Higher Coronary Plaque Burden in Psoriatic Arthritis Is Independent of Metabolic Syndrome and Associated With Underlying Disease Severity

被引:45
作者
Szentpetery, Agnes [1 ]
Healy, Gerard M. [1 ]
Brady, Darragh [1 ]
Haroon, Muhammad [1 ]
Gallagher, Phil [1 ]
Redmond, Ciaran E. [1 ]
Fleming, Hannah [1 ]
Duignan, John [1 ]
Dodd, Jonathan D. [1 ]
FitzGerald, Oliver [1 ,2 ]
机构
[1] St Vincents Univ Hosp, Dublin, Ireland
[2] Univ Coll Dublin, Conway Inst Biomol Res, Dublin, Ireland
关键词
COMPUTED TOMOGRAPHIC ANGIOGRAPHY; ARTERY-DISEASE; CARDIOVASCULAR-DISEASE; HIGH PREVALENCE; CT ANGIOGRAPHY; RISK-FACTORS; DIAGNOSTIC PERFORMANCE; RHEUMATOID-ARTHRITIS; AVAILABLE EVIDENCE; ACCURACY TRIAL;
D O I
10.1002/art.40389
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. To examine the effect of metabolic syndrome and psoriatic disease-related variables on coronary plaque burden in psoriatic arthritis (PsA) patients. Methods. Fifty PsA patients without symptoms of coronary artery disease (CAD) (25 with metabolic syndrome and 25 without metabolic syndrome) and 50 age- and sex-matched controls underwent 64-slice coronary computed tomography angiography. Plaque localization, segment involvement score (SIS), segment stenosis score (SSS), and total plaque volume (TPV) were calculated. Plaques were classified as calcified, mixed, or noncalcified. Kruskal-Wallis test, rank correlations, and linear regression analyses were used to study the relationship between PsA, metabolic syndrome, and plaque burden. Results. Plaques were found in 76% of PsA patients versus 44% of controls (P = 0.001), and a higher proportion of patients with PsA had affected coronary vessels (P = 0.007). SIS, SSS, and TPV were greater in PsA patients than controls (P = 0.003, P = 0.001, and P 0.001, respectively). More PsA patients had mixed plaques, and mixed plaque volume was higher than in controls (P <= 0.001). PsA patients with metabolic syndrome and those without metabolic syndrome had similar plaque burdens and types. SIS, SSS, and TPV did not show significant relationships with features of metabolic syndrome, but did significantly correlate with disease activity measures. TPV was associated with a diagnosis of PsA (B = 0.865, P = 0.008), but not with metabolic syndrome. Age, highest C-reactive protein level, highest swollen joint count, disease duration, and plasma glucose level were independent predictors of higher plaque burden in PsA. Conclusion. PsA is associated with accelerated coronary plaque formation, particularly mixed plaques, independent of metabolic disease. Psoriatic disease activity and severity may predict coronary plaque burden better than traditional risk factors.
引用
收藏
页码:396 / 407
页数:12
相关论文
共 50 条
[21]   Coronary Microvascular Dysfunction Is Associated With Significant Plaque Burden and Diffuse Epicardial Atherosclerotic Disease [J].
AlBadri, Ahmed ;
Eshtehardi, Parham ;
Hung, Olivia Y. ;
Bouchi, Yasir ;
Khawaja, Sameer ;
Mercado, Kalina ;
Corban, Michel T. ;
Mehta, Puja K. ;
Shaw, Leslee J. ;
Samady, Habib .
JACC-CARDIOVASCULAR INTERVENTIONS, 2019, 12 (15) :1519-1520
[22]   The metabolic syndrome and coronary artery disease: A structural equation modeling approach suggestive of a common underlying pathophysiology [J].
Steuenson, Jennifer E. ;
Wright, Bruce R. ;
Boydstun, Alan S. .
METABOLISM-CLINICAL AND EXPERIMENTAL, 2012, 61 (11) :1582-1588
[23]   Fragmented QRS complex is an independent predictor of plaque burden in patients at intermediate risk of coronary artery disease [J].
Mahfouz, Ragab A. ;
Arab, Mohamad ;
Abdelhamid, Mohamed ;
Elzayat, Ahmad .
INDIAN HEART JOURNAL, 2019, 71 (05) :394-399
[24]   Association of IL-10 to coronary disease severity in patients with metabolic syndrome [J].
Vargas Barcelos, Ana Leticia ;
de Oliveira, Eduardo Aires ;
Haute, Gabriela Viegas ;
Costa, Bruna Pasqualotto ;
Pedrazza, Leonardo ;
Fagundes Donadio, Marcio Vinicius ;
de Oliveira, Jarbas Rodrigues ;
Bodanese, Luiz Carlos .
CLINICA CHIMICA ACTA, 2019, 495 :394-398
[25]   Differences in Prevalence and Severity of Coronary Artery Disease by Three Metabolic Syndrome Definitions [J].
Chang, Jung-Jung ;
Chu, Chi-Ming ;
Wang, Po-Chang ;
Lin, Yu-Sheng ;
Pan, Kuo-Li ;
Jang, Shih-Jung ;
Chang, Shih-Tai .
CANADIAN JOURNAL OF CARDIOLOGY, 2012, 28 (02) :208-214
[26]   Total coronary atherosclerotic plaque burden assessment by CT angiography for detecting obstructive coronary artery disease associated with myocardial perfusion abnormalities [J].
Kishi, Satoru ;
Magalhaes, Tiago A. ;
Cerci, Rodrigo J. ;
Matheson, Matthew B. ;
Vavere, Andrea ;
Tanami, Yutaka ;
Kitslaar, Pieter H. ;
George, Richard T. ;
Brinker, Jeffrey ;
Miller, Julie M. ;
Clouse, Melvin E. ;
Lemos, Pedro A. ;
Niinuma, Hiroyuki ;
Reiber, Johan H. C. ;
Rochitte, Carlos E. ;
Rybicki, Frank J. ;
Di Carli, Marcelo F. ;
Cox, Christopher ;
Lima, Joao A. C. ;
Arbab-Zadeh, Armin .
JOURNAL OF CARDIOVASCULAR COMPUTED TOMOGRAPHY, 2016, 10 (02) :121-127
[27]   Achilles Tendon Thickning is Associated With Disease Severity and Plaque Vulnerability in Patients With Coronary Artery Disease. [J].
Hashimoto, Takuya ;
Minami, Yoshiyasu ;
Kakizaki, Ryota ;
Nemoto, Teruyoshi ;
Fujiyoshi, Kazuhiro ;
Meguro, Kentaro ;
Shimohama, Takao ;
Tojo, Taiki ;
Ako, Junya .
CIRCULATION, 2018, 138
[28]   Total coronary atherosclerotic plaque burden is associated with myocardial ischemia in non-obstructive coronary artery disease [J].
Eskerud, Ingeborg ;
Gerdts, Eva ;
Larsen, Terje H. ;
Simon, Judit ;
Maurovich-Horvat, Pal ;
Lonnebakken, Mai Tone .
IJC HEART & VASCULATURE, 2021, 35
[29]   Hyperhomocysteinemia as a metabolic disorder parameter is independently associated with the severity of coronary heart disease [J].
Liu, Chenggui ;
Yang, Yinzhong ;
Peng, Duanliang ;
Chen, Linong ;
Luo, Jun .
SAUDI MEDICAL JOURNAL, 2015, 36 (07) :839-846
[30]   Increased Prevalence of Metabolic Syndrome Associated with Rheumatoid Arthritis in Patients without Clinical Cardiovascular Disease [J].
Crowson, Cynthia S. ;
Myasoedova, Elena ;
Davis, John M., III ;
Matteson, Eric L. ;
Roger, Veronique L. ;
Therneau, Terry M. ;
Fitz-Gibbon, Patrick ;
Rodeheffer, Richard J. ;
Gabriel, Sherine E. .
JOURNAL OF RHEUMATOLOGY, 2011, 38 (01) :29-35