Ustekinumab treatment is associated with decreased systemic and vascular inflammation in patients with moderate-to-severe psoriasis: Feasibility study using <sup>18</sup>F-fluorodeoxyglucose PET/CT.
prospective_cohort · Level II
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- Record sourced from PubMed, PMID 29559399.
- Also identified by DOI 10.1016/j.jaad.2018.03.011.
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Abstract
Evidence suggests that psoriasis might be associated with metabolic syndrome and an increased risk for cardiovascular disease. To determine whether ustekinumab reduces systemic and vascular inflammation associated with metabolic syndrome and cardiovascular disease, measured using <sup>18</sup>F-fluorodeoxyglucose positron emission tomography-computed tomography (<sup>18</sup>F-FDG PET/CT). Patients with psoriasis and healthy controls underwent baseline <sup>18</sup>F-FDG PET/CT imaging. Patients with moderate-to-severe psoriasis were treated with ustekinumab and underwent <sup>18</sup>F-FDG PET/CT again after a Psoriasis Area and Severity Index of 75 was achieved. After a Psoriasis Area and Severity Index of 75 was achieved with ustekinumab treatment, standardized uptake values were reduced in the liver, spleen, and 5 parts of the aorta (P < .05). Our study does not provide outcome data concerning cardiovascular events or metabolic syndrome; it only shows surrogate markers in a limited (Korean) population. Ustekinumab treatment was significantly associated with decreased systemic and vascular inflammation related to metabolic syndrome and cardiovascular disease among patients with psoriasis.
Medical subject headings
- Dermatologic Agents
- Inflammation
- Positron Emission Tomography Computed Tomography
- Psoriasis
- Ustekinumab
- Vasculitis