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	<front>
		<journal-meta>
			<journal-id journal-id-type="publisher-id">rfmun</journal-id>
			<journal-title-group>
				<journal-title>Revista de la Facultad de Medicina</journal-title>
				<abbrev-journal-title abbrev-type="publisher">rev.fac.med.</abbrev-journal-title>
			</journal-title-group>
			<issn pub-type="ppub">0120-0011</issn>
			<publisher>
				<publisher-name>Universidad Nacional de Colombia</publisher-name>
			</publisher>
		</journal-meta>
		<article-meta>
			<article-id pub-id-type="doi">10.15446/revfacmed.v68n1.69979</article-id>
			<article-categories>
				<subj-group subj-group-type="heading">
					<subject>Original papers</subject>
				</subj-group>
			</article-categories>
			<title-group>
				<article-title>Cardiovascular disease risk markers in children under 10 years of age and their relationship with serum concentrations of IGF-1, IGFBP-1, IGFBP-2 and IGFBP-3</article-title>
				<trans-title-group xml:lang="es">
					<trans-title>Marcadores de riesgo cardiovascular en niños menores de 10 años y su relación con niveles séricos de IGF-1, IGFBP-1, IG-FBP-2 e IGFBP-3</trans-title>
				</trans-title-group>
			</title-group>
			<contrib-group>
				<contrib contrib-type="author">
					<name>
						<surname>Vera</surname>
						<given-names>Sorany</given-names>
					</name>
					<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
					<xref ref-type="corresp" rid="c1">*</xref>
				</contrib>
				<contrib contrib-type="author">
					<name>
						<surname>Figueroa</surname>
						<given-names>Tatiana</given-names>
					</name>
					<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
				</contrib>
				<contrib contrib-type="author">
					<name>
						<surname>Aranzalez</surname>
						<given-names>Luz Helena</given-names>
					</name>
					<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
				</contrib>
				<contrib contrib-type="author">
					<name>
						<surname>Mockus</surname>
						<given-names>Ismena</given-names>
					</name>
					<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
				</contrib>
				<aff id="aff1">
					<label>1</label>
					<institution content-type="original"> Universidad Nacional de Colombia - Bogotá Campus - Faculty of Medicine - Division of Lipids and Diabetes - Bogotá D.C. -Colombia.</institution>
					<institution content-type="normalized">Universidad Nacional de Colombia</institution>
					<institution content-type="orgname">Universidad Nacional de Colombia</institution>
					<addr-line>
						<city>Bogotá D.C</city>
					</addr-line>
					<country country="CO">Colombia</country>
				</aff>
			</contrib-group>
			<author-notes>
				<corresp id="c1">
					<label><sup>*</sup>Corresponding author:</label> Sorany Vera Barrios. División de Lípidos y Diabetes, Facultad de Medicina, Universidad Nacional de Colombia. Carrera 30 No. 45-03, building: 471, office: 418. Telephone number: +57 1 3165000, ext.: 15054. Bogotá D.C. Colombia. Email: <email>sverab@unal.edu.co</email>.</corresp>
			</author-notes>
			<pub-date pub-type="collection">
				<season>Jan-Mar</season>
				<year>2020</year>
			</pub-date>
			<volume>68</volume>
			<issue>1</issue>
			<fpage>51</fpage>
			<lpage>58</lpage>
			<history>
				<date date-type="received">
					<day>24</day>
					<month>01</month>
					<year>2018</year>
				</date>
				<date date-type="accepted">
					<day>07</day>
					<month>05</month>
					<year>2018</year>
				</date>
			</history>
			<permissions>
				<license license-type="open-access" xlink:href="https://creativecommons.org/licenses/by/4.0" xml:lang="en">
					<license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution License</license-p>
				</license>
			</permissions>
			<abstract>
				<title><italic>Abstract</italic></title>
				<sec>
					<title>Introduction: </title>
					<p>Any type of nutritional imbalance experienced during childhood will affect the health of an individual, both in their childhood and their adulthood. Several studies have proved that there is an association between cardiovascular disease (CVD) risk and endocrine and lipid markers at early stages of life.</p>
				</sec>
				<sec>
					<title>Objective: </title>
					<p>To establish the relationship between nutritional status (IGF-1 and serum levels of its binding proteins IGFBP-1, IGFBP-2 and IGFBP-3), and CVD risk markers in students aged 7 to 9 years. </p>
				</sec>
				<sec>
					<title>Materials and methods: </title>
					<p>Cross-sectional observational study conducted in 84 children attending two schools from Bogotá D.C. and Soacha, Colombia, to identify the relationship between possible variations in CVD risk markers and nutritional status. Sexual development stage, lipid profile, anthropometric data, blood sugar levels and IGF-1 and IGFBP serum levels of all participants were measured. Statistical analysis was conducted using the Pearson's correlation coefficient, the analysis of variance (ANOVA), and the Kruskall-Wallis, Games-Howell and Dunnett's tests. The confidence interval and statistical significance were 95% and p&lt;0.05, respectively.</p>
				</sec>
				<sec>
					<title>Results: </title>
					<p>IGFBP-1 and IGFBP-2 levels proportionally decreased as weight increased. An inverse correlation between both proteins and triglyceride levels was found, as well as a direct correlation with HDL cholesterol levels.</p>
				</sec>
				<sec>
					<title>Conclusions: </title>
					<p>Alterations in CVD risk markers can be identified during childhood. If said alterations are timely detected, it is possible to adopt preventive and therapeutic actions such as the promotion of public policies aimed at preventing childhood overweight and obesity, which in turn will reduce the risk of developing cardiovascular disease in adulthood.</p>
				</sec>
			</abstract>
			<trans-abstract xml:lang="es">
				<title><italic>Resumen</italic></title>
				<sec>
					<title>Introducción. </title>
					<p>Los desequilibrios nutricionales en la infancia afectan la salud tanto en la niñez como en la adultez. Estudios previos demuestran la asociación de marcadores endocrinos y lipídicos con riesgo cardiovascular (RCV) desde edades tempranas.</p>
				</sec>
				<sec>
					<title>Objetivo. </title>
					<p>Establecer la relación entre estado nutricional (niveles séricos de IGF-1 y sus proteínas enlazantes IGFBP-1, IGFBP-2 e IGFBP-3) y marcadores de RCV en estudiantes de 7 a 9 años. </p>
				</sec>
				<sec>
					<title>Materiales y métodos. </title>
					<p>Estudio observacional comparativo transversal realizado en 84 niños de 2 colegios de Bogotá D.C. y Soacha, Colombia, para identificar la relación entre posibles variaciones de marcadores de RCV y estado nutricional. Se midieron los niveles de glucemia y niveles séricos de IGF-1 e IGFBP, el nivel de desarrollo sexual, el perfil lipídico y los valores antropométricos. Para el análisis estadístico se utilizaron el coeficiente de correlación de Pearson, un análisis de varianza (ANOVA) y las pruebas de Kruskal Wallis, Games-Howell y Dunnett. El intervalo de confianza fue del 95% y la significancia estadística, de p&lt;0.05.</p>
				</sec>
				<sec>
					<title>Resultados. </title>
					<p>La reducción en los niveles de IGFB-1 e IGFBP-2 fue directamente proporcional al aumento de peso. Por otra parte, se observó una correlación inversa entre ambas proteínas y concentraciones de triglicéridos, y una directa con los niveles colesterol HDL.</p>
				</sec>
				<sec>
					<title>Conclusiones. </title>
					<p>Las alteraciones de marcadores de RCV se pueden identificar en la infancia. Si estas son detectadas a tiempo es posible adoptar medidas preventivas y terapéuticas como la promoción de políticas públicas dirigidas prevenir el sobrepeso infantil, lo que a su vez reducirá el riesgo de padecer enfermedades cardiovasculares en edades adultas.</p>
				</sec>
			</trans-abstract>
			<kwd-group xml:lang="en">
				<title>Keywords:</title>
				<kwd>Nutritional Status</kwd>
				<kwd>Insulin-Like Growth Factor Binding Protein 1</kwd>
				<kwd>Insulin-Like Growth Factor Binding Protein 2</kwd>
				<kwd>Insulin-Like Growth Factor Binding Protein 3</kwd>
				<kwd>Pediatric Obesity</kwd>
				<kwd>Dyslipidemias (MeSH)</kwd>
			</kwd-group>
			<kwd-group xml:lang="es">
				<title>Palabras clave:</title>
				<kwd>Estado nutricional</kwd>
				<kwd>Proteína 1 de unión a factor de crecimiento similar a la insulina</kwd>
				<kwd>Proteína 2 de unión a factor de crecimiento similar a la insulina</kwd>
				<kwd>Proteína 3 de unión a factor de crecimiento similar a la insulina</kwd>
				<kwd>Obesidad pediátrica</kwd>
				<kwd>Dislipidemias (DeCS)</kwd>
			</kwd-group>
			<counts>
				<fig-count count="3"/>
				<table-count count="3"/>
				<equation-count count="0"/>
				<ref-count count="51"/>
				<page-count count="8"/>
			</counts>
		</article-meta>
	</front>
	<body>
		<sec sec-type="intro">
			<title>Introduction</title>
			<p>Childhood obesity and overweight are highly prevalent in Colombia. Currently, 1 out of every 6 children between the ages of 5 and 17 has one of these conditions,<xref ref-type="bibr" rid="B1"><sup>1</sup></xref> situation that Fernández-Juan <italic>et al.</italic><xref ref-type="bibr" rid="B2"><sup>2</sup></xref> have reported on schoolchildren from Bogotá. Worldwide, several studies have discussed the relationship between childhood and adult lipid metabolism, and have reported that serum levels of total cholesterol, lipoproteins and body mass index (BMI) in children are predictors of cardiovascular disease (CVD) risk in adulthood.<xref ref-type="bibr" rid="B3"><sup>3</sup></xref><sup>-</sup><xref ref-type="bibr" rid="B5"><sup>5</sup></xref>
			</p>
			<p>Delgadillo-Guerra &amp; Romero-Hernández<xref ref-type="bibr" rid="B6"><sup>6</sup></xref> report that alterations in glucose and insulin metabolism associated with dyslipidemia and changes in blood pressure are risk factors for the development of cardiovascular disease (CVD) and type 2 diabetes, conditions that can occur at an early age and persist into adulthood. In addition, insulin resistance (IR) and hyperinsulinemia are risk factors for metabolic syndrome (MS) in puberty. <xref ref-type="bibr" rid="B7"><sup>7</sup></xref><sup>,</sup><xref ref-type="bibr" rid="B8"><sup>8</sup></xref>
			</p>
			<p>Considering the anabolic and mitogenic effects of insulin-like growth factor 1 (IGF-1) and its important role in development and growth, in recent years an association has been reported between this factor, as well as 3 of its binding proteins (IGFBP-1, IGFBP-2 and IGFBP-3), and the development of CVD. <xref ref-type="bibr" rid="B9"><sup>9</sup></xref><sup>,</sup><xref ref-type="bibr" rid="B10"><sup>10</sup></xref> It has also been suggested that the IGF/IGFBP axis may influence atherogenesis through the stimulation of vascular smooth muscle cells and foam cells proliferation, possibly by acting on lipid levels in blood and insulin sensitivity. <xref ref-type="bibr" rid="B11"><sup>11</sup></xref>
			</p>
			<p>IGF-1 is an effector hormone that is synthesized in multiple organs -especially the liver-, is essential for growth, and plays an important role in mediating growth hormone (GH) function; <xref ref-type="bibr" rid="B9"><sup>9</sup></xref><sup>,</sup><xref ref-type="bibr" rid="B12"><sup>12</sup></xref> it is also homologous to insulin and is capable of inhibiting proteolysis and stimulating glucose uptake, glycogen synthesis and lipogenesis. <xref ref-type="bibr" rid="B13"><sup>13</sup></xref><sup>,</sup><xref ref-type="bibr" rid="B14"><sup>14</sup></xref> In this regard, Mohanraj <italic>et al.</italic><xref ref-type="bibr" rid="B15"><sup>15</sup></xref> describe the relationship between obesity and circulating levels of IGFBP, while Akanji <italic>et al.</italic><xref ref-type="bibr" rid="B11"><sup>11</sup></xref> state that alterations in the IGF/IGFBP axis may increase the risk of CVD and that increased IGF-I is associated with premature atherosclerosis and increased risk of CVD.</p>
			<p>IGFBP-1 is one of six binding proteins that regulates IGF-1 bioactivity. Its production in the liver is regulated by insulin. <xref ref-type="bibr" rid="B16"><sup>16</sup></xref> Its plasma concentrations have been associated with metabolic, nutritional and anthropometric factors, <xref ref-type="bibr" rid="B17"><sup>17</sup></xref> and its levels are inversely proportional to adiposity and IR. <xref ref-type="bibr" rid="B18"><sup>18</sup></xref> Circulating concentrations of this protein are high during fasting, malnutrition and both types of diabetes, and are low in overweight cases. <xref ref-type="bibr" rid="B19"><sup>19</sup></xref><sup>,</sup><xref ref-type="bibr" rid="B20"><sup>20</sup></xref> There is also evidence that suggests that IGFBP-1 is a useful predictive marker of CVD risk given its relationship with BMI, circulating proinsulin levels, MS, <xref ref-type="bibr" rid="B21"><sup>21</sup></xref> IR<xref ref-type="bibr" rid="B11"><sup>11</sup></xref><sup>,</sup><xref ref-type="bibr" rid="B17"><sup>17</sup></xref><sup>,</sup><xref ref-type="bibr" rid="B22"><sup>22</sup></xref> and even fatty liver. <xref ref-type="bibr" rid="B9"><sup>9</sup></xref><sup>,</sup><xref ref-type="bibr" rid="B16"><sup>16</sup></xref>
			</p>
			<p>On the other hand, IGFBP-2 is a biomarker that allows identifying IR and high CVD risk in adults. It is the most common IGFBP expressed during childhood and the main IGFBP produced by adipocytes. Recent studies have shown an inverse correlation between the circulating levels of this protein and adiposity. A similar correlation between IR and adiposity has also been described. Determining the levels of IGFBP-2 is useful in order to deepen understanding of the correlation between nutrition, growth, obesity and CVD risk. <xref ref-type="bibr" rid="B23"><sup>23</sup></xref><sup>-</sup><xref ref-type="bibr" rid="B25"><sup>25</sup></xref>
			</p>
			<p>Regarding IGFBP-3 -protein synthesized mainly by the liver-, its circulating levels have been associated with CVD, obesity and IR. It has also been proven that it acts as an anti-inflammatory factor capable of inhibiting the pathway of nuclear factor kappa-light-chain-enhancer of activated B cells (NF-kB).<xref ref-type="bibr" rid="B15"><sup>15</sup></xref>
			</p>
			<p>Mohanraj <italic>et al.</italic><xref ref-type="bibr" rid="B15"><sup>15</sup></xref> reported that proteolytic IGFBP-3 is positively correlated with adiposity parameters such as waist circumference (WC), BMI, fasting insulin and IR in overweight and obese population. Moreover, several studies have described an increase in IGF-1 and IGFBP-3 levels in overweight and obese adolescents. <xref ref-type="bibr" rid="B15"><sup>15</sup></xref><sup>,</sup><xref ref-type="bibr" rid="B19"><sup>19</sup></xref><sup>,</sup><xref ref-type="bibr" rid="B20"><sup>20</sup></xref> This protein appears to have an antiproliferative action in vascular smooth muscle cells, <xref ref-type="bibr" rid="B11"><sup>11</sup></xref> which inhibits the formation of atheromatous plaque.</p>
			<p>With all this in mind, the aim of this study was to establish the correlation between nutritional status -determined by anthropometry and serum levels of IGF-1 and its binding proteins (IGFBP-1, IGFBP-2 and IGFBP-3)- and CVD risk markers in students aged between 7 and 9 years enrolled in 2 schools.</p>
		</sec>
		<sec sec-type="materials|methods">
			<title>Materials and methods</title>
			<p>Comparative cross-sectional observational study conducted in 84 children between 7 and 9 years of age to identify the correlation between possible variations in CVD risk markers and nutritional status.</p>
			<p>This research was carried out during the second half of 2014 in a school located in Bogotá D.C. and another in Soacha, and was approved by the Ethics Committee of the Faculty of Medicine of the Universidad Nacional de Colombia by means of Minutes No. 75 of November 28, 2013. The study complied with all ethical aspects and followed the principles of the Declaration of Helsinki; <xref ref-type="bibr" rid="B26"><sup>26</sup></xref> it was also classified as a minimal risk research according to Resolution 8430 of 1993<xref ref-type="bibr" rid="B27"><sup>27</sup></xref> of the Colombian Ministry of Health. Both children and their guardians signed an informed consent</p>
			<p>A non-probabilistic sample for convenience was selected; students enrolled at the Instituto Educativo Distrital Llano Oriental (Bogotá D.C.) and the Liceo Integral Los Alisos (Soacha) schools were included. The selection criteria were children aged between 7 and 9 years and 11 months, with no disease that could affect the results (diabetes, systemic arterial hypertension, hypoglycemia, hyperglycemia, hypercholesterolemia and growth hormone alteration), and children who had used medications in the last month. All the children were at stage 1 on the Tanner scale (no apparent sign of sexual maturation).</p>
			<p>Weight was measured on a Tanita scale, with the participants barefoot and dressed in light clothing; height was determined using a dry stadiometer according to the recommendations of the World Health Organization's (WHO) growth pattern instructions for Colombia.<xref ref-type="bibr" rid="B28"><sup>28</sup></xref> BMI or Quetelet index was defined as weight/height expressed in kg/m<sup>2</sup>, and WC was measured in a horizontal plane halfway between the last right rib and the iliac crest using an inelastic fiberglass tape.</p>
			<p>Blood samples were taken from the antecubital vein by venepuncture after 12 hours of fasting and centrifuged at 3 500 rpm for 5 minutes. The sera obtained were stored at -20°C in order to measure blood glucose levels and lipid profile, and at -80°C for determining IGF-1 and its 3 binding proteins.</p>
			<p>Total cholesterol (total-c), triglycerides (TG), high-density cholesterol (HDL-c) and blood glucose were measured using spectrophotometric enzymatic techniques; low-density cholesterol (LDL-c) was calculated using the Friedewald equation and non-HDL cholesterol (non-HDL-c) was defined as the difference between total-c and HDL-c. Serum levels of IGF-1, IGBP-1, IGFBP-2 and IGBP-3 were determined by double-binding enzyme immunoassay (ELISA) according to the manufacturer's instructions (DIAsource). This process was performed with the DS2/DSX automated equipment.</p>
			<p>The WHO growth reference data for children and adolescents (2007) were used to interpret anthropometric variables as set forth in Resolution 2465 of 2016. <xref ref-type="bibr" rid="B28"><sup>28</sup></xref> Moreover, weight/height, height/age and WC/age indicators were established and five subgroups with a similar number of children were formed: 1) low height-for-age and risk of low height-for-age, 2) eutrophic, 3) adequate weight and high WC, 4) overweight and 5) obese. WC in childhood was classified according to the percentiles established by McDowell <italic>et al.</italic><xref ref-type="bibr" rid="B29"><sup>29</sup></xref> and the lipid profile fractions were classified, as indicated by Bamba, <xref ref-type="bibr" rid="B30"><sup>30</sup></xref> according to the National Heart, Lung, and Blood Institute (NHLBI) cholesterol screening guidelines and cut-off points, <xref ref-type="bibr" rid="B30"><sup>30</sup></xref> which are also based on the National Cholesterol Education Program study.<xref ref-type="bibr" rid="B31"><sup>31</sup></xref>
			</p>
			<p>The statistical analysis was performed using the SPSS program version 18.0 after creating a database in Microsoft Excel 2013. The quantitative variables were mean, standard deviation of the mean, minimum and maximum values, percentiles and count of cases on which this calculation had been made; the frequency distributions of the continuous variables were represented in bar charts, box plots and histograms. Subsequently, an inferential statistic was made and anthropometric variables and lipid profile and glycaemia were described with means and standard deviation.</p>
			<p>Pearson's correlation coefficient was used to identify the linear relationship between two quantitative variables. Furthermore, for non-homoscedastic lipid variables, the Kruskal-Wallis test was used to find significant differences between the nutritional status groups. Likewise, an analysis of variance (ANOVA) was used to compare the means of IGF-1, IGFBP-1, IGFBP-2 and IGFBP-3 between the groups according to the nutritional status of their members. On the other hand, pairwise comparisons were applied using the Games-Howell method, which assumes different variances, in order to complement the contrasts between the groups. In addition, groups were assessed according to the nutritional status of their members using the Dunnett's test, and significant results were obtained.</p>
		</sec>
		<sec sec-type="results">
			<title>Results</title>
			<p>The average age of the children was 8.2±0.7 years; 49% attended the Liceo Integral Los Alisos school and 51% the Instituto Educativo Distrital Llano Oriental school. <xref ref-type="table" rid="t1">Table 1</xref> shows the anthropometric variables of the participants.</p>
			<p>
				<table-wrap id="t1">
					<label>Table 1</label>
					<caption>
						<title>Anthropometric, lipid profile and glycemic variables per nutritional classification group.</title>
					</caption>
					<graphic xlink:href="0120-0011-rfmun-68-01-51-gt1.gif"/>
					<table-wrap-foot>
						<fn id="TFN1">
							<p>BMI: body mass index; total-c: total cholesterol; HDL-c: HDL cholesterol; LDL-c: LDL cholesterol; TG: triglycerides; WC: waist circumference.</p>
						</fn>
						<fn id="TFN2">
							<p>* Significant difference (p&lt;0.05).</p>
						</fn>
						<fn id="TFN3">
							<p>Source: Own elaboration.</p>
						</fn>
					</table-wrap-foot>
				</table-wrap>
			</p>
			<p>The lipid profile of most children were within normal values (<xref ref-type="table" rid="t1">Table 1</xref>); however, a significant number had alarming (bordering) or elevated levels compared to the NHLBI recommended limits (<xref ref-type="fig" rid="f1">Figure 1</xref>). All participants had blood glucose levels within the reference values.</p>
			<p>
				<fig id="f1">
					<label>Figure 1</label>
					<caption>
						<title>Percentage of children classified according to the National Heart, Lung, and Blood Institute's lipid profile cut-off points. </title>
					</caption>
					<graphic xlink:href="0120-0011-rfmun-68-01-51-gf1.gif"/>
					<attrib>Total-c: total cholesterol; HDL-c: HDL cholesterol; LDL-c: LDL cholesterol; non-HDL-c: cholesterol no HDL; TG: triglycerides. Source: Own elaboration.</attrib>
				</fig>
			</p>
			<p>After analyzing anthropometric variables and the lipid profile, a significant difference was found between children in the overweight, obesity and adequate weight groups with high WC compared to children in the eutrophic and at risk of underweight groups (p&lt;0.05).</p>
			<p>Moreover, 62% of children with excess weight had alterations of at least one variable of the lipid profile and 26.7% were in the bordering cut-off point, which would indicate that the lipid profile values of 88.7% of the participants in this group had alterations. These results could indicate the possibility of being at risk of CVD in the long term.</p>
			<p>Also, using the Pearson's correlation coefficient, a direct association between IGF-1 and height was observed, while the ANOVA test, Kruskal Wallis'testandthe medians allowed finding the inferences (p&lt;0.05). The significant difference between individuals with adequate height and low height-for-age or at risk of low height-for-age was identified using the Dunnett's statistical method.</p>
			<p>
				<xref ref-type="fig" rid="f2">Figure 2</xref> shows IGFBP-1 and IGFBP-2 serum levels according to the BMI classification. The lowest IGFBP-1 values were found in overweight individuals and those with a higher WC index; the lowest IGFBP-2 values were also found in overweight children.</p>
			<p>
				<fig id="f2">
					<label>Figure 2</label>
					<caption>
						<title>Box plot according to nutritional status and the IGFBP-1 and IGFBP-2 variables. </title>
					</caption>
					<graphic xlink:href="0120-0011-rfmun-68-01-51-gf2.gif"/>
					<attrib>IGFBP-1: Insulin-like growth factor-binding protein 1; IGFBP-2: Insulin-like growth factor-binding protein 2 Source: Own elaboration.</attrib>
				</fig>
			</p>
			<p>With respect to IGFBP-1 levels, both the ANOVA test and the Games-Howell method established a significant difference between individuals with adequate BMI and those who are overweight or obese (p=0.000 and p&lt;0.05, respectively). Likewise, the ANOVA analysis allowed evidencing that children with lower IGFBP-2 values were obese and overweight (p=0.001), while the Dunnett's test found that the highest statistical significance for IGFBP-2 is in the obese group.</p>
			<p>The ANOVA analysis of the WC classification and the IGFBP-1 and IGFBP-2 levels revealed a significant difference (p=0.000), while the Games-Howell method identified that these proteins tend to decrease as the WC increases. On the other hand, IGFBP-3 did not show any significant difference according to nutritional status nor did it show any relationship with IGF-I levels.</p>
			<p>The relationships between IGFBP-1 and IGFBP-2 levels and the lipid profile variables (<xref ref-type="table" rid="t2">Table 2</xref>) were evaluated, finding that both proteins are inversely correlated with TG concentrations and directly correlated with HDL-c values. Some variables were also compared between eutrophic and obese children (<xref ref-type="table" rid="t3">Table 3</xref>).</p>
			<p>
				<table-wrap id="t2">
					<label>Table 2</label>
					<caption>
						<title>Correlation coefficients between IGFBP-1 and IGFBP-2 and lipid profile variables.</title>
					</caption>
					<graphic xlink:href="0120-0011-rfmun-68-01-51-gt2.gif"/>
					<table-wrap-foot>
						<fn id="TFN4">
							<p>IGFBP-1: insulin-like growth factor-binding protein 1; IGFBP-2: insulin-like growth factor-binding protein 2; Total-c: total cholesterol; HDL-c: HDL cholesterol; LDL-c: LDL cholesterol; TG: triglycerides.</p>
						</fn>
						<fn id="TFN5">
							<p>* Significant correlation (p&lt;0.05).</p>
						</fn>
						<fn id="TFN6">
							<p>Source: Own elaboration.</p>
						</fn>
					</table-wrap-foot>
				</table-wrap>
			</p>
			<p>
				<table-wrap id="t3">
					<label>Table 3</label>
					<caption>
						<title>Statistical summary of biochemical differences between eutrophic and obese children.</title>
					</caption>
					<table>
						<colgroup>
							<col/>
							<col/>
							<col/>
							<col/>
							<col/>
							<col/>
							<col/>
							<col/>
							<col/>
						</colgroup>
						<tbody>
							<tr>
								<td align="left">Characteristics of children</td>
								<td align="left">IGF-1</td>
								<td align="left">IGFBP-1</td>
								<td align="left">IGFBP-2</td>
								<td align="left">IGFBP-3</td>
								<td align="left">Total-c</td>
								<td align="left">HDL-c</td>
								<td align="left">LDL-c</td>
								<td align="left">TG</td>
							</tr>
							<tr>
								<td align="left">Eutrophic</td>
								<td align="left">244.9</td>
								<td align="left">14.4</td>
								<td align="left">266.5</td>
								<td align="left">3742.2</td>
								<td align="left">151.9</td>
								<td align="left">51.3</td>
								<td align="left">87.5</td>
								<td align="left">65.4</td>
							</tr>
							<tr>
								<td align="left">Obese</td>
								<td align="left">324.5</td>
								<td align="left">5.7</td>
								<td align="left">150.1</td>
								<td align="left">3605.1</td>
								<td align="left">160.7</td>
								<td align="left">42.5</td>
								<td align="left">96.3</td>
								<td align="left">109.5</td>
							</tr>
							<tr>
								<td align="left">p-value</td>
								<td align="left">0.035*</td>
								<td align="left">0.002 *</td>
								<td align="left">0.0000126 *</td>
								<td align="left">0.317</td>
								<td align="left">0.161</td>
								<td align="left">0.011 *</td>
								<td align="left">0.091</td>
								<td align="left">0.013 *</td>
							</tr>
						</tbody>
					</table>
					<table-wrap-foot>
						<fn id="TFN7">
							<p>IGF-1: insulin-like growth factor 1, IGFBP-1: insulin-like growth factor-binding protein 1; IGFBP-2: insulin-like growth factor-binding protein 2; IGFBP-3: insulin-like growth factor-binding protein 3; Total-c: total cholesterol; HDL-c: HDL cholesterol; LDL-c: LDL cholesterol; TG: triglycerides.</p>
						</fn>
						<fn id="TFN8">
							<p>* Significant difference (p&lt;0.05) when assessing the assumption of equality of means for the variables.</p>
						</fn>
						<fn id="TFN9">
							<p>Source: Own elaboration.</p>
						</fn>
					</table-wrap-foot>
				</table-wrap>
			</p>
			<p>In each case, the hypothesis of equality of means was evaluated (p&lt;0.05), finding that obese individuals had significantly lower IGFBP-1, IGFBP-2 and HDL-c levels compared to eutrophic individuals. In turn, significantly lower IGF-1 and TG levels were observed in the latter.</p>
			<p>No strong association between IGF-1 and BMI or WC was observed. Furthermore, an inverse relationship between IGFBP-1 and IGFBP-2 serum levels and BMI was identified. Finally, it was observed an increase in TG levels and a decrease in HDL-c levels in eutrophic children as weight increases leading to overweight and obesity (<xref ref-type="fig" rid="f3">Figure 3</xref>).</p>
			<p>
				<fig id="f3">
					<label>Figure 3</label>
					<caption>
						<title>Mean values and standard deviation of TG and HDL-c for each nutritional status.</title>
					</caption>
					<graphic xlink:href="0120-0011-rfmun-68-01-51-gf3.gif"/>
					<attrib>HDL-c: HDL cholesterol; TG: triglycerides; WC: waist circumference. Source: Own elaboration.</attrib>
				</fig>
			</p>
			<p>A linear relationship between WC and IGFBP-1 and IGFBP-2 was identified using the Pearson correlation coefficient, which was confirmed with a Games-Howell statistical test. The average level of these proteins decreases as the WC of the individuals increases.</p>
			<p>Finally, the relationship between TG and HDL-c was analyzed using the TG/HDL-c index; <xref ref-type="bibr" rid="B32"><sup>32</sup></xref> the latter was &gt;2 in 32 children, of whom 72% were in the high WC, overweight and obesity groups, suggesting a high risk of IR in this population.</p>
		</sec>
		<sec sec-type="discussion">
			<title>Discussion</title>
			<p>The results obtained show alterations in the lipid profile, particularly high concentrations of TG and low concentrations of HDL-c, which have been previously reported<xref ref-type="bibr" rid="B33"><sup>33</sup></xref><sup>-</sup><xref ref-type="bibr" rid="B36"><sup>36</sup></xref> and are constantly associated with future health risks. The most frequently reported risk factor for CVD is a decrease in HDL-c, which has protective functions at the endothelial level as it reduces the formation of foam cells and atheromatous plaques. Consequently, these alterations in early life are of particular concern, since they mean that individuals have a longer exposure time and, therefore, greater endothelial damage, which is considered a risk factor for IR in adolescents.</p>
			<p>When analyzing the TG/HDL-c ratio, values &gt;2 were observed, mostly in the overweight and obesity groups. In the study by Iwani <italic>et al.,</italic><xref ref-type="bibr" rid="B37"><sup>37</sup></xref> this indicator was significantly correlated with the value of the homeostatic model to assess IR (HOMA-IR) and WC, while the study by Soutelo <italic>et al.</italic><xref ref-type="bibr" rid="B32"><sup>32</sup></xref> established that it could facilitate timely decisions in health, even in children from 7 years of age.</p>
			<p>IGF-1 was not related to BMI, but it was related to height when comparing the 5 study groups, finding lower levels in children with low height-for-age and at risk of low height-for-age compared to children with adequate height. Although IGF-1 secretion is stimulated by GH in all tissues, the response depends on nutritional status. In addition, this factor also stimulates cartilage growth; the synthesis of RNA, DNA and protein; and anabolic processes.<xref ref-type="bibr" rid="B38"><sup>38</sup></xref><sup>,</sup><xref ref-type="bibr" rid="B39"><sup>39</sup></xref> In this sense, IGF-1 plays a key role in growth, so there is a positive correlation between its circulating concentrations and the growth rate of children.<xref ref-type="bibr" rid="B38"><sup>38</sup></xref>
			</p>
			<p>When comparing obese children with eutrophic children, IGF-1 levels were elevated in the first group and also had a significant difference. Mohanraj <italic>et al.</italic><xref ref-type="bibr" rid="B15"><sup>15</sup></xref> and Park <italic>et al.</italic><xref ref-type="bibr" rid="B40"><sup>40</sup></xref> reported similar findings. Although obese individuals have lower GH production, their circulating IGF-1 concentrations were high, which could be explained by increased pre-adipocyte expression of IGF-1 and its receptor due to the effects of insulin and cortisol; thus, IGF-1 activates the proliferation of pre-adipocytes and their differentiation into adipocytes.<xref ref-type="bibr" rid="B41"><sup>41</sup></xref>
			</p>
			<p>IGF-1 production in response to an increased number of adipocytes may play a role in the decreased output of GH observed in patients who suffer from obesity.<xref ref-type="bibr" rid="B20"><sup>20</sup></xref><sup>,</sup><xref ref-type="bibr" rid="B42"><sup>42</sup></xref><sup>,</sup><xref ref-type="bibr" rid="B43"><sup>43</sup></xref> However, this decrease in the secretion of this hormone is not associated with an alteration in the speed of growth, since obese children usually have a normal or even increased height for their age; for example, in this study, the obese group was 7cm taller than children of similar age with adequate weight.</p>
			<p>There was no significant difference in IGFBP-3 levels according to the nutritional status; however, obese children had the lowest average IGFBP-3 compared to other nutritional statuses. This finding has been reported in other studies in which IGFBP-3 levels in obese children and adolescents were reduced<xref ref-type="bibr" rid="B42"><sup>42</sup></xref> or did not change. <xref ref-type="bibr" rid="B42"><sup>42</sup></xref><sup>,</sup><xref ref-type="bibr" rid="B44"><sup>44</sup></xref><sup>,</sup><xref ref-type="bibr" rid="B45"><sup>45</sup></xref> In Switzerland, Lewitt <italic>et al.</italic><xref ref-type="bibr" rid="B46"><sup>46</sup></xref> linked this decrease in total IGFBP-3 in obese adolescents to increased protease activity of IGFBP-3 and increased circulating fragments of IGFBP-3, and in the US, Mohanraj <italic>et al.</italic><xref ref-type="bibr" rid="B15"><sup>15</sup></xref> reported, on the one hand, the same situation in adolescents in whom circulating levels of total IGFBP-3 were low and, on the other, the presence of proteolytic fragments of IGFBP-3 in overweight and obese subjects.</p>
			<p>The serum IGFBP-1 level observed in the children in this study was significantly lower in the obese than in the eutrophic children. Similar findings were reported by Martínez-de Icaya <italic>et al.</italic><xref ref-type="bibr" rid="B19"><sup>19</sup></xref> in Spain, Reinehr <italic>et al.</italic><xref ref-type="bibr" rid="B21"><sup>21</sup></xref> in Germany, Saitoh <italic>et al.</italic><xref ref-type="bibr" rid="B22"><sup>22</sup></xref> in Japan and Ricco <italic>et al.</italic><xref ref-type="bibr" rid="B44"><sup>44</sup></xref> in Brazil. Specifically in Spain, Martinez-de Icaya found in a group of 7-10-year-old children that overweight children had higher serum IGF-1 levels and lower serum IGFBP-1 levels compared to controls;<xref ref-type="bibr" rid="B19"><sup>19</sup></xref> these findings in children with obesity are related to being more prone to IR.</p>
			<p>Other relevant data reported in the present study were the relationships between IGFBP-1 and IGFBP-2 and the variables of the lipid profile. It was found that low levels of these proteins were associated with low levels of HDL-c and high levels of serum TG, which is similar to what was reported in adults by Ruan &amp; Lai<xref ref-type="bibr" rid="B13"><sup>13</sup></xref> and Heald <italic>et al.</italic><xref ref-type="bibr" rid="B47"><sup>47</sup></xref> These results suggest that low IGFBP-1 and IGFBP-2 levels may be associated with different factors that predispose to atherogenesis<xref ref-type="bibr" rid="B13"><sup>13</sup></xref><sup>,</sup><xref ref-type="bibr" rid="B48"><sup>48</sup></xref> and that low serum IGFBP-1 may be an early predictor of CVD in prepubertal obesity. <xref ref-type="bibr" rid="B13"><sup>13</sup></xref><sup>,</sup><xref ref-type="bibr" rid="B21"><sup>21</sup></xref>
			</p>
			<p>Furthermore, this study found an inverse relationship between circulating IGFBP-2 levels and nutritional status. The lowest values were found in children diagnosed with obesity, which is consistent with previously reported data.<xref ref-type="bibr" rid="B23"><sup>23</sup></xref><sup>,</sup><xref ref-type="bibr" rid="B47"><sup>47</sup></xref><sup>,</sup><xref ref-type="bibr" rid="B49"><sup>49</sup></xref><sup>,</sup><xref ref-type="bibr" rid="B50"><sup>50</sup></xref>
			</p>
			<p>IGFBP-2 has paracrine action and is the IGF-1 binding protein most expressed in the body and the main IGFBP secreted by white preadipocytes during adipogenesis.<xref ref-type="bibr" rid="B23"><sup>23</sup></xref><sup>,</sup><xref ref-type="bibr" rid="B24"><sup>24</sup></xref> The relationship found in the present study, between decreased circulating IGFBP-2 levels and overweight and obesity may be explained by an unfavorable secretion profile of this binding protein by adipocytes, which may be associated with increased leptin and decreased adiponectin levels.<xref ref-type="bibr" rid="B49"><sup>49</sup></xref> In this regard, Hedbacker <italic>et al.</italic><xref ref-type="bibr" rid="B51"><sup>51</sup></xref> demonstrated that leptin increases liver transcription of IGFBP2 when administered peripherally or centrally in mice with lipodystrophy.</p>
		</sec>
		<sec sec-type="conclusions">
			<title>Conclusions</title>
			<p>The presence of high levels of cholesterol and TG in children is a serious public health problem. In the present study, alterations in the lipid profile were evidenced in overweight and obese children, so early modifications in the metabolism regarding overweight and increased adiposity are recommended.</p>
			<p>Excess weight was positively related to TG and negatively related to HDL-c. This fact is associated with an increased risk of developing CVD, so it is necessary to promote the implementation of physical activity and nutrition education programs in schools to improve eating habits and the practice of physical activity in the child population.</p>
			<p>In overweight children, there are alterations at the lipid and protein-binding level of insulin-like growth factors, which increase the risk of vascular disease in adulthood. Therefore, public health strategies should be established to prevent and treat excess weight in childhood, which in turn will reduce the risk of these diseases in adulthood.</p>
		</sec>
	</body>
	<back>
		<ack>
			<title>Acknowledgements</title>
			<p>To the schools where the research was conducted and to their principals, boys, girls and parents, who allowed the development of the project.</p>
		</ack>
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				<p> None stated by the authors.</p>
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				<p> This research was financed by the Master's Degree in Physiology and by the Universidad Nacional de Colombia through the DIB-Hermes-21970 and 21971 calls.</p>
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