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Abstract Number: 0327

Clinical and Immunological Risk Factors Associated with Fybromialgia in Patients with Idiopathic Inflammatory Myopathies

Samuel Govea-Peláez1, Beatriz Alcalá-Carmona2, Jennifer Balderas Miranda3, Yatzil Reyna-Juárez2, María José Ostos-prado2, Nancy R Mejía-Domínguez2, Guillermo Juarez-Vega4, Jiram Torres Ruiz5 and Diana Gomez-martin6, 1INCMNSZ, Mexico City, Mexico, 2Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran, Mexico City, Distrito Federal, Mexico, 3Universidad Nacional Autónoma de México, Ciudad de México, Mexico, 4Red de Apoyo a la Investigación, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán and Universidad Nacional Autónoma de México, Mexico City, Distrito Federal, Mexico, 5INCMNSZ, Mexico, Federal District, Mexico, 6INCMNSZ, Mexico City, Federal District, Mexico

Meeting: ACR Convergence 2024

Keywords: B-Lymphocyte, cytokines, fibromyalgia, Myopathies, pain

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Session Information

Date: Saturday, November 16, 2024

Title: Muscle Biology, Myositis & Myopathies – Basic & Clinical Science Poster I

Session Type: Poster Session A

Session Time: 10:30AM-12:30PM

Background/Purpose: Patients with idiopathic inflammatory myopathies (IIM) have reported chronic pain despite having normal serum muscular enzymes, physician global assessment (PhGA) and MMT8 scores, thus becoming a priority in treatment and research. The prevalence, clinical and immunological factors associated with fibromyalgia (FM), a condition known for chronic pain in patients with IIM have not been previously addressed.

Methods: We performed a case-control study in a third-level referral center in Mexico City. We included patients from the institutional myositis cohort MYOTReCSZ who fulfilled EULAR/ACR 2017 criteria for IIM and had complete clinical response / remission for 6 months; patients with other autoimmune diseases were excluded. All subjects answered the PROMIS Pain Interference Short Form 8a; in case of a score >11, WPI and SSS were used for FM classification according to EULAR/ACR 2010 criteria. Activity and damage were evaluated by IMACS core set measurements. Peripheral blood mononuclear subsets were assessed by multiparametric flow cytometry and serum cytokines were measured by a multiplex luminometry assay.

Results: We included 49 IMM patients in complete clinical response; the prevalence of FM was 40.1% (20/29) and female sex was predominant (95% vs 68.9%, p=0.016). Main demographic, clinical and immunological features and depicted in Table 1. Dermatomyositis was the most prevalent subtype in both groups. We did not find any differences in MMT8 and PhGA scores. Interestingly, patients with IMM and FM displayed higher PtGA (3.5 vs 0.50, p=0.001), as well as muscular damage (1.5 vs. 1.0, p=0.023). Furthermore, the percentage and dosis of prednisone usage was more prevalent in IIM + FM (55% vs 17.2%, p=0.005). Immunologically, patients with IIM+ FM were characterized by lower amounts of T CD8+ cells (0.04 vs 0.13, p=0.045), B cells (58.4 vs. 152, p=0.052), and non classial monocytes (16.4 vs 28.5, p=0.027), as well as higher levels of serum IL-6 (0.111 vs. 0.003, p=0.232). Accordingly, the univariate analysis showed the following variables to be associated with FM in IIM patients: ptGA (OR 1.84, CI 95% 1.33-2.84), muscular damage score (OR 1.63, CI 95% 1.07-2.65), use of prednisone (OR 5.86, CI 95% 1.66-23.41), levels of IL-6 (OR 3.96, CI 95% 4.0-27.6) and MCP-1 (OR 1.07, CI 95% 1.0-1.75) and B cell count (OR 0.99, CI 95% 0.98-0.99). The univariate analysis showed a positive association between the presence of FM and the patient’s GA.

Conclusion: Our data suggests a high prevalence of FM in patients with IIM in complete clinical response, which might be a source of chronic pain and decreased quality of life in this population. The main risks factors associated with FM in IIM are PtGA, muscular damage score, use of prednisone as well as higher serum levels of pro-inflammatory cytokines IL-6 and MCP-1 and lower amounts of B cells, despite of being classified as complete clinical responders. Our findings suggest that persistent pain in patients with IIM should raise a suspicion for a diagnosis of fibromyalgia, remarking the importance of PROs for the comprehensive evaluation of this population, since it could suggest prescription of unnecessary therapy, thus translating in higher comorbidity.

Supporting image 1

Table 1. Demographic, clinical and immunological factors in IIM patients with or without a diagnosis of FM

Supporting image 2

Table 2. Univariate analysis


Disclosures: S. Govea-Peláez: None; B. Alcalá-Carmona: None; J. Balderas Miranda: None; Y. Reyna-Juárez: None; M. Ostos-prado: None; N. Mejía-Domínguez: None; G. Juarez-Vega: None; J. Torres Ruiz: None; D. Gomez-martin: None.

To cite this abstract in AMA style:

Govea-Peláez S, Alcalá-Carmona B, Balderas Miranda J, Reyna-Juárez Y, Ostos-prado M, Mejía-Domínguez N, Juarez-Vega G, Torres Ruiz J, Gomez-martin D. Clinical and Immunological Risk Factors Associated with Fybromialgia in Patients with Idiopathic Inflammatory Myopathies [abstract]. Arthritis Rheumatol. 2024; 76 (suppl 9). https://acrabstracts.org/abstract/clinical-and-immunological-risk-factors-associated-with-fybromialgia-in-patients-with-idiopathic-inflammatory-myopathies/. Accessed .
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