Key result
Serum ANGPTL8 concentrations differed significantly between patients with psoriasis and healthy controls (p < 0.05) and increased significantly after 3 months of acitretin treatment (p < 0.05).
Why the study?
The molecular targets of ANGPTL8 remain poorly defined, prompting evaluation of serum ANGPTL8 concentrations in psoriasis and the effect of systemic therapy.
Does systemic therapy with methotrexate or acitretin alter serum ANGPTL8 concentrations in patients with plaque-type psoriasis?
Observational (n=53)
Does systemic therapy with methotrexate or acitretin alter serum ANGPTL8 concentrations in patients with plaque-type psoriasis?
Elevated levels of ANGPTL8 may reduce the likelihood of atherogenic dyslipidemia in individuals with psoriasis, and acitretin treatment increases its concentration.
Answers are grounded in this paper and cite their sources.
Higher ANGPTL8 in psoriasis correlated inversely with lipids; hypothesis-generating for a protective metabolic role pending confirmatory studies.
Angiopoietin-like protein 8 (ANGPTL8) exerts pleiotropic effects, taking part in lipid and carbohydrate metabolism, inflammation, hematopoiesis and oncogenesis. So far, the exact molecular targets of ANGPTL8 remain poorly defined. We aimed to evaluate the serum concentration of ANGPTL8 in individuals with psoriasis and examine how systemic therapy affects the concentration of ANGPTL8. The study enrolled 35 patients with plaque-type psoriasis that were followed for 3 months of treatment with methotrexate or acitretin, and 18 healthy volunteers without psoriasis as controls. Serum ANGPTL8 concentrations were analyzed by ELISA and differences between groups were determined using Student’s t-test or the Mann–Whitney test, while correlations were assessed using Spearman’s rank test. The average concentration of ANGPTL8 differed significantly between the psoriasis group (before and after therapy) and the control group (p < 0.05). Significant negative correlations between ANGPTL8 and total cholesterol and LDL levels were noted (both p < 0.05). A significant increase in ANGPTL8 concentration was observed after acitretin (p < 0.05), whereas in patients treated with methotrexate the ANGPTL8 did not change significantly (p > 0.05). Additionally, a negative, statistically significant correlation with PASI was found after treatment (p < 0.05). Based on our study, it appears that elevated levels of ANGPTL8 may reduce the likelihood of atherogenic dyslipidemia in individuals with psoriasis, and treatment for psoriasis may impact the protective effects of ANGPTL8.
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Baran et al. (2023) conducted an observational in Psoriasis (n=53). Psoriasis vs. Healthy volunteers without psoriasis was evaluated on Serum ANGPTL8 concentration (p=< 0.05). Serum ANGPTL8 concentrations differed significantly between patients with psoriasis and healthy controls (p < 0.05) and increased significantly after 3 months of acitretin treatment (p < 0.05).
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