Massin Sophia Z, Suszko Adrian, Wright Stephen P, Billia Filo, Ha Andrew C T, Singh Sheldon M, Lawler Patrick R, Mak Susanna, Chauhan Vijay S
Division of Cardiology, Peter Munk Cardiac Centre, Toronto General Hospital, University Health Network, Toronto, Ontario, Canada.
Division of Cardiology, Mount Sinai Hospital, Toronto, Ontario, Canada.
Can J Cardiol. 2025 Jul 21. doi: 10.1016/j.cjca.2025.07.020.
Atrial low voltage areas (LVAs) provide the substrate for atrial fibrillation (AF). In AF patients with minimal left atrial (LA) LVAs, this substrate has not been well characterised. We determined whether LA myopathy is present in AF patients with minimal LA LVAs (mLVA) by evaluating LA mechanical function and blood biomarkers of structural remodelling.
AF patients undergoing pulmonary vein isolation (PVI) and control subjects without AF were prospectively enrolled. In AF patients, mLVA was defined by LA LVA cut points < 1% to < 5% (< 0.5 mV), and the remaining patients at each cut point were +LVA. LA systolic function was evaluated according to dP/dt of LA pressure. LA diastolic function was assessed according to LA wall compliance. Blood biomarkers were assayed with the use of immunosorbent techniques. Atrial arrhythmia (AA) recurrence was assessed 12 months after PVI.
Among 36 control subjects and 60 AF patients, LA dP/dt was lower in mLVA than in control subjects (P < 0.001). +LVA and mLVA had similar dP/dt. LA compliance was lower in mLVA compared with control subjects (P < 0.001), and lower in +LVA vs mLVA (P < 0.05). Patient groups were associated with mechanical function after adjusting for LVA risk factors. N-terminal pro-atrial natriuretic peptide (NT-proANP) was abnormally elevated in 32% of mLVA patients, and the levels were higher in +LVA than mLVA (P < 0.001). mLVA patients with AA recurrence had lower LA dP/dt than those without AA recurrence (P = 0.012).
mLVA patients have LA mechanical dysfunction and abnormal NT-proANP levels, which are not present in control subjects. AA recurrence in mLVA is associated with LA systolic dysfunction. These findings support the presence of early, diffuse LA myopathy in mLVA.
心房低电压区(LVAs)为房颤(AF)提供了基质。在左心房(LA)LVAs极少的房颤患者中,这种基质尚未得到充分表征。我们通过评估LA机械功能和结构重塑的血液生物标志物,来确定LA心肌病变是否存在于LA LVAs极少(mLVA)的房颤患者中。
前瞻性纳入接受肺静脉隔离(PVI)的房颤患者和无房颤的对照受试者。在房颤患者中,mLVA由LA LVA切点<1%至<5%(<0.5 mV)定义,每个切点处的其余患者为+LVA。根据LA压力的dP/dt评估LA收缩功能。根据LA壁顺应性评估LA舒张功能。使用免疫吸附技术检测血液生物标志物。在PVI后12个月评估房性心律失常(AA)复发情况。
在36名对照受试者和60名房颤患者中,mLVA患者的LA dP/dt低于对照受试者(P<0.001)。+LVA和mLVA的dP/dt相似。与对照受试者相比,mLVA患者的LA顺应性较低(P<0.001),+LVA患者的LA顺应性低于mLVA患者(P<0.05)。在调整LVA危险因素后,患者组与机械功能相关。32%的mLVA患者N末端前心房利钠肽(NT-proANP)异常升高,+LVA患者的NT-proANP水平高于mLVA患者(P<0.001)。AA复发的mLVA患者的LA dP/dt低于未复发AA的患者(P=0.012)。
mLVA患者存在LA机械功能障碍和NT-proANP水平异常,对照受试者中不存在这些情况。mLVA患者的AA复发与LA收缩功能障碍有关。这些发现支持mLVA中存在早期弥漫性LA心肌病变。