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Ann Rheum Dis 2010;69:202-205 doi:10.1136/ard.2008.096255
  • Clinical and epidemiological research
  • Concise report

Overlap of coronary disease and pulmonary arterial hypertension in systemic sclerosis

  1. A Komócsi1,
  2. T Pintér2,
  3. R Faludi1,
  4. B Magyari1,
  5. J Bozó1,
  6. G Kumánovics2,
  7. T Minier2,
  8. J Radics2,
  9. L Czirják2
  1. 1
    Heart Institute, University of Pécs, Pécs, Hungary
  2. 2
    Department of Immunology and Rheumatology, Faculty of Medicine, University of Pécs, Pécs, Hungary
  1. Correspondence to A Komócsi, University of Pécs, Heart Institute, H-7624 Pécs, Ifjúság u. 13, Hungary; andras.komocsi{at}aok.pte.hu
  • Accepted 11 January 2009
  • Published Online First 21 January 2009

Abstract

Objectives: Pulmonary arterial hypertension (PAH) is a common complication of systemic sclerosis (SSc). Symptoms of coronary artery disease (CAD) and PAH are closely related and cardiac catheterisation is needed to confirm their diagnosis. The aim of the present work was to investigate of the extent of overlap between CAD and PAH in patients with SSc.

Methods: Based on non-invasive investigations, 20 patients out of 120 were suspected to have PAH (“suspected PAH” group). Another 10 patients showed signs of coronary disease (“suspected CAD” Group). In these 30 patients, right heart catheterisation and coronary angiography were performed, and the coronary flow reserve (CFR) was assessed by thermodilution technique.

Results: In the “suspected PAH” and the “suspected CAD” groups, PAH was found in 12/20 and 2/10 cases, and coronary artery stenosis in 9/20 and 6/10 cases, respectively. Severely reduced CFR was revealed in 7/20 and 3/10 cases, respectively.

Conclusions: PAH, CAD and reduced CFR all show a considerable overlap in symptomatic patients with SSc. The current non-invasive investigations are neither sensitive nor specific enough to make an appropriate distinction between these different disease manifestations. A more invasive approach, such as coronary angiography at the initial catheterisation, is required to properly characterise and treat the different forms of cardiac involvement in SSc.

Footnotes

  • ‣ Additional data (supplementary tables 1 and 2) are published online only at http://ard.bmj.com/content/vol69/issue1

  • Competing interests None.

  • Ethics approval Ethics approval was granted by the Medical Research Council Scientific and Ethical Committee, Hungary.

  • Provenance and Peer review Not commissioned; externally peer reviewed.

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