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      <subfield code="a">Lurbe, Empar</subfield>
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      <subfield code="a">Kafatos, Anthony</subfield>
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      <subfield code="a">Molnár, Dénes</subfield>
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      <subfield code="a">Kersting, Mathilde</subfield>
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      <subfield code="a">Breidenassel, Christina</subfield>
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      <subfield code="a">Sinningen, Kathrin</subfield>
      <subfield code="e">author</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">De Ruyter, Thaïs</subfield>
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      <subfield code="a">Labayen, Idoia</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Rupérez, Azahara I</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Bueno-Lozano, Gloria</subfield>
      <subfield code="e">author</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Moreno, Luis A</subfield>
      <subfield code="e">author</subfield>
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      <subfield code="a">HELENA study group</subfield>
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      <subfield code="c">2023-06-01</subfield>
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      <subfield code="a">INTRODUCTION: From genome wide association study (GWAS) a large number of single nucleotide polymorphisms (SNPs) have previously been associated with blood pressure (BP) levels. A combination of SNPs, forming a genetic risk score (GRS) could be considered as a useful genetic tool to identify individuals at risk of developing hypertension from early stages in life. Therefore, the aim of our study was to build a GRS being able to predict the genetic predisposition to hypertension (HTN) in European adolescents. METHODS: Data were extracted from the Healthy Lifestyle in Europe by Nutrition in Adolescence (HELENA) cross-sectional study. A total of 869 adolescents (53% female), aged 12.5-17.5, with complete genetic and BP information were included. The sample was divided into altered (?130 mmHg for systolic and/or ?80 mmHg for diastolic) or normal BP. Based on the literature, a total of 1.534 SNPs from 57 candidate genes related with BP were selected from the HELENA GWAS database. RESULTS: From 1,534 SNPs available, An initial screening of SNPs univariately associated with HTN (p &lt; 0.10) was established, to finally obtain a number of 16 SNPs significantly associated with HTN (p &lt; 0.05) in the multivariate model. The unweighted GRS (uGRS) and weighted GRS (wGRS) were estimated. To validate the GRSs, the area under the curve (AUC) was explored using ten-fold internal cross-validation for uGRS (0.802) and wGRS (0.777). Further covariates of interest were added to the analyses, obtaining a higher predictive ability (AUC values of uGRS: 0.879; wGRS: 0.881 for BMI z-score). Furthermore, the differences between AUCs obtained with and without the addition of covariates were statistically significant (p &lt; 0.05). CONCLUSIONS: Both GRSs, the uGRS and wGRS, could be useful to evaluate the predisposition to hypertension in European adolescents.</subfield>
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      <subfield code="a">Front Cardiovasc Med  . 2023 :10:1118919</subfield>
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      <subfield code="a">10.3389/fcvm.2023.1118919</subfield>
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      <subfield code="a">2297-055X</subfield>
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      <subfield code="a">Frontiers in cardiovascular medicine</subfield>
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      <subfield code="a">37324619</subfield>
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      <subfield code="a">https://hdl.handle.net/20.500.12105/23124</subfield>
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   <datafield ind2="0" ind1="0" tag="245">
      <subfield code="a">Development of a genetic risk score to predict the risk of hypertension in European adolescents from the HELENA study</subfield>
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