Author:
Wang Bing,Deng Hui,Hu Yao,Han Ling,Huang Qiong,Fang Xu,Yang Ke,Wu Siyuan,Zheng Zhizhong,Yawalkar Nikhil,Zhang Zhenghua,Yan Kexiang
Abstract
Abstract
Background
Methotrexate (MTX) has a protective effect against cardiovascular diseases (CVD), but the mechanism is unclear.
Objective
To investigate the effect of MTX on lipid profiles and the difference between psoriasis without arthritis (PsO) and psoriatic arthritis (PsA).
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.
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.
Conclusion
PsA patients had a significantly higher percentage of concomitant disease than PsO. The decrease of MTX on CVD might be related with sex.
Trial registration
ChiCTR2000036192
Publisher
Springer Science and Business Media LLC
Cited by
6 articles.
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