Key result
Increased arterial stiffness driven by aging and comorbidities is linked to HFpEF.
Why the study?
Comorbidities and abnormal macrovascular and microvascular function may contribute to HFpEF, but whether increased arterial stiffness from comorbidities is associated with HFpEF remains to be investigated.
Does increased arterial stiffness associate with HFpEF, in addition to ageing and vascular effects of comorbidities?
Observational
No
Does increased arterial stiffness associate with HFpEF, in addition to ageing and vascular effects of comorbidities?
The IDENTIFY-HF study is designed to evaluate whether increased arterial stiffness and microvascular dysfunction driven by comorbidities are associated with the pathophysiology of HFpEF.
Observational design leaves open arterial stiffness as HFpEF contributor beyond aging and comorbidities; longitudinal studies needed.
AIMS: There has been a paradigm shift proposing that comorbidities are a major contributor towards the heart failure with preserved ejection fraction (HFpEF) syndrome. Furthermore, HFpEF patients have abnormal macrovascular and microvascular function, which may significantly contribute towards altered ventricular-vascular coupling in these patients. The IDENTIFY-HF study will investigate whether gradually increased arterial stiffness (in addition to ageing) as a result of increasing common comorbidities, such as hypertension and diabetes, is associated with HFpEF. METHODS AND ANALYSIS: In our observational study, arterial compliance and microvascular function will be assessed in five groups (Groups A to E) of age, sex and body mass index matched subjects (age ≥70 years in all groups):Group A; normal healthy volunteers without major comorbidities such as hypertension and diabetes mellitus (control). Group B; patients with hypertension without diabetes mellitus or heart failure (HF). Group C; patients with hypertension and diabetes mellitus without HF. Group D; patients with HFpEF. Group E; patients with heart failure and reduced ejection fraction (parallel group). Vascular function and arterial compliance will be assessed using pulse wave velocity, as the primary outcome measure. Further outcome measures include cutaneous laser Doppler flowmetry as a measure of endothelial function, transthoracic echocardiography and exercise tolerance measures. Biomarkers include NT-proBNP, high-sensitivity troponin T, as well as serum galectin-3 as a marker of fibrosis. ETHICS AND DISSEMINATION: The study was approved by the regional research ethics committee (REC), West Midland and Black Country 17/WM/0039, UK, and permission to conduct the study in the hospital was also obtained from the RDI, UHCW NHS Trust. The results will be published in peer-reviewed journals and presented in local, national and international medical society meetings. TRIAL REGISTRATION NUMBER: NCT03186833.
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Ali et al. (2019) conducted an observational in Heart failure with preserved ejection fraction (HFpEF). Assessment of arterial compliance and microvascular function vs. Healthy volunteers, hypertension, hypertension with diabetes, and HFrEF groups was evaluated on Vascular function and arterial compliance assessed using pulse wave velocity. The IDENTIFY-HF study is an observational trial designed to investigate whether increased arterial stiffness, driven by aging and comorbidities, is associated with HFpEF.
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