Method and apparatus for detection of vulnerable atherosclerotic plaque

• US 7,603,166 B2
• Filed: 08/12/2003
• Issued: 10/13/2009
• Est. Priority Date: 09/20/1996
• Status: Expired due to Fees

• Current Assignee: Board of Regents of the University of Texas System (University of Texas System)
• Original Assignee: Board of Regents of the University of Texas System (University of Texas System)
• Inventors: Guo, Bujin, Casscells, S. Ward III, Naghavi, Morteza, Willerson, James T.
• Primary Examiner(s): Winakur; Eric F
• Application Number:
  US10/640,570
• Publication Number:
  US 20040111016A1
• Time in Patent Office: 2,254 Days
• Field of Search: 600/310, 600/311, 600/317, 600/322, 600/342, 600/473, 600/476
• US Class Current: 600/473
• CPC Class Codes: A61B 1/044 for absorption imaging
• CPC Class Codes: A61B 1/046 for infrared imaging
• CPC Class Codes: A61B 5/01 Measuring temperature of body parts ; Diagnostic temperature sensing, e.g. for malignant or inflamed tissue clinical contact thermometers G01K13/20
• CPC Class Codes: A61B 5/0507 using microwaves or terahertz waves
• CPC Class Codes: A61B 5/14539 for measuring pH
• CPC Class Codes: A61B 5/1459 invasive, e.g. introduced into the body by a catheter A61B5/1464 takes precedence
• CPC Class Codes: A61B 5/6853 with a balloon

Abstract

Methods for the detection of inflammation associated with vulnerable atherosclerotic plaque to prevent heart attack and stroke are disclosed. The methods are also applicable to detection of infection, cancer, wounds or auto-immune disease in the body. Certain embodiments of the new methods provide a way of predicting the level of vulnerability of an atherosclerotic plaque to rupture or thrombus formation by assessing via fiber optic NIR spectrophotometry the status of two or more parameters associated with inflamed atherosclerotic plaque in a vessel of a living patient. From these measurements such conditions as low pH, hypoxia, low glucose, oxidative stress or compounds abundant in vulnerable plaque such as oxidized LDL cholesterol and oxidized metabolites of NO, significant active macrophage population, thin plaque cap, as well as senescence and/or apoptosis of smooth muscle or endothelial cells are determined with the assistance of a suitably programmed microprocessor. By considering together the status of some or all of these conditions with respect to successive sites along a vessel wall, particular plaques which are at significant risk of rupturing or thrombosing can be distinguished from “normal” vessel wall and from “intermediate” and relatively stable or “lower risk” plaques. Sites having more of the indicator conditions would be considered most in need of prompt intervention, and certain combinations of parameter levels would be suggestive of relatively stable plaque.

Also disclosed is a multi-parameter catheter and analytical processing assembly for use in the methods.

Claims

1. A method of simultaneously measuring in a living vessel at least two chemical parameters associated with inflamed vulnerable atherosclerotic plaque, the method comprising:

providing a fiber optic catheter having an illumination fiber bundle and a detection fiber bundle capable of, respectively, directing radiation onto or receiving radiation from a site on a vessel wall, said catheter having means for reducing optical interference by blood or other fluid within a vessel when undergoing examination;

providing a source of 400-2500 nm wavelength radiation operatively linked to said illumination fiber bundle;

providing a spectrometer operatively linked to the detection fiber bundle;

providing a processor operatively linked to said spectrometer containing algorithms and reference measurements for at least two chemical parameters associated with inflamed vulnerable atherosclerotic plaque, said spectrometer and processor together being capable of receiving and analyzing spectral data collected by said detection fiber bundle and reporting corresponding parameter measurements;

providing a display system capable of receiving and displaying a report from said processor;

measuring a first parameter at a multiplicity of sites on the vessel wall;

measuring at least one other parameter at said multiplicity of sites on a vessel wall;

analyzing a multiplicity of parameter measurements corresponding to said multiplicity of sites so that a qualitative or quantitative value for each said parameter is obtained; and

performing a determination regarding inflamed vulnerable atherosclerotic plaque at said multiplicity of sites based on the qualitative or quantitative value for each said parameter, wherein the results of said determination are reported on said display system, and wherein said first parameter is chosen from the group consisting of pH, oxyhemoglobin, deoxyhemoglobin, cytochrome oxidase aa₃, reduced cytochrome oxidase aa₃, nitrosyl hemoglobin, nitrosyl tyrosine, glucose, lactate, and oxidized collagen, and wherein said at least one other parameter is chosen from the group consisting of pH, oxyhemoglobin, deoxyhemoglobin, cytochrome oxidase aa₃, reduced cytochrome oxidase aa₃, nitrosyl hemoglobin, nitrosyl tyrosine, glucose, lactate, oxidized LDL cholesterol, and oxidized collagen.

2. The method of claim 1 wherein said first parameter is pH.

3. The method of claim 1 wherein said first parameter is oxyhemoglobin and said at least one other parameter comprises deoxyhemoglobin.

4. The method of claim 1 wherein said first parameter is cytochrome oxidase aa₃ and said at least one other parameter comprises reduced cytochrome oxidase aa₃.

5. The method of claim 1 wherein said first parameter is nitrosyl-hemoglobin or nitrosyl-tyrosine.

6. The method of claim 1 wherein said first parameter is oxidized collagen.

7. The method of claim 1 wherein said first parameter is glucose.

8. The method of claim 1 wherein said first parameter is pH, and said at least one other parameter includes oxidized collagen and a parameter chosen from the group consisting of oxyhemoglobin, deoxyhemoglobin, cytochrome oxidase aa₃, reduced cytochrome oxidase aa₃, nitrosyl hemoglobin, nitrosyl tyrosine, glucose, andlactate, and oxidized LDL cholesterol.

9. The method of claim 1 wherein said step of providing a processor includes:

providing a processor operatively linked to said spectrometer, said processor containing algorithms and reference measurements for at least two chemical parameters associated with inflamed vulnerable atherosclerotic plaque, and containing algorithms and reference measurements for colorimetric measurement of thrombi colored red, brown, greenish-brown and white, said spectrometer and processor together being capable of receiving and analyzing spectral data collected by said detection fiber bundle and reporting corresponding parameter and colorimetric measurements.

10. The method of claim 1 wherein providing said display system capable of receiving and displaying a report from said processor includes providing a monitor capable of displaying a color image of said vessel wall.

11. The method of claim 1 further comprising detecting an indicator dye associated with a plaque whereby a plaque cap fissure is revealed.

12. The method of claim 11 wherein said step of detecting an indicator dye comprises detecting a radiocontrast dye associated with a plaque by intraplaque leakage.

13. The method of claim 11 wherein said step of detecting an indicator dye comprises detecting a biocompatible molecule having a distinct NIR absorbance spectrum.

14. The method of claim 13 wherein said step of detecting an indicator dye comprises detecting a hydroxyethyl starch.

15. A method of detecting in a living vessel an atherosclerotic plaque at risk of rupturing or thrombosing, the method comprising:

qualitatively or quantitatively measuring at least two parameters associated with inflamed vulnerable plaque in accordance with the method of claim 1;

measuring dye sequestered beneath the surface of a site along a vessel wall; and

analyzing said dye measurement together with said parameter measurements to distinguish inflamed vulnerable plaque from relatively stable plaque and normal vessel wall and to determine predictive level of risk of rupture or thrombosis for at least one site or group of sites on a wall of said vessel.

16. The method of claim 15 wherein said measuring of dye sequestration is performed with said fiber optic catheter, said dye containing a 400-2,500 nm wavelength radiation absorbing chromophore, and said processor additionally containing algorithms and reference measurements for analysing reflected or scattered radiation from said chromophore.

17. The method of claim 15 wherein said measuring of dye sequestration is performed by angiography, said dye is radiopaque, and said signal processor is also capable of receiving and analyzing said angiographic measurement.

18. A method of detecting a vulnerable atherosclerotic plaque on a vessel wall comprising the method of claim 15 and additionally

monitoring the visible color image of said site;

and

analyzing said visual image together with said parameter and dye penetration measurements.

19. A method of treating a patient known to be suffering from atherosclerotic vessel disease and suspected of being at risk of experiencing a plaque rupture and/or an occlusive thrombotic event, the method comprising:

detecting an atherosclerotic plaque at risk of rupturing or thrombosing according to the method of claim 15, said method including monitoring the visible color image of said site and analyzing said visual image together with said parameter and dye measurements;

determining from said predicted level of risk for at least one site or group of sites on a wall of said vessel at least one vulnerable plaque for targeting treatment;

applying a local treatment to at least one so-determined target plaque, said treatment chosen from the group consisting of balloon angioplasty, laser angioplasty, heated balloon (RF, ultrasound or laser) angioplasty, surgical atherectomy, laser atherectomy, the placement of an appropriate stent, another conventional mechanical or irradiation treatment method, and pharmacological treatment regimens including anticoagulants, fibrinolytic, thrombolytic, anti-inflammatory, anti-proliferative, immunosuppressant, collagen-inhibiting, endothelial cell growth-promoting, and other conventional pharmacologically appropriate local treatments effective for reducing or eliminating inflamed plaque.

20. A method of distinguishing vulnerable plaque in need of therapeutic intervention from relatively stable plaque or non diseased tissue in a living vessel wall comprising the method of claim 1 wherein performing a determination includes comparing said qualitative or quantitative values for a site or group of adjacent sites to similarly obtained values for another site or group of sites along the vessel wall, so that a qualitative or quantitative value for each said parameter is reported by the display system for a particular site or region on a vessel wall expressed in terms relative to other sites or groups of sites along the same vessel wall.

21. A method of detecting an inflamed vulnerable atherosclerotic plaque on a vessel wall comprising:

providing a device comprising a spectrometer operatively linked to a fiber optic catheter and a processor, wherein the spectrometer and processor together are configured to receive and analyze spectral data collected by said fiber optic catheter and report corresponding parameter measurements;

operating said device to identify areas on said vessel wall having pH<

7.2;

operating said device to identify areas on said vessel wall having an amount of oxidized collagen indicative of a thin or weak plaque cap;

operating said device to identify areas on said vessel wall having red microthrombi;

operating said device to identify areas on said vessel wall that have taken up and sequestered an indicator dye beneath the surface of a vessel;

correlating at least two of said identified areas with a site or group of sites on said vessel wall; and

calculating a predictive level of risk of plaque rupture for each said site or group of sites.

22. An improved method of detecting vulnerable atherosclerotic plaque in vivo in which a chemical or biochemical component of a plaque is measured using a device comprising a fiber optic catheter operatively linked to a spectrometer, the improvement comprising measuring at least two different analytes associated with activated macrophages, said analytes chosen from the group consisting of pH, oxyhemoglobin, deoxyhemoglobin, nitrosyl hemoglobin, nitrosyl tyrosine, oxidized cytochrome aa₃, reduced cytochrome aa₃, glucose, lactate, oxidized LDL cholesterol and oxidized collagen;

and

detecting inflamed vulnerable atherosclerotic plaque at a multiplicity of sites based on a qualitative or quantitative value for each said measured analyte at said sites.

23. The method of claim 22 wherein said method includes using visible or near-infrared spectroscopy to measure said analytes.

24. The method of claim 22 wherein said method includes using magnetic resonance spectroscopy to measure said analytes.

25. An improved method of differentiating atherosclerotic plaque at risk of rupturing and occluding from plaque not presently at risk in which optical radiation from a site along a vessel wall is analyzed using a device comprising a fiber optic catheter operatively linked to a spectrometer, the improvement comprising identifying a site on said vessel wall by analyzing for indicia of actively metabolizing cells, wherein said indicia include a first parameter selected from the group consisting of pH, oxyhemoglobin, deoxyhemoglobin, cytochrome oxidase aa₃, reduced cytochrome oxidase aa₃, nitrosyl hemoglobin, nitrosyl tyrosine, glucose, lactate, and oxidized collagen, and at least a second parameter selected from the group consisting of pH, oxyhemoglobin, deoxyhemoglobin, cytochrome oxidase aa₃, reduced cytochrome oxidase aa₃, nitrosyl hemoglobin, nitrosyl tyrosine, glucose, lactate, oxidized LDL cholesterol, and oxidized collagen.

26. A method of detecting infection, cancer, wound or autoimmune disease comprising;

providing a device comprising a spectrometer operatively linked to a fiber optic catheter and a processor, wherein the spectrometer and processor together are configured to receive and analyze spectral data collected by said fiber optic catheter and report corresponding parameter measurements;

detecting with said device inflammation associated with said infection, cancer, wound or autoimmune disease, said detecting comprising measuring at a site in the body at least two different parameters chosen from the group consisting of pH, oxyhemoglobin, deoxyhemoglobin, cytochrome oxidase aa₃, reduced cytochrome oxidase aa₃, nitrosyl hemoglobin, nitrosyl tyrosine, glucose and lactate and performing a determination regarding infection, cancer, wound or autoimmune disease at said site based on a qualitative or quantitative value for each said measured parameter at said site.

27. A system for diagnosing an atherosclerotic plaque at risk of rupture or thrombosis, comprising:

a catheter having a proximal end and a distal end and having an illumination lumen and a detection lumen therein;

one or more optical illumination fibers within said illumination lumen, said optical illumination fibers capable of transmitting approximately 400 to 2500 nm wavelength radiation;

one or more optical detection fibers within said detection lumen, said optical detection fibers capable of transmitting approximately 400 to 2500 nm wavelength radiation;

a light source operatively linked to the proximal end of said catheter, said light source capable of emitting approximately 400 to 2500 nm wavelength radiation;

a spectrometer operatively linked to said one or more optical detection fibers;

a processor operatively linked to said spectrometer and containing algorithms and reference data for determining values for at least two different parameters associated with actively metabolizing cells of inflamed atherosclerotic plaque, wherein said at least two different parameters are selected from the group consisting of oxyhemoglobin, reduced hemoglobin, oxidized cytochrome oxidase aa₃, nitrosyl hemoglobin, nitrosyl tyrosine, pH, glucose, lactate, oxidized LDL cholesterol, and oxidized collagen, and for performing a determination regarding atherosclerotic plaque at risk of rupture or thrombosis based on the values for each said parameter.

28. A method of differentiating atherosclerotic plaque at risk of rupturing, comprising:

identifying sites containing indicia of highly metabolically active cells using the system of claim 27; and

differentiating the vulnerable atherosclerotic plaque based upon the location of said highly metabolically active cells.

29. A method of detecting vulnerable atherosclerotic plaque, comprising:

measuring analytes comprising a chemical or biochemical component of plaque with a device comprising a spectrometer operatively linked to a fiber optic catheter and a processor, wherein the spectrometer and processor together are configured to receive and analyze spectral data collected by said fiber optic catheter and report corresponding chemical or biochemical component measurements, wherein said analytes are associated with activated macrophages; and

identifying the vulnerable atherosclerotic plaque based upon the location and measurements of said analytes, wherein said analytes comprise a first analyte selected from the group consisting of pH, oxyhemoglobin, deoxyhemoglobin, cytochrome oxidase aa₃, reduced cytochrome oxidase aa₃, nitrosyl hemoglobin, nitrosyl tyrosine, glucose, lactate, and oxidized collagen, and at least a second analyte selected from the group consisting of pH, oxyhemoglobin, deoxyhemoglobin, cytochrome oxidase aa₃, reduced cytochrome oxidase aa₃, nitrosyl hemoglobin, nitrosyl tyrosine, glucose, lactate, oxidized LDL cholesterol, and oxidized collagen.

30. The method of claim 29 further comprising measuring said analytes by using visible and near-infrared spectroscopy.