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  1. 原著論文

4G/5G variant of plasminogen activator inhibitor-1 gene and severe pregnancy-induced hypertension: subgroup analyses with variants of angiotensinogen and endothelial nitoricoxide synthase.

https://repo.qst.go.jp/records/46136
https://repo.qst.go.jp/records/46136
c6cfd81e-6592-4c00-8ee9-cb7cd5f61e59
Item type 学術雑誌論文 / Journal Article(1)
公開日 2011-07-14
タイトル
タイトル 4G/5G variant of plasminogen activator inhibitor-1 gene and severe pregnancy-induced hypertension: subgroup analyses with variants of angiotensinogen and endothelial nitoricoxide synthase.
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Kobashi, Gen

× Kobashi, Gen

WEKO 459329

Kobashi, Gen

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Ohta, Kaori

× Ohta, Kaori

WEKO 459330

Ohta, Kaori

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Yamada, Hideto

× Yamada, Hideto

WEKO 459331

Yamada, Hideto

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Hata, Akira

× Hata, Akira

WEKO 459332

Hata, Akira

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Minakami, Hisanori

× Minakami, Hisanori

WEKO 459333

Minakami, Hisanori

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Sakuragi, Noriaki

× Sakuragi, Noriaki

WEKO 459334

Sakuragi, Noriaki

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Tamashiro, Hidehiko

× Tamashiro, Hidehiko

WEKO 459335

Tamashiro, Hidehiko

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Fujimoto, Seiichiro

× Fujimoto, Seiichiro

WEKO 459336

Fujimoto, Seiichiro

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et.al

× et.al

WEKO 459337

et.al

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小橋 元

× 小橋 元

WEKO 459338

en 小橋 元

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太田 薫里

× 太田 薫里

WEKO 459339

en 太田 薫里

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内容記述タイプ Abstract
内容記述 BACKGROUND: Pregnancy-induced hypertension (PIH) is a common cause of perinatal mortality. It is believed to result from the interaction of several factors, including those related to the blood coagulation system. We performed genotyping and subgroup analyses to determine if the 4G/5G genotypes of the plasminogen activator inhibitor-1 gene (PAI-1) play a role in the pathogenesis of PIH, and to evaluate possible interactions of the PAI-1 polymorphisms with those of the angiotensinogen gene (AGT) and the endothelial nitric oxide synthase gene (NOS3).
\nMETHODS: An association study of PAI-1 polymorphism, and subgroup analyses of common variants of AGT and NOS3, among 128 patients with PIH and 376 healthy pregnant controls.
\nRESULTS: No significant differences were found between the cases and controls in the frequencies of allele 4G or the 4G/4G genotype. In subgroup analyses, after adjustment for multiple comparison, a significant association with the AGT TT genotype was found among women with the PAI-1 4G/4G genotype, and an association with the NOS3 GA+AA genotype was found among women with the 5G/5G or 4G/5G genotypes.
\nCONCLUSIONS: Our findings suggest that there are at least 2 pathways in the pathogenesis of severe PIH. However, with respect to early prediction and prevention of severe PIH, although the PAI-1 4G/4G genotype alone was not a risk factor for severe PIH, the fact that PAI-1 genotypes are associated with varying risks for severe PIH suggests that PAI-1 genotyping of pregnant women, in combination with other tests, may be useful in the development of individualized measures that may prevent severe PIH.
書誌情報 Journal of Epidemiology

巻 19, 号 6, p. 275-280, 発行日 2009
ISSN
収録物識別子タイプ ISSN
収録物識別子 0917-5040
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