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Lipid profile disturbances may predispose psoriatic patients to liver dysfunction

Authors :
Dorota Kozłowska
Ewa Harasim-Symbor
Adrian Chabowski
Hanna Myśliwiec
Iwona Flisiak
Anna Justyna Milewska
Source :
Advances in Dermatology and Allergology, Vol 38, Iss 2, Pp 310-318 (2021), Advances in Dermatology and Allergology/Postȩpy Dermatologii i Alergologii
Publication Year :
2021
Publisher :
Termedia Sp. z.o.o., 2021.

Abstract

Introduction Psoriasis is a chronic inflammatory disease associated with metabolic disturbances and liver dysfunction. Both serum fatty acids (FA) and ceramides (Cer) have structural functions but also are signal molecules that could be involved in the pathogenesis of liver dysfunction. Aim To assess the concentration of the circulating FA and Cer in correlation with the alanine aminotransferase (ALT) blood level in psoriatic patients. In addition, we have examined the relationship between ALT concentration and severity of the disease and inflammation markers. Material and methods Eighty-five patients with psoriasis and 32 healthy controls were enrolled in the study. Patients were divided into 2 groups according to ALT blood levels. Serum concentration of 14 FA and 14 Cer were measured by gas-liquid chromatography. The results were correlated with the Psoriasis Area and Severity Index (PASI), serum lipid profile, and inflammatory markers. Results We observed higher PASI score (p = 0.01) and higher C-reactive protein (p = 0.02) concentration in the group of psoriatic patients with high ALT. Serum ALT positively correlated with saturated fatty acids (SFA) (p = 0.01, r = 0.27) and SFA/unsaturated fatty acids (UFA) ratio (p = 0.01, r = 0.26). ALT negatively correlated with UFA level (p = 0.008, r = –0.28). Lignoceric ceramide positively correlated with ALT level (r = 0.22; p = 0.045) in psoriatic patients. Conclusions Patients with severe psoriasis are predisposed to the development of liver dysfunction. We have demonstrated disturbances of serum fatty acid and sphingolipid profile in psoriatic patients, which may trigger liver disease.

Details

ISSN :
1642395X
Volume :
38
Database :
OpenAIRE
Journal :
Advances in Dermatology and Allergology
Accession number :
edsair.doi.dedup.....6745eea16a38423fc5ff38933ce3d59f
Full Text :
https://doi.org/10.5114/ada.2021.106209