CYP11B1 gene polymorphisms and susceptibility to ischemic stroke in a Chinese Han population
Ischemic stroke (IS) is the major cause of death and disability. While previous studies confirmed that is closely associated with IS, the present study aimed to analyze the impact of gene polymorphisms on the IS susceptibility. The present study genotyped six single nucleotide polymorphisms (SNPs) (...
Saved in:
Published in | Frontiers in neuroscience Vol. 16; p. 1030551 |
---|---|
Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media S.A
01.12.2022
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Ischemic stroke (IS) is the major cause of death and disability. While previous studies confirmed that
is closely associated with IS, the present study aimed to analyze the impact of
gene polymorphisms on the IS susceptibility.
The present study genotyped six single nucleotide polymorphisms (SNPs) (including rs4736312, rs5017238, rs5301, rs5283, rs6410, and rs4534) of
in peripheral blood samples from IS and control populations. Logistic regression analysis was used to analyze the association between the SNPs and IS risk. The multifactor dimensionality reduction (MDR) method was used to determine the roles of SNP-SNP interactions in IS.
The present study showed that rs5283 was associated with an increased susceptibility to IS [odds ratio (OR) 1.81,
= 0.012]. On the contrary, rs6410 had a protective influence on IS risk (OR 0.56,
= 0.020). Stratified analyses indicated that rs5283 could enhance the risk of IS in subjects aged >63 years (OR 2.41,
= 0.011), of female gender (OR 3.31,
= 0.001), that do not smoke (OR 1.64,
= 0.005), and with hypertension (OR 2.07,
= 0.003). Whereas, rs6410 was related to a lower susceptibility to IS in subjects aged >63 years (OR 0.43,
= 0.032), of female gender (OR 0.30,
= 0.006), do not smoke (OR 0.42,
= 0.017), and with hypertension (OR 0.52,
= 0.022). Besides, rs4736312 reduced the IS susceptibility in non-smokers (OR 0.69,
= 0.031). Rs4534 had a risk-decreasing impact on IS in non-drinking (OR 0.54,
= 0.016). Moreover, the results of the MDR analysis corroborate that the best prediction model for IS was rs5283.
This study revealed that
gene polymorphisms strongly correlated with IS in the Chinese Han population. |
---|---|
AbstractList | Ischemic stroke (IS) is the major cause of death and disability. While previous studies confirmed that CYP11B1 is closely associated with IS, the present study aimed to analyze the impact of CYP11B1 gene polymorphisms on the IS susceptibility.ObjectivesIschemic stroke (IS) is the major cause of death and disability. While previous studies confirmed that CYP11B1 is closely associated with IS, the present study aimed to analyze the impact of CYP11B1 gene polymorphisms on the IS susceptibility.The present study genotyped six single nucleotide polymorphisms (SNPs) (including rs4736312, rs5017238, rs5301, rs5283, rs6410, and rs4534) of CYP11B1 in peripheral blood samples from IS and control populations. Logistic regression analysis was used to analyze the association between the SNPs and IS risk. The multifactor dimensionality reduction (MDR) method was used to determine the roles of SNP-SNP interactions in IS.MethodsThe present study genotyped six single nucleotide polymorphisms (SNPs) (including rs4736312, rs5017238, rs5301, rs5283, rs6410, and rs4534) of CYP11B1 in peripheral blood samples from IS and control populations. Logistic regression analysis was used to analyze the association between the SNPs and IS risk. The multifactor dimensionality reduction (MDR) method was used to determine the roles of SNP-SNP interactions in IS.The present study showed that rs5283 was associated with an increased susceptibility to IS [odds ratio (OR) 1.81, p = 0.012]. On the contrary, rs6410 had a protective influence on IS risk (OR 0.56, p = 0.020). Stratified analyses indicated that rs5283 could enhance the risk of IS in subjects aged >63 years (OR 2.41, p = 0.011), of female gender (OR 3.31, p = 0.001), that do not smoke (OR 1.64, p = 0.005), and with hypertension (OR 2.07, p = 0.003). Whereas, rs6410 was related to a lower susceptibility to IS in subjects aged >63 years (OR 0.43, p = 0.032), of female gender (OR 0.30, p = 0.006), do not smoke (OR 0.42, p = 0.017), and with hypertension (OR 0.52, p = 0.022). Besides, rs4736312 reduced the IS susceptibility in non-smokers (OR 0.69, p = 0.031). Rs4534 had a risk-decreasing impact on IS in non-drinking (OR 0.54, p = 0.016). Moreover, the results of the MDR analysis corroborate that the best prediction model for IS was rs5283.ResultsThe present study showed that rs5283 was associated with an increased susceptibility to IS [odds ratio (OR) 1.81, p = 0.012]. On the contrary, rs6410 had a protective influence on IS risk (OR 0.56, p = 0.020). Stratified analyses indicated that rs5283 could enhance the risk of IS in subjects aged >63 years (OR 2.41, p = 0.011), of female gender (OR 3.31, p = 0.001), that do not smoke (OR 1.64, p = 0.005), and with hypertension (OR 2.07, p = 0.003). Whereas, rs6410 was related to a lower susceptibility to IS in subjects aged >63 years (OR 0.43, p = 0.032), of female gender (OR 0.30, p = 0.006), do not smoke (OR 0.42, p = 0.017), and with hypertension (OR 0.52, p = 0.022). Besides, rs4736312 reduced the IS susceptibility in non-smokers (OR 0.69, p = 0.031). Rs4534 had a risk-decreasing impact on IS in non-drinking (OR 0.54, p = 0.016). Moreover, the results of the MDR analysis corroborate that the best prediction model for IS was rs5283.This study revealed that CYP11B1 gene polymorphisms strongly correlated with IS in the Chinese Han population.ConclusionThis study revealed that CYP11B1 gene polymorphisms strongly correlated with IS in the Chinese Han population. ObjectivesIschemic stroke (IS) is the major cause of death and disability. While previous studies confirmed that CYP11B1 is closely associated with IS, the present study aimed to analyze the impact of CYP11B1 gene polymorphisms on the IS susceptibility.MethodsThe present study genotyped six single nucleotide polymorphisms (SNPs) (including rs4736312, rs5017238, rs5301, rs5283, rs6410, and rs4534) of CYP11B1 in peripheral blood samples from IS and control populations. Logistic regression analysis was used to analyze the association between the SNPs and IS risk. The multifactor dimensionality reduction (MDR) method was used to determine the roles of SNP–SNP interactions in IS.ResultsThe present study showed that rs5283 was associated with an increased susceptibility to IS [odds ratio (OR) 1.81, p = 0.012]. On the contrary, rs6410 had a protective influence on IS risk (OR 0.56, p = 0.020). Stratified analyses indicated that rs5283 could enhance the risk of IS in subjects aged >63 years (OR 2.41, p = 0.011), of female gender (OR 3.31, p = 0.001), that do not smoke (OR 1.64, p = 0.005), and with hypertension (OR 2.07, p = 0.003). Whereas, rs6410 was related to a lower susceptibility to IS in subjects aged >63 years (OR 0.43, p = 0.032), of female gender (OR 0.30, p = 0.006), do not smoke (OR 0.42, p = 0.017), and with hypertension (OR 0.52, p = 0.022). Besides, rs4736312 reduced the IS susceptibility in non-smokers (OR 0.69, p = 0.031). Rs4534 had a risk-decreasing impact on IS in non-drinking (OR 0.54, p = 0.016). Moreover, the results of the MDR analysis corroborate that the best prediction model for IS was rs5283.ConclusionThis study revealed that CYP11B1 gene polymorphisms strongly correlated with IS in the Chinese Han population. Ischemic stroke (IS) is the major cause of death and disability. While previous studies confirmed that is closely associated with IS, the present study aimed to analyze the impact of gene polymorphisms on the IS susceptibility. The present study genotyped six single nucleotide polymorphisms (SNPs) (including rs4736312, rs5017238, rs5301, rs5283, rs6410, and rs4534) of in peripheral blood samples from IS and control populations. Logistic regression analysis was used to analyze the association between the SNPs and IS risk. The multifactor dimensionality reduction (MDR) method was used to determine the roles of SNP-SNP interactions in IS. The present study showed that rs5283 was associated with an increased susceptibility to IS [odds ratio (OR) 1.81, = 0.012]. On the contrary, rs6410 had a protective influence on IS risk (OR 0.56, = 0.020). Stratified analyses indicated that rs5283 could enhance the risk of IS in subjects aged >63 years (OR 2.41, = 0.011), of female gender (OR 3.31, = 0.001), that do not smoke (OR 1.64, = 0.005), and with hypertension (OR 2.07, = 0.003). Whereas, rs6410 was related to a lower susceptibility to IS in subjects aged >63 years (OR 0.43, = 0.032), of female gender (OR 0.30, = 0.006), do not smoke (OR 0.42, = 0.017), and with hypertension (OR 0.52, = 0.022). Besides, rs4736312 reduced the IS susceptibility in non-smokers (OR 0.69, = 0.031). Rs4534 had a risk-decreasing impact on IS in non-drinking (OR 0.54, = 0.016). Moreover, the results of the MDR analysis corroborate that the best prediction model for IS was rs5283. This study revealed that gene polymorphisms strongly correlated with IS in the Chinese Han population. |
Author | Duan, Ying Liu, Gaowen |
AuthorAffiliation | Department of Critical Care Medicine, Xianyang Central Hospital , Xianyang , China |
AuthorAffiliation_xml | – name: Department of Critical Care Medicine, Xianyang Central Hospital , Xianyang , China |
Author_xml | – sequence: 1 givenname: Gaowen surname: Liu fullname: Liu, Gaowen – sequence: 2 givenname: Ying surname: Duan fullname: Duan, Ying |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/36532271$$D View this record in MEDLINE/PubMed |
BookMark | eNp9kktv1DAUhS1URJ9_gAXyks0MfsSJs0GCUaGVKsECJCpVshznZsbFsYPtIM2_x50ZqpYFK7_O-e6V7zlFRz54QOg1JUvOZftu8NanJSOMLSnhRAj6Ap3QumaLSvAfR0_2x-g0pXtCaiYr9god81pwxhp6gu5Wt18p_UjxGjzgKbjtGOK0sWlMWPsepzkZmLLtrLN5i3PANpkNjNbglGP4Cdh6rPFqYz0kwFfaF8g0O51t8Ofo5aBdgovDeoa-f7r8trpa3Hz5fL36cLMwVS3zQtaEci6A10a0fTUA1dBx2ZByoLp03RFdyQYkaXnbSmH6HmQ7MKMFKQrgZ-h6z-2DvldTtKOOWxW0VbuLENdKx2yNA0V0PRDd9FJ0rCJN35kOWDc0hplKt5UprPd71jR3I_QGfI7aPYM-f_F2o9bht2obwVoiCuDtARDDrxlSVmP5MnBOewhzUqwRQhIuOS3SN09rPRb5O54iYHuBiSGlCMOjhBL1kAG1y4B6yIA6ZKCY5D8mY_NuHqVf6_5n_QNiN7kk |
CitedBy_id | crossref_primary_10_1016_j_tiv_2024_105854 crossref_primary_10_3389_fstro_2024_1382379 |
Cites_doi | 10.1097/FJC.0000000000000793 10.1161/HYPERTENSIONAHA.112.200741 10.1097/FJC.0000000000001032 10.21203/rs.2.21934/v1 10.1007/s12017-018-8492-z 10.1016/S1474-4422(21)00252-0 10.2471/BLT.16.181636 10.1080/01616412.2018.1446281 10.18632/oncotarget.19991 10.1186/s12920-022-01307-8 10.1186/s12883-019-1285-7 10.1007/s12031-018-1221-0 10.1503/jpn.190177 10.1177/0271678X18793324 10.1155/2020/9358290 10.1161/CIRCULATIONAHA.116.025250 10.18632/oncotarget.18430 10.1002/brb3.1503 10.1007/s11886-016-0804-z 10.1016/j.arcmed.2017.03.015 10.1111/cen.13414 10.1038/hr.2010.21 10.1016/j.jnma.2019.02.004 10.1007/s12041-016-0635-0 10.1016/S2214-109X(13)70089-5 10.1186/s12967-021-02904-4 10.1080/10641963.2017.1377218 10.1097/MD.0000000000020830 10.1177/0883073815620672 10.1177/1941874416648198 10.1097/MD.0000000000006266 10.4103/0028-3886.103196 10.5455/JPMA.6666 10.1016/j.domaniend.2019.106430 10.1016/j.jns.2010.06.013 10.1161/CIRCULATIONAHA.118.035905 10.1016/j.jns.2021.118676 |
ContentType | Journal Article |
Copyright | Copyright © 2022 Liu and Duan. Copyright © 2022 Liu and Duan. 2022 Liu and Duan |
Copyright_xml | – notice: Copyright © 2022 Liu and Duan. – notice: Copyright © 2022 Liu and Duan. 2022 Liu and Duan |
DBID | AAYXX CITATION NPM 7X8 5PM DOA |
DOI | 10.3389/fnins.2022.1030551 |
DatabaseName | CrossRef PubMed MEDLINE - Academic PubMed Central (Full Participant titles) DOAJ - Directory of Open Access Journals |
DatabaseTitle | CrossRef PubMed MEDLINE - Academic |
DatabaseTitleList | MEDLINE - Academic PubMed |
Database_xml | – sequence: 1 dbid: DOA name: DOAJ Directory of Open Access Journals url: https://www.doaj.org/ sourceTypes: Open Website – sequence: 2 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Anatomy & Physiology |
EISSN | 1662-453X |
ExternalDocumentID | oai_doaj_org_article_0a6f0a7d85b2407dbcbe2bf7c2c4a94c PMC9752905 36532271 10_3389_fnins_2022_1030551 |
Genre | Journal Article |
GroupedDBID | --- 29H 2WC 53G 5GY 5VS 8FE 8FH 9T4 AAFWJ AAYXX ABUWG ACGFO ACGFS ACXDI ADRAZ AEGXH AENEX AFKRA AFPKN AIAGR ALMA_UNASSIGNED_HOLDINGS AZQEC BBNVY BENPR BHPHI BPHCQ CITATION CS3 DIK DU5 E3Z EBS EJD EMOBN F5P FRP GROUPED_DOAJ GX1 HCIFZ HYE KQ8 LK8 M2P M48 M7P O5R O5S OK1 OVT P2P PGMZT PIMPY PQQKQ PROAC RNS RPM W2D 88I C1A CCPQU DWQXO GNUQQ IAO IEA IHR ISR M~E NPM 7X8 5PM |
ID | FETCH-LOGICAL-c468t-8601335e36c59d4fe1aeb38709d41a006b0a487e80939985cdde89f2ca50d41e3 |
IEDL.DBID | M48 |
ISSN | 1662-453X 1662-4548 |
IngestDate | Wed Aug 27 01:27:59 EDT 2025 Thu Aug 21 18:39:15 EDT 2025 Fri Jul 11 07:56:19 EDT 2025 Thu Jan 02 22:54:36 EST 2025 Tue Jul 01 01:39:48 EDT 2025 Thu Apr 24 23:09:36 EDT 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Keywords | susceptibility case-control study CYP11B1 gene polymorphisms ischemic stroke |
Language | English |
License | Copyright © 2022 Liu and Duan. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c468t-8601335e36c59d4fe1aeb38709d41a006b0a487e80939985cdde89f2ca50d41e3 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Edited by: Jun Zhang, Texas Tech University Health Sciences Center, United States This article was submitted to Neurogenomics, a section of the journal Frontiers in Neuroscience Reviewed by: Yonggang Hao, Sir Run Run Shaw Hospital, China; Yipeng Ding, Hainan General Hospital, China |
OpenAccessLink | http://journals.scholarsportal.info/openUrl.xqy?doi=10.3389/fnins.2022.1030551 |
PMID | 36532271 |
PQID | 2755803831 |
PQPubID | 23479 |
ParticipantIDs | doaj_primary_oai_doaj_org_article_0a6f0a7d85b2407dbcbe2bf7c2c4a94c pubmedcentral_primary_oai_pubmedcentral_nih_gov_9752905 proquest_miscellaneous_2755803831 pubmed_primary_36532271 crossref_primary_10_3389_fnins_2022_1030551 crossref_citationtrail_10_3389_fnins_2022_1030551 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2022-12-01 |
PublicationDateYYYYMMDD | 2022-12-01 |
PublicationDate_xml | – month: 12 year: 2022 text: 2022-12-01 day: 01 |
PublicationDecade | 2020 |
PublicationPlace | Switzerland |
PublicationPlace_xml | – name: Switzerland |
PublicationTitle | Frontiers in neuroscience |
PublicationTitleAlternate | Front Neurosci |
PublicationYear | 2022 |
Publisher | Frontiers Media S.A |
Publisher_xml | – name: Frontiers Media S.A |
References | Wang (B30) 2017; 96 Song (B25) 2020; 72 Krishnamurthi (B18) 2013; 1 Lin (B20) 2021; 19 Yuan (B36) 2021; 78 Diakite (B8) 2016; 95 Yan (B33) 2012; 60 Ancelin (B2) 2021; 46 Gao (B10) 2019; 19 Mialovytska (B22) 2021; 319 Chauhan (B5) 2016; 18 Xu (B32) 2017; 48 Zhang (B38) 2019; 111 Hussain (B16) 2020; 70 Tu (B26) 2020; 2020 Wang (B31) 2017; 135 Huang (B14) 2022; 15 Zhang (B37) 2010; 33 Mackay (B21) 2004 Goyal (B12) 2021; 69 Johnson (B17) 2016; 94 Liberman (B19) 2016; 6 Wang (B29) 2019; 67 Munshi (B23) 2010; 296 Türkanoglu Özçelik (B27) 2018; 40 Georgakis (B11) 2019; 139 Cai (B4) 2020; 75 Bushnell (B3) 2018; 38 Zhuo (B39) 2020; 99 Rui (B24) 2020; 34 Yi (B35) 2017; 8 Alvarez-Madrazo (B1) 2013; 61 Gu (B13) 2018; 20 Deng (B7) 2016; 31 Valassi (B28) 2017; 87 Cheng (B6) 2017; 8 Feigin (B9) 2021; 20 Yang (B34) 2020; 10 Hussain (B15) 2018; 40 |
References_xml | – volume: 75 start-page: 344 year: 2020 ident: B4 article-title: Genetic variations of CYP19A1 gene and stroke susceptibility: a case-control study in the Chinese Han population publication-title: J. Cardiovasc. Pharmacol. doi: 10.1097/FJC.0000000000000793 – volume: 61 start-page: 232 year: 2013 ident: B1 article-title: Common polymorphisms in the CYP11B1 and CYP11B2 genes: evidence for a digenic influence on hypertension publication-title: Hypertension doi: 10.1161/HYPERTENSIONAHA.112.200741 – volume: 319 start-page: 87 year: 2021 ident: B22 article-title: Analysis of relationship between polymorphism of MTHFR (C677T), MTHFR (A1298C), MTR (A2756G) genes in the development of ischemic stroke in young patients publication-title: Georgian Med. News – volume: 78 start-page: e128 year: 2021 ident: B36 article-title: Contribution of WNT2B genetic variants to ischemic stroke occurrence in a Chinese Han population publication-title: J. Cardiovasc. Pharmacol. doi: 10.1097/FJC.0000000000001032 – volume: 34 start-page: 1445 year: 2020 ident: B24 article-title: Serum level of IL-10 and IL-10-1082G/A polymorphism are associated with the risk of ischemic stroke: a meta-analysis publication-title: J. Biol. Regul. Homeost. Agents doi: 10.21203/rs.2.21934/v1 – volume: 20 start-page: 271 year: 2018 ident: B13 article-title: Association of CALM1 rs3179089 polymorphism with ischemic stroke in Chinese Han population publication-title: Neuromol. Med. doi: 10.1007/s12017-018-8492-z – volume: 20 start-page: 795 year: 2021 ident: B9 article-title: Global, regional, and national burden of stroke and its risk factors, 1990-2019: a systematic analysis for the Global Burden of Disease Study 2019 publication-title: Lancet Neurol. doi: 10.1016/S1474-4422(21)00252-0 – volume: 94 start-page: 634 year: 2016 ident: B17 article-title: Stroke: a global response is needed publication-title: Bull. World Health Organ. doi: 10.2471/BLT.16.181636 – volume: 40 start-page: 364 year: 2018 ident: B27 article-title: O. Adali. Genetic polymorphisms of vitamin D3 metabolizing CYP24A1 and CYP2R1 enzymes in Turkish patients with ischemic stroke publication-title: Neurol. Res. doi: 10.1080/01616412.2018.1446281 – volume: 8 start-page: 70811 year: 2017 ident: B35 article-title: Interaction among CYP2C8, GPIIIa and P2Y12 variants increase susceptibility to ischemic stroke in Chinese population publication-title: Oncotarget doi: 10.18632/oncotarget.19991 – volume: 15 start-page: 158 year: 2022 ident: B14 article-title: Genetic variants in CYP11B1 influence the susceptibility to coronary heart disease publication-title: BMC Med. Genom. doi: 10.1186/s12920-022-01307-8 – volume: 19 start-page: 67 year: 2019 ident: B10 article-title: Association of the MMP-9 polymorphism and ischemic stroke risk in southern Chinese Han population publication-title: BMC Neurol. doi: 10.1186/s12883-019-1285-7 – volume: 67 start-page: 165 year: 2019 ident: B29 article-title: HDAC9 polymorphisms predict susceptibility, severity, and short-term outcome of large artery atherosclerotic stroke in chinese population publication-title: J. Mol. Neurosci. doi: 10.1007/s12031-018-1221-0 – volume: 46 start-page: E147 year: 2021 ident: B2 article-title: 11β-Hydroxylase (CYP11B1) gene variants and new-onset depression in later life publication-title: J. Psychiat. Neurosci. doi: 10.1503/jpn.190177 – volume: 38 start-page: 2179 year: 2018 ident: B3 article-title: Sex differences in stroke: challenges and opportunities publication-title: J. Cereb. Blood Flow Metab. doi: 10.1177/0271678X18793324 – volume-title: The Atlas of Heart Disease and Stroke. year: 2004 ident: B21 – volume: 2020 start-page: 9358290 year: 2020 ident: B26 article-title: Associations between aquaglyceroporin gene polymorphisms and risk of stroke among patients with hypertension publication-title: BioMed Res. Int. doi: 10.1155/2020/9358290 – volume: 135 start-page: 759 year: 2017 ident: B31 article-title: Prevalence, incidence, and mortality of stroke in China: results from a nationwide population-based survey of 480 687 adults publication-title: Circulation doi: 10.1161/CIRCULATIONAHA.116.025250 – volume: 8 start-page: 97913 year: 2017 ident: B6 article-title: Interactions between ACYP2 genetic polymorphisms and environment factors with susceptibility to ischemic stroke in a Han Chinese population publication-title: Oncotarget doi: 10.18632/oncotarget.18430 – volume: 10 start-page: e01503 year: 2020 ident: B34 article-title: The association analysis between CYP24A1 genetic polymorphisms and the risk of ischemic stroke in Chinese Han population publication-title: Brain Behav. doi: 10.1002/brb3.1503 – volume: 18 start-page: 124 year: 2016 ident: B5 article-title: Genetic risk factors for ischemic and hemorrhagic stroke publication-title: Curr. Cardiol. Rep. doi: 10.1007/s11886-016-0804-z – volume: 48 start-page: 203 year: 2017 ident: B32 article-title: ESR2 genetic variants and combined oral contraceptive use associated with the risk of stroke publication-title: Arch. Med. Res. doi: 10.1016/j.arcmed.2017.03.015 – volume: 87 start-page: 433 year: 2017 ident: B28 article-title: A polymorphism in the CYP17A1 gene influences the therapeutic response to steroidogenesis inhibitors in Cushing's syndrome publication-title: Clin. Endocrinol. doi: 10.1111/cen.13414 – volume: 33 start-page: 478 year: 2010 ident: B37 article-title: Polymorphisms in CYP11B2 and CYP11B1 genes associated with primary hyperaldosteronism publication-title: Hypertension Res. doi: 10.1038/hr.2010.21 – volume: 111 start-page: 447 year: 2019 ident: B38 article-title: Extended risk factors for stroke prevention publication-title: J. Natl. Med. Assoc. doi: 10.1016/j.jnma.2019.02.004 – volume: 95 start-page: 303 year: 2016 ident: B8 article-title: Genetic polymorphisms of T-1131C APOA5 and ALOX5AP SG13S114 with the susceptibility of ischaemic stroke in Morocco publication-title: J. Genet. doi: 10.1007/s12041-016-0635-0 – volume: 1 start-page: e259 year: 2013 ident: B18 article-title: Global and regional burden of first-ever ischaemic and haemorrhagic stroke during 1990–2010: findings from the Global Burden of Disease Study 2010 publication-title: Lancet doi: 10.1016/S2214-109X(13)70089-5 – volume: 19 start-page: 227 year: 2021 ident: B20 article-title: Association of ADH1B polymorphism and alcohol consumption with increased risk of intracerebral hemorrhagic stroke publication-title: J. Transl. Med. doi: 10.1186/s12967-021-02904-4 – volume: 40 start-page: 344 year: 2018 ident: B15 article-title: Hypertension regulating angiotensin peptides in the pathobiology of cardiovascular disease publication-title: Clin. Exp. Hypertens. doi: 10.1080/10641963.2017.1377218 – volume: 99 start-page: e20830 year: 2020 ident: B39 article-title: Clinical risk factors associated with recurrence of ischemic stroke within two years: a cohort study publication-title: Medicine doi: 10.1097/MD.0000000000020830 – volume: 31 start-page: 733 year: 2016 ident: B7 article-title: A family-based association study of CYP11A1 and CYP11B1 gene polymorphisms with autism in Chinese trios publication-title: J. Child Neurol. doi: 10.1177/0883073815620672 – volume: 6 start-page: 147 year: 2016 ident: B19 article-title: International classification of diseases, ninth revision (ICD-9) diagnosis codes can identify cerebral venous thrombosis in hospitalized adults publication-title: Neurohospitalist doi: 10.1177/1941874416648198 – volume: 96 start-page: e6266 year: 2017 ident: B30 article-title: Association of CYP2J2 gene polymorphisms with ischemic stroke and stroke subtypes in Chinese population publication-title: Medicine doi: 10.1097/MD.0000000000006266 – volume: 60 start-page: 504 year: 2012 ident: B33 article-title: Association of CYP11B2 gene polymorphism with ischemic stroke in the north Chinese Han population publication-title: Neurol. India doi: 10.4103/0028-3886.103196 – volume: 70 start-page: 624 year: 2020 ident: B16 article-title: Pharmacogenetic study of ACE, AGT, CYP11B1, CYP11B2 and eNOS gene variants in hypertensive patients from Faisalabad, Pakistan publication-title: JPMA doi: 10.5455/JPMA.6666 – volume: 72 start-page: 106430 year: 2020 ident: B25 article-title: A SNP in the 3'UTR of the porcine IGF-1 gene interacts with miR-new14 to affect IGF-1 expression, proliferation and apoptosis of PK-15 cells publication-title: Domest. Anim. Endocrinol. doi: 10.1016/j.domaniend.2019.106430 – volume: 296 start-page: 34 year: 2010 ident: B23 article-title: Association of the−344C/T aldosterone synthase (CYP11B2) gene variant with hypertension and stroke publication-title: J. Neurol. Sci. doi: 10.1016/j.jns.2010.06.013 – volume: 139 start-page: 256 year: 2019 ident: B11 article-title: Genetically determined levels of circulating cytokines and risk of stroke publication-title: Circulation doi: 10.1161/CIRCULATIONAHA.118.035905 – volume: 69 start-page: 1217 year: 2021 ident: B12 article-title: Role of ACE polymorphism in acute ischemic stroke publication-title: Neurol. India doi: 10.1016/j.jns.2021.118676 |
SSID | ssj0062842 |
Score | 2.318865 |
Snippet | Ischemic stroke (IS) is the major cause of death and disability. While previous studies confirmed that
is closely associated with IS, the present study aimed... Ischemic stroke (IS) is the major cause of death and disability. While previous studies confirmed that CYP11B1 is closely associated with IS, the present study... ObjectivesIschemic stroke (IS) is the major cause of death and disability. While previous studies confirmed that CYP11B1 is closely associated with IS, the... |
SourceID | doaj pubmedcentral proquest pubmed crossref |
SourceType | Open Website Open Access Repository Aggregation Database Index Database Enrichment Source |
StartPage | 1030551 |
SubjectTerms | case-control study CYP11B1 gene polymorphisms ischemic stroke Neuroscience susceptibility |
SummonAdditionalLinks | – databaseName: DOAJ - Directory of Open Access Journals dbid: DOA link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV3NSx0xEA_iyYu01bavthKh9CKL2XzsJkeVykOweFBQKCxJdpYu1ay4-w7-951k9z18Reqlx91kN2FmMjO_ZDJDyFdvhUOroLLC1SyTVkHmINeZAHBGFKzhacPt4kcxv5bnN-rmWamvGBM2pgceCXfEbNEwW9ZauQg-aucdcNeUnntpjfRR-6LNW4KpUQcXqHT5eEUGIZg5akIbYm5uzuMlc6ZUvmaGUrb-l1zMvyMln5meszdke_IZ6fE417dkA8I7snMcEC_fP9FvNEVxpu3xHfLz9PYyz09yioIB9KG7Q2yPpGz7-57aUNN-0adAlhQT-0SHjraIb2OEPO2Hx-430DZQS2NZbeiBzm3AnyxrfO2S67PvV6fzbKqgkHlZ6CHTCLeEUCAKr0wtG8gtgmdcoviQW6STYxYRC2hm0FHRyqOy06bhsU4C9gDxnmyGLsBHQqUSUAuHa1ZLabVEWMKEcqwxxvK6YTOSLwla-Sm9eKxycVchzIhMqBITqsiEamLCjByuvnkYk2v8s_dJ5NOqZ0yMnV6guFSTuFSvicuMHCy5XOFCiqcjNkC3wKFKpTRDwI4DfRi5vhpKFAoVX4kt5Zo8rM1lvSW0v1KyblMqbpj69D8mv0e2IkHGaJrPZHN4XMAX9IkGt5_E_w9CbAxd priority: 102 providerName: Directory of Open Access Journals |
Title | CYP11B1 gene polymorphisms and susceptibility to ischemic stroke in a Chinese Han population |
URI | https://www.ncbi.nlm.nih.gov/pubmed/36532271 https://www.proquest.com/docview/2755803831 https://pubmed.ncbi.nlm.nih.gov/PMC9752905 https://doaj.org/article/0a6f0a7d85b2407dbcbe2bf7c2c4a94c |
Volume | 16 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV3di9QwEA_HCXIvop4f6-kRQXyRatJ8NHkQuTs8F-HEBxdWEErSpmdxN73bdsH9752k7eLKnS-FtmnSzkdnfslkBqFXhWEWrIJIpC1Jwo1wiXVUJcw5q5kkVRon3C6-yOmMf56L-R4ayx0NBGxvhHahntRstXj7-3rzART-fUCcYG_fVb72IfN2moYt5ESEHdV3wDJloaLBBd-uKkj4FcfVTxl2CoGr3m-iuaWPA3SXSQHyntEdmxVT-9_kj_4bVvmXnTq_j-4NDiY-6SXiAdpz_iE6PPEArpcb_BrHkM84l36Ifpx9_0rpKcUgRQ5fNYvNsgG61-2yxcaXuF23MeolBtBucNfgGigWwulx262aXw7XHhscanC71uGp8dDJWBDsEZqdf_x2Nk2GcgtJwaXqEgXYjDHhmCyELnnlqAGkDfoMJ9QA-SwxAG-cIhq8GiUK-DMqXaWhqAK0cOwx2veNd08R5oK5kllQcMW5URwwDGHCkkprk5YVmSA6EjQvhlzkoSTGIgdMEviRR37kgR_5wI8JerN95qrPxPHf1qeBT9uWIYt2vNCsLvNBKXNiZEVMViphA7AtbWFdaqusSAtuNC8m6OXI5Ry0LiylGO-aNQyVCaEIoHsY6EnP9e1Qo9RMULYjDzvvsnvH1z9jZm-diVQT8ezWPo_QQfjKPp7mOdrvVmv3Aryizh7H2QQ4fprT4yj2fwAVugoA |
linkProvider | Scholars Portal |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=CYP11B1+gene+polymorphisms+and+susceptibility+to+ischemic+stroke+in+a+Chinese+Han+population&rft.jtitle=Frontiers+in+neuroscience&rft.au=Liu%2C+Gaowen&rft.au=Duan%2C+Ying&rft.date=2022-12-01&rft.issn=1662-4548&rft.volume=16&rft.spage=1030551&rft_id=info:doi/10.3389%2Ffnins.2022.1030551&rft_id=info%3Apmid%2F36532271&rft.externalDocID=36532271 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1662-453X&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1662-453X&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1662-453X&client=summon |