Skip to main content
Nephro-urology Monthly logoLink to Nephro-urology Monthly
. 2015 Jun 30;7(4):e28576. doi: 10.5812/numonthly.28576

Comparing the Levels of Trace Elements in Patients With Diabetic Nephropathy and Healthy Individuals

Atieh Makhlough 1, Marjan Makhlough 2,*, Mohammad Shokrzadeh 3, Mozhdeh Mohammadian 4,5, Omid Sedighi 5, Mansooreh Faghihan 6
PMCID: PMC4628134  PMID: 26539418

Abstract

Background:

Diabetic nephropathy is the most common cause of end stage renal disease (ESRD) in developed countries. Several trace elements were reported to be changed in diabetic nephropathy.

Objectives:

The aim of this study was to investigate changes in serum levels of zinc, copper and chromium and their association with the incidence of ESRD in patients with diabetes.

Patients and Methods:

This study was performed on 70 patients with type 2 diabetic nephropathy (macro and micro-albuminuria) and 70 healthy individuals. Samples were collected to survey metals by atomic absorption spectrophotometer. Data was analyzed by SPSS18 using descriptive and inferential analysis methods.

Results:

Mean ± SD levels of Zn, Cu and Cr were significantly decreased in blood samples of patients compared to healthy subjects (P < 0.01). Also the mean concentrations of Cu, Zn and Cr in drinking water of Sari were lower than the accepted limit. Only in one case, Cu was higher than the accepted limit, which was the possibility of contamination by water supply pipes.

Conclusions:

Cu, Zn and Cr play a specific role in the pathophysiology of diabetic nephropathy. Meanwhile in these patients, low serum levels of Cu, Zn and Cr were not associated with factors such as drinking water. Possible causes should be sought in other factors like urine, intervention factors in absorption and utilization and individual conditions.

Keywords: Diabetic Nephropathies, Zinc, Copper, Chromium, Atomic Absorption

1. Background

Diabetes mellitus is a group of metabolic disorders characterized by hyperglycemia. There are several types of diabetes caused by complicated genetic reactions and environmental factors. Hyperglycemia is caused by defects in insulin secretion, reduced glucose utilization and increased glucose production depending on the type of diabetes. End organ damage is the result of metabolic disorder in patients with diabetes, which is accompanied by other important problems for patients and health care system. In the USA, diabetes is the main cause of renal disease, also known as ESRD, non-traumatic lower extremity amputation and adults' blindness. It is the fourth reason of referring patients to physicians (1-5). Diabetes nephropathy occurs in both types 1 and 2 diabetes and also in genetic types of diabetes. It is the most common cause of ESRD in developed countries and includes 30% of these cases. Type 1 diabetes is usually easy to recognize and the epidemiology of diabetic nephropathy in type 1 has been more clarified. Micro-albuminuria occurs in almost 20% - 30% of patients with type 2 diabetes after 15 years. Less than a half of patients with micro-albuminuria would progress to end-stage renal disease (2, 3, 6).

Zinc (Zn) plays a functional act in nervous and immune systems, hormones activity, growth and development, taste and smells function and wound healing as well as proteins and nucleic acids synthesis (7-9), sexual maturation, release of vitamin A from the liver and cell wall structure (10). Zn is an important micronutrient, which has a major role in synthesis, storage, secretion and function of insulin and its metabolism is altered in diabetes (11, 12). Zn deficiency is correlated with insulin resistance (13, 14). In diabetic patients, chronic hyperglycemia due to glycosylation and peroxidation leads to increased oxidative stress and thereby proteins and lipids structure are changed (15). Lipid peroxidation produces toxic aldehydes; malondialdehyde (MDA) is one of the most poisonous molecules (16). Zn acts as a strong antioxidant (17, 18) and may decrease lipid peroxidation and improve antioxidant status in patients with diabetes (19, 20).

Hyperglycemia is the most important sign of diabetes induced by increased oxidative stress, free radicals production and proteins glycosylation. Copper (Cu) ions have more desire to bind to these proteins (15, 21). Cu binding glycosylated proteins can cause oxidative reactions, increased oxidative stress and free radicals production in diabetes (22, 23). The ceruloplasmin (Cu-carrying protein) can stimulate glycation and release Cu ions by accelerating oxidative stress in diabetes. Therefore, plasma level of Cu is increased (24), which can induce oxidative activity. In contrast, antioxidant defense system reduces damages by decreasing oxidative stress (25).

Chromium (Cr) is another element, which affects insulin action. The requirement of insulin would be reduced with sufficient dietary intake of Cr, which is very critical to prevent adverse effects of diabetes. Cr deficiency in diet causes impaired glucose tolerance. Chromium supplementation has an anti-diabetic effect and improves fasting blood sugar (FBS), insulin function, insulin-receptor binding, increased pancreas beta cells sensitivity and glucagon action (26). Cr plays a vital role in lipid and protein metabolism and regulation of water and also may decrease low density lipoprotein (LDL) and β lipoprotein. Cr is an inhibitor of oxidative stress. It can also reduce the effect of free radicals in type 2 diabetes (27, 28).

2. Objectives

Regarding trace element role in pathophysiology of renal dysfunction and their importance in diabetes, we measured these elements level (Zn, Cu and Cr) in patients with diabetic nephropathy and control subjects. In addition, we evaluated these elements levels in drinking water.

3. Patients and Methods

This study was performed at Mazandaran university of medical sciences, Sari city, during 2010 - 2011. Confirmation from ethical committee was taken before the study. The number of samples was selected based on the previous studies (22, 23). After obtaining informed consents, individuals were recruited for study groups. All participants in this study were subjected to complete history taking and thorough clinical examination. In case group, there was no history of type 1 diabetes, proteinuria with other reasons, hypertension more than 140/90, dialysis, transplantation, ARF (acute renal failure), malnutrition and use of supplementary such as Zn or other evaluated elements in mineral or purified water. Demographic characteristics were obtained through interviewing subjects. Weight was calculated using a balance standard measure. Systolic and diastolic blood pressures were measured using a standard mercury sphygmomanometer.

3.1. Biochemical Studies

24-hour urine samples were obtained from all subjects for evaluation of micro-albumin. Eventually, the term microalbuminuria is determined by a lower and upper limit for the urinary albumin concentration. Lower than 30 mg/day (or 20 mg/L) is assumed normal and above 300 mg/day (or 200 mg/L) considered as macroalbuminuria. The urinary albumin was evaluated by immunonephelometric testing.

After 12 hours overnight fasting, blood samples were taken through peripheral venous and serum was separated by centrifugation at 1500 rpm for 5 minutes and stored at 4°C until assayed. Serum FBS, Hb, HbA1c, uric acid, BUN (Blood Urea Nitrogen) and creatinine levels were measured by standard kits (Pars Azmoon, Iran) using an auto analyzer (prestige 24i, Japan).

3.2. Trace element Analysis

3.2.1. Serum Samples

Immediately after separating serum, each tube was diluted (1:3) with diluted glycerol and serum Zn, Cu and Cr were assessed using a varian atomic absorption spectrometer. The serum level of metals for each sample was obtained by calibration curve and dilution of samples.

3.2.2. Water Samples

Before collecting samples of drinking water, the water supply area of Sari city was detected coming from wells. Following chlorination, well water was pumped to distribution system. There are three water distribution supplies in Sari city. For sample collection, five points were chosen from each water distribution supply and samples (1 liter) were taken from the house water tap at 8 AM, 12 MD and 4PM. The samples were then transferred into a container of 3 liter and mixed. Then 1 liter was taken from the mixed samples and pH was adjusted between 4.6 and 6.4. Testing sample was sent to the toxicology laboratory and stored below 4°C. Before analysis, the samples were fixed by nitric acid 65% and stored in the refrigerator until analyzed. Finally, the levels of mentioned metals were evaluated by an atomic absorption spectrophotometer model A100.

3.3. Statistical Analysis

Data was analyzed using SPSS v.18. Independent-samples t-test was used to compare data between the two groups. P values less than 0.05 considered significant in all studies.

4. Results

The study population included 70 patients (30 - 60 years old) with type 2 diabetic nephropathy (micro and macroalbuminuria) (cases) and 70 healthy subjects (controls) matched for age and gender and other variables. Both case and control groups were subjected to complete history taking and clinical examination; individuals with complications mentioned above were excluded from the study. Demographic data, duration of diabetes and findings of clinical and laboratory examination of both case and control groups are presented in Table 1.

Table 1. Demographic Parameters, Clinical and Laboratory Findings and Duration of Disease in Cases and Controls.

Cases Controls P Value
Age, y 55.17 ± 3.71 51.16 ± 1.94 0.084
Weight, Kg 77.87 ± 8.09 75.59 ± 4.60 0.59
Hb, g/dL 13.08 ± 0.62 14.75 ± 1.34 0.110
FBS, mg/dL 197.62 ± 21.81 92.92 ± 9.72 0.001
SBP, mmHg 130.11 ± 0.34 120.04 ± 0.13 0.001
DBP, mmHg 80.35 ± 0.13 80.01 ± 0.06 0.004
Creatinine, mg/dL 1.01 ± 0.06 0.87 ± 0.04 0.09
BUN, mg/dL 22.82 ± 2.15 9.5 ± 1.75 <0.001
Microalbuminuria, mg/d 209.63 ± 16.39 13.58 ± 2.14 0.008
Uric acid, mg/dL 6.26 ± 1.30 4.90 ± 0.93 0.067
HbA1c,% 8.68 ± 0.40 5.53 ± 0.31 <0.001
Duration of diabetes 13.21 ± 2.84 - -

Cu, Cr and Zn were assessed in both case and control groups using a varian atomic absorption spectrometer model A100. Figure 1 demonstrated the values of these elements in case and control groups.

Figure 1. Comparison of Serum Trace Elements Level in Cases and Controls.

Figure 1.

Trace Elements in Cases are Significantly Lower Than Controls (*, P < 0.001). Errors Bars Represent Standard Deviation.

Albumin was evaluated on 24-hour urine samples of patients and healthy individuals. Urine protein in micro-albuminuria and macro-albuminuria were 113.43 ± 41.38 mg/dL and 514.35 ± 90.11 mg/dL, respectively. Figure 2 illustrated the comparison of serum trace elements level in patients with micro- and macro-albuminuria.

Figure 2. Comparison of Serum Trace Elements Level in Cases With Micro and Macro Albuminuria. Cu and Zn in Patients With Micro-Albuminuria are Significantly Higher than in Those With Macro-Albuminuria.

Figure 2.

There was no significant difference in Cr values in micro and macro albuminuria cases (*, P < 0.05). Errors bars represent standard deviation.

The values of trace elements in drinking water are represented in Table 2.

Table 2. Comparison of Serum Trace Elements Level (mean ± SD) in Drinking Water a.

Cu Zn Cr
Values 695.25 ± 11.57 1241.5 ± 9.59 28.6 ± 5.59
Iran Standard accepted limit 1000 accepted limit 3000 accepted limit 50
WHO Standard accepted limit 2000 accepted limit 3000 accepted limit 50

a All unit are based on µg/L.

5. Discussion

Several studies indicated that imbalance of some fundamental metals can adversely affect pancreatic islet that cause diabetes. However, imbalance of essential metals induced generation of some reactive oxygen species (ROS) during diabetes. Hyperglycemia causes oxidative stress that can lead to a reduction of gene promoter activity and expression of mRNA in pancreatic islet cells. Assessment of trace elements such as Zn, Cu and Cr in various diseases including diabetes remains contradictory with a lot of unanswered questions (6, 29).

According to the results in the present study, patients with diabetic nephropathy had lower serum concentrations of Zn, Cu and Cr than healthy individuals. Our data was in coordination with Jamshidi et al. study, which demonstrated a decrease in serum level of Zn in male and female with type 2 diabetes compared to both genders in healthy group (30). Kazi et al. reported a significant reduction in Zn level in blood and scalp hair samples and also its increase in urine of both genders in diabetic patients (31). In a study performed by Nasli-Esfahani et al. the level of elements in hair, nail, urine and serum were evaluated in type 2 diabetic patients; their results indicated a meaningful decrease in serum level of Zn in patients compared to healthy individuals (32). In a research performed by Adewumi et al. the serum level of Cu in type 2 diabetic patients of both genders was significantly decreased in patient groups compared with healthy individuals (33), which was in accordance with our study. Our results were in agreement with Kazi et al. study, in which type 2 diabetic patients had lower values of Cr in blood and scalp hair samples in men and women compared with healthy subjects (31). Nasli-Esfahani et al. and Saboori et al. demonstrated low serum Cr in diabetic patients compared to healthy individuals (32, 34), which is in accordance to our findings.

Our research displayed a significant difference in serum Cu and Zn levels between patients with macro and microalbuminuria; as serum copper and zinc concentrations in patients with microalbuminuria were remarkably higher than patients with macroalbuminuria. As well, Talaei et al. evaluated levels of proteinuria and Cu in diabetes and a positive association between microalbuminuria and urine Cu level has been found; as higher levels of urinary copper have been shown in diabetics (35). In diabetic patients with nephropathy, high levels of urinary copper may be associated with excretion of its carrier proteins, ceruloplasmin. Copper excretion in urine may also be caused by dissociations from both copper-albumin and ceruloplasmin-copper complexes filtered through the disturbed glomerulus. High urinary copper can damage renal tubules and play an important function in the development of nephropathy (35). A relationship between serum zinc and albuminuria has been detected in various researches for type 1 and type 2 diabetes (36). Decreased serum concentration of zinc assumed to be the result of increased urinary albumin excretion by microvascular injury. Regarding our survey and other studies, low levels of these elements can be considered as a risk factor for diabetes. There are inconsistent findings about the association of serum Cu level with diabetes incidence, which necessitates further investigations. In addition, results indicate that factors such as drinking water have no role in low serum levels of Cu, Zn and Cr in patients with diabetic nephropathy and the reason should be studied in other causes such as urinary excretion, amount of these elements in each meal, intervention factors in absorption and utilization and individual conditions. The dietary minerals and their effects on diabetic persons need more research and interventional studies. Excessive urination in diabetic subjects may be a potential cause fort these trace elements deficiency.

Regarding our study, serum Zn, Cu and Cr levels were low in patients with diabetic nephropathy, whereas no association was found between drinking water and serum concentration of these trace elements in patients with diabetic nephropathy. The mentioned trace elements are cofactors of different enzymes playing a major role in the etiology of diabetes. It is recommended to perform future studies to investigate the association between serum levels of these enzymes and other metals including selenium, magnesium and iron.

Acknowledgments

We would like to express our sincere appreciation to all participants and also researching vice-chancellor of Mazandaran university of medical sciences.

Footnotes

Authors’ Contributions:Study concept and design: Atieh Makhlough, Mohammad Shokrzadeh. Acquisition of data: Marjan Makhlough, Omid Sedighi, Mansooreh Faghihan. Analysis and interpretation of data: Marjan Makhlough, Mozhdeh Mohammadian. Drafting of the manuscript: Marjan Makhlough, Mozhdeh Mohammadian. Critical revision of the manuscript for important intellectual content: Atieh Makhlough, Mohammad Shokrzadeh. Statistical analysis: Mozhdeh Mohammadian, Administrative, technical, and material support: Marjan Makhlough. Study supervision: Marjan Makhlough.

Funding/Support:This study was supported by grant from Mazandaran university of medical sciences.

References

  • 1.Aryangat AV, Gerich JE. Type 2 diabetes: postprandial hyperglycemia and increased cardiovascular risk. Vasc Health Risk Manag. 2010;6:145–55. doi: 10.2147/vhrm.s8216. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.American Diabetes A. Diagnosis and classification of diabetes mellitus. Diabetes Care. 2010;33 Suppl 1:S62–9. doi: 10.2337/dc10-S062. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Foley RN, Collins AJ. End-stage renal disease in the United States: an update from the United States Renal Data System. J Am Soc Nephrol. 2007;18(10):2644–8. doi: 10.1681/ASN.2007020220. [DOI] [PubMed] [Google Scholar]
  • 4.Li Y, Burrows NR, Gregg EW, Albright A, Geiss LS. Declining rates of hospitalization for nontraumatic lower-extremity amputation in the diabetic population aged 40 years or older: U.S., 1988-2008. Diabetes Care. 2012;35(2):273–7. doi: 10.2337/dc11-1360. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Xu Y, Wang L, He J, Bi Y, Li M, Wang T, et al. Prevalence and control of diabetes in Chinese adults. JAMA. 2013;310(9):948–59. doi: 10.1001/jama.2013.168118. [DOI] [PubMed] [Google Scholar]
  • 6.Salem M, Kholoussi S, Kholoussi N, Fawzy R. Malondialdehyde and trace element levels in patients with type 2 diabetes mellitus. Arch Hellenic Med. 2011;28(Suppl 1):83–8. [Google Scholar]
  • 7.Mishra J, Carpenter S, Singh S. Low serum zinc levels in an endemic area of visceral leishmaniasis in Bihar, India. Indian J Med Res. 2010;131:793–8. [PubMed] [Google Scholar]
  • 8.Josko O. Copper and zinc, biological role and significance of copper/zinc imbalance. Journal of Clinical Toxicology. 2011 [Google Scholar]
  • 9.El Missiry M, Hamed Hussein M, Khalid S, Yaqub N, Khan S, Itrat F, et al. Assessment of serum zinc levels of patients with thalassemia compared to their siblings. Anemia. 2014;2014:125452. doi: 10.1155/2014/125452. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Charney P, Escott-Stump S, Mahan LK. Nutrition diagnosis and intervention. Krause's Food and Nutrition Therapy. 12th ed. St Louis, MO: Saunders Elsevier. 2008:454–69. [Google Scholar]
  • 11.Thomas B, Kumari S, Ramitha K, Ashwini Kumari MB. Comparative evaluation of micronutrient status in the serum of diabetes mellitus patients and healthy individuals with periodontitis. J Indian Soc Periodontol. 2010;14(1):46–9. doi: 10.4103/0972-124X.65439. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Li B, Tan Y, Sun W, Fu Y, Miao L, Cai L. The role of zinc in the prevention of diabetic cardiomyopathy and nephropathy. Toxicol Mech Methods. 2013;23(1):27–33. doi: 10.3109/15376516.2012.735277. [DOI] [PubMed] [Google Scholar]
  • 13.Marreiro DN, Geloneze B, Tambascia MA, Lerario AC, Halpern A, Cozzolino SM. Effect of zinc supplementation on serum leptin levels and insulin resistance of obese women. Biol Trace Elem Res. 2006;112(2):109–18. doi: 10.1385/bter:112:2:109. [DOI] [PubMed] [Google Scholar]
  • 14.Kim J, Lee S. Effect of zinc supplementation on insulin resistance and metabolic risk factors in obese Korean women. Nutr Res Pract. 2012;6(3):221–5. doi: 10.4162/nrp.2012.6.3.221. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Fiorentino TV, Prioletta A, Zuo P, Folli F. Hyperglycemia-induced oxidative stress and its role in diabetes mellitus related cardiovascular diseases. Curr Pharm Des. 2013;19(32):5695–703. doi: 10.2174/1381612811319320005. [DOI] [PubMed] [Google Scholar]
  • 16.Pizzimenti S, Ciamporcero E, Daga M, Pettazzoni P, Arcaro A, Cetrangolo G, et al. Interaction of aldehydes derived from lipid peroxidation and membrane proteins. Front Physiol. 2013;4:242. doi: 10.3389/fphys.2013.00242. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Miao X, Sun W, Miao L, Fu Y, Wang Y, Su G, et al. Zinc and diabetic retinopathy. Journal of diabetes research. 2013;2013 doi: 10.1155/2013/425854. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Prasad AS. Zinc is an Antioxidant and Anti-Inflammatory Agent: Its Role in Human Health. Front Nutr. 2014;1:14. doi: 10.3389/fnut.2014.00014. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Bao B, Prasad AS, Beck FW, Fitzgerald JT, Snell D, Bao GW, et al. Zinc decreases C-reactive protein, lipid peroxidation, and inflammatory cytokines in elderly subjects: a potential implication of zinc as an atheroprotective agent. Am J Clin Nutr. 2010;91(6):1634–41. doi: 10.3945/ajcn.2009.28836. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Song Y, Leonard SW, Traber MG, Ho E. Zinc deficiency affects DNA damage, oxidative stress, antioxidant defenses, and DNA repair in rats. J Nutr. 2009;139(9):1626–31. doi: 10.3945/jn.109.106369. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Giacco F, Brownlee M. Oxidative stress and diabetic complications. Circ Res. 2010;107(9):1058–70. doi: 10.1161/CIRCRESAHA.110.223545. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Puri M, Gujral U, Nayyar SB. Comparative study of serum zinc, magnesium and copper levels among patients of type 2 diabetes mellitus with and without microangiopathic complications. INNOVATIVE JOURNAL OF MEDICAL AND HEALTH SCIENCE. 2013;3(6) [Google Scholar]
  • 23.Eaton JW, Qian M. Interactions of copper with glycated proteins: possible involvement in the etiology of diabetic neuropathy. Mol Cell Biochem. 2002;234-235(1-2):135–42. [PubMed] [Google Scholar]
  • 24.Ahmadpour S, Sadeghi YOUSEF, Hami J, Haghir H. Effects of insulin and ascorbic acid therapy on plasma cu level in streptozotocin-induced diabetic rats. Journal of Birjand University of Medical Sciences. 2008;15(3):26–31. [Google Scholar]
  • 25.Sakamoto K, Brownlee M. Type 1 Diabetes. Springer; 2003. pp. 375–92.Biochemistry and Molecular Biology of Diabetic Complications. [Google Scholar]
  • 26.Guimaraes MM, Martins Silva Carvalho AC, Silva MS. Chromium nicotinate has no effect on insulin sensitivity, glycemic control, and lipid profile in subjects with type 2 diabetes. J Am Coll Nutr. 2013;32(4):243–50. doi: 10.1080/07315724.2013.816598. [DOI] [PubMed] [Google Scholar]
  • 27.Jain SK, Rains JL, Croad JL. Effect of chromium niacinate and chromium picolinate supplementation on lipid peroxidation, TNF-alpha, IL-6, CRP, glycated hemoglobin, triglycerides, and cholesterol levels in blood of streptozotocin-treated diabetic rats. Free Radic Biol Med. 2007;43(8):1124–31. doi: 10.1016/j.freeradbiomed.2007.05.019. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Cefalu WT, Hu FB. Role of chromium in human health and in diabetes. Diabetes Care. 2004;27(11):2741–51. doi: 10.2337/diacare.27.11.2741. [DOI] [PubMed] [Google Scholar]
  • 29.Khan AR, Awan FR. Metals in the pathogenesis of type 2 diabetes. J Diabetes Metab Disord. 2014;13(1):16. doi: 10.1186/2251-6581-13-16. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Jamshidi F, Tasallli E, Heshmat R, Kimiagar M, Larijanio B. Evaluation of Mg, Zn and Cu serum levels in Diabetic and nondiabetic persons and its relationship with anemic situation in food rejims. Diabetes and Lipid J. 9(3):249–59. [Google Scholar]
  • 31.Kazi TG, Afridi HI, Kazi N, Jamali MK, Arain MB, Jalbani N, et al. Copper, chromium, manganese, iron, nickel, and zinc levels in biological samples of diabetes mellitus patients. Biol Trace Elem Res. 2008;122(1):1–18. doi: 10.1007/s12011-007-8062-y. [DOI] [PubMed] [Google Scholar]
  • 32.Nasli-Esfahani E, Faridbod F, Larijani B, Ganjali MR, Norouzi P. Trace element analysis of hair, nail, serum and urine of diabetes mellitus patients by inductively coupled plasma atomic emission spectroscopy. Journal of Diabetes & Metabolic Disorders. 2011;10(1):5. [Google Scholar]
  • 33.Adewumi MT, Njoku CH, Saidu Y, Abubakar MK, Shehu RA, Bilbis LS. Serum chromium, copper, and manganese levels of diabetic subjects in Katsina, Nigeria. Asian J. Biochem. 2007;2:284–8. [Google Scholar]
  • 34.SABOURI SOMAYEH, Mohtadinia J, ALIASGARZADEH A, NOUMI GS, YOUSEFIRAD E. The relationship between serum level of chromium and serum malondialdehyde in patients with type II diabetes. 2010 [Google Scholar]
  • 35.Talaei A, Jabari S, Bigdeli MH, Farahani H, Siavash M. Correlation between microalbuminuria and urinary copper in type two diabetic patients. Indian J Endocrinol Metab. 2011;15(4):316–9. doi: 10.4103/2230-8210.85586. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Al-Timimi DJ, Sulieman DM, Hussen KR. Zinc status in type 2 diabetic patients: relation to the progression of diabetic nephropathy. J Clin Diagn Res. 2014;8(11):CC04–8. doi: 10.7860/JCDR/2014/10090.5082. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Nephro-urology Monthly are provided here courtesy of Brieflands

RESOURCES