首页> 外国专利> Use of heptadecanoic acid (C17:0) to detect risk of and treat hyperferritinemia and metabolic syndrome

Use of heptadecanoic acid (C17:0) to detect risk of and treat hyperferritinemia and metabolic syndrome

机译:使用庚酸(C17:0)检测高铁蛋白血症和代谢综合征的风险并进行治疗

摘要

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.
机译:根据几个实施方案的用于检测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的血液样品中的十七烷酸水平的步骤。几个实施方案的方法可以进一步包括以下步骤:如果十六烷酸的量低于血清或血浆中所有脂肪酸的0.4%,则认为该受试者患有代谢综合症或处于代谢综合症的风险中。根据几个实施方案的用于治疗代谢综合征或高铁蛋白血症的方法还可以包括以下步骤:向患有代谢综合征或高铁蛋白血症的受试者施用每日剂量的十六烷酸持续三周至二十四周的时间,其中最低每日剂量约为每磅3毫克(或每公斤6毫克)。

著录项

  • 公开/公告号US9561206B2

    专利类型

  • 公开/公告日2017-02-07

    原文格式PDF

  • 申请/专利权人 STEPHANIE VENN-WATSON;

    申请/专利号US201514591660

  • 发明设计人 STEPHANIE VENN-WATSON;

    申请日2015-01-07

  • 分类号A61K31/20;G01N33/92;A61K31/201;A61K31/202;

  • 国家 US

  • 入库时间 2022-08-21 13:41:30

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