Study of malondialdehyde and estimation of blood glucose levels in patients with diabetes mellitus with cataract

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Original Research Article DOI: 10.18231/2394-6377.2017.0074 Study of malondialdehyde and estimation of blood glucose levels in patients diabetes mellitus cataract Syeda Shahana Jalees 1,*, M. Rosaline 2 1 Assistant Professor, 2 Professor & HOD, Dept. of Biochemistry, Deccan College of Medical Sciences, Hyderabad, Telangana. *Corresponding Author: Email: drshahana.sj@gmail.com Abstract Increased oxidative stress may contribute to development of complications in diabetes may result from over production of precursors to reactive oxygen radicals and/ or decreased efficiency of inhibitory scavenger systems. Senile diabetic cataract is one of the chronic complications of diabetes mellitus. The present study has been carried out in patients suffering NIDDM (Type- 2) or out associated cataract. Hyperglycemia causes oxidative stress, as measured by malondialdehyde (MDA) (a lipid peroxidation product) is more in diabetic patients (370.80 n.mol/l) compared to the normal individuals (181.04 n.mol/l) whereas the oxidative stress in diabetics cataract is significantly more (399.12 n.mol/l) than that in diabetics out complications. Attempts have been made under present study to estimate serum MDA levels as a marker of free radical stress against free radical injury. Keywords: Diabetes mellitus,, Malondialdehyde Manuscript Received: 6 th May, 2017 Manuscript Accept: 11 th July, 2017 Introduction appear earlier in life and seem to progress more rapidly in diabetics than in non-diabetic persons (Brownlee 1981, Albert, 1982). Major emphasis has been placed on the polyol pathway wherein glucose is reduced to sorbitol by the enzyme aldose reductase. Diabetes mellitus can result in frequent periods of hyperglycemia allowing formation and accumulation of sorbitol. Sorbital which appears to function as a tissue toxin has been implicated in the pathogenesis of retinopathy, neuropathy, cataracts, nephropathy and aortic disease (Brownlee 1981, Albert 1982). Diabetes is associated two types of cataracts. 1. Senile cataract 2. True diabetic cataract:-it is also called snow flake cataract or snow -storm cataract. It is a rare condition, usually occurring in young adults due to osmotic over-hydration of the lens. (Comprehensive Ophthalmology, 4 th edn, pg. no.185). The term sugar cataract refers to the cataracts associated galactosemia and juvenile diabetes mellitus. It also include diabetic cataract in adult diabetes. Lipid peroxidation is a chain reaction providing a continuous supply of free radicals that initiate further peroxidation, malonaldehyde is a stable end product of lipid peroxidation. The reaction is initiated by an existing free radical (x ), by light, or by metal ions. Malondialdehyde is only formed by fatty acids three or more double bonds and is used as a measure of lipid peroxidation together ethane from the terminal two carbons of ω 3 fatty acids and pentane from the terminal five carbons of ω 6 fatty acids. Oxygen radicals are capable of damaging compounds of all biological molecules such as 1. Nucleic acids. 2. Proteins and free amino acids. 3. Lipids and lipoproteins. 4. Carbohydrates and 5. Connective tissue and macromolecules. An increase production of Malondialdehyde (MDA) a marker of lipid peroxidation has been found in RBC membranes of diabetic patients (Nagasaki Y, Fufiis, Kaneko T, 1989). The circulating levels of MDA are higher in the plasma of diabetic subjects as compared those in non-diabetic individuals (Nishigaki L, 1981; Altomare E, 1992). Lipid hydroperoxides decompose to many products including aldehydes such as Malondialdehyde, which can reflect the degree of oxidative stress. Oxidatively damaged lipids have been linked to cause coronary artery disease and degenerative disease of aging. Materials and Method The diabetic patients were divided into two groups; the diabetic complication as cataract and diabetics out complications. The oxidative stress as measured by MDA (A lipid peroxidation product) seen in 75 individuals. The analysis of serum MDA levels in these patients has compared healthy volunteers. The study has been done in the outpatient clinics of department of ophthalmology and internal medicine at Owaisi hospital and research center and Princess Esra hospital, Hyderabad. The following are the criteria for the selection of Test and Control groups. International Journal of Clinical Biochemistry and Research, July-September 2017;4(3):319-323 319

The diabetic subjects of age 40 to 70 of both sex and having complication diabetic cataract are included. The blood samples for the estimation of serum Malondialdehyde and Blood glucose was drawn in a fasting state. Estimation of blood glucose: By Harold Varley method (Asatoor et al., 1954). Estimation of malondialdehyde in serum: Thiobarbituric acid reactive substance assay [TBRAS] method. Statistical analysis: Statistical analysis was done by means of one way analysis of variance. The individual pair wise differences were seen by means of Duncan s multiple range test; the level of significance was set at P=0.05. Results Table 1: Descriptive of age of normal, diabetic out cataract and diabetic cataract subjects by sex Sex Group Age No. of Std. Std. Error Minimum Maximum Subjects Mean Deviation of Mean Age Age Normal 10 48.00 6.912 2.186 38 58 out 9 53.78 7.629 2.543 42 65 Male 14 61.93 3.912 1.045 54 68 Normal 15 45.80 5.894 1.522 36 56 out 16 49.50 6.314 1.579 42 64 Female 11 58.73 5.623 1.695 50 70 Normal 25 46.68 6.276 1.255 36 58 out 25 51.04 6.979 1.396 42 65 Total 25 60.52 4.908 0.982 50 70 Table 2: Descriptive of fasting blood sugar (mg/dl) and malondialdehyde (n.mol/l) of normal, diabetic out cataract and cataract subject by sex Parameter Sex Group No Mean SD Sem Min Max Normal 10 85.70 3.945 1.248 80 90 Male 156 out 9 145.22 10.072 3.357 129 14 162.07 7.437 1.988 150 172 FBS(mg/dl) Normal 15 86.40 3.542 0.914 80 90 out 16 147.63 7.839 1.960 135 160 Female 11 160.91 5.647 1.703 152 171 Total Normal 25 86.12 3.644 0.729 80 90 International Journal of Clinical Biochemistry and Research, July-September 2017;4(3):319-323 320

MDA (n.mol/l) Male Female Total out 25 146.76 8.579 1.716 129 160 25 161.56 6.602 1.320 150 172 Normal 10 183.50 19.208 6.074 147 213 out 9 388.33 65.276 21.759 293 480 14 427.50 77.217 20.637 267 540 Normal 15 179.40 24.377 6.294 149 214 out 16 360.94 90.485 22.621 196 507 11 363.00 97.149 29.292 213 533 Normal 25 181.04 22.118 4.424 147 214 out 25 370.80 81.961 16.392 196 507 25 399.12 90.719 18.144 213 540 FBS (mg/dl) MDA (n.mol/l) Table 3: ANOVA Sum of df Mean Square F Sig Squares Between 79895.360 2 39947.680 groups Within groups 3131.360 72 43.491 918.525 0.001 Total 83026.720 74 Between Groups 703081.39 2 351540.693 Within groups 370483.60 72 5145.606 Total 1073565.0 74 68.319 0.001 Table 4: Duncan s multiple range test for FBS (mg/dl) Group Mean± SD Normal 86.12 ± 3.644 a out 146.76±8.579 cataract ƅ cataract 161.56± 6.602 c NB: Different superscripts are significantly different (p 0.05) Table 5: Duncan s multiple range test for MDA (n.mol/l) Group Mean± SD Normal 181.04 ± 22.118 a out cataract cataract 370.80 ± 81.961 ƅ 399.12 ± 90.719 ƅ NB: Different superscripts are significantly different (P 0.05). Analysis of fasting Blood Sugar (mg/dl) and Serum MDA (n.mol/l) levels are seen in 75 individuals. Out of them 25 are normal subjects and 50 are diabetic subjects; out of which 25 diabetics out cataract and 25 diabetic cataract. The data is analyzed statistically and the results are tested by means of one way analysis of variance technique. The descriptive for fasting blood sugar and MDA levels for 25 normal subjects (out of which 10 are male and 15 female subjects) were shown in Table 2. The fasting blood sugar ranges between 80 to 90 mg/dl. The mean and SD for fasting blood sugar (mg/dl) is 86.12± 3.644 and for serum MDA (nmol/l) is 181.04 ± 22.118 respectively. Serum MDA levels are in normal range, ranging from 147-214 nmol/l in males and females. Table 2 gives the descriptive for fasting blood sugar (mg/dl) and MDA for the three categories of both International Journal of Clinical Biochemistry and Research, July-September 2017;4(3):319-323 321

sex. The fasting blood sugar (mg/dl) of 25 diabetic subjects out cataract (Table 2) ranged from 129-160 mg/dl. The mean and SD for FBS (mg/dl) is 146.76 8.579. The serum MDA (n.mol/l) levels for the same group are varying from 196-507. The mean and SD for serum MDA (n.mol) is 370.80 81.961. The values are above the normal range in the fasting Blood sugar (mg/dl) of 25 diabetic patients cataract (Table 2) range from 150-172. The mean and SD for FBS is 161.56 6.602. The Serum MDA (n.mol/l) levels for this group are ranging from 213-540. And the mean and SD for MDA (n.mol/l) is 399.12± 90.719. enzymes such as SOD, CAT, GP X have been reported to be increased, decreased or unaltered in various tissues of diabetics wide variation from one tissue to another. These discrepancies may depend on variation in enzyme activity over a time. Compensatory increase in enzyme activity to faced raised oxidative stress, as well as the type of tissue under examination. (Uzel N, 1987; Wolff SP, 1993; Yeh HC, 1987). The combination of antioxidants will improve the antioxidant status and help in prevention and postponing the onset of diabetic complications such as cataract. Senile diabetic cataract is one of the chronic complications of diabetes mellitus. Sorbitol is normally present in lens of eyes. But in diabetes mellitus, when glucose level is high, the sorbitol concentration also increases in the lens. This leads to osmotic damage of the tissue and development of cataract. The elevated level of sorbitol has been implicated in the development of neuropathy, cataract and retinopathy in diabetes mellitus. The early development of cataract of lens is due to the increased rate of sorbitol formation caused by the hyperglycemia. Fig. 1: Shows that there is a significantly high level of MDA in diabetics compared to normal subjects. There is not much difference in MDA levels between diabetics out complications and diabetics cataract subjects Conclusion The oxidative stress as measured by Serum MDA (a lipid peroxidation product) is significant in diabetic patients compared to the normal individuals, where as the oxidative stress in diabetes cataract is significantly more than that in diabetes out complications. Lipid peroxidation may also play a role in cataractogenesis. The Estimation of serum MDA is significant in diabetic patients & out cataract compared to normal subjects according to the study done. Discussion The TBARS (Thiobarbituric acid reactive substances) method is used to estimate malondialdehyde, which is a marker of lipid peroxidation. We have found that the levels of serum MDA were significantly elevated References 1. Akkus I, Kalak S, Vural H, Caglayan O, Menekse E, Can in patients diabetes compared to those in normal G, Durmus G. Leucocyte lipid peroxidation, superoxide subjects which supports the findings by others (Peuchant dismutase peroxidase and serum and leucocyte vitamin c E, 1997; Akkus I, 1996; Losada, 1996; Santini SA, 1996; level type II diabetes mellitus. Clin Chim Acta. 1996 Griesmacher A, 1995; Armstrong D, 1992; Nishigakil, Jan 31; 244(2):221-7. PMID: 8714439. 1981). We have seen that diabetes have increased 2. Albert. The biochemistry of complications of DM. In: H. oxidative stress and hence showed high levels of Serum Keen, J. Jarethi Eds. Complications of diabetes. 2 nd edn. London: Edward Arnold Ltd. 1982; pp 231-71. MDA compared to matched non-diabetics. The average 3. Altomare E, Vendamiale G, Chicco D, Procacci V, Cirelli serum MDA levels in Normal subjects is 181.04 n.mol/l, F. Increased Lipid peroxidation in Type-2 poorly in diabetics out complication it is 370.80 n mol/l and controlled patients. Metab. 1992; patients diabetic cataract it is 399.12 n mol/ l. The 18:264-271. data analysis revealed a significantly elevated serum 4. Armstrong D, Rauk A, Yud. Aminoalkyl and Alkylaminium free radicals and related species; structures, MDA levels in diabetic cataract patients (P 0.05) and thermodynamic properties, reduction potentials and diabetics out complications (P 0.05) compared to aqueous energies. J Am Chem Soc. 1992; 115:666-73. normal individuals. It has been reported that 5. Asatoor AM, King EJ. Simplified colorimetric blood sugar hyperglycemia increases lipid peroxidation and leads to method. Biochem J. 1954 Jan 16; XIIV:56. PMID: decrease in antioxidants (Auge N, 1995; Ferrari R, 13159933. 6. Auge N, 1995. 1991). 7. Brownlee. The Biochemistry of the complications of D. In studies focusing on a limited number of M. Ann Rev Biochem. 1981; 50:385. individuals, antioxidants may not reflect the real 8. Comprehensive Ophthalmology-Diseases of the lens- 4 th antioxidants status of patients. In general antioxidants edn. pg. 185. 9. Ferrari R, 1991. International Journal of Clinical Biochemistry and Research, July-September 2017;4(3):319-323 322

10. Griesmacher A, Hauser MK, Andert SE, Schreiner W, Toma C, Knoebl P, Pietschmann P, Prager R, Schnack C, Schemthaner G, Mueller MM. Enhanced Serum levels of Thiobarbituric acid reactive substances in diabetes mellitus. The American journal of Medicine. 1995. 11. Losada, 1996. 12. Nagasaki Y, Fufii S, Kaneko T. Effects of high Glucose and Sorbitol Pathway on Lipid peroxidation of Erythrocytes. Horm Metab Res. 1989;19:89-90. 13. Nishigakil, 1981. 14. Peuchant E, Poor glycemic control. Diabetes, oxidative stress and physical exercise. 1997. 15. Santini SA, Early increase of oxidative stress 1996. 16. Uzel N, Sivas A, Uysal M, Oz H. Erythrocyte lipid peroxidation and glutathione peroxidase activities in patients diabetes mellitus. Horm Metab Res.1987 Feb; 19 (2):89-90. PMID: 3557287. 17. Wolff SP. Diabetes mellitus and free radicals. Free radicles, transition metals and oxidative stress in the aetiology of diabetes mellitus and complications. British Medical Bulletin 1993 July; 49(3):642-52. PMID: 8221029. 18. Yeh HC, 1987. International Journal of Clinical Biochemistry and Research, July-September 2017;4(3):319-323 323