Official Journals By StatPerson Publication
Table of Content - Volume 9 Issue 1 - January 2019
Relevance of Lipoprotein (a) in predicting the diagnosis of type II diabetes mellitus
Amrita1, Amrendra Amar2*
1Ex PG, 2Final Year PG, Department of Biochemistry, M.G.M. Medical College and L.S.K. Hospital Kishanganj, Bihar, INDIA. Email: aseemhealthcare@yahoo.in
Abstract Lp(a) has atherogenic and thrombotic properties and is considered to be a major risk factor for the development of atherosclerotic disease. The risk of cardiovascular disease is increased in both insulin-dependent (IDDM) and non-insulin-dependent diabetes mellitus (NIDDM), and Lp(a) has attracted attention as a potential risk factor in diabetic patients. Methods: This study was a cross sectional study selected randomly and working in the department of Biochemistry and Medicine ward of M.G.M Medical College and L.S.K. Hospital Kishanganj, Bihar. The duration of study was from Oct 2017 to Nov 2018. The study group comprised of 50 - 50 each of IDDM and NIDDM patients and control 50 healthy individual persons. After following the exclusion and inclusion criteria. Result: After analysing all the data that we have collected throughout our study we found that, LP(a), Oxidative stress marker (MDA) level is increased in both IDDM and NIDDM patients. Conclusion: LP(a) is raised in DM in respect of case. The degree of rise is more is IDDM than NIDDM. Key Word: Lp(a) , IDDM, NIDDM.
INTRODUCTION The cause of type 1 diabetes is unknown.1 However, it is believed to involve a combination of genetic and environmental factors.2 Risk factors include having a family member with the condition.3 The underlying mechanism involves an autoimmune destruction of the insulin-producing beta cells in the pancreas. 4 Diabetes is diagnosed by testing the level of sugar or glycated hemoglobin (HbA1C) in the blood.3,5 Type 1 diabetes can be distinguished from type 2 by testing for the presence of autoantibodies. 3 There is no known way to prevent type 1 diabetes.1 Treatment with insulin is required for survival.2 Insulin therapy is usually given by injection just under the skin but can also be delivered by an insulin pump.6 A diabetic diet and exercise are important parts of management.4 If left untreated, diabetes can cause many complications.1 Complications of relatively rapid onset include diabetic ketoacidosis and nonketotic hyperosmolar coma.3 Long-term complications include heart disease, stroke, kidney failure, foot ulcers and damage to the eyes.1 Furthermore, complications may arise from low blood sugar caused by excessive dosing of insulin.3 Diabetes mellitus type 2 is a long-term metabolic disorder that is characterized by high blood sugar, insulin resistance, and relative lack of insulin. 7 Common symptoms include increased thirst, frequent urination, and unexplained weight loss. 8 Symptoms may also include increased hunger, feeling tired, and sores that do not heal.8 Often symptoms come on slowly.7 Long-term complications from high blood sugar include heart disease, strokes, diabetic retinopathy which can result in blindness, kidney failure, and poor blood flow in the limbs which may lead to amputations. The sudden onset of hyperosmolar hyperglycemic state may occur; however, ketoacidosis is uncommon.1,3 Lp(a) and diabetes, results of studies investigating Lp(a) levels in patients with Type 1 diabetes are inconsistent. Several studies have reported that Lp(a) levels were increased in patients with Type 1 diabetes 9 while in others, a significant relationship was not observed. It is also controversial as to whether Lp(a) levels are related to glycemic control in Type 1 diabetes. Although some studies suggested that Lp(a) levels decreased with improved metabolic and/or glycemic control 10, others reported that improved metabolic control did not change plasma Lp(a) levels in patients with Type 1 diabetes. For example, in the Diabetes Control and Complications Trial 10 , there was no difference in plasma Lp(a) levels between 1299 patients with Type 1 diabetes and 2158 nondiabetic controls at baseline. Patients receiving intensive insulin therapy showed lower Lp(a) levels compared with those receiving conventional insulin therapy, but Lp(a) levels was not correlated with glycemic control estimated by HbA1c levels 10.
METHODS This study was a cross sectional study selected randomly and working in the department of Biochemistry and Medicine ward of M.G.M Medical College and L.S.K. Hospital Kishanganj, Bihar. The duration of study was from Oct 2017 to Nov 2018. The study group comprised of 50 - 50 each of IDDM and NIDDM patients and control 50 healthy individual persons. After following the exclusion and inclusion criteria. A short history and clinical examination of the patients were obtained regarding the diabetes, blood pressure, Duration of diabetes, history of drug intake and after taking the verbal consent of the patient the blood samples were Collected and the blood samples were tested in the department of Biochemistry, M.G.M. Medical College and L.S.K. Hospital, Kishanganj, Bihar. Samples were collected for estimation of:
Study tools:
Inclusion criteria:- Insulin and Non Insulin dependent patients were included in our study. Exclusion Criteria:- Suffering from hepatic, muscular and cardiac disorders, Neonates are exclusion from our study group.
RESULTS Table 1: Age and sex wise distribution of IDDM patients among case group
Table 2: Age and sex wise distribution of NIDDM patients among case group
Table 3: Age and sex wise distribution of control group (Non Diabetic patients)
Table 4: Duration of Diabetes among IDDM and NIDDM patients
Table 5: Mean and SD value of Age among Case and Control group
Table 6: Mean and SD value of Glucose and HbA1c among Case and control group
Table 7: Mean and SD value of Lipid profile among Case and control group
Table 8: Mean and SD value of LP(a) and MDA among Case and control group
DISCUSSION Diabetes mellitus comprises of a group of disorders that share a phenotype of hyperglycemia. The complications are an important cause of morbidity and mortality in the diabetic patients. These complications are a result of interaction of multiple metabolic, genetic and other factors.11 In our study, distribution of IDDM patients according to their age and sex is mentioned in Table 1. The above table shows majority of patients belonged to 20-30 and 31-40 years age group. 20-30 years age group consisted 20 (40%) patients among them 11were male and 9 were female. 31-40 years age group consisted 22 (44%) patients among them 15 were male and 7 were female. Distribution of NIDDM patients according to their age and sex is mentioned in Table2. The above table shows majority of patients belonged 51-60 y ears age group. 28 (56%) patients belonged to this particular age group, among them 13 were male and 15 were female. 41-50 years age group consisted 12(24%) patients among them 7.were male and 5 were female. 31-40 years age group consisted only 4 (8%) patients among them 3 were male and female. Distribution of control group according to their age and sex is mentioned in Table3.The above table shows majority of patients belonged to 31-40 and41-50 years age group. 31-40 years age group consisted 18(36%) patients among them 11 were male and 7 were female. 41-50 years age group consisted 20(40%) patients among them 7 were male and 13 were female. Table 4 shows distribution of both IDDM and NIDDM patients according to the duration of diabetes. From the above table we can found that in case of IDDM majority of patients i.e. 34 (68%) patients were suffering from diabetes for 3-‹5 years. And in case of NIDDM majority of patients i.e.22 (44%) patients were suffering from diabetes for 5-10 years. Table 5 shows the mean and SD value of age among IDDM, NIDDM patients and control group. The mean age and SD value of IDDM patient was 33.06 and ±8.52. In case of NIDDM patients the mean age and SD value was 46.8 and ±9.76. The mean age and SD value for control group was 41.34 and ±8.34. The mean and SD value of glucose (fasting and PP) and HbA1c level of case (IDDM and NIDDM) and control group is shown in Table 6. After comparing the blood glucose level and HbA1c level of IDDM and NIDDM patients we found in case of IDDM patients Blood glucose and HbA1c level is elevated than that of NIDDM Patient. And we found the results statistically significant (p value = <0.001). The mean and SD value of lipid profile level of case (IDDM and NIDDM) and control group is shown in Table7. After comparing the Lipid profile level of IDDM and NIDDM patients we found in case of NIDDM patients Lipid profile level is elevated than that of IDDM Patient. Metabolic reasons for lower HDL levels have not been fully documented. Decreased synthesis of HDL has been found in one small study.12 Increased clearance of HDL particles from the plasma space may also be operative particularly in patients with hypertriglyceridemia.13 Schmitt et al.14 suggested that LDL uptake by fibroblasts may be impaired in type 2 diabetics. This leads to increase in LDL: HDL ratio in type 2 diabetics. In our study, LDL: HDL ratio did not differ significantly between controlled and uncontrolled diabetics (P>0.05). Similar results have also been forwarded by Haffner et al.15 However, Schmitt et al. 14 found that LDL: HDL ratio correlated with HbA1c better than any of the lipids or lipoprotein fractions. LDL: HDL ratio changed significantly than did its component fractions. We also did not find any significant association between the Lp(a) levels and LDL:HDL ratio. Ramirez et al.16 also found no significant correlation between Lp(a) and LDL levels, suggesting that the Lp(a) and the LDL levels are under different metabolic control. In this study LP(a) is significantly increased in both IDDM and NIDDM. The degree of rise is more in case of IDDM then in NIDDM. Heller et al. 17 suggested that hyperinsulinemia can be the causal factor for increase in the Lp(a) levels in type 2 diabetics. Similar results have also been reported by Wolffenbuttel et al.18 They reported that Lp(a) levels were elevated in diabetics as compared to non-diabetic subjects of similar age but did not change with insulin and there was no correlation with the degree of metabolic control and changes in Lp(a) levels.
CONCLUSION Our results suggest that lipid metabolism is important for the development of inflammation which is elevated in several complications associated with diabetes. LP(a) is raised in DM in respect of case. The degree of rise is more is IDDM than NIDDM.
REFERENCES
|