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Prognostic implications of surrogate markers of atherosclerosis in low to intermediate risk patients with type 2 diabetes.
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PMID:  22900680     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
BACKGROUND: Type 2 diabetes mellitus (T2DM) patients are at increased risk of developing cardiovascular events. Unfortunately traditional risk assessment scores, including the Framingham Risk Score (FRS), have only modest accuracy in cardiovascular risk prediction in these patients.
METHODS: We sought to determine the prognostic values of different non-invasive markers of atherosclerosis, including brachial artery endothelial function, carotid artery atheroma burden, ankle-brachial index, arterial stiffness and computed tomography coronary artery calcium score (CACS) in 151 T2DM Chinese patients that were identified low-intermediate risk from the FRS recalibrated for Chinese (<20% risk in 10 years). Patients were prospectively followed-up and presence of atherosclerotic events documented for a mean duration of 61 ± 16 months.
RESULTS: A total of 17 atherosclerotic events in 16 patients (11%) occurred during the follow-up period. The mean FRS of the study population was 5.0 ± 4.6% and area under curve (AUC) from receiver operating characteristic curve analysis for prediction of atherosclerotic events was 0.59 ± 0.07 (P = 0.21). Among different vascular assessments, CACS > 40 had the best prognostic value (AUC 0.81 ± 0.06, P < 0.01) and offered significantly better accuracy in prediction compared with FRS (P = 0.038 for AUC comparisons). Combination of FRS with CACS or other surrogate vascular markers did not further improve the prognostic values over CACS alone. Multivariate Cox regression analysis identified CACS > 40 as an independent predictor of atherosclerotic events in T2DM patients (Hazards Ratio 27.11, 95% Confidence Interval 3.36-218.81, P = 0.002).
CONCLUSIONS: In T2DM patients identified as low-intermediate risk by the FRS, a raised CACS > 40 was an independent predictor for atherosclerotic events.
Authors:
Kui-Kai Lau; Yuen-Kwun Wong; Yap-Hang Chan; Kai-Hang Yiu; Kay-Cheong Teo; Leonard Sheung-Wai Li; Shu-Leong Ho; Koon-Ho Chan; Chung-Wah Siu; Hung-Fat Tse
Publication Detail:
Type:  Journal Article     Date:  2012-08-18
Journal Detail:
Title:  Cardiovascular diabetology     Volume:  11     ISSN:  1475-2840     ISO Abbreviation:  Cardiovasc Diabetol     Publication Date:  2012  
Date Detail:
Created Date:  2012-09-18     Completed Date:  2012-12-21     Revised Date:  2013-07-12    
Medline Journal Info:
Nlm Unique ID:  101147637     Medline TA:  Cardiovasc Diabetol     Country:  England    
Other Details:
Languages:  eng     Pagination:  101     Citation Subset:  IM    
Affiliation:
Division of Neurology, Department of Medicine, Queen Mary Hospital, The University of Hong Kong, Hong Kong SAR, China.
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MeSH Terms
Descriptor/Qualifier:
Aged
Ankle Brachial Index
Area Under Curve
Atherosclerosis / diagnosis*,  epidemiology*,  physiopathology
Brachial Artery / physiopathology
Carotid Arteries / pathology
Carotid Artery Diseases / diagnosis*,  epidemiology*
Carotid Intima-Media Thickness
Chi-Square Distribution
Comorbidity
Coronary Angiography / methods
Coronary Artery Disease / diagnosis*,  epidemiology*
Diabetes Mellitus, Type 2 / epidemiology*
Diabetic Angiopathies / diagnosis*,  epidemiology*,  physiopathology
Disease-Free Survival
Endothelium, Vascular / physiopathology
Female
Follow-Up Studies
Hong Kong / epidemiology
Humans
Kaplan-Meier Estimate
Male
Middle Aged
Multivariate Analysis
Plaque, Atherosclerotic
Predictive Value of Tests
Prognosis
Proportional Hazards Models
Prospective Studies
Pulse Wave Analysis
Risk Assessment
Risk Factors
Time Factors
Tomography, X-Ray Computed
Vascular Calcification / diagnosis,  epidemiology
Vascular Stiffness
Comments/Corrections

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Journal Information
Journal ID (nlm-ta): Cardiovasc Diabetol
Journal ID (iso-abbrev): Cardiovasc Diabetol
ISSN: 1475-2840
Publisher: BioMed Central
Article Information
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Copyright ©2012 Lau et al.; licensee BioMed Central Ltd.
open-access:
Received Day: 13 Month: 4 Year: 2012
Accepted Day: 11 Month: 8 Year: 2012
collection publication date: Year: 2012
Electronic publication date: Day: 18 Month: 8 Year: 2012
Volume: 11First Page: 101 Last Page: 101
ID: 3444371
Publisher Id: 1475-2840-11-101
PubMed Id: 22900680
DOI: 10.1186/1475-2840-11-101

Prognostic implications of surrogate markers of atherosclerosis in low to intermediate risk patients with Type 2 Diabetes
Kui-Kai Lau12 Email: gkklau@hku.hk
Yuen-Kwun Wong1 Email: debbieyk@hku.hk
Yap-Hang Chan3 Email: chanwill@hku.hk
Kai-Hang Yiu24 Email: khkyiu@hku.hk
Kay-Cheong Teo1 Email: kaycteo@yahoo.com
Leonard Sheung-Wai Li5 Email: lswli@hku.hk
Shu-Leong Ho12 Email: slho@hku.hk
Koon-Ho Chan12 Email: koonho@hku.hk
Chung-Wah Siu24 Email: cwdsiu@hku.hk
Hung-Fat Tse24 Email: hftse@hku.hk
1Division of Neurology, Department of Medicine, Queen Mary Hospital, The University of Hong Kong, Hong Kong SAR, China
2Research Center of Heart, Brain, Hormone and Healthy Aging, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China
3School of Public Health, The University of Hong Kong, Hong Kong SAR, China
4Division of Cardiology, Department of Medicine, Queen Mary Hospital, The University of Hong Kong, Hong Kong SAR, China
5Division of Rehabilitation Medicine, Department of Medicine, Tung Wah Hospital, The University of Hong Kong, Hong Kong SAR, China

Background

Patients with type 2 diabetes mellitus (T2DM) are at increased risk of developing adverse atherosclerotic events including acute coronary syndrome (ACS) and ischemic stroke [1-3]. Various risk assessment algorithms, for example the Framingham Risk Score (FRS) and Systematic Coronary Risk Evaluation (SCORE), aim to predict the likelihood of developing cardiovascular events [4-6]. Some of these scores have also been recalibrated based on the ethnic differences in cardiovascular risk profile and incidences of cardiovascular diseases (CVD). Nonetheless only the Framingham Risk Score has been calibrated for use in the Chinese population [7]. Although these algorithms are considered a useful tool for risk stratification in the general population, they do not have sufficient power and lack accuracy in patients with T2DM [8-10]. Furthermore, whilst current guidelines provide clear recommendations on initiating anti-platelet therapy for primary prevention of CVD in diabetic patients with high cardiovascular risk, not those at low risk, there are no recommendations for those categorized as intermediate risk [11].

Surrogate markers of atherosclerosis, including brachial artery flow-mediated dilatation (FMD), carotid artery atheroma burden, ankle-brachial index (ABI), arterial stiffness and computed tomography coronary artery calcium score (CACS) have been increasingly used for the prediction of cardiovascular events [12-16]. Prior studies have demonstrated that such markers improve risk stratification of CVD in the general population when used in conjunction with the FRS [12,14,15,17-22]. Recent studies also support the use of carotid intima-media thickness (IMT) and CACS in conjunction with traditional risk scores to improve risk stratification in diabetics asymptomatic for CVD [16,23]. The prognostic values of surrogate markers of atherosclerosis in T2DM patients deemed low-intermediate risk is nevertheless currently unknown. The purpose of this prospective study was to compare the prognostic values of the FRS with a range of commonly used surrogate markers of atherosclerosis, used alone and in combination with the FRS, in Chinese T2DM patients identified as low-intermediate risk.


Methods
Subjects

Consecutive Chinese patients with T2DM as defined by the WHO criteria were prospectively recruited from the Medical Outpatient Clinics from July 2005 to December 2006 [24,25]. Patients calculated to be at high risk (≥20%) of developing a cardiovascular event within 10 years based on the recalibrated FRS for Chinese were excluded [7]. Patients with a history of prior athero-thrombotic events (including ACS, ischemic stroke, acute limb ischemia), stable angina, symptomatic peripheral vascular disease, creatinine level >220 μmol/L, severe hepatic disease, malignancy or connective tissue diseases were also excluded. A total of 151 patients with T2DM were thus eligible for this study. We obtained approval from the local institutional review board and all subjects gave written informed consent.

Study design

Baseline demographic data, cardiovascular risk factors and cardiovascular medication at the time of recruitment were documented. Cardiovascular risk factors including tobacco smoking, hypercholesterolemia, hypertension and family history of CVD diagnosed in first-degree relatives before 55 years of age were assessed. Hypertension was defined as either resting systolic or diastolic blood pressure ≥140 or ≥90 mmHg respectively, recorded at two different clinical visits or the prescription of anti-hypertensive medication [26]. Hypercholesterolemia was defined as fasting total plasma cholesterol ≥5.1 mmol/L or the prescription of lipid-lowering medication [27]. Smoking status was recorded as ever-smoker (past or current) or non-smoker.

Anthropometric measurements including body weight, height and waist-hip circumference ratio (WHR) were performed. Body-mass index (BMI) was calculated as kg/m2. Systolic and diastolic blood pressures were measured and fasting blood samples were obtained to measure serum levels of glucose, hemoglobin A1c (HbA1c), total cholesterol, triglyceride, low-density lipoprotein-cholesterol (LDL-C), high-density lipoprotein-cholesterol (HDL-C) and creatinine. Glomerular filtration rate (GFR) was calculated using the Modification of Diet in Renal Disease Study equation [28].

Vascular assessments

Vascular ultrasound examination for brachial endothelial function, carotid IMT and presence of carotid plaque was evaluated through a standard B-mode ultrasound examination with the use of a 7.5 MHz linear array transducer and a high resolution ultrasound system (Agilent Sonos 5500, Philips, Andover, Massachusetts, USA) as described previously [18]. Measurements of ABI and arterial stiffness were performed using a commercially available device based on the oscillometric method (VP-2000, Colin Corporation, Komaki, Japan) [25]. Arterial stiffness was represented by brachial to ankle pulse wave velocity (baPWV). This method has previously been validated and closely correlates with aortic PWV [29].

A single experienced operator blinded to the status of the study subjects performed all vascular ultrasound examinations. Another experienced operator, also blinded to the status of study subjects, operated on VP-2000 and obtained ABI and arterial stiffness parameters.

Brachial endothelial function

Patients were studied in the fasting state and vasoactive medications were withheld for 12 hours prior to the scans. Longitudinal brachial artery diameter was obtained at rest, and then during FMD, induced by inflation of a pneumatic tourniquet placed around the forearm to a pressure of 50 mmHg above systolic blood pressure for 5 minutes. The cuff was then released and serial imaging of the brachial artery was recorded for 5 minutes. FMD was defined as the percentage change in brachial artery diameter between 1 minute following cuff deflation and that on the baseline scan. All digital images were stored on optical diskettes for subsequent off-line analysis using a computer workstation (EchoPAC, GE Medical, Wisconsin, USA). A single operator measured the brachial artery diameter and an average value from three consecutive measurements was calculated. The intra-observer correlation coefficient for FMD was 0.90 (2 repeated measurements in 20 randomly chosen subjects).

Carotid intima-media thickness and plaque

Carotid IMT was determined by measuring manually the distance between the lumen-intima and media-adventia border of the vascular wall using electronic calipers. Each ultrasonic scan was performed in the anterior, lateral and posterior projections of the right and left carotid arteries. Three IMT measurements were made on the near and far wall of the common carotid arteries, carotid bifurcation and internal carotid arteries. The mean maximum IMT (mmIMT) was used for analysis and was calculated by averaging the values of maximum IMT from 12 pre-selected segments of the carotid arteries. Presence of carotid plaque was defined as an endoluminal protrusion of the arterial lumen of at least 0.5 mm or 50% of the surrounding IMT value or demonstration of an IMT of >1.5 mm [30]. The intra-observer correlation coefficient for mmIMT was 0.97 (2 repeated measurements in 20 randomly chosen subjects).

Ankle-brachial index and arterial stiffness

Measurements of ABI and arterial stiffness were performed with subjects in the supine resting position in a quiet and temperature-controlled room. Pneumatic pressure cuffs with oscillometric pressure sensors were wrapped tightly around both arms and both ankles. Electrocardiographic electrodes were attached to both wrists and a phonocardiogram was placed at the left second intercostal space, at the margin of the sternum. After ensuring that patients had rested for 15 minutes, fully automatic data acquisition began. Pressure waveforms of the brachial and posterior tibial arteries were recorded. Based on the height of the patient, the device estimated the path lengths from the brachial artery to the posterior tibial artery. BaPWV was calculated as the path length divided by the corresponding time interval (cm/s). The right and left baPWV were averaged and the resulting value selected as the representative baPWV.

The pneumatic cuffs over both arms and ankles enabled simultaneous measurement of systolic blood pressure at each limb. The right-and left-sided ABI were calculated as the ankle systolic blood pressure divided by the brachial systolic blood pressure measured from the right and left side, respectively. The right and left ABI were averaged and the resulting value selected as the representative ABI.

The intra-observer correlation coefficient for ABI was 0.85 and the intra-observer correlation coefficient for baPWV was 0.98 (2 repeated measurements in 20 randomly chosen subjects).

Computed tomography coronary artery calcium score

All subjects underwent computed tomography imaging of the coronary arteries using a 64 slice MDCT (Lightspeed, VCT, GE Healthcare, USA) as described previously [18,31]. All scans were performed with subjects in the supine position, and included regions from the arch of the aorta to the fundus of the heart. Prospective electrocardiogram-gated cardiac scan was obtained with the following scan variables: rotation time = 0.35 s, slice thickness = 2.5 mm; 120 kV; 250 mA; trigger delay = 70% R-R interval. Patients were instructed to breath hold for 30s during scanning.

The acquired MDCT images were reviewed at the post-processing image workstation (Advantage windows 4.02, GE Healthcare). Complete data were available from all scans, with no mis-registration of slices due to artifacts of motion, respiration, or asynchronous electrocardiographic triggering. To ensure continuity and consistency of interpretation of calcium scores, two expert investigators, who were unaware of subject’s clinical status, analyzed all scans. The inter-observer and intra-observer variability correlation coefficients of CACS measurements were 0.92 and 0.91, respectively.

Measurement of CACS was performed using a commercially available software “smart score” (GE Healthcare) using the threshold option set for pixels >130 Hounsefiled units and expressed in Agaston units. CACS was calculated as the sum of calcium scores in the left main coronary artery, left anterior descending artery, left circumflex coronary artery, right coronary artery, and posterior descending artery.

Clinical outcome

All patients were followed-up in our clinic every 3–4 months. Clinical data of all patients were retrieved from the medical records and subsequently during the most recent clinic visit. An adverse atherosclerotic event was defined as ACS, ischemic stroke, new onset symptomatic peripheral vascular disease, death due to ACS or ischemic stroke or symptom driven revascularization procedures of the carotid, coronary or peripheral arteries.

Statistical analysis

Power calculation was performed based on the prediction values of coronary artery calcium score for atherosclerotic events in patients with type 2 diabetes. Using an alpha of 0.05 and total sample size of 151 would give a power of 80%.

Data were expressed as mean ± standard deviation for continuous variables and proportions for categorical variables. Baseline characteristics were compared between groups using Student’s t-test or Chi-squared test, as appropriate. Pearson’s correlation was used to measure the correlations between vascular assessment variables. Area under receiver operating curves (AUC) were calculated and the cut-off values of the vascular assessments with optimal sensitivity and specificity were obtained. These cut-off values were then used in subsequent analysis to determine the prognostic role of these surrogate markers in the prediction of atherosclerotic events. Chi-squared test was also used to compare the predictive accuracy between FRS and vascular markers in atherosclerotic event prediction. The associations between vascular assessment parameters, categorized by AUC cut-off values, and event-free survival were evaluated using Cox regression models with adjustment for potential confounding variables. Only parameters with P < 0.1 in uni-variate analysis were entered into a multi-variate model to identify the independent predictors for atherosclerotic events. Cumulative event rates were estimated using the Kaplan-Meier method and compared using log-rank test.

All statistical analyses were performed using the statistical software SPSS for Windows (Version 15.0, SPSS, Chicago, USA) and STATA for Windows (Version 11.2, STATA Corp., College Station, TX). A P value <0.05 was considered statistically significant.


Results
Clinical characteristics

Clinical characteristics of the study population are summarized in Table 1. Their average age was 60.9 ± 10.0 years and 40% were men. Their mean duration of DM was 15.2 ± 7.5 years, 60% patients had hypertension, 56% had hypercholesterolemia, 18% were ever-smokers and 17% had a family history of CVD. The mean HbA1C was 7.7 ± 1.2%, 16% of patients had retinopathy and the average GFR was 84 ± 22 ml/min/1.73 m2. The mean FRS of the study population was 5.0 ± 4.6%. Results of the vascular assessment parameters are shown in Table 1.

Relationship between Framingham risk score and vascular assessment parameters

Table 2 shows the correlation coefficients between FRS and various vascular assessments. There was a modest but significant correlation between FRS and mmIMT, baPWV and CACS (all P < 0.01). CACS also correlated well with mmIMT, ABI and baPWV (all P < 0.05) and mmIMT correlated well with CACS, ABI and baPWV (all P < 0.01). FMD showed no correlation with the FRS nor with the other vascular markers.

Clinical outcomes

During a mean follow-up of 61 ± 16 months (range 3–75 months), 17 atherosclerotic events including 1 cardiovascular death, 1 ACS, three ischemic stroke, 2 new onset peripheral vascular disease and 11 percutaneous coronary interventions were observed in 16 patients (11% of the study population). Elective percutaneous coronary interventions were performed at a mean of 8 ± 4 months following CT examination. All percutaneous coronary interventions were performed for treatment of symptomatic coronary artery disease and / or based on the presence of inducible ischemia detected by functional assessment rather than the results of CACS.

Table 1 shows the clinical characteristics and vascular marker parameters in patients with and without atherosclerotic event. Patients with atherosclerotic events were more likely to be smokers (35% versus 16%, P = 0.047). There was also a trend for patients with atherosclerotic events to be older (64.9 ± 10.1 years versus 60.4 ± 9.9 years, P = 0.079), have a lower BMI (23.8 ± 3.3 kg/m2 versus 25.8 ± 4.1 kg/m2, P = 0.061) and a lower GFR (74 ± 27 ml/min/1.73 m2 versus 85 ± 21 ml/min/1.73 m2, P = 0.059). There were nonetheless no significant differences between the two groups in terms of gender, proportions with hypertension or hypercholesterolemia, duration of DM, HbA1c or use of medication.

Patients with atherosclerotic events had a significantly greater carotid artery mmIMT (1.1 ± 0.3 mm versus 0.9 ± 0.2 mm, P = 0.047) and CACS (374 ± 341 versus 120 ± 346, P = 0.011) than those without atherosclerotic events. No significant differences in FRS, brachial artery FMD, prevalence of carotid plaque, ABI or baPWV were observed between the two groups.

Prognostic values of vascular assessments

ROC curves were constructed to obtain the prognostic values and optimal cut-off values of the FRS as well as different vascular assessment parameters (Table 3). All of these parameters had good negative predictive values (90-100%) but poor positive predictive values (14-57%). The FRS had an AUC of 0.59 ± 0.07 (P = 0.21). In contrast, of all the vascular assessment parameters tested, CACS >40 had the best predictive power for an atherosclerotic event (AUC 0.81 ± 0.06, P < 0.01) followed by carotid artery mmIMT > 1.07 mm (AUC 0.67 ± 0.07, P = 0.02).

Uni-variate analysis identified age, male sex, BMI, WHR, hypertension, FMD ≤1.12%, mmIMT >1.07 mm, ABI ≤0.98 and CACS >40 as positive predictors for an atherosclerotic event (all P < 0.1). Multi-variate Cox regression analysis revealed that mean ABI ≤0.98 (Hazards ratio (HR) 7.17, 95% CI (confidence interval) 1.63-31.52, P = 0.009) and CACS >40 (HR 27.11, 95% CI 3.36-218.81, P = 0.002) were independent predictors of an atherosclerotic event (Table 4). There was also a trend for mmIMT >1.07 mm as an independent predictor of an atherosclerotic event (HR 2.76, 95% CI 0.90-8.46, P = 0.077). In Kaplan-Meier analysis, a raised CACS >40 was associated with the occurrence of an atherosclerotic event during follow-up (P < 0.0001, Figure 1).

Finally, we compared the predictive power of FRS for atherosclerotic events against other vascular assessment markers, alone and in combination with the FRS (Table 5). CACS had significantly greater AUC compared with FRS (AUC 0.81 versus 0.59, P = 0.038). There were no significant differences in AUC between other vascular markers and FRS (all P > 0.05). Combining CACS with FRS provided incremental benefit in risk prediction compared with FRS alone (AUC 0.77 versus 0.59, P = 0.013) but did not offer further benefit compared with CACS alone. Combination of FRS with other vascular markers also did not provide further incremental benefit.


Discussion

This study compared the diagnostic value of non-invasive markers of atherosclerosis, used alone and with the FRS, in the prediction of atherosclerotic events in Chinese T2DM deemed low-intermediate risk. The results of our study show that in Chinese T2DM patients of low-intermediate risk, 11% developed an atherosclerotic event during a mean follow-up of 61 ± 16 months. The FRS only had a modest accuracy in prediction of atherosclerotic events in our study. In contrast, among the different surrogate markers of atherosclerosis evaluated, a raised CACS > 40 offered the best prognostic value and was superior to FRS in risk prediction. It was also an independent predictor of a future atherosclerotic event. Although combination of CACS with FRS provided incremental benefit in risk prediction versus FRS alone, such a combination did not offer further prognostic value compared with CACS alone.

Limitations of traditional risk scores

The FRS has been successful in prediction of CVD in general populations. The risk algorithm nonetheless lacks accuracy in patients with diabetes [4,5]. Studies using the FRS in different population groups have found that the FRS has both under- and over-estimated CVD risk in patients with DM [8-10]. Such an observation has been postulated to be related to a small number of diabetic patients in the original Framingham cohort (4% of 5573 subjects) from which the equation was derived. Glycemic control as well as duration of diabetes are also considered important parameters in determining CVD risk and should be included in risk algorithms [8]. Among Chinese, the FRS also overestimates cardiovascular risk, leading to a recent recalibration to suit the Chinese population [7]. Although this has led to improved risk estimation, recent studies have further identified limitations of such a model due to the greater prevalence of stroke than coronary heart disease in China [32]. In this study, the average FRS of our study population was only 5.0 ± 4.6% for prediction of cardiovascular events in 10 years but up to 11% (16 out of 151) of patients developed an adverse cardiovascular event within a mean follow-up period of 61 ± 16 months, thus highlighting the limitations of the FRS.

Use of vascular markers in improving cardiovascular risk stratification

In view of the FRS’s drawbacks, further strategies to improve risk stratification should be implemented. Previous studies have identified that use of non-invasive surrogate markers of atherosclerosis including brachial artery FMD, carotid atheroma burden, ABI, arterial stiffness and CACS improve CVD risk stratification in the general population [12,14,15,17-22]. Fewer such studies have been performed in a population limited to patients with T2DM. Recent studies have shown that combination of the FRS with carotid artery IMT provides greater predictive power of cardiovascular events compared with FRS alone [23,33], but such a benefit was not observed when combining baPWV with FRS [23]. Similarly the PREDICT study provided evidence that measurement of the CACS was a powerful predictor of cardiovascular events in asymptomatic patients with T2DM and was able to improve risk prediction as calculated by the United Kingdom Prospective Diabetes Study risk model [16].

Amongst commonly used non-invasive surrogate markers of atherosclerosis, a raised CACS was determined to have the best prognostic value in this study with a high negative predictive value of 98.7%. This finding is consistent with similar studies that also showed CACS to be superior to other markers for CVD prediction in the general population [22,34]. It has been suggested that the superiority of CACS in coronary heart disease prediction is likely related to the direct measurement of atheroma burden in the vasculature bed of interest [22]. Nonetheless despite a range of end points related to atherosclerotic disease being used in this study, CACS remained superior to other vascular markers. The significant correlations of CACS with mmIMT, ABI and arterial stiffness suggests that CACS is not only a reflection of atheroma burden in the coronary arteries but of other vasculature beds including the carotid arteries and peripheral vasculatures.

The most recent international guidelines provide clear recommendations for initiation of antiplatelet therapy in diabetic patients considered to be at high cardiovascular risk (men >50 years or women >60 years with one additional major cardiovascular risk factor) and does not recommend such therapy for those at low risk (men <50 years or women <60 years with no major cardiovascular risk factors) [11]. Nonetheless the prescription of anti-platelet agents remains a matter of clinical judgment for those at intermediate risk e.g. young patients with cardiovascular risk factors or older patients with no risk factors [11]. Our results show that screening of atherosclerotic burden with CACS may identify a high risk subgroup of diabetic patients who have been classified as intermediate risk using FRS. This group of patients may benefit from more aggressive preventive measures, including lipid lowering and anti-platelet therapy for CVD. Our results echo those from previous studies that have also demonstrated CACS as a powerful predictor of CVD and all-cause mortality as well as enhancing risk prediction in asymptomatic diabetic patients [16,26,35,36].

Limitations

In this prospective observational study, there was a small sample size that of only 151 Chinese patients with T2DM resulting in 17 events. Further large scale studies replicated in other ethnic populations and using other risk algorithms are needed to confirm our findings. In addition, there is increasing interest in coronary artery plaque location and morphology as detected by contrast CT coronary angiogram but this was not assessed in the current study [35,37]. Finally, whilst serial monitoring of surrogate markers of atherosclerosis in diabetics have recently been studied to delineate the change in vascular parameters with treatment and time, this was not performed in our study [36,38].


Conclusions

In this small study, detection of CACS > 40 was an independent predictor for atherosclerotic events in T2DM patients identified as low-intermediate risk by the FRS.


Competing interest

The author(s) declare that they have no competing interests.


Authors’ contribution

KKL carried out the study and wrote the manuscript; YKW retrieved the follow-up data & performed the statistical analysis; YHC, KHY & KCT recruited the subjects & performed the vascular assessments; LSWL, SLH, KHC & CWS supervised the study; and HFT supervised the study design as well as writing of the manuscript. All authors read and approved the final manuscript.


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Figures

[Figure ID: F1]
Figure 1 

Kaplan-Meier curve for the development of atherosclerotic events in patients with CACS > 40 or CACS ≤ 40.



Tables
[TableWrap ID: T1] Table 1 

Clinical characteristics of the study population


Characteristic All With Atherosclerotic Event Without Atherosclerotic Event P-value
 
(N = 151)
(N = 17)
(N = 134)
 
Age, years
60.9 ± 10.0
64.9 ± 10.1
60.4 ± 9.9
0.079
Males, n (%)
61 (40)
10 (59)
51 (38)
0.10
Hypertension, n (%)
89 (60)
8 (47)
81 (62)
0.24
Hypercholesterolemia, n (%)
80 (56)
9 (60)
71 (55)
0.71
Ever-smokers, n (%)
27 (18)
6 (35)
21 (16)
0.047
Family history of CVD, n (%)
25 (17)
2 (12)
23 (17)
0.57
Duration of DM, years
15.2 ± 7.5
14.1 ± 7.8
15.3 ± 7.5
0.54
BMI, kg/m2
25.6 ± 4.1
23.8 ± 3.3
25.8 ± 4.1
0.061
WHR
88.5 ± 10.4
85.6 ± 8,5
88.9 ± 10.6
0.23
Systolic blood pressure, mmHg
140 ± 21
143 ± 21
139 ± 21
0.46
Diastolic blood pressure, mmHg
78 ± 9
76 ± 9
78 ± 9
0.49
Fasting blood glucose, mmol/L
7.5 ± 2.0
8.0 ± 2.9
7.5 ± 1.9
0.38
HbA1c, %
7.7 ± 1.2
7.7 ± 1.1
7.7 ± 1.3
0.94
Triglyceride, mmol/L
1.5 ± 1.2
1.5 ± 0.8
1.6 ± 1.2
0.77
Total cholesterol, mmol/L
4.9 ± 0.9
5.0 ± 1.1
4.9 ± 0.9
0.69
LDL-C, mmol/L
2.8 ± 0.8
3.0 ± 0.8
2.8 ± 0.7
0.46
HDL-C, mmol/L
1.4 ± 0.4
1.4 ± 0.3
1.4 ± 0.4
0.73
GFR, ml/min/1.73 m2
84 ± 22
74 ± 27
85 ± 21
0.059
Beta-blocker, n (%)
29 (21)
2 (13)
27 (22)
0.40
Calcium channel blocker, n (%)
50 (36)
4 (25)
46 (37)
0.35
ACEI/ARB, n (%)
44 (31)
6 (38)
38 (30)
0.56
Aspirin, n (%)
8 (6)
1 (6)
7 (6)
0.92
Statin, n (%)
30 (21)
5 (31)
25 (20)
0.31
Oral hypoglycemic agent, n (%)
115 (82)
13 (81)
102 (82)
0.92
Insulin, n (%)
24 (17)
2 (13)
22 (18)
0.60
Retinopathy, n (%)
23 (16)
3 (19)
20 (16)
0.76
Urine albumin g/l
0.07 ± 0.2
0.1 ± 0.3
0.1 ± 0.2
0.60
FRS, %
5.0 ± 4.6
5.9 ± 5.0
4.9 ± 4.5
0.41
FMD, %
2.8 ± 3.8
1.7 ± 3.9
2.9 ± 3.7
0.22
mmIMT, mm
0.9 ± 0.2
1.1 ± 0.3
0.9 ± 0.2
0.047
Carotid plaque, n (%)
85 (57)
12 (71)
73 (55)
0.22
ABI
1.1 ± 0.1
1.0 ± 0.2
1.1 ± 0.1
0.080
baPWV, cm/s
1752 ± 384
1897 ± 373
1732 ± 383
0.20
CACS 148 ± 353 374 ± 341 120 ± 346 0.011

Abbreviations: ABI = ankle brachial index; ACEI = angiotensin converting enzyme inhibitor; ARB = angiotensin receptor blocker; baPWV = brachial-ankle pulse wave velocity; BMI = body mass index; CACS = coronary artery calcium score; CVD = cardiovascular disease; DM = diabetes mellitus; FMD = flow mediated dilatation; FRS = Framingham Risk Score; GFR = glomerular filtration rate; HbA1c = haemoglobin A1c; HDL = high-density lipoprotein cholesterol; LDL-C = low-density lipoprotein cholesterol; mmIMT = mean maximum intima-media thickness; WHR = waist-hip circumference ratio.


[TableWrap ID: T2] Table 2 

Pearson correlation coefficients between FRS and vascular assessment parameters


  FMD mmIMT ABI baPWV CACS
mmIMT
−0.07
 
 
 
 
ABI
0.02
−0.42**
 
 
 
baPWV
0.10
0.36**
−0.22
 
 
CACS
0.03
0.35**
−0.29*
0.49**
 
FRS −0.06 0.31** −0.17 0.34** 0.33**

Abbreviations as in Table 1.

*P < 0.05, **P < 0.01.


[TableWrap ID: T3] Table 3 

Prognostic values of FRS and vascular assessments according to specified cut-off values


Markers AUC (SE) Cut-off values Sensitivity, % (95%CI) Specificity, % (95 % CI) PPV, % NPV, %
FRS
0.59 ± 0.07
>2.56 %
82.4 (56.6-96.2)
47.8 (39.1-56.6)
16.7
95.5
FMD
0.59 ± 0.08
≤1.12 %
52.9 (27.8-77.0)
72.4 (64.0-79.8)
19.6
92.4
mmIMT
0.67 ± 0.07*
>1.07 mm
41.2 (18.4-67.1)
85.7 (78.6-91.2)
26.9
91.9
Carotid plaque
0.58 ± 0.06
-
70.6 (44.0-89.7)
45.11 (36.5-54.0)
14.1
92.3
ABI
0.64 ± 0.10
≤0.98
33.3 (9.9-65.1)
95.9 (88.5-99.1)
57.1
89.7
baPWV
0.63 ± 0.09
>1467 cm/s
100.0 (69.2-100.0)
26.4 (16.7-38.1)
15.9
100
CACS 0.81 ± 0.06** >40 92.9 (66.1-99.8) 67.3 (57.8-75.8) 26.0 98.7

Abbreviations as in Table 1 and AUC = area under curve; SE = standard error; CI = confidence interval; PPV = positive predictive value; NPV = negative predictive value*P < 0.05, **P < 0.01.


[TableWrap ID: T4] Table 4 

Multivariate Cox regression for atherosclerotic events in relation to vascular markers and risk factors


Risk variable
mmIMT
ABI
CACS
  HR (95 % CI) P-value HR (95 % CI) P-value HR (95 % CI) P-value
mmIMT > 1.07 mm
2.76 (0.90-8.46)
0.077
-
-
-
-
ABI ≤ 0.98
-
-
7.17 (1.63-31.52)
0.009
-
-
CACS > 40
-
-
-
-
27.11 (3.36-218.81)
0.002
Age
1.05 (1.00-1.11)
0.079
1.03 (0.97-1.09)
0.33
1.01 (0.95-1.08)
0.70
Males
2.32 (0.79-6.78)
0.12
2.43 (0.81-7.25)
0.11
2.17 (0.64-7.41)
0.22
BMI
0.91 (0.67-1.24)
0.56
0.85 (0.63-1.15)
0.29
0.81 (0.58-1.12)
0.20
WHR
1.00 (0.89-1.12)
0.99
1.02 (0.91-1.14)
0.73
1.05 (0.93-1.19)
0.41
Hypertension 0.55 (0.20-1.51) 0.24 0.71 (0.25-2.00) 0.52 0.53 (0.18-1.60) 0.26

Abbreviations as in Tables 1, 2, 3.


[TableWrap ID: T5] Table 5 

Comparison of the AUC of FRS alone and in combination with vascular assessment markers for atherosclerotic events


  AUC (SE) P-Value
FRS
0.59 ± 0.07
-
FRS + FMD
0.62 ± 0.07
0.66
FRS + mmIMT
0.67 ± 0.07
0.34
FRS + carotid plaque
0.61 ± 0.07
0.77
FRS + ABI
0.67 ± 0.10
0.29
FRS + baPWV
0.66 ± 0.09
0.30
FRS + CACS 0.77 ± 0.06 0.013

Abbreviations as in Tables 1, 2, 3.



Article Categories:
  • Original Investigation

Keywords: Vascular markers of atherosclerosis, Type 2 diabetes mellitus.

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