System and method for non-invasive monitoring of advanced glycation end-products (AGE)

1. A system comprising:

a medical device comprising:

a light emitter configured to provide incident light to tissue of a patient at one excitation wavelength; at least one photodetector configured to monitor an emission response to the incident light at a first emission wavelength and at a second emission wavelength; and

one or more processors configured to:

determine a concentration of an advanced glycation end-product (AGE) based on a ratio of the emission response at the first emission wavelength to the emission response at the second emission wavelength, wherein the emission response at the first emission wavelength is associated with a maximum of the emission response and the emission response at the second emission wavelength is associated with a minimum of the emission response;

compare the determined concentration to a threshold; and

generate an alert based on the comparison.

2. The system of claim 1 , wherein the AGE is glycated hemoglobin (HbA1c).

3. The system of claim 2 , wherein the one or more processors are configured to determine a risk of diabetes based on the determined concentration of HbA1c.

4. The system of claim 1 , wherein the at least one photodetector is configured to monitor an autofluorescence decay of the emission response at the first emission wavelength and the emission response at the second emission wavelength.

5. The system of claim 4 , wherein the at least one photodetector is configured to measure a first rate of decay of the emission response at the first emission wavelength and a second rate of decay of the emission response at the second emission wavelength, and the one or more processors are configured to determine the concentration of the AGE based on a ratio of the first rate of decay to the second rate of decay.

6. The system of claim 1 , wherein the at least one photodetector is configured to monitor a first amplitude at the first emission wavelength and a second amplitude at the second emission wavelength.

7. The system of claim 1 , wherein the one or more processors comprises a processor of the medical device.

8. The system of claim 1 , wherein the medical device is configured for implantation in the patient.

9. A method performed by a medical device comprising processing circuitry and being configured to determine a concentration of an advanced glycation end-product (AGE), the method comprising:

providing incident light, by a light emitter of the medical device, to tissue of a patient at one excitation wavelength;

monitoring, by at least one photodetector of the medical device, an emission response to the incident light at a first emission wavelength and at a second emission wavelength;

determining, by the processing circuitry, a concentration of the AGE based on a ratio of the emission response at the first emission wavelength to the emission response at the second emission wavelength, wherein the emission response at the first emission wavelength is associated with a maximum of the emission response and the emission response at the second emission wavelength is associated with a minimum of the emission response;

comparing, by the processing circuitry, the determined concentration to a threshold; and

generating, by the processing circuitry, an alert based on the comparison.

10. The method of claim 9 , wherein the AGE is glycated hemoglobin (HbA1c).

11. The method of claim 10 , further comprising determining, by the processing circuitry, a risk of diabetes based on the determined concentration of HbA1c.

12. The method of claim 9 , wherein monitoring the emission response comprises monitoring an autofluorescence decay of the emission response at the first emission wavelength and the emission response at the second emission wavelength.

13. The method of claim 12 , wherein monitoring the autofluorescence decay comprises measuring a first rate of decay of the emission response at the first emission wavelength and a second rate of decay of the emission response at the second emission wavelength, and wherein determining the concentration of the AGE comprises calculating the concentration of the AGE based on a ratio of the first rate of decay to the second rate of decay.

14. The method of claim 9 , wherein monitoring the emission response comprises monitoring a first amplitude at the first emission wavelength and a second amplitude at the second emission wavelength.

15. The method of claim 9 , wherein providing the incident light and monitoring the emission response comprises providing the incident light and monitoring the emission response with the medical device implanted in the patient.

16. The method of claim 9 , wherein providing the incident light and monitoring the emission response comprises providing the incident light and monitoring the emission response with the medical device subcutaneously inserted in the patient.

17. A system comprising:

a medical device comprising:

a light emitter configured to provide incident light to tissue of a patient at one excitation wavelength; at least one photodetector configured to monitor a first rate of autofluorescence decay of an emission response to the incident light at a first emission wavelength and a second rate of autofluorescence decay of the emission response at a second emission wavelength; and

one or more processors configured to:

determine a concentration of an advanced glycation end-product (AGE) based on a ratio of the first rate of autofluorescence decay of the emission response at the first emission wavelength to the second rate of autofluorescence decay of the emission response at the second emission wavelength.

18. The system of claim 17 , wherein the AGE is glycated hemoglobin (HbA1c).