Method for Quantitative Diagnosis of Cerebrovascular, Neurovascular and Neurodegenerative Diseases via Computation of a CO2 Vasomotor Reactivity Index based on a Nonlinear Predictive Model

• US 20140278285A1
• Filed: 03/13/2013
• Published: 09/18/2014
• Est. Priority Date: 03/13/2013
• Status: Abandoned Application

• Current Assignee: Dae C. Shin, Melissa Emily Orme-Marmarelis, Vasilis Z. Marmarelis
• Original Assignee: Dae C. Shin, Melissa Emily Orme-Marmarelis, Vasilis Z. Marmarelis
• Inventors: Marmarelis, Vasilis Z., Orme-Marmarelis, Melissa Emily, Shin, Dae C.
• Application Number:
  US13/801,426
• Publication Number:
  US 20140278285A1
• Time in Patent Office: Days
• US Class Current: 703/2
• CPC Class Codes: G16H 50/30 for calculating health indices; for individual health risk assessment
• CPC Class Codes: G16H 50/50 for simulation or modelling of medical disorders
• CPC Class Codes: G16Z 99/00 Subject matter not provided for in other main groups of this subclass

Abstract

The present invention relates generally to a method for computer-aided quantitative diagnosis of cerebrovascular and neurodegenerative diseases (such as Alzheimer'"'"'s, vascular dementia, mild cognitive impairment, transient ischemia, stroke etc.) via a vasomotor reactivity index (VMRI) which is computed on the basis of a computational model of the dynamic nonlinear inter-relationships between beat-to-beat time-series measurements of cerebral blood flow velocity, arterial blood pressure and end-tidal CO2. This model is obtained by means of a method pioneered by the inventors and may incorporate additional physiological measurements from human subjects. Its purpose is to provide useful information to physicians involved in the diagnosis and treatment of cerebrovascular and neurodegenerative diseases with a significant neurovascular component by offering quantitative means of assessment of the effects of the disease or medication on cerebral vasomotor reactivity. Initial results from clinical data have corroborated the diagnostic potential of this approach.

Claims

1. A method for computing a subject-specific index of CO2 vasomotor reactivity of cerebral hemodynamics comprising the steps of:

estimation of a subject-specific data-based dynamic nonlinear model of cerebral hemodynamics with two inputs (arterial blood pressure and end-tidal CO2) and one output (cerebral flow velocity);

computation of a model-based vasomotor reactivity index (VMRI) as a “

physiomarker”

that quantifies the CO2 vasomotor reactivity of a subject on the basis of the model-predicted cerebral flow velocity response to a positive and a negative pulse change of the CO2 input.

2. The method as set forth in claim 1, wherein the method further comprises the means for diagnosing and assessing the severity of Alzheimer'"'"'s disease, mild cognitive impairment, and dementia, using the VMRI physiomarker.

3. The method as set forth in claim 1, wherein the method further comprises the means for assessing the cerebrovascular, neurovascular and neurological effects of hypertension, stroke, ischemia, subcortical infarctions, cerebral angiopathy and atrophy, and diabetes, using the VMRI physiomarker.

4. The method as set forth in claim 1, wherein the method further comprises the means for assessing the cerebrovascular, neurovascular and neurological effects of brain trauma and surgery, using the VMRI physiomarker.

5. The method as set forth in claim 1, wherein the method further comprises the means for assessing the effects of various medications on cerebrovascular, neurovascular and neurodegenerative diseases, as well as prescribing the proper dosage of such medications, using the VMRI physiomarker.

6. The method as set forth in claim 1, wherein the method further comprises the means for incorporating additional physiological variables in the model for the computation of the VMRI physiomarker that are measured by minimally-invasive and/or invasive procedures.

7. The method as set forth in claim 1, wherein the method further comprises the means for incorporating variables or parameters in the model for the computation of the VMRI that are measured at the molecular or cellular level.

8. A method for computing a subject-specific index of CO2 vasomotor reactivity of cerebral hemodynamics comprising the steps of:

estimation of a subject-specific data-based dynamic nonlinear model of cerebral hemodynamics with two inputs (arterial blood pressure and end-tidal CO2) and one output (cerebral flow velocity);

estimation of a subject-specific data-based dynamic nonlinear model of cerebral hemodynamics with two inputs (cerebral flow velocity and end-tidal CO2) and one output (arterial blood pressure);

computation of a model-based vasomotor reactivity index (VMRI) that quantifies the CO2 vasomotor reactivity of a subject on the basis of the model-predicted cerebral flow velocity response to a positive and negative pulse change of the CO2 in a closed-loop pressure-flow configuration that accounts for the mutual interdependence of blood pressure and cerebral flow.

9. The method as set forth in claim 8, wherein the method further comprises the means for incorporating additional physiological variables in the model, either in open-loop or closed-loop/nested-loop configurations utilizing feedback and cross-linking pathways that account for multiple physiological interactions, which influence cerebral hemodynamics and partake in the computation of the VMRI.

10. The method as set forth in claim 8, wherein the method further comprises the means for diagnosing and assessing the severity of Alzheimer'"'"'s disease, mild cognitive impairment, and dementia, using the VMRI physiomarker.

11. The method as set forth in claim 8, wherein the method further comprises the means for assessing the cerebrovascular, neurovascular and neurological effects of hypertension, stroke, ischemia, subcortical infarctions, cerebral angiopathy and atrophy, and diabetes, using the VMRI physiomarker.

12. The method as set forth in claim 8, wherein the method further comprises the means for assessing the cerebrovascular, neurovascular and neurological effects of brain trauma and surgery, using the VMRI physiomarker.

13. The method as set forth in claim 8, wherein the method further comprises the means for assessing the effects of various medications on cerebrovascular, neurovascular and neurodegenerative diseases, as well as prescribing the proper dosage of such medications, using the VMRI physiomarker.

14. A method for computing a subject-specific index of CO2 vasomotor reactivity of cerebral hemodynamics comprising the steps of:

estimation of subject-specific data-based dynamic nonlinear models of cerebral hemodynamics with a plurality of inputs and outputs, which are measured physiological variables that affect cerebral hemodynamics;

computation of a model-based vasomotor reactivity index (VMRI) that quantifies the CO2 vasomotor reactivity of a subject on the basis of the model-predicted cerebral flow velocity response to a positive and negative pulse change of the CO2 in a nested-loop configuration that accounts for the mutual interdependences of all these variables.

15. The method as set forth in claim 14, wherein the method further comprises the means for incorporating additional physiological variables in the model for the computation of the VMRI physiomarker that are measured by non-invasive, minimally-invasive or invasive procedures.

16. The method as set forth in claim 14, wherein the method further comprises the means for incorporating variables or parameters in the model for the computation of the VMRI that are measured at the molecular or cellular level.

17. The method as set forth in claim 14, wherein the method further comprises the means for diagnosing and assessing the severity of Alzheimer'"'"'s disease, Mild Cognitive Impairment, and dementia, using the VMRI physiomarker.

18. The method as set forth in claim 14, wherein the method further comprises the means for assessing the cerebrovascular, neurovascular and neurological effects of hypertension, stroke, ischemia, subcortical infarctions, cerebral angiopathy and atrophy, and diabetes, using the VMRI physiomarker.

19. The method as set forth in claim 14, wherein the method further comprises the means for assessing the cerebrovascular, neurovascular and neurological effects of brain trauma and surgery, using the VMRI physiomarker.

20. The method as set forth in claim 14, wherein the method further comprises the means for assessing the effects of various medications on cerebrovascular, neurovascular and neurodegenerative diseases, as well as prescribing the proper dosage of such medications, using the VMRI physiomarker.

21. The method as set forth in claim 14, wherein the method further comprises the means for incorporating additional physiological variables in the model for the computation of the VMRI physiomarker that are measured by non-invasive, minimally-invasive or invasive procedures.

22. The method as set forth in claim 14, wherein the method further comprises the means for incorporating variables or parameters in the model for the computation of the VMRI that are measured at the molecular or cellular level.