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      Ocular fundus changes and association with systemic conditions in systemic lupus erythematosus

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          Abstract

          Systemic lupus erythematosus (SLE) is an autoimmune disease that affects multiple organs and systems. Ocular involvement is estimated to manifest in one-third of individuals with SLE, of which lupus retinopathy and choroidopathy represent the severe subtype accompanied by vision impairment. Advancements in multimodal ophthalmic imaging have allowed ophthalmologists to reveal subclinical microvascular and structural changes in fundus of patients with SLE without ocular manifestations. Both ocular manifestations and subclinical fundus damage have been shown to correlate with SLE disease activity and, in some patients, even precede other systemic injuries as the first presentation of SLE. Moreover, ocular fundus might serve as a window into the state of systemic vasculitis in patients with SLE. Given the similarities of the anatomy, physiological and pathological processes shared among ocular fundus, and other vital organ damage in SLE, such as kidney and brain, it is assumed that ocular fundus involvement has implications in the diagnosis and evaluation of other systemic impairments. Therefore, evaluating the fundus characteristics of patients with SLE not only contributes to the early diagnosis and intervention of potential vision damage, but also holds considerate significance for the evaluation of SLE vasculitis state and prediction of other systemic injuries.

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          To describe the Systemic Lupus Erythematosus Disease Activity Index 2000 (SLEDAI-2K), a modification of SLEDAI to reflect persistent, active disease in those descriptors that had previously only considered new or recurrent occurrences, and to validate SLEDAI-2K against the original SLEDAI as a predictor for mortality and as a measure of global disease activity in the clinic. All visits in our cohort of 960 patients were used to correlate SLEDAI-2K against the original SLEDAI, and the whole cohort was used to validate SLEDAI-2K as a predictor of mortality. A subgroup of 212 patients with SLE followed at the Lupus Clinic who had 5 regular visits, 3-6 months apart, in 1991-93 was also included. An uninvolved clinician evaluated each patient record and assigned a clinical activity level. The SLEDAI score was calculated from the database according to both the original and modified definitions. SLEDAI-2K correlated highly (r = 0.97) with SLEDAI. Both methods for SLEDAI scoring predicted mortality equally (p = 0.0001), and described similarly the range of disease activity as recognized by the clinician. SLEDAI-2K, which allows for persistent activity in rash, mucous membranes, alopecia, and proteinuria, is suitable for use in clinical trials and studies of prognosis in SLE.
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            2019 European League Against Rheumatism/American College of Rheumatology classification criteria for systemic lupus erythematosus

            To develop new classification criteria for systemic lupus erythematosus (SLE) jointly supported by the European League Against Rheumatism (EULAR) and the American College of Rheumatology (ACR). This international initiative had four phases. (1) Evaluation of antinuclear antibody (ANA) as an entry criterion through systematic review and meta-regression of the literature and criteria generation through an international Delphi exercise, an early patient cohort and a patient survey. (2) Criteria reduction by Delphi and nominal group technique exercises. (3) Criteria definition and weighting based on criterion performance and on results of a multi-criteria decision analysis. (4) Refinement of weights and threshold scores in a new derivation cohort of 1001 subjects and validation compared with previous criteria in a new validation cohort of 1270 subjects. The 2019 EULAR/ACR classification criteria for SLE include positive ANA at least once as obligatory entry criterion; followed by additive weighted criteria grouped in seven clinical (constitutional, haematological, neuropsychiatric, mucocutaneous, serosal, musculoskeletal, renal) and three immunological (antiphospholipid antibodies, complement proteins, SLE-specific antibodies) domains, and weighted from 2 to 10. Patients accumulating ≥10 points are classified. In the validation cohort, the new criteria had a sensitivity of 96.1% and specificity of 93.4%, compared with 82.8% sensitivity and 93.4% specificity of the ACR 1997 and 96.7% sensitivity and 83.7% specificity of the Systemic Lupus International Collaborating Clinics 2012 criteria. These new classification criteria were developed using rigorous methodology with multidisciplinary and international input, and have excellent sensitivity and specificity. Use of ANA entry criterion, hierarchically clustered and weighted criteria reflect current thinking about SLE and provide an improved foundation for SLE research.
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              Recommendations on Screening for Chloroquine and Hydroxychloroquine Retinopathy (2016 Revision).

              The American Academy of Ophthalmology recommendations on screening for chloroquine (CQ) and hydroxychloroquine (HCQ) retinopathy are revised in light of new information about the prevalence of toxicity, risk factors, fundus distribution, and effectiveness of screening tools.
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                Author and article information

                Contributors
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                URI : https://loop.frontiersin.org/people/2728068Role: Role: Role: Role:
                URI : https://loop.frontiersin.org/people/1542270Role: Role: Role: Role: Role:
                Journal
                Front Immunol
                Front Immunol
                Front. Immunol.
                Frontiers in Immunology
                Frontiers Media S.A.
                1664-3224
                18 July 2024
                2024
                : 15
                : 1395609
                Affiliations
                [1] 1 Department of Ophthalmology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences , Beijing, China
                [2] 2 Key Lab of Ocular Fundus Diseases, Chinese Academy of Medical Sciences , Beijing, China
                Author notes

                Edited by: Pedro Mecê, UMR7587 Institut Langevin, France

                Reviewed by: Mohamed Tharwat Hegazy, Cairo University, Egypt

                Konstantinos Triantafyllias, Rheumatology Center Rhineland Palatinate, Germany

                *Correspondence: Youxin Chen, chenyx@ 123456pumch.cn ; Xinyu Zhao, zhaoxinyu@ 123456pumch.cn ; Huan Chen, chenhuan1@ 123456pumch.cn

                †These authors have contributed equally to this work and share first authorship

                ‡These authors have contributed equally to this work and share last authorship

                Article
                10.3389/fimmu.2024.1395609
                11291259
                39091490
                f3143000-136a-49a6-b820-6957e1e9036d
                Copyright © 2024 Meng, Wang, Yang, Lin, Wang, Chen, Zhao and Chen

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 04 March 2024
                : 26 June 2024
                Page count
                Figures: 4, Tables: 1, Equations: 0, References: 92, Pages: 12, Words: 5724
                Funding
                The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work was supported by the Peking Union Medical College Hospital Deposit Integration Commission Funds (ZC201904168) and Innovative and Training Program for College Students (2023zglc06008).
                Categories
                Immunology
                Review
                Custom metadata
                Autoimmune and Autoinflammatory Disorders : Autoimmune Disorders

                Immunology
                systemic lupus erythematosus,ocular fundus,multimodal imaging,systemic damage,kidney,central nervous system

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