TY - JOUR
T1 - Combined Brain/Heart Magnetic Resonance Imaging in Systemic Lupus Erythematosus
AU - Mavrogeni, Sophie
AU - Koutsogeorgopoulou, Loukia
AU - Dimitroulas, Theodoros
AU - Markousis-Mavrogenis, George
AU - Boki, Kyriaki
AU - Katsifis, Gikas
AU - Vartela, Vasiliki
AU - Kallenberg, Cees G.
AU - Kolovou, Genovefa
AU - Kitas, George
PY - 2020
Y1 - 2020
N2 - Cardiovascular Disease (CVD) in Systemic Lupus Erythematosus (SLE) and Neuropsychiatric SLE (NPSLE) has an estimated prevalence of 50% and 40%, respectively and both constitute major causes of death among SLE patients. In this review, we proposea combined brain/heart Magnetic Resonance Imaging (MRI) for SLE risk stratification has been proposed.The pathophysiologic background of NPSLE includes microangiopathy, macroscopic infarcts and accelerated atherosclerosis. Classic brain MRI findings demonstrate lesions suggestive of NPSLE in 50% of the NPSLE cases, while advanced MRI indices can detect pre-clinical lesions in the majority of them, but their clinical impact still remains unknown. Cardiac involvement in SLE includes myo-pericarditis, valvular disease/endocarditis, Heart Failure (HF), coronary macro-microvascular disease, vasculitis and pulmonary hypertension. Classic and advanced Cardiovascular Magnetic Resonance (CMR) indices allow function and tissue characterization for early diagnosis and treatment follow-up of CVD in SLE.Although currently, there are no clinical data supporting the combined use of brain/heart MRI in asymptomatic SLE, it may have a place in cases with clinical suspicion of brain/heart involvement, especially in patients at high risk for CVD/stroke such as SLE with antiphospholipid syndrome (SLE/APS), in whom concurrent cardiac and brain lesions have been identified. Furthermore, it may be of value in SLE with multi-organ involvement, NPSLE with concurrent cardiac involvement, and recent onset of arrhythmia and/or heart failure.
AB - Cardiovascular Disease (CVD) in Systemic Lupus Erythematosus (SLE) and Neuropsychiatric SLE (NPSLE) has an estimated prevalence of 50% and 40%, respectively and both constitute major causes of death among SLE patients. In this review, we proposea combined brain/heart Magnetic Resonance Imaging (MRI) for SLE risk stratification has been proposed.The pathophysiologic background of NPSLE includes microangiopathy, macroscopic infarcts and accelerated atherosclerosis. Classic brain MRI findings demonstrate lesions suggestive of NPSLE in 50% of the NPSLE cases, while advanced MRI indices can detect pre-clinical lesions in the majority of them, but their clinical impact still remains unknown. Cardiac involvement in SLE includes myo-pericarditis, valvular disease/endocarditis, Heart Failure (HF), coronary macro-microvascular disease, vasculitis and pulmonary hypertension. Classic and advanced Cardiovascular Magnetic Resonance (CMR) indices allow function and tissue characterization for early diagnosis and treatment follow-up of CVD in SLE.Although currently, there are no clinical data supporting the combined use of brain/heart MRI in asymptomatic SLE, it may have a place in cases with clinical suspicion of brain/heart involvement, especially in patients at high risk for CVD/stroke such as SLE with antiphospholipid syndrome (SLE/APS), in whom concurrent cardiac and brain lesions have been identified. Furthermore, it may be of value in SLE with multi-organ involvement, NPSLE with concurrent cardiac involvement, and recent onset of arrhythmia and/or heart failure.
KW - Magnetic resonance imaging
KW - systemic lupus erythematosus
KW - brain lesions
KW - cardiovascular disease
KW - neuropsychiatric symptoms
KW - cognitive dysfunction
KW - CORONARY-ARTERY-DISEASE
KW - RISK-FACTORS
KW - NEUROPSYCHIATRIC MANIFESTATIONS
KW - MYOCARDIAL INFLAMMATION
KW - HEART-DISEASE
KW - MRI
KW - PREDICTORS
KW - BRAIN
KW - PERFUSION
KW - SLE
U2 - 10.2174/1573403X15666190801122105
DO - 10.2174/1573403X15666190801122105
M3 - Review article
SN - 1573-403X
VL - 16
SP - 178
EP - 186
JO - Current cardiology reviews
JF - Current cardiology reviews
IS - 3
ER -