Urinary orosomucoid and retinol binding protein levels as early diagnostic markers for diabetic kidney Disease
Diabetic kidney disease (DKD) is the most common microvascular complication of diabetes, which has been a major cause of end-stage renal failure. Diagnosing diabetic kidney disease is important to prevent long-term kidney damage and determine the prognosis of patients with diabetes. In this study, w...
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Published in | BMC nephrology Vol. 24; no. 1; pp. 357 - 6 |
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Format | Journal Article |
Language | English |
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04.12.2023
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Abstract | Diabetic kidney disease (DKD) is the most common microvascular complication of diabetes, which has been a major cause of end-stage renal failure. Diagnosing diabetic kidney disease is important to prevent long-term kidney damage and determine the prognosis of patients with diabetes. In this study, we investigated the clinical significance of combined detection of urine orosomucoid and retinol-binding protein for early diagnosis of diabetic kidney disease.
We recruited 72 newly diagnosed patients with type 2 diabetes and 34 healthy persons from August 2016 to July 2018 at the First Affiliated Hospital of Henan Polytechnic University (Jiaozuo Second People's Hospital). Using the Mogensen grading criteria, participants were classified as having diabetes or diabetic kidney disease, and healthy persons constituted the control group. Urine orosomucoid and retinol-binding protein levels were measured and correlated with other variables.
With the aggravation of renal damage, the level of urinary mucoid protein gradually increased. Urinary retinol-binding protein and microalbumin levels were significantly higher in the diabetes group than in control and nephropathy groups. Orosomucoid and retinol-binding protein might be independent risk factors for diabetes and diabetic kidney disease. Urinary orosomucoid significantly correlated with retinol-binding protein and microalbumin levels in the diabetic kidney disease group.
Elevated urine orosomucoid and retinol-binding protein levels can be detected in the early stages of type 2 diabetic kidney disease. Both of these markers are important for diabetic kidney disease detection and early treatment. |
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AbstractList | Diabetic kidney disease (DKD) is the most common microvascular complication of diabetes, which has been a major cause of end-stage renal failure. Diagnosing diabetic kidney disease is important to prevent long-term kidney damage and determine the prognosis of patients with diabetes. In this study, we investigated the clinical significance of combined detection of urine orosomucoid and retinol-binding protein for early diagnosis of diabetic kidney disease.
We recruited 72 newly diagnosed patients with type 2 diabetes and 34 healthy persons from August 2016 to July 2018 at the First Affiliated Hospital of Henan Polytechnic University (Jiaozuo Second People's Hospital). Using the Mogensen grading criteria, participants were classified as having diabetes or diabetic kidney disease, and healthy persons constituted the control group. Urine orosomucoid and retinol-binding protein levels were measured and correlated with other variables.
With the aggravation of renal damage, the level of urinary mucoid protein gradually increased. Urinary retinol-binding protein and microalbumin levels were significantly higher in the diabetes group than in control and nephropathy groups. Orosomucoid and retinol-binding protein might be independent risk factors for diabetes and diabetic kidney disease. Urinary orosomucoid significantly correlated with retinol-binding protein and microalbumin levels in the diabetic kidney disease group.
Elevated urine orosomucoid and retinol-binding protein levels can be detected in the early stages of type 2 diabetic kidney disease. Both of these markers are important for diabetic kidney disease detection and early treatment. BackgroundDiabetic kidney disease (DKD) is the most common microvascular complication of diabetes, which has been a major cause of end-stage renal failure. Diagnosing diabetic kidney disease is important to prevent long-term kidney damage and determine the prognosis of patients with diabetes. In this study, we investigated the clinical significance of combined detection of urine orosomucoid and retinol-binding protein for early diagnosis of diabetic kidney disease.MethodsWe recruited 72 newly diagnosed patients with type 2 diabetes and 34 healthy persons from August 2016 to July 2018 at the First Affiliated Hospital of Henan Polytechnic University (Jiaozuo Second People’s Hospital). Using the Mogensen grading criteria, participants were classified as having diabetes or diabetic kidney disease, and healthy persons constituted the control group. Urine orosomucoid and retinol-binding protein levels were measured and correlated with other variables.ResultsWith the aggravation of renal damage, the level of urinary mucoid protein gradually increased. Urinary retinol-binding protein and microalbumin levels were significantly higher in the diabetes group than in control and nephropathy groups. Orosomucoid and retinol-binding protein might be independent risk factors for diabetes and diabetic kidney disease. Urinary orosomucoid significantly correlated with retinol-binding protein and microalbumin levels in the diabetic kidney disease group.ConclusionElevated urine orosomucoid and retinol-binding protein levels can be detected in the early stages of type 2 diabetic kidney disease. Both of these markers are important for diabetic kidney disease detection and early treatment. Diabetic kidney disease (DKD) is the most common microvascular complication of diabetes, which has been a major cause of end-stage renal failure. Diagnosing diabetic kidney disease is important to prevent long-term kidney damage and determine the prognosis of patients with diabetes. In this study, we investigated the clinical significance of combined detection of urine orosomucoid and retinol-binding protein for early diagnosis of diabetic kidney disease.BACKGROUNDDiabetic kidney disease (DKD) is the most common microvascular complication of diabetes, which has been a major cause of end-stage renal failure. Diagnosing diabetic kidney disease is important to prevent long-term kidney damage and determine the prognosis of patients with diabetes. In this study, we investigated the clinical significance of combined detection of urine orosomucoid and retinol-binding protein for early diagnosis of diabetic kidney disease.We recruited 72 newly diagnosed patients with type 2 diabetes and 34 healthy persons from August 2016 to July 2018 at the First Affiliated Hospital of Henan Polytechnic University (Jiaozuo Second People's Hospital). Using the Mogensen grading criteria, participants were classified as having diabetes or diabetic kidney disease, and healthy persons constituted the control group. Urine orosomucoid and retinol-binding protein levels were measured and correlated with other variables.METHODSWe recruited 72 newly diagnosed patients with type 2 diabetes and 34 healthy persons from August 2016 to July 2018 at the First Affiliated Hospital of Henan Polytechnic University (Jiaozuo Second People's Hospital). Using the Mogensen grading criteria, participants were classified as having diabetes or diabetic kidney disease, and healthy persons constituted the control group. Urine orosomucoid and retinol-binding protein levels were measured and correlated with other variables.With the aggravation of renal damage, the level of urinary mucoid protein gradually increased. Urinary retinol-binding protein and microalbumin levels were significantly higher in the diabetes group than in control and nephropathy groups. Orosomucoid and retinol-binding protein might be independent risk factors for diabetes and diabetic kidney disease. Urinary orosomucoid significantly correlated with retinol-binding protein and microalbumin levels in the diabetic kidney disease group.RESULTSWith the aggravation of renal damage, the level of urinary mucoid protein gradually increased. Urinary retinol-binding protein and microalbumin levels were significantly higher in the diabetes group than in control and nephropathy groups. Orosomucoid and retinol-binding protein might be independent risk factors for diabetes and diabetic kidney disease. Urinary orosomucoid significantly correlated with retinol-binding protein and microalbumin levels in the diabetic kidney disease group.Elevated urine orosomucoid and retinol-binding protein levels can be detected in the early stages of type 2 diabetic kidney disease. Both of these markers are important for diabetic kidney disease detection and early treatment.CONCLUSIONElevated urine orosomucoid and retinol-binding protein levels can be detected in the early stages of type 2 diabetic kidney disease. Both of these markers are important for diabetic kidney disease detection and early treatment. Diabetic kidney disease (DKD) is the most common microvascular complication of diabetes, which has been a major cause of end-stage renal failure. Diagnosing diabetic kidney disease is important to prevent long-term kidney damage and determine the prognosis of patients with diabetes. In this study, we investigated the clinical significance of combined detection of urine orosomucoid and retinol-binding protein for early diagnosis of diabetic kidney disease. We recruited 72 newly diagnosed patients with type 2 diabetes and 34 healthy persons from August 2016 to July 2018 at the First Affiliated Hospital of Henan Polytechnic University (Jiaozuo Second People's Hospital). Using the Mogensen grading criteria, participants were classified as having diabetes or diabetic kidney disease, and healthy persons constituted the control group. Urine orosomucoid and retinol-binding protein levels were measured and correlated with other variables. With the aggravation of renal damage, the level of urinary mucoid protein gradually increased. Urinary retinol-binding protein and microalbumin levels were significantly higher in the diabetes group than in control and nephropathy groups. Orosomucoid and retinol-binding protein might be independent risk factors for diabetes and diabetic kidney disease. Urinary orosomucoid significantly correlated with retinol-binding protein and microalbumin levels in the diabetic kidney disease group. Elevated urine orosomucoid and retinol-binding protein levels can be detected in the early stages of type 2 diabetic kidney disease. Both of these markers are important for diabetic kidney disease detection and early treatment. Background Diabetic kidney disease (DKD) is the most common microvascular complication of diabetes, which has been a major cause of end-stage renal failure. Diagnosing diabetic kidney disease is important to prevent long-term kidney damage and determine the prognosis of patients with diabetes. In this study, we investigated the clinical significance of combined detection of urine orosomucoid and retinol-binding protein for early diagnosis of diabetic kidney disease. Methods We recruited 72 newly diagnosed patients with type 2 diabetes and 34 healthy persons from August 2016 to July 2018 at the First Affiliated Hospital of Henan Polytechnic University (Jiaozuo Second People's Hospital). Using the Mogensen grading criteria, participants were classified as having diabetes or diabetic kidney disease, and healthy persons constituted the control group. Urine orosomucoid and retinol-binding protein levels were measured and correlated with other variables. Results With the aggravation of renal damage, the level of urinary mucoid protein gradually increased. Urinary retinol-binding protein and microalbumin levels were significantly higher in the diabetes group than in control and nephropathy groups. Orosomucoid and retinol-binding protein might be independent risk factors for diabetes and diabetic kidney disease. Urinary orosomucoid significantly correlated with retinol-binding protein and microalbumin levels in the diabetic kidney disease group. Conclusion Elevated urine orosomucoid and retinol-binding protein levels can be detected in the early stages of type 2 diabetic kidney disease. Both of these markers are important for diabetic kidney disease detection and early treatment. Keywords: Diabetic Nephropathy, Diagnosis, Urine microalbumin, Retinol-binding protein Abstract Background Diabetic kidney disease (DKD) is the most common microvascular complication of diabetes, which has been a major cause of end-stage renal failure. Diagnosing diabetic kidney disease is important to prevent long-term kidney damage and determine the prognosis of patients with diabetes. In this study, we investigated the clinical significance of combined detection of urine orosomucoid and retinol-binding protein for early diagnosis of diabetic kidney disease. Methods We recruited 72 newly diagnosed patients with type 2 diabetes and 34 healthy persons from August 2016 to July 2018 at the First Affiliated Hospital of Henan Polytechnic University (Jiaozuo Second People’s Hospital). Using the Mogensen grading criteria, participants were classified as having diabetes or diabetic kidney disease, and healthy persons constituted the control group. Urine orosomucoid and retinol-binding protein levels were measured and correlated with other variables. Results With the aggravation of renal damage, the level of urinary mucoid protein gradually increased. Urinary retinol-binding protein and microalbumin levels were significantly higher in the diabetes group than in control and nephropathy groups. Orosomucoid and retinol-binding protein might be independent risk factors for diabetes and diabetic kidney disease. Urinary orosomucoid significantly correlated with retinol-binding protein and microalbumin levels in the diabetic kidney disease group. Conclusion Elevated urine orosomucoid and retinol-binding protein levels can be detected in the early stages of type 2 diabetic kidney disease. Both of these markers are important for diabetic kidney disease detection and early treatment. |
ArticleNumber | 357 |
Audience | Academic |
Author | Yang, Bo Hou, Bao-hua Li, Yong-feng Liu, Shu-yan Zhou, Xue-hong |
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Keywords | Diagnosis Urine microalbumin Diabetic Nephropathy Retinol-binding protein |
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References | S Varghese (3363_CR4) 2007; 18 J Wu (3363_CR22) 2017; 42 K Furuichi (3363_CR2) 2018; 57 S Liu (3363_CR12) 2018; 9 A Schwandt (3363_CR10) 2017; 31 A Lewandowicz (3363_CR5) 2015; 125 H Wang (3363_CR7) 2020; 25 GV Kapoula (3363_CR1) 2019; 4 G Nichols (3363_CR11) 2011; 34 N Pallet (3363_CR21) 2014; 9 M Mahfouz (3363_CR8) 2016; 11 R Lage (3363_CR14) 2015; 416 NMS El-Beblawy (3363_CR6) 2016; 22 J Harreiter (3363_CR9) 2023; 135 Z Luo (3363_CR13) 2015; 71 A Klisic (3363_CR19) 2018; 23 N Papadopoulou-Marketou (3363_CR3) 2017; 54 R Fandiño-Vaquero (3363_CR16) 2014; 235 M Andreucci (3363_CR17) 2017; 39 N El-Beblawy (3363_CR15) 2016; 22 S Adiyanti (3363_CR18) 2012; 44 3363_CR20 |
References_xml | – volume: 22 start-page: 718 issue: 8 year: 2016 ident: 3363_CR15 publication-title: Clin Appl thrombosis/hemostasis: Official J Int Acad Clin Appl Thrombosis/Hemostasis doi: 10.1177/1076029616637185 – volume: 135 start-page: 7 year: 2023 ident: 3363_CR9 publication-title: Wiener Klinische Wochenschrift doi: 10.1007/s00508-022-02122-y – volume: 54 start-page: 326 issue: 5 year: 2017 ident: 3363_CR3 publication-title: Crit Rev Clin Lab Sci doi: 10.1080/10408363.2017.1377682 – volume: 34 start-page: 2374 issue: 11 year: 2011 ident: 3363_CR11 publication-title: Diabetes Care doi: 10.2337/dc11-0475 – volume: 125 start-page: 27 issue: 1–2 year: 2015 ident: 3363_CR5 publication-title: Pol Arch Med Wewn doi: 10.20452/pamw.2640 – volume: 25 start-page: 667 issue: 9 year: 2020 ident: 3363_CR7 publication-title: Nephrol (Carlton Vic) doi: 10.1111/nep.13707 – volume: 31 start-page: 1376 issue: 9 year: 2017 ident: 3363_CR10 publication-title: J Diabetes Complicat doi: 10.1016/j.jdiacomp.2017.06.016 – volume: 9 start-page: 1182 issue: 5 year: 2018 ident: 3363_CR12 publication-title: J Diabetes Invest doi: 10.1111/jdi.12828 – volume: 23 start-page: 44 year: 2018 ident: 3363_CR19 publication-title: J Res Med Sciences: Official J Isfahan Univ Med Sci doi: 10.4103/jrms.JRMS_893_17 – volume: 22 start-page: 718 issue: 8 year: 2016 ident: 3363_CR6 publication-title: Clin Appl Thromb Hemost doi: 10.1177/1076029616637185 – volume: 9 start-page: e84708 issue: 1 year: 2014 ident: 3363_CR21 publication-title: PLoS ONE doi: 10.1371/journal.pone.0084708 – volume: 4 start-page: 78 issue: 1 year: 2019 ident: 3363_CR1 publication-title: J Appl Lab Med doi: 10.1373/jalm.2018.028530 – volume: 235 start-page: 281 issue: 2 year: 2014 ident: 3363_CR16 publication-title: Atherosclerosis doi: 10.1016/j.atherosclerosis.2014.05.921 – ident: 3363_CR20 doi: 10.1155/2018/4578140 – volume: 11 start-page: 31 year: 2016 ident: 3363_CR8 publication-title: Biomark Insights doi: 10.4137/BMI.S33191 – volume: 416 start-page: 77 year: 2015 ident: 3363_CR14 publication-title: Mol Cell Endocrinol doi: 10.1016/j.mce.2015.08.025 – volume: 57 start-page: 3346 issue: 23 year: 2018 ident: 3363_CR2 publication-title: Intern Med doi: 10.2169/internalmedicine.1132-18 – volume: 42 start-page: 594 issue: 2 year: 2017 ident: 3363_CR22 publication-title: Cell Physiol Biochemistry: Int J Experimental Cell Physiol Biochem Pharmacol doi: 10.1159/000477860 – volume: 39 start-page: 1 year: 2017 ident: 3363_CR17 publication-title: Eur J Intern Med doi: 10.1016/j.ejim.2016.12.001 – volume: 71 start-page: 329 issue: 2 year: 2015 ident: 3363_CR13 publication-title: J Physiol Biochem doi: 10.1007/s13105-015-0389-9 – volume: 44 start-page: 246 issue: 3 year: 2012 ident: 3363_CR18 publication-title: Acta Med Indones – volume: 18 start-page: 913 issue: 3 year: 2007 ident: 3363_CR4 publication-title: J Am Soc Nephrology: JASN doi: 10.1681/ASN.2006070767 |
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Snippet | Diabetic kidney disease (DKD) is the most common microvascular complication of diabetes, which has been a major cause of end-stage renal failure. Diagnosing... Background Diabetic kidney disease (DKD) is the most common microvascular complication of diabetes, which has been a major cause of end-stage renal failure.... BackgroundDiabetic kidney disease (DKD) is the most common microvascular complication of diabetes, which has been a major cause of end-stage renal failure.... Abstract Background Diabetic kidney disease (DKD) is the most common microvascular complication of diabetes, which has been a major cause of end-stage renal... |
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SubjectTerms | Analysis Binding proteins Biomarkers Blood pressure Calibration Care and treatment Creatinine Diabetes Diabetes mellitus (non-insulin dependent) Diabetes Mellitus, Type 2 - complications Diabetes Mellitus, Type 2 - diagnosis Diabetic Nephropathies Diabetic Nephropathy Diagnosis End-stage renal disease Females Humans Kidney Kidney diseases Microvasculature Nephrology Nephropathy Orosomucoid - metabolism Patients Proteins Proteomics Regression analysis Renal failure Retinoids Retinol-binding protein Retinol-Binding Proteins - urine Risk factors Urine Urine microalbumin Variables Vitamin A |
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Title | Urinary orosomucoid and retinol binding protein levels as early diagnostic markers for diabetic kidney Disease |
URI | https://www.ncbi.nlm.nih.gov/pubmed/38049745 https://www.proquest.com/docview/2902115377 https://www.proquest.com/docview/2898312906 https://pubmed.ncbi.nlm.nih.gov/PMC10696675 https://doaj.org/article/b5266e837381492fab1a713e6a7d9fdc |
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