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Review
. 2024 May 25;403(10441):2326-2338.
doi: 10.1016/S0140-6736(24)00398-2. Epub 2024 Apr 17.

Systemic lupus erythematosus

Affiliations
Review

Systemic lupus erythematosus

Alberta Hoi et al. Lancet. .

Erratum in

  • Department of Error.
    [No authors listed] [No authors listed] Lancet. 2024 May 25;403(10441):2292. doi: 10.1016/S0140-6736(24)01044-4. Lancet. 2024. PMID: 38796208 No abstract available.

Abstract

Systemic lupus erythematosus (SLE) is a multisystemic autoimmune disease characterised by the presence of autoantibodies towards nuclear antigens, immune complex deposition, and chronic inflammation at classic target organs such as skin, joints, and kidneys. Despite substantial advances in the diagnosis and management of SLE, the burden of disease remains high. It is important to appreciate the typical presentations and the diagnostic process to facilitate early referral and diagnosis for patients. In most patients, constitutional, mucocutaneous, and musculoskeletal symptoms represent the earliest complaints; these symptoms can include fatigue, lupus-specific rash, mouth ulcers, alopecia, joint pain, and myalgia. In this Seminar we will discuss a diagnostic approach to symptoms in light of the latest classification criteria, which include a systematic evaluation of clinical manifestations (weighted within each domain) and autoantibody profiles (such as anti-double-stranded DNA, anti-Sm, hypocomplementaemia, or antiphospholipid antibodies). Non-pharmacotherapy management is tailored to the individual, with specific lifestyle interventions and patient education to improve quality of life and medication (such as hydroxychloroquine or immunosuppressant) adherence. In the last decade, there have been a few major breakthroughs in approved treatments for SLE and lupus nephritis, such as belimumab, anifrolumab, and voclosporin. However the disease course remains variable and mortality unacceptably high. Access to these expensive medications has also been restricted across different regions of the world. Nonetheless, understanding of treatment goals and strategies has improved. We recognise that the main goal of treatment is the achievement of remission or low disease activity. Comorbidities due to both disease activity and treatment adverse effects, especially infections, osteoporosis, and cardiovascular disease, necessitate vigilant prevention and management strategies. Tailoring treatment options to achieve remission, while balancing treatment-related comorbidities, are priority areas of SLE management.

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Conflict of interest statement

Declaration of interests AH reports grants from Arthritis Australia, AstraZeneca, Perpetual IMPACT fund, Bristol Myers Squibb, Merck Serono, GSK, and Janssen; received sponsorship for the Australian Lupus Registry and Biobank to their institution from AstraZeneca, Bristol Myers Squibb, GSK, Eli Lilly, and UCB; and reports honoraria or speaker fees from Novartis, Janssen, and Recordati, all outside of the submitted work. CCM reports honoraria or speaker fees from GSK and Pfizer; received research funding as part of the participating site of BLISS-LN, sponsored by GSK; and is a member of the drug advisory committee of the hospital authority of Hong Kong, all outside of the submitted work. LA reports consulting fees from Alpine Pharmaceuticals, AstraZeneca, Bristol Myers Squibb, Kezar, and Novartis; reports honoraria or speaker fees from Alexion, Alpine Pharmaceuticals, Amgen, AstraZeneca, AbbVie, Biogen, Bristol Myers Squibb, Boehringer Ingelheim, Chugai, GSK, Grifols, Janssen, Kezar, LFB, Eli Lilly, Medac, Novartis, Ono Pharmaceuticals, Pfizer, Roche, and UCB; and received research funding from GSK and AstraZeneca paid to their institution, all outside of the submitted work. All other authors declare no competing interests.

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