Biomedical Research

Research Article - Biomedical Research (2018) Volume 29, Issue 3

Serum levels of advanced glycation end products in type II diabetic patients with acute cerebral infarction

Hao Ju1, Qingshi Zhao2*, Wei Li3, Haiyan Liu4, Yan Gao5, Lin Yi2, Hongyan Wang6, Zhaohui Wang6, Chuan Liu6, Fanhua Meng6, Haiping Li6 and Ligang Jiang6

1Department of Endocrinology, Affiliated Hospital of Beihua University, Jilin, PR China

2Stroke Ward, Affiliated Hospital of Beihua University, Jilin, PR China

3Department of Neurology, Affiliated Hospital of Beihua University, Jilin, PR China

4Department of Neurology, Jilin people's Hospital, Jilin, PR China

5Stroke Unit, Affiliated Hospital of Beihua University, Jilin, PR China

6Affiliated Hospital of Beihua University, Jilin, PR China

*Corresponding Author:
Qingshi Zhao
Stroke Ward
Affiliated Hospital of Beihua University, PR China

Accepted date: November 10, 2017

DOI: 10.4066/biomedicalresearch.29-17-2611

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Abstract

Background: Advanced glycation end products (AGEs) are reported to be associated with diabetic vascular complications. However, the role of AGEs in the pathogenesis of cerebral thrombosis remains unclear. This study aimed to investigate the relationship between advanced glycation end products (AGEs) generation and pathogenesis of cerebral thrombosis.

Methods: 100 patients with cerebral thrombosis were recruited and 50 healthy controlled individuals were served as a control group. Enzyme Linked Immunosorbent Assay (ELISA) was applied for measuring serum AGEs level. The condition of carotid intima was examined by carotid ultrasonography. Serum AGEs levels were compared among patients with certain conditions of carotid atherosclerosis.

Results: AGEs levels in carotid plaque or thickening groups showed significant difference compared with those in control group. Carotid plaque patients showed remarkably different AGEs levels compared to thickening patients. AGEs levels were significantly elevated with higher severity of carotid plaque. Moderate or severe stenosis patients, or blocked group showed significantly different AGEs compared to mild stenosis group. Severe stenosis or blockade group showed remarkably different AGEs compared with moderate stenosis patients. In addition, severe stenosis group had statistically different AGEs compared with blockade group.

Conclusion: AGEs level is correlated with pathogenesis of cerebral thrombosis and they are further elevated with aggravation of carotid atherosclerosis in patients, suggesting they might be used as a biomarker to evaluate the severity of atherosclerosis.

Keywords

Advanced glycation end products, Pathogenesis of cerebral thrombosis, Carotid atherosclerosis

Introduction

Cerebral thrombosis severely threatens public health, and it is critical to investigate its risk factors for further prevention and treatment [1-4]. Advanced Glycation End Products (AGEs) are heterogeneous, long-lived protein adducts which are generated from a nonenzymatic chemical reaction between sugars and the amino acid [5]. The formation and accumulation of AGEs have been demonstrated to progress during normal aging process as well as at an accelerated rate under diabetes [6]. Circulating levels of AGEs, also known as hemoglobin A1C, might be used as important biomarkers in clinic for monitoring diabetes therapy. Under pathological conditions, cellular interactions with AGEs induce biologic responses that have been linked directly to the development of diabetic vascular complications. Via interacting with AGEs (RAGE) receptor, AGEs are demonstrated to be involved in the generation of oxidative stress in various types of cells and subsequently triggering vascular inflammation [7,8], promoting the proliferation of vascular smooth muscle cells [9,10], potentiating adhesion, aggregation and activation of leukocyte [11], accelerating platelet aggregation and fibronectin formation, elevating macrophage infiltration [12], leading to the occurrence of lipid metabolic disorder, thus facilitating atherosclerosis [13,14]. However, the exact role of AGEs in the pathogenesis of cerebral thrombosis remains poorly understood. This study aimed to investigate the relationship between serum AGEs levels and carotid Inner-Middle Membrane Thickness (IMT) as well as the incidence of carotid cavity stenosis in cerebral thrombosis patients.

Patients and Methods

Research subject

A total of 100 cerebral thrombosis patients admitted between November 2012 and November 2013 were recruited. Meanwhile, 50 healthy individuals from normal body examination were served as a control group. Inclusive criteria: Admitted in our department, following the diagnostic criteria of cerebral thrombosis stipulated by 4th Cerebral Vascular Disease Symposium of China. Healthy control group was recruited from out-patient individuals receiving normal body examination. Exclusive criteria: Individuals having acute disease of liver, heart, kidney, and gastrointestinal disease, with recent history of surgery, trauma, infection, malignant tumor, diabetic ketosis, or connective tissue diseases. Those recently taken drugs affecting glucose metabolism or oxidative stress functions were also excluded. This study has been approved by the Ethnic Committee of the Affiliated Hospital of Beihua University, Jilin, China and all individuals signed the informed consents before enrolment.

Collection of clinical information

100 cerebral thrombosis patients were recruited, including 50 cases with single cerebral thrombosis (27 males and 23 females, aged between 40 and 78 y, average age=54 y) and 50 cases with cerebral thrombosis with diabetes (31 males and 19 females, aged between 40 and 78 y, average age=54 y). 50 healthy controlled individuals (24 males and 26 females, aging between 40 and 71 y, average age=53.5 y) were also recruited. All individuals were further divided into pure cerebral thrombosis, cerebral thrombosis with diabetes and healthy controlled groups (N=50 each). All patients were further divided into normal, thickening and plaque sub-groups based on Inner-Middle Membrane Thickness (IMT) acquired from carotid ultrasonography. Grouping criteria were: (1) Normal group (IMT<1.0 mm); (2) Thickening group (1.0 mm<IMT<1.5 mm); (3) Plaque group (IMT>1.5 mm). Based on stenosis condition of focal carotid cavity, all plaque tissues were further divided into group groups: (1) Mild stenosis, with less than 50% of stenosis rate in focal cavity caused by the plaque; (2) Moderate stenosis, with 50%~69% stenosis rate in plaque-induced lesion; (3) Severe stenosis group, with 70%~99% stenosis rate caused by focal plaque in carotid cavity; (4) Complete blockade group. All these groups showed no significant difference of sex ratio or age distribution (p>0.05).

Sample collection and assays

4 ml blood samples were collected from elbow veins of patients after 12 h fasting. Blood samples were incubated for 20 min at room temperature, and centrifuged for 20 min (2000~3000 rpm) at room temperature. 200 μL serum samples were aliquoted and stored at -20°C. ELISA was applied to measure serum AGEs level using test kit (Dongge Boye Biotech, China) following the manual protocols.

Carotid ultrasonography examination

ACUSON X300 ultrasound apparatus (Siemens, Germany) with VF10-5 and CH5-2 probes was used for carotid ultrasonography examination by clinicians from department of neurology. Patients were placed in supine position with neck extension and head inclined toward the side of examiner. Ultrasonography was performed on bilateral common carotid, internal/external carotid, spinal artery, subclavian artery to examine vascular morphology, structure and plaque formation. IMT was measured simultaneously at 1.0~1.5 cm inferior of the branching point of internal and external carotid artery on the distal site of common carotid artery.

Blood pressure measurement

All individuals were prohibited from smoking within 30 min before testing. After 10 min general break, patients were placed in supine or sitting position, with right elbow at identical level of the heart. Table sphygmomanometer was used to measure systolic and diabolic pressure of patients. Blood pressures were measured in three times on different days. All measurements were averaged for calculating Pulse Pressure (PP).

Biochemical index assay

All individuals were measured for those biochemical indexes by our laboratory: fasted blood Glucose (GLU), Triglyceride (TG), Total Cholesterol (CHO), Low Density Lipoprotein (LDC-C) and High Density Lipoprotein (HDL-C).

Statistical analysis

SPSS 18.0 software was used to process all data, which were presented as mean ± Standard Deviation (SD). Measurement data were compared and analysed by one-way Analysis of Variance (ANOVA) with Newman-Keuls multiple comparison post-hoc analysis. A statistical analysis was defined when p<0.05. All statistical analysis was performed using SPSS 18.0 software.

Results

Comparison of clinical data and AGEs levels

No statistical significance was found regarding the HDL-C levels in cerebral thrombosis group and control group (p>0.05). However, PP, CHO, LDL-C and AGEs were all significantly higher in cerebral thrombosis than those in control group (p<0.01). AGEs and PP also showed statistically significant difference among these two groups (p<0.01, Table 1).

Group N PP CHO TG LDL-C HDL-C AGEs
mmHg mmol/L mmol/L mmol/L mmol/L pg/ml
Control group 50 53.0 ± 10.7 4.8 ± 0.7 1.2 ± 0.5 2.5 ± 0.4 1.1 ± 0.4 30.4 ± 6.9
Pure cerebral thrombosis 50 62.3 ± 13.5 * 5.5 ± 0.7* 1.6 ± 0.7* 2.7 ± 0.6* 1.1 ± 0.3 34.2 ± 7.8*
Cerebral thrombosis with diabetes 50 73.4 ± 14.5*@ 5.5 ± 0.8* 1.8 ± 0.6* 2.8 ± 0.7*@ 1.1 ± 0.3 38.4 ± 7.8*@

Table 1. Comparison of clinical information and AGEs.

Comparison of AGEs and PP among different IMT patients

Compared with control group, plaque and thickening group all showed statistically significant difference of AGEs and PP levels. Comparison between plaque and thickening groups also showed statistically significant difference of AGEs and PP levels (Table 2).

IMT condition N AGEs PP
(μg/ml) (mmHg)
Control group 35 25.6 ± 2.8 61.3 ± 14.2
Thickening group 65 36.4 ± 6.8* 70.5 ± 12.3*
Plaque group 50 43.0 ± 4.5**@ 80.2 ± 13.0*@

Table 2. Comparison of AGEs and PP levels among IMT patients.

Comparison of AGEs and PP

AGEs level was elevated along with aggravation of carotid plaque. In moderate and severe stenosis groups, or complete blockade group, both AGEs and PP levels showed statistically significance compared to those in mild stenosis group. Severe stenosis and blockade groups further had remarkably different AGEs and PP levels against those in moderate stenosis group. Moreover, severe stenosis group showed statistically significant difference of AGEs or PP levels compared to complete blockade group (Table 3).

Degree of stenosis N AGEs PP
(μg/ml) (mmHg)
Mild stenosis 15 32.3 ± 5.7 62.3 ± 13.5
Moderate stenosis 15 35.9 ± 6.8* 68.5 ± 11.3*
Severe stenosis 12 39.3 ± 5.8**@ 74.9 ± 12.0*@
Complete blockade 8 43.4 ± 8.1**@@# 80.5 ± 7.3*@@#

Table 3. Comparison of AGEs and PP among patients with different stenosis conditions.

Discussion

Carotid Atherosclerosis (AS) is common disorder in elder patients. Mild AS usually does not affect brain blood supply. Under severe conditions, however, AS may lead to restricted blood supply toward the brain, leading to symptoms including headache and dazedness. Further activity of neck may further aggravate blood ischemia, or even lead to the formation of cerebral thrombosis [15,16]. AS is the basic pathogenic factor for cerebral thrombosis, and is caused by deposition of lipid components of blood onto artery endothelial layer under various stimuli. Such lipid deposition may cause fibrous thickened lesion of endothelial tissues, leading to necrosis and breakdown of deeper tissues, thus causing the formation of plaque-like lesion, and subsequent rigidity of artery walls. Various factors including hypertension, high blood lipid and diabetes all can accelerate AS progression [17-19]. Due to blood flow restriction inside artery with thrombosis, innervated cerebral tissues may not obtain sufficient blood or oxygen supply, leading to tissue softening and necrosis. Clinical manifestations include symptoms and body signs of focal cerebral dysfunction, such as cognitive disorder, sensory dysfunction, paralysis, or aphasia. The observation of carotid artery AS plaque is an important indicator for preventing the development of cerebral thrombosis [20-22].

Currently many reports showed the important role of AGEs in the pathogenesis of AS [21-23]. Related functions mainly include the following contents: Firstly, AGEs may lead to instability and secondary rupture of plaque surface fibrous layer. Previous study showed 3-5 folds higher activity of MMP-9 protein in the shoulder area of unstable plaque compared to those in stable plaques. AGE can facilitate AS pathogenesis progression via high glucose-induced expression of lipoprotein esterase from macrophage, and finally cause the rupture of AS plaque on diabetic patients through facilitating the secretion of inflammatory cytokines such as TNF-A and interleukin-1B from monocytes. Secondly, AGEs can facilitate the generation of oxidative stress, which further accelerates AS. Recent in vitro studies [24-26] also confirmed that AGE could stimulate oxidative oxygen production within circulation and vascular cells, and reactive oxygen level is an important factor catalysing AGE generation. Inside AS plaque, upregulation of AGE receptor expression inside monocytes facilitates cellular binding to more AGEs to stimulate the release of pro-inflammatory factors, forming a positive feedback loop of inflammation. Such process can further aggravate pro-inflammatory effects of AGE at local circulation or deposition, thus aggravating the instability of AS plaque. In a word, AGEs showed a wide spectrum of pathogenic roles.

Our results showed significantly higher serum AGEs levels in carotid AS patients, especially those with carotid artery plaque, than those without AS or plaque. Further comparison among different grades of cavity stenosis showed aggravated AGEs displayed higher severity of carotid AS, indicating the association of serum AGEs level with carotid AS or plaque formation. Meanwhile, sub-grouping of patients based on disease conditions showed higher AGEs levels in cerebral thrombosis patients with diabetes compared to those with pure cerebral thrombosis formation or healthy individuals, and those pure thrombosis patients had higher AGEs levels than control group, indicating important roles of AGEs in the formation of cerebral thrombosis. Meanwhile, we also showed that individuals having carotid AS, especially with carotid artery plaque, had significantly higher PP levels than those without carotid AS or plaque. Disease-based grouping showed higher PP levels in cerebral thrombosis patients complicated with diabetes compared to those having pure cerebral thrombosis, which further showed higher PP levels than control group. These results showed the involvement of PP in carotid AS, plaque or cerebral thrombosis formation. PP level is an important indicator reflecting major artery AS, as elevated PP level could accelerate AS progression, and aggravate carotid artery IMT. This study also found better blood pressure management in IMT thickening and control groups compared to plaque group, indicating important roles of PP in AS pathogenesis. In this study, some patients were complicated with diabetes and no significant difference was found in fasted blood glucose level among all groups, probably due to blood glucose management by insulin or oral medicines. However, due to limited number of patients enrolled in this study, large cohort clinical study is required to confirm these findings in the future [27,28].

Conclusion

AGEs level is correlated with cerebral thrombosis and might work as an indicator for evaluating carotid artery AS condition. Further study on functional roles and mechanism of AGEs in AS probably will provide novel targets for clinical prevention and treatment of AS or cerebral thrombosis. Meanwhile, identification of drugs inhibiting AGEs production or functions also has critical importance for preventing and treatment of cerebral vascular disease.

Acknowledgements

This work was supported by Jilin Provincial Education Department “12th Five-Year” science and technology research project, Ji Jiao Ke 2014 (No.498).

References