lgsIs8wQpJwjltXUbI5c3lKzImtK7bqoZo0c_CEePokdwUBZk2IxJWMrDECTMZ0Hs3rfN2oN2u68iVswE3d-bn1dMefMYXt8-j6sfnT99Pvy7Ov305O_1wvuiEZNNCLwVQpmreNn2LwHoqNWUIHXBUDJjWAmm3BCktkxS5oKxuqNVLJYTqG82PqrOd10a4NGNyA6SNieDMdiOmlYFUxvNoQCmGyKVtVNug4LqvqWppu-St4kLx4nq_c43r5YC2K3eewD-QPvwS3IVZxWujWy0Zo0Xw5laQ4q815skMLnfltiBgXGfDZCPbhrVtW9DXj9DLuJ5_bKGUprJmVNeFevX3RPej3BWkAGIHdCnmnLC_R2pq5iKauyKauYjmtogl9-5RrnPTtk3lYM7_N32yS7tQyjXATUzemgk2PqY-QehcNvzfij9EzvlE |
| CitedBy_id | crossref_primary_10_15446_revfacmed_v71n3_107190 crossref_primary_10_1080_0886022X_2022_2158102 crossref_primary_10_1097_MD_0000000000034878 crossref_primary_10_2478_acph_2025_0002 crossref_primary_10_4108_eetpht_10_5691 crossref_primary_10_1371_journal_pone_0321258 crossref_primary_10_1007_s12012_024_09880_3 crossref_primary_10_1155_2024_8857453 crossref_primary_10_1080_0886022X_2023_2257808 crossref_primary_10_2147_DMSO_S451628 crossref_primary_10_4103_ijem_ijem_183_24 crossref_primary_10_1186_s12882_023_03424_7 crossref_primary_10_2147_IJGM_S462896 crossref_primary_10_4239_wjd_v14_i12_1793 crossref_primary_10_7759_cureus_60145 crossref_primary_10_1111_dom_15933 crossref_primary_10_1186_s12916_024_03649_9 crossref_primary_10_1371_journal_pone_0329269 crossref_primary_10_1038_s41598_023_47449_2 crossref_primary_10_3389_fendo_2025_1552772 crossref_primary_10_14814_phy2_15579 crossref_primary_10_3389_fendo_2024_1406442 crossref_primary_10_1109_ACCESS_2024_3432118 crossref_primary_10_3389_fmed_2023_1155426 crossref_primary_10_1136_bmjopen_2024_086032 crossref_primary_10_1016_j_artmed_2023_102696 crossref_primary_10_1016_j_endmts_2024_100212 crossref_primary_10_1177_20552076251335705 crossref_primary_10_1016_j_amjms_2024_01_018 crossref_primary_10_1109_ACCESS_2023_3299866 crossref_primary_10_3389_fpubh_2023_1331517 crossref_primary_10_3389_fendo_2025_1538704 crossref_primary_10_1007_s00592_025_02529_9 crossref_primary_10_1007_s11655_023_3639_7 crossref_primary_10_3389_fnut_2024_1322229 crossref_primary_10_1002_clc_24104 crossref_primary_10_1177_19322968221124583 crossref_primary_10_1016_j_diabet_2024_101536 crossref_primary_10_2147_IJGM_S449397 crossref_primary_10_2196_47833 crossref_primary_10_1186_s13098_023_01216_5 crossref_primary_10_1177_20552076251355448 crossref_primary_10_1007_s12020_023_03637_8 crossref_primary_10_1007_s40200_025_01621_9 crossref_primary_10_1016_j_jff_2024_106188 crossref_primary_10_32604_biocell_2023_027373 crossref_primary_10_1016_j_phymed_2023_155162 crossref_primary_10_1016_j_ijmedinf_2024_105546 crossref_primary_10_3389_fendo_2024_1320335 crossref_primary_10_1080_03007995_2024_2423737 crossref_primary_10_1186_s12920_023_01497_9 crossref_primary_10_1111_jdi_14401 crossref_primary_10_1007_s00259_025_07081_w crossref_primary_10_1016_j_jad_2022_08_070 crossref_primary_10_1186_s12902_024_01698_y crossref_primary_10_1002_ctd2_355 crossref_primary_10_1177_20552076241238093 |
| Cites_doi | 10.1155/2019/7825804 10.1038/s41591-018-0239-8 10.1111/j.1523-1755.2005.09909.x 10.1016/j.clinimag.2018.04.015 10.1080/03007995.2019.1682981 10.7717/peerj.8499 10.1007/s00125-006-0247-y 10.1681/ASN.2010010010 10.1016/j.freeradbiomed.2013.02.005 10.1016/j.mcna.2012.10.001 10.1097/JCMA.0000000000000175 10.1136/bmjopen-2019-035308 10.1111/dom.14178 10.1186/s12882-017-0671-x 10.4158/EP-2019-0238 10.1155/2019/4354061 10.1097/MNH.0000000000000341 10.1186/1471-2369-6-8 10.3390/jcm10010003 10.1111/jdi.12533 10.1016/j.bbrc.2010.09.027 10.1111/j.1523-1755.2004.00863.x 10.1038/ncpneph0378 10.1371/journal.pone.0190930 10.1053/j.ackd.2017.12.005 10.5888/pcd17.200076 10.1016/j.brat.2016.11.008 10.1159/000101958 10.1053/j.ajkd.2020.04.016 10.1371/journal.pone.0177799 |
| ContentType | Journal Article |
| Copyright | 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. 2022 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. This work is licensed under the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. 2022 The Author(s) |
| Copyright_xml | – notice: 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. 2022 – notice: 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. This work is licensed under the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. – notice: 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. 2022 The Author(s) |
| DBID | 0YH AAYXX CITATION CGR CUY CVF ECM EIF NPM 3V. 7T5 7X7 7XB 88E 8FI 8FJ 8FK 8G5 ABUWG AFKRA AZQEC BENPR CCPQU DWQXO FYUFA GHDGH GNUQQ GUQSH H94 K9. M0S M1P M2O MBDVC PHGZM PHGZT PIMPY PJZUB PKEHL PPXIY PQEST PQQKQ PQUKI PRINS Q9U 7X8 5PM DOA |
| DOI | 10.1080/0886022X.2022.2056053 |
| DatabaseName | Taylor & Francis Open Access CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed ProQuest Central (Corporate) Immunology Abstracts Health & Medical Collection ProQuest Central (purchase pre-March 2016) Medical Database (Alumni Edition) ProQuest Hospital Collection Hospital Premium Collection (Alumni Edition) ProQuest Central (Alumni) (purchase pre-March 2016) Research Library (Alumni) ProQuest Central (Alumni) ProQuest Central UK/Ireland ProQuest Central Essentials ProQuest Central ProQuest One Community College ProQuest Central Health Research Premium Collection Health Research Premium Collection (Alumni) ProQuest Central Student ProQuest Research Library AIDS and Cancer Research Abstracts ProQuest Health & Medical Complete (Alumni) ProQuest Health & Medical Collection Medical Database Research Library Research Library (Corporate) ProQuest Central Premium ProQuest One Academic (New) ProQuest Publicly Available Content Database ProQuest Health & Medical Research Collection ProQuest One Academic Middle East (New) One Health & Nursing ProQuest One Academic Eastern Edition (DO NOT USE) ProQuest One Academic (retired) ProQuest One Academic UKI Edition ProQuest Central China ProQuest Central Basic MEDLINE - Academic PubMed Central (Full Participant titles) DOAJ Directory of Open Access Journals |
| DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) Publicly Available Content Database Research Library Prep ProQuest Central Student ProQuest One Academic Middle East (New) ProQuest Central Essentials ProQuest Health & Medical Complete (Alumni) ProQuest Central (Alumni Edition) ProQuest One Community College ProQuest One Health & Nursing Research Library (Alumni Edition) ProQuest Central China ProQuest Central ProQuest Health & Medical Research Collection Health Research Premium Collection Health and Medicine Complete (Alumni Edition) ProQuest Central Korea Health & Medical Research Collection AIDS and Cancer Research Abstracts ProQuest Research Library ProQuest Central (New) ProQuest Medical Library (Alumni) ProQuest Central Basic ProQuest One Academic Eastern Edition ProQuest Hospital Collection Health Research Premium Collection (Alumni) ProQuest Hospital Collection (Alumni) ProQuest Health & Medical Complete ProQuest Medical Library ProQuest One Academic UKI Edition Immunology Abstracts ProQuest One Academic ProQuest One Academic (New) ProQuest Central (Alumni) MEDLINE - Academic |
| DatabaseTitleList | Publicly Available Content Database MEDLINE MEDLINE - Academic |
| Database_xml | – sequence: 1 dbid: DOA name: DOAJ Directory of Open Access Journals url: https://www.doaj.org/ sourceTypes: Open Website – sequence: 2 dbid: NPM name: PubMed url: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 3 dbid: 0YH name: Taylor & Francis Open Access url: https://www.tandfonline.com sourceTypes: Publisher – sequence: 4 dbid: PIMPY name: ProQuest Publicly Available Content Database url: http://search.proquest.com/publiccontent sourceTypes: Aggregation Database |
| DeliveryMethod | fulltext_linktorsrc |
| Discipline | Medicine |
| DocumentTitleAlternate | Y. Zou et al |
| EISSN | 1525-6049 |
| EndPage | 570 |
| ExternalDocumentID | oai_doaj_org_article_a772ee36d4794e538f107909b3973573 PMC8986220 35373711 10_1080_0886022X_2022_2056053 2056053 |
| Genre | Research Article Journal Article |
| GroupedDBID | --- 00X 0YH 123 29P 36B 4.4 53G 5RE 7X7 88E 8FI 8FJ 8G5 ABDBF ABUWG ACGEJ ACGFS ACUHS ADBBV ADCVX ADRBQ ADXPE AENEX AFKRA AFKVX AJWEG ALMA_UNASSIGNED_HOLDINGS AOIJS AQTUD ARJSQ AZQEC BABNJ BCNDV BENPR BLEHA CCPQU CS3 DWQXO EAP EBC EBD EBS EMB EMK EMOBN EPL ESX F5P FYUFA GNUQQ GROUPED_DOAJ GUQSH H13 HMCUK HZ~ M1P M2O M4Z O9- P2P PHGZM PHGZT PIMPY PJZUB PPXIY PROAC PSQYO RPM SV3 TDBHL TFDNU TFL TFW TUS UKHRP V1S ~1N AAYXX AFFHD CITATION .GJ 5VS AALIY AAORF AAPXX ABWCV AFLEI AJVHN AWYRJ BPHCQ BRMBE CAG CGR COF CUY CVF CYYVM CZDIS DRXRE DWTOO ECM EIF EJD HYE JENTW M44 NPM NUSFT PQQKQ QQXMO ZGI ZXP 3V. 7T5 7XB 8FK H94 K9. MBDVC PKEHL PQEST PQUKI PRINS Q9U 7X8 PUEGO 5PM |
| ID | FETCH-LOGICAL-c562t-8b5a0271394f9ea2f06802eaca3e72a2885e0cba66d260e3502140d8b7557f483 |
| IEDL.DBID | 0YH |
| ISICitedReferencesCount | 67 |
| ISICitedReferencesURI | http://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestLinkType=CitingArticles&DestApp=WOS_CPL&KeyUT=000778107800001&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D |
| ISSN | 0886-022X 1525-6049 |
| IngestDate | Mon Nov 10 04:35:56 EST 2025 Tue Nov 04 02:01:08 EST 2025 Thu Oct 02 11:25:48 EDT 2025 Tue Oct 07 06:56:46 EDT 2025 Mon Jul 21 05:45:49 EDT 2025 Sat Nov 29 02:26:01 EST 2025 Tue Nov 18 22:18:56 EST 2025 Mon Oct 20 23:46:15 EDT 2025 |
| IsDoiOpenAccess | true |
| IsOpenAccess | true |
| IsPeerReviewed | true |
| IsScholarly | true |
| Issue | 1 |
| Keywords | diabetic kidney disease risk prediction model Type 2 diabetes mellitus end-stage renal disease machine learning |
| Language | English |
| License | open-access: http://creativecommons.org/licenses/by/4.0/: This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
| LinkModel | DirectLink |
| MergedId | FETCHMERGED-LOGICAL-c562t-8b5a0271394f9ea2f06802eaca3e72a2885e0cba66d260e3502140d8b7557f483 |
| Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Supplemental data for this article can be accessed here. |
| ORCID | 0000-0003-1121-3004 0000-0001-7750-1864 |
| OpenAccessLink | https://www.tandfonline.com/doi/abs/10.1080/0886022X.2022.2056053 |
| PMID | 35373711 |
| PQID | 2780612081 |
| PQPubID | 3933335 |
| PageCount | 9 |
| ParticipantIDs | crossref_primary_10_1080_0886022X_2022_2056053 crossref_citationtrail_10_1080_0886022X_2022_2056053 doaj_primary_oai_doaj_org_article_a772ee36d4794e538f107909b3973573 proquest_miscellaneous_2646942999 pubmedcentral_primary_oai_pubmedcentral_nih_gov_8986220 proquest_journals_2780612081 pubmed_primary_35373711 informaworld_taylorfrancis_310_1080_0886022X_2022_2056053 |
| PublicationCentury | 2000 |
| PublicationDate | 2022-Dec |
| PublicationDateYYYYMMDD | 2022-12-01 |
| PublicationDate_xml | – month: 12 year: 2022 text: 2022-Dec |
| PublicationDecade | 2020 |
| PublicationPlace | England |
| PublicationPlace_xml | – name: England – name: New York |
| PublicationTitle | Renal failure |
| PublicationTitleAlternate | Ren Fail |
| PublicationYear | 2022 |
| Publisher | Taylor & Francis Taylor & Francis Ltd Taylor & Francis Group |
| Publisher_xml | – name: Taylor & Francis – name: Taylor & Francis Ltd – name: Taylor & Francis Group |
| References | e_1_3_5_29_1 e_1_3_5_28_1 Wang Y (e_1_3_5_15_1) 2019; 2019 e_1_3_5_26_1 e_1_3_5_25_1 e_1_3_5_24_1 e_1_3_5_23_1 e_1_3_5_22_1 e_1_3_5_3_1 e_1_3_5_2_1 e_1_3_5_9_1 e_1_3_5_21_1 Zhang J (e_1_3_5_6_1) 2019; 2019 e_1_3_5_8_1 e_1_3_5_20_1 e_1_3_5_5_1 e_1_3_5_4_1 e_1_3_5_7_1 e_1_3_5_18_1 e_1_3_5_17_1 e_1_3_5_16_1 e_1_3_5_13_1 e_1_3_5_14_1 e_1_3_5_11_1 e_1_3_5_33_1 Pinsker JE (e_1_3_5_12_1) 2015; 38 e_1_3_5_19_1 He BB (e_1_3_5_27_1) 2015; 18 e_1_3_5_32_1 e_1_3_5_10_1 e_1_3_5_31_1 e_1_3_5_30_1 |
| References_xml | – volume: 2019 start-page: 1 year: 2019 ident: e_1_3_5_6_1 article-title: The level of serum albumin is associated with renal prognosis in patients with diabetic nephropathy publication-title: J Diabetes Res doi: 10.1155/2019/7825804 – ident: e_1_3_5_11_1 doi: 10.1038/s41591-018-0239-8 – ident: e_1_3_5_25_1 doi: 10.1111/j.1523-1755.2005.09909.x – ident: e_1_3_5_28_1 doi: 10.1016/j.clinimag.2018.04.015 – ident: e_1_3_5_4_1 doi: 10.1080/03007995.2019.1682981 – ident: e_1_3_5_10_1 doi: 10.7717/peerj.8499 – ident: e_1_3_5_24_1 doi: 10.1007/s00125-006-0247-y – ident: e_1_3_5_13_1 doi: 10.1681/ASN.2010010010 – ident: e_1_3_5_18_1 doi: 10.1016/j.freeradbiomed.2013.02.005 – volume: 18 start-page: 277 issue: 5 year: 2015 ident: e_1_3_5_27_1 article-title: Relationship between anemia and chronic complications in Chinese patients with type 2 diabetes mellitus publication-title: Arch Iran Med – ident: e_1_3_5_2_1 doi: 10.1016/j.mcna.2012.10.001 – ident: e_1_3_5_26_1 doi: 10.1097/JCMA.0000000000000175 – ident: e_1_3_5_5_1 doi: 10.1136/bmjopen-2019-035308 – volume: 38 start-page: S41–S48 issue: 1 year: 2015 ident: e_1_3_5_12_1 article-title: Comment on American Diabetes Association. Approaches to glycemic treatment. Sec. 7. In standards of medical care in diabetes-2015 publication-title: Diabetes Care – ident: e_1_3_5_17_1 doi: 10.1111/dom.14178 – ident: e_1_3_5_3_1 doi: 10.1186/s12882-017-0671-x – ident: e_1_3_5_32_1 doi: 10.4158/EP-2019-0238 – volume: 2019 start-page: 1 year: 2019 ident: e_1_3_5_15_1 article-title: Comparison of performance of equations for estimated glomerular filtration rate in Chinese patients with biopsy-proven diabetic nephropathy publication-title: Dis Markers doi: 10.1155/2019/4354061 – ident: e_1_3_5_29_1 doi: 10.1097/MNH.0000000000000341 – ident: e_1_3_5_21_1 doi: 10.1186/1471-2369-6-8 – ident: e_1_3_5_8_1 doi: 10.3390/jcm10010003 – ident: e_1_3_5_9_1 doi: 10.1111/jdi.12533 – ident: e_1_3_5_19_1 doi: 10.1016/j.bbrc.2010.09.027 – ident: e_1_3_5_23_1 doi: 10.1111/j.1523-1755.2004.00863.x – ident: e_1_3_5_22_1 doi: 10.1038/ncpneph0378 – ident: e_1_3_5_31_1 doi: 10.1371/journal.pone.0190930 – ident: e_1_3_5_33_1 doi: 10.1053/j.ackd.2017.12.005 – ident: e_1_3_5_7_1 doi: 10.5888/pcd17.200076 – ident: e_1_3_5_14_1 doi: 10.1016/j.brat.2016.11.008 – ident: e_1_3_5_16_1 doi: 10.1159/000101958 – ident: e_1_3_5_30_1 doi: 10.1053/j.ajkd.2020.04.016 – ident: e_1_3_5_20_1 doi: 10.1371/journal.pone.0177799 |
| SSID | ssj0015872 |
| Score | 2.5644872 |
| Snippet | Diabetic kidney disease (DKD) is the most common cause of end-stage renal disease (ESRD) and is associated with increased morbidity and mortality in patients... AimsDiabetic kidney disease (DKD) is the most common cause of end-stage renal disease (ESRD) and is associated with increased morbidity and mortality in... Aims Diabetic kidney disease (DKD) is the most common cause of end-stage renal disease (ESRD) and is associated with increased morbidity and mortality in... |
| SourceID | doaj pubmedcentral proquest pubmed crossref informaworld |
| SourceType | Open Website Open Access Repository Aggregation Database Index Database Enrichment Source Publisher |
| StartPage | 562 |
| SubjectTerms | Algorithms Biopsy Blood glucose Clinical Study Diabetes Diabetes mellitus (non-insulin dependent) Diabetes Mellitus, Type 2 - complications Diabetes Mellitus, Type 2 - pathology diabetic kidney disease Diabetic Nephropathies - diagnosis Diabetic Nephropathies - etiology Diabetic Nephropathies - metabolism End-stage renal disease Glomerular filtration rate Hemoglobin Humans Kidney diseases Kidney Failure, Chronic - diagnosis Kidney Failure, Chronic - epidemiology Kidney Failure, Chronic - etiology Learning algorithms Machine Learning Morbidity Patients Prediction models Prognosis Proteinuria Risk factors risk prediction model Type 2 diabetes mellitus |
| SummonAdditionalLinks | – databaseName: DOAJ Directory of Open Access Journals dbid: DOA link: http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1Nj9MwELXQCiEuiG8CCzIS10Brx7F9BMSKCysOIPVmOcmkG9GmqzRdiX_Gz2PGdqp2hdQL1yR27PjZM2NP3mPsncT5X6Klym1d-bzw1Tw34MscNNriompLo6sgNqEvL81iYb8fSH1RTlikB44f7oNH9w9Alg1RoQNOzxYDFjuzFRpSqXTg-USvZwqm0vmBMkG2CacQpdiKxfTvDrFqG5JdEguMDQX9iYUmX8kjqxTI-29Rl_7LAb2dR3lgmC4esgfJo-QfY08esTvQP2b3vqUz8yfsz0FeEPd9w7u4CbjiCLIuSirxTcvXIa0SeNKRWHK_Wm6Gbrxabzm2kEPf5OhKLoEPQKXT0Q6n5HR-PdD7QlVBW4cqjMnpnHZ6Oe30csGnnV6-Jh7QcbcNDYpXu5r_6poefk81P2U_L778-Pw1T3oNeY1e1JibSnmMctGnLFoLXrSk6yFwZfcStPDCGAUzhERZNhhFgVTE1zZrTKWV0m1h5DN21m96eMG4klDYWetbaaDwc7BGFbVscGU2dVkrkbFiGi9XJzJz0tRYufnEeZqG2dEwuzTMGXu_L3Yd2TxOFfhEYNg_TGTc4QJC1CWIulMQzZg9hJIbw15MG4VTnDzRgPMJdy6tLlsntCHPFL25jL3d38Z1gQ57fA-bHT5TFqUlZ8Nm7HmE6b4XUkkt9RxL6yMAH3Xz-E7fXQXucWMxBBazl__ju7xi96mrMTnonJ2Nww5es7v1zdhthzdhQv8F-dVKug priority: 102 providerName: Directory of Open Access Journals – databaseName: ProQuest Central dbid: BENPR link: http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1Lj9MwELagixAX3o_CgozENdDacWyfEIt2xYVqhUDqLXKSSTfaNilNisQ_4-cx4zilXSH2wDWJHY8ynpcn38fYG4n7P0FPFdk8c1HssmlkwCURaPTFcVYmRmeebELPZmY-t-eh4NaGtsrBJnpDXTQ51cjfCW3IG6MHe7_-HhFrFJ2uBgqNm-yIkMriETs6OZ2df9mdIyjj6ZtwK1GrrZgP__AQurYh-iUxxxxR0B9Z6PqVPPBOHsT_CoTp3wLRq_2Uew7q7N7_inaf3Q2hKf_Q69IDdgPqh-z253D4_oj92msw4q4ueNVXE5cctbXquZl4U_KV788EHggpFtwtF_i67mLVchSRQ11EGJMugG-ARoczIk5d7ny9off5qTxJD03Yd7lzKhlzKhlzwYeSMV8RoGi3bf2C-qtVzi-rooafw8yP2bez068fP0WB-CHKMRzrIpMph-kyBqdxacGJkghCBLoIJ0ELJ4xRMEHdSpIC0zGQioDfJoXJtFK6jI18wkZ1U8MzxpWE2E5KV0oDsZuCNSrOZYEm3uRJrsSYxcMHT_OAik7kHMt0OoCnBj1JSU_SoCdj9nY3bN3Dglw34IS0afcwoXr7C81mkQYjkTpMdQBkUhDsP6ArKjE5txObYdAolcZJ7L4upp0v6pQ9A0sqr1nA8aB8aTBTbfpH88bs9e42Ghg6NXI1NFt8JokTS1GLHbOnvZ7vpJBKaqmnOFof7IADMQ_v1NWFBzE3FnNpMXn-72W9YHdIiL5_6JiNus0WXrJb-Y-uajevwm7_DZurW6E priority: 102 providerName: ProQuest |
| Title | Development and internal validation of machine learning algorithms for end-stage renal disease risk prediction model of people with type 2 diabetes mellitus and diabetic kidney disease |
| URI | https://www.tandfonline.com/doi/abs/10.1080/0886022X.2022.2056053 https://www.ncbi.nlm.nih.gov/pubmed/35373711 https://www.proquest.com/docview/2780612081 https://www.proquest.com/docview/2646942999 https://pubmed.ncbi.nlm.nih.gov/PMC8986220 https://doaj.org/article/a772ee36d4794e538f107909b3973573 |
| Volume | 44 |
| WOSCitedRecordID | wos000778107800001&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D |
| hasFullText | 1 |
| inHoldings | 1 |
| isFullTextHit | |
| isPrint | |
| journalDatabaseRights | – providerCode: PRVAON databaseName: DOAJ Directory of Open Access Journals customDbUrl: eissn: 1525-6049 dateEnd: 99991231 omitProxy: false ssIdentifier: ssj0015872 issn: 0886-022X databaseCode: DOA dateStart: 20160101 isFulltext: true titleUrlDefault: https://www.doaj.org/ providerName: Directory of Open Access Journals – providerCode: PRVPQU databaseName: Health & Medical Collection customDbUrl: eissn: 1525-6049 dateEnd: 99991231 omitProxy: false ssIdentifier: ssj0015872 issn: 0886-022X databaseCode: 7X7 dateStart: 20171101 isFulltext: true titleUrlDefault: https://search.proquest.com/healthcomplete providerName: ProQuest – providerCode: PRVPQU databaseName: ProQuest Central - New (Subscription) customDbUrl: eissn: 1525-6049 dateEnd: 99991231 omitProxy: false ssIdentifier: ssj0015872 issn: 0886-022X databaseCode: BENPR dateStart: 20171101 isFulltext: true titleUrlDefault: https://www.proquest.com/central providerName: ProQuest – providerCode: PRVPQU databaseName: ProQuest Publicly Available Content Database customDbUrl: eissn: 1525-6049 dateEnd: 99991231 omitProxy: false ssIdentifier: ssj0015872 issn: 0886-022X databaseCode: PIMPY dateStart: 20171101 isFulltext: true titleUrlDefault: http://search.proquest.com/publiccontent providerName: ProQuest – providerCode: PRVPQU databaseName: Research Library customDbUrl: eissn: 1525-6049 dateEnd: 99991231 omitProxy: false ssIdentifier: ssj0015872 issn: 0886-022X databaseCode: M2O dateStart: 20171101 isFulltext: true titleUrlDefault: https://search.proquest.com/pqrl providerName: ProQuest – providerCode: PRVAWR databaseName: Taylor & Francis customDbUrl: eissn: 1525-6049 dateEnd: 99991231 omitProxy: false ssIdentifier: ssj0015872 issn: 0886-022X databaseCode: TFW dateStart: 20170101 isFulltext: true titleUrlDefault: https://www.tandfonline.com providerName: Taylor & Francis – providerCode: PRVAWR databaseName: Taylor & Francis Open Access customDbUrl: eissn: 1525-6049 dateEnd: 99991231 omitProxy: false ssIdentifier: ssj0015872 issn: 0886-022X databaseCode: 0YH dateStart: 19870101 isFulltext: true titleUrlDefault: https://www.tandfonline.com providerName: Taylor & Francis |
| link | http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV3Nb9MwFLdgQ4gL37DCqIzENZDacWwfGVo1Di0VGqI7RU7idBFtOiXpJP4z_jzec5yqnUA7wMVSnDwnlp_fl19-j5B3HPZ_DJoq0Flqgsiko0BZEwdWgi6O0iJWMnXFJuR0quZzPfPZhI1Pq0QfuuiAIpysxs1t0qbPiPsAGyMG1TMH747hv1SgtAW_Sw4ZuCaY1RVenG0PEoRy9ZuQJECa_ieevw2zp54civ8NDNM_WaI3Eyp3NNT40X-Y22Py0Jun9GPHT0_IHVs9Jfcn_gD-Gfm1k2RE4SW07CKKSwocW3b1mei6oCuXo2mpL0qxoGa5WNdle7lqKMyS2ioPwC5dWFpbpPbnRBQz3elVje9zQ7lCPThgl-lOMWxMMWxMGe3DxnSFoKLtpnEf1PWWGf1R5pX92Y_8nHwbn55_Ogt88YcgA5OsDVQqDLjMYKBGhbaGFVgkhIGaMNxKZphSwobAX3Gcg0tmuUDwtzBXqRRCFpHiL8hBta7sEaGC20iHhSm4spEZWa1ElPEcxLzK4kywAYn6NU8yj4yOBTqWyagHUPWrkuCqJH5VBuT9luyqgwa5jeAEGWr7MCJ7u451vUi8oEgMuDvW8jhH6H8L6qgAB12HOgXDkQsJg-hddkxaF9gpuiosCb_lA4573k28qGoSJhWauWAaDsjb7W0QMnhyZCq73sAzcRRrtFz0gLzsWH07Cy645HIE1HJvE-xNc_9OVV46IHOlwZ9m4at_mNJr8gAvuwSjY3LQ1hv7htzLrtuyqYdOFkAr59K1akgOT06ns69DF3uBdsK-QN_s82R2AVfn4--_AdnnZO4 |
| linkProvider | Taylor & Francis |
| linkToHtml | http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMw1V1Lj9MwELaWLgIuvB-FBYwEx0Bix7FzQIjXaqvdVj0sUjkZJ3G6EW1a2hS0f4ozP4-ZxCntCrGnPXBNYtd2v3l4PJ6PkOcc5D8CS-XFaWK80CSBp6yJPCvBFodJHimZ1GQTcjBQo1E83CE_27swmFbZ6sRaUWezFGPkr5hUaI3Bgr2Zf_OQNQpPV1sKjQYWh_b0B2zZlq97H-D_fcHY_sfj9weeYxXwUrD1lacSYWAvBp5PmMfWsBzZJxjoH8OtZIYpJawPA4-iDHx9ywVWFfMzlUghZB4qDv1eIrshgF11yO6w1x9-Xp9bCFXTRYHoYmovG7V3hrCat0K6JzaCPSnDG2Dgagi-ZQ1r0oAzJVP_5viezd_cMIj7N_63pbxJrjvXm75tZOUW2bHlbXKl75IL7pBfGwlU1JQZLZpo6YSCNBYN9xSd5XRa559a6gg3xtRMxjC96mS6pLCk1JaZBz732NKFxdbuDIxiFj-dL_D36q5qEiLssMnipxgSpxgSp4y2IXE6xYKp1WpZD6h5WqT0a5GV9rTt-S75dCHrdo90yllpHxAquA1jPzc5VzY0gY2VCFOegQlTaZQK1iVhCzCduqrvSD4y0UFbHNbhUiMutcNll7xcN5s3ZU_Oa_AO0bv-GKuW1w9mi7F2SlAb2MpZy6MMaQ0smNo88GXsxwk4xVxI6CTexL6u6qBV3jDMaH7OAPZasGunhpf6D9K75Nn6NShQPBUzpZ2t4JsojGL0yuIuud_I1XoWXHDJZQCt5ZbEbU1z-01ZnNRF2lWsIsb8h_8e1lNy9eC4f6SPeoPDR-QaTqjJldojnWqxso_J5fR7VSwXT5ymoeTLRUvkb9uMtp8 |
| linkToPdf | http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1Lj9MwELZgQau98F62sICRuAbaOI7tI68KBFR7WERvlpPY3Yg2rZIUiX_Gz2PGcaJ2BdoDXOOMk5HH8_L4G0JeMNj_KViqSOWZiRKTTSJpTRpZAbY4yVwqReabTYjZTM7n6ixUEzahrBJjaNcBRXhdjZt7U7i-Iu4VbIwUTM8corsY71KB0ebsOrnhwbFApM-n34aDBC59_yYkiZCmv8Tzt2n2zJNH8b-EYfonT_RyQeWOhZre_g-83SG3gntKX3fydJdcs9U9cvglHMDfJ792iowofISWXUZxSUFiy64_E107uvI1mpaGphQLapaLdV22F6uGApfUVkUEfunC0toidTgnoljpTjc1fs9P5Rv14IRdpTvFtDHFtDGNaZ82pisEFW23jf-h7mmZ0-9lUdmf_cwPyNfp-_O3H6LQ_CHKwSVrI5lxAyEzOKiJU9bEDpuExGAmDLMiNrGU3I5BvtK0gJDMMo7gb-NCZoJz4RLJjslBta7sCaGc2USNnXFM2sRMrJI8yVkBal7mac7jEUn6Ndd5QEbHBh1LPekBVMOqaFwVHVZlRF4OZJsOGuQqgjcoUMPLiOztH6zrhQ6KQhsId6xlaYHQ_xbMkYMAXY1VBo4j4wImUbviqFuf2HFdFxbNrviB0152dVBVjY6FRDcXXMMReT4Mg5LBkyNT2fUW3kmTVKHnokbkYSfqAxeMM8HEBKjF3ibYY3N_pCovPJC5VBBPx-NH_8DSM3J49m6qP3-cfXpMjnCkqzU6JQdtvbVPyM38R1s29VOvFn4DDOxfqw |
| openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Development+and+internal+validation+of+machine+learning+algorithms+for+end-stage+renal+disease+risk+prediction+model+of+people+with+type+2+diabetes+mellitus+and+diabetic+kidney+disease&rft.jtitle=Renal+failure&rft.au=Zou%2C+Yutong&rft.au=Zhao%2C+Lijun&rft.au=Zhang%2C+Junlin&rft.au=Wang%2C+Yiting&rft.date=2022-12-01&rft.issn=1525-6049&rft.eissn=1525-6049&rft.volume=44&rft.issue=1&rft.spage=562&rft_id=info:doi/10.1080%2F0886022X.2022.2056053&rft.externalDBID=NO_FULL_TEXT |
| thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0886-022X&client=summon |
| thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0886-022X&client=summon |
| thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0886-022X&client=summon |