ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstract Number: 1640

Psoriatic Disease Associated with Neuroconnectivity Alterations in the Default Mode Network

Rebecca Haberman1, Sydney Catron1, Yu Veronica Sui1, Sarah Moussavi1, Soumya Reddy2, Eileen Lydon3, Andrea Neimann1, Alexis R Ogdie4, Mariana Lazar1 and Jose Scher5, 1NYU Grossman School of Medicine, New York, NY, 2NYU School of Medicine, New York, NY, 3New York University, New York, NY, 4University of Pennsylvania, Philadelphia, PA, 5New York University School of Medicine, New York, NY

Meeting: ACR Convergence 2023

Keywords: depression, Neuroimaging, pain, Psoriatic arthritis

  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print
Session Information

Date: Monday, November 13, 2023

Title: Abstracts: Spondyloarthritis Including Psoriatic Arthritis – Diagnosis, Manifestations, & Outcomes II: Psoriatic Arthritis

Session Type: Abstract Session

Session Time: 2:00PM-3:30PM

Background/Purpose: Despite significant advances in psoriatic disease (PsD) therapeutics, treatment response remains suboptimal. Even in patients with psoriatic arthritis (PSA) that achieve seemingly controlled inflammation, up to half continue to experience residual symptoms, notably pain and fatigue, which can prevent meaningful improvement in symptoms and quality of life. However, the pathophysiology and effectors of residual pain are not well understood. Functional brain MRI (fMRI) can be used to identify alterations in brain connectivity as a possible basis for residual pain and have the potential to discern inflammatory driven pain from centrally-provoked pain. Here we describe pilot fMRI data showing neuroconnectivity changes in those with PsD.

Methods: Seven patients with PsD were enrolled from the NYU Psoriatic Arthritis Center (PAC). Patients on psychotropic medications were excluded. Demographics, medical history, and medication use were recorded and focused musculoskeletal and skin exams were performed. Participants completed patient reported outcomes including the SF-36, Beck Depression Index, fatigue numeric rating score, and RAPID 3. Four healthy controls were used as a comparison group. fMRI sequences were obtained in all participants at both rest and with a fatigue inducing task (Paced Auditory Serial Addition Test) using a 3 Tesla Siemens Prisma scanner. fMRI time series were analyzed using the independent component analysis, with a focus on connectivity within the default mode network (DMN, Figure 1) which has been previously implicated in depression and chronic pain states such as fibromyalgia.

Results: Compared to healthy controls, those with PsD had decreased connectivity between the DMN’s posteromedial cortex node and the superior parietal lobule (p= < 0.05 FDR-corrected at cluster level) (Figure 2). Additionally, for the 7 participants with PsD, levels of pain, depression, and fatigue all correlated with strength of connectivity in pathways of the DMN (Figure 3).

Conclusion: This initial data demonstrates the feasibility and acceptability of using fMRI to characterize neuroconnectivity in patients with PsD. We observed differences in functional connectivity between healthy participants and patients with PsD, even with well controlled disease. Furthermore, identifying networks and connections associated with pain, depression, and fatigue may ultimately help in identifying and characterizing residual pain that contributes to worse clinical outcomes. Future studies will confirm and further characterize these findings using larger sample sizes.

Supporting image 1

Supporting image 2

Supporting image 3


Disclosures: R. Haberman: Janssen, 1, 5, UCB, 1; S. Catron: None; Y. Sui: None; S. Moussavi: None; S. Reddy: AbbVie, 2, Amgen, 2, Fresenius Kabi, 2, Janssen, 2, Novartis, 2, UCB, 2; E. Lydon: Aurinia, 1, GlaxoSmithKlein(GSK), 1, UCB, 1; A. Neimann: Sun Pharma, 1, UCB, 1; A. Ogdie: AbbVie/Abbott, 2, 5, Amgen, 2, 5, Bristol-Myers Squibb(BMS), 2, Celgene, 2, CorEvitas, 2, Eli Lilly, 2, Gilead, 2, GSK, 2, Janssen, 2, 5, Novartis, 2, 5, Pfizer, 2, 5, Takeda, 2, UCB, 2; M. Lazar: None; J. Scher: AbbVie, 2, Janssen, 2, 5, Novartis, 5, Pfizer, 2, 5, Sanofi, 2, UCB, 2.

To cite this abstract in AMA style:

Haberman R, Catron S, Sui Y, Moussavi S, Reddy S, Lydon E, Neimann A, Ogdie A, Lazar M, Scher J. Psoriatic Disease Associated with Neuroconnectivity Alterations in the Default Mode Network [abstract]. Arthritis Rheumatol. 2023; 75 (suppl 9). https://acrabstracts.org/abstract/psoriatic-disease-associated-with-neuroconnectivity-alterations-in-the-default-mode-network/. Accessed .
  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print

« Back to ACR Convergence 2023

ACR Meeting Abstracts - https://acrabstracts.org/abstract/psoriatic-disease-associated-with-neuroconnectivity-alterations-in-the-default-mode-network/

Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM ET on November 14, 2024. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology