Correlation between coronary atherosclerosis calcification and epicardial adipose tissue volume in patients with nephropathy
- Authors:
- Published online on: September 27, 2018 https://doi.org/10.3892/etm.2018.6801
- Pages: 4669-4673
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Copyright: © Zuo et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
Abstract
Introduction
The adipose tissue between epicardium and the myocardial surface is called epicardial adipose tissue (EAT) (1). EAT is rich in heart arteries and is one of the most important types of tissues in the human body (2). At present, studies (3–5) have proven that local inflammatory mediator produced by EAT is closely related to the occurrence and development of coronary atherosclerosis, and its mechanism of action is not yet clear. With the increased incidence of coronary atherosclerosis in recent years (6), the studies on correlations between coronary atherosclerosis and EAT have attracted increased attention. Tsushima et al (7) have shown that measuring the EAT volume can effectively predict coronary artery disease. However, measurement of EAT was not accurate in the past due to the technical difficulties (8). With the rapid development of modern technology, EAT now can be accurately measured by CT. The most serious and common complications of chronic kidney disease are cardiovascular and cerebrovascular diseases (9). Carlsson et al (10) showed that the main causes of death in patients with chronic kidney disease in 2015 were acute coronary syndrome, and heart failure and sudden death after myocardial infarction. However, there is no effective indicator for the detection of sudden cardiovascular disease in patients with chronic kidney disease. Therefore, we speculate that EAT may be used as an indicator of coronary atherosclerosis in patients with renal disease to monitor the occurrence of sudden cardiovascular and cerebrovascular condition. Correlation between EAT and atherosclerosis in patients with nephropathy are not yet clear. Therefore, we analyzed the correlation between EAT and coronary atherosclerosis, calcification, and the number of lesions in patients with nephropathy to evaluate the possible application of EAT as an indicator of atherosclerotic conditions in patients with nephropathy. Our study provided reference for future clinical studies.
Materials and methods
General information
A retrospective analysis was performed on 529 patients with chronic kidney disease who were highly suspected to have coronary atherosclerosis during preliminary examination in Xianyang Central Hospital (Xianyang, China) from August 2013 to September 2016. Those patients included 354 males and 175 females, and the age ranged from 30 to 60 years, with a mean age of 43.75±9.62 years. Inclusion criteria: patients diagnosed with chronic kidney disease in Xianyang Central Hospital; patients aged from 30 to 60 years; patients with complete clinical case, and patients with clinical symptoms of coronary atherosclerosis. Exclusion criteria: patients with cardiovascular and cerebrovascular disease; patients with other respiratory diseases; drug-sensitive patients; pregnant patients; patients with a family history; patients with a history of cancer, and patients with iodine allergy.
The study was approved by the Ethics Committee of Xianyang Central Hospital. The patients signed an informed consent.
Method
CT was performed in strict accordance with operation guideline of 2010 CT examination of the coronary artery (11). Parameter settings are shown in Table I.
Calcification integral scan was performed first, and the heart was scanned from the point 1 cm below the trachea towards feet. The enhanced scan was preceded by injection of 60–80 ml of umbilical non-ionic iopromide contrast agent with a speed of 5 ml/sec, followed by another 30–40 ml with a speed of 5 ml/sec. Bolus tracking was used to determine scan trigger time, and the optimal diastolic and systolic periods were automatically reconstructed, with a tolerance of 0.75 mm and overlap of 0.5 mm.
Interpretation of results
The 2015 CT coronary angiography guidelines were used as the diagnostic criteria for atherosclerosis (12). A CT value of ≥130 HU and image showing a red color was judged as calcification. Imaging results were double-blindly reviewed by three senior imaging physicians in Xianyang Central Hospital. A right coronary artery, left anterior descending, and left circumflex coronary artery lesion was counted as one coronary artery disease, while left main coronary artery l lesion was counted as 2 coronary artery lesions. Degree of coronary calcification was divided into ≤50 group, 51–200 group, 201–500 group, 501–1,000 group, and >1,000 group.
Statistical analysis
SPSS 22.0 statistical software (IBM Corp., Armonk, NY, USA) was used to analyze and process data. Measurement data are expressed as mean ± standard deviation and t-tests were used. Analysis of variance followed by post hoc test (Least Significant Difference) was used for comparisons among multiple groups. Correlation analysis was performed using linear correlation analysis. P<0.05 was considered to be statistically significant.
Results
EAT volume in patients with different BMI
Mean EAT volume of the 529 patients with nephropathy was 97.81±49.31 mm3, and the maximum volume was 742 mm3, and the minimum volume was 26.57 mm3. Mean BMI of the 529 patients was 22.37±9.63 kg/m2, the highest was 38.74 kg/m2, and the lowest was 15.23 kg/m2. Coronary atherosclerosis was seen in 319 out of 529 patients. Mean EAT volume in patients with coronary atherosclerosis was 81.42±29.68 mm3, and mean EAT volume in patients without coronary atherosclerosis was 62.15±36.16 mm3, significant differences were found between them (p<0.01). According to the median BMI, patients were divided into BMI <22 kg/m2 group (221 cases) and BMI >22 kg/m2 group (308 cases). EAT volume in patients with BMI <22 kg/m2 was 95.23±40.53 mm3, which was significantly higher than that in patients with BMI ≥22 kg/m2 112.61±48.17 mm3 (p<0.01). Linear correlation analysis showed a positive correlation between EAT volume and BMI (r=0.61, p<0.05) (Tables II and III, Fig. 1).
EAT volume in patients with different calcification scores
There were 447 cases of atherosclerosis calcification in 529 patients with nephropathy, of which 243 patients had calcification score <50, and mean EAT volume was 82.34±49.78 mm3, 62 patients had calcification score between 51–200, and mean EAT volume was 91.33±51.67 mm3, 73 patients had calcification score between 201–500, and mean EAT volume was 113.82±62.02 mm3, 57 patients had calcification score between 501–1,000, and mean EAT volume was (13.82±62.02 mm3, 57 patients had calcification score >1,000, and mean EAT volume was 104.69±59.68 mm3. EAT volume in patients with calcification integral ≤50 was the smallest, followed by 51–200 group and 201–500 group, and the volume in 501–1,000 group was the largest. EAT volume of >1,000 group was significantly lower than that of the 501–1,000 group and significantly higher than that of 201–500 group (p<0.05). Linear correlation analysis showed a positive correlation between EAT volume and calcification score (r=0.72, p<0.05) (Table IV and Fig. 2).
EAT volume in patients with different numbers of coronary artery lesions
Coronary lesions were seen in 315 patients with 529 nephropathy, and mean EAT volume in non-lesioned patients was 80.71±53.27 mm3. There were 117 patients with 1 lesion and the mean EAT volume was 80.71±53.27 mm3. There were 94 patients with 2 lesions and mean EAT volume was 94.84±52.33 mm3. There were 72 patients with 3 lesions and mean EAT volume was 101.37±54.08 mm3. There were 32 patients with 4 lesions and mean EAT volume was 104.74±36.68 mm3. EAT volume increased with the number of lesions (p<0.05). Linear correlation analysis showed that the EAT volume was positively correlated with the number of coronary lesions (r=0.64, p<0.05) (Table V and Fig. 3).
Discussion
After the report of the role of EAT in inducing coronary atherosclerosis by local inflammatory mediators, detecting EAT volume has been widely used as a predictor of coronary atherosclerosis. EAT develops from embryonic adipose tissue and shares homology with mesenteric and omental adipose tissue (13,14). Studies have shown that EAT can secrete and synthesize a variety of types of cell adipokines and related inflammatory factors to act on the surface of coronary arteries and enhance atherosclerosis (6,15–17). In this study, high-resolution dual-source CT was used to examine the EAT volume in patients with suspected coronary atherosclerosis, which not only provided a better assessment of the coronary artery lesions, but also improved the accuracy of the measurement of the volume of EAT.
Results of this study indicate that the EAT volume is positively correlated with BMI, coronary artery calcification, and the number of coronary artery lesions in patients with nephropathy, which is basically consistent with the findings of Mazurek and Opolski (18) and Pawar et al (19), indicating that EAT volume can be used as an independent indicator to predict the occurrence and development of coronary arteriosclerosis. Higher BMI was accompanied with larger EAT volume. High BMI can increase the level of plasma positive cytokine to promote the process of atherosclerosis (4), but the mechanism of action still needs to be further studied. EAT not only reserves energy, but also serves as an endocrine organ to secrete large amounts of free fatty acids (20). The secreted cytokines affect the metabolism of heart muscle by regulating heart morphology, so as to promote the proliferation of smooth muscle cells of the coronary vascular wall, and accelerate the process of coronary artery stenosis (21). Free fatty acids released by EAT not only induce apoptosis of vascular endothelial cells, but also impair intravascular endothelium relaxation and contraction. Secretion of excessive inflammatory factors such as TNF-α and MCP-1 accelerate the process of coronary atherosclerosis (22). The degree of coronary artery calcification is positively correlated with the severity of lesions and EAT volume. Patients with calcification score >1,000 patients had a decreased EAT volume compared with patients with a calcification score of 501–1,000. The reason may be the bias caused by the small number of cases in this study, but the overall correlation between calcification and EAT volume is still positive. Our future studies are expected to confirm the findings. Chaowalit et al (23) showed that there was no significant correlation between calcification and the volume, possibly due to the different detection methods. Chaowalit et al used ultrasound as the main measurement instrument. Ultrasound was only accurate for the measurement of local thickness of EAT. Distribution of EAT thickness on the surface of the heart varies from individual to individual. Ultrasound may not be an appropriate imaging method for measurement of EAT.
In this study, CT was used to detect EAT volume in patients with suspected coronary atherosclerotic nephropathy, and correlations of EAT with BMI, calcification, and pathological conditions were analyzed. There are still deficiencies, such as the small sample size. Our future studies will solve these problems.
In summary, coronary atherosclerosis, BMI, calcification, and number of lesions are positively correlated with the volume of EAT in patients with nephropathy. Detection of EAT volume may serve as an indicator of the occurrence and development of coronary atherosclerosis in the future.
Acknowledgements
Not applicable.
Funding
No funding was received.
Availability of data and materials
The datasets used and/or analyzed during the present study are available from the corresponding author on reasonable request.
Authors' contributions
HZ and YZ drafted the manuscript. HZ and QM analyzed and interpreted calcification integral scan. YZ and QM treated patients and were responsible for statistical analysis. All authors read and approved the final manuscript.
Ethics approval and consent to participate
The study was approved by the Ethics Committee of Xianyang Central Hospital (Xianyang, China). Signed informed consents were obtained from the patients or guardians.
Patient consent for publication
Not applicable.
Competing interests
The authors declare that they have no competing interests.
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