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Intracranial Aneurysm Risk Locus 5q23.2 Is Associated with Elevated Systolic Blood Pressure

Although genome-wide association studies (GWAS) have identified hundreds of complex trait loci, the pathomechanisms of most remain elusive. Studying the genetics of risk factors predisposing to disease is an attractive approach to identify targets for functional studies. Intracranial aneurysms (IA)...

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Autores principales: Gaál, Emília Ilona, Salo, Perttu, Kristiansson, Kati, Rehnström, Karola, Kettunen, Johannes, Sarin, Antti-Pekka, Niemelä, Mika, Jula, Antti, Raitakari, Olli T., Lehtimäki, Terho, Eriksson, Johan G., Widen, Elisabeth, Günel, Murat, Kurki, Mitja, von und zu Fraunberg, Mikael, Jääskeläinen, Juha E., Hernesniemi, Juha, Järvelin, Marjo-Riitta, Pouta, Anneli, Newton-Cheh, Christopher, Salomaa, Veikko, Palotie, Aarno, Perola, Markus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3305343/
https://www.ncbi.nlm.nih.gov/pubmed/22438818
http://dx.doi.org/10.1371/journal.pgen.1002563
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author Gaál, Emília Ilona
Salo, Perttu
Kristiansson, Kati
Rehnström, Karola
Kettunen, Johannes
Sarin, Antti-Pekka
Niemelä, Mika
Jula, Antti
Raitakari, Olli T.
Lehtimäki, Terho
Eriksson, Johan G.
Widen, Elisabeth
Günel, Murat
Kurki, Mitja
von und zu Fraunberg, Mikael
Jääskeläinen, Juha E.
Hernesniemi, Juha
Järvelin, Marjo-Riitta
Pouta, Anneli
Newton-Cheh, Christopher
Salomaa, Veikko
Palotie, Aarno
Perola, Markus
author_facet Gaál, Emília Ilona
Salo, Perttu
Kristiansson, Kati
Rehnström, Karola
Kettunen, Johannes
Sarin, Antti-Pekka
Niemelä, Mika
Jula, Antti
Raitakari, Olli T.
Lehtimäki, Terho
Eriksson, Johan G.
Widen, Elisabeth
Günel, Murat
Kurki, Mitja
von und zu Fraunberg, Mikael
Jääskeläinen, Juha E.
Hernesniemi, Juha
Järvelin, Marjo-Riitta
Pouta, Anneli
Newton-Cheh, Christopher
Salomaa, Veikko
Palotie, Aarno
Perola, Markus
author_sort Gaál, Emília Ilona
collection PubMed
description Although genome-wide association studies (GWAS) have identified hundreds of complex trait loci, the pathomechanisms of most remain elusive. Studying the genetics of risk factors predisposing to disease is an attractive approach to identify targets for functional studies. Intracranial aneurysms (IA) are rupture-prone pouches at cerebral artery branching sites. IA is a complex disease for which GWAS have identified five loci with strong association and a further 14 loci with suggestive association. To decipher potential underlying disease mechanisms, we tested whether there are IA loci that convey their effect through elevating blood pressure (BP), a strong risk factor of IA. We performed a meta-analysis of four population-based Finnish cohorts (n(FIN) = 11 266) not selected for IA, to assess the association of previously identified IA candidate loci (n = 19) with BP. We defined systolic BP (SBP), diastolic BP, mean arterial pressure, and pulse pressure as quantitative outcome variables. The most significant result was further tested for association in the ICBP-GWAS cohort of 200 000 individuals. We found that the suggestive IA locus at 5q23.2 in PRDM6 was significantly associated with SBP in individuals of European descent (p(FIN) = 3.01E-05, p(ICBP-GWAS) = 0.0007, p(ALL) = 8.13E-07). The risk allele of IA was associated with higher SBP. PRDM6 encodes a protein predominantly expressed in vascular smooth muscle cells. Our study connects a complex disease (IA) locus with a common risk factor for the disease (SBP). We hypothesize that common variants in PRDM6 can contribute to altered vascular wall structure, hence increasing SBP and predisposing to IA. True positive associations often fail to reach genome-wide significance in GWAS. Our findings show that analysis of traditional risk factors as intermediate phenotypes is an effective tool for deciphering hidden heritability. Further, we demonstrate that common disease loci identified in a population isolate may bear wider significance.
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spelling pubmed-33053432012-03-21 Intracranial Aneurysm Risk Locus 5q23.2 Is Associated with Elevated Systolic Blood Pressure Gaál, Emília Ilona Salo, Perttu Kristiansson, Kati Rehnström, Karola Kettunen, Johannes Sarin, Antti-Pekka Niemelä, Mika Jula, Antti Raitakari, Olli T. Lehtimäki, Terho Eriksson, Johan G. Widen, Elisabeth Günel, Murat Kurki, Mitja von und zu Fraunberg, Mikael Jääskeläinen, Juha E. Hernesniemi, Juha Järvelin, Marjo-Riitta Pouta, Anneli Newton-Cheh, Christopher Salomaa, Veikko Palotie, Aarno Perola, Markus PLoS Genet Research Article Although genome-wide association studies (GWAS) have identified hundreds of complex trait loci, the pathomechanisms of most remain elusive. Studying the genetics of risk factors predisposing to disease is an attractive approach to identify targets for functional studies. Intracranial aneurysms (IA) are rupture-prone pouches at cerebral artery branching sites. IA is a complex disease for which GWAS have identified five loci with strong association and a further 14 loci with suggestive association. To decipher potential underlying disease mechanisms, we tested whether there are IA loci that convey their effect through elevating blood pressure (BP), a strong risk factor of IA. We performed a meta-analysis of four population-based Finnish cohorts (n(FIN) = 11 266) not selected for IA, to assess the association of previously identified IA candidate loci (n = 19) with BP. We defined systolic BP (SBP), diastolic BP, mean arterial pressure, and pulse pressure as quantitative outcome variables. The most significant result was further tested for association in the ICBP-GWAS cohort of 200 000 individuals. We found that the suggestive IA locus at 5q23.2 in PRDM6 was significantly associated with SBP in individuals of European descent (p(FIN) = 3.01E-05, p(ICBP-GWAS) = 0.0007, p(ALL) = 8.13E-07). The risk allele of IA was associated with higher SBP. PRDM6 encodes a protein predominantly expressed in vascular smooth muscle cells. Our study connects a complex disease (IA) locus with a common risk factor for the disease (SBP). We hypothesize that common variants in PRDM6 can contribute to altered vascular wall structure, hence increasing SBP and predisposing to IA. True positive associations often fail to reach genome-wide significance in GWAS. Our findings show that analysis of traditional risk factors as intermediate phenotypes is an effective tool for deciphering hidden heritability. Further, we demonstrate that common disease loci identified in a population isolate may bear wider significance. Public Library of Science 2012-03-15 /pmc/articles/PMC3305343/ /pubmed/22438818 http://dx.doi.org/10.1371/journal.pgen.1002563 Text en Gaál et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Gaál, Emília Ilona
Salo, Perttu
Kristiansson, Kati
Rehnström, Karola
Kettunen, Johannes
Sarin, Antti-Pekka
Niemelä, Mika
Jula, Antti
Raitakari, Olli T.
Lehtimäki, Terho
Eriksson, Johan G.
Widen, Elisabeth
Günel, Murat
Kurki, Mitja
von und zu Fraunberg, Mikael
Jääskeläinen, Juha E.
Hernesniemi, Juha
Järvelin, Marjo-Riitta
Pouta, Anneli
Newton-Cheh, Christopher
Salomaa, Veikko
Palotie, Aarno
Perola, Markus
Intracranial Aneurysm Risk Locus 5q23.2 Is Associated with Elevated Systolic Blood Pressure
title Intracranial Aneurysm Risk Locus 5q23.2 Is Associated with Elevated Systolic Blood Pressure
title_full Intracranial Aneurysm Risk Locus 5q23.2 Is Associated with Elevated Systolic Blood Pressure
title_fullStr Intracranial Aneurysm Risk Locus 5q23.2 Is Associated with Elevated Systolic Blood Pressure
title_full_unstemmed Intracranial Aneurysm Risk Locus 5q23.2 Is Associated with Elevated Systolic Blood Pressure
title_short Intracranial Aneurysm Risk Locus 5q23.2 Is Associated with Elevated Systolic Blood Pressure
title_sort intracranial aneurysm risk locus 5q23.2 is associated with elevated systolic blood pressure
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3305343/
https://www.ncbi.nlm.nih.gov/pubmed/22438818
http://dx.doi.org/10.1371/journal.pgen.1002563
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