Metabolic Syndrome, Clusterin and Elafin in Patients with Psoriasis Vulgaris
Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články
Grantová podpora
Q40-09
Charles University, Faculty of Medicine in Hradec Kralove, the Czech Republic
Q40-10
Charles University, Faculty of Medicine in Hradec Kralove, the Czech Republic
Q40-11
Charles University, Faculty of Medicine in Hradec Kralove, the Czech Republic
SVV-260543/2020
Charles University, Faculty of Medicine in Hradec Kralove, the Czech Republic
PubMed
32764517
PubMed Central
PMC7460615
DOI
10.3390/ijms21165617
PII: ijms21165617
Knihovny.cz E-zdroje
- Klíčová slova
- clusterin, elafin, metabolic syndrome, psoriasis,
- MeSH
- dospělí MeSH
- elafin genetika MeSH
- index tělesné hmotnosti MeSH
- klusterin genetika MeSH
- komorbidita MeSH
- lidé středního věku MeSH
- lidé MeSH
- metabolický syndrom komplikace genetika metabolismus patologie MeSH
- psoriáza komplikace genetika metabolismus patologie MeSH
- regulace genové exprese genetika MeSH
- studie případů a kontrol MeSH
- stupeň závažnosti nemoci MeSH
- zánět genetika metabolismus patologie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- CLU protein, human MeSH Prohlížeč
- elafin MeSH
- klusterin MeSH
- PI3 protein, human MeSH Prohlížeč
BACKGROUND: Psoriasis is a pathological condition characterized by immune system dysfunction and inflammation. Patients with psoriasis are more likely to develop a wide range of disorders associated with inflammation. Serum levels of various substances and their combinations have been associated with the presence of the disease (psoriasis) and have shown the potential to reflect its activity. The aim of the present study is to contribute to the elucidation of pathophysiological links between psoriasis, its pro-inflammatory comorbidity metabolic syndrome (MetS), and the expression of clusterin and elafin, which are reflected in the pathophysiological "portfolio" of both diseases. MATERIAL AND METHODS: Clinical examinations (PASI score), ELISA (clusterin, elafin), and biochemical analyses (parameters of MetS) were performed. RESULTS: We found that patients with psoriasis were more often afflicted by MetS, compared to the healthy controls. Clusterin and elafin levels were higher in the patients than in the controls but did not correlate to the severity of psoriasis. CONCLUSION: Our data suggest that patients with psoriasis are more susceptible to developing other systemic inflammatory diseases, such as MetS. The levels of clusterin and elafin, which are tightly linked to inflammation, were significantly increased in the patients, compared to the controls, but the presence of MetS in patients did not further increase these levels.
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