SYSTEM AND METHOD FOR TARGETING RELEVANT RESEARCH ACTIVITY IN RESPONSE TO ANGIOGENIC REGULATOR ANALYSES

• US 20110231104A1
• Filed: 03/18/2011
• Published: 09/22/2011
• Est. Priority Date: 03/19/2010
• Status: Active Grant

• Current Assignee: Rebecca Lambert
• Original Assignee: Rebecca Lambert
• Inventors: Lambert, Rebecca
• Granted Patent: US 8,874,378 B2
• Time in Patent Office: Days
• US Class Current: 702/19
• CPC Class Codes: G01N 2800/60 Complex ways of combining multiple protein biomarkers for diagnosis
• CPC Class Codes: G16B 20/00 ICT specially adapted for functional genomics or proteomics, e.g. genotype-phenotype associations
• CPC Class Codes: G16B 50/00 ICT programming tools or database systems specially adapted for bioinformatics
• CPC Class Codes: G16H 70/60 relating to pathologies

Abstract

A system and method for targeting relevant research activity for clinical application in response to angiogenic regulator analyses. An angiogenic analysis is performed on a patient blood sample in order to detect the level of each of at least ten angiogenic regulators. The levels of the tested regulators are used as indexes to identify relevant peer-reviewed research publications from among a large database of articles. The most relevant peer-reviewed literature reporting research and studies that have been conducted to identify, moderate, and define the mechanisms unique to individual and combinations of angiogenic regulators for various disease states are then provided to the patient and/or to the patient'"'"'s physician, optionally in conjunction with a summarization of the treatment recommendations gleaned from the provided literature. The customized information delivery provides the patient and physician a range of published peer-reviewed therapeutic options and published research studies for moderating the out of range regulators to within normal range or other diagnostic significant range.

Claims

1. A system for targeting relevant research activity in response to angiogenic regulator analyses, comprising:

an angiogenic analyzer for receiving at least one patient blood sample, for measuring in a single patient blood sample the level of each of at least ten angiogenic regulators, and for generating a data output indicative of the respective level of each of the at least ten measured angiogenic regulators;

a database unit comprising plural entries, each entry corresponding to a respective publication and indexed at least according to a range of levels for each of at least one angiogenic regulator; and

a data processing unit in communication with the angiogenic analyzer and the database unit for receiving the data output from the angiogenic analyzer, for identifying entries in the database unit for which one or more of the patient angiogenic regulator levels are addressed therein, and for providing an identification of the identified database entries.

2. The system of claim 1, wherein the at least ten angiogenic regulators are selected from the group consisting of Vascular Endothelial Growth Factor, Epidermal Growth Factor, Fibroblast Growth Factor-Basic, Interleukin-2, Platelet-derived Growth Factor-BB, Tumor Necrosis Factor-alpha, Interleukin-1 beta, Interleukin-8, Interleukin-10, Thrombospondin-1, Cyclooxygenase, Hepatocyte Growth Factor, Insulin like Growth Factor, Matrix Metalloproteinase-2, Matrix Metalloproteinase-9, Tumor Necrosis Factor-beta, Transforming Growth Factor-beta, Angiogenin, Granulocyte Macrophage Colony-Stimulating Factor, Endostatin (collagen XVIII fragment), Angiostatin (plasminogen fragment), Interleukin-6, Granulocyte Colony-Stimulating Factor, Interleukin-7, Kringle 5 (plasminogen fragment), Angiopoitin-1, and Fibrinogen.

3. The system of claim 1, wherein the data output is provided on a removable data carrier.

4. The system of claim 1, wherein the data output is received by the data processing unit as a sequence of electromagnetic signals transmitted over a transmission medium.

5. The system of claim 1, wherein the database unit and the data processing element are integrated within a common physical enclosure.

6. The system of claim 1, wherein the angiogenic analyzer measures the level of each of the at least ten angiogenic regulators via a technique selected from the group consisting of enzyme-linked immunosorbent assay (ELISA), planar microarray, bead-based assays, magnetic particle assays, and chemiluminescence immunoassays.

7. The system of claim 1, wherein the database unit further comprises, in conjunction with each of the plural entries, the text, data and images, as such exist, of the respective publication.

8. The system of claim 7, wherein the data processing unit is further for providing, in conjunction with the identification of the identified database entries, the text, data and images, as such exist, of each of the respective publications.

9. The system of claim 1, wherein each identification of the identified database entries is provided as an address of the respective publication in a database of publications accessible by a communications network.

10. The system of claim 1, wherein each publication is a peer-reviewed research study from which the levels of at least one angiogenic regulator is correlated with a recommended treatment option.

11. The system of claim 10, wherein the recommended treatment regime is selected from the group consisting of specific pharmaceutical, chemo- or radiation therapies, specific naturally occurring compound therapies, diet programs, exercise programs, meditation-based therapies, and integrative, complimentary, and alternative therapies.

12. The system of claim 10, wherein the recommended treatment regime is for the purpose of angiogenesis inhibition.

13. The system of claim 1, wherein the data processing unit is further for providing the indication of the identified database entries to the patient from whom the blood sample was obtained or to a physician caring for the patient.

14. The system of claim 1, wherein the data processing unit is further for receiving from the patient from whom the blood sample was drawn, or a physician caring for the patient, additional information and for identifying from among the database unit entries for which the patient additional information is relevant.

15. The system of claim 14, wherein the additional information is selected from the group consisting of a diagnosed patient condition, a suspected patient condition, a diagnosed disease stage, mitotic count, radiologic or biologic test results, current and prior medications prescribed, allergies, and family medical history.

16. The system of claim 1, wherein the data processing unit is further for extracting treatment recommendations from the identified database entries and for providing a summarization of the treatment recommendations in conjunction with the identification of the identified database entries.

17. A method of targeting relevant research activity in response to angiogenic regulator analyses, comprising:

providing a patient blood sample to an angiogenic analyzer;

measuring the level of each of at least ten angiogenic regulators in the blood sample;

generating a data output indicative of the respective level of each of the at least ten measured angiogenic regulators;

providing a database unit comprising plural entries, each entry corresponding to a respective publication and indexed at least according to a range of levels for each of at least one angiogenic regulator;

identifying, with a data processor, each entry in the database unit for which the patient angiogenic regulator levels in the data output are within the respective ranges of levels; and

providing an identification of the identified database entries.

18. The method of claim 17, wherein the at least ten angiogenic regulators are selected from the group consisting of Vascular Endothelial Growth Factor, Epidermal Growth Factor, Fibroblast Growth Factor-Basic, Interleukin-2, Platelet-derived Growth Factor-BB, Tumor Necrosis Factor-alpha, Interleukin-1 beta, Interleukin-8, Interleukin-10, Thrombospondin-1, Cyclooxygenase, Hepatocyte Growth Factor, Insulin like Growth Factor, Matrix Metalloproteinase-2, Matrix Metalloproteinase-9, Tumor Necrosis Factor-beta, Transforming Growth Factor-beta, Angiogenin, Granulocyte Macrophage Colony-Stimulating Factor, Endostatin (collagen XVIII fragment), Angiostatin (plasminogen fragment), Interleukin-6, Granulocyte Colony-Stimulating Factor, Interleukin-7, Kringle 5 (plasminogen fragment), Angiopoitin-1, and Fibrinogen.

19. The method of claim 17, wherein the data output is generated by the angiogenic analyzer on a removable data carrier.

20. The method of claim 17, wherein the data output is generated by the angiogenic analyzer and received by the data processor as a sequence of electromagnetic signals transmitted over a transmission medium.

21. The method of claim 17, wherein the database unit and the data processor are provided as an integrated device.

22. The method of claim 17, wherein the angiogenic analyzer measures the level of each of the at least ten angiogenic regulators via a technique selected from the group consisting of enzyme-linked immunosorbent assay (ELISA), planar microarray, bead-based assays, magnetic particle assays, and chemiluminescence immunoassays.

23. The method of claim 17, wherein the database unit is provided, in conjunction with each of the plural entries, the text, data and images, as such exist, of the respective publication.

24. The method of claim 23, wherein the database unit is further for providing, in conjunction with the identification of the identified database entries, the text, data and images, as such exist, of each of the respective publications.

25. The method of claim 17, wherein the database unit is further for providing, in conjunction with each of the plural entries, an address of the respective publication in a database of publications accessible by a communications network.

26. The method of claim 17, wherein the database unit is further for corresponding each of the plural entries with a respective peer-reviewed research study from which levels of at least one angiogenic regulator is correlated with a recommended treatment option.

27. The method of claim 26, wherein the recommended treatment regime is selected from the group consisting of specific pharmaceutical, chemo- or radiation therapies, specific naturally occurring compound therapies, diet programs, exercise programs, meditation-based therapies, and integrative, complimentary, and alternative therapies.

28. The method of claim 17, wherein the recommended treatment regime is for the purpose of angiogenesis inhibition.

29. The method of claim 17, further comprising providing the indication of the identified database entries to the patient from whom the blood sample was obtained or to a physician caring for the patient.

30. The method of claim 17, further comprising receiving from the patient from whom the blood sample was drawn, or a physician caring for the patient, additional information in the data processor and identifying from among the identified database unit entries for which the patient additional information is relevant.

31. The method of claim 30, wherein the additional information is selected from the group consisting of a diagnosed patient condition, a suspected patient condition, a diagnosed disease stage, mitotic count, radiologic or biologic test results, current and prior medications prescribed, allergies, and family medical history.

32. The method of claim 17, further comprising extracting treatment recommendations from the identified database entries and providing a summarization of the treatment recommendations in conjunction with the identification of the identified database entries.