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Cardiovascular involvement in systemic rheumatic diseases: An integrated view for the treating physicians
Authors:Kwang Seob Lee  Andreas Kronbichler  Michael Eisenhut  Keum Hwa Lee  Jae Il Shin
Affiliation:1. Yonsei University College of Medicine, Seoul, Republic of Korea;2. Department of Internal Medicine IV (Nephrology and Hypertension), Medical University Innsbruck, Innsbruck, Austria;3. Department of Pediatrics, Luton & Dunstable University Hospital NHS Foundation Trust, Luton, UK;4. Department of Pediatrics, Yonsei University College of Medicine, Seoul, Republic of Korea;5. Department of Pediatric Nephrology, Severance Children’s Hospital, Seoul, Republic of Korea;6. Institute of Kidney Disease Research, Yonsei University College of Medicine, Seoul, Republic of Korea
Abstract:Systemic autoimmune diseases can affect various kinds of organs including the kidney, the skin, soft tissue and the bone. Among others, cardiovascular involvement in rheumatic diseases has been shown to affect myocardium, pericardium, cardiac vessels, conduction system and valves, eventually leading to increased mortality. In general, underlying chronic inflammation leads to premature atherosclerosis, but also other manifestations such as arrhythmia and heart failure may have a ‘silent’ progress. Traditional cardiovascular risk factors play a secondary role, while disease-specific factors (i.e. disease duration, severity, antibody positivity, persistent disease activity) can directly influence the cardiovascular system. Therefore, early diagnosis is critical to optimize management and to control inflammatory activity and recent data suggest that risk factors (i.e. hypercholesterolemia and hypertension) need intensive treatment as well. With the advent of immunosuppressive agents, most rheumatic diseases are well controlled on treatment, but information related to their cardioprotective efficacy is not well-defined. In this review, we focus on cardiovascular involvement in rheumatic diseases and highlight current evidence which should be of help for the treating physicians. Moreover, cardiotoxicity of immunosuppressive drugs is a rare issue and such potential adverse events will be briefly discussed.
Keywords:SLE  systemic lupus erythematosus  RA  rheumatoid arthritis  C3  complement factor 3  IgM, IgG  IgA immunoglobulin M, G, A  APS  antiphospholipid syndrome  anti-Ro/SSA  anti-Sjögren syndrome-related antigen A  HF  heart failure  CVD  cardiovascular disease  CIMT  carotid intima-media thickness  HDLc  high-density lipoprotein cholesterol  TG  triglyceride  ESR  erythrocyte sedimentation rate  SLEDAI  systemic lupus erythematosus disease activity index  ACE  angiotensin converting enzyme  LDLc  low-density lipoprotein cholesterol  MI  myocardial infarction  AMI  acute myocardial infarction  PCI  percutaneous coronary intervention  QTc  corrected QT  CQ  chloroquine  AV  atrioventricular  PE  pericardial effusion  RF  rheumatoid factor  CAD  coronary artery disease  IHD  ischemic heart disease  FMD  flow-mediated dilation  anti-CCP  anti-cyclic citrullinated peptide  DAS28  disease activity score in 28 joints  CRP  C-reactive protein  ACS  acute coronary syndrome  CHF  congestive heart failure  IL  interleukin  LV  left ventricle  AF  atrial fibrillation  SCD  sudden cardiac death  ANS  autonomic nervous system  TNF- α  tumor necrosis factor- α  dc/lcSSc  diffuse cutaneous/limited cutaneous systemic sclerosis  CFR  coronary flow reserve  ANA  anti-nuclear antibody  ACA  anti-centromere antibody  Scl-70  anti-topoisomerase I antibody  RBBB  right bundle branch block  HRV  heart rate variability  HRT  heart rate turbulence  GCA  giant cell arteritis  TAK  Takayasu's arteritis  NT-pro BNP  N-terminal pro b-type natriuretic peptide  CVE  cardiovascular event  CABG  coronary artery bypass grafting  KD  Kawasaki disease  WBC  white blood cell  cTnI  coronary troponin I  IVIG  intravenous immunoglobulin  ANCA  anti-neutrophil cytoplasmic antibody  GPA  granulomatosis with polyangiitis  MPA  microscopic polyangiitis  EGPA  eosinophilic granulomatosis with polyangiitis  HSP  Henoch-Schönlein purpura  BD  Behcet's disease  PSS  primary Sjögren syndrome  AS  ankylosing spondylitis  NSAID  non-steroidal anti-inflammatory drug  IIM  idiopathic inflammatory myopathy  DMARD  disease-modifying anti-rheumatic drug  MTX  methotrexate  Systemic rheumatic disease  Cardiovascular involvement  Disease-modifying anti-rheumatic drug  Toxicity
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