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: 1667

Efficacy of Plasma Phosphoethanolamine as a Biomarker for Rheumatoid Arthritis-associated Depression

Yusuke Miwa1, Yoshiaki Ohashi2, Hajime Tomatsu3 and Yuko Mitamura4, 1Division of Rheumatology, Department of Medicine, School of Medicine, Showa University, Tokyo, Japan, 2HMT Biomedical Inc., Yokohama, Japan, 3HMT Biomedical Inc., Chuo, Japan, 4Department of Nursing, Showa University School of Nursing and Rehabilitation Sciences, Shinagawa-ku, Japan

Meeting: ACR Convergence 2021

Keywords: Biomarkers, depression, rheumatoid 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: Tuesday, November 9, 2021

Title: RA – Diagnosis, Manifestations, & Outcomes Poster IV: Outcomes, Trajectory of Disease, & Epidemiology (1645–1673)

Session Type: Poster Session D

Session Time: 8:30AM-10:30AM

Background/Purpose: The odds of patients with rheumatoid arthritis (RA) experiencing depression is 1.42 (95% CI: 1.3–1.5; approximately 15% of patients) compared with healthy individuals. Diagnosis of depression is based on an interview, which is subjective to both psychiatrist and patient, and auxiliary diagnoses such as a self-rating scale for depression are uncertainty. Phosphoethanolamine (PEA), a plasma biomarker, has been reported to be a useful diagnostic biomarker for depression. We examined the efficacy of PEA as a biomarker for RA-associated depression.

Methods: This study included 52 registered RA patients who were recruited between 2019 and 2020. Patients provided written informed consent to participate and the study was approved by the Institutional Ethics Committee of the Showa University. The following background factors were investigated: age, sex, and disease duration. RA disease activity was evaluated using the Simplified Disease Activity Index. The depression status was evaluated using the Patient Health Questionnaire (PHQ)-9 as a standard scale. Questionnaires for depression, anxiety, and ego were also performed. Items of these questionnaire were converted into Scale A (depression/anxiety scale) and Scale B (adaptation scale). Plasma PEA was measured in Human Metabolome Technologies Inc. Statistical analysis was performed using the chi-square test and one-way analysis of variance.

Results: Forty-nine RA patients with no missing data were included in the analysis. The PHQ-9 score, the gold standard, was used to stratify patients by disease severity—normal, 33; mild depression, 12; moderate depression, 3; and severe depression, 1. Each group was compared between groups.

①The patient visual analog scale (VAS) score was significantly high among patients with depression (p = 0.00157). The difference in VAS scores of patients and doctors was significantly high considering patients with depression (p = 0.00409).

②The Scale A score was significantly high among patients with depression (p = 1.19 × 10−10), and the ratio of Scale A score to PEA was significantly high (p = 1.64 × 10−7) among patients.

③A significant difference was noted between the groups for the plasma PEA concentration (p = 0.0272). The plasma PEA concentration was low in patients with mild and moderate depression and high in a patient with severe depression.

④The Scale B score tended to be higher among patients with depression compared with others, without significant difference.

Conclusion: Plasma PEA alone presents a weak performance as a diagnostic biomarker for depression in patients with RA. However, a composite measure for diagnosing depression, including questionnaires for depression, anxiety, and ego may be used as an auxiliary diagnosis.


Disclosures: Y. Miwa, Pfizer Japan Inc., 5; Y. Ohashi, None; H. Tomatsu, None; Y. Mitamura, None.

To cite this abstract in AMA style:

Miwa Y, Ohashi Y, Tomatsu H, Mitamura Y. Efficacy of Plasma Phosphoethanolamine as a Biomarker for Rheumatoid Arthritis-associated Depression [abstract]. Arthritis Rheumatol. 2021; 73 (suppl 9). https://acrabstracts.org/abstract/efficacy-of-plasma-phosphoethanolamine-as-a-biomarker-for-rheumatoid-arthritis-associated-depression/. 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 2021

ACR Meeting Abstracts - https://acrabstracts.org/abstract/efficacy-of-plasma-phosphoethanolamine-as-a-biomarker-for-rheumatoid-arthritis-associated-depression/

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