Factors associated with high cardiovascular risk in psoriatic arthritis and non-psoriatic spondyloarthritis

被引:4
|
作者
Kavadichanda, Chengappa [1 ]
Shanoj, K. C. [1 ]
Ganapathy, Sachit [2 ]
Shah, Sanket, I [1 ]
Ananthakrishnan, Ramesh [3 ]
Sahoo, Jayprakash [4 ]
Negi, Vir Singh [1 ]
机构
[1] Jawaharlal Inst Postgrad Med Educ & Res, Dept Clin Immunol, Pondicherry 605005, India
[2] Jawaharlal Inst Postgrad Med Educ & Res, Dept Biostat, Pondicherry, India
[3] Jawaharlal Inst Postgrad Med Educ & Res, Dept Radiodiag, Pondicherry, India
[4] Jawaharlal Inst Postgrad Med Educ & Res, Dept Endocrinol, Pondicherry, India
关键词
Sarcopenia; MACE; Atherosclerosis; Arthritis; Inflammation; Visceral fat; Adipokines; ACTIVITY SCORE ASDAS; DISEASE-ACTIVITY; CAROTID ULTRASOUND; METABOLIC SYNDROME; RESISTIN; LEPTIN; MASS;
D O I
10.1007/s00296-021-05064-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To identify the association between traditional cardiovascular risk factors, diseases related factors, body composition and adipokines with high cardiovascular risk (HCVR) in psoriatic arthritis and non-psoriatic spondyloarthritis. This was a cross-sectional study involving age and BMI matched adults with psoriatic arthritis (PsA) (n = 56) and non-psoriatic spondyloarthritis (nPsA-SpA) (n = 58). Body composition using whole-body dual energy X-ray absorptiometry, adipokines and disease characteristics along with cardiovascular risk scoring QRISK3 and carotid intimal medial thickness (CIMT) was collected. Individuals with a QRISK3 >= 10% or CIMT of >= 75 percentile of the general population were categorised as HCVR. Predictors of HCVR were determined by logistic regression. HCVR was detected in 39 (34.2%) of the patients. After adjusting for all the factors, sarcopenia (aOR-15.83; 95% CI 1.16-215.48; p = 0.038) and presence of any traditional CV comorbidity (aOR: 18.97; 95% CI 1.63-221.29; p = 0.019) were associated with HCVR. nPsA-SpA had a 97% lesser chance of having HCVR as compared to PsA. The ROC curve analysis for the multiple logistic regression model which estimated the AUC as 0.787 (95% CI 0.701-0.874) and a P value < 0.001. Adipokine levels correlated well with body composition, but not with HCVR. PsA has a higher CV risk and the mechanisms for the same are poorly understood. Sarcopenia is an important determinant of HCVR and may be due to ectopic adipose tissue deposition in skeletal muscles. Focused physical therapy to prevent sarcopenia, optimum treatment of traditional CV risk factors and adequate disease control may help in preventing atherosclerosis in SpA.
引用
收藏
页码:251 / 260
页数:10
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