PCSK9 阻害およびスタチン療法による残留炎症リスク
Aruna D Pradhan1,2, Aaron W Aday2,3, Lynda M Rose2
1Department of Medicine, Division of Cardiovascular Medicine, VA Boston Healthcare System, West Roxbury Campus, MA (A.D.P.). apradhan@bwh.harvard.edu.
Circulation
|May 3, 2018
まとめ
スタチンとPCSK9阻害剤による治療は,LDLコレステロールを著しく低下させるが,hsCRP値によって示される残留炎症リスクは持続する. 治療中のhsCRP濃度の上昇は,両方の治療を受けた患者の心血管疾患発生率の増加と関連していました.
科学分野:
- 心臓病科
- 薬理学について
- 炎症に関する研究
背景:
- PCSK9抑制と併用されたスタチンの治療は,LDLコレステロールと心血管疾患を効果的に減少させる.
- 治療中の高感度C反応性タンパク質 (hsCRP) で測定された,残留炎症リスクの役割はよく定義されていません.
研究 の 目的:
- スタチン療法とPCSK9阻害剤のボコシズマブを併用した患者の残留炎症リスクを評価する.
- この患者集団における治療中のhsCRPレベルと心血管疾患発生率との関連性を評価する.
主な方法:
- SPIRE-1およびSPIRE-2試験の9738人の患者のポストホック分析が行われました.
- 治療中のhsCRP (hsCRPOT) とLDL- C (LDL- COT) を測定した.
- 心血管疾患 (心筋梗塞,脳卒中,不安定な胸痛,心血管疾患による死亡) を追跡した.
主要な成果:
- ボコシズマブは14週間でLDL- Cを - 60. 5% 減少させ,hsCRPは最小限の変化を示した.
- hsCRP< sub>OT sub>レベル (> 3 mg/ L) が高かった患者は,hsCRP< sub>OT sub>< 1 mg/ Lの患者と比較して,心血管疾患のリスクが著しく高かった (HR1. 62).
- hsCRP< sub>OT sub>レベルとボコシズマブで達成された相対的なリスク低下との間に有意な相互作用は観察されなかった.
結論:
- スタチンとPCSK9阻害で治療された患者では,治療中のhsCRPの増加によって示される残留炎症リスクが持続する.
- 高度なhsCRPOTレベルは,強烈なLDL- C低下であっても,心血管疾患のリスクが高くなります.
- これらの発見は,併用療法を受けている患者のLDL- Cレベルとは無関係に,炎症経路が心血管リスクに寄与することを示唆しています.
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