“…We analyzed and compared the following data: gender, age at SLE onset, age at admission to PUMCH, disease duration, serositis, nephropathy, hematological disturbance, nervous system disturbance (including all the neuropsychiatric syndromes defined by the 1999 ACR criteria for NPSLE), microscopic hematuria, albuminuria, erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), hypocomplimentemia, thrombocytopenia (classified as severe (platelet count: < 20 Â 10 9 /l), moderate (platelet count: 20-50 Â 10 9 /l), and mild (platelet count > 50 Â 10 9 /l and <100 Â 10 9 /l)), prolonged prothrombin time (PT, defined as 3 seconds (s) longer than the reference), lupus anticoagulant (LA), anti-nuclear antibody, anti-double-stranded DNA (anti-dsDNA) antibody, anti-ENA antibodies (including anti-SSA, anti-SSB, anti-Sm, anti-RNP, and anti-rRNP antibody), anti-cardiolipin (IgG-aCL) antibody, SLE disease activity index (SLEDAI, stratified to stable (<5), mild active (5)(6)(7)(8)(9), moderate active (10)(11)(12)(13)(14), and severe active (>14)), 17 antiphospholipid syndrome diagnosed according to revised classification criteria for antiphospholipid syndrome, 18 hypertension (defined as systolic blood pressure !140 mmHg and/or diastolic blood pressure !90 mmHg), diabetes (defined as fasting glucose level !126 mg per deciliter, twohour glucose level !200 mg per deciliter, or both), personal history of smoking (defined as having smoked at least 100 cigarettes), 19 and family history of cerebrovascular disease. Two or more occasions of IgG-aCL and LA, at least 12 weeks apart, were recorded.…”