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Genetic Determinants of Serum Calcification Propensity and Cardiovascular Outcomes in the General Population

BACKGROUND: Serum calciprotein particle maturation time (T(50)), a measure of vascular calcification propensity, is associated with cardiovascular morbidity and mortality. We aimed to identify genetic loci associated with serum T(50) and study their association with cardiovascular disease and mortal...

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Autores principales: de Haan, Amber, Ahmadizar, Fariba, van der Most, Peter J., Thio, Chris H. L., Kamali, Zoha, Ani, Alireza, Ghanbari, Mohsen, Chaker, Layal, van Meurs, Joyce, Ikram, M. Kamran, van Goor, Harry, Bakker, Stephan J. L., van der Harst, Pim, Snieder, Harold, Kavousi, Maryam, Pasch, Andreas, Eijgelsheim, Mark, de Borst, Martin H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8795369/
https://www.ncbi.nlm.nih.gov/pubmed/35097025
http://dx.doi.org/10.3389/fcvm.2021.809717
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author de Haan, Amber
Ahmadizar, Fariba
van der Most, Peter J.
Thio, Chris H. L.
Kamali, Zoha
Ani, Alireza
Ghanbari, Mohsen
Chaker, Layal
van Meurs, Joyce
Ikram, M. Kamran
van Goor, Harry
Bakker, Stephan J. L.
van der Harst, Pim
Snieder, Harold
Kavousi, Maryam
Pasch, Andreas
Eijgelsheim, Mark
de Borst, Martin H.
author_facet de Haan, Amber
Ahmadizar, Fariba
van der Most, Peter J.
Thio, Chris H. L.
Kamali, Zoha
Ani, Alireza
Ghanbari, Mohsen
Chaker, Layal
van Meurs, Joyce
Ikram, M. Kamran
van Goor, Harry
Bakker, Stephan J. L.
van der Harst, Pim
Snieder, Harold
Kavousi, Maryam
Pasch, Andreas
Eijgelsheim, Mark
de Borst, Martin H.
author_sort de Haan, Amber
collection PubMed
description BACKGROUND: Serum calciprotein particle maturation time (T(50)), a measure of vascular calcification propensity, is associated with cardiovascular morbidity and mortality. We aimed to identify genetic loci associated with serum T(50) and study their association with cardiovascular disease and mortality. METHODS: We performed a genome-wide association study of serum T(50) in 2,739 individuals of European descent participating in the Prevention of REnal and Vascular ENd-stage Disease (PREVEND) study, followed by a two-sample Mendelian randomization (MR) study to examine causal effects of T(50) on cardiovascular outcomes. Finally, we examined associations between T(50) loci and cardiovascular outcomes in 8,566 community-dwelling participants in the Rotterdam study. RESULTS: We identified three independent genome-wide significant single nucleotide polymorphism (SNPs) in the AHSG gene encoding fetuin-A: rs4917 (p = 1.72 × 10(−101)), rs2077119 (p = 3.34 × 10(−18)), and rs9870756 (p = 3.10 × 10(−8)), together explaining 18.3% of variation in serum T(50). MR did not demonstrate a causal effect of T(50) on cardiovascular outcomes in the general population. Patient-level analyses revealed that the minor allele of rs9870756, which explained 9.1% of variation in T(50), was associated with a primary composite endpoint of all-cause mortality or cardiovascular disease [odds ratio (95% CI) 1.14 (1.01–1.28)] and all-cause mortality alone [1.14 (1.00–1.31)]. The other variants were not associated with clinical outcomes. In patients with type 2 diabetes or chronic kidney disease, the association between rs9870756 and the primary composite endpoint was stronger [OR 1.40 (1.06–1.84), relative excess risk due to interaction 0.54 (0.01–1.08)]. CONCLUSIONS: We identified three SNPs in the AHSG gene that explained 18.3% of variability in serum T(50) levels. Only one SNP was associated with cardiovascular outcomes, particularly in individuals with type 2 diabetes or chronic kidney disease.
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spelling pubmed-87953692022-01-29 Genetic Determinants of Serum Calcification Propensity and Cardiovascular Outcomes in the General Population de Haan, Amber Ahmadizar, Fariba van der Most, Peter J. Thio, Chris H. L. Kamali, Zoha Ani, Alireza Ghanbari, Mohsen Chaker, Layal van Meurs, Joyce Ikram, M. Kamran van Goor, Harry Bakker, Stephan J. L. van der Harst, Pim Snieder, Harold Kavousi, Maryam Pasch, Andreas Eijgelsheim, Mark de Borst, Martin H. Front Cardiovasc Med Cardiovascular Medicine BACKGROUND: Serum calciprotein particle maturation time (T(50)), a measure of vascular calcification propensity, is associated with cardiovascular morbidity and mortality. We aimed to identify genetic loci associated with serum T(50) and study their association with cardiovascular disease and mortality. METHODS: We performed a genome-wide association study of serum T(50) in 2,739 individuals of European descent participating in the Prevention of REnal and Vascular ENd-stage Disease (PREVEND) study, followed by a two-sample Mendelian randomization (MR) study to examine causal effects of T(50) on cardiovascular outcomes. Finally, we examined associations between T(50) loci and cardiovascular outcomes in 8,566 community-dwelling participants in the Rotterdam study. RESULTS: We identified three independent genome-wide significant single nucleotide polymorphism (SNPs) in the AHSG gene encoding fetuin-A: rs4917 (p = 1.72 × 10(−101)), rs2077119 (p = 3.34 × 10(−18)), and rs9870756 (p = 3.10 × 10(−8)), together explaining 18.3% of variation in serum T(50). MR did not demonstrate a causal effect of T(50) on cardiovascular outcomes in the general population. Patient-level analyses revealed that the minor allele of rs9870756, which explained 9.1% of variation in T(50), was associated with a primary composite endpoint of all-cause mortality or cardiovascular disease [odds ratio (95% CI) 1.14 (1.01–1.28)] and all-cause mortality alone [1.14 (1.00–1.31)]. The other variants were not associated with clinical outcomes. In patients with type 2 diabetes or chronic kidney disease, the association between rs9870756 and the primary composite endpoint was stronger [OR 1.40 (1.06–1.84), relative excess risk due to interaction 0.54 (0.01–1.08)]. CONCLUSIONS: We identified three SNPs in the AHSG gene that explained 18.3% of variability in serum T(50) levels. Only one SNP was associated with cardiovascular outcomes, particularly in individuals with type 2 diabetes or chronic kidney disease. Frontiers Media S.A. 2022-01-14 /pmc/articles/PMC8795369/ /pubmed/35097025 http://dx.doi.org/10.3389/fcvm.2021.809717 Text en Copyright © 2022 de Haan, Ahmadizar, van der Most, Thio, Kamali, Ani, Ghanbari, Chaker, van Meurs, Ikram, van Goor, Bakker, van der Harst, Snieder, Kavousi, Pasch, Eijgelsheim and de Borst. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cardiovascular Medicine
de Haan, Amber
Ahmadizar, Fariba
van der Most, Peter J.
Thio, Chris H. L.
Kamali, Zoha
Ani, Alireza
Ghanbari, Mohsen
Chaker, Layal
van Meurs, Joyce
Ikram, M. Kamran
van Goor, Harry
Bakker, Stephan J. L.
van der Harst, Pim
Snieder, Harold
Kavousi, Maryam
Pasch, Andreas
Eijgelsheim, Mark
de Borst, Martin H.
Genetic Determinants of Serum Calcification Propensity and Cardiovascular Outcomes in the General Population
title Genetic Determinants of Serum Calcification Propensity and Cardiovascular Outcomes in the General Population
title_full Genetic Determinants of Serum Calcification Propensity and Cardiovascular Outcomes in the General Population
title_fullStr Genetic Determinants of Serum Calcification Propensity and Cardiovascular Outcomes in the General Population
title_full_unstemmed Genetic Determinants of Serum Calcification Propensity and Cardiovascular Outcomes in the General Population
title_short Genetic Determinants of Serum Calcification Propensity and Cardiovascular Outcomes in the General Population
title_sort genetic determinants of serum calcification propensity and cardiovascular outcomes in the general population
topic Cardiovascular Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8795369/
https://www.ncbi.nlm.nih.gov/pubmed/35097025
http://dx.doi.org/10.3389/fcvm.2021.809717
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