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Genetic and clinical determinants of abdominal aortic diameter: genome-wide association studies, exome array data and Mendelian randomization study

Progressive dilation of the infrarenal aortic diameter is a consequence of the ageing process and is considered the main determinant of abdominal aortic aneurysm (AAA). We aimed to investigate the genetic and clinical determinants of abdominal aortic diameter (AAD). We conducted a meta-analysis of g...

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Autores principales: Portilla-Fernandez, Eliana, Klarin, Derek, Hwang, Shih-Jen, Biggs, Mary L, Bis, Joshua C, Weiss, Stefan, Rospleszcz, Susanne, Natarajan, Pradeep, Hoffmann, Udo, Rogers, Ian S, Truong, Quynh A, Völker, Uwe, Dörr, Marcus, Bülow, Robin, Criqui, Michael H, Allison, Matthew, Ganesh, Santhi K, Yao, Jie, Waldenberger, Melanie, Bamberg, Fabian, Rice, Kenneth M, Essers, Jeroen, Kapteijn, Daniek M C, van der Laan, Sander W, de Knegt, Rob J, Ghanbari, Mohsen, Felix, Janine F, Ikram, M Arfan, Kavousi, Maryam, Uitterlinden, Andre G, Roks, Anton J M, Danser, A H Jan, Tsao, Philip S, Damrauer, Scott M, Guo, Xiuqing, Rotter, Jerome I, Psaty, Bruce M, Kathiresan, Sekar, Völzke, Henry, Peters, Annette, Johnson, Craig, Strauch, Konstantin, Meitinger, Thomas, O’Donnell, Christopher J, Dehghan, Abbas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9558840/
https://www.ncbi.nlm.nih.gov/pubmed/35234888
http://dx.doi.org/10.1093/hmg/ddac051
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author Portilla-Fernandez, Eliana
Klarin, Derek
Hwang, Shih-Jen
Biggs, Mary L
Bis, Joshua C
Weiss, Stefan
Rospleszcz, Susanne
Natarajan, Pradeep
Hoffmann, Udo
Rogers, Ian S
Truong, Quynh A
Völker, Uwe
Dörr, Marcus
Bülow, Robin
Criqui, Michael H
Allison, Matthew
Ganesh, Santhi K
Yao, Jie
Waldenberger, Melanie
Bamberg, Fabian
Rice, Kenneth M
Essers, Jeroen
Kapteijn, Daniek M C
van der Laan, Sander W
de Knegt, Rob J
Ghanbari, Mohsen
Felix, Janine F
Ikram, M Arfan
Kavousi, Maryam
Uitterlinden, Andre G
Roks, Anton J M
Danser, A H Jan
Tsao, Philip S
Damrauer, Scott M
Guo, Xiuqing
Rotter, Jerome I
Psaty, Bruce M
Kathiresan, Sekar
Völzke, Henry
Peters, Annette
Johnson, Craig
Strauch, Konstantin
Meitinger, Thomas
O’Donnell, Christopher J
Dehghan, Abbas
author_facet Portilla-Fernandez, Eliana
Klarin, Derek
Hwang, Shih-Jen
Biggs, Mary L
Bis, Joshua C
Weiss, Stefan
Rospleszcz, Susanne
Natarajan, Pradeep
Hoffmann, Udo
Rogers, Ian S
Truong, Quynh A
Völker, Uwe
Dörr, Marcus
Bülow, Robin
Criqui, Michael H
Allison, Matthew
Ganesh, Santhi K
Yao, Jie
Waldenberger, Melanie
Bamberg, Fabian
Rice, Kenneth M
Essers, Jeroen
Kapteijn, Daniek M C
van der Laan, Sander W
de Knegt, Rob J
Ghanbari, Mohsen
Felix, Janine F
Ikram, M Arfan
Kavousi, Maryam
Uitterlinden, Andre G
Roks, Anton J M
Danser, A H Jan
Tsao, Philip S
Damrauer, Scott M
Guo, Xiuqing
Rotter, Jerome I
Psaty, Bruce M
Kathiresan, Sekar
Völzke, Henry
Peters, Annette
Johnson, Craig
Strauch, Konstantin
Meitinger, Thomas
O’Donnell, Christopher J
Dehghan, Abbas
author_sort Portilla-Fernandez, Eliana
collection PubMed
description Progressive dilation of the infrarenal aortic diameter is a consequence of the ageing process and is considered the main determinant of abdominal aortic aneurysm (AAA). We aimed to investigate the genetic and clinical determinants of abdominal aortic diameter (AAD). We conducted a meta-analysis of genome-wide association studies in 10 cohorts (n = 13 542) imputed to the 1000 Genome Project reference panel including 12 815 subjects in the discovery phase and 727 subjects [Partners Biobank cohort 1 (PBIO)] as replication. Maximum anterior–posterior diameter of the infrarenal aorta was used as AAD. We also included exome array data (n = 14 480) from seven epidemiologic studies. Single-variant and gene-based associations were done using SeqMeta package. A Mendelian randomization analysis was applied to investigate the causal effect of a number of clinical risk factors on AAD. In genome-wide association study (GWAS) on AAD, rs74448815 in the intronic region of LDLRAD4 reached genome-wide significance (beta = −0.02, SE = 0.004, P-value = 2.10 × 10(−8)). The association replicated in the PBIO1 cohort (P-value = 8.19 × 10(−4)). In exome-array single-variant analysis (P-value threshold = 9 × 10(−7)), the lowest P-value was found for rs239259 located in SLC22A20 (beta = 0.007, P-value = 1.2 × 10(−5)). In the gene-based analysis (P-value threshold = 1.85 × 10(−6)), PCSK5 showed an association with AAD (P-value = 8.03 × 10(−7)). Furthermore, in Mendelian randomization analyses, we found evidence for genetic association of pulse pressure (beta = −0.003, P-value = 0.02), triglycerides (beta = −0.16, P-value = 0.008) and height (beta = 0.03, P-value < 0.0001), known risk factors for AAA, consistent with a causal association with AAD. Our findings point to new biology as well as highlighting gene regions in mechanisms that have previously been implicated in the genetics of other vascular diseases.
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spelling pubmed-95588402022-10-18 Genetic and clinical determinants of abdominal aortic diameter: genome-wide association studies, exome array data and Mendelian randomization study Portilla-Fernandez, Eliana Klarin, Derek Hwang, Shih-Jen Biggs, Mary L Bis, Joshua C Weiss, Stefan Rospleszcz, Susanne Natarajan, Pradeep Hoffmann, Udo Rogers, Ian S Truong, Quynh A Völker, Uwe Dörr, Marcus Bülow, Robin Criqui, Michael H Allison, Matthew Ganesh, Santhi K Yao, Jie Waldenberger, Melanie Bamberg, Fabian Rice, Kenneth M Essers, Jeroen Kapteijn, Daniek M C van der Laan, Sander W de Knegt, Rob J Ghanbari, Mohsen Felix, Janine F Ikram, M Arfan Kavousi, Maryam Uitterlinden, Andre G Roks, Anton J M Danser, A H Jan Tsao, Philip S Damrauer, Scott M Guo, Xiuqing Rotter, Jerome I Psaty, Bruce M Kathiresan, Sekar Völzke, Henry Peters, Annette Johnson, Craig Strauch, Konstantin Meitinger, Thomas O’Donnell, Christopher J Dehghan, Abbas Hum Mol Genet Association Studies Article Progressive dilation of the infrarenal aortic diameter is a consequence of the ageing process and is considered the main determinant of abdominal aortic aneurysm (AAA). We aimed to investigate the genetic and clinical determinants of abdominal aortic diameter (AAD). We conducted a meta-analysis of genome-wide association studies in 10 cohorts (n = 13 542) imputed to the 1000 Genome Project reference panel including 12 815 subjects in the discovery phase and 727 subjects [Partners Biobank cohort 1 (PBIO)] as replication. Maximum anterior–posterior diameter of the infrarenal aorta was used as AAD. We also included exome array data (n = 14 480) from seven epidemiologic studies. Single-variant and gene-based associations were done using SeqMeta package. A Mendelian randomization analysis was applied to investigate the causal effect of a number of clinical risk factors on AAD. In genome-wide association study (GWAS) on AAD, rs74448815 in the intronic region of LDLRAD4 reached genome-wide significance (beta = −0.02, SE = 0.004, P-value = 2.10 × 10(−8)). The association replicated in the PBIO1 cohort (P-value = 8.19 × 10(−4)). In exome-array single-variant analysis (P-value threshold = 9 × 10(−7)), the lowest P-value was found for rs239259 located in SLC22A20 (beta = 0.007, P-value = 1.2 × 10(−5)). In the gene-based analysis (P-value threshold = 1.85 × 10(−6)), PCSK5 showed an association with AAD (P-value = 8.03 × 10(−7)). Furthermore, in Mendelian randomization analyses, we found evidence for genetic association of pulse pressure (beta = −0.003, P-value = 0.02), triglycerides (beta = −0.16, P-value = 0.008) and height (beta = 0.03, P-value < 0.0001), known risk factors for AAA, consistent with a causal association with AAD. Our findings point to new biology as well as highlighting gene regions in mechanisms that have previously been implicated in the genetics of other vascular diseases. Oxford University Press 2022-03-02 /pmc/articles/PMC9558840/ /pubmed/35234888 http://dx.doi.org/10.1093/hmg/ddac051 Text en © The Author(s) 2022. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Association Studies Article
Portilla-Fernandez, Eliana
Klarin, Derek
Hwang, Shih-Jen
Biggs, Mary L
Bis, Joshua C
Weiss, Stefan
Rospleszcz, Susanne
Natarajan, Pradeep
Hoffmann, Udo
Rogers, Ian S
Truong, Quynh A
Völker, Uwe
Dörr, Marcus
Bülow, Robin
Criqui, Michael H
Allison, Matthew
Ganesh, Santhi K
Yao, Jie
Waldenberger, Melanie
Bamberg, Fabian
Rice, Kenneth M
Essers, Jeroen
Kapteijn, Daniek M C
van der Laan, Sander W
de Knegt, Rob J
Ghanbari, Mohsen
Felix, Janine F
Ikram, M Arfan
Kavousi, Maryam
Uitterlinden, Andre G
Roks, Anton J M
Danser, A H Jan
Tsao, Philip S
Damrauer, Scott M
Guo, Xiuqing
Rotter, Jerome I
Psaty, Bruce M
Kathiresan, Sekar
Völzke, Henry
Peters, Annette
Johnson, Craig
Strauch, Konstantin
Meitinger, Thomas
O’Donnell, Christopher J
Dehghan, Abbas
Genetic and clinical determinants of abdominal aortic diameter: genome-wide association studies, exome array data and Mendelian randomization study
title Genetic and clinical determinants of abdominal aortic diameter: genome-wide association studies, exome array data and Mendelian randomization study
title_full Genetic and clinical determinants of abdominal aortic diameter: genome-wide association studies, exome array data and Mendelian randomization study
title_fullStr Genetic and clinical determinants of abdominal aortic diameter: genome-wide association studies, exome array data and Mendelian randomization study
title_full_unstemmed Genetic and clinical determinants of abdominal aortic diameter: genome-wide association studies, exome array data and Mendelian randomization study
title_short Genetic and clinical determinants of abdominal aortic diameter: genome-wide association studies, exome array data and Mendelian randomization study
title_sort genetic and clinical determinants of abdominal aortic diameter: genome-wide association studies, exome array data and mendelian randomization study
topic Association Studies Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9558840/
https://www.ncbi.nlm.nih.gov/pubmed/35234888
http://dx.doi.org/10.1093/hmg/ddac051
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