ABFM KSA - Diabetes Flashcards
Question: 1 of 60
True statements regarding nonpharmacologic therapy to reduce insulin resistance include which of the following? (Mark all that are true.)
- Decreasing caloric intake will increase insulin sensitivity independent of weight loss
- Moderate alcohol intake increases insulin resistance
- Exercise has been shown to enhance insulin action in skeletal muscle
- A decrease of as little as 5% in body weight can result in a substantial reduction in insulin resistance
- If there are no contraindications, patients with insulin resistance syndrome should be advised to engage in 30 minutes of modest aerobic exercise at least 4–5 times/week
- Decreasing caloric intake will increase insulin sensitivity independent of weight loss
- Moderate alcohol intake increases insulin resistance
- Exercise has been shown to enhance insulin action in skeletal muscle
- A decrease of as little as 5% in body weight can result in a substantial reduction in insulin resistance
- If there are no contraindications, patients with insulin resistance syndrome should be advised to engage in 30 minutes of modest aerobic exercise at least 4–5 times/week
Critique:
Lifestyle interventions play a pivotal role in the management of insulin resistance syndrome. Losing even 5% of body weight has been shown to substantially reduce insulin resistance. In addition, insulin sensitivity can be increased by reducing caloric intake, even if no weight is lost. Exercise is an important adjunct to weight loss, since it has been shown to enhance insulin action in skeletal muscle not only during physical activity but for up to a week following exercise. All patients with insulin resistance syndrome should be advised to engage in 30 minutes of aerobic exercise at least 4–5 times/week. Moderate alcohol intake lowers insulin resistance.
Question: 2 of 60
Which one of the following neurologic tests is most useful for predicting the future occurrence of a diabetic foot ulcer?
- Pressure sensation with Semmes-Weinstein monofilament (10 g)
- Deep tendon reflexes of the ankle
- Proprioception
- Vibratory sensation with a 128-mHz tuning fork
- Light touch with a wisp of cotton
- Pressure sensation with Semmes-Weinstein monofilament (10 g)
- Deep tendon reflexes of the ankle
- Proprioception
- Vibratory sensation with a 128-mHz tuning fork
- Light touch with a wisp of cotton
Critique:
Failure to perceive a pressure sensation produced by Semmes-Weinstein monofilament indicates a loss of protective sensation in the diabetic foot and is highly predictive of foot ulceration. Traditional neurologic examination techniques for evaluating reflexes, proprioception, vibration, or light touch are highly subjective and less predictive of future ulceration.
Question: 3 of 60
Which of the following lipid-lowering agents can worsen glycemic control? (Mark all that are true.)
- Colestipol (Colestid)
- Ezetimibe (Zetia)
- Gemfibrozil (Lopid)
- Niacin
- Atorvastatin (Lipitor)
- Colestipol (Colestid)
- Ezetimibe (Zetia)
- Gemfibrozil (Lopid)
- Niacin
- Atorvastatin (Lipitor)
Critique:
Niacin is the most effective agent for raising HDL-cholesterol, producing an increase of 15%–35%, it also reduces triglycerides by 20%–50% and LDL-cholesterol by 5%–25%.
Hyperglycemia is a side effect of niacin therapy, particularly at high doses. A dosage of 750–2000 mg/day is associated with only moderate rises in blood glucose, and at one time was considered a treatment option in patients with diabetes, particularly those with low HDL-cholesterol levels. However, the recommendations for niacin use were changed as a result of the AIM-HIGH trial (Atherothrombosis Intervention in Metabolic Syndrome with Low HDL/High Triglycerides: Impact on Global Health Outcomes), which found no incremental clinical benefit from the addition of niacin to statin therapy in patients with coronary heart disease and LDL-cholesterol levels >70 mg/dL.
Recent studies support a link between statin use and the development of diabetes mellitus. In a meta-analysis of 13 studies, statin therapy was associated with a 9% increased risk for incident diabetes. Another meta-analysis corroborated this result and found that intensive-dose statin therapy was associated with a higher risk of new-onset diabetes compared with moderate-dose statin therapy. In 2012, the FDA modified the package labeling of statins to include the risk of increased blood glucose levels and the development of type 2 diabetes. The benefit of statin therapy, however, outweighs the risk; it was estimated there would be 1 additional case of diabetes for every 498 patients treated for 1 year, compared with 1 less patient experiencing a cardiovascular event for every 155 patients treated for 1 year.
Question: 4 of 60
A 58-year-old male with type 2 diabetes mellitus comes in during the early afternoon for his annual physical examination. His current medication regimen consists of insulin glargine (Lantus), 18 units in the evening; glipizide (Glucotrol), 20 mg/day; metformin (Glucophage), 1000 mg twice a day; and acarbose (Precose), 100 mg three times a day. He suddenly becomes shaky, diaphoretic, and pale, and tells you he thinks it is because he skipped lunch before his appointment.
Which of the following would be effective for managing this episode? (Mark all that are true.)
- Glucose tablets
- A sugar cube
- A banana
- A soft drink containing sugar
- Raisins
- Glucagon
- Glucose tablets
- A sugar cube
- A banana
- A soft drink containing sugar
- Raisins
- Glucagon
Critique:
Acarbose, an α-glucosidase inhibitor, inhibits an enzyme present in the brush border of the proximal intestinal epithelium that breaks down disaccharides and more complex carbohydrates. As a result, if hypoglycemia were to occur in a patient on an α-glucosidase inhibitor, reversal requires either the consumption of glucose itself (as opposed to complex carbohydrates) or the injection of glucagon.
Question: 5 of 60
Which of the following medications can cause hyperglycemia? (Mark all that are true.)
- Niacin
- Clozapine (Clozaril)
- Prednisone
- Spironolactone
- Ramipril (Altace)
- Niacin
- Clozapine (Clozaril)
- Prednisone
- Spironolactone
- Ramipril (Altace)
Critique:
Several medications have been shown to affect glucose homeostasis, resulting in impaired glucose tolerance and hyperglycemia. Agents associated with the development of hyperglycemia include
- pentamidine,
- niacin,
- glucocorticoids,
- thyroid hormone,
- diazoxide,
- β-adrenergic agonists,
- thiazide diuretics,
- phenytoin, and
- α-interferon.
In addition, second-generation antipsychotic agents, particularly clozapine and olanzapine, have also been linked to the development of hyperglycemia and diabetes mellitus.
Spironolactone and ramipril have not been linked to the development of diabetes. In fact, in the HOPE (Heart Outcomes Prevention Evaluation) study, the use of ramipril, an ACE inhibitor, appeared to reduce the risk for developing type 2 diabetes mellitus by 20%–35%.
Question: 6 of 60
A 55-year-old African-American male sees you for a routine visit. His past medical history is notable for an 8-year history of diabetes mellitus and a past history of hypercholesterolemia. His current medications are atorvastatin (Lipitor), 20 mg/day, and extended-release metformin (Glucophage XR), 1000 mg/day. He also reports a history of peanut allergy manifested by lip angioedema, and carries an epinephrine auto-injector (EpiPen).
On examination he has a blood pressure of 124/80 mm Hg. His hemoglobin A1c is 6.7%. A spot urine sample contains 40 µg albumin/mg creatinine.
You see the patient 6 months later for a follow-up visit, and a spot urine sample has an albumin/creatinine ratio of 45 µg/mg.
Which one of the following would be most appropriate initially?
- Have the patient return in 6 months for a repeat urine test for albumin and creatinine
- Order a 24-hour urine collection for creatinine
- Recommend that the patient reduce his daily protein intake to 1.5 g/kg/day
- Begin an ACE inhibitor
- Begin an angiotensin receptor blocker
- Have the patient return in 6 months for a repeat urine test for albumin and creatinine
- Order a 24-hour urine collection for creatinine
- Recommend that the patient reduce his daily protein intake to 1.5 g/kg/day
- Begin an ACE inhibitor
- Begin an angiotensin receptor blocker
Critique:
Diabetic nephropathy develops in 20%–40% of patients with diabetes, and is the leading cause of end-stage renal disease. Persistent albuminuria in the range of 30–200 mg/24 hr (microalbuminuria) is the earliest sign of nephropathy in patients with type 1 diabetes, and is a marker for nephropathy in type 2 diabetes. Patients with microalbuminuria who progress to macroalbuminuria (>300 mg/24 hr) are likely to progress to end-stage renal disease over a period of years.
Although timed 4- and 24-hour urine collections for creatinine can be used to screen for microalbuminuria, a random spot urine specimen for measurement of the albumin-to-creatinine ratio is the preferred method. A minimum of two of three tests showing a urine albumin level >30 µg/mg creatinine or more over a 6-month period confirms the diagnosis of microalbuminuria.
Intensive diabetic management and the use of ACE inhibitors and angiotensin receptor blockers (ARBs) have been shown to delay the progression from microalbuminuria to macroalbuminuria in patients with type 1 or type 2 diabetes. Since the antiproteinuric effect is believed to be independent of blood pressure, current ADA guidelines recommend the use of ACE inhibitors or ARBs as first-line therapy for both type 1 and type 2 diabetic patients with microalbuminuria, even if their blood pressure is normal. Some studies, however, have raised questions about the value of early renin-angiotensin blockade for preventing microalbuminuria in normotensive patients with type 1 or type 2 diabetes, and ADA guidelines recommend against the use of these drugs for patients with normal blood pressure and no albuminuria.
Compared to whites, African-Americans and Asians have a three- to fourfold higher risk of angioedema associated with the use of ACE inhibitors. The American Heart Association recommends that ACE inhibitors not be initiated in any patient with a history of angioedema.
Reduction of protein intake to 0.8–1.0 g/kg/day in the early stages of chronic kidney disease, and to 0.8 g/kg/day in the late stages, may improve renal function and should be considered in patients whose nephropathy seems to be progressive despite optimal glucose and blood pressure control and the use of an ACE inhibitor and/or an ARB.
Question: 7 of 60
True statements regarding carbohydrate intake and diabetes mellitus include which of the following? (Mark all that are true.)
- The glycemic index is not useful in the management of diabetes mellitus
- Carbohydrate sources high in protein are effective for treating hypoglycemia
- Low-fat diets are more effective for achieving weight loss than low-carbohydrate diets (<130 g/day)
- Excessive intake of sugar-sweetened beverages has been shown to increase the risk for diabetes mellitus
- Carbohydrates have fewer calories per gram than alcohol
- The glycemic index is not useful in the management of diabetes mellitus
- Carbohydrate sources high in protein are effective for treating hypoglycemia
- Low-fat diets are more effective for achieving weight loss than low-carbohydrate diets (<130 g/day)
- Excessive intake of sugar-sweetened beverages has been shown to increase the risk for diabetes mellitus
- Carbohydrates have fewer calories per gram than alcohol
Question: 8 of 60
A 51-year-old male with type 2 diabetes mellitus controlled with diet is found to have a serum triglyceride level of 350 mg/dL, an LDL-cholesterol level of 101 mg/dL, and an HDL-cholesterol level of 45 mg/dL.
Which one of the following supplements would most likely reduce his serum triglyceride levels?
- Vitamin E
- Vitamin C
- Omega-3 fatty acids
- Folate
- Chromium
- Vitamin E
- Vitamin C
- Omega-3 fatty acids @ 3 g/day
- Folate
- Chromium
Critique:
At a dosage of approximately 3 g/day, omega-3 (or n-3) fatty acids have been reported to reduce serum triglyceride concentrations by 25%–30%, with accompanying increases in LDL-cholesterol of 5%–10%, and in HDL-cholesterol of 1%–3%.
Question: 9 of 60
Which one of the following is INEFFECTIVE for treating pain syndromes arising from diabetic neuropathy?
- Tricyclic antidepressants
- SSRIs
- Duloxetine (Cymbalta)
- Pregabalin (Lyrica)
- Tricyclic antidepressants
- SSRIs
- Duloxetine (Cymbalta)
- Pregabalin (Lyrica)
Critique:
Control of pain represents one of the most challenging management issues in patients with diabetic neuropathy. Tricyclic antidepressants, anticonvulsants, and topical capsaicin have been shown to reduce the pain of diabetic neuropathy.
Pregabalin and duloxetine are both FDA-approved for the treatment of diabetic peripheral neuropathy.
Limited evidence suggests that SSRIs are no more effective than placebo. Although interventions with NSAIDs, transcutaneous electrical nerve stimulation (TENS), ACE inhibitors, and tramadol have been reported for diabetic neuropathy, systematic evaluations have not been published.
Question: 10 of 60
At a routine health maintenance visit, a 42-year-old obese male is found to have a fasting plasma glucose level of 118 mg/dL. Which one of the following is the most appropriate initial intervention for preventing or delaying the development of diabetes mellitus in this patient?
- Lifestyle modification
- Metformin (Glucophage)
- A thiazolidinedione
- An oral sulfonylurea agent
- An ACE inhibitor
- Lifestyle modification
- Metformin (Glucophage)
- A thiazolidinedione
- An oral sulfonylurea agent
- An ACE inhibitor
Critique:
Based on the clinical practice guidelines of the American Diabetes Association, impaired fasting glucose (IFG) is defined as a fasting plasma glucose of 100–125 mg/dL, and impaired glucose tolerance (IGT) as a 2-hour plasma glucose of 140–199 mg/dL. These two categories have been officially termed prediabetes and are considered risk factors for future diabetes and cardiovascular disease. Lifestyle modification focusing on weight loss and physical exercise is regarded as first-line therapy for preventing or delaying diabetes mellitus in patients with prediabetes.
In the Diabetes Prevention Program (DPP), lifestyle modification (5%–10% weight loss and moderate physical activity of 30 min/day) was associated with a 58% reduction of risk for developing diabetes.
Metformin can be considered for very high-risk individuals (elevation of both IFG and IGT and at least one other risk factor such as hemoglobin A1C >6%, hypertension, low HDL-cholesterol, elevated serum triglycerides, or family history of type 2 diabetes mellitus in a first degree relative); in the DPP it was associated with a 31% reduction in risk. It was most effective in patients with a BMI of at least 35 kg/m2 who were under age 60.
Question: 11 of 60
A 77-year-old obese male sees you for a routine visit. He has a 20-year history of hypertension, a 12-year history of type 2 diabetes mellitus complicated by the development of microalbuminuria and proliferative diabetic retinopathy, and a history of an inferior myocardial infarction 2 years ago. Although his diabetes had been adequately controlled with extended-release metformin (Glucophage XR), 500 mg twice daily, you recently added extended-release glipizide (Glucotrol XL), 2.5 mg once daily in the morning, because his hemoglobin A1c rose to 7.1%. He reports that since then he has episodically experienced shakiness and diaphoresis in the late morning, relieved by drinking orange juice. Several of these episodes have occurred during walks he takes with his wife before eating lunch.
Which one of the following would be the most appropriate management?
- Reducing his metformin dosage to 500 mg in the morning
- Discontinuing glipizide and keeping the patient on his previous drug regimen
- Discontinuing glipizide and substituting nateglinide (Starlix)
- Advising the patient to eat lunch earlier in the day
- Advising the patient to delay his walk until after lunch
- Reducing his metformin dosage to 500 mg in the morning
- Discontinuing glipizide and keeping the patient on his previous drug regimen
- Discontinuing glipizide and substituting nateglinide (Starlix)
- Advising the patient to eat lunch earlier in the day
- Advising the patient to delay his walk until after lunch
Critique:
Although studies have clearly shown that intensive glycemic control reduces the risk for microvascular complications in patients with diabetes, it remains unclear whether it reduces the risk for cardiovascular disease as well. ACCORD, ADVANCE, and the Veterans Affairs Diabetes Trial have failed to show benefit, and the ACCORD trial actually reported an increased mortality rate in patients with type 2 diabetes treated with intensive therapy with a target hemoglobin A1c of <6.0%. Subjects in the ACCORD trial averaged 62 years of age and had diabetes for a mean duration of 10 years. Subjects either had a history of a cardiovascular disease (CVD) event between the ages 40 and 79, or had significant CVD risk and were between the ages 55 and 79. Based on the data available, the American Diabetes Association, in association with the American College of Cardiology Foundation and the American Heart Association, issued a position statement advising that less stringent hemoglobin A1c goals may be appropriate for patients with a history of severe hypoglycemia, limited life expectancy, advanced microvascular or macrovascular complications, poor health, or long-standing diabetes mellitus recalcitrant to therapy. A hemoglobin A1c of <7.0% is still recommended for the majority of patients with diabetes mellitus, with a target hemoglobin A1c closer to normal reserved for healthy patients with a short duration of disease and a long life expectancy (SOR C).
Question: 12 of 60
True statments regarding dipeptidyl peptidase-4 inhibitors include which of the following? (Mark all that are true.)
- They are more effective than metformin for lowering hemoglobin A1c
- They reduce insulin resistance
- They augment glucagon secretion
- They are weight neutral
- They are not associated with hypoglycemia
- They are more effective than metformin for lowering hemoglobin A1c
- They reduce insulin resistance
- They augment glucagon secretion
- They are weight neutral
- They are not associated with hypoglycemia
Critique:
Oral dipeptidyl peptidase-4 (DPP-4) inhibitors are oral hypoglycemic agents that work by enhancing circulating concentrations of active glucagon-like peptide 1 (GLP-1) and glucose-dependent insulinotropic peptide (GIP). These agents lower glucose by increasing insulin secretion and reducing glucagon secretion in a glucose-dependent manner. Oral DPP-4 inhibitors are generally felt to be less effective than metformin and the sulfonylureas for lowering glucose, with an expected HbA1c reduction in the range of 0.5%–1.0% compared to 1.0%–1.5% for metformin and the sulfonylureas. DPP-4 inhibitors are considered weight neutral and are not associated with hypoglycemia. Side effects include nasopharyngitis, upper respiratory tract infection, and headache.
Question: 13 of 60
A 62-year-old male sees you for the first time. His past medical history is notable for a long history of type 2 diabetes and hypertension, as well as a history of myocardial infarction 5 years ago and New York Heart Association class III heart failure. His current medications are hydrochlorothiazide, 25 mg daily; valsartan (Diovan), 320 mg daily; metoprolol succinate (Toprol XL), 50 mg daily, metformin (Glucophage), 850 mg twice daily; rosuvastatin (Crestor), 20 mg daily; and aspirin, 81 mg daily. Notable findings on examination include a blood pressure of 135/84 mm Hg and a heart rate of 58 beats/min. Laboratory findings include a hemoglobin A1C of 7.8%, an LDL-cholesterol level of 70 mg/dL, an HDL-cholesterol level of 35 mg/dL, a serum triglyceride level of 210 mg/dL, and an estimated glomerular filtration rate of 71 mL/min/1.73 m2.
Which one of the following has been shown to reduce cardiovascular risk in patients such as this?
- Glipizide extended-release (Glucotrol XL)
- Liraglutide (Victoza)
- Niacin
- Pioglitazone (Actos)
- Saxagliptin (Onglyza)
- Glipizide extended-release (Glucotrol XL)
- Liraglutide (Victoza) – only FDA approved hypoglycemic agent for LOWERING risk of cardiovascular event.
- Niacin
- Pioglitazone (Actos)
- Saxagliptin (Onglyza)
Critique:
The LEADER trial (Liraglutide Effect and Action in Diabetes: Evaluation of Cardiovascular Outcome Results) was a double-blind trial that compared the use of liraglutide, a GLP-1 analogue, to placebo in 9340 patients with type 2 diabetes at high cardiovascular risk. After a mean follow-up of 3.8 years, liraglutide was found to significantly reduce the rate of death from cardiovascular causes, as well as the first occurrence of nonfatal myocardial infarction and nonfatal stroke (hazard ratio, 0.87; 95% confidence interval [CI], 0.78 to 0.97). The rate of death from any cause was also reduced (SOR B).
Cardiovascular outcome studies evaluating DPP-4 inhibitors such as sitagliptin, saxagliptin, and alogliptin have yet to demonstrate a significant reduction in adverse cardiovascular events in patients with diabetes. In addition, the SAVOR-TIMI trial (Saxagliptin Assessment of Vascular Outcomes Recorded in Patients with Diabetes Mellitus—TIMI 53) reported a higher risk for hospitalization for heart failure associated with saxagliptin treatment compared to placebo. Although a reduced risk for stroke has been reported with pioglitazone, thiozolidenediones are associated with fluid retention, which can lead to weight gain, edema, and heart failure. Their use is contraindicated in patients with New York Heart Association class III or IV heart failure. Oral sulfonylureas are potent glucose-lowering agents associated with a higher risk for hypoglycemia. Studies have not shown a reduced cardiovascular risk with their use, and the University Group Diabetes Program (UGDP) trial reported a higher risk of cardiovascular death associated with the use of tolbutamide.
Although niacin might have been a consideration in the past in an effort to raise HDL-cholesterol and lower triglycerides, support for its use was dampened by the findings of the AIM-HIGH trial (Atherothrombosis Intervention in Metabolic Syndrome with Low HDL/High Triglycerides: Impact on Global Health Outcomes), which found no clinical benefit from adding sustained-release niacin to a statin in patients with known coronary heart disease and low HDL-cholesterol.
Question: 14 of 60
A 66-year-old male who was hospitalized because of a TIA 3 months ago sees you for a follow-up visit. His past medical history is notable for impaired fasting glucose and mild hypertension. His current medications are valsartan (Diovan), 160 mg daily; rosuvastatin (Crestor), 20 mg daily; and aspirin, 81 mg daily. On examination his BMI is 30.2 kg/m2, his blood pressure is 134/86 mm Hg, and he has brown, velvety, hyperkeratotic plaques on the back of his neck and in his axilla. His laboratory studies are notable for an LDL-cholesterol level of 85 mg/dL, an HDL-cholesterol level of 35 mg/dL, and a serum triglyceride level of 174 mg/dL.
Which one of the following agents may reduce his risk for stroke and myocardial infarction?
- Basal insulin
- Acarbose (Precose)
- Glipizide (Glucotrol)
- Pioglitazone (Actos)
- Sitagliptin (Januvia)
- Basal insulin
- Acarbose (Precose)
- Glipizide (Glucotrol)
- Pioglitazone (Actos)
- Sitagliptin (Januvia)
Critique:
In addition to playing a primary role in the development of type 2 diabetes, insulin resistance is also found in more than half of patients without diabetes who experience an ischemic stroke or TIA. Although treatment of individual cardiovascular risk factors plays a major role in the management of these patients, treatment directly targeted at reducing insulin resistance may also have a role.
The Insulin Resistance Intervention in Stroke (IRIS) trial was a 4.8-year multicenter double-blind study that investigated the role of pioglitazone in nondiabetic stroke and TIA patients determined to have insulin resistance based on the homeostasis model assessment of insulin resistance (HOMA-IR) index.
- In this trial, the use of pioglitazone was associated with a 24% reduction in stroke and myocardial infarction and a 52% reduction in the risk of developing type 2 diabetes.
This potential benefit should be balanced against possible adverse events linked to thiazolidinedione use, including weight gain, edema, bone fracture, and bladder cancer.
Question: 15 of 60
Hypoglycemia is a possible side effect of which of the following diabetes agents? (Mark all that are true.)
- Insulin
- Pioglitazone (Actos)
- Metformin (Glucophage)
- Sulfonylureas
- Repaglinide (Prandin)
- Acarbose (Precose)
- Insulin
- Pioglitazone (Actos)
- Metformin (Glucophage)
- Sulfonylureas
- Repaglinide (Prandin)
- Acarbose (Precose)
Critique:
Hypoglycemia is a well-known complication of insulin therapy. Since sulfonylureas (SU’s) and repaglinide (Meglitinide) work by enhancing insulin secretion, hypoglycemia is a complication of these two agents as well.
Used alone, acarbose, metformin, and thiazolidinediones (e.g., pioglitazone) are not associated with the development of hypoglycemia. It should be noted, however, that in June 2011, the FDA issued a drug safety alert reporting that use of pioglitazone for more than 1 year may be associated with an increased risk of bladder cancer.
Question: 16 of 60
True statements regarding dietary fat intake in patients with diabetes mellitus include which of the following? (Mark all that are true.)
- A Mediterranean-style diet rich in monounsaturated fats has been shown to improve glycemic control in patients with diabetes
- Trans fatty acids have been shown to lower LDL-cholesterol and raise HDL-cholesterol
- Saturated fats should provide 10% of caloric intake
- Omega-3 (or n-3) fatty acid supplementation is associated with a cardioprotective effect
- A gram of fat contains 50% more calories than a gram of carbohydrate
- A Mediterranean-style diet rich in monounsaturated fats has been shown to improve glycemic control in patients with diabetes
- Trans fatty acids have been shown to lower LDL-cholesterol and raise HDL-cholesterol
- Saturated fats should provide 10% of caloric intake
- Omega-3 (or n-3) fatty acid supplementation is associated with a cardioprotective effect
- A gram of fat contains 50% more calories than a gram of carbohydrate
Critique:
The primary goal with regard to fat intake in patients with diabetes is to limit saturated fat and trans fatty acids.
- National dietary guidelines recommend that intake of saturated fat be limited to <10% of daily calories.
Intake of trans unsaturated fatty acids should be minimized, since they have been shown to raise LDL-cholesterol and lower HDL-cholesterol.
A Mediterranean-style diet rich in monunsaturated fats has been found to improve both glycemic control and lipid levels in patients with diabetes.
Randomized, controlled trials do NOT support recommending omega-3 supplements for primary or secondary prevention of cardiovascular disease.
A gram of fat contains more than twice the calories of a gram of carbohydrate.
Question: 17 of 60
True statements regarding coronary heart disease in patients with diabetes mellitus include which of the following? (Mark all that are true.)
- Routine screening with a cardiac stress test is recommended in asymptomatic patients with diabetes who are at increased cardiovascular risk
- β-Blockers should be avoided in diabetic patients with coronary artery disease, due to the risk of masking hypoglycemia and reducing insulin secretion
- Long-term outcomes following percutaneous transluminal coronary angioplasty are as good in diabetic patients as in nondiabetic patients
- The survival of diabetic patients with multivessel disease is better with coronary revascularization with coronary artery bypass graft (CABG) surgery than with percutaneous transluminal coronary angioplasty
- Optimal glycemic control has been shown to reduce the risk of coronary heart disease in patients with type 2 diabetes
- Routine screening with a cardiac stress test is recommended in asymptomatic patients with diabetes who are at increased cardiovascular risk
- β-Blockers should be avoided in diabetic patients with coronary artery disease, due to the risk of masking hypoglycemia and reducing insulin secretion
- Long-term outcomes following percutaneous transluminal coronary angioplasty are as good in diabetic patients as in nondiabetic patients
- The survival of diabetic patients with multivessel disease is better with coronary revascularization with coronary artery bypass graft (CABG) surgery than with percutaneous transluminal coronary angioplasty
- Optimal glycemic control has been shown to reduce the risk of coronary heart disease in patients with type 2 diabetes
Critique:
Although atherosclerotic cardiovascular disease is the leading cause of morbidity and mortality in patients with diabetes, routine screening for coronary heart disease is NOT recommended since it has not been shown to improve cardiovascular outcomes provided cardiovascular risk factors are treated (SOR A).
The potential benefit of β-blockers in the diabetic patient with coronary artery disease outweighs the potential risk of masking hypoglycemia or reducing insulin secretion (SOR A).
Good glycemic control has been shown to reduce microvascular complications in patients with diabetes mellitus. Although the Diabetes Control and Complications Trial and the Epidemiology of Diabetes Interventions and Complications study found that intensive glycemic control initiated soon after the diagnosis of type 1 diabetes produced long-term protection from cardiovascular disease, the results of three large trials (ACCORD, ADVANCE, and VADT) published in 2008 suggested no reduction in cardiovascular disease risk with intensive glycemic control in patients with type 2 diabetes.
Mortality rates after percutaneous transluminal coronary angioplasty (PTCA) are generally higher in patients with diabetes mellitus than in nondiabetic patients.
The survival of diabetic patients with multivessel disease is better after coronary artery bypass graft (CABG) surgery than after PTCA. This was shown in the FREEDOM trial (Future Revascularization Evaluation in Patients with Diabetes Mellitus: Optimal Management of Multivessel Disease), a randomized trial of 1900 patients with diabetes and multivessel coronary heart disease.
Treatment with CABG was associated with both a lower rate of myocardial infarction and lower mortality compared to PCI with drug-eluting stents (SOR A).
Question: 18 of 60
The threshold fasting plasma glucose level recommended for confirming the diagnosis of diabetes mellitus is ________ mg/dL
Fast BSL 126 mg/dL (or HA1c > 6.5)
Critique:
According to the current criteria of the American Diabetes Association, the diagnosis of diabetes mellitus should be made if any one of the following criteria is met:
- fasting plasma glucose ≥126 mg/dL
- 2-hour post load glucose ≥200 mg/dL on oral glucose tolerance testing
- hemoglobin A1c ≥6.5%
- symptoms of diabetes plus a casual plasma glucose level ≥200 mg/dL
Question: 19 of 60
A 62-year-old African-American male with a 10-year history of type 2 diabetes is diagnosed with hypertension. His current medications include metformin (Glucophage XR), 1500 mg daily; sitagliptin (Januvia), 100 mg daily; and simvastatin (Zocor), 40 mg daily. His blood pressure at today’s visit is 154/94 mm Hg. His urine is negative for microalbuminuria.
Which one of the following is true regarding treatment recommendations for this patient?
- Current American Diabetes Association (ADA) guidelines recommend treatment to a systolic blood pressure goal of <130 mm Hg and a diastolic blood pressure goal of <85 mm Hg
- JNC 8 guidelines recommend treatment to a systolic blood pressure goal <150 mm Hg and a diastolic blood pressure goal of <90 mm Hg
- The SPRINT trial supports targeting a systolic blood pressure goal of <120 mm Hg
- ADA guidelines recommend initiating therapy with either an ACE inhibitor or an angiotensin receptor blocker
- JNC 8 guidelines recommend initiating therapy with either a thiazide-like diuretic or a dihydropyridine calcium channel blocker
- Current American Diabetes Association (ADA) guidelines recommend treatment to a systolic blood pressure goal of <130 mm Hg and a diastolic blood pressure goal of <85 mm Hg
- JNC 8 guidelines recommend treatment to a systolic blood pressure goal <150 mm Hg and a diastolic blood pressure goal of <90 mm Hg
- The SPRINT trial supports targeting a systolic blood pressure goal of <120 mm Hg
- ADA guidelines recommend initiating therapy with either an ACE inhibitor or an angiotensin receptor blocker
- JNC 8 guidelines recommend initiating therapy with either a thiazide-like diuretic or a dihydropyridine calcium channel blocker
Critique:
Although randomized clinical trials have shown the cardiovascular and renal benefit of antihypertensive treatment targeting a systolic blood pressure <140 mm Hg and a diastolic blood pressure <90 mm Hg, they have not generally demonstrated additional benefit with more intensive therapy (targeting a systolic blood pressure <120–30 mm Hg and a diastolic blood pressure <80 mm Hg) in patients with diabetes.
JNC 8 guidelines recommend a target systolic blood pressure of <150 mm Hg and a target diastolic blood pressure of <90 mm Hg in individuals over 60 years of age, but the guidelines recommend a target systolic blood pressure of <140 mm Hg in individuals over 18 years of age with diabetes mellitus (SOR C).
Current American Diabetes Association (ADA) guidelines generally recommend a target systolic blood pressure of <140 mm Hg and a target diastolic blood pressure of <90 mm Hg (SOR A), with lower targets, such as 130/80 mm Hg, for high-risk patients with diabetes if these goals are achievable without undue treatment burden (SOR C). The 2017 ACC/AHA hypertension guidelines take a more aggressive approach, recommending antihypertensive drug treatment be initiated at a blood pressure of 130/80 mm Hg or higher, with a treatment goal of <130/80 mm Hg in patients with diabetes.
With the exception of the diabetic patients with albuminuria, ADA guidelines recommend initiating therapy with any of the antihypertensive agents shown to reduce cardiovascular events in patients with diabetes, which includes ACE inhibitors, angiotensin receptor blockers (ARBs), thiazide-like diuretics, and dihydropyridine calcium channel blockers. First-line treatment with an ACE inhibitor or ARB is recommended by the ADA for diabetic individuals with albuminuria (SOR B). In the general African-American population, including those with diabetes, JNC 8 guidelines favor initial treatment with a thiazide-like diuretic or dihydropyridine calcium channel blocker; however, in patients with chronic kidney disease, regardless of race or diabetes status, both JNC 8 and the ADA recommend initial therapy with an ACE inhibitor or ARB.
SPRINT (Systolic Blood Pressure Intervention Trial) was a randomized, controlled, open-label trial that compared aggressive treatment to a target systolic blood pressure <120 mm Hg with a target of <140 mm Hg in patients at increased cardiovascular risk. Although it did find that targeting a systolic blood pressure of <120 mm Hg resulted in lower rates of fatal and nonfatal major cardiovascular events, patients with diabetes or history of previous stroke were specifically excluded from the study.
Question: 20 of 60
Endocrinopathies associated with diabetes mellitus include which of the following? (Mark all that are true.)
- Cushing’s syndrome
- Acromegaly
- Pheochromocytoma
- Gastrinoma
- Glucagonoma
- Cushing’s syndrome
- Acromegaly
- Pheochromocytoma
- Gastrinoma
- Glucagonoma
Critique:
Endogenous gluconeogenic hormones include cortisol, norepinephrine, epinephrine, glucagon, and growth hormone. Accordingly, endocrinopathies associated with excessive levels of these hormones can cause glucose intolerance and diabetes; such disorders include
- acromegaly,
- Cushing’s syndrome,
- glucagonoma, and
- pheochromocytoma.
- Hyperthyroidism has also been shown to be associated with diabetes mellitus. In addition,
- somatostatinomas and
- aldosteronomas can cause diabetes, most likely by inhibiting insulin secretion.
Question: 21 of 60
According to National Cholesterol Education Program guidelines, criteria for the diagnosis of metabolic syndrome include which of the following? (Mark all that are true.)
- A waist circumference >40 inches in males
- An HDL-cholesterol level <50 mg/dL in females
- An LDL-cholesterol level ≥160 mg/dL
- A serum triglyceride level ≥150 mg/dL
- Diastolic blood pressure ≥85 mm Hg
- A waist circumference >40 inches in males
- An HDL-cholesterol level <50 mg/dL in females
- An LDL-cholesterol level ≥160 mg/dL
- A serum triglyceride level ≥150 mg/dL
- Diastolic blood pressure ≥85 mm Hg
Critique:
Metabolic syndrome is a constellation of cardiovascular risk factors related to hypertension, abdominal obesity, dyslipidemia, and insulin resistance.
Diagnostic criteria for metabolic syndrome, according to the National Cholesterol Education Program (Adult Treatment Panel III Guidelines), include the presence of three or more of the following:
- obesity, with a waist circumference exceeding 102 cm (40 inches) in men or 88 cm (35 inches) in women;
- blood pressure ≥130 mm Hg systolic and/or 85 mm Hg diastolic;
- a fasting glucose level ≥110 mg/dL;
- a serum triglyceride level ≥150 mg/dL; and
- an HDL-cholesterol level <40 mg/dL in men or <50 mg/dL in women.
Question: 22 of 60
A 62-year-old female is diagnosed with type 2 diabetes mellitus on the basis of consecutive fasting plasma glucose levels of 138 mg/dL and 143 mg/dL. Current American Diabetes Association guidelines recommend which of the following as part of her initial management? (Mark all that are true.)
- Lifestyle intervention
- Metformin (Glucophage)
- An oral sulfonylurea
- A thiazolidinedione
- Pramlintide (Symlin)
- Lifestyle intervention
- Metformin (Glucophage)
- An oral sulfonylurea
- A thiazolidinedione
- Pramlintide (Symlin)
Critique:
Most individuals with type 2 diabetes mellitus fail to achieve or maintain metabolic goals with only lifestyle intervention, because of failure to lose or maintain weight loss, progressive disease, or a combination of factors. As a result, current American Diabetes Association treatment guidelines recommend that metformin be initiated concurrently with lifestyle intervention at the time of diagnosis of type 2 diabetes mellitus.
Question: 23 of 60
Pharmacologic agents found to be effective in reducing the progression of impaired glucose tolerance to overt diabetes include which of the following? (Mark all that are true.)
- Acarbose (Precose)
- Metformin (Glucophage)
- Repaglinide (Prandin)
- Pioglitazone (Actos)
- Orlistat (Alli, Xenical)
- Acarbose (Precose)
- Metformin (Glucophage)
- Repaglinide (Prandin)
- Pioglitazone (Actos)
- Orlistat (Alli, Xenical)
Critique:
There is evidence that a number of pharmacologic interventions may be of value in preventing the development of type 2 diabetes mellitus in patients with impaired glucose tolerance (or prediabetes). Drug therapy with
- metformin (a biguanide),
- orlistat (a lipase inhibitor),
- GLP-1 receptor agonists, or
- acarbose (an α-glucosidase inhibitor)
has been shown to delay or prevent the progression of impaired glucose tolerance to type 2 diabetes.
The ACT NOW study reported a reduction of incident type 2 diabetes in patients with impaired glucose tolerance or impaired fasting glucose treated with pioglitazone. In addition, the ACT NOW study recently reported that compared to placebo, pioglitazone reduced the risk of conversion of impaired glucose tolerance to type 2 diabetes by 72%.
It should be noted, however, that in June 2011, the FDA issued a drug safety alert reporting that use of pioglitazone for more than 1 year may be associated with an increased risk of bladder cancer. After factoring in cost, side effects, and evidence of long-term effect, American Diabetes Association guidelines recommended metformin as the only drug for use in diabetes prevention.
Question: 24 of 60
A 29-year-old female with polycystic ovary syndrome (PCOS) asks if you can correct her oligomenorrhea. Her fasting glucose level is 100 mg/dL and her hemoglobin A1c is in the desirable range.
Which one of the following diabetes medications would be most appropriate for managing her oligomenorrhea?
- Glyburide (DiaBeta)
- Metformin (Glucophage)
- Pioglitazone (Actos)
- Miglitol (Glyset)
- Repaglinide (Prandin)
- Glyburide (DiaBeta)
- Metformin (Glucophage)
- Pioglitazone (Actos)
- Miglitol (Glyset)
- Repaglinide (Prandin)
Critique:
Polycystic ovary syndrome affects an estimated 6% of women of reproductive age. Insulin resistance with compensatory hyperinsulinemia is thought to play a major role in the etiology of this syndrome, which is characterized by anovulation and hyperandrogenism. Metformin and thiazolidinediones (i.e., pioglitazone and rosiglitazone) are oral hypoglycemic agents that reduce insulin resistance and have been shown to increase the frequency of ovulation in patients with this syndrome.
Caution is advised with the use of thiazolidenediones, however. In addition to troglitazone being withdrawn from the market, a meta-analysis of 42 studies found a 43% increased risk of myocardial infarction in patients taking rosiglitazone compared with other antidiabetic agents. This increased risk was subsequently corroborated by another published meta-analysis. In addition, the FDA issued a drug safety alert in 2011 reporting that use of pioglitazone for more than 1 year may be associated with an increased risk of bladder cancer. However, in November 2013 the FDA determined that more recent data indicates that rosiglitazone-containing drugs do not increase the risk of heart attack when compared to metformin and sulfonylurea, and removed the prescribing and dispensing restrictions.