Diabetes and Renal Complications: An Overview on Pathophysiology, Biomarkers and Therapeutic Interventions
Open accessAbstract
Diabetic kidney disease (DKD) is a major microvascular complication of both type 1 and type 2 diabetes. DKD is characterised by injury to both glomerular and tubular compartments, leading to kidney dysfunction over time. It is one of the most common causes of chronic kidney disease (CKD) and end-stage renal disease (ESRD). Persistent high blood glucose levels can damage the small blood vessels in the kidneys, impairing their ability to filter waste and fluids from the blood effectively. Other factors like high blood pressure (hypertension), genetics, and lifestyle habits can also contribute to the development and progression of DKD. The key features of renal complications of diabetes include morphological and functional alterations to renal glomeruli and tubules leading to mesangial expansion, glomerulosclerosis, homogenous thickening of the glomerular basement membrane (GBM), albuminuria, tubulointerstitial fibrosis and progressive decline in renal function. In advanced stages, DKD may require treatments such as dialysis or kidney transplant to sustain life. Therefore, early detection and proactive management of diabetes and its complications are crucial in preventing DKD and preserving kidney function.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
These complications serve as hallmarks of systemic microvascular pathology, indicating an increased likelihood of renal impairment.
“These complications serve as hallmarks of systemic microvascular pathology, indicating an increased likelihood of renal impairment (85).”
From Machine learning-based risk predictive models for diabetic kidney disease in type 2 diabetes mellitus patients: a systematic review and meta-analysis (2025) · cites this paper as [85]
The Abstract describes diabetic kidney disease as a microvascular complication that leads to kidney dysfunction, supporting the general link between microvascular damage and renal impairment. It does not say that the unspecified “these complications” are hallmarks of systemic microvascular pathology or that their presence indicates an increased likelihood of renal impairment; searches for retinopathy and neuropathy did not establish that link. (LLM, conf=0.76)
Experimental — accuracy not yet measuredDiabetic retinopathy and peripheral vascular disease are closely associated with an increased risk of DKD.
“Furthermore, complications, such as diabetic retinopathy and peripheral vascular disease are also closely associated with an increased risk of DKD.”
From Machine learning-based risk predictive models for diabetic kidney disease in type 2 diabetes mellitus patients: a systematic review and meta-analysis (2025) · cites this paper as [85]
The Abstract and Section 2 discuss DKD and its renal mechanisms but do not link diabetic retinopathy or peripheral vascular disease to increased DKD risk. Searches of our copy for “retinopathy” and “peripheral vascular disease” found no passage addressing either association; the indexed passages have no page numbers. (LLM, conf=0.76)
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
The citation lists haven’t been fetched yet
References 195 · Cited by 144
Research works printed but not linked: 186
- [1]De Boer I.H. Rue T.C. Hall Y.N. Heagerty P.J. Weiss N.S. Himmelfarb J. Temporal trends in the prevalence of diabetic kidney disease in the United States JAMA 2011 305 2532 2539 10.1001/jama.2011.861 21693741 PMC3731378 · DOI · Paper page
- [2]Sukkar L. Kang A. Hockham C. Young T. Jun M. Foote C. Pecoits-Filho R. Neuen B. Rogers K. Pollock C. Incidence and Associations of Chronic Kidney Disease in Community Participants with Diabetes: A 5-Year Prospective Analysis of the EXTEND45 Study Diabetes Care 2020 43 982 990 10.2337/dc19-1803 32161053 PMC7809711 · DOI
- [3]Wen H. Yang D. Xie C. Shi F. Liu Y. Zhang J. Yu C. Comparison of trend in chronic kidney disease burden between China, Japan, the United Kingdom, and the United States Front. Public Health 2022 10 999848 10.3389/fpubh.2022.999848 36159316 PMC9499831 · DOI
- [5]Rossing K. Christensen P.K. Jensen B.R. Parving H.H. Dual blockade of the renin-angiotensin system in diabetic nephropathy: A randomized double-blind crossover study Diabetes Care 2002 25 95 100 10.2337/diacare.25.1.95 11772908 · DOI
- [6]Ortiz A. Ferro C.J. Balafa O. Burnier M. Ekart R. Halimi J.M. Kreutz R. Mark P.B. Persu A. Rossignol P. Mineralocorticoid receptor antagonists for nephroprotection and cardioprotection in patients with diabetes mellitus and chronic kidney disease Nephrol. Dial. Transplant. 2023 38 10 25 10.1093/ndt/gfab167 33944938 · DOI
- [7]Goldfarb-Rumyantzev A. Hurdle J.F. Scandling J. Wang Z. Baird B. Barenbaum L. Cheung A.K. Duration of end-stage renal disease and kidney transplant outcome Nephrol. Dial. Transplant. 2005 20 167 175 10.1093/ndt/gfh541 15546892 · DOI
- [8]Rudberg S. Persson B. Dahlquist G. Increased glomerular filtration rate as a predictor of diabetic nephropathy--an 8-year prospective study Kidney Int. 1992 41 822 828 10.1038/ki.1992.126 1513104 · DOI
- [9]Chiarelli F. Cipollone F. Romano F. Tumini S. Costantini F. di Ricco L. Pomilio M. Pierdomenico S.D. Marini M. Cuccurullo F. Increased circulating nitric oxide in young patients with type 1 diabetes and persistent microalbuminuria: Relation to glomerular hyperfiltration Diabetes 2000 49 1258 1263 10.2337/diabetes.49.7.1258 10909986 · DOI
- [10]Palygin O. Spires D. Levchenko V. Bohovyk R. Fedoriuk M. Klemens C.A. Sykes O. Bukowy J.D. Cowley A.W. Jr. Lazar J. Progression of diabetic kidney disease in T2DN rats Am. J. Physiol. Ren. Physiol. 2019 317 F1450 F1461 10.1152/ajprenal.00246.2019 PMC6960784 31566426 · DOI
- [11]Tai H. Jiang X.-L. Kuang J.-S. Yu J.J.J. Ju Y.-T. Cao W.-C. Chen W. Cui X.-Y. Zhang L.-D. Fu X. Early changes in pulmonary function and intrarenal haemodynamics and the correlation between these sets of parameters in patients with T2DM PLoS ONE 2019 14 e0224923 10.1371/journal.pone.0224923 31851677 PMC6919602 · DOI
- [12]Jha J.C. Dai A. Garzarella J. Charlton A. Urner S. Østergaard J.A. Okabe J. Holterman C.E. Skene A. Power D.A. Independent of Renox, NOX5 Promotes Renal Inflammation and Fibrosis in Diabetes by Activating ROS-Sensitive Pathways Diabetes 2022 71 1282 1298 10.2337/db21-1079 35275988 · DOI
- [13]Lovshin J.A. Boulet G. Lytvyn Y. Lovblom L.E. Bjornstad P. Farooqi M.A. Lai V. Cham L. Tse J. Orszag A. Renin-angiotensin-aldosterone system activation in long-standing type 1 diabetes JCI Insight 2018 3 e96968 10.1172/jci.insight.96968 29321380 PMC5821172 · DOI
- [14]Jha J.C. Banal C. Chow B.S. Cooper M.E. Jandeleit-Dahm K. Diabetes and Kidney Disease: Role of Oxidative Stress Antioxid. Redox Signal. 2016 25 657 684 10.1089/ars.2016.6664 26906673 PMC5069735 · DOI · Paper page
- [15]Hashimoto Y. Yamagishi S. Mizukami H. Yabe-Nishimura C. Lim S.W. Kwon H.M. Yagihashi S. Polyol pathway and diabetic nephropathy revisited: Early tubular cell changes and glomerulopathy in diabetic mice overexpressing human aldose reductase J. Diabetes Investig. 2011 2 111 122 10.1111/j.2040-1124.2010.00071.x 24843470 PMC4015536 · DOI
- [16]Tuttle K.R. Anderberg R.J. Cooney S.K. Meek R.L. Oxidative stress mediates protein kinase C activation and advanced glycation end product formation in a mesangial cell model of diabetes and high protein diet Am. J. Nephrol. 2009 29 171 180 10.1159/000154470 18781061 · DOI
- [17]Nosadini R. Velussi M. Brocco E. Abaterusso C. Carraro A. Piarulli F. Morgia G. Satta A. Faedda R. Abhyankar A. Increased renal arterial resistance predicts the course of renal function in type 2 diabetes with microalbuminuria Diabetes 2006 55 234 239 10.2337/diabetes.55.01.06.db05-0881 16380498 · DOI
- [18]Zhang J. Jiang S. Wei J. Yip K.P. Wang L. Lai E.Y. Liu R. Glucose dilates renal afferent arterioles via glucose transporter-1 Am. J. Physiol. Ren. Physiol. 2018 315 F123 F129 10.1152/ajprenal.00409.2017 29513069 PMC6335005 · DOI
- [19]Nagahama T. Hayashi K. Ozawa Y. Takenaka T. Saruta T. Role of protein kinase C in angiotensin II-induced constriction of renal microvessels Kidney Int. 2000 57 215 223 10.1046/j.1523-1755.2000.00822.x 10620202 · DOI
- [20]Tuttle K.R. Agarwal R. Alpers C.E. Bakris G.L. Brosius F.C. Kolkhof P. Uribarri J. Molecular mechanisms and therapeutic targets for diabetic kidney disease Kidney Int. 2022 102 248 260 10.1016/j.kint.2022.05.012 35661785 · DOI
- [21]Fioretto P. Zambon A. Rossato M. Busetto L. Vettor R. SGLT2 Inhibitors and the Diabetic Kidney Diabetes Care 2016 39 S165 S171 10.2337/dcS15-3006 27440829 · DOI
- [22]Kawanami D. Matoba K. Takeda Y. Nagai Y. Akamine T. Yokota T. Sango K. Utsunomiya K. SGLT2 Inhibitors as a Therapeutic Option for Diabetic Nephropathy Int. J. Mol. Sci. 2017 18 1083 10.3390/ijms18051083 28524098 PMC5454992 · DOI
- [23]Ding M. Tang Z. Liu W. Shao T. Yuan P. Chen K. Zhou Y. Han J. Zhang J. Wang G. Burdock Fructooligosaccharide Attenuates High Glucose-Induced Apoptosis and Oxidative Stress Injury in Renal Tubular Epithelial Cells Front. Pharmacol. 2021 12 784187 10.3389/fphar.2021.784187 34955856 PMC8695902 · DOI
- [24]DeFronzo R.A. Reeves W.B. Awad A.S. Pathophysiology of diabetic kidney disease: Impact of SGLT2 inhibitors Nat. Rev. Nephrol. 2021 17 319 334 10.1038/s41581-021-00393-8 33547417 · DOI
- [25]Hernandez L.F. Eguchi N. Whaley D. Alexander M. Tantisattamo E. Ichii H. Anti-Oxidative Therapy in Diabetic Nephropathy Front Biosci (Sch. Ed.) 2022 14 14 10.31083/j.fbs1402014 35730439 · DOI
- [26]Asaba K. Tojo A. Onozato M.L. Goto A. Quinn M.T. Fujita T. Wilcox C.S. Effects of NADPH oxidase inhibitor in diabetic nephropathy Kidney Int. 2005 67 1890 1898 10.1111/j.1523-1755.2005.00287.x 15840036 · DOI
- [27]Etoh T. Inoguchi T. Kakimoto M. Sonoda N. Kobayashi K. Kuroda J. Sumimoto H. Nawata H. Increased expression of NAD(P)H oxidase subunits, NOX4 and p22phox, in the kidney of streptozotocin-induced diabetic rats and its reversibity by interventive insulin treatment Diabetologia 2003 46 1428 1437 10.1007/s00125-003-1205-6 13680125 · DOI
- [28]Jha J.C. Gray S.P. Barit D. Okabe J. El-Osta A. Namikoshi T. Thallas-Bonke V. Wingler K. Szyndralewiez C. Heitz F. Genetic targeting or pharmacologic inhibition of NADPH oxidase nox4 provides renoprotection in long-term diabetic nephropathy J. Am. Soc. Nephrol. 2014 25 1237 1254 10.1681/asn.2013070810 24511132 PMC4033375 · DOI · Paper page
- [29]Jha J.C. Banal C. Okabe J. Gray S.P. Hettige T. Chow B.S.M. Thallas-Bonke V. De Vos L. Holterman C.E. Coughlan M.T. NADPH Oxidase Nox5 Accelerates Renal Injury in Diabetic Nephropathy Diabetes 2017 66 2691 2703 10.2337/db16-1585 28747378 · DOI
- [30]Carlström M. Lai E.Y. Ma Z. Patzak A. Brown R.D. Persson A.E. Role of NOX2 in the regulation of afferent arteriole responsiveness Am. J. Physiol. Regul. Integr. Comp. Physiol. 2009 296 R72 R79 10.1152/ajpregu.90718.2008 18987286 · DOI · Paper page
- [31]Jha J.C. Thallas-Bonke V. Banal C. Gray S.P. Chow B.S. Ramm G. Quaggin S.E. Cooper M.E. Schmidt H.H. Jandeleit-Dahm K.A. Podocyte-specific Nox4 deletion affords renoprotection in a mouse model of diabetic nephropathy Diabetologia 2016 59 379 389 10.1007/s00125-015-3796-0 26508318 PMC6450410 · DOI
- [32]Rinaldi Tosi M.E. Bocanegra V. Manucha W. Gil Lorenzo A. Vallés P.G. The Nrf2-Keap1 cellular defense pathway and heat shock protein 70 (Hsp70) response. Role in protection against oxidative stress in early neonatal unilateral ureteral obstruction (UUO) Cell Stress. Chaperones 2011 16 57 68 10.1007/s12192-010-0221-y 20734248 PMC3024087 · DOI
- [33]Jha J.C. Dai A. Holterman C.E. Cooper M.E. Touyz R.M. Kennedy C.R. Jandeleit-Dahm K.A.M. Endothelial or vascular smooth muscle cell-specific expression of human NOX5 exacerbates renal inflammation, fibrosis and albuminuria in the Akita mouse Diabetologia 2019 62 1712 1726 10.1007/s00125-019-4924-z 31222503 · DOI
- [34]Foresto-Neto O. Albino A.H. Arias S.C.A. Faustino V.D. Zambom F.F.F. Cenedeze M.A. Elias R.M. Malheiros D. Camara N.O.S. Fujihara C.K. NF-κB System Is Chronically Activated and Promotes Glomerular Injury in Experimental Type 1 Diabetic Kidney Disease Front. Physiol. 2020 11 84 10.3389/fphys.2020.00084 32116790 PMC7026681 · DOI
- [35]Ha H. Yu M.R. Choi Y.J. Kitamura M. Lee H.B. Role of high glucose-induced nuclear factor-kappaB activation in monocyte chemoattractant protein-1 expression by mesangial cells J. Am. Soc. Nephrol. 2002 13 894 902 10.1681/asn.V134894 11912248 · DOI
- [36]Araújo L.S. Torquato B.G.S. da Silva C.A. Dos Reis Monteiro M.L.G. Dos Santos Martins A.L.M. da Silva M.V. Dos Reis M.A. Machado J.R. Renal expression of cytokines and chemokines in diabetic nephropathy BMC Nephrol. 2020 21 308 10.1186/s12882-020-01960-0 32723296 PMC7389446 · DOI
- [37]Fufaa G.D. Weil E.J. Nelson R.G. Hanson R.L. Knowler W.C. Rovin B.H. Wu H. Klein J.B. Mifflin T.E. Feldman H.I. Urinary monocyte chemoattractant protein-1 and hepcidin and early diabetic nephropathy lesions in type 1 diabetes mellitus Nephrol. Dial. Transplant. 2015 30 599 606 10.1093/ndt/gfv012 25648911 PMC4402379 · DOI
- [38]Pérez-Morales R.E. Del Pino M.D. Valdivielso J.M. Ortiz A. Mora-Fernández C. Navarro-González J.F. Inflammation in Diabetic Kidney Disease Nephron 2019 143 12 16 10.1159/000493278 30273931 · DOI
- [39]García-García P.M. Getino-Melián M.A. Domínguez-Pimentel V. Navarro-González J.F. Inflammation in diabetic kidney disease World J. Diabetes 2014 5 431 443 10.4239/wjd.v5.i4.431 25126391 PMC4127580 · DOI
- [40]Vallon V. Komers R. Pathophysiology of the diabetic kidney Compr. Physiol. 2011 1 1175 1232 10.1002/cphy.c100049 23733640 PMC6029262 · DOI
- [41]Watanabe K. Sato E. Mishima E. Miyazaki M. Tanaka T. What’s New in the Molecular Mechanisms of Diabetic Kidney Disease: Recent Advances Int. J. Mol. Sci. 2022 24 570 10.3390/ijms24010570 36614011 PMC9820354 · DOI
- [42]Jung S.W. Moon J.Y. The role of inflammation in diabetic kidney disease Korean J. Intern. Med. 2021 36 753 766 10.3904/kjim.2021.174 34237822 PMC8273831 · DOI
- [43]Hills C.E. Siamantouras E. Smith S.W. Cockwell P. Liu K.K. Squires P.E. TGFβ modulates cell-to-cell communication in early epithelial-to-mesenchymal transition Diabetologia 2012 55 812 824 10.1007/s00125-011-2409-9 22215279 · DOI
- [44]Putta S. Lanting L. Sun G. Lawson G. Kato M. Natarajan R. Inhibiting microRNA-192 ameliorates renal fibrosis in diabetic nephropathy J. Am. Soc. Nephrol. 2012 23 458 469 10.1681/asn.2011050485 22223877 PMC3294315 · DOI
- [45]Mahimainathan L. Das F. Venkatesan B. Choudhury G.G. Mesangial cell hypertrophy by high glucose is mediated by downregulation of the tumor suppressor PTEN Diabetes 2006 55 2115 2125 10.2337/db05-1326 16804083 · DOI
- [46]Nalin N. Al Dhanhani A. AlBawardi A. Sharma C. Chandran S. Yasin J. Bakoush O. Effect of angiotensin II on diabetic glomerular hyperpermeability: An in vivo permeability study in rats Am. J. Physiol. Ren. Physiol. 2020 319 F833 F838 10.1152/ajprenal.00259.2020 33017190 · DOI
- [47]Holterman C.E. Thibodeau J.F. Towaij C. Gutsol A. Montezano A.C. Parks R.J. Cooper M.E. Touyz R.M. Kennedy C.R. Nephropathy and elevated BP in mice with podocyte-specific NADPH oxidase 5 expression J. Am. Soc. Nephrol. 2014 25 784 797 10.1681/asn.2013040371 24262797 PMC3968494 · DOI
- [48]Eijkelkamp W.B. Zhang Z. Remuzzi G. Parving H.H. Cooper M.E. Keane W.F. Shahinfar S. Gleim G.W. Weir M.R. Brenner B.M. Albuminuria is a target for renoprotective therapy independent from blood pressure in patients with type 2 diabetic nephropathy: Post hoc analysis from the Reduction of Endpoints in NIDDM with the Angiotensin II Antagonist Losartan (RENAAL) trial J. Am. Soc. Nephrol. 2007 18 1540 1546 10.1681/asn.2006050445 17409317 · DOI
- [49]Toto R.D. Microalbuminuria: Definition, detection, and clinical significance J. Clin. Hypertens 2004 6 2 7 10.1111/j.1524-6175.2004.4064.x PMC8109505 15538104 · DOI
- [50]Lee S.R. An E.J. Kim J. Bae Y.S. Function of NADPH Oxidases in Diabetic Nephropathy and Development of Nox Inhibitors Biomol. Ther. 2020 28 25 33 10.4062/biomolther.2019.188 31875663 PMC6939690 · DOI
- [51]Zimnol A. Spicker N. Balhorn R. Schröder K. Schupp N. The NADPH Oxidase Isoform 1 Contributes to Angiotensin II-Mediated DNA Damage in the Kidney Antioxidants 2020 9 586 10.3390/antiox9070586 32635630 PMC7402089 · DOI
- [52]Gesualdo L. Fiorentino M. Conserva F. Pontrelli P. Should we enlarge the indication for kidney biopsy in patients with diabetes? The pro part Clin. Kidney J. 2024 17 sfad266 10.1093/ckj/sfad266 38186902 PMC10768746 · DOI
- [53]Di Paolo S. Fiorentino M. De Nicola L. Reboldi G. Gesualdo L. Barutta F. Natali A. Penno G. Fioretto P. Pugliese G. Indications for renal biopsy in patients with diabetes. Joint position statement of the Italian Society of Nephrology and the Italian Diabetes Society Nutr. Metab. Cardiovasc. Dis. 2020 30 2123 2132 10.1016/j.numecd.2020.09.013 33239162 · DOI
- [55]Tsalamandris C. Allen T.J. Gilbert R.E. Sinha A. Panagiotopoulos S. Cooper M.E. Jerums G. Progressive decline in renal function in diabetic patients with and without albuminuria Diabetes 1994 43 649 655 10.2337/diab.43.5.649 8168641 · DOI
- [56]Brenner B.M. Hostetter T.H. Humes H.D. Molecular basis of proteinuria of glomerular origin N. Engl. J. Med. 1978 298 826 833 10.1056/nejm197804132981507 634317 · DOI
- [57]Hovind P. Tarnow L. Rossing P. Graae M. Torp I. Binder C. Parving H.-H. Predictors for the development of microalbuminuria and macroalbuminuria in patients with type 1 diabetes: Inception cohort study BMJ 2004 328 1105 10.1136/bmj.38070.450891.FE 15096438 PMC406322 · DOI
- [58]Vistisen D. Andersen G.S. Hulman A. Persson F. Rossing P. Jørgensen M.E. Progressive Decline in Estimated Glomerular Filtration Rate in Patients with Diabetes after Moderate Loss in Kidney Function—Even without Albuminuria Diabetes Care 2019 42 1886 1894 10.2337/dc19-0349 31221677 · DOI · Paper page
- [59]Hasanato R.M. Diagnostic efficacy of random albumin creatinine ratio for detection of micro and macro-albuminuria in type 2 diabetes mellitus Saudi Med. J. 2016 37 268 273 10.15537/smj.2016.3.13567 26905348 PMC4800890 · DOI
- [60]Rondeau P. Bourdon E. The glycation of albumin: Structural and functional impacts Biochimie 2011 93 645 658 10.1016/j.biochi.2010.12.003 21167901 · DOI · Paper page
- [61]Freitas P.A.C. Ehlert L.R. Camargo J.L. Glycated albumin: A potential biomarker in diabetes Arch. Endocrinol. Metab. 2017 61 296 304 10.1590/2359-3997000000272 28699985 PMC10118799 · DOI
- [62]Kohzuma T. Tao X. Koga M. Glycated albumin as biomarker: Evidence and its outcomes J. Diabetes Complicat. 2021 35 108040 10.1016/j.jdiacomp.2021.108040 34507877 · DOI
- [63]Fang M. Daya N. Coresh J. Christenson R.H. Selvin E. Glycated Albumin for the Diagnosis of Diabetes in US Adults Clin. Chem. 2022 68 413 421 10.1093/clinchem/hvab231 35092266 PMC8897243 · DOI
- [65]Zacharski L.R. Shamayeva G. Chow B.K. DePalma R.G. Ferritin and Percent Transferrin Saturation Levels Predict Type 2 Diabetes Risk and Cardiovascular Disease Outcomes Curr. Diabetes Rev. 2017 13 428 436 10.2174/1573399813666170504163138 28474556 · DOI
- [66]Cho M.E. Hansen J.L. Peters C.B. Cheung A.K. Greene T. Sauer B.C. An increased mortality risk is associated with abnormal iron status in diabetic and non-diabetic Veterans with predialysis chronic kidney disease Kidney Int. 2019 96 750 760 10.1016/j.kint.2019.04.029 31345582 · DOI
- [67]Hansen J.B. Moen I.W. Mandrup-Poulsen T. Iron: The hard player in diabetes pathophysiology Acta Physiol. 2014 210 717 732 10.1111/apha.12256 24521359 · DOI
- [68]Zhao L. Zou Y. Zhang J. Zhang R. Ren H. Li L. Guo R. Zhang J. Liu F. Serum transferrin predicts end-stage Renal Disease in Type 2 Diabetes Mellitus patients Int. J. Med. Sci. 2020 17 2113 2124 10.7150/ijms.46259 32922172 PMC7484672 · DOI
- [70]Kawabata H. Transferrin and transferrin receptors update Free Radic. Biol. Med. 2019 133 46 54 10.1016/j.freeradbiomed.2018.06.037 29969719 · DOI
- [71]Quinlan G.J. Martin G.S. Evans T.W. Albumin: Biochemical properties and therapeutic potential Hepatology 2005 41 1211 1219 10.1002/hep.20720 15915465 · DOI
- [72]Bernard A.M. Amor A.A. Goemaere-Vanneste J. Antoine J.L. Lauwerys R.R. Lambert A. Vandeleene B. Microtransferrinuria is a more sensitive indicator of early glomerular damage in diabetes than microalbuminuria Clin. Chem. 1988 34 1920 1921 10.1093/clinchem/34.9.1920a 3416456 · DOI
- [73]Li B. Wang J. Ye W. A meta-analysis of urinary transferrin for early diagnosis of diabetic nephropathy Lab. Med. 2024 lmad115 10.1093/labmed/lmad115 38335130 · DOI
- [74]Abdalla M.M.I. Therapeutic potential of adiponectin in prediabetes: Strategies, challenges, and future directions Ther. Adv. Endocrinol. Metab. 2024 15 20420188231222371 10.1177/20420188231222371 38250316 PMC10798122 · DOI
- [75]Wang Z.V. Scherer P.E. Adiponectin, the past two decades J. Mol. Cell Biol. 2016 8 93 100 10.1093/jmcb/mjw011 26993047 PMC4816148 · DOI · Paper page
- [76]Yamauchi T. Kamon J. Minokoshi Y. Ito Y. Waki H. Uchida S. Yamashita S. Noda M. Kita S. Ueki K. Adiponectin stimulates glucose utilization and fatty-acid oxidation by activating AMP-activated protein kinase Nat. Med. 2002 8 1288 1295 10.1038/nm788 12368907 · DOI · Paper page
- [77]Shinnosuke Y. Hiroki C. Mikio I. Mika M. Yong-Huang J. Kenji S. Kazunari N. Satoshi W. Hitomi T. Mugiho K. Urinary adiponectin as a new diagnostic index for chronic kidney disease due to diabetic nephropathy BMJ Open Diabetes Res. Care 2019 7 e000661 10.1136/bmjdrc-2019-000661 PMC6557464 31245009 · DOI
- [78]Gitlin J.D. Transcriptional regulation of ceruloplasmin gene expression during inflammation J. Biol. Chem. 1988 263 6281 6287 10.1016/S0021-9258(18)68783-6 3360784 · DOI
- [79]Gembillo G. Labbozzetta V. Giuffrida A.E. Peritore L. Calabrese V. Spinella C. Stancanelli M.R. Spallino E. Visconti L. Santoro D. Potential Role of Copper in Diabetes and Diabetic Kidney Disease Metabolites 2023 13 17 10.3390/metabo13010017 36676942 PMC9866181 · DOI
- [80]de Paula Silva L. de Moraes Rego F.G. Picheth G. Müller-Santos M. Alberton D. Prospection of plasma proteins as biomarkers for diabetes mellitus monitoring J. Diabetes Metab. Disord. 2021 20 611 620 10.1007/s40200-021-00788-1 34222081 PMC8212233 · DOI
- [81]Sokolov A.V. Zakahrova E.T. Kostevich V.A. Samygina V.R. Vasilyev V.B. Lactoferrin, myeloperoxidase, and ceruloplasmin: Complementary gearwheels cranking physiological and pathological processes BioMetals 2014 27 815 828 10.1007/s10534-014-9755-2 24966132 · DOI
- [82]Sharma V.K. Tumbapo A. Pant V. Aryal B. Shrestha S. Yadav B.K. Tuladhar E.T. Bhattarai A. Raut M. Ceruloplasmin, a potential marker for glycemic status and its relationship with lipid profile in Type II diabetes mellitus Asian J. Med. Sci. 2018 9 13 18 10.3126/ajms.v9i2.19003 · DOI
- [83]Setty S. Michael A.A. Fish A.J. Michael Mauer S. Butkowski R.J. Virtanen I. Kim Y. Differential expression of laminin isoforms in diabetic nephropathy and other renal diseases Mod. Pathol. 2012 25 859 868 10.1038/modpathol.2011.216 22343787 PMC3698943 · DOI
- [84]Lehmann R. Schleicher E.D. Molecular mechanism of diabetic nephropathy Clin. Chim. Acta 2000 297 135 144 10.1016/S0009-8981(00)00240-0 10841915 · DOI
- [85]Shi R. Zhao W.M. Zhu L. Wang R.F. Wang D.G. Identification of basement membrane markers in diabetic kidney disease and immune infiltration by using bioinformatics analysis and experimental verification IET Syst. Biol. 2023 17 316 326 10.1049/syb2.12078 37776100 PMC10725710 · DOI
- [86]Yang M.T. Chang W.H. Kuo T.F. Shen M.Y. Yang C.W. Tien Y.J. Lai B.Y. Chen Y.R. Chang Y.C. Yang W.C. Identification of Novel Biomarkers for Pre-diabetic Diagnosis Using a Combinational Approach Front. Endocrinol. 2021 12 641336 10.3389/fendo.2021.641336 33995275 PMC8113970 · DOI
- [87]Menon M.C. Chuang P.Y. He C.J. The Glomerular Filtration Barrier: Components and Crosstalk Int. J. Nephrol. 2012 2012 749010 10.1155/2012/749010 22934182 PMC3426247 · DOI
- [88]Kopp J.B. Anders H.-J. Susztak K. Podestà M.A. Remuzzi G. Hildebrandt F. Romagnani P. Podocytopathies Nat. Rev. Dis. Primers 2020 6 68 10.1038/s41572-020-0196-7 32792490 PMC8162925 · DOI
- [89]Susztak K. Raff A.C. Schiffer M. Böttinger E.P. Glucose-Induced Reactive Oxygen Species Cause Apoptosis of Podocytes and Podocyte Depletion at the Onset of Diabetic Nephropathy Diabetes 2006 55 225 233 10.2337/diabetes.55.01.06.db05-0894 16380497 · DOI
- [90]Nakamura T. Ushiyama C. Suzuki S. Hara M. Shimada N. Ebihara I. Koide H. Urinary excretion of podocytes in patients with diabetic nephropathy Nephrol. Dial. Transplant. 2000 15 1379 1383 10.1093/ndt/15.9.1379 10978394 · DOI
- [91]Wang G. Lai F.M.-M. Lai K.-B. Chow K.-M. Li K.-T.P. Szeto C.-C. Messenger RNA Expression of Podocyte-Associated Molecules in the Urinary Sediment of Patients with Diabetic Nephropathy Nephron Clin. Pract. 2007 106 c169 c179 10.1159/000104428 17596726 · DOI
- [92]Hara M. Yamagata K. Tomino Y. Saito A. Hirayama Y. Ogasawara S. Kurosawa H. Sekine S. Yan K. Urinary podocalyxin is an early marker for podocyte injury in patients with diabetes: Establishment of a highly sensitive ELISA to detect urinary podocalyxin Diabetologia 2012 55 2913 2919 10.1007/s00125-012-2661-7 22854890 PMC3464371 · DOI
- [93]Pätäri A. Forsblom C. Havana M. Taipale H. Groop P.-H. Holthöfer H. FinnDiane Study Group Nephrinuria in Diabetic Nephropathy of Type 1 Diabetes Diabetes 2003 52 2969 2974 10.2337/diabetes.52.12.2969 14633858 · DOI
- [94]Zeng L. Szeto C.-C. Urinary podocyte markers in kidney diseases Clin. Chim. Acta 2021 523 315 324 10.1016/j.cca.2021.10.017 34666027 · DOI
- [95]Mårtensson J. Bellomo R. The Rise and Fall of NGAL in Acute Kidney Injury Blood Purif. 2014 37 304 310 10.1159/000364937 25170751 · DOI
- [96]Devarajan P. Neutrophil gelatinase-associated lipocalin (NGAL): A new marker of kidney disease Scand. J. Clin. Lab. Investig. Suppl. 2008 241 89 94 10.1080/00365510802150158 18569973 PMC2528839 · DOI
- [97]Li A. Yi B. Liu Y. Wang J. Dai Q. Huang Y. Li Y.C. Zhang H. Urinary NGAL and RBP Are Biomarkers of Normoalbuminuric Renal Insufficiency in Type 2 Diabetes Mellitus J. Immunol. Res. 2019 2019 5063089 10.1155/2019/5063089 31637265 PMC6766169 · DOI
- [98]Haase M. Bellomo R. Devarajan P. Ma Q. Bennett M.R. Möckel M. Matalanis G. Dragun D. Haase-Fielitz A. Novel biomarkers early predict the severity of acute kidney injury after cardiac surgery in adults Ann. Thorac. Surg. 2009 88 124 130 10.1016/j.athoracsur.2009.04.023 19559209 · DOI
- [99]Mishra J. Dent C. Tarabishi R. Mitsnefes M.M. Ma Q. Kelly C. Ruff S.M. Zahedi K. Shao M. Bean J. Neutrophil gelatinase-associated lipocalin (NGAL) as a biomarker for acute renal injury after cardiac surgery Lancet 2005 365 1231 1238 10.1016/S0140-6736(05)74811-X 15811456 · DOI · Paper page
- [100]Duan S. Chen J. Wu L. Nie G. Sun L. Zhang C. Huang Z. Xing C. Zhang B. Yuan Y. Assessment of urinary NGAL for differential diagnosis and progression of diabetic kidney disease J. Diabetes Complicat. 2020 34 107665 10.1016/j.jdiacomp.2020.107665 32653382 · DOI
- [101]Currie G. McKay G. Delles C. Biomarkers in diabetic nephropathy: Present and future World J. Diabetes 2014 5 763 776 10.4239/wjd.v5.i6.763 25512779 PMC4265863 · DOI
- [102]Phanish M.K. Chapman A.N. Yates S. Price R. Hendry B.M. Roderick P.J. Dockrell M.E.C. Evaluation of Urinary Biomarkers of Proximal Tubular Injury, Inflammation, and Fibrosis in Patients with Albuminuric and Nonalbuminuric Diabetic Kidney Disease Kidney Int. Rep. 2021 6 1355 1367 10.1016/j.ekir.2021.01.012 34013114 PMC8116913 · DOI
- [103]Sheira G. Noreldin N. Tamer A. Saad M. Urinary biomarker N-acetyl-β-D-glucosaminidase can predict severity of renal damage in diabetic nephropathy J. Diabetes Metab. Disord. 2015 14 4 10.1186/s40200-015-0133-6 25717442 PMC4340101 · DOI
- [104]Ghobrial E.E. Said A.M. Abd El Shaheed G.F. Shaalan Y.M. Urinary N-Acetyl-β-D glucosaminidase (uNAG) levels as an early marker for diabetic nephropathy in children with type 1 diabetes Egypt. Pediatr. Assoc. Gaz. 2022 70 31 10.1186/s43054-022-00126-x · DOI
- [105]Siddiqui K. Al-Malki B. George T.P. Nawaz S.S. Rubeaan K.A. Urinary N-acetyl-beta-d-glucosaminidase (NAG) with neutrophil gelatinase-associated lipocalin (NGAL) improves the diagnostic value for proximal tubule damage in diabetic kidney disease 3 Biotech. 2019 9 66 10.1007/s13205-019-1593-z 30729090 PMC6364253 · DOI
- [106]Ichimura T. Bonventre J.V. Bailly V. Wei H. Hession C.A. Cate R.L. Sanicola M. Kidney Injury Molecule-1 (KIM-1), a Putative Epithelial Cell Adhesion Molecule Containing a Novel Immunoglobulin Domain, Is Up-regulated in Renal Cells after Injury J. Biol. Chem. 1998 273 4135 4142 10.1074/jbc.273.7.4135 9461608 · DOI
- [107]Vaidya V.S. Niewczas M.A. Ficociello L.H. Johnson A.C. Collings F.B. Warram J.H. Krolewski A.S. Bonventre J.V. Regression of microalbuminuria in type 1 diabetes is associated with lower levels of urinary tubular injury biomarkers, kidney injury molecule-1, and N-acetyl-β-D-glucosaminidase Kidney Int. 2011 79 464 470 10.1038/ki.2010.404 20980978 PMC3033751 · DOI
- [108]Sabbisetti V.S. Waikar S.S. Antoine D.J. Smiles A. Wang C. Ravisankar A. Ito K. Sharma S. Ramadesikan S. Lee M. Blood kidney injury molecule-1 is a biomarker of acute and chronic kidney injury and predicts progression to ESRD in type I diabetes J. Am. Soc. Nephrol. 2014 25 2177 2186 10.1681/asn.2013070758 24904085 PMC4178434 · DOI
- [109]Ichimura T. Asseldonk E.J. Humphreys B.D. Gunaratnam L. Duffield J.S. Bonventre J.V. Kidney injury molecule-1 is a phosphatidylserine receptor that confers a phagocytic phenotype on epithelial cells J. Clin. Investig. 2008 118 1657 1668 10.1172/jci34487 18414680 PMC2293335 · DOI
- [110]Mori Y. Ajay A.K. Chang J.H. Mou S. Zhao H. Kishi S. Li J. Brooks C.R. Xiao S. Woo H.M. KIM-1 mediates fatty acid uptake by renal tubular cells to promote progressive diabetic kidney disease Cell Metab. 2021 33 1042 1061.e1047 10.1016/j.cmet.2021.04.004 33951465 PMC8132466 · DOI
- [111]Kim S.S. Song S.H. Kim I.J. Jeon Y.K. Kim B.H. Kwak I.S. Lee E.K. Kim Y.K. Urinary cystatin C and tubular proteinuria predict progression of diabetic nephropathy Diabetes Care 2013 36 656 661 10.2337/dc12-0849 23093662 PMC3579333 · DOI
- [112]Schrauben S.J. Shou H. Zhang X. Anderson A.H. Bonventre J.V. Chen J. Coca S. Furth S.L. Greenberg J.H. Gutierrez O.M. Association of Multiple Plasma Biomarker Concentrations with Progression of Prevalent Diabetic Kidney Disease: Findings from the Chronic Renal Insufficiency Cohort (CRIC) Study J. Am. Soc. Nephrol. 2021 32 115 126 10.1681/asn.2020040487 33122288 PMC7894671 · DOI
- [113]Kusano E. Suzuki M. Asano Y. Itoh Y. Takagi K. Kawai T. Human alpha 1-microglobulin and its relationship to renal function Nephron 1985 41 320 324 10.1159/000183608 2415841 · DOI
- [114]Ekrikpo U.E. Effa E.E. Akpan E.E. Obot A.S. Kadiri S. Clinical Utility of Urinary β2-Microglobulin in Detection of Early Nephropathy in African Diabetes Mellitus Patients Int. J. Nephrol. 2017 2017 4093171 10.1155/2017/4093171 28250988 PMC5303867 · DOI
- [115]Hong C.-Y. Hughes K. Chia K.-S. Ng V. Ling S.-L. Urinary α1-Microglobulin as a Marker of Nephropathy in Type 2 Diabetic Asian Subjects in Singapore Diabetes Care 2003 26 338 342 10.2337/diacare.26.2.338 12547859 · DOI
- [116]Zhang X. Zhou H. Li Y. Combined Detection of Urinary Micro Albumin, α1-microglobulin and N-acetyl-β-D-glucosaminidase in the Early Diagnosis of Diabetic Nephropathy Pak. J. Med. Sci. 2017 33 1324 1327 10.12669/pjms.336.13168 29492052 PMC5768818 · DOI
- [117]Kamijo-Ikemori A. Sugaya T. Kimura K. Urinary fatty acid binding protein in renal disease Clin. Chim. Acta 2006 374 1 7 10.1016/j.cca.2006.05.038 16860300 · DOI
- [118]Nakamura T. Sugaya T. Kawagoe Y. Ueda Y. Koide H. Effect of pioglitazone on urinary liver-type fatty acid-binding protein concentrations in diabetes patients with microalbuminuria Diabetes Metab. Res. Rev. 2006 22 385 389 10.1002/dmrr.633 16506273 · DOI
- [119]Kamijo-Ikemori A. Sugaya T. Sekizuka A. Hirata K. Kimura K. Amelioration of diabetic tubulointerstitial damage in liver-type fatty acid-binding protein transgenic mice Nephrol. Dial. Transplant. 2008 24 788 800 10.1093/ndt/gfn573 18854419 · DOI
- [120]Steinhoff J.S. Lass A. Schupp M. Biological Functions of RBP4 and Its Relevance for Human Diseases Front. Physiol. 2021 12 659977 10.3389/fphys.2021.659977 33790810 PMC8006376 · DOI
- [121]Basualdo C.G. Wein E.E. Basu T.K. Vitamin A (retinol) status of first nation adults with non-insulin-dependent diabetes mellitus J. Am. Coll. Nutr. 1997 16 39 45 10.1080/07315724.1997.10718647 9013432 · DOI
- [123]Norseen J. Hosooka T. Hammarstedt A. Yore M.M. Kant S. Aryal P. Kiernan U.A. Phillips D.A. Maruyama H. Kraus B.J. Retinol-Binding Protein 4 Inhibits Insulin Signaling in Adipocytes by Inducing Proinflammatory Cytokines in Macrophages through a c-Jun N-Terminal Kinase- and Toll-Like Receptor 4-Dependent and Retinol-Independent Mechanism Mol. Cell. Biol. 2012 32 2010 2019 10.1128/MCB.06193-11 22431523 PMC3347417 · DOI
- [124]Zhang L. Cheng Y.-L. Xue S. Xu Z.-G. The Role of Circulating RBP4 in the Type 2 Diabetes Patients with Kidney Diseases: A Systematic Review and Meta-Analysis Dis. Markers 2020 2020 8830471 10.1155/2020/8830471 33082885 PMC7556081 · DOI
- [125]Timpl R. Brown J.C. Supramolecular assembly of basement membranes Bioessays 1996 18 123 132 10.1002/bies.950180208 8851045 · DOI
- [126]Hudson B.G. Reeders S.T. Tryggvason K. Type IV collagen: Structure, gene organization, and role in human diseases. Molecular basis of Goodpasture and Alport syndromes and diffuse leiomyomatosis J. Biol. Chem. 1993 268 26033 26036 10.1016/S0021-9258(19)74270-7 8253711 · DOI
- [127]Ziyadeh F.N. Sharma K. Ericksen M. Wolf G. Stimulation of collagen gene expression and protein synthesis in murine mesangial cells by high glucose is mediated by autocrine activation of transforming growth factor-beta J. Clin. Investig. 1994 93 536 542 10.1172/jci117004 8113392 PMC293875 · DOI
- [128]Mahendran K.B. Bhaskar M.V. Santha K. Inmozhi R. Perumal K.K. Plasma and Urinary Type IV Collagen Levels for Early Detection of Nephropathy in Type 2 Diabetes Mellitus Patients Int. J. Health Sci. 2016 10 492 498 PMC5085343 27833513
- [129]Cohen M.P. Lautenslager G.T. Shearman C.W. Increased Collagen IV Excretion in Diabetes: A marker of compromised filtration function Diabetes Care 2001 24 914 918 10.2337/diacare.24.5.914 11347754 · DOI
- [130]Salem R.M. Todd J.N. Sandholm N. Cole J.B. Chen W.M. Andrews D. Pezzolesi M.G. McKeigue P.M. Hiraki L.T. Qiu C. Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen J. Am. Soc. Nephrol. 2019 30 2000 2016 10.1681/asn.2019030218 31537649 PMC6779358 · DOI
- [131]Carlsson A.C. Östgren C.J. Nystrom F.H. Länne T. Jennersjö P. Larsson A. Ärnlöv J. Association of soluble tumor necrosis factor receptors 1 and 2 with nephropathy, cardiovascular events, and total mortality in type 2 diabetes Cardiovasc. Diabetol. 2016 15 40 10.1186/s12933-016-0359-8 26928194 PMC4770690 · DOI
- [132]Gómez-Banoy N. Cuevas V. Higuita A. Aranzález L.H. Mockus I. Soluble tumor necrosis factor receptor 1 is associated with diminished estimated glomerular filtration rate in colombian patients with type 2 diabetes J. Diabetes Complicat. 2016 30 852 857 10.1016/j.jdiacomp.2016.03.015 27068267 · DOI
- [133]Doody A. Jackson S. Elliott J.A. Canavan R.J. Godson C. Slattery D. Twomey P.J. McKenna M.J. le Roux C.W. Docherty N.G. Validating the association between plasma tumour necrosis factor receptor 1 levels and the presence of renal injury and functional decline in patients with Type 2 diabetes J. Diabetes Complicat. 2018 32 95 99 10.1016/j.jdiacomp.2017.09.007 29122448 · DOI
- [134]Perlman A.S. Chevalier J.M. Wilkinson P. Liu H. Parker T. Levine D.M. Sloan B.J. Gong A. Sherman R. Farrell F.X. Serum Inflammatory and Immune Mediators Are Elevated in Early Stage Diabetic Nephropathy Ann. Clin. Lab. Sci. 2015 45 256 263 26116588
- [135]Shoukry A. Bdeer Sel A. El-Sokkary R.H. Urinary monocyte chemoattractant protein-1 and vitamin D-binding protein as biomarkers for early detection of diabetic nephropathy in type 2 diabetes mellitus Mol. Cell Biochem. 2015 408 25 35 10.1007/s11010-015-2479-y 26104579 · DOI
- [136]Wada T. Furuichi K. Sakai N. Iwata Y. Yoshimoto K. Shimizu M. Takeda S.-I. Takasawa K. Yoshimura M. Kida H. Up-regulation of monocyte chemoattractant protein-1 in tubulointerstitial lesions of human diabetic nephropathy Kidney Int. 2000 58 1492 1499 10.1046/j.1523-1755.2000.00311.x 11012884 · DOI
- [137]Shikano M. Sobajima H. Yoshikawa H. Toba T. Kushimoto H. Katsumata H. Tomita M. Kawashima S. Usefulness of a highly sensitive urinary and serum IL-6 assay in patients with diabetic nephropathy Nephron 2000 85 81 85 10.1159/000045634 10773760 · DOI
- [138]Sanchez-Alamo B. Shabaka A. Cachofeiro V. Cases-Corona C. Fernandez-Juarez G. Serum interleukin-6 levels predict kidney disease progression in diabetic nephropathy Clin. Nephrol. 2022 97 1 9 10.5414/CN110223 34753557 · DOI
- [139]Vodošek Hojs N. Bevc S. Ekart R. Hojs R. Oxidative Stress Markers in Chronic Kidney Disease with Emphasis on Diabetic Nephropathy Antioxidants 2020 9 925 10.3390/antiox9100925 32992565 PMC7600946 · DOI
- [140]Calabrese V. Mancuso C. Sapienza M. Puleo E. Calafato S. Cornelius C. Finocchiaro M. Mangiameli A. Di Mauro M. Stella A.M. Oxidative stress and cellular stress response in diabetic nephropathy Cell Stress Chaperones 2007 12 299 306 10.1379/csc-270.1 18229449 PMC2134792 · DOI
- [141]Chawla D. Bansal S. Banerjee B.D. Madhu S.V. Kalra O.P. Tripathi A.K. Role of advanced glycation end product (AGE)-induced receptor (RAGE) expression in diabetic vascular complications Microvasc. Res. 2014 95 1 6 10.1016/j.mvr.2014.06.010 24984291 · DOI
- [142]Pan H.-Z. Zhang L. Guo M.-Y. Sui H. Li H. Wu W.-H. Qu N.-Q. Liang M.-H. Chang D. The oxidative stress status in diabetes mellitus and diabetic nephropathy Acta Diabetol. 2010 47 71 76 10.1007/s00592-009-0128-1 19475334 · DOI
- [143]Tatsch E. Carvalho J.A.M.D. Hausen B.S. Bollick Y.S. Torbitz V.D. Duarte T. Scolari R. Duarte M.M.M.F. Londero S.W.K. Vaucher R.A. Oxidative DNA damage is associated with inflammatory response, insulin resistance and microvascular complications in type 2 diabetes Mutat. Res./Fundam. Mol. Mech. Mutagen. 2015 782 17 22 10.1016/j.mrfmmm.2015.10.003 26520687 · DOI
- [144]Good D.M. Zürbig P. Argilés A. Bauer H.W. Behrens G. Coon J.J. Dakna M. Decramer S. Delles C. Dominiczak A.F. Naturally occurring human urinary peptides for use in diagnosis of chronic kidney disease Mol. Cell Proteom. 2010 9 2424 2437 10.1074/mcp.M110.001917 20616184 PMC2984241 · DOI
- [145]Tofte N. Persson F. Rossing P. Omics research in diabetic kidney disease: New biomarker dimensions and new understandings? J. Nephrol. 2020 33 931 948 10.1007/s40620-020-00759-4 32474762 · DOI
- [146]Sandholm N. Cole J.B. Nair V. Sheng X. Liu H. Ahlqvist E. van Zuydam N. Dahlström E.H. Fermin D. Smyth L.J. Genome-wide meta-analysis and omics integration identifies novel genes associated with diabetic kidney disease Diabetologia 2022 65 1495 1509 10.1007/s00125-022-05735-0 35763030 PMC9345823 · DOI
- [147]Wei L. Gao J. Wang L. Tao Q. Tu C. Multi-omics analysis reveals the potential pathogenesis and therapeutic targets of diabetic kidney disease Human Mol. Genet. 2024 33 122 137 10.1093/hmg/ddad166 37774345 · DOI
- [148]Manrique C. Lastra G. Gardner M. Sowers J.R. The renin angiotensin aldosterone system in hypertension: Roles of insulin resistance and oxidative stress Med. Clin. N. Am. 2009 93 569 582 10.1016/j.mcna.2009.02.014 19427492 PMC2828938 · DOI
- [149]Cleveland K.H. Schnellmann R.G. Pharmacological Targeting of Mitochondria in Diabetic Kidney Disease Pharmacol. Rev. 2023 75 250 262 10.1124/pharmrev.122.000560 36781216 · DOI
- [150]Petrie J.R. Guzik T.J. Touyz R.M. Diabetes, Hypertension, and Cardiovascular Disease: Clinical Insights and Vascular Mechanisms Can. J. Cardiol. 2018 34 575 584 10.1016/j.cjca.2017.12.005 29459239 PMC5953551 · DOI · Paper page
- [151]Kim Y. Kim W. Kim J.K. Moon J.Y. Park S. Park C.W. Park H.S. Song S.H. Yoo T.H. Lee S.Y. Blood Pressure Control in Patients with Diabetic Kidney Disease Electrolyte Blood Press. 2022 20 39 48 10.5049/ebp.2022.20.2.39 36688208 PMC9827046 · DOI
- [152]Burnier M. Renin-Angiotensin System Blockade in Advanced Kidney Disease: Stop or Continue? Kidney Med. 2020 2 231 234 10.1016/j.xkme.2020.04.002 32734939 PMC7380388 · DOI
- [155]United States Renal Data System 2019 USRDS Annual Data Report: Epidemiology of Kidney Disease in the United States Am. J. Kidney Dis. 2020 75 A6 A7 10.1053/j.ajkd.2019.09.003 31704083 · DOI
- [156]Charlton A. Garzarella J. Jandeleit-Dahm K.A.M. Jha J.C. Oxidative Stress and Inflammation in Renal and Cardiovascular Complications of Diabetes Biology 2020 10 18 10.3390/biology10010018 33396868 PMC7830433 · DOI
- [157]De Boer I.H. Caramori M.L. Chan J.C. Heerspink H.J. Hurst C. Khunti K. Rossing P. KDIGO 2020 Clinical Practice Guideline for Diabetes Management in Chronic Kidney Disease Kidney Int. 2020 98 S1 S115 10.1016/j.kint.2020.06.019 32998798 · DOI · Paper page
- [159]Tong L.L. Adler S.G. Diabetic kidney disease treatment: New perspectives Kidney Res. Clin. Pract. 2022 41 S63 S73 10.23876/j.krcp.21.288 36239062 PMC9590300 · DOI
- [160]Anfossi G. Russo I. Bonomo K. Trovati M. The cardiovascular effects of metformin: Further reasons to consider an old drug as a cornerstone in the therapy of type 2 diabetes mellitus Curr. Vasc. Pharmacol. 2010 8 327 337 10.2174/157016110791112359 19485923 · DOI
- [161]Lee M.Y. Wang Y. Vanhoutte P.M. Senescence of cultured porcine coronary arterial endothelial cells is associated with accelerated oxidative stress and activation of NFkB J. Vasc. Res. 2010 47 287 298 10.1159/000265563 20016203 · DOI
- [162]Kleibert M. Zygmunciak P. Łakomska K. Mila K. Zgliczyński W. Mrozikiewicz-Rakowska B. Insight into the Molecular Mechanism of Diabetic Kidney Disease and the Role of Metformin in Its Pathogenesis Int. J. Mol. Sci. 2023 24 13038 10.3390/ijms241713038 37685845 PMC10487922 · DOI
- [163]Margonato D. Galati G. Mazzetti S. Cannistraci R. Perseghin G. Margonato A. Mortara A. Renal protection: A leading mechanism for cardiovascular benefit in patients treated with SGLT2 inhibitors Heart Fail. Rev. 2021 26 337 345 10.1007/s10741-020-10024-2 32901315 PMC7895775 · DOI
- [164]Tong L. Adler S. Glycemic control of type 2 diabetes mellitus across stages of renal impairment: Information for primary care providers Postgrad. Med. 2018 130 381 393 10.1080/00325481.2018.1457397 29667921 · DOI
- [165]Parab P. Chaudhary P. Mukhtar S. Moradi A. Kodali A. Okoye C. Klein D. Mohamoud I. Olanisa O.O. Hamid P. Role of Glucagon-Like Peptide-1 (GLP-1) Receptor Agonists in Cardiovascular Risk Management in Patients with Type 2 Diabetes Mellitus: A Systematic Review Cureus 2023 15 e45487 10.7759/cureus.45487 37859909 PMC10584355 · DOI
- [166]Collins L. Costello R.A. Glucagon-like Peptide-1 Receptor Agonists StatPearls StatPearls Publishing LLC. Treasure Island, FL, USA 2024 31855395
- [167]Daza-Arnedo R. Rico-Fontalvo J.-E. Pájaro-Galvis N. Leal-Martínez V. Abuabara-Franco E. Raad-Sarabia M. Montejo-Hernández J. Cardona-Blanco M. Cabrales-Juan J. Uparella-Gulfo I. Dipeptidyl Peptidase-4 Inhibitors and Diabetic Kidney Disease: A Narrative Review Kidney Med. 2021 3 1065 1073 10.1016/j.xkme.2021.07.007 34939016 PMC8664739 · DOI
- [168]Lerma E. White W.B. Bakris G. Effectiveness of nonsteroidal mineralocorticoid receptor antagonists in patients with diabetic kidney disease Postgrad. Med. 2023 135 224 233 10.1080/00325481.2022.2060598 35392754 · DOI · Paper page
- [169]Bauersachs J. Jaisser F. Toto R. Mineralocorticoid receptor activation and mineralocorticoid receptor antagonist treatment in cardiac and renal diseases Hypertension 2015 65 257 263 10.1161/hypertensionaha.114.04488 25368026 · DOI
- [170]Crook M. Type 2 diabetes mellitus: A disease of the innate immune system? An update Diabet. Med. 2004 21 203 207 10.1046/j.1464-5491.2003.01030.x 15008827 · DOI
- [171]Navarro J.F. Mora C. Role of inflammation in diabetic complications Nephrol. Dial. Transplant. 2005 20 2601 2604 10.1093/ndt/gfi155 16188894 · DOI
- [172]Hofherr A. Williams J. Gan L.M. Söderberg M. Hansen P.B.L. Woollard K.J. Targeting inflammation for the treatment of Diabetic Kidney Disease: A five-compartment mechanistic model BMC Nephrol. 2022 23 208 10.1186/s12882-022-02794-8 35698028 PMC9190142 · DOI
- [173]Perakakis N. Bornstein S.R. Birkenfeld A.L. Linkermann A. Demir M. Anker S.D. Filippatos G. Pitt B. Rossing P. Ruilope L.M. Efficacy of finerenone in patients with type 2 diabetes, chronic kidney disease and altered markers of liver steatosis and fibrosis: A FIDELITY subgroup analysis Diabetes Obes. Metab. 2024 26 191 200 10.1111/dom.15305 37814928 · DOI
- [174]Hudkins K.L. Li X. Holland A.L. Swaminathan S. Alpers C.E. Regression of diabetic nephropathy by treatment with empagliflozin in BTBR ob/ob mice Nephrol. Dial. Transplant. 2022 37 847 859 10.1093/ndt/gfab330 34865099 · DOI
- [175]He L. Li Y. Zhang D. Song H. Xu D. Song Z. Dapagliflozin improves endothelial cell dysfunction by regulating mitochondrial production via the SIRT1/PGC-1α pathway in obese mice Biochem. Biophys. Res. Commun. 2022 615 123 130 10.1016/j.bbrc.2022.05.022 35609417 · DOI
- [176]Budge K. Dellepiane S. Yu S.M. Cravedi P. Complement, a Therapeutic Target in Diabetic Kidney Disease Front. Med. 2020 7 599236 10.3389/fmed.2020.599236 33553201 PMC7858668 · DOI
- [177]Trambas I.A. Coughlan M.T. Tan S.M. Therapeutic Potential of Targeting Complement C5a Receptors in Diabetic Kidney Disease Int. J. Mol. Sci. 2023 24 8758 10.3390/ijms24108758 37240105 PMC10218149 · DOI
- [178]Tan S.M. Snelson M. Østergaard J.A. Coughlan M.T. The Complement Pathway: New Insights into Immunometabolic Signaling in Diabetic Kidney Disease Antioxid. Redox Signal. 2022 37 781 801 10.1089/ars.2021.0125 34806406 PMC9587781 · DOI
- [179]Bruchfeld A. Magin H. Nachman P. Parikh S. Lafayette R. Potarca A. Miao S. Bekker P. C5a receptor inhibitor avacopan in immunoglobulin A nephropathy-an open-label pilot study Clin. Kidney J. 2022 15 922 928 10.1093/ckj/sfab294 35498891 PMC9050557 · DOI
- [180]Jha J.C. Ho F. Dan C. Jandeleit-Dahm K. A causal link between oxidative stress and inflammation in cardiovascular and renal complications of diabetes Clin. Sci. 2018 132 1811 1836 10.1042/cs20171459 30166499 · DOI
- [181]Navarro-González J.F. Mora-Fernández C. Muros de Fuentes M. Chahin J. Méndez M.L. Gallego E. Macía M. del Castillo N. Rivero A. Getino M.A. Effect of pentoxifylline on renal function and urinary albumin excretion in patients with diabetic kidney disease: The PREDIAN trial J. Am. Soc. Nephrol. 2015 26 220 229 10.1681/asn.2014010012 24970885 PMC4279740 · DOI
- [182]Aranda-Rivera A.K. Cruz-Gregorio A. Pedraza-Chaverri J. Scholze A. Nrf2 Activation in Chronic Kidney Disease: Promises and Pitfalls Antioxidants 2022 11 1112 10.3390/antiox11061112 35740009 PMC9220138 · DOI
- [183]Robledinos-Antón N. Fernández-Ginés R. Manda G. Cuadrado A. Activators and Inhibitors of NRF2: A Review of Their Potential for Clinical Development Oxid. Med. Cell. Longev. 2019 2019 9372182 10.1155/2019/9372182 31396308 PMC6664516 · DOI
- [184]Tanase D.M. Gosav E.M. Anton M.I. Floria M. Seritean Isac P.N. Hurjui L.L. Tarniceriu C.C. Costea C.F. Ciocoiu M. Rezus C. Oxidative Stress and NRF2/KEAP1/ARE Pathway in Diabetic Kidney Disease (DKD): New Perspectives Biomolecules 2022 12 1227 10.3390/biom12091227 36139066 PMC9496369 · DOI
- [185]Ruggenenti P. The CARDINAL Trial of Bardoxolone Methyl in Alport Syndrome: When Marketing Interests Prevail over Patients Clinical Needs Nephron 2023 147 465 469 10.1159/000529471 36731435 · DOI
- [186]Al-Waili N. Al-Waili H. Al-Waili T. Salom K. Natural antioxidants in the treatment and prevention of diabetic nephropathy; a potential approach that warrants clinical trials Redox Rep. 2017 22 99 118 10.1080/13510002.2017.1297885 28276289 PMC6837693 · DOI
- [187]Ashrafizadeh M. Ahmadi Z. Mohammadinejad R. Farkhondeh T. Samarghandian S. Curcumin Activates the Nrf2 Pathway and Induces Cellular Protection Against Oxidative Injury Curr. Mol. Med. 2020 20 116 133 10.2174/1566524019666191016150757 31622191 · DOI
- [188]Hasheminasabgorji E. Jha J.C. Dyslipidemia, Diabetes and Atherosclerosis: Role of Inflammation and ROS-Redox-Sensitive Factors Biomedicines 2021 9 1602 10.3390/biomedicines9111602 34829831 PMC8615779 · DOI
- [189]Huang R. Fu P. Ma L. Kidney fibrosis: From mechanisms to therapeutic medicines Signal Transduct. Target. Ther. 2023 8 129 10.1038/s41392-023-01379-7 36932062 PMC10023808 · DOI
- [190]Nathan S.D. Costabel U. Albera C. Behr J. Wuyts W.A. Kirchgaessler K.U. Stauffer J.L. Morgenthien E. Chou W. Limb S.L. Pirfenidone in patients with idiopathic pulmonary fibrosis and more advanced lung function impairment Respir. Med. 2019 153 44 51 10.1016/j.rmed.2019.04.016 31153107 · DOI
- [191]Sharma K. Ix J.H. Mathew A.V. Cho M. Pflueger A. Dunn S.R. Francos B. Sharma S. Falkner B. McGowan T.A. Pirfenidone for diabetic nephropathy J. Am. Soc. Nephrol. 2011 22 1144 1151 10.1681/asn.2010101049 21511828 PMC3103734 · DOI
- [192]Adler S.G. Schwartz S. Williams M.E. Arauz-Pacheco C. Bolton W.K. Lee T. Li D. Neff T.B. Urquilla P.R. Sewell K.L. Phase 1 study of anti-CTGF monoclonal antibody in patients with diabetes and microalbuminuria Clin. J. Am. Soc. Nephrol. 2010 5 1420 1428 10.2215/cjn.09321209 20522536 PMC2924405 · DOI
- [193]Wang S. Li B. Li C. Cui W. Miao L. Potential Renoprotective Agents through Inhibiting CTGF/CCN2 in Diabetic Nephropathy J. Diabetes Res. 2015 2015 962383 10.1155/2015/962383 26421309 PMC4572424 · DOI
- [194]Sun X. Liu Y. Matrix Metalloproteinase-10 in Kidney Injury Repair and Disease Int. J. Mol. Sci. 2022 23 2131 10.3390/ijms23042131 35216251 PMC8877639 · DOI
- Authors
- Jha, R., Lopez-Trevino, S., Kankanamalage, H. R., & Jha, J. C.
- Affiliations
- Kansas College of Osteopathic Medicine, Wichita, KS 67202, USA
- Monash University (AU)
- Corresponding author
- Jha, Jay C.
- Venue
- Biomedicines
- Publisher
- MDPI AG
- Published
- 2024-05-15
- Volume
- 12
- Issue
- 5
- Pages
- 1098
- ISSN
- 2227-9059 (ISSN-L)
- PMC
- PMC11118045
- OpenAlex
- W4396918818
- Cited by
- 144
- References
- 195
- Citations by year
- 2026: 73 · 2025: 63 · 2024: 8
- FWCI
- 9.37
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Biomedicines (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- Topics
- Health Sciences › Medicine › Nephrology › Chronic Kidney Disease and Diabetes
- Health Sciences › Medicine › Nephrology › Renal Diseases and Glomerulopathies
- Health Sciences › Medicine › Nephrology › Acute Kidney Injury Research
- Keywords
- diabetic nephropathy, type 1 diabetes, type 2 diabetes, microvascular complications, chronic kidney disease, end-stage renal disease, glomerular injury, tubulointerstitial fibrosis, albuminuria, glomerulosclerosis, glomerular basement membrane thickening, mesangial expansion, hypertension, biomarkers, pathophysiology, therapeutic interventions, early detection
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review