Svitlana I. Smiyan , Anastasia V. Bilukha , Bohdan O. Koshak
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Disease activity PsA (DAPSA) and psoriasis area and severity index (PASI) were recorded.</p></div><div><h3>Results</h3><p>Reduced EDVD (<10 %) was significantly more frequent in PsA compared to control (75.3 % vs. 6.7 %, p < 0.001), with significant differences in lipid profile (p < 0.001), homocysteine (p < 0.001), QRISK (p < 0.001), CRP (p < 0.001), DAPSA (p < 0.001), and disease duration (p < 0.001) between PsA patients with reduced and normal EDVD. Average CV risk was 7.7 times higher than in control, and the classical risk factors did not account for the reduced EDVD. Linear regression analysis identified disease duration (β 0.5; OR 1.65, p < 0.001) and disease activity (β 0.09; OR 1.09, p < 0.001) as significant predictors of CV risk in PsA patients. The predictive accuracy of DAPSA (sensitivity 69 %, specificity 86.4 %, 95 % CI: 0.7–0.9; p < 0.001) and disease duration (sensitivity 91 %, specificity 55 %, 95 % CI: 0.95–1; p < 0.001) for CV risk was determined.</p></div><div><h3>Conclusion</h3><p>A heightened CV risk in PsA patients is highlightened independent of traditional risk factors. The significance of disease activity and disease duration as robust predictors of CV risk in PsA patients is emphasized. The data on hyperhomocysteinemia and its association with endothelial dysfunction emphasize the intricate link between PsA, homocysteine levels, and increased CV risk.</p></div>","PeriodicalId":46152,"journal":{"name":"Egyptian Rheumatologist","volume":null,"pages":null},"PeriodicalIF":1.0000,"publicationDate":"2023-11-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S111011642300090X/pdfft?md5=a3afc620119305fa7a6cd62c52aa644e&pid=1-s2.0-S111011642300090X-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Modern determinants of cardiovascular risk factors in patients with psoriatic arthritis: Relation to disease activity and severity\",\"authors\":\"Svitlana I. Smiyan , Anastasia V. Bilukha , Bohdan O. 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Average CV risk was 7.7 times higher than in control, and the classical risk factors did not account for the reduced EDVD. Linear regression analysis identified disease duration (β 0.5; OR 1.65, p < 0.001) and disease activity (β 0.09; OR 1.09, p < 0.001) as significant predictors of CV risk in PsA patients. The predictive accuracy of DAPSA (sensitivity 69 %, specificity 86.4 %, 95 % CI: 0.7–0.9; p < 0.001) and disease duration (sensitivity 91 %, specificity 55 %, 95 % CI: 0.95–1; p < 0.001) for CV risk was determined.</p></div><div><h3>Conclusion</h3><p>A heightened CV risk in PsA patients is highlightened independent of traditional risk factors. The significance of disease activity and disease duration as robust predictors of CV risk in PsA patients is emphasized. 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引用次数: 0
摘要
目的探讨银屑病关节炎(PsA)患者心血管(CV)危险因素的发生频率。患者与方法本研究纳入97例PsA患者和30例对照组。评估血脂和血清同型半胱氨酸水平。内皮依赖性血管舒张(EDVD)评估。采用QRISK-3量表评估心血管风险。记录疾病活动性PsA (DAPSA)和银屑病面积及严重程度指数(PASI)。结果与对照组相比,PsA中EDVD降低(< 10%)的发生率明显更高(75.3% vs. 6.7%, p <0.001),血脂水平有显著差异(p <0.001),同型半胱氨酸(p <0.001), QRISK (p <0.001), CRP (p <0.001), DAPSA (p <0.001)和病程(p <0.001), PsA降低和正常EDVD患者之间的差异。平均CV风险是对照组的7.7倍,传统的危险因素并不能解释EDVD的降低。线性回归分析确定疾病持续时间(β 0.5;OR 1.65, p <0.001)和疾病活动性(β 0.09;OR 1.09, p <0.001)作为PsA患者CV风险的重要预测因子。DAPSA的预测准确性(敏感性69%,特异性86.4%,95% CI: 0.7-0.9;p & lt;0.001)和病程(敏感性91%,特异性55%,95% CI: 0.95-1;p & lt;0.001)的CV风险。结论PsA患者的心血管风险升高与传统危险因素无关。强调疾病活动性和病程作为PsA患者心血管风险的可靠预测因子的重要性。高同型半胱氨酸血症及其与内皮功能障碍相关的数据强调了PsA、同型半胱氨酸水平和心血管风险增加之间的复杂联系。
Modern determinants of cardiovascular risk factors in patients with psoriatic arthritis: Relation to disease activity and severity
Aim of the work
To evaluate the frequency of cardiovascular (CV) risk factors in psoriatic arthritis (PsA) patients.
Patients and methods
The study included 97 PsA patients and 30 control. Lipid profile and serum homocysteine level were assessed. The endothelium-dependent vasodilation (EDVD) evaluated. The QRISK-3 scale was used to assess CV risk. Disease activity PsA (DAPSA) and psoriasis area and severity index (PASI) were recorded.
Results
Reduced EDVD (<10 %) was significantly more frequent in PsA compared to control (75.3 % vs. 6.7 %, p < 0.001), with significant differences in lipid profile (p < 0.001), homocysteine (p < 0.001), QRISK (p < 0.001), CRP (p < 0.001), DAPSA (p < 0.001), and disease duration (p < 0.001) between PsA patients with reduced and normal EDVD. Average CV risk was 7.7 times higher than in control, and the classical risk factors did not account for the reduced EDVD. Linear regression analysis identified disease duration (β 0.5; OR 1.65, p < 0.001) and disease activity (β 0.09; OR 1.09, p < 0.001) as significant predictors of CV risk in PsA patients. The predictive accuracy of DAPSA (sensitivity 69 %, specificity 86.4 %, 95 % CI: 0.7–0.9; p < 0.001) and disease duration (sensitivity 91 %, specificity 55 %, 95 % CI: 0.95–1; p < 0.001) for CV risk was determined.
Conclusion
A heightened CV risk in PsA patients is highlightened independent of traditional risk factors. The significance of disease activity and disease duration as robust predictors of CV risk in PsA patients is emphasized. The data on hyperhomocysteinemia and its association with endothelial dysfunction emphasize the intricate link between PsA, homocysteine levels, and increased CV risk.