Uncovering Proteins Commonly Expressed Between Heart Failure and Dementia Using Bioinformatic Tools
Filipa J Costa1, Rui Vitorino1,2,3, Fernando Ribeiro4
1Institute of Biomedicine (iBiMED), Department of Medical Science, University of Aveiro, 3810-193 Aveiro, Portugal.
Insights
Heart failure and dementia share common risk factors in older adults. This study identifies key proteins like APOE and ACE involved in the heart-brain axis, offering potential biomarkers for these conditions.
Area of Science:
- Gerontology
- Neuroscience
- Cardiology
Background:
- Heart failure (HF) and dementia are prevalent in the elderly, with HF patients facing increased cognitive decline risk.
- Cognitive impairment is a shared comorbidity, yet underlying mechanisms linking HF and dementia remain unclear.
Purpose of the Study:
- To identify proteins that potentially modulate the relationship between heart failure and dementia.
- To investigate molecular players in the heart-brain axis relevant to aging-related cognitive and cardiovascular diseases.
Main Methods:
- Utilized a bioinformatic pipeline for comprehensive literature searching.
- Applied computational tools to analyze and synthesize existing research data.
Main Results:
- Identified apolipoprotein E (APOE), c-reactive protein (CRP), interleukin 6 (IL6), renin (REN), and angiotensin-converting enzyme (ACE) as key proteins.
- These proteins are crucial for heart-brain axis homeostasis; their dysregulation is linked to neuronal and cardiovascular diseases.
Conclusions:
- Highlighted specific proteins that may elucidate the pathophysiology linking heart failure and dementia.
- These identified proteins represent potential biomarkers and therapeutic targets for co-occurring cardiovascular and neurological conditions.
Abstract:
(1) Background: Heart failure (HF) and dementia are commonly associated with the elderly. A significant percentage of patients with HF are at high risk of cognitive decline and progression to dementia. Cognitive impairment is associated with both diseases. However, the molecules and mechanisms that affect the HF-dementia axis are poorly understood. (2) Objective: In this work, we aim to identify potential proteins that modulate HF and dementia. (3) Methods: We applied a pipeline using bioinformatic tools that robustly perform a literature search. (4) Results: Our results show that apolipoprotein E (APOE), c-reactive protein (CRP), interleukin 6 (IL6), renin (REN), and angiotensin-converting enzyme (ACE) proteins are important for maintaining homeostasis in the heart-brain axis. Additionally, deregulated levels of these proteins are associated with neuronal and cardiovascular diseases. (5) Conclusions: Our work highlights proteins that may help in understanding the pathophysiological relationship between HF and dementia. Moreover, these proteins may also be potential biomarkers and/or therapeutic targets.
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