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...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:Renal failure Ročník 44; číslo 1; s. 562 - 570
Hlavní autoři: Zou, Yutong, Zhao, Lijun, Zhang, Junlin, Wang, Yiting, Wu, Yucheng, Ren, Honghong, Wang, Tingli, Zhang, Rui, Wang, Jiali, Zhao, Yuancheng, Qin, Chunmei, Xu, Huan, Li, Lin, Chai, Zhonglin, Cooper, Mark E., Tong, Nanwei, Liu, Fang
Médium: Journal Article
Jazyk:angličtina
Vydáno: England Taylor & Francis 01.12.2022
Taylor & Francis Ltd
Taylor & Francis Group
Témata:
ISSN:0886-022X, 1525-6049, 1525-6049
On-line přístup:Získat plný text
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo vytvoří štítek k tomuto záznamu!
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
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)
Publicly Available Content Database
ProQuest Health & Medical Research Collection
ProQuest One Academic Middle East (New)
ProQuest 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: 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/eLvHCXMwrV1Lj9MwELbQCiEuiDeBBRmJayC187CPgFhxgBUHkHqzHGfcjWjTVZsi8c_4eczYTtWukHrhmsSOH188M_bk-xh7A5Q7g4Ynx1hAYIDSQW7RLuaudrJrEUCuCySuX5rLSzWf628HUl-UExbpgePAvbPo_gHIuiMqdMDP02PAogvdoiGVVRN4PtHrmYKpdH5QqSDbhO2gFFsxn_7dIVZtRbJLYo6xoaA_sdDkV_LIKgXy_hvUpf9yQG_mUR4Ypov77F7yKPn72JMH7BYMD9mdr-nM_BH7c5AXxO3Q8T5uAi45gqyPkkp87fkqpFUCTzoSC26Xi_WmH69WW44t5DB0ObqSC-AboNLpaIdTcjq_3tD7QlVBW4cqjMnpnHZ6Oe30csGnnV6-Ih7QcbcNDYpXe8d_9t0Av6eaH7MfF5--f_ycJ72G3KEXNeaqrSxGuehTll6DFZ50PQSu7FZCI6xQqoLCtbauO4yiQFbE11Z0qm2qqvGlkk_Y2bAe4Bnjha1gZp0G37rSe7BKWdvV3omibXXZZKyc5su4RGZOmhpLM5s4T9M0G5pmk6Y5Y2_3xa4jm8epAh8IDPuHiYw7XECImgRRcwqiGdOHUDJj2IvxUTjFyBMNOJ9wZ9LqsjWiUeSZojeXsdf727gu0GGPHWC9w2fqstbkbOiMPY0w3fdCVrKRzQxLN0cAPurm8Z2hvwrc40pjCCyK5_9jXF6wu9TVmBx0zs7GzQ5estvu19hvN6_CB_0XPiVLkQ
  priority: 102
  providerName: Directory of Open Access Journals
– databaseName: ProQuest Central
  dbid: BENPR
  link: http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV3LjtMwFLWggxAb3o_CgIzENpDaeTgrxKAZsYBqhEDqLnLsm05Em5YkReLP-DzudZzQjhCzYJvEjq2c-D58fQ5jr4BqZ9DwBBgLCAxQLAQa7WJgEiNtgQAy1pG4fkznc7VYZOc-4db6ssphTXQLtd0YypG_Eakia4wW7O32e0CqUbS76iU0rrMjYiqLJuzo5HR-_nncR4iVk2_C8VCprVgMZ3iIXVuR_JJYYIwo6EQWmv5YHlgnR-J_icL0b47o5XrKPQN1dud_p3aX3fauKX_XY-keuwb1fXbzk998f8B-7RUYcV1bXvXZxBVHtFa9NhPflHzt6jOBe0GKJderJb6uu1i3HKfIobYB-qRL4A1Qa79HxKnKnW8bep_ryon0UId9lTunlDGnlDEXfEgZ8zURina71g2ov1oZ_q2yNfwcen7Ivp6dfnn_IfDCD4FBd6wLVBFrDJfROY3KDLQoSSBEoInQElKhhVIxhKbQSWIxHAMZE_FbaFWRxnFaRko-YpN6U8MTxkMdw0ybDMrCRGUJWimtbVIaERZFFqVTFg0fPDeeFZ3EOVb5bCBP9TjJCSe5x8mUvR6bbXtakKsanBCaxoeJ1dtd2DTL3C8SucZQB0Amlmj_AU1RicF5FmYFOo0yTrGTbB-LeeeSOmWvwJLLKwZwPIAv98tUm_9B3pS9HG_jAkO7RrqGzQ6fSaIkI68lm7LHPc7HWchYpjKdYev04A84mObhnbq6cCTmKsNYWoRP_z2sZ-wWTaKvHzpmk67ZwXN2w_zoqrZ54f_235V9XHg
  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
  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 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: PRVPQU
  databaseName: 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: PRVAWR
  databaseName: Taylor & Francis Online Journals
  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/eLvHCXMwrV3db9MwELdgQ4gXvgeFURmJ10BqJ7HzyNCqIdFSoSG6p8hx7C6iTackReI_48_jznGqdgLtAV4sxcmdY_ni-_Dld4S8MZg7A4onAF-AgYNSmECBXgx0onmRgwDpwoG4fhLTqZzP05nPJmx8WiX60LYDinB7NX7cKm_6jLh3wD0B1TMH747hv1SgtGN-mxwycE0wqyu8ONseJMTS1W9CkgBp-p94_sZmTz05FP9rGKZ_skSvJ1TuaKjxg_8wt4fkvjdP6ftOnh6RW6Z6TO5O_AH8E_JrJ8mIwiC07CKKSwoSW3b1meja0pXL0TTUF6VYULVcrOuyvVw1FGZJTVUEYJcuDK0NUvtzIoqZ7vSqxvEcK1eoBxl2me4Uw8YUw8aU0T5sTFcIKtpuGvdCXW-p6feyqMzPnvNT8nV8ev7hLPDFHwINJlkbyDxW4DKDgRrZ1ChmsUgIAzWhuBFMMSljE-pcJUkBLpnhMYK_hYXMRRwLG0l-RA6qdWWeExqq2IyUTo3NdWStUVIqVSRWszDP00gMSNSveaY9MjoW6Fhmox5A1a9KhquS-VUZkLdbsqsOGuQmghMUqO3DiOztOtb1IvMbRabA3TGGJwVC_xtQRxYc9DRMczAceSyASborjlnrAju2q8KS8Rte4LiX3cxvVU3GhEQzF0zDAXm9vQ2bDJ4cqcqsN_BMEiUpWi7pgDzrRH07Cx5zwcUIqMXeR7A3zf07VXnpgMxlCv40C1_8w5Reknt42SUYHZODtt6YV-SO_tGWTT10ewG0Yi5cK4fk8OR0OvsydLEXaCfsM_TNPk5mF3B1Pv72Gw6rZcU
linkProvider Taylor & Francis
linkToHtml http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMw1V1Lj9MwELaWLgIuvFkKCxgJjoHUeTkHhHitttq26mGRyik4zqQbbZuWNgXtn-LMz2PGcUq7QuxpD1yT2LXdz_PyeD7GXgDlzqDicdAXEOigZOAo1IuODrWXpQggnZkirr1oMJCjUTzcYT-buzCUVtnIRCOos5mmGPlrEUnSxqjB3s6_OcQaRaerDYVGDYsjOPuBLtvyTfcj_r8vhTj4dPzh0LGsAo5GXV85Mg0U-mJo-fh5DErkxD4hUP4oDyKhhJQBuDpVYZihrQ9eQFXF3EymURBEuS897PcK2_UR7LLFdofd_vDL-twikIYuCudPqb1i1NwZomrekuiexAh9UkE3wNDUCLwtbWhIA86VTP2b4Xs-f3NDIR7c-t-W8ja7aU1v_q7eK3fYDpR32bW-TS64x35tJFBxVWa8qKOlE467sai5p_gs51OTfwrcEm6MuZqMcXrVyXTJcUk5lJmDNvcY-AKotT0D45TFz-cL-j3TlSEhog7rLH5OIXFOIXEueBMS51MqmFqtlmZA9dNC89MiK-Gs6fk--3wp6_aAtcpZCQ8Zd1UAHaVjyFPt5zkoKZXKwlwLN01jP2ozvwFYom3VdyIfmSSdpjisxWVCuEwsLtvs1brZvC57clGD94Te9cdUtdw8mC3GiRWCiUJXDsALM6I1AFS1eceNYjdO0Sj2ggg7iTexn1QmaJXXDDOJd8EA9huwJ1YML5M_SG-z5-vXKEDpVEyVMFvhN6EfxmSVxW22V--r9Sy8wIu8qIOto60dtzXN7TdlcWKKtMtYhkK4j_49rGfs-uFxv5f0uoOjx-wGTajOldpnrWqxgifsqv5eFcvFUytpOPt62TvyN6r3t3Y
linkToPdf http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1Lj9MwELZgQSsuvGELCxiJayCN83COvCoQS7WHRfRmOc64G9EmVZquxD_j5zHjOFW7Au0BrnFmkpEn8_LkG8ZeAfXOoOMJMBeIMEEpIdDoFwOTGlEWqECmdCCuJ9l0Kmez_NR3E659WyXl0LYHinC2mj7uVWmHjrg3yD1F1zPD7C6if6nQaSfiOrvhwLFQpc8m37cHCYl085uIJCCa4Seev7HZc08Oxf8ShumfItHLDZU7Hmpy5z_Idpfd9uEpf9vr0z12Der77PCrP4B_wH7tNBlxfAiv-origqPGVv18Jt5YvnQ9msD9UIo514t501bd-XLNUUoOdRlgXDoH3gJR-3MiTp3ufNXS8xwrN6iHGPad7pzKxpzKxjziQ9mYLwlUtNus3Qv1VyvDf1RlDT8Hzg_Zt8nHs_efAj_8ITAYknWBLBKNKTMGqLHNQUeWhoRE6Ca0gCzSkZQJhKbQaVpiSgYiIfC3sJRFliSZjaV4xA7qpoYjxkOdwFibHGxhYmtBS6l1mVoThUWRx9mIxcOeK-OR0WlAx0KNBwBVvyuKdkX5XRmx11uyVQ8NchXBO1Ko7c2E7O0uNO1ceUOhNKY7ACItCfof0B1ZTNDzMC8wcBRJhkzyXXVUnSvs2H4KixJXvMDxoLvKm6q1ijJJYS6GhiP2cruMRoZOjnQNzQbvSeM0p8glH7HHvapvpRCJyEQ2Rups7yPYE3N_pa7OHZC5zDGfjsIn_yDSC3Z4-mGiTj5Pvzxlt2il7zU6Zgddu4Fn7Ka56Kp1-9yZhd8kPGCC
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.eissn=1525-6049&rft.volume=44&rft.issue=1&rft.spage=562&rft_id=info:doi/10.1080%2F0886022X.2022.2056053&rft_id=info%3Apmid%2F35373711&rft.externalDocID=35373711
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