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Ocular microvascular alterations in patients with heart failure with preserved ejection fraction
Yoichiro Shinohara1, Masaru Obokata2, Ryo Mukai3,4
1Department of Ophthalmology, Gunma University Graduate School of Medicine, 3-39-15 Showa machi, Maebashi, Gunma, 371-8511, Japan. shinohara@gunma-u.ac.jp.
Insights
Ocular blood flow and retinal thickness are reduced in heart failure with preserved ejection fraction (HFpEF) patients. These changes correlate with cardiac function, suggesting LSFG and OCT/OCTA can detect HFpEF-related ocular alterations.
Area of Science:
- Ophthalmology
- Cardiology
- Medical Imaging
Background:
- Heart failure with preserved ejection fraction (HFpEF) affects cardiac function.
- Ocular circulation may reflect systemic cardiovascular health.
Purpose of the Study:
- To investigate ocular circulation and structure in HFpEF patients.
- To assess the association between ocular findings and cardiac function in HFpEF.
Main Methods:
- Prospective observational study of 15 HFpEF patients and 15 controls.
- Evaluated best-corrected visual acuity (BCVA), retinal and choroidal thickness, laser speckle flowgraphy (LSFG), and optical coherence tomography angiography (OCTA).
- Echocardiography assessed cardiac function, including E/e' for diastolic dysfunction.
Main Results:
- Reduced mean blur rate (MBR) in optic nerve head (ONH) and macula in HFpEF patients.
- ONH-MBR correlated with E/e' (left ventricular diastolic dysfunction marker).
- Enlarged foveal avascular zone and thinner central retinal thickness (CRT) and choroidal thickness (CCT) in HFpEF patients.
Conclusions:
- Ocular circulatory and structural changes are detectable in HFpEF.
- LSFG and OCT/OCTA can identify these changes, potentially linking ocular findings to cardiac function.
Purpose:
To investigate ocular circulation characteristics and their association with cardiac function in patients with heart failure with preserved ejection fraction (HFpEF).
Study Design:
Prospective observational study.
Methods:
This prospective study included 15 patients with and 15 individuals without HFpEF. Best-corrected visual acuity (BCVA), central retinal thickness (CRT), central choroidal thickness (CCT), laser speckle flowgraphy (LSFG), and optical coherence tomography angiography (OCTA) were assessed. LSFG was performed to evaluate blood flow in the optic nerve head (ONH) and macula; OCTA was performed to evaluate macular microvascular parameters. Patients with HFpEF underwent echocardiography to evaluate their cardiac function.
Results:
Mean blur rate (MBR), a blood flow parameter of LSFG, in HFpEF eyes was significantly reduced in the ONH and macula compared with individuals without HFpEF (p=0.0002; ONH, p=0.0012; macula). ONH-MBR correlated with E/e', a marker for left ventricular diastolic dysfunction measured using echocardiography (r=-0.67, p=0.011). The foveal avascular zone, measured using OCTA, was significantly enlarged in patients with HFpEF (p=0.018) and correlated with BCVA (r=0.58, p=0.0009). CRT and CCT in patients with HFpEF were significantly thinner compared with those in individuals without HFpEF (p=0.011, CRT; p=0.010, CCT).
Conclusion:
Ocular circulatory and chorioretinal structural changes may be detectable in patients with HFpEF using LSFG and OCT/OCTA.
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