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Association of the Complement System with Subclinical Atherosclerosis in Psoriasis: Findings from an Observational
Laura Mourino-Alvarez1, Inés Perales-Sanchez1, Emilio Berna-Rico2
1Department of Vascular Physiopathology, Hospital Nacional de Paraplejicos, SESCAM, Toledo, Spain; Department of Vascular Physiopathology, Hospital Nacional de Paraplejicos, IDISCAM, Toledo, Spain.
Insights
This study identified 11 key proteins linked to complement cascades, revealing their role in developing atherosclerosis in psoriasis patients. These findings offer insights into cardiovascular risk and potential new therapies for psoriasis.
Area of Science:
- Immunodermatology
- Cardiovascular Science
- Proteomics
Background:
- Psoriasis is a chronic inflammatory skin and joint disease.
- Psoriasis patients face increased cardiovascular disease (CVD) risk, particularly atherosclerosis.
- Shared inflammatory pathways link psoriasis and atherosclerosis, including vascular inflammation and complement activation.
Purpose of the Study:
- To investigate the relationship between psoriasis and atherosclerosis.
- To identify specific protein biomarkers associated with subclinical atherosclerosis in psoriasis patients.
Main Methods:
- Proteomics analysis of plasma from psoriasis patients.
- Bioinformatics analysis to identify differentially expressed proteins.
- Validation using ELISA and western blotting.
Main Results:
- 31 proteins related to complement system and oxygen transport were identified.
- 11 proteins were validated as indicators of subclinical atherosclerosis in psoriasis patients.
- Complement cascades play a significant role in atherosclerotic plaque development in psoriasis.
Conclusions:
- The study identified novel protein biomarkers for subclinical atherosclerosis in psoriasis.
- Findings enhance understanding of cardiovascular risk pathways in psoriasis.
- Results may inform predictive tools and therapeutic strategies for managing psoriasis comorbidities.
Abstract:
Psoriasis is a chronic and inflammatory disease that affects the skin and joints and is associated with multiple comorbidities and cardiovascular risk factors. Consequently, patients with psoriasis have an increased risk of cardiovascular diseases such as atherosclerosis, a chronic pathology that shares common inflammatory and immune-response mechanisms with psoriasis, including vascular inflammation and complement activation. To better understand the relationship between atherosclerosis and psoriasis, a proteomics study followed by a bioinformatics analysis was carried out, with a subsequent validation step using ELISA and western blotting. When the plasma from patients with psoriasis alone was compared with that from patients with psoriasis and atherosclerosis, 31 proteins of interest related to the complement system and oxygen transport were identified. After the validation phase, 11 proteins appeared to define the presence of subclinical atherosclerosis in patients with psoriasis, indicating the importance of complement cascades in the development of atherosclerotic plaques in individuals with psoriasis. These results are a step forward in understanding the pathological pathways implicated in the cardiovascular risk associated with this population, which may represent an interesting starting point for developing predictive tools that improve the follow-up of these patients and design more effective therapies.
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