首页> 外国专利> COMPOSITION, CONTAINING SUBLIMED SULPHUR, FOR ALTERING PLASMA HOMODYST(E) LEVELS IN HUMANS

COMPOSITION, CONTAINING SUBLIMED SULPHUR, FOR ALTERING PLASMA HOMODYST(E) LEVELS IN HUMANS

机译:包含取代硫的组合物,用于改变人类血浆中的同种异体水平

摘要

Plasma homocysteine values 10.2νmol per litre are associated with an increased risk of atherothrombosis, but normal values are considered to be 4 to 15 νmol per litre. An initial test subject with Hyper-homocystinemia and lactose intolerance was treated with Sublimed Sulfur 300 mg orally twice daily for 45 days. An additional 46 randomly selected subjects were treated with Sublimed Sulfur 200 mg orally daily for 30 days. Basal control plasma homocysteine, erythrocyte folic acid and serum vitamin B12 and lipids were compared with follow-up results obtained 24 hours and 30 days after discontinuation of Sublimed Sulfur. In the initial test subject, basal plasma homocysteine of 77 νmol per litre decreased by 95.7 percent. In the 46 patients, the effect of Sublimed Sulfur varied according to the initial basal plasma homocysteine concentration; basal levels of 2.3 to 7 νmol per litre increased by 58.5 percent (p 0.001) 24 hours after discontinuation of treatment, and by 85.4 percent 30 days later; basal levels of 7.1 to 9.9 νmol per litre showed no consistent changes, and basal levels of 9.9 to 22.1 νmol per litre decreased to 63.9 percent (p 0.005) of basal levels 24 hours after discontinuation of Sublimed Sulfur, and to 70.7 percent of basal levels 30 days later. Sublimed Sulfur therapy eliminated the initial plasma homocysteine differences between low, intermediate and high basal levels. Sublimed Sulfur therapy normalized plasma homocysteine by causing a regression towards the mean of basal plasma homocysteine levels.
机译:血浆同型半胱氨酸值>10.2νmol/升与动脉粥样硬化血栓形成的风险增加有关,但正常值被认为是4-15νmol/升。最初对患有高同型胱氨酸血症和乳糖不耐症的受试者进行口服升华硫300 mg的治疗,每天两次,持续45天。每天对另外46名随机选择的受试者口服升华硫200 mg,治疗30天。将基础对照血浆同型半胱氨酸,红细胞叶酸,血清维生素B12和脂质与升华硫磺停用后24小时和30天获得的随访结果进行比较。在最初的测试对象中,基础血浆高半胱氨酸为每升77νmol下降了95.7%。在这46例患者中,升华硫磺的作用因基础血浆血浆同型半胱氨酸的初始浓度而异。在停止治疗后24小时,基础水平为2.3至7 vmol /升,增加了58.5%(p <0.001),在30天后增加了85.4%;升华硫停止后24小时的基础水平为7.1至9.9νmol/升,未显示出一致的变化,基础水平为9.9至22.1νmol/升,降至基础水平的63.9%(p <0.005),降至基础水平的70.7% 30天后达到水平。升华硫疗法消除了低,中和高基础水平之间的初始血浆高半胱氨酸差异。升华硫疗法通过使基础血浆同型半胱氨酸水平的平均值回归来使血浆同型半胱氨酸正常化。

著录项

  • 公开/公告号WO0061154A1

    专利类型

  • 公开/公告日2000-10-19

    原文格式PDF

  • 申请/专利权人 KHAN AIRUDIN S.;

    申请/专利号WO1999CA00892

  • 发明设计人 KHAN AIRUDIN S.;

    申请日1999-09-27

  • 分类号A61K33/04;

  • 国家 WO

  • 入库时间 2022-08-22 01:49:28

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号