Primary Prevention Clinical Trial
Official title:
Subclinical Atherosclerosis: Biomarkers of Early Disease
Subclinical atherosclerosis is the atherosclerotic process identified before clinical symptoms and thus it can be a useful marker of future cardiovascular events. It can be evaluated by many methods. This study included the diagnosis of subclincal atherosclerosis by four different methods: coronary calcium score, carotid doppler ultrasound to quantify intima media thickness and carotid plaques, exercise stress test and ankle brachial index. Clinical data, anthropometric measures (body mass index, abdominal circumference), markers of inflammation (high sensitive - C reactive protein, TNF alfa and Lipoprotein Associated Phospholipase A2), fat tissue function (leptin, resistin and adiponectin), glucose metabolism (fasting plasma glucose, glycated hemoglobin and insulin) and genetics markers of atherosclerotic process were evaluated as biomarkers of subclinical atherosclerosis in a uneventful population.
This study cross-sectionally evaluated consecutive patients at the outpatient clinic of
Dyslipidemia and of Hypertension and Nephrology Medical Sections of Dante Pazzanese
Institute of Cardiology, a cardiologic tertiary hospital in São Paulo - Brazil. After they
fulfilled inclusion criteria and signed an informed consent, a brief medical history and
anthropometric data (abdominal circumference, height and weight for body mass index
calculation) were collected. Within of a month after inclusion, all patients underwent blood
sample collection for dosing fast plasma glucose and insulin and 2 hours after 75g of
dextrose test glucose and insulin, fast serum triglycerides, total cholesterol, HDL
cholesterol, creatinine, high sensitive c-reactive protein (hs-CRP), HbA1c, thyroid
stimulating hormone (TSH), free thyroxin (fT4), creatine kinase, adiponectin, resistin,
leptin, tumor necrosis factor alpha (TNF-α), lipoprotein associated phospholipase A2
(Lp-PLA2). Blood sample was also stored for DNA (rs2383206, rs10757274, rs10757278,
rs1051931, rs16874954 and rs1799724) and RNA PLA2G7 (2-ΔCT), TNF-α (2-ΔCT), LEP (2-ΔCT),
LEPR (2-ΔCT) extraction and analyses.
Subclinical atherosclerosis was evaluated by four methods: carotid doppler ultrasound,
cardiac computed tomography, exercise stress test and ankle-brachial index (ABI). All above
tests were performed at the same day.
Carotid Doppler ultrasound was performed by using high-resolution Vivid 7 ultrasound (GE,
USA) and high-frequency linear transducer type 9 MHz with automated measurement. Carotid
Intima media thickness (cIMT) was evaluated 1 cm distal of the posterior wall of the left
and right common carotid arteries and the presence of atherosclerotic plaques in common,
internal and external carotid arteries was assessed. Carotid plaque was defined by the
presence of focal wall thickening at least 50% greater than that of the surrounding vessel
wall, or as a focal region with IMT greater than 1.5 mm, which protrude into the lumen and
that is distinct from the adjacent boundary.
Cardiac Computed Tomography was performed to determine coronary calcium score (CAC) and
calcium distribution. Hepatic density was performed to evaluate the presence of hepatic
steatosis with Aquilion apparatus (Toshiba Medical, Tochigi, Japan) with 64 rows of
detectors. The acquisition of tomographic data was represented by images of average
thickness (3 mm) and low intensity (50 milliamps, 120 kV) and coupled to the
electrocardiogram. Calcium score was considered present when its density in the coronary
artery was above 130 Housfield units (HU) for at least 3 continuous pixels (> 1 mm2) of the
same coronary artery. Calcium score comprised the sum of individual scores of the left and
right coronary arteries.
Exercise stress test was performed following under one of following protocols: Bruce,
modified Bruce or Ellestad treadmill. The test was interrupted if maximum heart rate was
reached or if clinical symptoms installed, including exhaustion. The exam was considered
positive when there were: negative horizontal/descending deflection of ST segment measured
at the J point ≥1 mm, pain suggestive of coronary artery disease, complex and sustained
ventricular arrhythmias, plateau or drop in systolic blood pressure in effort and/or
functional capacity lower than 5 METS.
ABI tests were performed with the patient in the supine position after resting for five
minutes. Palpation of bilateral arterial pulses of pedial, posterior tibial, popliteal and
brachial were performed. Measures of systolic pressures were made by a 5 MHz
ultrasonography. The relationship between systolic and diastolic pressures of upper and
lower limbs was used for calculating the ABI. The test was considered positive when at least
one of the relationships was less than 0.9.
Personal and clinical characteristics of the patients will be described according to group
using absolute and relative frequencies for qualitative characteristics and summary measures
(mean, standard deviation, median, minimum and maximum) for quantitative characteristics.
Distribution of the variables will be tested using Kolmogorov-Smirnov test. Comparative
analyses for non-normal data will be performed using Kruskal-Wallis test and expressed as
median (interquartile range). Normal data will be evaluated using analyses of variance
(ANOVA) and expressed as mean ± standard deviation. To evaluate associations between
categorical variables chi-square test and Fisher's Exact test will be used. Analysis of
covariance (ANCOVA) adjusted for age and sex will be used to compare clinical and
biochemical measures between groups (glucose, insulin, Homa-R, hs-PCR, HDL-c, triglycerides,
LDL-c, HbA1c, TNF-α, leptin, 2 hours glucose and regular use of medication). Ordinal
logistic regression will be used to evaluate subclinical atherosclerosis. A two-tailed P
value < 0.05 will be considered statistically significant.
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Observational Model: Cohort, Time Perspective: Cross-Sectional
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