The blood proteomic signature of prurigo nodularis reveals distinct inflammatory and neuropathic endotypes: A cluster analysis

被引:10
|
作者
Parthasarathy, Varsha [1 ]
Cravero, Karen [1 ]
Xu, Lillian [1 ]
Deng, Junwen [1 ]
Sun, Zhe [2 ]
Engle, Sarah M. [2 ]
Sims, Jonathan T. [2 ]
Okragly, Angela J. [2 ]
Kwatra, Shawn G. [1 ,3 ]
机构
[1] Johns Hopkins Sch Med, Dept Dermatol, Baltimore, MD USA
[2] Eli Lilly & Co, Indianapolis, IN USA
[3] Johns Hopkins Univ, Sch Med, Canc Res Bldg II,Suite 206,1550 Orleans St, Baltimore, MD 21231 USA
关键词
clustering; endotypes; itch; multiplex; Olink; proteomic; pruritus; prurigo nodularis; ATOPIC-DERMATITIS; TNF-ALPHA; BURDEN; SKIN; REGULATOR; LIGAND; IMMUNE; SERUM; TH1;
D O I
10.1016/j.jaad.2023.01.042
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Prurigo nodularis (PN) is an extremely pruritic, chronic inflammatory skin disease. Little is known about systemic inflammation in PN. Objective: To characterize plasma inflammatory biomarkers in patients with PN and investigate the presence of disease endotypes. Methods: In this cross-sectional study, Olink proteomic analysis was performed on plasma samples from patients with PN (n = 29) and healthy controls (n = 18). Results: Patients with PN had increased levels of 8 circulating biomarkers compared to controls, including tumor necrosis factor, C-X-C Motif Chemokine Ligand 9, interleukin-12B, and tumor necrosis factor receptor superfamily member 9 (P \.05). Two PN clusters were identified in cluster 1 (n = 13) and cluster 2 (n = 16). Cluster 2 had higher levels of 25 inflammatory markers than cluster 1. Cluster 1 had a greater percentage of patients with a history of myelopathy and spinal disc disease compared with cluster 2 (69% vs 25%, P = .03). Patients in cluster 2 were more likely to have a history of atopy (38% in cluster 2 vs 8% in cluster 1, P = .09). Limitations: Small sample size precludes robust subgroup analyses. Conclusion: This study provides evidence of neuroimmune-biased endotypes in PN and can aid clinicians in managing patients with PN that are nonresponsive to traditional therapies. ( J Am Acad Dermatol 2023;88:1101-9.)
引用
收藏
页码:1101 / 1109
页数:9
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