ログイン
言語:

WEKO3

  • トップ
  • ランキング
To
lat lon distance
To

Field does not validate



インデックスリンク

インデックスツリー

メールアドレスを入力してください。

WEKO

One fine body…

WEKO

One fine body…

アイテム

  1. C. 医薬保健学域; 医学類・薬学類・医薬科学類・保健学類
  2. c 10. 学術雑誌掲載論文(医・保健)
  3. 1. 査読済論文(医学・保健)

Comparison of effects of bezafibrate and fenofibrate on circulating proprotein convertase subtilisin/kexin type 9 and adipocytokine levels in dyslipidemic subjects with impaired glucose tolerance or type 2 diabetes mellitus: Results from a crossover study

http://hdl.handle.net/2297/27306
http://hdl.handle.net/2297/27306
4bea5029-e614-4e8e-9316-9d05757b0fa8
名前 / ファイル ライセンス アクション
ME-PR-KOBAYASHI-J-165 ME-PR-KOBAYASHI-J-165 (167.4 kB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2017-10-03
タイトル
タイトル Comparison of effects of bezafibrate and fenofibrate on circulating proprotein convertase subtilisin/kexin type 9 and adipocytokine levels in dyslipidemic subjects with impaired glucose tolerance or type 2 diabetes mellitus: Results from a crossover study
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
著者 Noguchi, Tohru

× Noguchi, Tohru

WEKO 21334
研究者番号 40456421

Noguchi, Tohru

Search repository
Kobayashi, Junji

× Kobayashi, Junji

WEKO 477
e-Rad 60302577
研究者番号 60302577

Kobayashi, Junji

Search repository
Yagi, Kunimasa

× Yagi, Kunimasa

WEKO 438
e-Rad 30293343
金沢大学研究者情報 30293343
研究者番号 30293343

Yagi, Kunimasa

Search repository
Nohara, Atsushi

× Nohara, Atsushi

WEKO 342
e-Rad 50313648
金沢大学研究者情報 50313648
研究者番号 50313648

Nohara, Atsushi

Search repository
Yamaaki, Naoto

× Yamaaki, Naoto

WEKO 22103

Yamaaki, Naoto

Search repository
Sugihara, Masako

× Sugihara, Masako

WEKO 22104

Sugihara, Masako

Search repository
Ito, Naoko

× Ito, Naoko

WEKO 1206
金沢大学研究者情報 46182858
研究者番号 46182858

Ito, Naoko

Search repository
Oka, Rie

× Oka, Rie

WEKO 22105

Oka, Rie

Search repository
Kawashiri, Masaaki

× Kawashiri, Masaaki

WEKO 333
e-Rad 90345637
金沢大学研究者情報 90345637
研究者番号 90345637

Kawashiri, Masaaki

Search repository
Tada, Hayato

× Tada, Hayato

WEKO 22106

Tada, Hayato

Search repository
Takata, Mutsuko

× Takata, Mutsuko

WEKO 22107

Takata, Mutsuko

Search repository
Inazu, Akihiro

× Inazu, Akihiro

WEKO 539
e-Rad 80293348
金沢大学研究者情報 80293348
研究者番号 80293348

Inazu, Akihiro

Search repository
Yamagishi, Masakazu

× Yamagishi, Masakazu

WEKO 265
e-Rad 70393238
金沢大学研究者情報 70393238
研究者番号 70393238

Yamagishi, Masakazu

Search repository
Mabuchi, Hiroshi

× Mabuchi, Hiroshi

WEKO 389
e-Rad 00019960
研究者番号 00019960

Mabuchi, Hiroshi

Search repository
提供者所属
内容記述タイプ Other
内容記述 金沢大学医学系研究科
書誌情報 Atherosclerosis 217 (1), pp. 165-170

巻 217, 号 1, p. 165-170, 発行日 2011-07-01
ISSN
収録物識別子タイプ ISSN
収録物識別子 0021-9150
NCID
収録物識別子タイプ NCID
収録物識別子 AA00553457
DOI
関連タイプ isVersionOf
識別子タイプ DOI
関連識別子 10.1016/j.atherosclerosis.2011.02.012
出版者
出版者 Elsevier Ireland Ltd
抄録
内容記述タイプ Abstract
内容記述 Background: Bezafibrate and fenofibrate show different binding properties against peroxisome proliferator-activated receptor subtypes, which could cause different clinical effects on circulating proprotein convertase subtilisin/kexin type 9 (PCSK9) levels and on various metabolic markers. Methods: An open, randomized, four-phased crossover study using 400 mg of bezafibrate or 200 mg of fenofibrate was performed. Study subjects were 14 dyslipidemia with impaired glucose tolerance or type 2 diabetes mellitus (61 ± 16 years, body mass index (BMI) 26 ± 3 kg/m2, total cholesterol (TC) 219 ± 53 mg/dL, triglyceride (TG) 183 ± 83 mg/dL, high-density lipoprotein-cholesterol (HDL-C) 46 ± 8 mg/dL, fasting plasma glucose 133 ± 31 mg/dL and HbA1c 6.2 ± 0.8%). Subjects were given either bezafibrate or fenofibrate for 8 weeks, discontinued for 4 weeks and then switched to the other fibrate for 8 weeks. Circulating PCSK9 levels and other metabolic parameters, including adiponectin, leptin and urine 8-hydroxy-2′-deoxyguanosine (8-OHdG) were measured at 0, 8, 12 and 20 weeks. Results: Plasma PCSK9 concentrations were significantly increased (+39.7% for bezafibrate and +66.8% for fenofibrate, p < 0.001) in all patients except for one subject when treated with bezafibrate. Both bezafibrate and fenofibrate caused reductions in TG (-38.3%, p < 0.001 vs. -32.9%, p < 0.01) and increases in HDL-C (+18.0%, p < 0.001 vs. +11.7%, p < 0.001). Fenofibrate significantly reduced serum cholesterol levels (TC, -11.2%, p < 0.01; non-HDL-C, -17.3%, p < 0.01; apolipoprotein B, -15.1%, p < 0.01), whereas bezafibrate significantly improved glucose tolerance (insulin, -17.0%, p < 0.05) and metabolic markers (γ-GTP, -38.9%, p < 0.01; adiponectin, +15.4%, p < 0.05; urine 8-OHdG/Cre, -9.5%, p < 0.05). Conclusion: Both bezafibrate and fenofibrate increased plasma PCSK9 concentrations. The addition of a PCSK9 inhibitor to each fibrate therapy may achieve beneficial cholesterol lowering along with desirable effects of respective fibrates. © 2011 Elsevier Ireland Ltd. All rights reserved.
著者版フラグ
出版タイプ AM
出版タイプResource http://purl.org/coar/version/c_ab4af688f83e57aa
関連URI
識別子タイプ URI
関連識別子 http://www.elsevier.com/locate/issn/00219150
戻る
0
views
See details
Views

Versions

Ver.1 2023-07-28 01:04:38.156749
Show All versions

Share

Mendeley Twitter Facebook Print Addthis

Cite as

エクスポート

OAI-PMH
  • OAI-PMH JPCOAR 2.0
  • OAI-PMH JPCOAR 1.0
  • OAI-PMH DublinCore
  • OAI-PMH DDI
Other Formats
  • JSON
  • BIBTEX

Confirm


Powered by WEKO3


Powered by WEKO3