Paediatric Obesity and Cardiovascular Dysfunction
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|ClinicalTrials.gov Identifier: NCT03169257|
Recruitment Status : Active, not recruiting
First Posted : May 30, 2017
Last Update Posted : November 28, 2018
|First Submitted Date ICMJE||May 24, 2017|
|First Posted Date ICMJE||May 30, 2017|
|Last Update Posted Date||November 28, 2018|
|Actual Study Start Date ICMJE||January 15, 2015|
|Actual Primary Completion Date||February 8, 2017 (Final data collection date for primary outcome measure)|
|Current Primary Outcome Measures ICMJE
||Early cardiovascular abnormalities in OB patients compared with NW subjects [ Time Frame: Baseline: at study entry ]
We performed transthoracic echocardiogram to all subjects. Measurements of left ventricle (LV), left atrium diameter (LAD), LA and LV volumes, LV systolic and diastolic function, LV mass and relative wall thickness were obtained and compared between OB and matched NW subjects. A vascular assessment was also performed which included carotid artery intima-media thickness (CIMT), abdominal aortic strain and stiffness and brachial artery flow-mediated dilation (FMD). All these measurements were compared between OB and NW subjects. A sample of 15 individuals has been estimated to be sufficient to demonstrate a difference of 10% in LV diameter with a standard deviation (SD) of 0.44 cm with 90% power and a significance level of 95% in the Student t-test between OB and NW according to published data.
|Original Primary Outcome Measures ICMJE||Same as current|
|Change History||Complete list of historical versions of study NCT03169257 on ClinicalTrials.gov Archive Site|
|Current Secondary Outcome Measures ICMJE
|Original Secondary Outcome Measures ICMJE||Same as current|
|Current Other Pre-specified Outcome Measures||Not Provided|
|Original Other Pre-specified Outcome Measures||Not Provided|
|Brief Title ICMJE||Paediatric Obesity and Cardiovascular Dysfunction|
|Official Title ICMJE||Paediatric Obesity and Cardiovascular Dysfunction: Searching for Early Markers of Damage|
Background Childhood obesity has been related to an impaired cardiovascular structure and function. Aims of this study will be to evaluate early cardiovascular abnormalities in a large population of obese children and adolescents compared with a normal weight counterpart, to investigate the potential association with insulin resistance (IR), serum uric acid (sUA), metabolic syndrome (MetS), plasmatic markers of inflammation and oxidative stress and adipokines, to evaluate changes in cardiovascular dysfunction after 6 and 12 months of a behavioral treatment (isocaloric Mediterranean balanced diet plus daily aerobic physical activity).
Subjects and methods This was a single-center case-control study. Eighty obese (OB) subjects (6-16 years) and 20 normal weight (NW) matched controls were consecutively recruited. In the whole population we will perform an anthropometric and a cardiovascular assessment. OB patients will also undergo an OGTT and biochemical evaluations. In the OB group, all these evaluations will be performed at baseline and after 6 (T6) and 12 months (T12) of diet plus aerobic training.
Background Childhood obesity causes a wide range of severe complications, increasing the risk of premature morbidity and mortality and raising public-health concerns. In addition, obese children are more prone to become obese adults, with higher risk of cardiovascular diseases (CVD). A cluster of CVD risk factors has been identified in children as young as 5 years of age. Furthermore, among adolescents and young adults, the presence of CVD risk factors correlates with asymptomatic coronary atherosclerosis. Childhood obesity has been related to an impaired cardiac structure and function.
Atherogenesis and arterial wall damage begin during childhood and, there is evolving evidence that clinical indicators of atherosclerosis such as carotid artery intima-media thickness (CIMT), arterial stiffness, and endothelial function are altered in obese children. In addition, little is known on the potential association between early cardiovascular alterations and metabolic abnormalities in obese children. Metabolic syndrome (MetS) is a cluster of features, which includes dyslipidemia, hypertension, and visceral obesity, conferring with a higher risk of CVD and type 2 diabetes. Few studies investigated the association of MetS with cardiovascular changes during childhood. Hyperuricemia has been recognized as a risk factor for CVD in adults with a negative impact on longevity. However, data in pediatric age are still lacking and the association between hyperuricaemia and cardiovascular abnormalities in obese children is still unknown. Furthermore, obesity is a state of chronic low-level inflammation and increased oxidative stress. Oxidative stress plays an important role in the pathogenesis of cardiovascular alterations by either triggering or exacerbating the biochemical processes accompanying endothelial dysfunction.
Moreover, adipose tissue acts as a secretory gland, releasing hormones and adipokines with pro- or anti-inflammatory activity. Clinical studies of obese adults have observed an association between plasma levels of adipokines and markers of inflammation and/or oxidative stress. Among various adipokines, adiponectin seems to play an important role. Indeed, in contrast to other adipokines which are up-regulated in obesity, secretion of adiponectin is markedly reduced in obese subjects. Second, adiponectin seems to exert mainly positive activities on metabolism, vascular tone and inflammatory reaction. Consequently, in contrast to other adipokines, which circulate in excess in obese subjects and exert unbeneficial effects when chronically elevated, deficiency rather than excess of adiponectin is implicated in obesity-associated complications. Finally, serum concentration of adiponectin is very high in comparison to other hormones and cytokines, which suggests that apart from binding to specific high-affinity receptors, this protein may also have some less specific low affinity targets. Adiponectin has been associated with endothelial improvement and vascular protection through the activation of an endothelial isoform of nitric oxide (eNOS)-related signalling and with anti-inflammatory properties and antiatherogenic effects. Thus, an impaired production of adipokines may be a key mechanism linking obesity with inflammation and oxidative stress. The understanding of these complex mechanisms and the identification of possible early markers of cardiovascular damage are therefore necessary in order to establish preventive and therapeutic measures in childhood and to decrease cardiovascular morbidity and mortality in adulthood.
Subjects and methods This study is a single-centre longitudinal study. Subjects were recruited at Division of Pediatrics, Department of Health Sciences, University of Piedmont Orientale, Novara (Italy). The study protocol was in accordance with the ethical guidelines of the Declaration of Helsinki and has been approved by the local Ethical Committee. Informed written consent was obtained from all subjects and their parents before study. The investigators consecutively enrolled 80 Caucasian obese (OB) children and adolescents, aged 6 to 16 years, and 20 normal weight, age and sex matched controls (NW). NW patients were evaluated only at baseline while OB subjects will be evaluated at baseline and after 6 (T6) and 12 months (T12) of an isocaloric Mediterranean balanced diet plus aerobic training.
Assessment in both groups (OB and NW)
Echocardiographic assessment Transthoracic echocardiogram using a Vivid 7 Pro ultrasound scanner (General Electric Healthcare, USA) will be performed by a sonographer and the images will be reviewed by an expert pediatric cardiologist, blinded to patients' clinical data. Measurements of left ventricle (LV end-diastolic diameter, LVEDD; LV end-systolic diameter, LVESD; interventricular septum at end diastole, IVSD; LV posterior wall at end diastole, LVPWD) and left atrium diameter (LAD) will be obtained according to established standards. The maximum LA volume will be calculated from apical 4- and 2-chamber zoomed views of the LA. LV end-diastolic and end-systolic volumes and the LV ejection fraction at rest will be computed from 2- and 4-chamber views, using a modified Simpson's biplane method. LV mass (LVM) will be derived from the Devereux formula and indexed to body surface area (left ventricular mass index [LVMI]). Relative wall thickness (RWT) will be calculated as the ratio (LVPWD x 2)/LVEDD. Using pulsed wave Doppler, mitral inflow velocities, peak early diastolic velocity (E), peak late diastolic velocity (A), E/A ratio, will be measured.
Vascular assessment Vascular measurements will be performed with a high-resolution ultrasonography (Esaote MyLab25TM Gold, Esaote, Italy) using a 8-megaHertz (mHz) linear transducer and a 5 mHz convex transducer for the abdominal aorta, by an expert sonographer and images will be then reviewed offline by an expert vascular surgeon blinded to patients clinical status. Ultrasonography of the right and left carotid arteries will be performed in the supine position with the head turned 45° away from the side being imaged. CIMT will be defined as the mean distance from the leading edge of the lumen-intima interface to the leading edge of the media-adventitia interface of the far wall, approximately 10 mm distal to the common carotid artery. CIMT will be calculated by the average of three measurements performed at 0.2 mm intervals.
The abdominal aortic diameter will be measured at maximum systolic expansion (Ds) and minimum diastolic expansion (Dd) at the mid-point between renal arteries origin and iliac carrefour. Aortic strain (S) will be calculated using the formula (S = (Ds-Dd)/Dd). Pressure strain elastic modulus (Ep) will be calculated from S using the formula (Ep=(Ps-Pd)/S; Ps= aortic systolic pressure; Pd= aortic diastolic pressure). Pressure strain normalized by diastolic pressure (Ep*), will be calculated using the formula (Ep* = Ep/Pd). While S is the mean strain of the aortic wall, Ep and Ep* are the mean stiffness of the aorta. To measure brachial artery flow-mediated dilation (FMD), a pneumatic cuff will be placed on the right forearm, 2 cm above the antecubital fossa and inflated to a suprasystolic level (300 mmHg) for 5 minutes. A continuous Doppler velocity assessment will be obtained simultaneously, and data will be collected using the lowest insonation angle (between 30° and 60°). Brachial artery diameters, peak systolic velocity (PSV) and end diastolic velocity (EDV) will be measured immediately after and 2 minutes after the cuff release and then compared to basal values taken immediately before the inflation. The maximum diameter recorded following reactive hyperemia will be reported as a percentage change of resting diameter (FMD = peak diameter - baseline diameter/baseline diameter).
Anthropometric variables Height will be measured to the nearest 0.1 cm using a Harpenden stadiometer, and body weight to the nearest 0.1 kg using a manual weighing scale. Body mass index (BMI) will be calculated as body weight divided by squared height (kg/m2). Waist circumference (WC) will be measured at the high point of the iliac crest around the abdomen and was recorded to the nearest 0.1 cm. Hip circumference will be measured over the widest part of the gluteal region. Pubertal stages will be determined by physical examination, using the criteria of Marshall and Tanner. Systolic (SBP) and diastolic (DBP) blood pressure will be measured three times at 2-minute intervals using a standard mercury sphygmomanometer with an appropriate cuff size. Mean values will be used for the analysis.
Assessment only in the OB group
Biochemical variables After a 12-h overnight fast, blood samples will be taken for measurement of: glucose (mg/dL), insulin (μUI/mL), total cholesterol (mg/dL), high density lipoprotein-cholesterol (HDL-c, mg/dL), triglycerides (mg/dL), sUA (mg/dL), using standardized methods in the Hospital's Laboratory. Low density lipoprotein-cholesterol (LDL-c) will be calculated by the Friedwald formula. sUA (mg/dL) will be measured by Fossati method reaction using uricase with a Trinder-like endpoint.
OB subjects will also undergo an oral glucose tolerance test (1.75 g of glucose solution per kg, maximum 75 g) and samples will be drawn for the determination of glucose and insulin every 30 min. Insulin-resistance at fasting will be calculated using the formula of homeostasis model assessment (HOMA)-IR. Insulin sensitivity at fasting and during OGTT will be calculated as the formula of the Quantitative Insulin-Sensitivity Check Index (QUICKI) and Matsuda index (ISI).
Determination of interleukins (IL), tumor necrosis factor (TNF)α, plasminogen activator inhibitor-1 (PAI1), adiponectin and plasmatic markers of oxidative stress IL-8, IL-10, IL-6, TNFα, PAI-1, adiponectin, 3-nitrotyrosine, malondialdehyde (MDA), reactive oxygen species (ROS) generation, myeloperoxidase (MPO), reduced glutathione (GSH) and superoxide dismutase (SOD) will be measured using specific kits. NO will be quantified from blood samples by using the Griess reagent.
Mitochondria morphology and function Mitochondria will be isolated from monocytes. Ultrastructural analyses of mitochondria (through transmission electron microscope ZEISS 109) will be performed to assess morphologic mitochondrial changes (mitochondrial swelling, decrease in matrix density, possible difference in the sub-plasmalemmal and intrafibrillar sub-fraction of mitochondria, fission-fusion dynamic mitochondrial propriety, mitophagy). Moreover, mitochondria will be used for in vitro assays of mitochondrial oxygen consumption, complex I activity (NAD+/NADH), transmembrane potential and mitochondrial dynamic proteins expression (fusion and fission ratio through mitofusin 1 and 2 Western blot analysis).
Time course of measurements in the OB group All the evaluations previously described will be performed at baseline and after 6 (T6) and 12 months (T12) of an isocaloric Mediterranean balanced diet plus aerobic training.
Nutritional analysis and interventions A well-trained and experienced clinical paediatric endocrinologist will assess food consumption in all subjects and will administer an isocaloric Mediterranean balanced diet in OB children. To assess food consumption, foods will be divided according to the classic basic food groups by the Italian Institute of Research on Food and Nutrition. Food frequencies questionnaires, validated for a wide range of ages, will be also completed by parents. The nutritional counselling will be performed at baseline and after 6 and 12 months, according to Italian LARN (Livelli di Assunzione di Riferimento di Nutrienti) Guidelines and the Italian food pyramid.
Moreover, obese subjects will undergo an exercise training regimen. Exercise will be conducted daily and will consist of 60 minutes of aerobic physical activity. Parents will record every day, on a specific questionnaire, the training performed.
|Study Type ICMJE||Interventional|
|Study Phase ICMJE||Not Applicable|
|Study Design ICMJE||Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Intervention Model Description:
Only one group, the obese children group (OB) will be followed for one year. At baseline they received a behavioral intervention which comprises a Mediterranean balanced diet plus daily aerobic training.Masking: Single (Outcomes Assessor)
A sonographer will perform cardiovascular imaging. Images will be reviewed by an expert pediatric cardiologist and an expert vascular surgeon blinded to patients' clinical data.Primary Purpose: Treatment
|Intervention ICMJE||Behavioral: diet plus physical activity
OB subjects will undergo an isocaloric Mediterranen balanced diet plus a daily aerobic training for at least 60 minutes. All the evaluations will be performed at baseline and after 6 and 12 months of this behavioral therapy. To assess food consumption, foods will be divided according to the classic basic food groups by the Italian Institute of Research on Food and Nutrition. Food frequencies questionnaires, validated for a wide range of ages, will be also completed by parents. Physical activity will be recorded by parents daily on a specific questionnaire.
|Study Arms ICMJE||
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
|Recruitment Status ICMJE||Active, not recruiting|
|Actual Enrollment ICMJE
|Original Actual Enrollment ICMJE||Same as current|
|Estimated Study Completion Date ICMJE||December 2019|
|Actual Primary Completion Date||February 8, 2017 (Final data collection date for primary outcome measure)|
|Eligibility Criteria ICMJE||
|Ages ICMJE||6 Years to 16 Years (Child)|
|Accepts Healthy Volunteers ICMJE||Yes|
|Contacts ICMJE||Contact information is only displayed when the study is recruiting subjects|
|Listed Location Countries ICMJE||Not Provided|
|Removed Location Countries|
|NCT Number ICMJE||NCT03169257|
|Other Study ID Numbers ICMJE||CE 95/12|
|Has Data Monitoring Committee||Not Provided|
|U.S. FDA-regulated Product||
|IPD Sharing Statement ICMJE||
|Responsible Party||Flavia Prodam, Azienda Ospedaliero Universitaria Maggiore della Carita|
|Study Sponsor ICMJE||Azienda Ospedaliero Universitaria Maggiore della Carita|
|Collaborators ICMJE||Not Provided|
|PRS Account||Azienda Ospedaliero Universitaria Maggiore della Carita|
|Verification Date||November 2018|
ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP