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  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)

Changes in lipoprotein lipase and endothelial lipase mass in familial hypercholesterolemia during three-drug lipid-lowering combination therapy.

http://hdl.handle.net/2297/48355
http://hdl.handle.net/2297/48355
78f456b9-330a-43b4-806e-a20ed4f3a835
名前 / ファイル ライセンス アクション
ME=PR-YAMAGISHI-M-66.pdf ME=PR-YAMAGISHI-M-66.pdf (1.2 MB)
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 Changes in lipoprotein lipase and endothelial lipase mass in familial hypercholesterolemia during three-drug lipid-lowering combination therapy.
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 Tada, Hayato

× Tada, Hayato

WEKO 513
e-Rad 90623653
金沢大学研究者情報 90623653
研究者番号 90623653

Tada, Hayato

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Kobayashi, Junji

× Kobayashi, Junji

WEKO 477
e-Rad 60302577
研究者番号 60302577

Kobayashi, Junji

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Kawashiri, Masa-aki

× Kawashiri, Masa-aki

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

Kawashiri, Masa-aki

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Miyashita, Kazuya

× Miyashita, Kazuya

WEKO 25189

Miyashita, Kazuya

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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

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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

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Nakajima, Katsuyuki

× Nakajima, Katsuyuki

WEKO 25190

Nakajima, Katsuyuki

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Mabuchi, Hiroshi

× Mabuchi, Hiroshi

WEKO 389
e-Rad 00019960
研究者番号 00019960

Mabuchi, Hiroshi

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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

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書誌情報 Lipids in Health and Disease

巻 15, p. 66, 発行日 2016-04-02
ISSN
収録物識別子タイプ ISSN
収録物識別子 1476-511X
NCID
収録物識別子タイプ NCID
収録物識別子 AA1203677X
DOI
関連タイプ isIdenticalTo
識別子タイプ DOI
関連識別子 10.1186/s12944-016-0238-z
出版者
出版者 BioMed Central
抄録
内容記述タイプ Abstract
内容記述 Background: This study was performed to compare the effects of three different lipid-lowering therapies (statins, ezetimibe, and colestimide) on lipoprotein lipase and endothelial lipase masses in pre-heparin plasma (pre-heparin LPL and EL mass, respectively) from patients with familial hypercholesterolemia (FH). FH is usually treated by coadministration of these three drugs. Methods: The pre-heparin LPL and EL masses were measured in fresh frozen plasma drawn and stored at various time points during coadministration of the three drugs from patients with heterozygous FH harboring a single mutation in the LDL receptor (n = 16, mean age 63 years). The patients were randomly divided into two groups based on the timing when ezetimibe was added. Results: Plasma LPL mass concentration was significantly reduced by rosuvastatin at 20 mg/day (median = 87.4 [IQR: 71.4-124.7] to 67.5 [IQR: 62.1-114.3] ng/ml, P < 0.05). In contrast, ezetimibe at 10 mg/day as well as colestimide at 3.62 g/day did not alter its level substantially (median = 67.5 [IQR: 62.1-114.3] to 70.2 [IQR: 58.3-106.2], and to 74.9 [IQR: 55.6-101.3] ng/ml, respectively) in the group starting with rosuvastatin followed by the addition of ezetimibe and colestimide. On the other hand, the magnitude in LPL mass reduction was lower in the group starting with ezetimibe at 10 mg/day before reaching the maximum dose of 20 mg/day of rosuvastatin. Plasma EL mass concentration was significantly increased by rosuvastatin at 20 mg/day (median = 278.8 [IQR: 186.7-288.7] to 297.0 [IQR: 266.2-300.2] ng/ml, P < 0.05), whereas other drugs did not significantly alter its level. Conclusion: The effects on changes of LPL and EL mass differed depending on the lipid-lowering therapy, which may impact the prevention of atherosclerosis differently. © 2016 Tada et al.
著者版フラグ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
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