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Abstract Number: 3099

Higher Prevalence and Severity of Coronary Atherosclerosis in Psa Patients

Lydia Ho Pui TAM1,2, Tsz Ho CHENG1, Ho Man LAM1, Ka Tat WONG3, Qing SHANG4, Edmund LI1, Wang Kit LI5, Man Fei CHEUNG5, Uen-Lam MING1, Tin-Long LUI5, Wing-Lam TAO1, SY TSANG1 and Lai-Shan TAM6, 1Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong, Hong Kong, 2Department of Medicine and Therapeutics, Prince of Wales Hospital, Hong Kong, Hong Kong, 3Prince of Wales Hospital, Hong Kong, Hong Kong, 4Department of Medicine & Therapeutics, The Chinese University of Hong Kong, Hong Kong, Hong Kong, 5The Chinese University of Hong Kong, Hong Kong, Hong Kong, 6Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong, China

Meeting: 2016 ACR/ARHP Annual Meeting

Date of first publication: September 28, 2016

Keywords: Atherosclerosis, coronary artery disease and psoriatic arthritis

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Session Information

Date: Tuesday, November 15, 2016

Title: Spondylarthropathies and Psoriatic Arthritis – Clinical Aspects and Treatment IV: Psoriatic Arthritis – Clinical

Session Type: ACR Concurrent Abstract Session

Session Time: 4:30PM-6:00PM

Background/Purpose: Patients with psoriatic arthritis (PsA) have increased risk in cardiovascular diseases (CVD) including subclinical atherosclerosis. However, previous knowledge was limited to carotid atherosclerosis. The aim of this study was to determine whether PsA patients had a higher prevalence and severity of coronary atherosclerosis compared to control subjects. We also aimed to test the association between the disease characteristics and coronary atherosclerosis in PsA patients.

Methods: 82 PsA patients [male: 51 (62%); 51±11 years] were recruited. Coronary atherosclerosis was evaluated by computed tomography angiography (CTA). 231 control subjects [male: 155 (67%); 49±10 years] without known CVD and rheumatic diseases, who were referred to receive CTA scan due to chest pain and/or multiple CVD risk factors, were also recruited.

Results: PsA patients and controls were well matched in age, gender, smoking status, history of hypertension and dyslipidemia, lipid profile and fasting glucose (p ranged from 0.158 to 0.978). PsA patients had a higher prevalence of diabetes mellitus than controls [13 (16%) vs 15 (7%), p=0.012]. The prevalence of overall coronary plaque [52 (63%) vs 74 (32%), p<0.001], calcified plaque (CP) [27 (33%) vs 30 (13%), p<0.001], mixed plaque (MP) [19 (23%) vs 13 (6%), p<0.001], non-calcified plaque (NCP) [38 (46%) vs. 51 (22%), p<0.001], and combined MP/NCP [45 (55%) vs. 57 (25%), p<0.001] were all significantly higher in PsA patients. PsA patients also had higher coronary calcium score (CAC) compared with control subjects (46±151 vs 5±19, p=0.018). In patients with coronary plaque, 3-vessle diseases were seen in 11 (21%) PsA patients and 4 (5%) controls (p=0.007); while severe stenosis was seen in 7 (13%) PsA patients and 1 (1%) controls (p=0.008). After adjusting for traditional CVD risk factors, PsA remained the strongest predictor for all types of coronary plaques (Table 1). In all subjects with plaque (52 PsA patients and 74 controls), PsA was the only independent predictor for 3-vessel disease after adjusting for CVD risk factors [odd ratio: 5.724 (1.506-21.759), p=0.010]. In PsA patients, the PsA disease duration was the only disease specific characteristic which was correlated with the more vulnerable plaque types (MP/NCP) in univariate [1.057 (1.003-1.113), p=0.037] and multivariate analysis [1.067 (1.010-1.127), p=0.020; adjusted for age, gender, hypertension, diabetes, hyperlipidemia, family history of CVD and smoking]. The other independent predictor was male gender [3.519 (1.306-9.480), p=0.013].

Conclusion: PsA patients had higher prevalence and severity of coronary atherosclerosis compared with control subjects. Longer disease duration, but not older age, was independently correlated with the more vulnerable MP/NCP in PsA patients. Table 1. Independent predictors in multivariate analysis for coronary plaque in PsA patients and control subjects.

Odd ratio

95% CI

p

All plaque PsA

4.552

2.517-8.232

<0.001

Age

1.095

1.059-1.132

<0.001

Male gender

2.538

1.350-4.769

0.004

CP PsA

3.708

1.870-7.351

<0.001

Age

1.107

1.057-1.159

<0.001

Male gender

2.386

1.044-5.453

0.039

Dyslipidemia

2.808

1.261-6.254

0.012

MP PsA

4.523

2.048-9.991

<0.001

Age

1.077

1.024-1.132

0.004

Male gender

3.099

1.158-8.293

0.024

NCP PsA

3.283

1.886-5.715

<0.001

Age

1.039

1.008-1.070

0.012

MP or NCP PsA

4.120

2.349-7.228

<0.001

Age

1.061

1.029-1.094

<0.001

Male gender

2.231

1.194-4.167

0.012

Adjusted for age, gender, hypertension, diabetes, hyperlipidemia, and smoking


Disclosure: L. H. P. TAM, None; T. H. CHENG, None; H. M. LAM, None; K. T. WONG, None; Q. SHANG, None; E. LI, None; W. K. LI, None; M. F. CHEUNG, None; U. L. MING, None; T. L. LUI, None; W. L. TAO, None; S. TSANG, None; L. S. TAM, None.

To cite this abstract in AMA style:

TAM LHP, CHENG TH, LAM HM, WONG KT, SHANG Q, LI E, LI WK, CHEUNG MF, MING UL, LUI TL, TAO WL, TSANG S, TAM LS. Higher Prevalence and Severity of Coronary Atherosclerosis in Psa Patients [abstract]. Arthritis Rheumatol. 2016; 68 (suppl 10). https://acrabstracts.org/abstract/higher-prevalence-and-severity-of-coronary-atherosclerosis-in-psa-patients/. Accessed .
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