Ustekinumab treatment is associated with decreased systemic and vascular inflammation in patients with moderate-to-severe psoriasis: Feasibility study using


Journal

Journal of the American Academy of Dermatology
ISSN: 1097-6787
Titre abrégé: J Am Acad Dermatol
Pays: United States
ID NLM: 7907132

Informations de publication

Date de publication:
May 2019
Historique:
received: 27 04 2017
revised: 04 03 2018
accepted: 11 03 2018
pubmed: 22 3 2018
medline: 30 4 2019
entrez: 22 3 2018
Statut: ppublish

Résumé

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 Patients with psoriasis and healthy controls underwent baseline 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.

Sections du résumé

BACKGROUND BACKGROUND
Evidence suggests that psoriasis might be associated with metabolic syndrome and an increased risk for cardiovascular disease.
OBJECTIVE OBJECTIVE
To determine whether ustekinumab reduces systemic and vascular inflammation associated with metabolic syndrome and cardiovascular disease, measured using
METHODS METHODS
Patients with psoriasis and healthy controls underwent baseline
RESULTS RESULTS
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).
LIMITATIONS CONCLUSIONS
Our study does not provide outcome data concerning cardiovascular events or metabolic syndrome; it only shows surrogate markers in a limited (Korean) population.
CONCLUSION CONCLUSIONS
Ustekinumab treatment was significantly associated with decreased systemic and vascular inflammation related to metabolic syndrome and cardiovascular disease among patients with psoriasis.

Identifiants

pubmed: 29559399
pii: S0190-9622(18)30461-4
doi: 10.1016/j.jaad.2018.03.011
pii:
doi:

Substances chimiques

Dermatologic Agents 0
Radiopharmaceuticals 0
Fluorodeoxyglucose F18 0Z5B2CJX4D
Ustekinumab FU77B4U5Z0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1322-1331

Informations de copyright

Copyright © 2018 American Academy of Dermatology, Inc. Published by Elsevier Inc. All rights reserved.

Auteurs

Byung-Soo Kim (BS)

Department of Dermatology, School of Medicine, Pusan National University, Busan, Korea; Biomedical Research Institute, Pusan National University Hospital, Busan, Korea.

Won-Ku Lee (WK)

Department of Dermatology, School of Medicine, Pusan National University, Busan, Korea; Department of Dermatology, Pusan National University Yangsan Hospital, Yangsan, Korea; Research Institute for Convergence of Biomedical Science and Technology, Pusan National University Yangsan Hospital, Yangsan, Korea.

Kyoungjune Pak (K)

Biomedical Research Institute, Pusan National University Hospital, Busan, Korea; Department of Nuclear Medicine, Pusan National University Hospital, Busan, Korea.

Junhee Han (J)

Department of Statistics, Hallym University, Chuncheon, Korea.

Gun-Wook Kim (GW)

Department of Dermatology, School of Medicine, Pusan National University, Busan, Korea.

Hoon-Soo Kim (HS)

Department of Dermatology, School of Medicine, Pusan National University, Busan, Korea.

Hyun-Chang Ko (HC)

Department of Dermatology, School of Medicine, Pusan National University, Busan, Korea; Department of Dermatology, Pusan National University Yangsan Hospital, Yangsan, Korea; Research Institute for Convergence of Biomedical Science and Technology, Pusan National University Yangsan Hospital, Yangsan, Korea.

Moon-Bum Kim (MB)

Department of Dermatology, School of Medicine, Pusan National University, Busan, Korea; Biomedical Research Institute, Pusan National University Hospital, Busan, Korea.

Seong-Jang Kim (SJ)

Department of Nuclear Medicine, Pusan National University Hospital, Busan, Korea; Department of Nuclear Medicine, College of Medicine, Pusan National University, Busan, Korea; Department of Nuclear Medicine, Pusan National University Yangsan Hospital, Yangsan, Korea. Electronic address: growthkim@daum.net.

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Classifications MeSH