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  1. C100 医学部/医学系研究科
  2. C100b 刊行物
  3. Nagoya journal of medical science
  4. 75(1-2)

No Association between MTHFR C677T and Serum Uric Acid Levels among Japanese with ABCG2 126QQ and SLC22A12 258WW

https://doi.org/10.18999/nagjms.75.1-2.93
https://doi.org/10.18999/nagjms.75.1-2.93
cdeacf08-987a-4ed7-80da-797c2ff3366f
名前 / ファイル ライセンス アクション
10_Hinohara.pdf 10_Hinohara.pdf (130.9 kB)
アイテムタイプ 紀要論文 / Departmental Bulletin Paper(1)
公開日 2013-03-01
タイトル
タイトル No Association between MTHFR C677T and Serum Uric Acid Levels among Japanese with ABCG2 126QQ and SLC22A12 258WW
言語 en
著者 HINOHARA, YUKAKO

× HINOHARA, YUKAKO

WEKO 47483

en HINOHARA, YUKAKO

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NAITO, MARIKO

× NAITO, MARIKO

WEKO 47484

en NAITO, MARIKO

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OKADA, RIEKO

× OKADA, RIEKO

WEKO 47485

en OKADA, RIEKO

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YIN, GUAN

× YIN, GUAN

WEKO 47486

en YIN, GUAN

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HIGASHIBATA, TAKAHIRO

× HIGASHIBATA, TAKAHIRO

WEKO 47487

en HIGASHIBATA, TAKAHIRO

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TAMURA, TAKASHI

× TAMURA, TAKASHI

WEKO 47488

en TAMURA, TAKASHI

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KAWAI, SAYO

× KAWAI, SAYO

WEKO 47489

en KAWAI, SAYO

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MORITA, EMI

× MORITA, EMI

WEKO 47490

en MORITA, EMI

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WAKAI, KENJI

× WAKAI, KENJI

WEKO 47491

en WAKAI, KENJI

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MATSUO, HIROTAKA

× MATSUO, HIROTAKA

WEKO 47492

en MATSUO, HIROTAKA

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MORI, ATSUYOSHI

× MORI, ATSUYOSHI

WEKO 47493

en MORI, ATSUYOSHI

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HAMAJIMA, NOBUYUKI

× HAMAJIMA, NOBUYUKI

WEKO 47494

en HAMAJIMA, NOBUYUKI

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アクセス権
アクセス権 open access
アクセス権URI http://purl.org/coar/access_right/c_abf2
キーワード
主題Scheme Other
主題 Serum uric acid
キーワード
主題Scheme Other
主題 Urate transporter polymorphisms
キーワード
主題Scheme Other
主題 MTHFR C677T
抄録
内容記述タイプ Abstract
内容記述 Several genome-wide association studies (GWAS) have revealed that single nucleotide polymorphisms (SNPs) of ABCG2 and SLC22A12 were strongly associated with serum uric acid (SUA), but those of methylene tetrahydrofolate reductase (MTHFR) were not. However, there were several studies indicating the association with MTHFR C677T polymorphism. This study examined the association with the polymorphism, taking into account the genotypes of ABCG2 Q126X and SLC22A12 W258X. Subjects were 5,028 health checkup examinees of Seirei Preventive Health Care Center (3,416 males and 1,612 females) aged 35 to 69 years, who participated in the Japan Multi-Institutional Collaborative Cohort Study (J-MICC Study). Hyperuricemia was defined as SUA equal to 7 mg/dL or over. The genotype frequency was 35.9% for CC, 48.1% for CT, and 16.0% for TT, being in Hardy-Weinberg equilibrium (p=0.90). Among 4,425 participants with ABCG2 126QQ and SLC22A12 258WW who were not under medication for hyperuricemia, the mean SUA was 5.6 mg/dL, 5.6 mg/dL, and 5.7 mg/dL, respectively. When 114 participants with ABCG2 126QQ and SLC22A12 258WW under medication for hyperuricemia were included in hyperuricemia cases, the sex-age adjusted odds ratio (OR) of hyperuricemia was not significant; OR=1.00 (95% confidence interval, 0.89–1.24) for CT genotype and OR=0.98 (0.84–1.32) for TT genotype, relative to CC genotype. The present study indicated no association between SUA and MTHFR C677T genotype, after the influences of ABCG2 Q126X and SLC22A12 W258X were removed.
言語 en
出版者
出版者 Nagoya University School of Medicine
言語 en
言語
言語 eng
資源タイプ
資源 http://purl.org/coar/resource_type/c_6501
タイプ departmental bulletin paper
出版タイプ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
ID登録
ID登録 10.18999/nagjms.75.1-2.93
ID登録タイプ JaLC
関連情報
関連タイプ isVersionOf
識別子タイプ URI
関連識別子 http://www.med.nagoya-u.ac.jp/medlib/nagoya_j_med_sci/7512/7512.html
ISSN(print)
収録物識別子タイプ PISSN
収録物識別子 0027-7622
ISSN(Online)
収録物識別子タイプ EISSN
収録物識別子 2186-3326
書誌情報 en : Nagoya Journal of Medical Science

巻 75, 号 1-2, p. 93-100, 発行日 2013-02
著者版フラグ
値 publisher
URI
識別子 http://hdl.handle.net/2237/17605
識別子タイプ HDL
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