Zoriy I.A., Pashkovskaya N.V.
PECULIARITIES OF CARBOHYDRATE METABOLISM EXPERIENCINGBY PATIENTS
DIABETES MELLITUS TYPE 2 COMPLICATED WITH DIABETIC POLYNEUROPATHY
Introduction. The number of people
with diabetes worldwide continues to increase. Diabetes mellitus (DM) is one of
the most important problems of clinical medicine, because of its wide
distribution, clinical polymorphism, complications (Law D.W., 2012). One of the
most spread and difficult in the treatment complication of diabetes is diabetic
polyneuropathy (DP), that significantly reduces the quality of life,
contributes to the neuropathic forms of diabetic foot syndrome development,
Charcot arthropathy (Tesfaye S., 2010, Ndip A. et al., 2012 ).
The aim of the study: Study of peculiarities
of carbohydrate metabolism experiencing by patients diabetes mellitus type 2
complicated with diabetic polyneuropathy.
Material and methods.
110 patients with DM type 2,
complicated DP were examined (average age is 56,6±2,79 years) who were on
treatment at the Chernivtsi Regional Endocrinology center and 20 almost healthy
persons, included the control group. Patients distribution was carried out
taking into account the level of DP: mild DP (31%) was diagnosed for 34
patients with, moderate (52,7 %) – for 58 patients and in severe patients with
DP -18 (16,3%).
To establish DP severity all patients were neurologically examined according to the scale of Neuropathic Symptomatic
Score (NSS), the Modified Neuropathic Dysfunctional Score (NDS), Total Symptoms
Score (TSS) (Solomon T. et al., 2010).
The level of glycemia was studied by the glucose oxidase method using
standard reagent kits produced by “Phyllis Diagnostics” company (Ukraine). Glycated
hemoglobin (HbA1c) was determined by liquid
chromatography of high pressure on the automatic analyzer of glycated hemoglobin D10 of the company “Bio-Rad
Laboratories Inc.”(France), using the reagents by firm “Biomedinvest”
(Ukraine). The level of immunoreactive insulin (IRI) and C-peptide was
determined using the immunosorbent
method on the analyzer STAT-Fax Plus-303 (USA), using the reagents of firm “DRG
International Inc.” (the USA).
Statistical processing was performed
using MS® Excel® 2003tm, Biostat®, Statistika® 6. Reliability of the received
data was calculated by using Student t-criteria. Possible difference in the
samples distribution was determined by χ2. P-value <0.05 was considered correct.
Results and discussion.
It is generally known that first of
all the DP is the consequence of metabolic disorders in peripheral nerves, in
particular, caused by hyperglycemia, the activation of the polyol way of
glucose exchange accumulating osmotically
active substances in the nerve cells; oxidative stress with
activating, formation of free radical compounds, increasing nonenzymatic
glycosylation of proteins nerves, nerve ischemia and many other factors (Won J.C. et al., 2012).
It should be noted that the
initially DM type 2 for 13% of examined patients was displayed with features of
neurological injury of peripheral nerves. We compared each stage of DP
depending on the degree of metabolic control of diabetes. Determination of
HbA1c was performed for all patients. It’s worth to underline that the adequate
metabolic control (HbA1c <7%) was observed only for 4,8% of diabetic
patients, the rest was in the process of sub-and decompensated disease.
The characteristics of carbohydrate
metabolism in the studied groups are shown in Table 1. Comparing the control
group and patients with DM type 2 complicated by DP
depending on the levels of severity of changes in fasting glucose, HOMA
index-IR, glycated hemoglobin (HbA1c), immunoreactive insulin and C-peptide
were observed.
Table 1.
Indicators of Carbon Metabolism for Patients with Diabetes Mellitus Type
2 in Accordance with the Severity of Diabetic Polyneuropathy
|
Indicators |
Controls n = 20 |
Mild DP n = 34 |
Moderate DP n = 58 |
Severe DP n = 18 |
|
Glucose, mmol/l |
5,1±0,356 |
9,06±0,537* |
11,72±0,431*/** |
12,64±0,456*/** |
|
Glycated hemoglobin (HbA1c),% |
5,7±0,79 |
8,36±0,357* |
9,31±0,342* |
10,92±0,658*/** |
|
ÍÎÌÀ-IR |
1,31±0,183 |
5,10±0,776* |
8,15±0,837*/** |
8,49±1,710*/** |
|
Immunoreactive insulin, lU/ml |
12,92±1,078 |
19,10±1,829* |
26,51±2,121*/** |
28,14±1,239*/** |
|
C-peptide, ng/ml |
1,34±0,136 |
2,43±0,015* |
2,78±0,634* |
3,44±0,082*/** |
Note: * - p <0.05 -
significant difference compared with the control group, ** - p <0.05 -
significant difference in comparison with mild DP.
The data of Table 1 show that all DP
stages are characterized by statistically high rates of indicators of HbA1c,
fasting glucose, the IRI and C-peptide comparison with control. These
indicators are progradiently increasing due to severity of DP. Patients with
mild DP had HbA1c level 32,1% higher than the control group, with moderate DP –
39,0% higher, and with severe DP – 46,2% higher (p <0,05). It also observed
a significant growth of fasting and postprandial blood glucose for 43,2%, 56,4%
and 59,5%, respectively.
According to the indicator index
HOMA-IR, the examined patients had severe tissue insulin resistance (IR) that
is connected with much higher levels of insulin and elevated acute
glucose-stimulated insulin secretion in response to glycaemia. Increasing IRI
fasting indicators were observed for patients with moderate (24,5%) and severe
PD (32,4 %). These parameters were significantly higher compared with controls
and patients with mild DP (p<0.05). The level of C-peptide is more stable
indicator of insulin secretion than the rapidly changing insulin level. During
our research, the highest level of C-peptide, that was beyond the limit of norm
was observed for patients with severe DP (p<0.05).
Conclusion. Diabetic polyneuropathy of diabetes mellitus type 2 is
associated with high rates of indicators glycated hemoglobin, fasting glucose,
immunoreactive insulin and C-peptide. These violations are strengthening in
proportion to the stages of diabetic polyneuropathy development.