Abstract:Background: Patients with plaque psoriasis have an increased risk of metabolic syndrome. However, no studies have assessed the nutritional status or screening methods of this population. Aims: This review aimed to identify and summarise metabolic syndrome screening criteria and the tools/methods used in nutrition assessment in patients with plaque psoriasis. Data synthesis: PubMed, Web of Science, Ovid and Scopus were searched from inception to March 2023, following the Arkensey and O’Malley framework, to iden… Show more
“…Proinflammatory cytokines (e.g., TNF-a and IL-12/23) are shown to be related to renal inflammation and hemodynamics alterations, thus favoring sodium retention and hypertension. In addition, psoriasis is often accompanied with comorbidities such as obesity, insulin resistance, diabetes and NAFLD due to an increased levels of such proinflammatory cytokines (e.g., TNFa, IL-6 and IL-17) [1] [9] [10] .…”
Section: Discussionmentioning
confidence: 99%
“…In the current study the PCA extracted 4 factors consisted of metabolic and redox status parameters in a group of psoriasis patients as following: oxidative stress-inflammation related factor (i.e., HDL-c, CAT, AOPP and CRP), renal function related factor (i.e., creatinine and urea), metabolic related factor (i.e., glucose and TG) and oxidative stress-hepatic related factor (i.e., MDA, ALT). Indeed, previous data in literature have shown the evident interconnection between psoriasis and related comorbidities, such as dyslipidemia, insulin resistance, NAFLD, CKD (1,(9)(10)(11).…”
Section: Discussionmentioning
confidence: 99%
“…Like in many other chronic diseases (i.e., diabetes mellitus, hypertension, obesity, cardiovascular disease, etc.) [4] [5] [6] , oxidative stress and inflammation play the major role in the pathogenesis of psoriasis [7] [8] [9] . The impaired redox balance in favor of pro-oxidants [i.e., reactive oxygen species (ROS) and reactive nitrogen species (RNS)] leads to oxidative modifications and destruction of lipids, proteins and DNA structures in almost all cells and tissues [8] .…”
Section: Introductionmentioning
confidence: 99%
“…Given the fact that psoriasis is a systemic disease, biomolecules’ alterations related to cholesterol metabolism are correlated with comorbidities such as obesity, dyslipidemia, hypertension, insulin resistance, non-alcoholic fatty liver disease (NAFLD) and diabetes [1] [9] [10] . Patients with psoriasis are also at increased risk of chronic kidney disease (CKD) and end-stage renal disease since proinflammatory cytokines influence renal hemodynamics, favor the retention of sodium and lead to hypertension onset and renal injury [11] .…”
Background: Psoriasis is an autoinflammatory disease that affects not only skin, but multiple organs thus being associated with many comorbidities. Oxidative stress and inflammation play the major role in the pathogenesis of this disease. Studies that examined by-products of oxidative stress in psoriasis show discrepant results. Hence, we aimed to examine the oxidative stress, inflammation and metabolic markers and to explore their potential relationship with disease severity in patients with psoriasis.
Methods: This case-control study comprised of 35 patients with psoriasis and 35 age, sex and body mass index-matched healthy controls. Metabolic and oxidative stress biomarkers [i.e., malondialdehyde (MDA), advanced oxidation protein products (AOPP), and catalase (CAT)] were measured. The principal component analysis (PCA) was employed to reduce the number of measured variables into smaller number of factors.
Results: Higher AOPP levels (p<0.01) and CAT activity (p<0.001), but no difference in MDA levels in psoriasis patients vs. healthy controls were shown. Multivariate binary logistic regression analysis showed that a combination of metabolic related factor (i.e., glucose and triglycerides) and renal function related factor (i.e., creatinine and urea) was the best model for Psoriasis Area and Severity Index (PASI) >10 prediction, while oxidative stress-hepatic related factor (i.e., MDA, alanine aminotransferase) was selected as the best predictor for Dermatology Life Quality Index (DLQI) >20.
Conclusion: Multimarker approach showed that metabolic and renal function related factor and oxidative stress-hepatic related factor were better predictors of psoriasis severity than each single examined biomarker.
“…Proinflammatory cytokines (e.g., TNF-a and IL-12/23) are shown to be related to renal inflammation and hemodynamics alterations, thus favoring sodium retention and hypertension. In addition, psoriasis is often accompanied with comorbidities such as obesity, insulin resistance, diabetes and NAFLD due to an increased levels of such proinflammatory cytokines (e.g., TNFa, IL-6 and IL-17) [1] [9] [10] .…”
Section: Discussionmentioning
confidence: 99%
“…In the current study the PCA extracted 4 factors consisted of metabolic and redox status parameters in a group of psoriasis patients as following: oxidative stress-inflammation related factor (i.e., HDL-c, CAT, AOPP and CRP), renal function related factor (i.e., creatinine and urea), metabolic related factor (i.e., glucose and TG) and oxidative stress-hepatic related factor (i.e., MDA, ALT). Indeed, previous data in literature have shown the evident interconnection between psoriasis and related comorbidities, such as dyslipidemia, insulin resistance, NAFLD, CKD (1,(9)(10)(11).…”
Section: Discussionmentioning
confidence: 99%
“…Like in many other chronic diseases (i.e., diabetes mellitus, hypertension, obesity, cardiovascular disease, etc.) [4] [5] [6] , oxidative stress and inflammation play the major role in the pathogenesis of psoriasis [7] [8] [9] . The impaired redox balance in favor of pro-oxidants [i.e., reactive oxygen species (ROS) and reactive nitrogen species (RNS)] leads to oxidative modifications and destruction of lipids, proteins and DNA structures in almost all cells and tissues [8] .…”
Section: Introductionmentioning
confidence: 99%
“…Given the fact that psoriasis is a systemic disease, biomolecules’ alterations related to cholesterol metabolism are correlated with comorbidities such as obesity, dyslipidemia, hypertension, insulin resistance, non-alcoholic fatty liver disease (NAFLD) and diabetes [1] [9] [10] . Patients with psoriasis are also at increased risk of chronic kidney disease (CKD) and end-stage renal disease since proinflammatory cytokines influence renal hemodynamics, favor the retention of sodium and lead to hypertension onset and renal injury [11] .…”
Background: Psoriasis is an autoinflammatory disease that affects not only skin, but multiple organs thus being associated with many comorbidities. Oxidative stress and inflammation play the major role in the pathogenesis of this disease. Studies that examined by-products of oxidative stress in psoriasis show discrepant results. Hence, we aimed to examine the oxidative stress, inflammation and metabolic markers and to explore their potential relationship with disease severity in patients with psoriasis.
Methods: This case-control study comprised of 35 patients with psoriasis and 35 age, sex and body mass index-matched healthy controls. Metabolic and oxidative stress biomarkers [i.e., malondialdehyde (MDA), advanced oxidation protein products (AOPP), and catalase (CAT)] were measured. The principal component analysis (PCA) was employed to reduce the number of measured variables into smaller number of factors.
Results: Higher AOPP levels (p<0.01) and CAT activity (p<0.001), but no difference in MDA levels in psoriasis patients vs. healthy controls were shown. Multivariate binary logistic regression analysis showed that a combination of metabolic related factor (i.e., glucose and triglycerides) and renal function related factor (i.e., creatinine and urea) was the best model for Psoriasis Area and Severity Index (PASI) >10 prediction, while oxidative stress-hepatic related factor (i.e., MDA, alanine aminotransferase) was selected as the best predictor for Dermatology Life Quality Index (DLQI) >20.
Conclusion: Multimarker approach showed that metabolic and renal function related factor and oxidative stress-hepatic related factor were better predictors of psoriasis severity than each single examined biomarker.
BackgroundPsoriasis is a chronic inflammatory disease that causes significant disability. However, little is known about the underlying metabolic mechanisms of psoriasis. Our study aims to investigate the causality of 975 blood metabolites with the risk of psoriasis.Materials and MethodsWe mainly applied genetic analysis to explore the possible associations between 975 blood metabolites and psoriasis. The inverse variance weighted (IVW) method was used as the primary analysis to assess the possible association of blood metabolites with psoriasis. Moreover, generalized summary‐data‐based Mendelian randomization (GSMR) was used as a supplementary analysis. In addition, linkage disequilibrium score regression (LDSC) was used to investigate their genetic correction further. Metabolic pathway analysis of the most suggested metabolites was also performed using MetaboAnalyst 5.0.ResultsIn our primary analysis, 17 metabolites, including unsaturated fatty acids, phospholipids, and triglycerides traits, were selected as potential factors in psoriasis, with odd ratios (OR) ranging from 0.986 to 1.01. The GSMR method confirmed the above results (β = 0.001, p < 0.05). LDSC analysis mainly suggested the genetic correlation of psoriasis with genetic correlations (rg) from 0.088 to 0.155. Based on the selected metabolites, metabolic pathway analysis suggested seven metabolic pathways including ketone body that may be prominent pathways for metabolites in psoriasis.ConclusionOur study supports the causal role of unsaturated fatty acid properties and lipid traits with psoriasis. These properties may be regulated by the ketone body metabolic pathway.
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