リポラライゼーション・アルターナンは,人間の心房細動に対する脆弱性を明らかにする
Sanjiv M Narayan1, Michael R Franz, Paul Clopton
1VAMC/Cardiology, University of California-San Diego, 3350 La Jolla Village Dr., San Diego, CA 92161, USA. snarayan@ucsd.edu
Circulation
|June 8, 2011
まとめ
アクションポテンシャル持続時間 (APD) の変数におけるビート・トゥ・ビートの振動は,心房動 (AF) の動的基板を明らかにする. これらの代替薬は,対照群と比較して,持続性およびパラキシズム性AF患者においてより容易に発生し,より低い割合で発生します.
科学分野:
- 心臓病学 心臓病学
- 電気生理学 電気生理学
- 心律不整症とは,心律不整症のこと.
背景:
- 人間の心房細動 (AF) の根本的なメカニズムは,異常な再極化,特にアクションポテンシャル持続 (APD) が関与しているため,まだ完全に理解されていません.
- AFの脆弱性のスペクトルが存在し,AFのない個体から,パラキシズマルおよび持続的な形態を持つ個人に及ぶ.
研究 の 目的:
- APDのビート・トゥ・ビート振動,APDのアルターナーと呼ばれる振動がAF基板に寄与するという仮説を検証する.
- APDの代替薬が,異なる患者グループにおけるAFに対する異なる感受性を説明できるかどうかを判断する.
主な方法:
- プログラムされた電気刺激中に33人の被験者 (12人の持続性AF,13人のパラキシズム性AF,8人の対照) の左および右心房APDを記録した.
- ペースは,APDの復元と代替を評価するために,減速するサイクルの長さ (600〜500 ms,その後AFの開始までより速く) で実行されました.
- APDの変数,複雑な振動,および異なるペースでAFの開始の間の関係を分析した.
主要な成果:
- APDの代替薬は,パラキシズム性AF (372±72 ms) と持続性AF (411±94 ms) の患者と比較して,コントロール群 (サイクル長さ218±33 ms) で著しく速い割合で発現しました.
- AF患者では,APDのアルターナーが100-120bpmのペースで発生し,APDの回復とは無関係であった.
- AFに先立つ複雑な振動は,パロキシズム性AFと持続性AFの患者と比較して,対照群で漸進的により速い割合で発生しました.
結論:
- アトリアルAPDの代替剤はAFのダイナミックな基板として機能し,AFがコントロールと比較して持続的および症候性AF患者でより低い割合で最も容易に現れます.
- APDの代替は,一貫してすべての観察されたAFエピソードに先行し,AFが開始されなかったときに欠席していました.
- 細胞メカニズムを明らかにするためにさらなる研究が必要で,APDの代替体は生理学的心拍数に近い.
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