E059 Identifying the associations between anxiety/depression and disease activity in idiopathic inflammatory myopathy

Bibliographic Details
Title: E059 Identifying the associations between anxiety/depression and disease activity in idiopathic inflammatory myopathy
Authors: Nadir Z Aziz, Alexander Oldroyd, Francisca Bozan, Xia Lyu, Janine A Lamb, Patrick Gordon, David A Isenberg, Neil McHugh, Harsha Gunawardena, Patrick Kiely, Pedro M Machado, James Miller, Sarah Tansley, Anurag Bharadwaj, Ramasharan Laxminarayan, Natasha Jordan, Chee-Seng Yee, Damodar Makkuni, James Taylor, Peter C Lanyon, Voon H Ong, Athiveeraramapandian Prabu, Mohammed Akil, Karen M Douglas, Eleni Stathopoulou, Marian Regan, Hector Chinoy
Source: Rheumatology. 63
Publisher Information: Oxford University Press (OUP), 2024.
Publication Year: 2024
Subject Terms: 03 medical and health sciences, 0302 clinical medicine, 16. Peace & justice, 3. Good health
Description: Background/Aims Idiopathic inflammatory myopathy (IIM) is characterised by myositis, which can impact activities of daily living. The 2022 BSR IIM management guideline recommends assessing/managing factors associated with poor mental wellbeing and quality of life. Research into anxiety and depression associated with IIM is limited. This study aims to investigate associations between anxiety/depression and IIM disease activity. Methods The MYOPROSP study recruited UK adults with verified IIM throughout a 36 month period between 2016 and 2020. Patient questionnaires were collected at three, six, and 12 months. Participants completed the EQ-5D-5L questionnaire, which includes a question relating to anxiety and depression with five possible responses: “I am (not/slightly/moderately/severely/extremely) anxious or depressed”. The cohort was divided by response to the EQ-5D-5L anxiety/depression question at the time of recruitment. Disease activity was assessed using International Myositis Assessment & Clinical Studies Group (IMACS) Disease Activity Core Set Measures (see Table 1) and summarised across each EQ-5D-5L anxiety/depression group. The EQ-5D-5L visual analogue scale (VAS) relating to “overall health” (higher values correspond to better health) this value was summarised across each EQ-5D-5L anxiety/depression group. Only participants with complete data at recruitment were included in analysis. One-way ANOVA was performed to determine statistical significance (p Results Complete data on 35 participants (71% female) was collected. All participants reported to have no, slight, or moderate anxiety/depression (i.e. no participant reported severe or extreme anxiety/depression) (Table 1). The “not anxious/depressed” group demonstrated higher EQ-5D VAS values (reflecting better perceived health), shorter disease duration, and higher CK levels, compared to groups with “slight” and “moderate” anxiety/depression. All other investigated variables did not consistently vary across anxiety/depression groups. One-way ANOVA identified that only disease duration and EQ-5D VAS were significantly associated with EQ-5D-5L anxiety/depression group. Conclusion Anxiety and depression are associated with longer disease duration and poorer overall health in adults with IIM. These findings suggest that anxiety/depression in adults with IIM may be due to sustained muscle damage and resulting impacts upon activities of daily living and quality of life, rather than disease activity. Disclosure N.Z. Aziz: None. A. Oldroyd: None. F. Bozan: None. X. Lyu: None. J.A. Lamb: None. P. Gordon: None. D.A. Isenberg: None. N. McHugh: None. H. Gunawardena: None. P. Kiely: None. P.M. Machado: Consultancies; PMM has received consulting/speaker’s fees from Abbvie, BMS, Celgene, Eli Lilly, Janssen, MSD, Novartis, Orphazyme, Pfizer, Roche and UCB. J. Miller: None. S. Tansley: None. A. Bharadwaj: None. R. Laxminarayan: None. N. Jordan: None. C. Yee: None. D. Makkuni: None. J. Taylor: None. P.C. Lanyon: Consultancies; PCL has received consultancy fees from Pfizer. Grants/research support; PCL has received research grants, speaker fees and conference attendance support from CSL Vifor. V.H. Ong: None. A. Prabu: None. M. Akil: None. K.M. Douglas: None. E. Stathopoulou: None. M. Regan: None. H. Chinoy: None.
Document Type: Article
Language: English
ISSN: 1462-0332
1462-0324
DOI: 10.1093/rheumatology/keae163.286
Rights: OUP Standard Publication Reuse
Accession Number: edsair.doi...........b82e7290e6c82626c621e397845522b7
Database: OpenAIRE
Description
ISSN:14620332
14620324
DOI:10.1093/rheumatology/keae163.286