Get Permission Analike, Ihim, Iweanya, Ogbodo, Onah, Asomugha, Amah, Obi, Nwobodo, and Timothy: Assessment of glycated haemoglobin, total protein and albumin levels in patients with type 2 diabetes mellitus visiting NAUTH, Nnewi


Introduction

Diabetes mellitus (DM) is a chronic metabolic disease which results from diminished or absent secretion of insulin or even by reduced tissue sensitivity to insulin (Report of WHO Consultation, 1999;1 International Diabetes Federation, 2015; American Diabetes Association, 2016).2 Diabetes is a global endemic with rapidly increasing prevalence in developing countries such as Nigeria. Type 2 diabetes mellitus is one of the leading causes of preventable death in the world, with stroke, myocardial infarction and other cardiovascular diseases being the most common causes of death for adults with diabetes (Newman et al., 2017).3 A number of factors including less glycemic control, smoking, high blood pressure, elevated cholesterol levels, obesity, and lack of regular exercise are considered to be risk factors that accelerate the deleterious effects of diabetes (Elfaki et al., 2014).4 According to International Diabetes Federation (IDF), in 2017, approximately 425 million adults were living with diabetes and it is estimated to affect up to 629 million people by the year 2045 (IDF, 2017).5 Diabetes Mellitus has become a major public health problem in Nigeria accounting for a prevalence of 2.4% with total number of mortality amounting to 3028 deaths in 2017 (IDF, 2017).5 In the world, WHO estimates that, globally, 422 million adults aged over 18 years were living with diabetes in 2014 accounting for a prevalence of 8.5% among the adult population (WHO, 2016).6 Therefore, this continued increase in the prevalence of diabetes globally has become a matter of great concern, and hence, the management of diabetic complications is particularly important. (Yang et al., 2010; Danaei et al., 2011; Soriguer et al., 2012). 7,8,9

In individuals diagnosed of diabetes mellitus, glucose monitoring is essential for glycemic control (Yoon et al., 2015). Also, in diabetes mellitus, compared with non-diabetes, glycation of various proteins is known to be increased, and some of these glycated proteins are thought to be involved in the onset and progression of chronic diabetic complications (Cohen, 1998).10 Currently, the laboratory tests used to diagnose Diabetes Mellitus are glycated hemoglobin (A1C), fasting plasma glucose (FG) and two-hour plasma glucose (2hG) after a 75g oral glucose tolerance test (OGTT) (Sacks et al., 2011; ADA, 2016).11 Of the glycemic indices, the American Diabetes Association recommends glycated hemoglobin (HbA1 c) testing in all diabetic patients as an initial assessment and then as a part of continuing care (ADA, 2014). 12

This recommendation is derived from clinical data that shows that HbA1 c reflects average glycemicstatus over 2-3 months and predicts diabetic complications (Lee et al., 2013). 13

Albumin is one of the most abundant plasma proteins (Tiwari et al., 2015).14 The glycation of albumin to form glycated albumin (GA) is ten times more than the glycation of hemoglobin in type 2 DM (Tahara et al., 1995).15 GA is a marker reflects a short-term glycemic control (Yoon et al., 2015).16 One advantage of utilizing serum albumin as a measure of glycemic control is its shorter half-life of 21 days, which renders its serum concentration more sensitive to recent change in average blood glucose level than HbA1C (Guerin-Dubourg et al., 2012).17 Studies have shown decreased albumin levels associated with increased HbA1c and total protein (Shalbha et al., 2015; Malawadi and Adiga, 2016; Nazki et al., 2017).18,19 Therefore, the present study evaluated the glycated haemoglobin, total protein and albumin levels in patients with type 2 diabetes mellitus visiting NAUTH, Nnewi.

Materials and Methods

Study Site

This study was carried out at Nnamdi Azikiwe University Teaching Hospital (NAUTH), Nnewi.

Study design

The present study is a case control study aimed at evaluating the glycated haemoglobin, total protein and albumin levels in patients with type 2 diabetes mellitus visiting NAUTH, Nnewi. The protocol was explained to the subjects and those who gave their informed consent were recruited for the study. A total of 114 subjects comprising of 57 diabetic subjects and 57 controls aged between 40 and 73 years were recruited for the study. The patients and controls were aged and sex matched. Subsequently, structured questionnaire were used to obtain patients’ biodata and thereafter, 5mls of blood sample was collected from each patients and 1ml was dispensed into EDTA for the estimation of glycated haemoglobin, and 4ml was dispensed into plain containers for estimation of serum albumin and total protein levels.

Inclusion and exclusion criteria

Known diabetic subjects aged between 40 and 73 years were recruited for the study, whereas those younger than 40 or older than 73years and non-diabetic subjects were excluded from the study.

Ethical consideration

The ethical clearance for this study was obtained from the Ethics Committee of Nnamdi Azikiwe University Teaching Hospital (NAUTH), Nnewi.

Determination of glycated haemoglobin level

Glycated Haemoglobin level was determined using immunoturbidimetric method as described by Wolf et al., (1984).20

Estimation of serum albumin level

Serum albumin level was estimated Bromo Cresol green Method as described by Doumas et al., (1971).21

Estimation of total protein

Estimation of serum total protein level was done using Biuret Method according to Weichselbaum, (1946).22

Statistical analysis

The data were presented as mean±SD and the mean values of the control and test group were compared by Students t-test and pearson correlation using Statistical package for social sciences (SPSS) (Version 20) software. Statistical significance was tested at P<0.05.

Results

The mean level of HbA1c was significantly higher in the diabetic subjects when compared with control group (9.71±1.30Vs 5.58±0.65; p=0.000). There was no significant differences observed between the age, the serum levels of Albumin and Total protein in the test and control subjects (p>0.05).Table 1

Table 1
Parameters Control Diabetic subject t-test p-value
Age(years) 57.69±8.89 57.51±8.85 -0.082 0.935
HbA1c(%) 5.58±0.65 9.71±1.30 1.712 0.000*
Protein(g/L) 74.25±3.80 72.86±3.36 1.649 0.104
Albumin(g/L) 38.23±3.35 38.38±3.24 0.191 0.849

Levels of HbA1c, total protein and albumin in diabetic and control subjects

[i] *Statistically significant at P<0.05.

Table 2 shows that there is no significant correlation between age, HbA1c, total protein and albumin in diabetic subjects.

Table 2
Parameters R p-value
HbA1c Vs age 0.078 0.647
HbA1c Vs Total protein 0.096 0.571
HbA1c Vs Albumin -0.162 0.338
Age Vs Total protein -0.044 0.797
Age Vs Albumin 0.085 0.615
Total protein Vs Albumin -0.007 0.966

Correlation of HbA1c with age, total protein and albumin in diabetic subjects

[i] *Statistically significant at P<0.05.

Discussion

In this study, the mean level of HbA1c was significantly higher in the diabetic subjects than in control. This is in consonance with the report of some previous similar studies (Shalbha et al., 2015; Malawadi and Adiga, 2016; Nazki et al., 2017). This increase can be attributed to hyperglycaemia and disturbances of carbohydrate, fat and protein metabolism that results from abnormalities in insulin secretion, insulin action or even both (IDF, 2015; ADA, 2016).23,5 This finding implies that there is a poor glycemic control in the diabetic subjects under study. Furthermore, our finding shows a higher mean value of HbA1c (9.71±1.30) than the recommended cut-point (<7%) in diabetic patients (ADA, 2010).24 It follows therefore, that these patients may be at greater risk of long-term complications due to diabetes if the glycemic level is not properly controlled and this call for concern in the management of diabetic patients.

However, there was no significant difference between the mean serum level of Albumin in the test subjects when compared with control subjects (p>0.05). This is in line with the report of previous studies (Malawadi and Adiga, 2016). This may be as a result of Insulin resistance which is a principal cause of type 2 diabetes (Kahn, 1994)25 and previously, serum albumin has been associated with insulin resistance (Hostmark et al., 2005; Ishizaka et al., 2007).26,27 In diabetic patients, plasma albumin concentration has been reported to be inversely related with HbA1c levels, revealing a large proportion of poorly controlled diabetes in patients with lower plasma albumin concentrations (Rodriguez-Segade et al., 2005; Hemangi et al., 2012).28,29 This inverse relationship may also be explained by the fact that poorly controlled type 2 diabetes has been associated with a further decrease in insulin production and secretion by the pancreatic β-cell (Marshak et al., 1999; Kahn, 2003).30,31

Furthermore, our finding shows no significant difference between the serum levels of total protein in the diabetic patients and control subjects (p>0.05). This is in contrast with the findings of (Malawadi and Adiga, 2016; Nazki et al., 2017).18,19

There is no significant correlation between age, HbA1c, total protein and albumin in diabetic subjects. This finding is not in agreement with the finding of Hemangi et al., (2012)28 in which plasma albumin levels were negatively correlated with HbA1c and low albumin levels was associated with increased plasma protein glycation and that albumin competes for glycation with other plasma proteins in diabetes.

Conclusion

In conclusion, the present study showed significantly higher mean levels of HbA1c in the diabetic patients compared with the control subjects. However, the mean serum of levels of Albumin and total protein did not differ significantly when compared between the diabetic patients and controls. This finding implies that there was a poor glycemic control in the diabetic subjects studied. Therefore, there is need for better management of diabetic patients through medication and use of diet and exercise.

Source of funding

None.

Conflict of interest

None.

References

1 

World Health Organization, Definition, Diagnosis and Classification of Diabetes Mellitus and its complicationsWHOGeneva19992929Report of a WHO Consultation

2 

American Diabetes Association. Standards of Medical Care in Diabetes - 2016Diabetes Care201639Supplement11112

3 

J D Newman A Z Schwartzbard H Weintraub Primary prevention of cardiovascular disease in diabetes mellitusJ Am College Cardiol201770883893

4 

M E Raheem A M Ahmed E . Evaluation of Lipid Metabolism among Sudanese Patients with Type 2 Diabetes MellitusInt J Pure Appl Sci Technol20142312833

5 

International Diabetes Federation: IDF Diabetes Atlas2017Belgium: International Diabetes Federation

7 

G Danaei M M Finucane Y Lu G M Singh M J Cowan National, regional, and global trends in fasting plasma glucose and diabetes prevalence since 1980: systematic analysis of health examination surveys and epidemiological studies with 370 country-years and 2?7 million participantsLancet20113783140

8 

F Soriguer A Goday A Bosch-Comas E Bordiu A Calle-Pascual Prevalence of diabetes mellitus and impaired glucose regulation in Spain: the Diabetes StudyDiabetologia2012558893

9 

S H Yang K F Dou W J Song Prevalence of diabetes among men and women in ChinaNew Engl J Med201036224252426

10 

Nonenzymatic glycation: a central mechanism in diabetic microvasculopathyJ Diabetes Complications19982214217

11 

D B Sacks D E Bruns D E Goldstein N K Maclaren J M Mcdonald M Parrott Guidelines and recommendations for laboratory analysis in the diagnosis and management of diabetes mellitusClin Chem2011576147

12 

Standards of medical care in diabetes-2014Diabetes Care2014371480American Diabetes Associationsupplement 1

13 

E J Lee Y J Kim T Kim A1c variability can predict coronary artery disease in patients with type 2 diabetes with mean A1c levels greater than 7Endocrinol Metabol2013282125132

14 

S Tiwari M Bothale I Hasan M Kulkarni M Sayyad A Basu Association between serum albumin and glycated hemoglobin in Asian Indian subjectsIndian J Endocrinol Metabol20151915255

15 

Y Tahara K Shima Kinetics of HbA1c, Glycated albumin, and fructosamine and analysis of their weight functions against preceding plasma glucose levelDiabetes Care199518440447

16 

H Yoon Y Lee K Kim S Kim E Kang B Cha Glycated Albumin Levels in Patients with Type 2 Diabetes Increase Relative to HbA1C with TimeBioMed Res Int2015576306576306

17 

A Guerin-Dubourg A Catan E Bourdon P Rondeau Structural modifications of human albumin in diabetesDiabetes Metabol2012382171178

18 

B N Malawadi U Adiga Plasma proteins in Type 2DMIOSR J Biotechnol Biochem201625103

19 

F A Nazki A Syyeda S Mohammed Total proteins, albumin and HBA1c in type 2 diabetes mellitusMedpulse Int J Biochem2017334042

20 

H U Wolf W Lang R Zander Alkaline haematin D-575, a new tool for the determination of haemoglobin as an alternative to the cyanhaemiglobin method. II. Standardization of the method using pure chlorohaeminClinica Chimica Acta198413695104

21 

B T Doumas W A Watson H G Biggs Albumin standards and the measurement of serum albumin with bromcresol greenClinica Chimica Acta1971318796

22 

T E Weichselbaum An accurate and rapid method for the determination of proteins in small amounts of blood serum and plasmaAm J Clin Pathol1946104049

23 

International Diabetes Federation: IDF Diabetes Atlas. 7th ed. Belgium: International Diabetes Federation2015

24 

C R Kahn Banting Lecture Insulin action, diabetogenes, and the cause of type II diabetesDiabetes19944310661084

25 

A T Hostmark S E Tomten J E Berg Serum albumin and blood pressure: a population-based, cross-sectional studyJ Hypertens200523725730

26 

N Ishizaka Y Ishizaka R Nagai E Toda H Hashimoto M Yamakado Association between serum albumin, carotid atherosclerosis, and metabolic syndrome in Japanese individualsAtheroscler2007193373379

27 

S B Hemangi M K Arvind S K Sachin B G Sandeep D C Ashok L S Mahemud Low Plasma Albumin Levels Are Associated with Increased Plasma Protein Glycation and HbA1c in DiabetesJ Proteome Res201211213911396

28 

S Rodriguez-Segade J Rodriguez D Mayan F Camina Plasma albumin concentration is a predictor of HbA1c among type 2 diabetic patients, independently of fasting plasma glucose and fructosamineDiabetes Care200528437439

29 

S E Kahn The relative contributions of insulin resistance and beta-cell dysfunction to the pathophysiology of type 2 diabetesDiabetol200346319

30 

S Marshak G Leibowitz F Bertuzzi C Socci N Kaiser D J Gross Impaired beta-cell functions induced by chronic exposure of cultured human pancreatic islets to high glucoseDiabetes19994812301236



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https://doi.org/ 10.18231/j.ijpo.2019.132


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