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The difference of lipid profiles between psoriasis with arthritis and psoriasis without arthritis and sex-specific downregulation of methotrexate on the apolipoprotein B/apolipoprotein A-1 ratio.

Authors :
Wang B
Deng H
Hu Y
Han L
Huang Q
Fang X
Yang K
Wu S
Zheng Z
Yawalkar N
Zhang Z
Yan K
Source :
Arthritis research & therapy [Arthritis Res Ther] 2022 Jan 07; Vol. 24 (1), pp. 17. Date of Electronic Publication: 2022 Jan 07.
Publication Year :
2022

Abstract

Background: Methotrexate (MTX) has a protective effect against cardiovascular diseases (CVD), but the mechanism is unclear.<br />Objective: To investigate the effect of MTX on lipid profiles and the difference between psoriasis without arthritis (PsO) and psoriatic arthritis (PsA).<br />Methods: In this prospective study, we recruited 288 psoriatic patients (136 PsA and 152 PsO) who completed 12 weeks of MTX treatment. Total cholesterol (TC), triglycerides (TG), lipoprotein A [LP(a)], high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein (LDL), apolipoprotein A1 (ApoA1), and ApoB were measured.<br />Results: Compared with sex- and age-matched healthy controls, psoriatic patients had significantly (p < 0.0001) higher levels of proatherogenic lipids and lower levels of anti-atherogenic lipids. PsA patients had a higher ApoB/ApoA1 ratio than PsO patients (p < 0.05). Stepwise regression analysis found a positive correlation between the inflammatory marker hCRP and the Psoriasis Area Severity Index (PASI), ApoB/ApoA1 ratio, BMI, and smoking. ApoB was positively associated with concomitant arthritis, diabetes, and hypertension. MTX decreased the levels of pro-atherogenic and anti-atherogenic lipids. However, a significant reduction of the ApoB/ApoA1 ratio by MTX was only observed in male patients.<br />Conclusion: PsA patients had a significantly higher percentage of concomitant disease than PsO. The decrease of MTX on CVD might be related with sex.<br />Trial Registration: ChiCTR2000036192.<br /> (© 2022. The Author(s).)

Details

Language :
English
ISSN :
1478-6362
Volume :
24
Issue :
1
Database :
MEDLINE
Journal :
Arthritis research & therapy
Publication Type :
Academic Journal
Accession number :
34996506
Full Text :
https://doi.org/10.1186/s13075-021-02715-4