Non-alcoholic fatty liver disease (NAFLD) and atherosclerosis-related cardiovascular diseases (CVD) share common metabolic pathways. We explored the association between three NAFLD-associated single nucleotide polymorphisms (SNPs) rs738409, rs10401969, and rs1260326 with sub-clinical atherosclerosis estimated by the carotid intima-media thickness (c-IMT) and the inter-adventitia common carotid artery diameter (ICCAD) in patients free from clinically overt NAFLD and CVD. The study population is the IMPROVE, a multicenter European study (n = 3711). C-IMT measures and ICCAD were recorded using a standardized protocol. Linear regression with an additive genetic model was used to test for association of the three SNPs with c-IMT and ICCAD. In secondary analyses, the association of the three SNPs with c-IMT and ICCAD was tested after stratification by alanine aminotransferase levels (ALT). No associations were found between rs738409, rs1260326, rs10401969, and c-IMT or ICCAD. Rs738409-G and rs10401969-C were associated with ALT levels (p < 0.001). In patients with ALT levels above 28 U/L (highest quartile), we observed an association between rs10401969-C and c-IMT measures of c-IMTmax and c-IMTmean-max (p = 0.018 and 0.021, respectively). In conclusion, NAFLD-associated SNPs do not associate with sub-clinical atherosclerosis measures. However, our results suggest a possible mediating function of impaired liver function on atherosclerosis development.

Genetic Variants Associated with Non-Alcoholic Fatty Liver Disease Do Not Associate with Measures of Sub-Clinical Atherosclerosis: Results from the IMPROVE Study / L. Castaldo, F. Laguzzi, R.J. Strawbridge, D. Baldassarre, F. Veglia, L. Vigo, E. Tremoli, U. de Faire, P. Eriksson, A.J. Smit, J. Aubrecht, K. Leander, M. Pirro, P. Giral, A. Ritieni, G. Di Minno, A. Mälarstig, B. Gigante. - In: GENES. - ISSN 2073-4425. - 11:11(2020 Oct).

Genetic Variants Associated with Non-Alcoholic Fatty Liver Disease Do Not Associate with Measures of Sub-Clinical Atherosclerosis: Results from the IMPROVE Study

D. Baldassarre;F. Veglia;E. Tremoli;
2020

Abstract

Non-alcoholic fatty liver disease (NAFLD) and atherosclerosis-related cardiovascular diseases (CVD) share common metabolic pathways. We explored the association between three NAFLD-associated single nucleotide polymorphisms (SNPs) rs738409, rs10401969, and rs1260326 with sub-clinical atherosclerosis estimated by the carotid intima-media thickness (c-IMT) and the inter-adventitia common carotid artery diameter (ICCAD) in patients free from clinically overt NAFLD and CVD. The study population is the IMPROVE, a multicenter European study (n = 3711). C-IMT measures and ICCAD were recorded using a standardized protocol. Linear regression with an additive genetic model was used to test for association of the three SNPs with c-IMT and ICCAD. In secondary analyses, the association of the three SNPs with c-IMT and ICCAD was tested after stratification by alanine aminotransferase levels (ALT). No associations were found between rs738409, rs1260326, rs10401969, and c-IMT or ICCAD. Rs738409-G and rs10401969-C were associated with ALT levels (p < 0.001). In patients with ALT levels above 28 U/L (highest quartile), we observed an association between rs10401969-C and c-IMT measures of c-IMTmax and c-IMTmean-max (p = 0.018 and 0.021, respectively). In conclusion, NAFLD-associated SNPs do not associate with sub-clinical atherosclerosis measures. However, our results suggest a possible mediating function of impaired liver function on atherosclerosis development.
English
alanine aminotransferase and genetic association study; carotid intima-media thickness; non-alcoholic fatty liver disease
Settore BIO/14 - Farmacologia
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ott-2020
MDPI
11
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1243
11
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Periodico con rilevanza internazionale
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info:eu-repo/semantics/article
Genetic Variants Associated with Non-Alcoholic Fatty Liver Disease Do Not Associate with Measures of Sub-Clinical Atherosclerosis: Results from the IMPROVE Study / L. Castaldo, F. Laguzzi, R.J. Strawbridge, D. Baldassarre, F. Veglia, L. Vigo, E. Tremoli, U. de Faire, P. Eriksson, A.J. Smit, J. Aubrecht, K. Leander, M. Pirro, P. Giral, A. Ritieni, G. Di Minno, A. Mälarstig, B. Gigante. - In: GENES. - ISSN 2073-4425. - 11:11(2020 Oct).
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L. Castaldo, F. Laguzzi, R.J. Strawbridge, D. Baldassarre, F. Veglia, L. Vigo, E. Tremoli, U. de Faire, P. Eriksson, A.J. Smit, J. Aubrecht, K. Leande...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/780142
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