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http://hdl.handle.net/2445/189145
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DC Field | Value | Language |
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dc.contributor.author | Esteve Luque, Virginia | - |
dc.contributor.author | Fanlo Maresma, Marta | - |
dc.contributor.author | Padró i Miquel, Ariadna | - |
dc.contributor.author | Corbella, Emili | - |
dc.contributor.author | Rivas Regaira, Maite | - |
dc.contributor.author | Pintó Sala, Xavier | - |
dc.contributor.author | Candás Estébanez, Beatriz | - |
dc.date.accessioned | 2022-09-19T12:42:00Z | - |
dc.date.available | 2022-09-19T12:42:00Z | - |
dc.date.issued | 2022-08-30 | - |
dc.identifier.issn | 1422-0067 | - |
dc.identifier.uri | http://hdl.handle.net/2445/189145 | - |
dc.description.abstract | Background: Genetic risk scores (GRSs) have partially improved the understanding of the etiology of moderate hypertriglyceridemia (HTG), which until recently was mainly assessed by secondary predisposing causes. The main objective of this study was to assess whether this variability is due to the interaction between clinical variables and GRS. Methods: We analyzed 276 patients with suspected polygenic HTG. An unweighted GRS was developed with the following variants: c.724C > G (ZPR1 gene), c.56C > G (APOA5 gene), c.1337T > C (GCKR gene), g.19986711A > G (LPL gene), c.107 + 1647T > C (BAZ1B gene) and g.125478730A > T (TRIB gene). Interactions between the GRS and clinical variables (body mass index (BMI), diabetes mellitus, diet, physical activity, alcohol consumption, age and gender) were evaluated. Results: The GRS was associated with triglyceride (TG) concentrations. There was a significant interaction between BMI and GRS, with the intensity of the relationship between the number of alleles and the TG concentration being greater in individuals with a higher BMI. Conclusions: GRS is associated with plasma TG concentrations and is markedly influenced by BMI. This finding could improve the stratification of patients with a high genetic risk for HTG who could benefit from more intensive healthcare interventions. | - |
dc.format.extent | 11 p. | - |
dc.format.mimetype | application/pdf | - |
dc.language.iso | eng | - |
dc.publisher | MDPI AG | - |
dc.relation.isformatof | Reproducció del document publicat a: https://doi.org/10.3390/ijms23179837 | - |
dc.relation.ispartof | International Journal of Molecular Sciences, 2022, vol. 23, núm. 17, p. 9837 | - |
dc.relation.uri | https://doi.org/10.3390/ijms23179837 | - |
dc.rights | cc by (c) Esteve Luque, Virginia et al., 2022 | - |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/es/ | * |
dc.source | Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL)) | - |
dc.subject.classification | Obesitat | - |
dc.subject.classification | Triglicèrids | - |
dc.subject.other | Obesity | - |
dc.subject.other | Triglycerides | - |
dc.title | Polygenic Risk of Hypertriglyceridemia Is Modified by BMI | - |
dc.type | info:eu-repo/semantics/article | - |
dc.type | info:eu-repo/semantics/publishedVersion | - |
dc.date.updated | 2022-09-16T10:02:40Z | - |
dc.rights.accessRights | info:eu-repo/semantics/openAccess | - |
dc.identifier.pmid | 36077235 | - |
Appears in Collections: | Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL)) Articles publicats en revistes (Ciències Clíniques) |
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ijms-23-09837.pdf | 588.89 kB | Adobe PDF | View/Open |
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