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    • 31. 发明申请
    • ASSESSING THE RISK OF A MAJOR ADVERSE CARDIAC EVENT IN PATIENTS WITH CHEST PAIN
    • 评估患者与主要疼痛患者的主要不良心脏事件的风险
    • US20160266121A1
    • 2016-09-15
    • US15164205
    • 2016-05-25
    • THE CLEVELAND CLINIC FOUNDATION
    • Stanley L. HazenRenliang Zhang
    • G01N33/573
    • G01N33/573C12Q1/28G01N33/6893G01N2333/908G01N2800/32G01N2800/50G01N2800/56
    • Methods for characterizing the near terns risk of experiencing a major adverse cardiac event in a patient presenting with chest pain are provided. In one embodiment the method comprises determining the level of myeloperoxidase (MPO) activity in a bodily sample obtained. from the patient. In another embodiment, the method comprises determining the level of MPO mass in a bodily sample obtained from the patient. In another embodiment, the method comprises determining the level of one or more select MPO-generated oxidation products in a bodily sample obtained from the patient. The select MPO-generated oxidation products are dityrosine, nitrotyrosine, chlorotyrosine, methionine sulphoxide or an MPO-generated lipid peroxidation product. Levels of MPO activity, MPO mass, or the select MPO-generated oxidation product in bodily samples from the test subject are then compared to a control value that is derived from measurements of MPO activity, MPO mass, or the select MPO-generated oxidation product in comparable bodily samples obtained from control population. Such comparison can also be used to determine the near term treatment of the patient.
    • 提供了表征患有胸痛的患者的主要不良心脏事件的近端子风险的方法。 在一个实施方案中,该方法包括确定所获得的身体样品中髓过氧化物酶(MPO)活性的水平。 来自病人。 在另一个实施方案中,该方法包括确定从患者获得的身体样品中的MPO质量的水平。 在另一个实施方案中,该方法包括确定从患者获得的身体样品中的一种或多种选择的MPO产生的氧化产物的水平。 选择的MPO生成的氧化产物是二酪氨酸,硝基酪氨酸,氯酪氨酸,甲硫氨酸亚砜或MPO产生的脂质过氧化产物。 然后将来自测试受试者的身体样品中的MPO活性,MPO质量或选择的MPO生成的氧化产物的水平与从MPO活性,MPO质量或选择的MPO产生的氧化产物的测量结果相关的对照值进行比较 在从对照群体获得的可比较的身体样品中。 这种比较也可用于确定患者的近期治疗。
    • 33. 发明申请
    • RISK MARKERS FOR CARDIOVASCULAR DISEASE
    • 心血管疾病危险标志
    • US20150037905A1
    • 2015-02-05
    • US14275307
    • 2014-05-12
    • THE CLEVELAND CLINIC FOUNDATION
    • Stanley L. HazenMichael KinterMarc S. PennJonathan SmithLemin Zheng
    • G01N33/561C07K16/18
    • G01N33/561C07K16/18G01N33/6893G01N33/92G01N2333/775G01N2800/32
    • Provided herein methods for determining whether a subject, particularly a human subject, is at risk of developing, having, or experiencing a complication of cardiovascular disease, and methods of treating subjects who are identified by the current methods of being at risk for cardiovascular disease. In one embodiment, the method comprises determining levels of one or more oxidized apolipoprotein A-I related biomolecules in a bodily sample from the subject. Also, provided are kits and reagents for use in the present methods. Also provided are methods for monitoring the status of cardiovascular disease in a subject or the effects of therapeutic agents on subjects with cardiovascular disease. Such method comprising determining levels of one or more oxidized apolipoprotein A-I related molecules in bodily samples taken from the subject over time or before and after therapy.
    • 本文提供用于确定受试者,特别是人类受试者是否处于发展,具有或经历心血管疾病并发症的风险的方法,以及治疗由目前的心血管疾病风险的方法鉴定的受试者的方法。 在一个实施方案中,该方法包括确定来自受试者的身体样品中一种或多种氧化的载脂蛋白A-1相关生物分子的水平。 此外,提供了用于本方法的试剂盒和试剂。 还提供了用于监测受试者心血管疾病状态或治疗剂对心血管疾病受试者的影响的方法。 这种方法包括测定在受试者随时间或治疗之前或之后取自受试者的身体样品中一种或多种氧化的载脂蛋白A-1相关分子的水平。