Granted Patent B2

US 8,420,344 · App. 12/421,784 · Granted Apr 16, 2013

Abstract

Claims (40)

1. A method for predicting the risk of acute coronary syndrome (ACS) in a human subject, comprising:

(a) measuring, in a fatty acid sample isolated from red blood cells from a human subject, an amount of:

(i) linoleic acid and gamma-linolenic acid; and

(ii) docosahexaenoic acid (DHA) and optionally eicosapentaenoic acid (EPA);

(b) comparing the amount of (a)(i) and (a)(ii) in the fatty acid sample to an amount of (a)(i) and (a)(ii) in a control; and

(c) predicting a risk of ACS,

wherein the amount of each of the fatty acids measured in (a) is inversely correlated with the risk of ACS.

2. The method of claim 1 , wherein the measuring comprises measuring an amount of linoleic acid, gamma-linolenic acid, DHA, and EPA in the fatty acid sample.

3. The method of claim 1 , further comprising

(d) measuring an amount of one or more fatty acids selected from the group consisting of alpha-linolenic acid, palmitic acid, stearic acid, trans-oleic acid, n-6 docosapentaenoic acid, docosatetraenoic acid, arachidonic acid, oleic acid, n-3 docosapentaenoic acid, palmitoleic acid, trans-palmitoleic acid, and eicosadienoic acid in the fatty acid sample;

(e) comparing the amount the one or more fatty acids selected from the group to an amount of the one or more fatty acids selected from the group in the control; and

(f) using the comparison in step (e) in the predicting the risk of ACS.

4. The method of claim 1 further comprising

(d) measuring an amount of one or more fatty acids selected from the group consisting of stearic acid, alpha-linoleic acid, palmitoleic acid, arachidonic acid, trans-palmitoleic acid, eicosadienoic acid and trans-oleic acid in the fatty acid sample;

(e) comparing the amount of the one or more fatty acids measured in step (d) to an amount of the one or more fatty acids selected from the group in the control; and

(f) using the comparison in step (e) in the predicting the risk of ACS.

5. The method of claim 1 , further comprising

(d) measuring an amount of one or more fatty acids selected from the group consisting of alpha-linolenic acid, palmitic acid, stearic acid, trans-oleic acid, n-6 docosapentaenoic acid, docosatetraenoic acid, arachidonic acid, oleic acid, n-3 docosapentaenoic acid, palmitoleic acid, trans palmitoleic, and eicosadienoic acid in the fatty acid sample; and

(e) comparing the amount the one or more fatty acids measured in step (d) to an amount of the one or more fatty acids in the control; and

(f) using the comparison in step (e) in the predicting the risk of ACS.

6. The method of claim 1 , further comprising

(d) measuring an amount of one or more fatty acids selected from the group consisting of palmitic acid, alpha-linolenic acid, oleic acid and palmitoleic acid in the fatty acid sample; and

(e) comparing the amount the one or more fatty acids measured in step (d) to an amount of the one or more fatty acids in the control; and

(f) using the comparison in step (e) in the predicting the risk of ACS.

7. The method of claim 1 , wherein the measuring comprises measuring a percent total of the (a)(i) fatty acids and the (a)(ii) fatty acids in the fatty acid sample as a percent of total fatty acids in the fatty acid sample.

8. The method of claim 7 , wherein comparing the amount of the one or more fatty acids to a control comprises

(a) multiplying the percent total of the (a)(i) fatty acids and the (a)(ii) fatty acids in the fatty acid sample by a predetermined weighting coefficient to produce an individual fatty acid score; and

(b) summing the individual fatty acid scores to produce a risk score, wherein the risk score is used to correlate with ACS in the human subject.

9. The method of claim 7 , further comprising subjecting the percent total of the (a)(i) fatty acids and the (a)(ii) fatty acids in the fatty acid sample to an analysis selected from the group consisting of generalized models, multivariate analysis, and time-to-event survival analysis, to produce a modified risk score; wherein the modified risk score is used to correlate with ACS in the human subject.

10. The method of claim 1 , further comprising determining a Framingham risk score for the subject.

11. The method of claim 1 , wherein the subject has a family history of ACS, a genetic predisposition to ACS, and/or has previously suffered from ACS.

12. The method of claim 1 wherein the acute coronary syndrome is myocardial infarction or unstable angina.

13. A method for predicting the risk of acute coronary syndrome (ACS) in a human subject, comprising:

(a′) identifying a combination of fatty acids that discriminate the ACS cases from a control, said combination of fatty acids comprising linoleic acid, alpha-linolenic acid, arachidonic acid, eicosapentaenoic acid (EPA), and docosahexaenoic acid (DHA);

(a) measuring, in a fatty acid sample isolated from red blood cells from a subject, an amount comprising the fatty acids identified in (a′);

(b) comparing the amount of (a) in the fatty acid sample to an amount of (a) in a control; and

(c) predicting a risk of ACS.

14. The method of claim 1 , wherein the measuring further comprises measuring an amount of alpha-linolenic acid and arachidonic acid in the fatty acid sample.

15. The method of claim 1 , wherein the measuring further comprises measuring an amount of stearic acid, alpha-linoleic acid, palmitoleic acid, arachidonic acid, trans-palmitoleic acid, eicosadienoic acid and trans-oleic acid in the fatty acid sample.

16. The method of claim 13 , wherein the combination of fatty acids identified in (a′) further comprises stearic acid, palmitoleic acid, trans-palmitoleic acid, eicosadienoic acid and trans-oleic acid.

Assignments (9)