A pharmacologic agent that inhibits the activity of a-glucosidase. Oral use of these agents results in a significant delay in the digestion of carbohydrates, with a significant decrease in the rise in plasma glucose after a mixed carbohydrate meal.
A skin disease characterized by a hyperpigmentation and thickening of the skin. It may be associated with severe hyperinsulinemia and insulin resistance.
Acarbose (Precose®) is indicated as monotherapy as an adjunct to diet and exercise to lower blood glucose levels in patients with type 2 diabetes whose hyperglycemia cannot be controlled by diet and exercise alone. Acarbose may also be used in combination with a sulfonylurea when diet and exercise plus either acarbose or a sulfonylurea does not result in adequate glycemic control. In addition, acarbose may be used in combination with insulin or metformin.
Full Name: Action to Control Cardiovascular Risk in Diabetes
ACCORD was designed to determine 1) whether lowering blood glucose to a level closer to normal than called for in current guidelines reduces cardiovascular (CVD) risk (2) the effects of lowering blood pressure in the context of good blood sugar control, and (3) the effects of lowering LDL cholesterol and blood triglycerides and increasing HDL cholesterol compared to an intervention that only lowers LDL cholesterol, all in the context of good blood sugar control. The purpose of ACCORD is to prevent major cardiovascular events (heart attack, stroke, or cardiovascular death) in adults with type 2 diabetes mellitus using intensive glycemic control, intensive blood pressure control, and intensive lipid management. ACCORD commenced in 1999. A total of 10,000 patients with type 2 diabetes were expected to enroll in this study.
A randomized, double-blind, placebo-controlled, parallel assignment, safety/efficacy study designed to examine whether pioglitazone versus placebo can reduce the conversion rate of impaired glucose tolerance to type 2 diabetes mellitus. ACT NOW commenced in 2004. A total of 600 participants were expected to enroll in this study.
Published annually in the journal Diabetes Care, these are diabetes-related clinical practice recommendations developed by the American Diabetes Association. They are one of the gold standards upon which diabetes care and treatment are based.
A class of drugs that inhibit the interaction of neurotransmitters with certain nerve fibers of the autonomic nervous system. Administered to alleviate hypertension and other conditions, these drugs decrease the heart rate and force of heart contractions.
The nonenzymatic glycosylation of protein exposed to hyperglycemic blood for long periods results in formation of AGE. AGEs accumulate over time and induce cross-linking of collagen and other matrix proteins in vascular walls and other tissues. LDLs can then become covalently trapped and accumulate. AGEs in vascular walls may also contribute to thickening, loss of elasticity, and increased permeability of the vascular wall. AGEs stimulate the release of cytokines and induce cell proliferation and inflammatory effects.
Alanine transaminase, also called alanine aminotransferase, is an enzyme that is released into the plasma by liver cell death, a normal occurrence. When liver cell death increases, ALT levels rise above the normal range. The spillover of this enzyme into blood is measured as a marker of abnormal liver-cell damage.
Appearance of albumin in the urine. Some albumin normally appears in the urine. Increased albumin excretion above normal may be a sign of kidney disease, often a complication of diabetes.
A steroid hormone produced by the adrenal gland. Aldosterone acts on the kidney to retain sodium ions and water and excrete potassium and hydrogen ions. Aldosterone secretion is increased by angiotensin II.
(Glimepiride:Amaryl; Glipizide:Glucotrol; Glyburide:DiaBeta, Micronase, Glynase) A type of oral antidiabetic drug that stimulates insulin secretion from the pancreatic ß-cells.
First-Generation Agents Tolbutamide (Orinase®), tolazamide (Tolinase®), or chlorpropamide (Diabinese®). Indicated as an adjunct to diet and exercise to lower blood glucose levels in patients with type 2 diabetes whose hyperglycemia cannot be controlled by diet and exercise alone. Tolbutamide, tolazamide, or chlorpropamide may be used in combination with insulin when sulfonylurea monotherapy fails to reduce symptoms and/or blood glucose levels.
Second-Generation Agents Glipizide (Glucotrol®), glyburide, or glimepiride. Indicated as an adjunct to diet and exercise to lower blood glucose levels in patients with type 2 diabetes whose hyperglycemia cannot be controlled by diet and exercise alone. Glipizide, glyburide, or glimepiride may be used in combination with insulin when sulfonylurea monotherapy fails to reduce symptoms and/or blood glucose levels.
Angiotensin receptor blockers are medications that modulate the renin-angiotensin-aldosterone system. These drugs block the action of angiotensin II, permitting the blood vessels to relax and dilate, which lowers blood pressure. ARBs are primarily used for the treatment of hypertension when ACE inhibitor therapy cannot be tolerated by the patient.
A protein that converts angiotensin I to angiotensin II. Angiotensin II is the active form of angiotensin and plays an important role in vasoconstriction. The action of angiotensin II results in an increase in blood pressure and a decrease in glomerular filtration rate.
A protein found in the serum that blocks the conversion of angiotensin I to angiotensin II. This results in a decrease in sodium and water retention and a decrease in blood pressure. ACE-inhibitors are used to treat hypertension, a frequent concomitant of diabetes, as well as other conditions.
The ASCOT multicenter trial compared two antihypertensive treatment strategies to prevent coronary heart disease (CHD) in hypertensive patients (N=19,342) with no history of CHD.
The lipid-lowering arm of the Anglo-Scandinavian Cardiac Outcomes Trial was a randomized, double-blind, placebo-controlled study undertaken to examine whether lipid lowering with a statin provides additional benefits in treated hypertensive patients with total cholesterol concentrations not conventionally considered dyslipidemic. Despite the presence of 3 or more risk factors, these patients were deemed to be at moderate cardiovascular risk. The primary endpoint was nonfatal myocardial infarction (MI) (including silent MI) and fatal coronary heart disease.
This study compared lisinopril (an ACE inhibitor) and amlodipine (a calcium channel blocker) with chlorthalidone (a thiazide-type diuretic) to measure their efficacy in reducing clinical complications in normoglycemic (n=17,012) patients, patients with impaired fasting glucose (n=1,399), or with type 2 diabetes (n=13,101). The primary outcome measure was incidence of fatal coronary heart disease and nonfatal myocardial infarction.
A class of apolipoprotein that occurs primarily in HDL and in lesser amounts in chylomicrons. Apo E is the activator of lecithin-cholesterol acyltransferase (LCAT), which forms cholesteryl esters in HDL.
A group of diseases (including atherosclerosis) in which the arterial walls become thickened and lose elasticity. It is often associated with hypertension and diabetes.
Aspartate transaminase, also called aspartate aminotransferase, is an enzyme normally present in the liver, heart, and other tissues. A high level of AST released into the blood may be a sign of liver or heart damage, or other diseases.
Aspirin, or acetylsalicylic acid (acetosal) is a drug in the family of salicylates, often used as an analgesic (to relieve minor aches and pains), antipyretic (to reduce fever), and as an anti-inflammatory. It also has an antiplatelet ("blood-thinning") effect and is used in long-term, low doses to prevent heart attacks and thrombus formation in hypercoaguable states (e.g.in cancer).
A disorder of the arteries in which deposits (plaques) of cholesterol, lipids, and cellular debris line the inner layers of arterial walls. It is a major cause of serious heart disease and is associated with increasing age, obesity, tobacco use, hypertension, elevated cholesterol, dyslipidemia, and diabetes mellitus.
An immunologic disorder that results in the production of antibodies that react against an individual's own cells or cell products. Type 1 diabetes mellitus is often associated with autoantibody production, resulting in the destruction of the b-cells of the pancreas.
A class of drugs that inhibit the interaction of neurotransmitters with certain nerve fibers of the autonomic nervous system. Administered to alleviate hypertension and other conditions, these drugs decrease the heart rate and force of heart contractions.
Full Name: Bypass Angioplasty Revascularization Investigation in Type 2 Diabetics
The BARI 2D trial was a multicenter study that used a 2x2 factorial design, with patients assigned at randomization to initial elective revascularization with aggressive medical therapy or aggressive medical therapy alone with equal probability, and simultaneously assigned at randomization to an insulin providing or insulin sensitizing strategy of glycemic control (with a target value for A1C of <7.0% for all patients). This study was designed to determine in patients with type 2 diabetes and stable CAD: 1) the efficacy of initial elective coronary revascularization combined with aggressive medical therapy, compared to an initial strategy of aggressive medical therapy alone; and 2) the efficacy of a strategy of providing more insulin (endogenous or exogenous), versus a strategy of increasing sensitivity to insulin (reducing insulin resistance), in the management of hyperglycemia, with a target A1C level of < 7.0% for each strategy. BARI 2D commenced in 2000. A total of 2,800 patients were expected to enroll in this study.
The concentration of glucose (“blood sugar”) in the bloodstream. Blood glucose levels are usually determined after an overnight fast, but can also be determined randomly or at set times after the ingestion of glucose. A fasting plasma glucose level of less than 100 mg/dL is considered normal. Elevated levels of glucose may be indicative of diabetes mellitus. (See fasting plasma glucose test, hyperglycemia, oral glucose tolerance test.)
Exenatide is an injectable drug that reduces the level of glucose in the blood. It is used for treating type 2 diabetes. Exenatide belongs in a class of drugs called incretin mimetics.
Exenatide (Byetta®) is indicated as adjunctive therapy to improve glycemic control in patients with type 2 diabetes mellitus who are taking metformin, a sulfonylurea, a thiazolidinedione, a combination of metformin and a sulfonylurea, or a combination of metformin and a thiazolidinedione, but have not achieved adequate glycemic control.
A by-product of insulin production. Plasma C-peptide has a longer half-life than insulin and is often used to provide an indication of endogenous insulin secretion.
A measure of the cardiac output of a patient per square meter of body surface area. It is obtained by dividing the cardiac output in liters per minute by the body surface area. Normal range for a healthy adult is 2.8 to 4.2 L/min/m2.
Primary noninflammatory disease of the heart muscle, often of obscure or unknown etiology and not the result of ischemic, hypertensive, congenital, valvular, or pericardal disease.
Full Name: A Study of Pioglitazone HCl Versus Glimepiride in Subjects With Type 2 Diabetes Measuring the Progression of Atherosclerosis (CHICAGO)
A double-blind, randomized, comparator-controlled study in subjects with type 2 diabetes comparing the effects of pioglitazone HCl versus glimepiride on the rate of progression of atherosclerotic disease as measured by carotid intima-media thickness. This study commenced in 2003. A total of 462 participants were expected to enroll in this study.
A waxy lipid. Cholesterol circulates in the blood as part of a lipoprotein complex. High cholesterol levels put one at increased risk for atherosclerosis. (See high-density lipoprotein cholesterol, low-density lipoprotein cholesterol.)
A globule of lipoprotein in the serum measuring less than 0.5 mm in diameter and consisting predominantly of triglycerides. Chylomicrons transport fat from the intestine to the liver or adipose tissue.
The Collaborative Atorvastatin Diabetes Study was a primary cardiovascular prevention study using atorvastatin in patients with type 2 diabetes. Patients aged 40 to 75 years were randomized to atorvastatin 10 mg (n=1,428) or placebo (n=1,410) given once daily. The primary endpoint was occurrence of first acute cardiovascular event.
The use of a battery-powered pump system to deliver insulin into body via a needle or catheter placed in the subcutaneous tissue. It can be used by patients with type 1 diabetes as an alternative to daily injections of insulin. (See insulin pump.)
A disorder of the arteries of the heart, usually resulting from atherosclerosis. Deposits of plaque on the arterial wall cause narrowing of the lumen, thus preventing an adequate flow of oxygen and nutrients to the heart muscle.
Abbreviation for Clinical Trial of Reviparin and Metabolic Modulation in Acute Myocardial Infarction Treatment Evaluation-Estudios Cardiologicos Latin America.
A diagnostic measurement of kidney function used to estimate the glomerular filtration rate. Creatinine is a metabolic breakdown product of creatine and is found in the blood and urine. Normal blood levels range between 0.5 and 1.2 mg/dL.
(Glimepiride:Amaryl; Glipizide:Glucotrol; Glyburide:DiaBeta, Micronase, Glynase) A type of oral antidiabetic drug that stimulates insulin secretion from the pancreatic ß-cells.
First-Generation Agents Tolbutamide (Orinase®), tolazamide (Tolinase®), or chlorpropamide (Diabinese®). Indicated as an adjunct to diet and exercise to lower blood glucose levels in patients with type 2 diabetes whose hyperglycemia cannot be controlled by diet and exercise alone. Tolbutamide, tolazamide, or chlorpropamide may be used in combination with insulin when sulfonylurea monotherapy fails to reduce symptoms and/or blood glucose levels.
Second-Generation Agents Glipizide (Glucotrol®), glyburide, or glimepiride. Indicated as an adjunct to diet and exercise to lower blood glucose levels in patients with type 2 diabetes whose hyperglycemia cannot be controlled by diet and exercise alone. Glipizide, glyburide, or glimepiride may be used in combination with insulin when sulfonylurea monotherapy fails to reduce symptoms and/or blood glucose levels.
A 10-year study of more than 1,400 people with type 1 diabetes that was sponsored by the National Institutes of Health. It showed that team management to achieve tight blood glucose control significantly reduces the risk of diabetic retinopathy, neuropathy, and nephropathy.
A disease of carbohydrate, protein, and fat metabolism brought on by relative or absolute insulin deficiency. The disease is characterized by chronic hyperglycemia, which can result in damage to the kidneys, eyes, heart, blood vessels, and other organs. (Seetype 1 diabetes, type 2 diabetes, gestational diabetes.)
The US Diabetes Prevention Program was designed to compare incidence rates of diabetes among groups of individuals (N=3,234) with impaired glucose tolerance randomized to placebo, intensive lifestyle modification with diet and exercise, or metformin.
A life-threatening condition of decompensated diabetes mellitus. Diabetic coma can result from severe hyperglycemia and dehydration with our without diabetic ketoacidosis (See diabetic ketoacidosis). Unless treated immediately with insulin and fluid and electrolyte replacement, the person will not survive.
A disorder of acid-base balance in which severe or absolute insulin deficiency leads to unrestrained lipolysis and ketone body production that leads to accumulation of keto-acids in the bloodstream and acidosis. Diabetic ketoacidosis is usually associated with other electrolyte and fluid imbalances. The condition is fatal if not treated with fluids, electrolytes, and insulin (Seediabetic coma.)
Kidney disease resulting from years of poorly controlled diabetes. The main disease occurs in the glomerulus, where there is basement membrane thickening and mesangial overgrowth leading to proteinuria and reduced glomerular filtration, respectively. Some renal tubular disease may be found as well.
Damage to the nervous system resulting from poorly controlled diabetes. Four different forms of neuropathy can be distinguished: peripheral sensorimotor neuropathy, autonomic neuropathy, mononeuritis simplex, and polyradiculopathy, The first two forms are much more common that the second two. Peripheral neuropathy affects the motor and sensory nerves that control sensation and motor tone. Autonomic neuropathy affects the nerves involved in such involuntary functions as digestion.
(Glimepiride:Amaryl; Glipizide:Glucotrol; Glyburide:DiaBeta, Micronase, Glynase) A type of oral antidiabetic drug that stimulates insulin secretion from the pancreatic ß-cells.
First-Generation Agents Tolbutamide (Orinase®), tolazamide (Tolinase®), or chlorpropamide (Diabinese®). Indicated as an adjunct to diet and exercise to lower blood glucose levels in patients with type 2 diabetes whose hyperglycemia cannot be controlled by diet and exercise alone. Tolbutamide, tolazamide, or chlorpropamide may be used in combination with insulin when sulfonylurea monotherapy fails to reduce symptoms and/or blood glucose levels.
Second-Generation Agents Glipizide (Glucotrol®), glyburide, or glimepiride. Indicated as an adjunct to diet and exercise to lower blood glucose levels in patients with type 2 diabetes whose hyperglycemia cannot be controlled by diet and exercise alone. Glipizide, glyburide, or glimepiride may be used in combination with insulin when sulfonylurea monotherapy fails to reduce symptoms and/or blood glucose levels.
Full name: The DREAM (Diabetes Reduction Assessment With Ramipril and Rosiglitazone Medication) Trial
The DREAM trial was a large, international, multi-centre, randomized double-blind controlled trial to determine if ramipril and/or rosiglitazone prevented the onset of type 2 diabetes. DREAM commenced in 2001. A total of 5,269 participants were enrolled in the study.
An abnormal profile of blood lipids. The characteristic dyslipidemia associated with insulin resistance and poorly controlled diabetes includes high levels of triglycerides, low levels of HDL-C, and partitioning of LDL-C into relatively small and dense particles.
The most severe, fully developed phase of renal disease, in which the kidneys have lost so much function that dialysis or kidney transplantation is needed for patient survival.
Insulin secreted by the pancreatic b-cells. In patients with type 1 diabetes, endogenous insulin is virtually undetectable because of immune damage to the b-cell. Patients with type 2 diabetes have detectable insulin levels, but they are insufficient to overcome the increased insulin needs caused by insulin resistance.
Abnormal function of endothelial cells that may be detected by reduced ability to stimulate vascular dilation in response to ischemia and/or sheer stress. Endothelial function is known to be abnormal in diabetes and may be an early step in the development of atherosclerotic lesions.
The Epidemiology of Diabetes Interventions and Complications study is a long-term observational follow-up (mean 17 years) to the Diabetes Control and Complications Trial (DCCT), which studied whether the use of intensive therapy as compared with conventional therapy affected the incidence of cardiovascular disease in patients with type 1 diabetes. Ninety-seven percent of the original DCCT cohort joined the EDIC follow-up (N=1,394).
A hormone secreted by the adrenal gland during stress and when blood glucose levels are low. It has many actions, one of which is to counteracts the action of insulin by promoting glycogen breakdown in the liver and the release of fatty acids from adipose tissue.
Physiologic studies used to measure insulin resistance in a research setting, Insulin is infused to create matched insulin levels in all subjects. Glucose is infused to maintain matched glucose levels as well. Glucose requirements are used as a measure of insulin sensitivity. Clamps can be performed with isotope-labeled glucose to separately assess the effects of insulin on glucose production and glucose utilization.
Lists of foods—such as starch/bread, meat, vegetable, fruit, milk, and fat—and their quantity, which may be exchanged with other foods on the same list without changing the nutritional content of the diet.
Exenatide is an injectable drug that reduces the level of glucose in the blood. It is used for treating type 2 diabetes. Exenatide belongs in a class of drugs called incretin mimetics.
Exenatide (Byetta®) is indicated as adjunctive therapy to improve glycemic control in patients with type 2 diabetes mellitus who are taking metformin, a sulfonylurea, a thiazolidinedione, a combination of metformin and a sulfonylurea, or a combination of metformin and a thiazolidinedione, but have not achieved adequate glycemic control.
Glucose concentration in plasma obtained after an 8 to 10 hours overnight fast An FPG level less than 100 mg/dL is normal; one of 101-26 mg/dL is impaired; and one greater than or equal to 126 mg/dL indicated diabetes if it is reproducible and not found during an acute illness.
The test is taken after fasting for 8 to 10 hours, typically overnight. An FPG level less than 110 mg/dL is normal; one between 110 and 126 mg/dL indicates impaired glucose tolerance; and one greater than 126 mg/dL supports a provisional diagnosis of diabetes.
An oral medication of the fibrate class, it is mainly used with diet changes (restriction of cholesterol and fat intake) to reduce the amount of cholesterol and triglycerides (fatty substances) in blood. Like other fibrates, fenofibrate acts on PPAR-alpha to reduce cholesterol levels.
The insoluble protein formed from fibrinogen by the proteolytic action of thrombin during the normal clotting of blood. Fibrin forms the essential portion of blood clots.
Abbreviation for the Fenofibrate Intervention and Event Lowering in Diabetes study. In this study, investigators carried out a multinational, randomized controlled trial of 9,795 patients 50 to 75 years of age with type 2 diabetes. The patient population consisted of 2,131 individuals with previous CVD and 7,664 without. Following a placebo or fenofibrate run-in phase, patients were randomly assigned to treatment with micronized fenofibrate 200 mg daily (n=4,895) or to matching placebo (n=4,900).
Carbohydrate intolerance that comes on or is first recognized during pregnancy. Gestational diabetes increases the risk of perinatal morbidity in the infant and the later development of diabetes in both infant and mother.
(Glimepiride:Amaryl; Glipizide:Glucotrol; Glyburide:DiaBeta, Micronase, Glynase) A type of oral antidiabetic drug that stimulates insulin secretion from the pancreatic ß-cells.
First-Generation Agents Tolbutamide (Orinase®), tolazamide (Tolinase®), or chlorpropamide (Diabinese®). Indicated as an adjunct to diet and exercise to lower blood glucose levels in patients with type 2 diabetes whose hyperglycemia cannot be controlled by diet and exercise alone. Tolbutamide, tolazamide, or chlorpropamide may be used in combination with insulin when sulfonylurea monotherapy fails to reduce symptoms and/or blood glucose levels.
Second-Generation Agents Glipizide (Glucotrol®), glyburide, or glimepiride. Indicated as an adjunct to diet and exercise to lower blood glucose levels in patients with type 2 diabetes whose hyperglycemia cannot be controlled by diet and exercise alone. Glipizide, glyburide, or glimepiride may be used in combination with insulin when sulfonylurea monotherapy fails to reduce symptoms and/or blood glucose levels.