CardioAdvocate
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The Sweet Spot

Dr. Ian Riddock
Why type 2 diabetes patients continue to fall through the cracks
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Case Presentations

Patient A: 

49 year old male with Type 2 diabetes mellitus (T2DM) and CAD with a previous stent to the LAD presents for routine endocrinology visit to discuss his diabetes management. 

His A1C is 7.5% and stable compared to last year. He is on metformin and glimepiride. 

He asks about new medications he saw on television which may be good for his heart.

He is advised that he is doing great, with his A1C right in the “sweet spot”

Years ago, his doctor attended a lecture at a national conference where they discussed studies showing that overaggressive management of blood sugar, with an A1C less than 7%, was associated with an increase in adverse cardiac events. Similarly, undertreatment of blood sugar, with an A1C greater than 8% showed an increase in adverse outcome. 

With his A1C of 7.5% right in the “sweet spot” he is encouraged to continue his present management.

Patient B: 

A 42 year old female with Type 2 diabetes mellitus and obesity with BMI 31kg/m2 presents for a primary care visit to discuss her cholesterol management. 

Her LDL-C is 77 mg/dL, HDL-C 37 mg/dL, TG 213 mg/dL. 

She is informed that her LDL-C numbers are outstanding and at her age, she does not need to start taking a statin. 

However, her TGs are a little high and she was encouraged to work harder on a low carb diet.

Patient C: 

A 57 year old male with T2DM and a recent heart attack (STEMI) treated with a stent to the LAD 6 months ago, presents to his cardiologist to review his progress. He has finished cardiac rehab, has been adhering to a Mediterranean diet and been faithfully taking the maximum dose of rosuvastatin at 40 mg daily, which was initiated in the hospital, without any side effects.

Labs from 1 week prior to the visit reveal an LDL-C is 68 mg/dL, TG 216 mg/dL, HDL-C 40 mg/dL. 

He is told no additional treatments are needed for his lipids since his LDL-C is below the recommended goal of 70 mg/dL. 

Patient D:

A 57 year old female with T2DM, Heart Failure with a Preserved Ejection Fraction (HFpEF) and obesity with BMI 31 kg/m2, presents to her cardiologist following a recent stay in the hospital for 4 days for heart failure, characterized by shortness of breath with fluid in her lungs (pulmonary vascular congestion) and legs (edema). 

She was placed on furosemide and instructed to follow up with her cardiologist. 

Since then she has lost 8 lbs and feels much better. 

On exam, her cardiologist notes that her lungs are clear and the lower extremity edema has resolved. 

She is congratulated on the weight loss and her furosemide is reduced to once daily. She is advised to avoid salt and weigh herself daily, while keeping track in a diary. 

She asks about newer diabetes drugs she heard about on TV that reduce risk for heart failure hospitalization, such as Farxiga, Jardiance, Invokana and others that reduce cardiovascular risk and help with weight loss such as Ozempic.

Her cardiologist informs her that the drugs are expensive but she can talk to her primary care doctor or endocrinologist about them, since those are not drugs that cardiologists prescribe.

Flying Under the Radar

Why do these cases go undertreated?

The cases above represent some of the most frequent lapses and missed opportunities in the cardiometabolic care of the diabetic patient:

Patient A: 

  • Missing the point of landmark clinical trials
    • It’s about how you get to euglycemia
    • The failure of previous therapies employed to achieve intense glucose lowering is not a free pass to undertreat. An A1C of 7.5% is not desirable.
  • Taking the easy way out by persisting with outdated, yet inexpensive (and therefore easier to prescribe) sulfonylurea drugs that have been relegated below several other proven therapies in just about every guideline. 
    • Yes, new branded medications can be expensive and may require labor intensive prior authorizations, but the patient needs to be informed.
    • Help is on the way with Federal initiative to make branded diabetes drugs cheaper
    • Farxiga (dapagliflozin) now has a generic
  • It’s not always about the sugar anymore. 
    • Several clinical trials have now shown that glycemic control has little impact on major cardiovascular events.
  • Thankfully, we now have many therapies that, independent of glycemic improvement, also improve cardiovascular endpoints



Patient B: 

  • Lack of awareness of guideline recommendations
  • Reliance on suboptimal metrics - in this case, LDL-C is less accurate and underestimates risk compared with nonHDL-C when TGs are elevated (see Atherogenic Triad article in Phenotypes)
  • Failure to appreciate high lifetime risk and implementing early prevention - another example of undertreating cardiovascular risk in the female (diabetic) patient.

Patient C: 

  • Applying outdated and more conservative guidelines to our highest risk patients - LDL-C needs to be much lower
  • Failing to appropriately inform patients of potentially life saving therapies they may be eligible for
    • Even if some practitioners feel there is controversy with the REDUCE-IT Trial (see Something Smells Fishy - The Controversy with Fish Oil) , patients ought to be informed of icosapent ethyl (Vascepa) when they fit the indications for it. That’s part of shared decision making.

Patient D: 

  • Passing the buck - assuming some other specialist will take care of it.
  • We are in an interesting time in medicine, where multiple classes of diabetes medications now have separate indications for improving cardiovascular disease risk - independent of glycemic control. 
  • “I don’t treat diabetes”
    • It’s not acceptable for a cardiologist to fail to treat the underlying cardiovascular risk in a high risk heart failure patient recently hospitalized, simply out of misplaced fear about a “diabetes” drug.

To put it bluntly, the diabetic patient is left behind due to a lack of cohesiveness across medical disciplines. The PCP, already burdened with everything else, is left holding the bag when the specialists (cardiologists, endocrinologists and nephrologists) assume that the other is going to act. So, nobody acts, and the diabetic patient is exposed to unnecessary “residual risk” when there are potentially effective treatments available. Far too often the patient is left in the dark and never finds out about these therapies. 

Instead of fostering mutual trust and building a multidisciplinary community that agrees to take advantage of every opportunity to attack this risk, at every encounter, the opposite often occurs. The cardiologist doesn’t want to step on the endocrinologist’s toes and vice versa. The PCP may yield to the specialist, assuming they had a reason not to act, rather than seeing it as a missed opportunity. 

This is why some are trying to create a “cardiometabolic” subspecialty in its own right. Someone needs to put it all together.

Read more in Deep Dive.

Recommendations

A checklist of targeted recommendations based on published guidelines

Cholesterol Management:

  • Check ApoB 
    • May be used as the preferred biomarker for all patients with high TG, diabetes, obesity, metabolic syndrome or “very low LDL-C” for screening, diagnosis, risk management (Ia ESC/EAS)

European Guidelines:

  • T2DM at very high risk
    • LDL-C ≥ 50% reduction, and
    • LDL-C

No advice set

Deep Dive

Going into detail on the evidence behind the recommendations and history of treatment for this phenotype.

Patient A: 

The #1 killer in diabetic patients is heart disease, particularly coronary artery disease and heart failure. 

So, what has been the primary objective in treating diabetes? Controlling blood sugar, right?

One would think that if you optimally control blood sugar then you should see benefits in its worst outcome - cardiovascular disease, right? Wrong. 

Intense Glucose Lowering:

The UKPDS Trial: (The UK Prospective Diabetes Study (UKPDS): clinical and therapeutic implications for type 2 diabetes) failed to show reduction in cardiovascular events in those treated to reduce an A1C from 8.0% to 7.0% (although, a subset of patients treated with metformin had lower event rates.) 

Too many practitioners remain under the outdated impression that they dare not treat type 2 diabetic too aggressively, as this leads to an increase in mortality.  

This notion is born out of older randomized controlled trials, such as the ACCORD Trial: (Effects of Intensive Glucose Lowering in Type 2 Diabetes | NEJM), showing that the “intensive” therapy arm in diabetes did worse than the “standard” treatment arm, and the ADVANCE Trial: (Intensive Blood Glucose Control and Vascular Outcomes in Patients with Type 2 Diabetes | NEJM) which showed no significant difference in major cardiovascular events but did show a difference in microvascular outcomes (nephropathy) when randomized to an “intensive” therapy of sulfonylurea plus other medications as needed to achieve an A1C of 6.5% or less. 

A breakdown of these two trials is well summarized in this editorial: Intensive Glycemic Control in the ACCORD and ADVANCE Trials | NEJM.

In brief, the ACCORD trial randomized ~10,000 type 2 diabetics with A1C of 8.1% at baseline to an “intensive” treatment arm aimed at achieving an A1C


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