Introduction Drug-induced lupus (DIL) is an autoimmune condition triggered by exposure to certain medications, leading to the emergence of clinical features that resemble those of systemic lupus erythematosus (SLE). This study aims to investigate the clinical characteristics, management strategies, and outcomes of patients who develop DIL during tumor necrosis factor inhibitor (TNFi) therapy. Methods We conducted a retrospective case series involving 15 patients who developed positive anti-double-stranded DNA (anti-dsDNA) antibodies while undergoing TNFi therapy between 2015 and 2023. Clinical data were collected and analyzed to assess the relationship between TNFi therapy and the onset of DIL symptoms. Results The case series included 15 patients (13 females and two males) with a mean age of 42.13 years. The primary diagnoses were ankylosing spondylitis (AS) (46.66%), rheumatoid arthritis (RA) (40%), and psoriatic arthritis (PsA) (13.33%). The mean duration from TNFi initiation to the detection of anti-dsDNA positivity was 5.13 years. Two patients (13.33%) exhibited clinical manifestations of DIL; however, no major organ involvement was observed. Sixty percent of patients continued with the same TNFi without disease activation, while 33% switched medications. Conclusion TNFi-induced DIL typically presents with mild symptoms. Both continuation and switching of TNFi therapy can be considered without significant exacerbation of symptoms. Management should be individualized based on clinical and laboratory findings. Further research with larger patient cohorts is warranted to determine optimal management strategies.
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http://dx.doi.org/10.7759/cureus.72388 | DOI Listing |
Dermatol Ther (Heidelb)
January 2025
Department of Biomedical and Dental Sciences and Morphofunctional Imaging, Section of Dermatology, University of Messina, 98125, Messina, Italy.
Introduction: Patients with psoriasis (PsO) and permanent spinal cord injuries (SCI) resulting in paraplegia and tetraplegia may experience a higher rate of infections compared to patients with PsO without SCI. It can result in further challenges for therapeutic management with immunosuppressants (biological and non-biological treatments). Thus, we aimed to evaluate the rate of infections in patients with PsO and SCI treated with systemic immunosuppressants.
View Article and Find Full Text PDFAliment Pharmacol Ther
January 2025
Division of Gastroenterology, Hepatology, and Nutrition, Allegheny Health Network, Pittsburgh, Pennsylvania, USA.
Background: Obesity has been linked to a more severe phenotype in patients with ulcerative colitis (UC).
Aim: To evaluate the impact of obesity on outcomes of advanced therapies in UC.
Methods: We conducted a retrospective cohort study utilising the TriNetX database comparing the composite score of corticosteroid use, change in advanced therapy or colectomy within two years between two cohorts of patients with UC-those with obesity (BMI ≥ 30 kg/m) and those without (BMI 18.
Int J Rheum Dis
January 2025
Institute of Medicine, Chung Shan Medical University, Taichung, Taiwan.
Chronic inflammation is a major characteristic of ankylosing spondylitis (AS) and is closely related to the mechanisms of cancer development. Persistent inflammatory responses can lead to DNA damage, gene mutations, and abnormal cell proliferation, all of which may increase the risk of cancer. We also explore the use of biologic therapy of AS and their potential cancer risks.
View Article and Find Full Text PDFArch Dermatol Res
January 2025
Lűbeck Institute of Experimental Dermatology, University of Lübeck, Ratzeburger Allee 160, 23562, Lübeck, Germany.
Background: A low risk of cardiovascular and metabolic outcomes was found in the randomized clinical trials of dupilumab in atopic dermatitis (AD). Dupilumab-associated real-life long-term cardiometabolic risk relative to other systemic agents is yet to be precisely investigated.
Objective: To assess the risk of cardiometabolic outcomes in patients with AD treated with dupilumab relative to those treated with methotrexate and cyclosporine.
Int J Rheum Dis
January 2025
Japan Drug Information Institute in Pregnancy, National Center for Child Health and Development, Tokyo, Japan.
Aim: Uncontrolled chronic inflammatory diseases (CIDs) before, during, and after pregnancy, as well as some CID medications, can increase the risk of impaired fertility in addition to adverse maternal/pregnancy outcomes in women of childbearing age. We report pregnancy outcomes from prospectively reported pregnancies in Japanese women treated with certolizumab pegol (CZP).
Methods: Data from July 2001 to November 2020 on CZP-exposed pregnancies from the CZP Pharmacovigilance safety database were reviewed.
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