Loading…

Association of SNP41, SNP56 and a novel SNP in PDE4D gene with stroke and its subtypes

An association between phosphodiesterase 4D (PDE4D) gene and risk of stroke has been suggested by deCODE group in an Icelandic population. In the present case–control study we investigated the association of SNP41 (rs12153798) and SNP56 (rs702553) with ischemic stroke and stroke subtypes. Five hundr...

Full description

Saved in:
Bibliographic Details
Published in:Gene 2012-09, Vol.506 (1), p.31-35
Main Authors: Munshi, Anjana, Roy, Sitara, Thangaraj, Kumarasamy, Kaul, Subash, Babu, M. Sai, Jyothy, Akka
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c380t-556e3618e960d2ec7c82715b246e477113986109a2c89f1703a8d524f8c2c9063
cites cdi_FETCH-LOGICAL-c380t-556e3618e960d2ec7c82715b246e477113986109a2c89f1703a8d524f8c2c9063
container_end_page 35
container_issue 1
container_start_page 31
container_title Gene
container_volume 506
creator Munshi, Anjana
Roy, Sitara
Thangaraj, Kumarasamy
Kaul, Subash
Babu, M. Sai
Jyothy, Akka
description An association between phosphodiesterase 4D (PDE4D) gene and risk of stroke has been suggested by deCODE group in an Icelandic population. In the present case–control study we investigated the association of SNP41 (rs12153798) and SNP56 (rs702553) with ischemic stroke and stroke subtypes. Five hundred and sixteen ischemic stroke patients and 513 healthy age and sex matched controls were included in the study. The genotypes were determined by subjecting the PCR products to sequencing. Both the SNPs 56 and 41 associated significantly with stroke [adjusted OR=1.97; 95% CI (1.262–3.082); p=0.003: adjusted OR=5.42; 95% CI (3.45–8.5); pG was found while sequencing the PCR products including SNP56. This novel SNP was found in patients as well as controls but did not show a significant association with the disease. We found significant association of SNPs 56 and 41 with large artery atherosclerosis, lacunar and cardioembolic stroke. In conclusion PDE4D gene plays a key part in the pathogenesis of ischemic stroke in the South Indian population from Andhra Pradesh. ► We evaluated the association of variants of PDE4D gene with ischemic stroke. ► SNP41 and SNP56 associated significantly with the disease. ► A novel SNP was found but did not associate with the disease.
doi_str_mv 10.1016/j.gene.2012.06.079
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1032610345</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0378111912007895</els_id><sourcerecordid>1032610345</sourcerecordid><originalsourceid>FETCH-LOGICAL-c380t-556e3618e960d2ec7c82715b246e477113986109a2c89f1703a8d524f8c2c9063</originalsourceid><addsrcrecordid>eNp9kE1P3DAQhq2qVdkCf6CH1kcOTRjbsWNLvSCgHxIqSHxcLa8zAS-78WJnQfx7HJb2WF9Gsp55Z-Yh5DODmgFTh4v6FgesOTBeg6qhNe_IjOnWVABCvyczEK2uGGNmh3zKeQHlSck_kh3O25YZJmfk5ijn6IMbQxxo7Onln4uGfZuKVNQNHXV0iI-4nH5oGOjFyWlzQqe59CmMdzSPKd7jKxnGTPNmPj6vMe-RD71bZtx_q7vk-sfp1fGv6uz85-_jo7PKCw1jJaVCoZhGo6Dj6FuvecvknDcKm7IiE0YrBsZxr03PWhBOd5I3vfbcG1Bilxxsc9cpPmwwj3YVssfl0g0YN9kyELwEiEYWlG9Rn2LOCXu7TmHl0nOB7OTTLux0l518WlC2-CxNX97yN_MVdv9a_goswNct0Lto3W0K2V5flgRZXDdCaSjE9y2BxcNjwGSzDzh47EJCP9ouhv9t8AKkAYsH</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1032610345</pqid></control><display><type>article</type><title>Association of SNP41, SNP56 and a novel SNP in PDE4D gene with stroke and its subtypes</title><source>ScienceDirect Journals</source><creator>Munshi, Anjana ; Roy, Sitara ; Thangaraj, Kumarasamy ; Kaul, Subash ; Babu, M. Sai ; Jyothy, Akka</creator><creatorcontrib>Munshi, Anjana ; Roy, Sitara ; Thangaraj, Kumarasamy ; Kaul, Subash ; Babu, M. Sai ; Jyothy, Akka</creatorcontrib><description>An association between phosphodiesterase 4D (PDE4D) gene and risk of stroke has been suggested by deCODE group in an Icelandic population. In the present case–control study we investigated the association of SNP41 (rs12153798) and SNP56 (rs702553) with ischemic stroke and stroke subtypes. Five hundred and sixteen ischemic stroke patients and 513 healthy age and sex matched controls were included in the study. The genotypes were determined by subjecting the PCR products to sequencing. Both the SNPs 56 and 41 associated significantly with stroke [adjusted OR=1.97; 95% CI (1.262–3.082); p=0.003: adjusted OR=5.42; 95% CI (3.45–8.5); p&lt;0.001 respectively]. In addition to this, a novel SNP at position 59736747 T&gt;G was found while sequencing the PCR products including SNP56. This novel SNP was found in patients as well as controls but did not show a significant association with the disease. We found significant association of SNPs 56 and 41 with large artery atherosclerosis, lacunar and cardioembolic stroke. In conclusion PDE4D gene plays a key part in the pathogenesis of ischemic stroke in the South Indian population from Andhra Pradesh. ► We evaluated the association of variants of PDE4D gene with ischemic stroke. ► SNP41 and SNP56 associated significantly with the disease. ► A novel SNP was found but did not associate with the disease.</description><identifier>ISSN: 0378-1119</identifier><identifier>EISSN: 1879-0038</identifier><identifier>DOI: 10.1016/j.gene.2012.06.079</identifier><identifier>PMID: 22771915</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Adult ; Aged ; atherosclerosis ; Atherosclerosis - complications ; Atherosclerosis - enzymology ; Atherosclerosis - genetics ; Base Sequence ; Case-Control Studies ; Cyclic Nucleotide Phosphodiesterases, Type 3 - genetics ; Cyclic Nucleotide Phosphodiesterases, Type 4 ; Embolism - complications ; Embolism - enzymology ; Embolism - genetics ; Female ; Gene Frequency ; genes ; Genetic Association Studies ; genotype ; Heart Diseases - complications ; Heart Diseases - enzymology ; Heart Diseases - genetics ; Heterozygote ; Homozygote ; Humans ; India ; Ischemic stroke ; Male ; Middle Aged ; Novel SNP ; pathogenesis ; patients ; Phosphodiesterase 4D ; Polymerase Chain Reaction ; Polymorphism, Single Nucleotide ; risk ; Single nucleotide polymorphism ; stroke ; Stroke - classification ; Stroke - enzymology ; Stroke - etiology ; Stroke - genetics ; Stroke subtypes ; Stroke, Lacunar - enzymology ; Stroke, Lacunar - genetics</subject><ispartof>Gene, 2012-09, Vol.506 (1), p.31-35</ispartof><rights>2012 Elsevier B.V.</rights><rights>Copyright © 2012 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c380t-556e3618e960d2ec7c82715b246e477113986109a2c89f1703a8d524f8c2c9063</citedby><cites>FETCH-LOGICAL-c380t-556e3618e960d2ec7c82715b246e477113986109a2c89f1703a8d524f8c2c9063</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22771915$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Munshi, Anjana</creatorcontrib><creatorcontrib>Roy, Sitara</creatorcontrib><creatorcontrib>Thangaraj, Kumarasamy</creatorcontrib><creatorcontrib>Kaul, Subash</creatorcontrib><creatorcontrib>Babu, M. Sai</creatorcontrib><creatorcontrib>Jyothy, Akka</creatorcontrib><title>Association of SNP41, SNP56 and a novel SNP in PDE4D gene with stroke and its subtypes</title><title>Gene</title><addtitle>Gene</addtitle><description>An association between phosphodiesterase 4D (PDE4D) gene and risk of stroke has been suggested by deCODE group in an Icelandic population. In the present case–control study we investigated the association of SNP41 (rs12153798) and SNP56 (rs702553) with ischemic stroke and stroke subtypes. Five hundred and sixteen ischemic stroke patients and 513 healthy age and sex matched controls were included in the study. The genotypes were determined by subjecting the PCR products to sequencing. Both the SNPs 56 and 41 associated significantly with stroke [adjusted OR=1.97; 95% CI (1.262–3.082); p=0.003: adjusted OR=5.42; 95% CI (3.45–8.5); p&lt;0.001 respectively]. In addition to this, a novel SNP at position 59736747 T&gt;G was found while sequencing the PCR products including SNP56. This novel SNP was found in patients as well as controls but did not show a significant association with the disease. We found significant association of SNPs 56 and 41 with large artery atherosclerosis, lacunar and cardioembolic stroke. In conclusion PDE4D gene plays a key part in the pathogenesis of ischemic stroke in the South Indian population from Andhra Pradesh. ► We evaluated the association of variants of PDE4D gene with ischemic stroke. ► SNP41 and SNP56 associated significantly with the disease. ► A novel SNP was found but did not associate with the disease.</description><subject>Adult</subject><subject>Aged</subject><subject>atherosclerosis</subject><subject>Atherosclerosis - complications</subject><subject>Atherosclerosis - enzymology</subject><subject>Atherosclerosis - genetics</subject><subject>Base Sequence</subject><subject>Case-Control Studies</subject><subject>Cyclic Nucleotide Phosphodiesterases, Type 3 - genetics</subject><subject>Cyclic Nucleotide Phosphodiesterases, Type 4</subject><subject>Embolism - complications</subject><subject>Embolism - enzymology</subject><subject>Embolism - genetics</subject><subject>Female</subject><subject>Gene Frequency</subject><subject>genes</subject><subject>Genetic Association Studies</subject><subject>genotype</subject><subject>Heart Diseases - complications</subject><subject>Heart Diseases - enzymology</subject><subject>Heart Diseases - genetics</subject><subject>Heterozygote</subject><subject>Homozygote</subject><subject>Humans</subject><subject>India</subject><subject>Ischemic stroke</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Novel SNP</subject><subject>pathogenesis</subject><subject>patients</subject><subject>Phosphodiesterase 4D</subject><subject>Polymerase Chain Reaction</subject><subject>Polymorphism, Single Nucleotide</subject><subject>risk</subject><subject>Single nucleotide polymorphism</subject><subject>stroke</subject><subject>Stroke - classification</subject><subject>Stroke - enzymology</subject><subject>Stroke - etiology</subject><subject>Stroke - genetics</subject><subject>Stroke subtypes</subject><subject>Stroke, Lacunar - enzymology</subject><subject>Stroke, Lacunar - genetics</subject><issn>0378-1119</issn><issn>1879-0038</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNp9kE1P3DAQhq2qVdkCf6CH1kcOTRjbsWNLvSCgHxIqSHxcLa8zAS-78WJnQfx7HJb2WF9Gsp55Z-Yh5DODmgFTh4v6FgesOTBeg6qhNe_IjOnWVABCvyczEK2uGGNmh3zKeQHlSck_kh3O25YZJmfk5ijn6IMbQxxo7Onln4uGfZuKVNQNHXV0iI-4nH5oGOjFyWlzQqe59CmMdzSPKd7jKxnGTPNmPj6vMe-RD71bZtx_q7vk-sfp1fGv6uz85-_jo7PKCw1jJaVCoZhGo6Dj6FuvecvknDcKm7IiE0YrBsZxr03PWhBOd5I3vfbcG1Bilxxsc9cpPmwwj3YVssfl0g0YN9kyELwEiEYWlG9Rn2LOCXu7TmHl0nOB7OTTLux0l518WlC2-CxNX97yN_MVdv9a_goswNct0Lto3W0K2V5flgRZXDdCaSjE9y2BxcNjwGSzDzh47EJCP9ouhv9t8AKkAYsH</recordid><startdate>20120910</startdate><enddate>20120910</enddate><creator>Munshi, Anjana</creator><creator>Roy, Sitara</creator><creator>Thangaraj, Kumarasamy</creator><creator>Kaul, Subash</creator><creator>Babu, M. Sai</creator><creator>Jyothy, Akka</creator><general>Elsevier B.V</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20120910</creationdate><title>Association of SNP41, SNP56 and a novel SNP in PDE4D gene with stroke and its subtypes</title><author>Munshi, Anjana ; Roy, Sitara ; Thangaraj, Kumarasamy ; Kaul, Subash ; Babu, M. Sai ; Jyothy, Akka</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c380t-556e3618e960d2ec7c82715b246e477113986109a2c89f1703a8d524f8c2c9063</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adult</topic><topic>Aged</topic><topic>atherosclerosis</topic><topic>Atherosclerosis - complications</topic><topic>Atherosclerosis - enzymology</topic><topic>Atherosclerosis - genetics</topic><topic>Base Sequence</topic><topic>Case-Control Studies</topic><topic>Cyclic Nucleotide Phosphodiesterases, Type 3 - genetics</topic><topic>Cyclic Nucleotide Phosphodiesterases, Type 4</topic><topic>Embolism - complications</topic><topic>Embolism - enzymology</topic><topic>Embolism - genetics</topic><topic>Female</topic><topic>Gene Frequency</topic><topic>genes</topic><topic>Genetic Association Studies</topic><topic>genotype</topic><topic>Heart Diseases - complications</topic><topic>Heart Diseases - enzymology</topic><topic>Heart Diseases - genetics</topic><topic>Heterozygote</topic><topic>Homozygote</topic><topic>Humans</topic><topic>India</topic><topic>Ischemic stroke</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Novel SNP</topic><topic>pathogenesis</topic><topic>patients</topic><topic>Phosphodiesterase 4D</topic><topic>Polymerase Chain Reaction</topic><topic>Polymorphism, Single Nucleotide</topic><topic>risk</topic><topic>Single nucleotide polymorphism</topic><topic>stroke</topic><topic>Stroke - classification</topic><topic>Stroke - enzymology</topic><topic>Stroke - etiology</topic><topic>Stroke - genetics</topic><topic>Stroke subtypes</topic><topic>Stroke, Lacunar - enzymology</topic><topic>Stroke, Lacunar - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Munshi, Anjana</creatorcontrib><creatorcontrib>Roy, Sitara</creatorcontrib><creatorcontrib>Thangaraj, Kumarasamy</creatorcontrib><creatorcontrib>Kaul, Subash</creatorcontrib><creatorcontrib>Babu, M. Sai</creatorcontrib><creatorcontrib>Jyothy, Akka</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Gene</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Munshi, Anjana</au><au>Roy, Sitara</au><au>Thangaraj, Kumarasamy</au><au>Kaul, Subash</au><au>Babu, M. Sai</au><au>Jyothy, Akka</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association of SNP41, SNP56 and a novel SNP in PDE4D gene with stroke and its subtypes</atitle><jtitle>Gene</jtitle><addtitle>Gene</addtitle><date>2012-09-10</date><risdate>2012</risdate><volume>506</volume><issue>1</issue><spage>31</spage><epage>35</epage><pages>31-35</pages><issn>0378-1119</issn><eissn>1879-0038</eissn><abstract>An association between phosphodiesterase 4D (PDE4D) gene and risk of stroke has been suggested by deCODE group in an Icelandic population. In the present case–control study we investigated the association of SNP41 (rs12153798) and SNP56 (rs702553) with ischemic stroke and stroke subtypes. Five hundred and sixteen ischemic stroke patients and 513 healthy age and sex matched controls were included in the study. The genotypes were determined by subjecting the PCR products to sequencing. Both the SNPs 56 and 41 associated significantly with stroke [adjusted OR=1.97; 95% CI (1.262–3.082); p=0.003: adjusted OR=5.42; 95% CI (3.45–8.5); p&lt;0.001 respectively]. In addition to this, a novel SNP at position 59736747 T&gt;G was found while sequencing the PCR products including SNP56. This novel SNP was found in patients as well as controls but did not show a significant association with the disease. We found significant association of SNPs 56 and 41 with large artery atherosclerosis, lacunar and cardioembolic stroke. In conclusion PDE4D gene plays a key part in the pathogenesis of ischemic stroke in the South Indian population from Andhra Pradesh. ► We evaluated the association of variants of PDE4D gene with ischemic stroke. ► SNP41 and SNP56 associated significantly with the disease. ► A novel SNP was found but did not associate with the disease.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>22771915</pmid><doi>10.1016/j.gene.2012.06.079</doi><tpages>5</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0378-1119
ispartof Gene, 2012-09, Vol.506 (1), p.31-35
issn 0378-1119
1879-0038
language eng
recordid cdi_proquest_miscellaneous_1032610345
source ScienceDirect Journals
subjects Adult
Aged
atherosclerosis
Atherosclerosis - complications
Atherosclerosis - enzymology
Atherosclerosis - genetics
Base Sequence
Case-Control Studies
Cyclic Nucleotide Phosphodiesterases, Type 3 - genetics
Cyclic Nucleotide Phosphodiesterases, Type 4
Embolism - complications
Embolism - enzymology
Embolism - genetics
Female
Gene Frequency
genes
Genetic Association Studies
genotype
Heart Diseases - complications
Heart Diseases - enzymology
Heart Diseases - genetics
Heterozygote
Homozygote
Humans
India
Ischemic stroke
Male
Middle Aged
Novel SNP
pathogenesis
patients
Phosphodiesterase 4D
Polymerase Chain Reaction
Polymorphism, Single Nucleotide
risk
Single nucleotide polymorphism
stroke
Stroke - classification
Stroke - enzymology
Stroke - etiology
Stroke - genetics
Stroke subtypes
Stroke, Lacunar - enzymology
Stroke, Lacunar - genetics
title Association of SNP41, SNP56 and a novel SNP in PDE4D gene with stroke and its subtypes
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-24T03%3A19%3A13IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Association%20of%20SNP41,%20SNP56%20and%20a%20novel%20SNP%20in%20PDE4D%20gene%20with%20stroke%20and%20its%20subtypes&rft.jtitle=Gene&rft.au=Munshi,%20Anjana&rft.date=2012-09-10&rft.volume=506&rft.issue=1&rft.spage=31&rft.epage=35&rft.pages=31-35&rft.issn=0378-1119&rft.eissn=1879-0038&rft_id=info:doi/10.1016/j.gene.2012.06.079&rft_dat=%3Cproquest_cross%3E1032610345%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c380t-556e3618e960d2ec7c82715b246e477113986109a2c89f1703a8d524f8c2c9063%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1032610345&rft_id=info:pmid/22771915&rfr_iscdi=true