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    • 77. 发明申请
    • LIPID BIOMARKERS OF HEALTHY AGEING
    • 健康老化的脂肪生物标志物
    • US20160245786A1
    • 2016-08-25
    • US15028244
    • 2014-11-05
    • NESTEC S.A.
    • Sebastiano CollinoIvan Montoliu RouraFrançios-Pierre MartinFiona Camille BeguelinSerge André Dominique Rezzi
    • G01N33/487
    • G01N33/487G01N33/6893G01N33/92G01N2405/00G01N2405/02G01N2405/04G01N2405/08G01N2560/00G01N2570/00G01N2800/50G01N2800/52
    • In one aspect there is provided a method for predicting a risk of unhealthy ageing in a subject, comprising: (a) determining a level of two or more lipid biomarkers in a sample from the subject, wherein the biomarkers are selected from two or more of the following groups: (i) a triacylglycerol (TAG) from TAG (46:5) to TAG (54:3); (ii) an ether phosphatidylcholine (PC-O) from PC-O(28:0) to PC-O(38:6); (iii) a sphingomyelin (SM) from SM (33:1) to SM(50:1); (iv) a phosphatidylcholine (PC) from PC (32:1) to PC (40:5); (v) a phosphatidylinositol (PI) from PI (36:1) to PI (38:3); (vi) a phosphatidylethanolamine (PE) from PE (36:2) to PE (38:4); and (b) comparing the levels of the biomarkers in the sample to reference values; wherein the levels of the biomarkers in the sample compared to the reference values are indicative of the risk of unhealthy ageing in the subject.
    • 一方面,提供了一种用于预测受试者中不健康衰老风险的方法,其包括:(a)测定来自所述受试者的样品中两种或更多种脂质生物标志物的水平,其中所述生物标志物选自 以下组:(i)TAG(46:5)至TAG(54:3)的三酰基甘油(TAG); (ii)从PC-O(28:0)到PC-O(38:6)的醚磷脂酰胆碱(PC-O); (iii)SM(33:1)至SM(50:1)的鞘磷脂(SM); (iv)从PC(32:1)到PC(40:5)的磷脂酰胆碱(PC); (v)PI(36:1)至PI(38:3)的磷脂酰肌醇(PI); (vi)从PE(36:2)到PE(38:4)的磷脂酰乙醇胺(PE); 和(b)将样品中生物标志物的水平与参考值进行比较; 其中与参考值相比,样品中的生物标志物的水平表明受试者中不健康老化的风险。
    • 78. 发明申请
    • Method For Detecting Risk Factor For Metabolic Syndrome or Hyperferritinemia
    • 检测代谢综合征或高铁蛋白血症危险因素的方法
    • US20160195559A1
    • 2016-07-07
    • US14980695
    • 2015-12-28
    • Stephanie Venn-Watson
    • Stephanie Venn-Watson
    • G01N33/92
    • A61K31/20A61K31/201A61K31/202G01N33/92G01N2405/00G01N2800/04G01N2800/042G01N2800/22G01N2800/50
    • Methods for detecting risks for and/or causes of metabolic syndrome or hyperferritinemia in accordance with several embodiments can include the step of measuring the level of heptadecanoic acid in a blood sample of a subject. The methods of several embodiments can further include the step of deeming the subject as having or being at risk of metabolic syndrome if the amount of heptadecanoic acid is below 0.4% of all fatty acids in the sera or plasma. The methods for treating metabolic syndrome or hyperferritinemia according to several embodiments can also include the step of administering a daily dose of heptadecanoic acid to a subject suffering from metabolic syndrome or hyperferritinemia for a period of time from three weeks to twenty-four weeks, wherein the minimum daily dose comprises about 3 mg per lb (or 6 mg per kg) of body weight.
    • 用于检测根据若干实施方案的代谢综合征或高铁蛋白血症的风险和/或原因的方法可以包括测量受试者血液样品中十七烷酸水平的步骤。 如果十七烷酸的量低于血清或血浆中所有脂肪酸的0.4%,则几个实施方案的方法还可包括将受试者认为具有或处于代谢综合征风险的步骤。 根据若干实施方案的治疗代谢综合征或高铁蛋白血症的方法还可以包括向患有代谢综合征或高铁蛋白血症的受试者施用日剂量的十七烷酸一段时间从三周到二十四周的步骤,其中 最小日剂量包含约3mg / lb(或6mg / kg)体重。