Publication number | USH2246 H1 |
Publication type | Grant |
Application number | US 11/713,965 |
Publication date | 3 Aug 2010 |
Filing date | 28 Feb 2007 |
Priority date | 31 Oct 2006 |
Publication number | 11713965, 713965, US H2246 H1, US H2246H1, US-H1-H2246, USH2246 H1, USH2246H1 |
Inventors | Michael Franklin Miller, Poul Strange |
Original Assignee | Aventis Pharmaceuticals Inc. |
Export Citation | BiBTeX, EndNote, RefMan |
Patent Citations (4), Referenced by (1), Classifications (13), Legal Events (3) | |
External Links: USPTO, USPTO Assignment, Espacenet | |
This application is related to U.S. application Ser. No. 60/863,673, filed Oct. 31, 2006, the entire disclosure of which is hereby incorporated herein by reference.
The present invention relates, generally, to methods for analyzing continuous glucose monitoring data. More specifically, the invention relates to methods for determining a patient's susceptibility to hypoglycemic events and methods for predicting the effectiveness of insulin therapy in lowering average blood glucose levels in a diabetic patient.
Diabetics must monitor their own blood glucose levels, often several times a day, to determine how far above or below a normal level their glucose level is and to determine what oral medications or insulin(s) they may need. This is often done by placing a drop of blood from a skin prick onto a glucose strip and then inserting the strip into a glucose meter, which is a small machine that provides a digital readout of the blood glucose level.
Recently, continuous glucose monitoring systems (CGMS) have been developed that continuously record a patient's glucose levels throughout the day. Generally speaking, these devices work by inserting a small sensor into subcutaneous tissues. The sensor measures the level of glucose in the tissue and sends this information to a monitor worn by the patient which stores the results, In order to determine blood glucose levels, the monitor must be calibrated daily by entering at least three blood glucose readings obtained at different times, using a standard blood glucose meter. For example, Medtronic, Inc. of Minneapolis, Minn., sells an approved MinMed® device which can provide up to 288 glucose measurements every 24 hours for up to 72 hours.
One problem with the blood glucose level data obtained from continuous glucose monitoring systems is that there is a lot of variability in the data. The glucose level data shows a lot of sharp fluctuations, or signal noise, that is most likely not indicative of the average blood glucose levels, but rather is likely due to variability in the measurements.
Because of the lack of accurate diary data from patients and the lack of mealtime synchronization, another problem with CGMS data is the inability to aggregate the data easily to facilitate treatment group comparisons and to visualize the average treatment group curves.
As a result of the problems indicated above, a further problem is the lack of CGMS data indicators that would be useful for diagnosing and treating hypoglycemia and diabetes.
Therefore, there is a need to aggregate continuous blood glucose level data and to identify prognostic indicators for diagnosing and treating hypoglycemia and diabetes.
One aspect of the present invention relates to a method for predicting the effectiveness of medication-based therapy in lowering average blood glucose levels in a diabetic patient comprising the steps of: measuring the patient's blood glucose levels continuously for a period of time to obtain blood glucose level data; applying a Fourier approximation to develop a continuous oscillating blood glucose curve approximately representing the blood glucose level data; mathematically decomposing oscillation of the blood glucose curve into at least one respective component harmonic curve; calculating an amplitude of a composite curve that is a function of the at least one respective component harmonic curve; and correlating the amplitude of the composite curve with an expectation that medication-based therapy will lower the average blood glucose levels in a diabetic patient. This method may further comprise selectively recommending a medication-based therapy on the basis of the arithmetic average of the relative minima.
Another aspect of the invention is a method for determining susceptibility to symptomatic hypoglycemia in a patient comprising the steps of: measuring the patient's blood glucose levels continuously for a period of time to obtain blood glucose level data; applying a Fourier approximation to develop a continuous oscillating blood glucose curve approximately representing the blood glucose level data; identifying areas of the curve having steepest descent, the areas of steepest descent corresponding to relative minima of a first derivative of the curve; calculating an arithmetic average of the relative minima; and correlating a high arithmetic average of the relative minima with an increased susceptibility to symptomatic hypoglycemia. This method may further comprise selectively recommending a medication-based therapy on the basis of the arithmetic average of the relative minima.
Another aspect of the invention is a device for continuously monitoring blood glucose levels in a patient comprising: a sensor for measuring blood glucose levels in said patient; a monitor for recording blood glucose levels at regular intervals; and software executable by said monitor for applying a Fourier approximation to said blood glucose levels.
The present invention relates, generally, to methods for analyzing continuous glucose monitoring data. In order to minimize the impact of sharp fluctuations in CGMS data and to have the ability to aggregate CGMS data from various patient populations, applicants have applied the Fourier approximation method to patient CGMS data.
The Fourier approximation method provides a statistical model for assessing a patient's whole blood glucose profile over a period of time. The Fourier approximation method results in the smoothing out of extraneous variability in the CGMS data via dimension reduction. By applying a Fourier approximation to CGMS data, one can separate the blood glucose profile into a mean level and variability components which can be further partitioned into component harmonics.
The Fourier approximation method can be applied to blood glucose levels in the following manner. For example, levels of blood glucose over a given period of time can be defined as the function CGMS(t). The Fourier approximation of the function CGMS(t) can be designated as FR(t|k) where CGMS(t)=FR(t|k). Where t is measured in hours and ranges from 0 to 24 and harmonic term i oscillates through exactly i cycles in 24 hours, the Fourier approximation is calculated as follows:
=μ+Σ_{i}AMP(i)cos(2πi (t−PHS (i))/24)
=μ+Σ_{i}{A(i)cos(2πi t/24)+B(i)sin(2πi t/24)}
where
μ=CGMS 24-hour mean=AUC/24
A(i), B(i) regression coefficients for cycle i, i=l to k
Amplitude of harmonic term i=sqrt(A(i)^{2}+B(i)^{2})
Phase shift for harmonic term i=arctan(B(i)/A(i))
Individual components of the Fourier approximation can be used to measure the clinical outcomes for the treatment of hypoglycemia or diabetes. For example, if the clinical outcome is reducing the blood glucose levels, one would measure the first term in the Fourier expansion, the twenty-four hour mean blood glucose level. Similarly, if the goal is to reduce the risk of hypoglycemic and hyperglycemic events, one would measure the harmonic amplitudes. Furthermore, the CGMS twenty-four hour standard deviation is proportional to the square root of the sum of the squares of the individual amplitudes of all component harmonic functions. Thus, a reduction of the standard deviation of CGMS levels can be measured by a reduction of the Fourier harmonic component amplitudes.
A Fourier approximation is applied to the observed CGMS blood glucose data for one patient with type 2 diabetes mellitus.
This study employs CGMS 24-hour blood glucose profiles from the following patient populations:
For each subject, a seven cycle Fourier approximation is applied to twenty-four hour CGMS data. An aggregate curve is created for each patient population by averaging the subject Fourier coefficients and producing a graph determined by these averages.
This study employs CGMS 24-hour blood glucose profiles from the pediatric patients with type 1 diabetes mellitus (T1DM), N=90; half of the patients are on a typical insulin therapy regimen while half of the patients are using Lantus®. For each subject, a Fourier approximation is applied to twenty-four hour CGMS data. An aggregate curve is created for the patient population by averaging the subject Fourier coefficients and producing a graph determined by these averages. The Fourier approximation is decomposed into its component harmonics.
This correlation may be used, for example, as a basis for selectively recommending a medication-based therapy on the basis of the amplitude of the composite curve, e.g. to recommend the medication-based therapy if the amplitude exceeds a predetermined, empirically set, amplitude threshold. For example, the threshold and decision-based logic may be implemented by software executable by a special-purpose CGMS device configured in accordance with the present invention or a conventional personal computer (collectively, a “PC”), and the recommendation may be textual, graphical or other indicia displayed on a display screen of the PC, etc. to a prescribing physician, etc.
This study employs CGMS 24-hour blood glucose profiles from the pediatric patients with type 1 diabetes mellitus (T1DM), N=90; half of the patients are on a typical insulin therapy regimen while half of the patients are using Lantus®. For each patient, Fourier approximation using 3 cycles is applied to a 24-hour CGMS profile. The areas of the curve having the steepest descent are identified, the areas of steepest descent corresponding to the relative minima of a first derivative of the curve (e.g., as determined by zeros of the second derivative of the curve). The average steepest descent is calculated by mathematically calculating the arithmetic average of the relative minima.
This determination for susceptibility may be used, for example, as a basis for selectively recommending a medication-based therapy on the basis of the arithmetic average of the relative minima, e.g. to recommend the medication-based therapy if the average exceeds a predetermined, empirically set, average threshold. For example, the threshold and decision- based logic may be implemented by software executable by a special-purpose CGMS device configured in accordance with the present invention, a conventional personal computer (collectively, a “PC”), and the recommendation may be textual, graphical or other indicia displayed on a display screen of the PC, etc. to a prescribing physician, etc.
A device for continuously monitoring blood glucose levels in a patient may include a conventional sensor for measuring blood glucose levels in the patient and a conventional monitor for recording blood glucose levels at regular intervals. In accordance with the present invention, a substantially conventional CGMS device may be specially configured in accordance with the present invention to include software executable by the monitor for applying a Fourier approximation to the blood glucose level data, determining composite harmonic curve amplitudes, determining average steepest descent, determining susceptibility to symptomatic hypoglycemia, storing threshold data, selectively recommending medication-based therapy as a function of a relationship to stored threshold data, etc., as discussed in greater detail above. By way of further example, the device may be capable of exporting gathered data to a personal computer or other external computing device configured with similar specially configured software for providing such functionality.
While certain of the preferred embodiments of the present invention have been described and specifically exemplified above, it is not intended that the invention be limited to such embodiments. Various modifications may be made thereto without departing from the scope and spirit of the present invention, as set forth in the following claims.
Cited Patent | Filing date | Publication date | Applicant | Title |
---|---|---|---|---|
US5533509 * | 12 Aug 1993 | 9 Jul 1996 | Kurashiki Boseki Kabushiki Kaisha | Method and apparatus for non-invasive measurement of blood sugar level |
US6370407 * | 12 Jun 2000 | 9 Apr 2002 | Tecmed, Incorporated | System for improving the sensitivity and stability of optical polarimetric measurements |
US6574490 * | 11 Apr 2001 | 3 Jun 2003 | Rio Grande Medical Technologies, Inc. | System for non-invasive measurement of glucose in humans |
US6650915 * | 22 Oct 2001 | 18 Nov 2003 | Fovioptics, Inc. | Non-invasive measurement of blood analytes using photodynamics |
Citing Patent | Filing date | Publication date | Applicant | Title |
---|---|---|---|---|
US20110319322 * | 29 Dec 2011 | Hygieia, Inc. | Systems, Methods and Devices for Achieving Glycemic Balance |
U.S. Classification | 600/365, 600/347, 600/366, 600/319, 600/316 |
International Classification | A61B5/00 |
Cooperative Classification | G06F19/3437, A61B5/7275, A61B5/4848, A61B5/14532 |
European Classification | A61B5/72M2, A61B5/48M, A61B5/145G |
Date | Code | Event | Description |
---|---|---|---|
9 May 2007 | AS | Assignment | Owner name: SANOFI-AVENTIS U.S. LLC, NEW JERSEY Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:MILLER, MICHAEL FRANKLIN;STRANGE, POUL;SIGNING DATES FROM 20070504 TO 20070507;REEL/FRAME:019268/0977 |
15 May 2007 | AS | Assignment | Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:SANOFI-AVENTIS U.S. LLC.;REEL/FRAME:019293/0088 Owner name: SANOFI-AVENTIS, FRANCE Effective date: 20070507 |
2 Aug 2011 | AS | Assignment | Effective date: 20110511 Owner name: SANOFI, FRANCE Free format text: CHANGE OF NAME;ASSIGNOR:SANOFI-AVENTIS;REEL/FRAME:026686/0522 |