Hopkins Lupus Cohort

霍普金斯狼疮队列

• 批准号: 7466207
• 负责人: MICHELLE A PETRI
• 金额: $ 66.27万
• 依托单位: JOHNS HOPKINS UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 1996
• 资助国家: 美国
• 起止时间: 1996-09-30 至 2013-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7466207
• 关键词: Accounting; Acute; Address; African American; Antiphospholipid Antibodies; Arteries; Arts; Aspirin; Atherosclerosis; Autoantibodies; Basic Science; Biological Assay; Biological Markers; Biopsy; Blood Clot; Blood Platelets; Blood coagulation; Cardiac; Caring; Cause of Death; Class; Clinical; Coagulation Process; Collaborations; Complement; Complement Activation; Coronary; Coronary Arteriosclerosis; Data; Development; Event; Future; General Population; Gold; Hemostatic function; High Density Lipoproteins; Homocysteine; Homocystine; Human; Hydroxychloroquine; Hyperlipidemia; Hypertension; Individual; Inflammation; Inflammatory; Invasive; Kidney; Kidney Diseases; Kidney Failure; Kidney Transplantation; Laboratories; Lead; Lupus; Lupus Coagulation Inhibitor; Lupus Nephritis; Measures; Mediator of activation protein; Modeling; Mus; Obesity; Organ; Outcome; Pathway interactions; Patients; Phenotype; Prevention strategy; Principal Investigator; Proteins; Public Health; Risk; Risk Factors; Score; Spiral Computed Tomography; Standards of Weights and Measures; Statistical Methods; Stem cells; Systemic Lupus Erythematosus; Testing; Thrombophilia; Thrombosis; Transplant Recipients; Urine; Validation; Venous Thrombosis; Warfarin; Work; cardiovascular risk factor; chemokine; cohort; cytokine; experience; follow-up; improved; mortality; novel strategies; programs; prophylactic; radiologist; response; urinary

DESCRIPTION (provided by applicant): Traditional cardiovascular risk factors do not entirely account for the increased risk of atherosclerosis, the major cause of death, in systemic lupus erythematosus (SLE). In this project we want to identify new pathogenic pathways of atherosclerosis in SLE patients, by assessing the association between newly identified potential risk factors and a refined measure of subclinical atherosclerosis, soft (noncalcified) coronary plaque. Similarly over 50% of SLE patients develop lupus nephritis, including 75% of African-American SLE patients. Renal biopsy is the gold standard to determine renal activity, but is expensive, invasive, and has real risk to the patient. We hypothesize that urinary markers of renal activity will have clinical utility in human lupus nephritis, as they have in renal transplant patients and murine models of SLE. In addition we want to develop and study three new approaches to assess hypercoagulability risk (endogenous thrombogenic potential, complement activation, and platelet microparticles) to determine if these markers can predict future thrombotic events or associated with antiphospholipid antibodies. PUBLIC HEALTH RELEVANCE: Although the survival of SLE patients has greatly improved, permanent organ damage continues to occur in the general public. This project addresses three challenges: hardening of the arteries, blood clots, and lupus kidney disease in collaboration with other rheumatologists and radiologists.

描述（由申请人提供）：传统的心血管危险因素不能完全解释系统性红斑狼疮（SLE）患者动脉粥样硬化（死亡的主要原因）风险增加的原因。在这个项目中，我们希望通过评估新发现的潜在危险因素与亚临床动脉粥样硬化、软（非钙化）冠状动脉斑块之间的相关性，来确定SLE患者动脉粥样硬化的新致病途径。类似地，超过50%的SLE患者发展为狼疮性肾炎，包括75%的非裔美国SLE患者。肾活检是确定肾活性的金标准，但是昂贵、侵入性，并且对患者具有真实的风险。我们假设尿中的肾活动标志物在人类狼疮性肾炎中具有临床实用性，就像它们在肾移植患者和SLE小鼠模型中一样。此外，我们想开发和研究三种新的方法来评估高凝风险（内源性血栓形成潜力，补体激活和血小板微粒），以确定这些标志物是否可以预测未来的血栓形成事件或与抗磷脂抗体相关。 公共卫生相关性：虽然SLE患者的生存率大大提高，但永久性器官损伤仍在公众中发生。该项目解决了三个挑战：动脉硬化，血凝块和狼疮肾病与其他风湿病学家和放射科医生合作。