Inflammatory markers as tools in the detection and prevention of diabetes mellitus and as tools to aid in the selection of agents to be used for the prevention and treatment of diabetes
The invention involves methods for characterizing an individual's risk profile of developing future diabetes or complications of diabetes by obtaining a level of an inflammatory marker in the individual. Preferred inflammatory markers according to the present invention include C reactive protein and interleukin-6. The invention also involves methods for evaluating the likelihood that an individual will benefit from treatment with an agent for reducing the risk of future diabetes.
1. A method for predicting an individual's risk profile of developing future diabetes or a diabetic complication, comprising:
selecting an individual who is free of diabetes,
obtaining a level of C-reactive protein in a blood sample from the individual,
comparing the level of C-reactive protein in the blood sample from the individual to a predetermined value of 0.30 mg/dl, and if said level of C-reactive protein is about 0.30 mg/dl or higher in the blood sample from the individual, then
predicting said individual as having an increased risk of developing future diabetes or a diabetic complication, wherein the diabetic complication is diabetic ketoacidosis, hyperosmolar coma, retinopathy, diabetic nephropathy, diabetic neuropathy, or diabetic foot ulcers.
2. The method of claim 1 , wherein the level of C-reactive protein is about 0.60 mg/dl or higher in the blood sample from the individual.
3. A method for predicting an individual's risk profile of developing future diabetes or a diabetic complication, comprising:
selecting an individual who is free of diabetes,
obtaining a level of C-reactive protein in a blood sample from the individual, wherein a level of C-reactive protein about 0.30 mg/dl or higher in the blood sample from the individual establishes a first risk value,
obtaining a level of a glycosylated hemoglobin in a blood sample from the individual,
comparing the level of the glycosylated hemoglobin to a second predetermined value specific for the diagnosis of diabetes or a diabetic complication to establish a second risk value, and
predicting the individual's risk profile of developing diabetes or a diabetic complication based upon the combination of the first risk value and the second risk value, wherein the combination of the first risk value and second risk value establishes a third risk value different from said first and second risk values.
4. The method of claim 3 , wherein the level of C-reactive protein is about 0.60 mg/dl or higher in the blood sample of the individual.
5. A method for evaluating the likelihood that an individual will benefit from treatment with an agent for reducing the risk of diabetes, wherein the agent is insulin, a hypoglycemic agent, an anti-inflammatory agent, a lipid lowering agent, a calcium channel blocker, a beta-adrenergic receptor blocker, a cyclooxygenase-2 inhibitor, or an angiotensin system inhibitor, comprising:
selecting an individual who is free of diabetes,
obtaining a level of C-reactive protein in a blood sample from the individual,
comparing the level of C-reactive protein in the blood sample from the individual to a predetermined value of 0.30 mg/dl, and if said level of C-reactive protein is about 0.30 mg/dl or higher in the blood sample from the individual, then
predicting said individual as likely to benefit from treatment with said agents, wherein the lipid lowering agent is not an HMG-CoA reductase inhibitor.
6. The method of claim 5 , wherein the agent is a hypoglycemic agent.
7. The method of claim 5 , wherein the level of C-reactive protein is about 0.60 mg/dL or higher in the blood sample from the individual.
8. The method of claim 5 , wherein the agent is insulin.
9. The method of claim 5 , wherein the agent is an anti-inflammatory agent.
10. The method of claim 5 , wherein the agent is a lipid lowering agent.
11. The method of claim 5 , wherein the agent is a calcium channel blocker.
12. The method of claim 5 , wherein the agent is a beta-adrenergic receptor blocker.
13. The method of claim 5 , wherein the agent is a cyclooxygenase-2 inhibitor.
14. The method of claim 5 , wherein the agent is an angiotensin system inhibitor.
15. The method of claim 1 , wherein the diabetes or a diabetic complication is diabetes.
16. The method of claim 1 , wherein the diabetes or a diabetic complication is a diabetic complication.
17. The method of claim 3 , wherein the diabetes or a diabetic complication is diabetes.
18. The method of claim 3 , wherein the diabetes or a diabetic complication is a diabetic complication.
19. The method of claim 5 , wherein the agent is an agent for reducing the risk of diabetes.