Genetic variants within Ninjurin 2 gene are associated with risk of ischemic stroke in Iranian population.
Saved in:
| Title: | Genetic variants within Ninjurin 2 gene are associated with risk of ischemic stroke in Iranian population. |
|---|---|
| Authors: | Malekzadeh, Vadoud (AUTHOR), Azari, Iman (AUTHOR), Noroozi, Rezvan (AUTHOR), Shams, Roshanak (AUTHOR), Farzaneh, Mina (AUTHOR), Taheri, Mohammad (AUTHOR), Ghafouri-Fard, Soudeh (AUTHOR) |
| Source: | Neurological Sciences. Dec2019, Vol. 40 Issue 12, p2603-2607. 5p. 5 Charts. |
| Subjects: | Glycoproteins, Relative medical risk, Genetic polymorphisms, Case-control method, Cerebral ischemia, Stroke |
| Geographic Terms: | Iran |
| Abstract: | Previous genetic and epidemiological studies have shown the contribution of genetic factors in conferring the risk of ischemic stroke. Among the acknowledged risk factors of stroke are the single nucleotide polymorphisms (SNPs) near Ninjurin 2 (NINJ2) gene which encodes a surface adhesion protein. In the current study, we investigated the role of two SNPs near this gene in ischemic stroke in Iranian population. The frequency of the A allele of the rs11833579 was significantly lower in cases compared with controls (OR (95% CI) = 0.68 (0.54-0.86), adjusted P value = 0.002). The rs11833579 was significantly associated with risk of stroke in co-dominant (AA vs. GG: OR (95% CI) = 0.39 (0.23-0.66), adjusted P value = 0.003) and recessive (OR (95% CI) = 0.44 (0.27-0.72), adjusted P value = 0.001) models. The rs3809263 was associated with risk of stroke in dominant model (OR (95% CI) = 1.5 (1.09-2.06), adjusted P value = 0.02). The A C haplotype (rs11833579 and rs3809263) decreased the risk of stroke (OR (95% CI) = 0.72 (0.57-0.91), adjusted P value = 0.03), while the G T haplotype conferred susceptibility to stroke (OR (95% CI) = 1.42 (1.11-1.82), adjusted P value = 0.02). Consequently, the present case-control study supports the role of NINJ2 as a risk locus for ischemic stroke in Iranian population. [ABSTRACT FROM AUTHOR] |
| Copyright of Neurological Sciences is the property of Springer Nature and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) | |
| Database: | Psychology and Behavioral Sciences Collection |
|
Full text is not displayed to guests.
Login for full access.
|
|
| FullText | Links: – Type: pdflink Text: Availability: 1 |
|---|---|
| Header | DbId: pbh DbLabel: Psychology and Behavioral Sciences Collection An: 139600137 AccessLevel: 6 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
| IllustrationInfo | |
| Items | – Name: Title Label: Title Group: Ti Data: Genetic variants within Ninjurin 2 gene are associated with risk of ischemic stroke in Iranian population. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Malekzadeh%2C+Vadoud%22">Malekzadeh, Vadoud</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Azari%2C+Iman%22">Azari, Iman</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Noroozi%2C+Rezvan%22">Noroozi, Rezvan</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Shams%2C+Roshanak%22">Shams, Roshanak</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Farzaneh%2C+Mina%22">Farzaneh, Mina</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Taheri%2C+Mohammad%22">Taheri, Mohammad</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Ghafouri-Fard%2C+Soudeh%22">Ghafouri-Fard, Soudeh</searchLink> (AUTHOR) – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Neurological+Sciences%22">Neurological Sciences</searchLink>. Dec2019, Vol. 40 Issue 12, p2603-2607. 5p. 5 Charts. – Name: Subject Label: Subjects Group: Su Data: <searchLink fieldCode="DE" term="%22Glycoproteins%22">Glycoproteins</searchLink><br /><searchLink fieldCode="DE" term="%22Relative+medical+risk%22">Relative medical risk</searchLink><br /><searchLink fieldCode="DE" term="%22Genetic+polymorphisms%22">Genetic polymorphisms</searchLink><br /><searchLink fieldCode="DE" term="%22Case-control+method%22">Case-control method</searchLink><br /><searchLink fieldCode="DE" term="%22Cerebral+ischemia%22">Cerebral ischemia</searchLink><br /><searchLink fieldCode="DE" term="%22Stroke%22">Stroke</searchLink> – Name: SubjectGeographic Label: Geographic Terms Group: Su Data: <searchLink fieldCode="DE" term="%22Iran%22">Iran</searchLink> – Name: Abstract Label: Abstract Group: Ab Data: Previous genetic and epidemiological studies have shown the contribution of genetic factors in conferring the risk of ischemic stroke. Among the acknowledged risk factors of stroke are the single nucleotide polymorphisms (SNPs) near Ninjurin 2 (NINJ2) gene which encodes a surface adhesion protein. In the current study, we investigated the role of two SNPs near this gene in ischemic stroke in Iranian population. The frequency of the A allele of the rs11833579 was significantly lower in cases compared with controls (OR (95% CI) = 0.68 (0.54-0.86), adjusted P value = 0.002). The rs11833579 was significantly associated with risk of stroke in co-dominant (AA vs. GG: OR (95% CI) = 0.39 (0.23-0.66), adjusted P value = 0.003) and recessive (OR (95% CI) = 0.44 (0.27-0.72), adjusted P value = 0.001) models. The rs3809263 was associated with risk of stroke in dominant model (OR (95% CI) = 1.5 (1.09-2.06), adjusted P value = 0.02). The A C haplotype (rs11833579 and rs3809263) decreased the risk of stroke (OR (95% CI) = 0.72 (0.57-0.91), adjusted P value = 0.03), while the G T haplotype conferred susceptibility to stroke (OR (95% CI) = 1.42 (1.11-1.82), adjusted P value = 0.02). Consequently, the present case-control study supports the role of NINJ2 as a risk locus for ischemic stroke in Iranian population. [ABSTRACT FROM AUTHOR] – Name: AbstractSuppliedCopyright Label: Group: Ab Data: <i>Copyright of Neurological Sciences is the property of Springer Nature and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.) |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=pbh&AN=139600137 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1007/s10072-019-04023-x Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 5 StartPage: 2603 Subjects: – SubjectFull: Glycoproteins Type: general – SubjectFull: Relative medical risk Type: general – SubjectFull: Genetic polymorphisms Type: general – SubjectFull: Case-control method Type: general – SubjectFull: Cerebral ischemia Type: general – SubjectFull: Stroke Type: general – SubjectFull: Iran Type: general Titles: – TitleFull: Genetic variants within Ninjurin 2 gene are associated with risk of ischemic stroke in Iranian population. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Malekzadeh, Vadoud – PersonEntity: Name: NameFull: Azari, Iman – PersonEntity: Name: NameFull: Noroozi, Rezvan – PersonEntity: Name: NameFull: Shams, Roshanak – PersonEntity: Name: NameFull: Farzaneh, Mina – PersonEntity: Name: NameFull: Taheri, Mohammad – PersonEntity: Name: NameFull: Ghafouri-Fard, Soudeh IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 12 Text: Dec2019 Type: published Y: 2019 Identifiers: – Type: issn-print Value: 15901874 Numbering: – Type: volume Value: 40 – Type: issue Value: 12 Titles: – TitleFull: Neurological Sciences Type: main |
| ResultId | 1 |