发明名称 |
DIAGNOSING MULTIPLE SCLEROSIS |
摘要 |
There is provided an in vitro method for diagnosing Multiple Sclerosis (MS) in a human test subject, comprising (i) determining the concentrations of two or more metabolites in a sample from said subject, wherein said two or more metabolites are selected from: blood metabolites, wherein said blood metabolites comprise: alanine, ascorbic acid, choline, fatty acid, glucose, lactate, N-acetyl aspartate, N-acetyl glycoprotein, n-butyrate, oxyglutaric acid, phosphocholine, taurinebetaine, tyrosine, L-glutamine, N-acetyl species, and beta-hydroxybutyrate; and/or urine metabolites, wherein said urine metabolites comprise: citrate, creatinine, inositol, lactate and trimethylamine N-oxide (TMAO); (ii) comparing the concentrations of said two or more metabolites in the sample with the concentrations of the same metabolites in at least one reference standard; and (iii) identifying a concentration difference for each of said two or more metabolites in the sample relative to the reference standard; wherein said concentration differences correlate with the presence of MS. |
申请公布号 |
US2015338389(A1) |
申请公布日期 |
2015.11.26 |
申请号 |
US201314377454 |
申请日期 |
2013.02.07 |
申请人 |
ISIS INNOVATION LIMITED |
发明人 |
Anthony Daniel;Sibson Nicola;Palace Jacqueline |
分类号 |
G01N33/49;G01N33/493;G01N33/50 |
主分类号 |
G01N33/49 |
代理机构 |
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代理人 |
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主权项 |
1. An in vitro method for diagnosing Multiple Sclerosis (MS) in a human test subject, comprising
(i) determining the concentrations of two or more metabolites in a sample from said subject, wherein said two or more metabolites are selected from:
blood metabolites, wherein said blood metabolites comprise: phosphocholine, lactate, N-acetyl species, beta-hydroxybutyrate, alanine, ascorbic acid, choline, fatty acid, glucose, N-acetyl aspartate, N-acetyl glycoprotein, n-butyrate, oxyglutaric acid, taurinebetaine, tyrosine, and L-glutamine;and/orurine metabolites, wherein said urine metabolites comprise: citrate, creatinine, inositol, lactate and trimethylamine N-oxide (TMAO); (ii) comparing the concentrations of said two or more metabolites in the sample with the concentrations of the same metabolites in at least one reference standard;
and (iii) identifying a concentration difference for each of said two or more metabolites in the sample relative to the reference standard; wherein said concentration differences correlate with the presence of MS. |
地址 |
Oxford Oxfordshire GB |