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A Common Missense Variant in the ATP Receptor P2X7 Is Associated with Reduced Risk of Cardiovascular Events.

Gidlöf, Olof LU ; Smith, Gustav LU ; Melander, Olle LU ; Lövkvist, Håkan LU ; Hedblad, Bo LU ; Engström, Gunnar LU ; Nilsson, Peter LU ; Carlson, Joyce LU ; Berglund, Göran LU and Olsson, Sandra LU , et al. (2012) In PLoS One 7(5).
Abstract
BACKGROUND AND PURPOSE:

Extracellular adenosine triphosphate (ATP) regulates inflammatory cells by activation of the P2X(7) receptor. We hypothesized that polymorphisms in P2RX7 influence the risk of ischemic heart disease (IHD), ischemic stroke (IS) and cardiovascular risk factors and tested this hypothesis using genetic association studies.



METHODS:

Two loss-of-function SNPs in P2RX7 were genotyped in 1244 IHD cases and 2488 controls as well as 5969 individuals with cardiovascular risk factors. Eleven SNPs in a 250 kb region on chromosome 12 spanning P2RX7 as well as neighboring genes OASL, P2RX4 and CAMKK2 were genotyped in 4138 individuals with IS and 2528 controls. Association was examined using... (More)
BACKGROUND AND PURPOSE:

Extracellular adenosine triphosphate (ATP) regulates inflammatory cells by activation of the P2X(7) receptor. We hypothesized that polymorphisms in P2RX7 influence the risk of ischemic heart disease (IHD), ischemic stroke (IS) and cardiovascular risk factors and tested this hypothesis using genetic association studies.



METHODS:

Two loss-of-function SNPs in P2RX7 were genotyped in 1244 IHD cases and 2488 controls as well as 5969 individuals with cardiovascular risk factors. Eleven SNPs in a 250 kb region on chromosome 12 spanning P2RX7 as well as neighboring genes OASL, P2RX4 and CAMKK2 were genotyped in 4138 individuals with IS and 2528 controls. Association was examined using linear and logistic regression models with an additive genetic model.



RESULTS:

The common loss-of-function variant rs3751143 was significantly associated with a decreased risk of IHD in smokers (P = 0.03) as well as decreased risk of IS (OR 0.89; 95% CI = 0.81-0.97; P = 0.012). In addition, an intronic SNP in CAMKK2, rs2686342, were associated with a decreased risk of IS (OR 0.89; 95% CI = 0.82-0.97; P = 0.011). In subgroup analyses, both SNPs were associated with decreased risk of IS in individuals with hypertension (P = 0.045 and 0.015, respectively).



CONCLUSIONS:

A common loss-of-function missense variant in the gene encoding the P2X(7) receptor is associated with reduced risk of IS and with IHD in smokers. These findings might implicate a role of purinergic signaling in atherogenesis or atherothrombosis. (Less)
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organization
publishing date
type
Contribution to journal
publication status
published
subject
in
PLoS One
volume
7
issue
5
publisher
Public Library of Science
external identifiers
  • WOS:000305342300050
  • PMID:22662160
  • Scopus:84861472676
ISSN
1932-6203
DOI
10.1371/journal.pone.0037491
language
English
LU publication?
yes
id
4c246922-1c49-4c8d-b53c-9c7cf39f1968 (old id 2859840)
alternative location
http://www.ncbi.nlm.nih.gov/pubmed/22662160?dopt=Abstract
date added to LUP
2012-07-04 12:19:31
date last changed
2016-12-04 04:38:23
@misc{4c246922-1c49-4c8d-b53c-9c7cf39f1968,
  abstract     = {BACKGROUND AND PURPOSE:<br/><br>
Extracellular adenosine triphosphate (ATP) regulates inflammatory cells by activation of the P2X(7) receptor. We hypothesized that polymorphisms in P2RX7 influence the risk of ischemic heart disease (IHD), ischemic stroke (IS) and cardiovascular risk factors and tested this hypothesis using genetic association studies.<br/><br>
<br/><br>
METHODS:<br/><br>
Two loss-of-function SNPs in P2RX7 were genotyped in 1244 IHD cases and 2488 controls as well as 5969 individuals with cardiovascular risk factors. Eleven SNPs in a 250 kb region on chromosome 12 spanning P2RX7 as well as neighboring genes OASL, P2RX4 and CAMKK2 were genotyped in 4138 individuals with IS and 2528 controls. Association was examined using linear and logistic regression models with an additive genetic model.<br/><br>
<br/><br>
RESULTS:<br/><br>
The common loss-of-function variant rs3751143 was significantly associated with a decreased risk of IHD in smokers (P = 0.03) as well as decreased risk of IS (OR 0.89; 95% CI = 0.81-0.97; P = 0.012). In addition, an intronic SNP in CAMKK2, rs2686342, were associated with a decreased risk of IS (OR 0.89; 95% CI = 0.82-0.97; P = 0.011). In subgroup analyses, both SNPs were associated with decreased risk of IS in individuals with hypertension (P = 0.045 and 0.015, respectively).<br/><br>
<br/><br>
CONCLUSIONS:<br/><br>
A common loss-of-function missense variant in the gene encoding the P2X(7) receptor is associated with reduced risk of IS and with IHD in smokers. These findings might implicate a role of purinergic signaling in atherogenesis or atherothrombosis.},
  author       = {Gidlöf, Olof and Smith, Gustav and Melander, Olle and Lövkvist, Håkan and Hedblad, Bo and Engström, Gunnar and Nilsson, Peter and Carlson, Joyce and Berglund, Göran and Olsson, Sandra and Jood, Katarina and Jern, Christina and Norrving, Bo and Lindgren, Arne and Erlinge, David},
  issn         = {1932-6203},
  language     = {eng},
  number       = {5},
  publisher    = {ARRAY(0x81a5da0)},
  series       = {PLoS One},
  title        = {A Common Missense Variant in the ATP Receptor P2X7 Is Associated with Reduced Risk of Cardiovascular Events.},
  url          = {http://dx.doi.org/10.1371/journal.pone.0037491},
  volume       = {7},
  year         = {2012},
}