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Published on: August 17, 2022
Oxidative Stress Is Associated With Diastolic Dysfunction in Women With Ischemia With No Obstructive Coronary Artery
Mohamad Raad1, Ahmed AlBadri1, Janet Wei2
1Emory Clinical Cardiovascular Research Institute Emory University School of Medicine Atlanta GA.
Insights
Elevated oxidative stress, indicated by cystine levels, is linked to diastolic dysfunction in women with ischemia but no obstructive coronary artery disease. This suggests oxidative stress plays a role in their cardiovascular issues.
Area of Science:
- Cardiology
- Cardiovascular Research
- Biomarkers
Background:
- Women with ischemia and no obstructive coronary artery disease often exhibit diastolic dysfunction.
- Oxidative stress (OS) is a known cardiovascular risk factor, but its link to diastolic dysfunction in this population is unclear.
Purpose of the Study:
- To investigate the association between systemic oxidative stress and diastolic dysfunction in women with suspected ischemia and no obstructive coronary artery disease.
Main Methods:
- A subgroup of 75 women from the WISE-CVD study underwent cardiac MRI for diastolic function assessment (left ventricular end-diastolic volume, peak filling rate) and plasma aminothiol levels (cystine, glutathione) for OS measurement.
- Invasive left ventricular end-diastolic pressure was also recorded.
- Statistical analyses included Spearman correlation and multivariate linear regression.
Main Results:
- Higher plasma cystine levels (a marker of OS) were significantly correlated with impaired diastolic function, specifically a lower peak filling rate and higher left ventricular end-diastolic pressure.
- These associations remained significant after adjusting for cardiovascular risk factors and medications.
- Glutathione levels showed no significant association with diastolic function indices.
Conclusions:
- Systemic oxidative stress, as indicated by elevated cystine levels, is associated with diastolic dysfunction in women with ischemia and no obstructive coronary artery disease.
- These findings highlight a potential role for OS in the pathophysiology of this condition.
- Further research is warranted to explore OS's role in the progression of heart failure with preserved ejection fraction in this patient group.
Abstract:
Background Women with signs and symptoms of ischemia and no obstructive coronary artery disease often have evidence of diastolic dysfunction. Oxidative stress (OS) is associated with cardiovascular risk factors and adverse outcomes. The relationship between systemic OS and diastolic dysfunction is unknown. Methods and Results A subgroup of women (n=75) with suspected ischemia and no obstructive coronary artery disease who had both cardiac magnetic resonance imaging and OS measurements were enrolled in the WISE-CVD (Women Ischemia Syndrome Evaluation-Coronary Vascular Dysfunction) study. Left ventricular end-diastolic pressure was measured invasively. Left ventricular end-diastolic volume and peak filling rate were assessed using cardiac magnetic resonance imaging. Aminothiol levels of plasma cystine and glutathione were measured as markers of OS. Spearman correlation and linear regression analyses were conducted. The group mean age was 54±11 years, and 61% had a resting left ventricular end-diastolic pressure >12 mm Hg. Cystine levels correlated negatively with the peak filling rate (r=-0.31, P=0.007) and positively with left ventricular end-diastolic pressure (r=0.25; P=0.038), indicating that increased OS was associated with diastolic dysfunction. After multivariate adjustment including multiple known risk factors for diastolic dysfunction and cardiovascular medications, cystine levels continued to be associated with peak filling rate (β=-0.27, P=0.049) and left ventricular end-diastolic pressure (β=0.25; P=0.035). Glutathione levels were not associated with indices of diastolic function. Conclusions OS, measured by elevated levels of cystine, is associated with diastolic dysfunction in women with evidence of ischemia and no obstructive coronary artery disease, indicating the role of OS in patients with ischemia and no obstructive coronary artery disease. Its role in the progression of heart failure with preserved ejection fraction should be explored further.
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