The Chromosome 9p21 CVD- and T2D-Associated Regions in a Norwegian Population (The HUNT2 Survey)
Background. Two adjacent regions upstream CDKN2B on chromosome 9p21 have been associated with type 2 diabetes (T2D) and progression of cardiovascular disease (CVD).The precise location and number of risk variants have not been completely delineated and a possible synergistic relationship between the...
Published in: | International Journal of Endocrinology |
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Online Access: | http://hdl.handle.net/11250/2357317 https://doi.org/10.1155/2015/164652 |
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ftntnutrondheimi:oai:ntnuopen.ntnu.no:11250/2357317 2023-05-15T16:34:11+02:00 The Chromosome 9p21 CVD- and T2D-Associated Regions in a Norwegian Population (The HUNT2 Survey) Helgeland, Øyvind Hertel, Jens Kristoffer Molven, Anders Ræder, Helge Platou, Carl Geoffrey Parrinder Midthjell, Kristian Hveem, Kristian Nygård, Ottar Njølstad, Pål Rasmus Johansson, Stefan 2015-04-08T12:02:01Z http://hdl.handle.net/11250/2357317 https://doi.org/10.1155/2015/164652 eng eng Hindawi Publishing Corporation International Journal of Endocrinology 2015 urn:issn:1687-8345 http://hdl.handle.net/11250/2357317 https://doi.org/10.1155/2015/164652 cristin:1229721 International Journal of Endocrinology VDP::Medisinske fag: 700::Klinisk medisinske fag: 750::Endokrinologi: 774 VDP::Midical sciences: 700::Clinical medical sciences: 750::Endocrinology: 774 VDP::Medisinske fag: 700::Basale medisinske odontologiske og veterinærmedisinske fag: 710::Medisinsk genetikk: 714 VDP::Midical sciences: 700::Basic medical dental and veterinary sciences: 710::Medical genetics: 714 Journal article Peer reviewed 2015 ftntnutrondheimi https://doi.org/10.1155/2015/164652 2019-09-17T06:50:39Z Background. Two adjacent regions upstream CDKN2B on chromosome 9p21 have been associated with type 2 diabetes (T2D) and progression of cardiovascular disease (CVD).The precise location and number of risk variants have not been completely delineated and a possible synergistic relationship between the adjacent regions is not fully addressed. By a population based cross-sectional case-control design, we genotyped 18 SNPs upstream of CDKN2B tagging 138 kb in and around two LD-blocks associated with CVD and T2D and investigated associations with T2D, angina pectoris (AP), myocardial infarction (MI), coronary heart disease (CHD; AP or AMI), and stroke using 5,564 subjects from HUNT2. Results. Single point and haplotype analysis showed evidence for only one common T2D risk haplotype (rs10757282|rs10811661: OR = 1.19, ????? = 2.0 × 10−3) in the region.We confirmed the strong association between SNPs in the 60 kb CVD region with AP, MI, and CHD(????? < 0.01). Conditioning on the lead SNPs in the region, we observed two suggestive independent single SNP association signals for MI, rs2065501 (????? = 0.03) and rs3217986 (????? = 0.04). Conclusions. We confirmed the association of known variants within the 9p21 interval with T2D and CHD. Our results further suggest that additional CHD susceptibility variants exist in this region. Copyright © Øyvind Helgeland et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Article in Journal/Newspaper Helgeland NTNU Open Archive (Norwegian University of Science and Technology) Helgeland International Journal of Endocrinology 2015 1 9 |
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Open Polar |
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NTNU Open Archive (Norwegian University of Science and Technology) |
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ftntnutrondheimi |
language |
English |
topic |
VDP::Medisinske fag: 700::Klinisk medisinske fag: 750::Endokrinologi: 774 VDP::Midical sciences: 700::Clinical medical sciences: 750::Endocrinology: 774 VDP::Medisinske fag: 700::Basale medisinske odontologiske og veterinærmedisinske fag: 710::Medisinsk genetikk: 714 VDP::Midical sciences: 700::Basic medical dental and veterinary sciences: 710::Medical genetics: 714 |
spellingShingle |
VDP::Medisinske fag: 700::Klinisk medisinske fag: 750::Endokrinologi: 774 VDP::Midical sciences: 700::Clinical medical sciences: 750::Endocrinology: 774 VDP::Medisinske fag: 700::Basale medisinske odontologiske og veterinærmedisinske fag: 710::Medisinsk genetikk: 714 VDP::Midical sciences: 700::Basic medical dental and veterinary sciences: 710::Medical genetics: 714 Helgeland, Øyvind Hertel, Jens Kristoffer Molven, Anders Ræder, Helge Platou, Carl Geoffrey Parrinder Midthjell, Kristian Hveem, Kristian Nygård, Ottar Njølstad, Pål Rasmus Johansson, Stefan The Chromosome 9p21 CVD- and T2D-Associated Regions in a Norwegian Population (The HUNT2 Survey) |
topic_facet |
VDP::Medisinske fag: 700::Klinisk medisinske fag: 750::Endokrinologi: 774 VDP::Midical sciences: 700::Clinical medical sciences: 750::Endocrinology: 774 VDP::Medisinske fag: 700::Basale medisinske odontologiske og veterinærmedisinske fag: 710::Medisinsk genetikk: 714 VDP::Midical sciences: 700::Basic medical dental and veterinary sciences: 710::Medical genetics: 714 |
description |
Background. Two adjacent regions upstream CDKN2B on chromosome 9p21 have been associated with type 2 diabetes (T2D) and progression of cardiovascular disease (CVD).The precise location and number of risk variants have not been completely delineated and a possible synergistic relationship between the adjacent regions is not fully addressed. By a population based cross-sectional case-control design, we genotyped 18 SNPs upstream of CDKN2B tagging 138 kb in and around two LD-blocks associated with CVD and T2D and investigated associations with T2D, angina pectoris (AP), myocardial infarction (MI), coronary heart disease (CHD; AP or AMI), and stroke using 5,564 subjects from HUNT2. Results. Single point and haplotype analysis showed evidence for only one common T2D risk haplotype (rs10757282|rs10811661: OR = 1.19, ????? = 2.0 × 10−3) in the region.We confirmed the strong association between SNPs in the 60 kb CVD region with AP, MI, and CHD(????? < 0.01). Conditioning on the lead SNPs in the region, we observed two suggestive independent single SNP association signals for MI, rs2065501 (????? = 0.03) and rs3217986 (????? = 0.04). Conclusions. We confirmed the association of known variants within the 9p21 interval with T2D and CHD. Our results further suggest that additional CHD susceptibility variants exist in this region. Copyright © Øyvind Helgeland et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
format |
Article in Journal/Newspaper |
author |
Helgeland, Øyvind Hertel, Jens Kristoffer Molven, Anders Ræder, Helge Platou, Carl Geoffrey Parrinder Midthjell, Kristian Hveem, Kristian Nygård, Ottar Njølstad, Pål Rasmus Johansson, Stefan |
author_facet |
Helgeland, Øyvind Hertel, Jens Kristoffer Molven, Anders Ræder, Helge Platou, Carl Geoffrey Parrinder Midthjell, Kristian Hveem, Kristian Nygård, Ottar Njølstad, Pål Rasmus Johansson, Stefan |
author_sort |
Helgeland, Øyvind |
title |
The Chromosome 9p21 CVD- and T2D-Associated Regions in a Norwegian Population (The HUNT2 Survey) |
title_short |
The Chromosome 9p21 CVD- and T2D-Associated Regions in a Norwegian Population (The HUNT2 Survey) |
title_full |
The Chromosome 9p21 CVD- and T2D-Associated Regions in a Norwegian Population (The HUNT2 Survey) |
title_fullStr |
The Chromosome 9p21 CVD- and T2D-Associated Regions in a Norwegian Population (The HUNT2 Survey) |
title_full_unstemmed |
The Chromosome 9p21 CVD- and T2D-Associated Regions in a Norwegian Population (The HUNT2 Survey) |
title_sort |
chromosome 9p21 cvd- and t2d-associated regions in a norwegian population (the hunt2 survey) |
publisher |
Hindawi Publishing Corporation |
publishDate |
2015 |
url |
http://hdl.handle.net/11250/2357317 https://doi.org/10.1155/2015/164652 |
geographic |
Helgeland |
geographic_facet |
Helgeland |
genre |
Helgeland |
genre_facet |
Helgeland |
op_source |
International Journal of Endocrinology |
op_relation |
International Journal of Endocrinology 2015 urn:issn:1687-8345 http://hdl.handle.net/11250/2357317 https://doi.org/10.1155/2015/164652 cristin:1229721 |
op_doi |
https://doi.org/10.1155/2015/164652 |
container_title |
International Journal of Endocrinology |
container_volume |
2015 |
container_start_page |
1 |
op_container_end_page |
9 |
_version_ |
1766023933653417984 |