TY - JOUR
T1 - EULAR recommendations for cardiovascular risk management in rheumatic and musculoskeletal diseases, including systemic lupus erythematosus and antiphospholipid syndrome
AU - Drosos, George C.
AU - Vedder, Daisy
AU - Houben, Eline
AU - Boekel, Laura
AU - Atzeni, Fabiola
AU - Badreh, Sara
AU - Boumpas, Dimitrios T.
AU - Brodin, Nina
AU - Bruce, Ian N.
AU - Gonzalez-Gay, Miguel Angel
AU - Jacobsen, Soren
AU - Kerekes, Gyorgy
AU - Marchiori, Francesca
AU - Mukhtyar, Chetan
AU - Ramos-Casals, Manuel
AU - Sattar, Naveed
AU - Schreiber, Karen
AU - Sciascia, Savino
AU - Svenungsson, Elisabet
AU - Szekanecz, Zoltan
AU - Tausche, Anne-Kathrin
AU - Tyndall, Alan
AU - van Halm, Vokko
AU - Voskuyl, Alexandre
AU - Macfarlane, Gary J.
AU - Ward, Michael M.
AU - Nurmohamed, Michael T.
AU - Tektonidou, Maria G.
N1 - Funding: This study was funded by European Alliance of Associations for Rheumatology, EULAR. Project number: CLI112.
PY - 2022/5/16
Y1 - 2022/5/16
N2 - OBJECTIVE: To develop recommendations for cardiovascular risk (CVR) management in gout, vasculitis, systemic sclerosis (SSc), myositis, mixed connective tissue disease (MCTD), Sjögren's syndrome (SS), systemic lupus erythematosus (SLE) and antiphospholipid syndrome (APS). METHODS: Following European League against Rheumatism (EULAR) standardised procedures, a multidisciplinary task force formulated recommendations for CVR prediction and management based on systematic literature reviews and expert opinion. RESULTS: Four overarching principles emphasising the need of regular screening and management of modifiable CVR factors and patient education were endorsed. Nineteen recommendations (eleven for gout, vasculitis, SSc, MCTD, myositis, SS; eight for SLE, APS) were developed covering three topics: (1) CVR prediction tools; (2) interventions on traditional CVR factors and (3) interventions on disease-related CVR factors. Several statements relied on expert opinion because high-quality evidence was lacking. Use of generic CVR prediction tools is recommended due to lack of validated rheumatic diseases-specific tools. Diuretics should be avoided in gout and beta-blockers in SSc, and a blood pressure target <130/80 mm Hg should be considered in SLE. Lipid management should follow general population guidelines, and antiplatelet use in SLE, APS and large-vessel vasculitis should follow prior EULAR recommendations. A serum uric acid level <0.36 mmol/L (<6 mg/dL) in gout, and disease activity control and glucocorticoid dose minimisation in SLE and vasculitis, are recommended. Hydroxychloroquine is recommended in SLE because it may also reduce CVR, while no particular immunosuppressive treatment in SLE or urate-lowering therapy in gout has been associated with CVR lowering. CONCLUSION: These recommendations can guide clinical practice and future research for improving CVR management in rheumatic and musculoskeletal diseases.
AB - OBJECTIVE: To develop recommendations for cardiovascular risk (CVR) management in gout, vasculitis, systemic sclerosis (SSc), myositis, mixed connective tissue disease (MCTD), Sjögren's syndrome (SS), systemic lupus erythematosus (SLE) and antiphospholipid syndrome (APS). METHODS: Following European League against Rheumatism (EULAR) standardised procedures, a multidisciplinary task force formulated recommendations for CVR prediction and management based on systematic literature reviews and expert opinion. RESULTS: Four overarching principles emphasising the need of regular screening and management of modifiable CVR factors and patient education were endorsed. Nineteen recommendations (eleven for gout, vasculitis, SSc, MCTD, myositis, SS; eight for SLE, APS) were developed covering three topics: (1) CVR prediction tools; (2) interventions on traditional CVR factors and (3) interventions on disease-related CVR factors. Several statements relied on expert opinion because high-quality evidence was lacking. Use of generic CVR prediction tools is recommended due to lack of validated rheumatic diseases-specific tools. Diuretics should be avoided in gout and beta-blockers in SSc, and a blood pressure target <130/80 mm Hg should be considered in SLE. Lipid management should follow general population guidelines, and antiplatelet use in SLE, APS and large-vessel vasculitis should follow prior EULAR recommendations. A serum uric acid level <0.36 mmol/L (<6 mg/dL) in gout, and disease activity control and glucocorticoid dose minimisation in SLE and vasculitis, are recommended. Hydroxychloroquine is recommended in SLE because it may also reduce CVR, while no particular immunosuppressive treatment in SLE or urate-lowering therapy in gout has been associated with CVR lowering. CONCLUSION: These recommendations can guide clinical practice and future research for improving CVR management in rheumatic and musculoskeletal diseases.
KW - autoimmune diseases
KW - cardiovascular diseases
KW - lupus erythematosus
KW - systemic
KW - systemic vasculitis
KW - antiphospholipid syndrome
KW - GIANT-CELL ARTERITIS
KW - C-REACTIVE PROTEIN
KW - CORONARY-HEART-DISEASE
KW - MYOCARDIAL-INFARCTION
KW - VASCULAR EVENTS
KW - GOUT
KW - MORTALITY
KW - PREDICTORS
KW - COHORT
KW - DAMAGE
UR - http://www.scopus.com/inward/record.url?scp=85125531096&partnerID=8YFLogxK
U2 - 10.1136/annrheumdis-2021-221733
DO - 10.1136/annrheumdis-2021-221733
M3 - Article
VL - 81
SP - 768
EP - 779
JO - Annals of the Rheumatic Diseases
JF - Annals of the Rheumatic Diseases
SN - 0003-4967
IS - 6
M1 - 221733
ER -