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Association Between Coronary and Peripheral Vascular Injury in Heart Failure Patients With Preserved Ejection Fraction.

Association Between Coronary and Peripheral Vascular Injury in Heart Failure Patients With Preserved Ejection Fraction.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05884346
Acronym
COROVASC
Enrollment
84
Registered
2023-06-01
Start date
2023-06-30
Completion date
2024-05-31
Last updated
2023-06-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure With Preserved Ejection Fraction

Keywords

Ultrahigh-frequency ultrasound, Heart Failure with Preserved Ejection Fraction, Microcirculation, Arterial remodeling, Small arteries, Ischemia

Brief summary

Heart failure with preserved ejection fraction (HPEF, defined as LVEF ≥50%) represents 50% of hospital admissions for heart failure. Although its morbi-mortality is similar to that of heart failure with reduced ejection fraction (HFPEF), it remains an unknown disease with limited data especially from an etiological point of view. The underlying causes are imperfectly understood, and more than half of the patients have HPEF labeled idiopathic. A non-hierarchical clustering study of HPEF patients led to the identification of a subgroup of patients (25%) with a predominant coronary vascular phenotype (i.e., a history of coronary stenosis with or without the need for revascularization). In these patients, vascular endothelial dysfunction would play a central role in the development and progression of heart failure.One of the mechanisms leading to HPEF could be a decrease in the bioavailability of nitric oxide (NO) involved in the relaxation of the cardiac muscle. As the mechanism of action of NO is pleiotropic, a decrease in NO bioavailability could also be observed at the peripheral level, favoring in the long term the development of unfavorable vascular remodeling, for example in the small digital or retinal arteries.Some HPEF patients could thus be distinguished from others by their predominant vascular profile. The link between HPEF and endothelial dysfunction has been suspected but never clearly demonstrated. Ultra-high frequency ultrasound is an innovative technology to estimate the remodeling of small distal arteries in a non-invasive way. The investigators propose to use this imaging on digital arteries in HPEF patients and to study the association with known coronary macrovascular damage.The remodeling parameters will be measured and compared in patients with HPEF with or without identified macrovascular coronary disease.This characterization of arterial remodeling on the digital arteries could be a powerful tool for non-invasive screening in the identification of a subgroup of HPEF that is still considered idiopathic.

Interventions

OTHERUltrahigh-frequency ultrasound

Arterial remodeling of the digital arteries will be measured by ultrahigh-frequency ultrasound and will be compared in heart failure patients with preserved ejection fraction with and without identified macroscopic coronary disease

Sponsors

Institut National de la Santé Et de la Recherche Médicale, France
CollaboratorOTHER_GOV
Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

: Group 1 : * Patients who are ≥ 18 years old * Heart failure with preserved ejection fraction (LVEF ≥ 50%) * B-type natriuretic peptide (BNP) \> 35 pg/mL at inclusion * Coronary macrovascular disease (significant coronary stenosis, which may have required revascularization by stenting or coronary bypass surgery). Group 2 : * Patients who are ≥ 18 years old * Heart failure with preserved ejection fraction (LVEF ≥ 50%) * B-type natriuretic peptide (BNP) \> 35 pg/mL at screening * Absence of coronary macrovascular disease (no significant coronary atheroma (\< 30%) or history of stenting or coronary bypass surgery). Non-inclusion Criteria : Group 1 and group 2 : * Patients under legal protection * Patients not affiliated to a Social Security system * Patient under State Medical Help (France - AME) * Pregnancy or breastfeeding * Refusal or inability to sign consent * Known and treated retinal vasculopathy * Severe or non-stabilized hypertension (BP \> 180/100 mmHg at screening) * History of LVEF \< 40%.

Design outcomes

Primary

MeasureTime frameDescription
Digital vascular remodeling by ultrahigh-frequency ultrasoundDay 1The wall-to-lumen ratio of digital arteries recorded with ultrahigh-frequency ultrasound.

Secondary

MeasureTime frameDescription
Carotid vascular remodeling by echo-trackingDay 1Measurement of peripheral vascular remodeling on carotid arteries by arterial distension parameters.
Endothelial dysfunctionDay 1Level of endothelial function measured by arterial flow-mediated vasodilation (FMD, expressed in %).
Radial vascular remodeling by echo-trackingDay 1Measurement of peripheral vascular remodeling on radial arteries by arterial distension parameters.
Retinal microvascularizationDay 1To study the retinal microvascularization by Optical Coherence Tomography Angiography (OCT-A) : density measurement per sector (% per studied area).
Calcium scoreDay 1Compare the calcium score (expressed by the Agatston score) in patients with heart failure with preserved ejection fraction with or without a priori coronary artery disease.
Pulse wave velocityDay 1Pulse wave velocity (PWV, velocity expressed in m/s) carotid-femoral (aortic elasticity).

Countries

France

Contacts

Primary ContactAnnie BERGERA
gestion-locale.drc@aphp.fr(0)1 44 84 17 24
Backup ContactNatacha NOHILE
natacha.nohile@aphp.fr

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026