Distinct Biomarkers for Early Diagnosis of Diabetic Nephropathy

2017 ◽  
Vol 13 (6) ◽  
Author(s):  
Lalit Kishore ◽  
Navpreet Kaur ◽  
Randhir Singh
2019 ◽  
Vol 22 (07) ◽  
pp. 28-33
Author(s):  
Rawaa Behlul Al-Fatlawi ◽  
Kifah Jabbar Al-Yaqoobi ◽  
Ameera A Alsadawi ◽  
Najah R. Hadi ◽  
Kareem Ghaly ◽  
...  

2020 ◽  
Vol 2020 ◽  
pp. 1-7
Author(s):  
Mostafa Abdelsalam ◽  
A. M. Wahab ◽  
Maysaa El Sayed Zaki ◽  
Mohamad Motawea

Background. Diabetes mellitus is the leading cause of end-stage renal disease worldwide. Microalbuminuria is the cornerstone for the diagnosis of diabetic nephropathy. However, it is an inadequate marker for early diagnosis. MicroRNAs are not only new and promising markers for early diagnosis but also, but they may also play a role in the prevention of disease progression. Methods. This study included ninety patients with type 2 DM in addition to 30 control subjects. MicroRNA-451 expression in blood and plasma using real-time PCR was evaluated in addition to the classic diabetic nephropathy markers (serum creatinine, urinary albumin, and eGFR). Results. There was a significant difference between the studied groups versus control regarding serum creatinine, eGFR, urinary, and plasma microRNA-451 with p=0.0001. Patients with eGFR 60 ml/min/1.73 m2 showed a significantly higher plasma microRNA-451 (29.6 ± 1.6) and significantly lower urinary microRNA-451 (21 ± 0.9) in comparison to patients with eGFR >60 ml/min/1.73 m2 and p=0.0001. eGFR showed a positive correlation with urinary microRNA-451 and negative correlation with both plasma microRNA-451 and urinary albumin. Both plasma and urinary microRNA-451 are highly sensitive and specific markers for chronicity in diabetic nephropathy patients with sensitivity of 90.9% and 95.5% and specificity of 67.6% and 95.6%, respectively. Conclusion. MicroRNA-451 is a promising early biomarker for chronic kidney disease in diabetic nephropathy with high sensitivity and specificity.


2016 ◽  
Vol 2016 ◽  
pp. 1-13 ◽  
Author(s):  
Cristina Gluhovschi ◽  
Gheorghe Gluhovschi ◽  
Ligia Petrica ◽  
Romulus Timar ◽  
Silvia Velciov ◽  
...  

Diabetic nephropathy (DN) is a frequent and severe complication of diabetes mellitus (DM). Its diagnosis in incipient stages may allow prompt interventions and an improved prognosis. Towards this aim, biomarkers for detecting early DN can be used. Microalbuminuria has been proven a remarkably useful biomarker, being used for diagnosis of DN, for assessing its associated condition—mainly cardiovascular ones—and for monitoring its progression. New researches are pointing that some of these biomarkers (i.e., glomerular, tubular, inflammation markers, and biomarkers of oxidative stress) precede albuminuria in some patients. However, their usefulness is widely debated in the literature and has not yet led to the validation of a new “gold standard” biomarker for the early diagnosis of DN. Currently, microalbuminuria is an important biomarker for both glomerular and tubular injury. Other glomerular biomarkers (transferrin and ceruloplasmin) are under evaluation. Tubular biomarkers in DN seem to be of a paramount importance in the early diagnosis of DN since tubular lesions occur early. Additionally, biomarkers of inflammation, oxidative stress, podocyte biomarkers, and vascular biomarkers have been employed for assessing early DN. The purpose of this review is to provide an overview of the current biomarkers used for the diagnosis of early DN.


2019 ◽  
Vol 9 (1) ◽  
pp. 01-04
Author(s):  
Ketham Veera Sudhakar ◽  
◽  
B Ravindra Reddy ◽  
A Padma Vijaya Sree ◽  
◽  
...  

Author(s):  
T.T. Yarmola ◽  
L. Tkachenko ◽  
N. Mohilnik ◽  
A. Chernobay ◽  
A. Mohnachov

The aim of our research was to prove the feasibility of early diagnosis of diabetic nephropathy (DN), to optimize the treatment policy in the management ofpatients in I - II stage of chronic renal failure with hypertension. Materials and methods. We examined 43 patients with DN and chronic renal failure in I - II stages. Age fluctuations were in the range of 31 - 67 years. The ratio of male to female is, respectively, 1: 3. The disease duration of type 2 diabetes ranges from 2 to 15 years. Patients were evaluated after 1, 3 and 6 months. They were divided into two groups: the control group - 20patients treated: ACE inhibitor enalapril (active ingredient enalapril maleate, a daily dose of10 mg twice daily), if necessary, by combining with a blocker of slow calcium channels dihydropyridine amlodipine (active substance S - amlodipine 5 mg) and a diuretic (hydrochlorothiazide - 12.5 mg daily in the morning) or an aldosterone antagonist (spironolactone - 25 mg daily in the morning); main group - 23patients received an angiotensin IIreceptor antagonist type AT1 valsartan 80 mg or 160 mg or combined preparation  - 80mg, 160 mg of valsartan hydrochlorothiazide - 12.5 mg, if needed and / or early treatment combining amlodipine. Mandatory was to determine the level of daily proteinuria, serum creatinine and GFR calculation of sample Rehberg. The results of research. Source circadian AH type «dipper» is fixed in 62,8%, «non - dipper» - 27,9%, «over - dipper» - 7,0%, and «night - peaker» - 2,3% ofpatients. In 6 months were fixed an increasing number ofpatients with hypertension daily profile «dipper» up to 76.7%, the lack ofpatients with «night - peaker» and a decrease in the number ofpatients with «over - dipper» to 2.1%, and «non - dipper» - up to 21, 0% in the study group. In the control group these indicators were less pronounced. Statistically, there were no changes in the level of proteinuria as well as a decrease in the index of left ventricular mass in the control and in the main groups. Conclusions. In the absence of significant differences between the comparison groups of antihypertensive effect nephroprotective action, reducing the index of left ventricular mass, tolerability of treatment in the study group was significantly better than the control. Patients of the main group is significantly less needed for supplemental amlodipine. The use of valsartan hydrochlorothiazide had its preferences: BP control during the day and a single dose of the drug daily. It is known that patients category «non - dipper» have a worse prognosis than the category «dipper»; valsartan eliminates this effect in 76.7% ofpatients of the category «non - dipper», making them comparable to those forecasts in patients category «dipper». All of the above gives grounds to recommend these drugs to general practitioners (family medicine) as the drug of choice for the management ofpatients with chronic renal failure in I - II stages and hypertension with DN proves the need for comprehensive early diagnosis (including the identification of not only the common analyzes, microalbuminuria and proteinuria daily, and mandatory definition GFR)


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