Literature DB >> 32419071

Coronary microvascular dysfunction in patients with psoriasis.

Brittany Weber1, Lourdes M Perez-Chada2, Sanjay Divakaran1, Jenifer M Brown1, Viviany Taqueti1, Sharmila Dorbala1, Ron Blankstein1, Katherine Liao3, Joseph F Merola2, Marcelo Di Carli4.   

Abstract

BACKGROUND: Psoriasis is a common chronic inflammatory skin disorder that is associated with excess cardiovascular risk. Inflammation is a key mediator in the onset and progression of these cardiometabolic abnormalities; however, the excess cardiovascular risk conferred by psoriatic disease remains understudied. We investigated the prevalence and severity of CMD in patients with psoriasis and determined whether CMD is a result of CV risk factors and atherosclerotic burden.
METHODS: This was a consecutive retrospective cohort study of patients with psoriasis, normal myocardial perfusion, and LV ejection fraction (EF) > 50% (N = 62) and matched controls without psoriasis (N = 112). Myocardial perfusion and myocardial flow reserve (MFR) were quantified using PET imaging. Atherosclerotic burden was determined by semi-quantitative computed tomography (CT) coronary calcium assessment.
RESULTS: The prevalence of CMD (defined as MFR < 2) was 61.3% in patients with psoriatic disease, compared to 38.4% in a matched control population (P = .004). Furthermore, patients with psoriasis had a more severe reduction in adjusted MFR (2.3 ± .81 vs 1.92 ± .65, respectively, P = .001). The degree of atherosclerotic burden, as assessed by qualitative calcium score, was similar between psoriasis and controls.
CONCLUSIONS: Patients with psoriasis without overt CAD demonstrated a high prevalence of coronary vasomotor abnormalities that are not entirely accounted for by the commonly associated coronary risk factors or the burden of atherosclerosis.
© 2020. American Society of Nuclear Cardiology.

Entities:  

Keywords:  Inflammation; PET; microvascular dysfunction

Mesh:

Substances:

Year:  2020        PMID: 32419071      PMCID: PMC9202505          DOI: 10.1007/s12350-020-02166-5

Source DB:  PubMed          Journal:  J Nucl Cardiol        ISSN: 1071-3581            Impact factor:   3.872


  23 in total

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