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Sex-specific difference in the association between arterial stiffness and subclinical left ventricular dysfunction
Yuriko Yoshida1, Koki Nakanishi1, Masao Daimon1,2
1Department of Cardiovascular Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8655, Japan.
European Heart Journal. Cardiovascular Imaging
|June 29, 2020
Summary
Arterial stiffness is linked to early heart dysfunction, especially in women. This study found a stronger connection between arterial stiffness and reduced left ventricular function in women, potentially explaining their higher risk for heart failure.
Area of Science:
- Cardiology
- Vascular Biology
- Echocardiography
Background:
- Increased arterial stiffness is a key factor in heart failure with preserved ejection fraction (HFpEF).
- Subclinical left ventricular (LV) dysfunction and its sex-specific differences in relation to arterial stiffness are not well understood.
- Left ventricular (LV) strain analysis offers a sensitive method for detecting early LV abnormalities.
Purpose of the Study:
- To investigate the association between arterial stiffness and subclinical LV dysfunction.
- To explore potential sex-specific differences in this association.
- To determine if arterial stiffness predicts LV dysfunction independent of traditional risk factors.
Main Methods:
- Examined 1155 participants without overt cardiovascular disease.
- Assessed arterial stiffness using cardio-ankle vascular index (CAVI).
- Evaluated LV global longitudinal strain (LVGLS) and global circumferential strain (GCS) via speckle-tracking echocardiography.
Main Results:
- Arterial stiffness (CAVI) was associated with abnormal LVGLS, but not LVGCS, independent of risk factors.
- The association between CAVI and abnormal LVGLS was more pronounced in women than in men.
- This independent association persisted in women after adjusting for LV mass and diastolic parameters, but not in men.
Conclusions:
- Increased arterial stiffness is independently linked to reduced LVGLS, even in individuals without overt cardiovascular disease.
- A sex-specific pattern in vascular-ventricular coupling alterations was observed.
- These findings may contribute to understanding the higher susceptibility to HFpEF in women.
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