» Articles » PMID: 30760013

Inflammasome Signaling and Impaired Vascular Health in Psoriasis

Abstract

Objective- Psoriasis is an inflammatory skin disease which heightens the risk of cardiovascular disease. This study directly investigated vascular endothelial health and systemically altered pathways in psoriasis and matched controls. Approach and Results- Twenty patients (mean age, 40 years; 50% male) with active psoriasis and 10 age-, sex-matched controls were recruited. To investigate systemically alerted pathways, a deep sequencing omics approach was applied, including unbiased blood transcriptomic and targeted proteomic analysis. Vascular endothelial health was assessed by transcriptomic profiling of endothelial cells obtained from the brachial veins of recruited participants. Blood transcriptomic profiling identified inflammasome signaling as the highest differentially expressed canonical pathway ( Z score 1.6; P=1×10) including upregulation of CASP5 and interleukin ( IL) -1β. Proteomic panels revealed IL-6 as a top differentially expressed cytokine in psoriasis with pathway analysis highlighting IL-1β ( Z score 3.7; P=1.02×10) as an upstream activator of the observed upregulated proteins. Direct profiling of harvested brachial vein endothelial cells demonstrated inflammatory transcript (eg, IL-1β, CXCL10, VCAM-1, IL-8, CXCL1, Lymphotoxin beta, ICAM-1, COX-2, and CCL3) upregulation between psoriasis versus controls. A linear relationship was seen between differentially expressed endothelial inflammatory transcripts and psoriasis disease severity. IL-6 levels correlated with inflammatory endothelial cell transcripts and whole blood inflammasome-associated transcripts, including CASP5 and IL-1β. Conclusions- An unbiased sequencing approach demonstrated the inflammasome as the most differentially altered pathway in psoriasis versus controls. Inflammasome signaling correlated with psoriasis disease severity, circulating IL-6, and proinflammatory endothelial transcripts. These findings help better explain the heightened risk of cardiovascular disease in psoriasis. Clinical Trial Registration- URL: http://www.clinicaltrials.gov . Unique identifier: NCT03228017.

Citing Articles

Vascular Cell Adhesion Molecule 1 and E-Selectin as Potential Cardiovascular Risk Biomarkers in Psoriasis.

Machon N, Zdanowska N, Klimek-Trojan P, Owczarczyk-Saczonek A Int J Mol Sci. 2025; 26(2).

PMID: 39859506 PMC: 11765541. DOI: 10.3390/ijms26020792.


Cardiovascular Complications During Delivery Hospitalization in Patients With Psoriasis.

Agrawal A, Sorathia S, Bhagat U, Zahid S, Arockiam A, Bayat A JACC Adv. 2025; 4(2):101562.

PMID: 39837132 PMC: 11787633. DOI: 10.1016/j.jacadv.2024.101562.


Bioinformatics analysis reveals potential crosstalk genes and molecular mechanisms between ulcerative colitis and psoriasis.

Luo Q, An M, Wu Y, Wang J, Mao Y, Zhang L Arch Dermatol Res. 2024; 317(1):118.

PMID: 39673621 DOI: 10.1007/s00403-024-03617-6.


Efficient screening and discovery of umami peptides in Douchi enhanced by molecular dynamics simulations.

Guo W, Ren K, Long Z, Fu X, Zhang J, Liu M Food Chem X. 2024; 24:101940.

PMID: 39559460 PMC: 11570484. DOI: 10.1016/j.fochx.2024.101940.


Cardiodermatology: the heart of the connection between the skin and cardiovascular disease.

Gelfand J, Song W, Langan S, Garshick M Nat Rev Cardiol. 2024; .

PMID: 39537837 DOI: 10.1038/s41569-024-01097-9.


References
1.
van den Borne P, Quax P, Hoefer I, Pasterkamp G . The multifaceted functions of CXCL10 in cardiovascular disease. Biomed Res Int. 2014; 2014:893106. PMC: 4017714. DOI: 10.1155/2014/893106. View

2.
Yu G, Wang L, Han Y, He Q . clusterProfiler: an R package for comparing biological themes among gene clusters. OMICS. 2012; 16(5):284-7. PMC: 3339379. DOI: 10.1089/omi.2011.0118. View

3.
Salskov-Iversen M, Johansen C, Kragballe K, Iversen L . Caspase-5 expression is upregulated in lesional psoriatic skin. J Invest Dermatol. 2010; 131(3):670-6. DOI: 10.1038/jid.2010.370. View

4.
Libby P . Inflammation in atherosclerosis. Arterioscler Thromb Vasc Biol. 2012; 32(9):2045-51. PMC: 3422754. DOI: 10.1161/ATVBAHA.108.179705. View

5.
Hot A, Lavocat F, Lenief V, Miossec P . Simvastatin inhibits the pro-inflammatory and pro-thrombotic effects of IL-17 and TNF-α on endothelial cells. Ann Rheum Dis. 2012; 72(5):754-60. DOI: 10.1136/annrheumdis-2012-201887. View