A Practical Guide for Cardiologists to the Pharmacological Treatment of Patients with Type 2 Diabetes and Cardiovascular Disease

Abstract

Patients with type 2 diabetes are at increased cardiovascular risk. Until recently, reductions in HbA_1c and the use of specific glucose-lowering agents have not had a clear, reproducible benefit in reducing the incidence of cardiovascular disease. However, over the past 5 years, members of two categories of diabetes medications, sodium–glucose cotransporter 2 inhibitors and glucagon-like peptide-1 receptor agonists, have been associated with improved rates of major adverse cardiovascular events when used in high-risk type 2 diabetes patients. Importantly, these effects are not necessarily linked to these agents’ effects on HbA_1c. Sodium–glucose cotransporter 2 inhibitors have also been associated with reductions in heart failure hospitalization, a benefit that appears to extend to individuals without diabetes with established heart failure. Cardiovascular specialists should become familiar with these emerging data and be prepared to implement corresponding strategies in their practice to improve the cardiovascular outcomes of their patients. Recent clinical trial data and the changing landscape of corresponding professional guidelines are reviewed. Practical recommendations for safe prescribing of these anti-diabetes drugs are provided.

Patients with cardiovascular disease (CVD) and type 2 diabetes (T2D) suffer very high rates of cardiovascular (CV) morbidity and mortality.[1] Traditional paradigms for their treatments focus on the management of blood pressure and hyperlipidaemia by primary care physicians and/or cardiologists, and glucose control by primary care physicians and/or endocrinologists. As the ultimate goal of caring for these patients is to improve clinical outcomes, there has been a recent focus on alignment of goals, especially after the realisation that improvements in glucose management alone do not necessarily translate into the avoidance of adverse CV events.[2] One reason for these efforts was a mandate by the Food and Drug Administration (FDA) in 2008 to require an assessment of CV outcomes predominantly for the purpose of ensuring safety prior to approval of new glucose-lowering therapies for T2D. This requirement has resulted in the discovery of several novel agents to have significant benefits in the risk of major adverse CV events (MACE), a goal that had been previously largely elusive with older, traditional antihyperglycaemic medications.[3]

The greatly expanded therapeutic armamentarium for the treatment of patients with CVD and T2D has also stimulated a re-examination of the conventional roles of various medical specialties in their management. In a patient-centred model of care, all clinicians taking care of these high-risk patients should be comfortable prescribing therapies that improve outcomes – even if they have traditionally existed within disciplines. The goal of this review is to provide a brief history of the development of therapies for T2D, in the context of attempting to improve CV outcomes. We then provide a practical guide to the management of these patients that integrates the best available contemporary understanding and results from clinical trials, allowing the reader to be comfortable with the use of diabetes therapies that can now be used to address CVD risk.

Drug Development for Type 2 Diabetes: Focus on CVD

There has been a long track record in cardiology of therapies that improve surrogate measures of disease, but do not necessarily translate to better patient outcomes.[4] As a result, the threshold for therapeutic approval of cardiac medications by regulatory agencies has generally required a large, randomised controlled trial with clear, demonstrable benefits of actual clinical events. Until recently, however, this was not the case in drug development for diabetes medications. There was an assumption that tight glucose control, as reflected by improved HbA_1c, would lead not only to reductions in microvascular outcomes, such as retinopathy and diabetic kidney disease, but would also reduce macrovascular complications – despite a lack of definitive support for the latter. In fact, the ACCORD trial revealed increased CV mortality for patients assigned to a more intensive glucose-lowering strategy.[5] Other studies, such as ADVANCE and VADT, demonstrated no improvement in CV outcomes with more stringent glucose control.[6,7] These and other data have called into question the utility of the surrogate measure of HbA_1c for CV risk.[8]

Despite long-standing controversies regarding the link between glucose control and CV disease, it had always been presumed that glucose-lowering therapies would at least not increase adverse CV events. Indeed, prior to 2008, approval of T2D therapies was largely contingent on evidence of glycaemic efficacy based on HbA_1c reductions alone. An inflection point came when two meta-analyses raised concerns about the potential for increased CV risk with the thiazolidinedione rosiglitazone and an investigational dual peroxisome proliferator-activated receptor alpha/gamma agonist.[9,10] Although the overall CV safety of rosiglitazone was later mostly proved by a randomised clinical trial, concerns about diabetes drug safety stemming from these retrospective data sets persisted. In response, the FDA issued a guidance statement to the pharmaceutical industry in 2008, outlining expectations for the development of new antihyperglycaemic agents for T2D. This document essentially required all such therapies to demonstrate, at the minimum, CV safety when compared with a placebo.[3] Similar requirements were subsequently issued by the European Medicines Agency.

Rather than suppress innovation, as was once feared, many new therapies have since been evaluated under this new guidance with one or more dedicated CV safety studies. The results from these trials have provided unprecedented information about the CV impact of therapies tailored to target one of the most important risk factors for coronary artery disease and heart failure (HF).

In the decade since the FDA guidance was issued, there have been 25 long-term prospective clinical trials involving >200,000 participants. While some are yet to report, the available data have already transformed the management of patients with T2D and CVD. Trials showing reductions in MACE with two newer classes, sodium–glucose cotransporter 2 (SGLT-2) inhibitors and glucagon-like peptide-1 (GLP-1) receptor agonists, have in fact prompted a paradigm shift beyond a focus on glucose control alone towards more comprehensive CV risk reduction.[11] In accordance with these insights, there has been a call for cardiologists to play a more active role in prescribing medications for diabetes management, especially since their mechanism of benefit appears beyond merely lowering glucose.[12] Furthermore, these findings have streamlined the recommendations for therapies, as improvement in such hard outcomes has surpassed lowering of glycaemia as a therapeutic goal.

Modes of Action of Commonly Used Glucose-lowering Medications

Pharmacological advances in recent years have led to several mechanistically distinct therapies for T2D. The most commonly used classes of antihyperglycaemic agents can be broadly subdivided into those that increase insulin supply, improve the body’s response to insulin (insulin sensitisers), enhance incretin levels or promote urinary excretion of glucose (Figure 1).[13]

Figure 1: The Most Common Glucose-lowering Drug Classes Used in Type 2 Diabetes and Their Sites of Action.

DPP-4 = dipeptidyl peptidase-4; T2D = type 2 diabetes; GLP-1R = glucagon-like peptide-1 receptor; SGLT-2 = sodium–glucose cotransporter 2; SUs = sulfonylureas; TZD = thiazolidinedione.

Sulfonylureas work by stimulating insulin secretion and require residual beta cell function. The sulfonylurea receptor is a component of the adenosine triphosphate-sensitive potassium channel in the pancreatic beta cells. The triphosphate-sensitive potassium channel regulates insulin release from pancreatic beta cells. Sulfonylurea binding inhibits these channels, altering cell resting potential, leading to calcium influx, thereby stimulating insulin secretion. The net effect is increased beta cell responsiveness, promoting greater insulin release at any blood glucose concentration, with the consequent risk of hypoglycaemia.

Metformin, a biguanide, works mainly in the liver to reduce hepatic glucose production, and may be considered a liver insulin sensitiser. The precise mode of action at a cellular level remains controversial, but most likely involves alterations in mitochondrial respiration. When renal function is severely reduced, metformin accumulates in the plasma, and may predispose to lactic acidosis.

Thiazolidinediones reduce insulin resistance by binding to the peroxisome proliferator-activated receptor gamma nuclear receptor, which is found at the highest concentrations in adipocytes, promoting adipocyte differentiation, reducing hepatic fat accumulation and increasing fatty acid storage in peripheral, rather than central, locations. Glucose uptake into skeletal muscle increases and circulating insulin levels decrease with the use of thiazolidinediones, indicating a reduction in insulin resistance.

Pioglitazone has been shown to reduce MACE in high-risk T2D patients, as a secondary outcome in the PROactive study, and in insulin-resistant stroke patients without diabetes in the IRIS trial.[14,15] These drugs result in weight gain and oedema, and increase the risk of HF.

The three newest glucose-lowering drug categories include dipeptidyl peptidase-4 (DPP-4) inhibitors, GLP-1 receptor agonists and SGLT2 inhibitors. DPP-4 inhibitors reduce the degradation of the incretins – GLP-1 and glucose-dependent insulinotropic peptide – thus increasing insulin release, especially in the postprandial state, and suppressing glucagon release as well.[16] They are generally well tolerated. GLP-1 receptor agonists act directly on this pathway, and as more powerful agents, not only beneficially modulate pancreatic insulin and glucagon secretion, but also slow gastric emptying and decrease appetite, the latter probably through central mechanisms.[17] Major side-effects pertain to the gastrointestinal system. SGLT-2 inhibitors lower blood glucose by selectively inhibiting a cotransporter expressed in the proximal convoluted tubule of the nephron. This blocks glucose reabsorption, thereby reducing the renal threshold for glucose and leading to increased urinary glucose excretion.[18] Their major side-effects are genitourinary in nature.

Results from Cardiovascular Outcomes Trials

As noted, since the FDA guidance statement for CV safety with glucose-lowering therapies, several large, industry-sponsored, placebo-controlled trials have tested the safety and efficacy of these latter three groups of medications (Table 1). Most participants had established T2D and either overt CVD or were at high CVD risk owing to multiple concomitant risk factors.

Table 1: Overview of Cardiovascular Outcome Trials with Glucose-lowering Therapies.

Agent	Trial	Population	n	Median Follow-up (Years)	MACE Outcome, HR [95% CI]
Dipeptidyl Peptidase-4 Inhibitors
Saxagliptin	SAVOR	Age ≥40 years with ASCVD; ≥55 years men or ≥60 years women with ≥1 CV risk factor	16,492	2.1	HR 1.00 [0.89–1.12]
Alogliptin	EXAMINE	Age ≥18 years with recent ACS	5,380	1.5	HR 0.96 [≤1.16]
Sitagliptin	TECOS	Age ≥50 years with ASCVD	14,671	3.0	HR 0.98 [0.88–1.09]
Linagliptin	CARMELINA	History of ASCVD and micro- or macro-albuminuria	6,979	2.2	HR 1.02 [0.89–1.17]
Linagliptin	CAROLINA*	ASCVD; ≥2 CV risk factors; age ≥70 years and microvascular complications	6,042	6.3	HR 0.98 [0.84–1.14]
Glucagon-like Peptide-1 Receptor Agonists
Lixisenatide	ELIXA	Age ≥30 years with ASCVD	6,068	2.1	HR 1.02 [0.89–1.17]
Liraglutide	LEADER	Age ≥50 years with ASCVD; age ≥60 years with ≥1 CV risk factor	9,340	3.8	HR 0.87 [0.78–0.97]
Semaglutide	SUSTAIN-6	Age ≥50 years with ASCVD; CHF or stage 3–5 CKD; age ≥60 years with ≥1 CV risk factor	3,297	2	HR 0.74 [0.58–0.95]
Semaglutide (oral)	PIONEER-6	Age ≥50 years with ASCVD or CKD; ≥60 years with ≥1 CV risk factor	3,183	1.3	HR 0.79 [0.57–1.11]
Exenatide XR	EXSCEL	73% had ASCVD	14,752	3.2	HR 0.91 [0.83–1.00]
Albiglutide†	Harmony Outcomes	Age ≥40 years with ASCVD	9,463	1.6	HR 0.78 [0.68–0.90]
Dulaglitide	REWIND	Age ≥50 years with ASCVD, age ≥55 years with ASCVD or 1 CV risk factor; age ≥60 years with ≥2 CV risk factors	9,901	5.4	HR 0.88 [0.79–0.99]
Sodium–Glucose Cotransporter 2 Inhibitors
Empagliflozin	EMPA-REG OUTCOME	Age ≥18 years with ASCVD	7,020	3.1	HR 0.86 [0.744–0.99]
Canagliflozin	CANVAS	Age ≥30 years with ASCVD; age ≥50 years with ≥2 risk factors	10,142	3.6‡	HR 0.86 [0.75–0.97]
Canagliflozin	CREDENCE	eGFR 30–90 and albumin:creatinine ratio >300	4,401	2.6	HR 0.70 [0.59–0.82]
Dapagliflozin	DECLARE	Age ≥40 years with. ASCVD; age ≥55 years men with ≥2 CV risk factors; age ≥60 years women with ≥1 CV risk factor	17,160	4.2	HR 0.93 [0.84–1.03]
Dapagliflozin	DAPA-HF	NYHA class II–IV HF with LVEF ≤40%	4,744	1.5	HR 0.74 [0.65–0.85]
Ertugliflozin	VERTIS-CV	Age ≥40 years with ASCVD	9,463	1.6	HR 0.95 [0.85–1.11]

*Compared with glimepiride; all other trials are compared with placebo. †Removed from the market by the manufacturer due to poor penetration. ‡Data expressed as the mean. ACS = acute coronary syndrome; ASCVD = atherosclerotic cardiovascular disease; CHF = congestive heart failure; CKD = chronic kidney disease; CV = cardiovascular; eGFR = estimated glomerular filtration rate; HF = heart failure; LVEF = left ventricular ejection fraction; NYHA = New York Heart Association.

Dipeptidyl Peptidase-4 Inhibitors

Several DPP-4 inhibitor trials have been completed, showing neither inferiority nor superiority compared with a placebo with respect to MACE risk. Of note, however, saxagliptin was associated with an increased incidence of hospitalisation for HF in the SAVOR–TIMI 53 trial.[19]

There was also a non-statistically significant increase in hospitalisations for HF with alogliptin in the EXAMINE trial.[20] Such trends for HF were noted in neither the TECOS nor CARMELINA, large CV outcome trials involving two additional DPP-4 inhibitors versus a placebo, but also, neither was able to establish any CV superiority.[21,22] Finally, the CAROLINA demonstrated no differences in CV risk for linagliptin versus glimepiride in the only active comparator CV outcome trial for a DPP-4 inhibitor.[23]

As a result of these studies, DPP-4 inhibitors are deemed to be generally safe for use in high-risk CV patients, perhaps with the exception of saxagliptin and potentially alogliptin with regard to possible HF risk. However, this class clearly does not prevent CV events in high-risk patients with T2D.

Glucagon-like Peptide-1 Receptor Agonists

Several GLP-1 receptor agonists have demonstrated benefits for the reduction of adverse CV events among patients with T2D. Seven CV outcomes studies evaluating GLP-1 receptor agonists have been reported to date, with several showing superior CV outcomes.

The LEADER trial randomised 9,340 patients with T2D and high CV risk (the majority with established CVD) to liraglutide or a placebo in addition to standard of care.[24] After a median follow-up duration of 3.8 years, participants in the liraglutide group experienced a significantly reduced risk versus placebo for the primary composite three-point MACE outcome (CV death, non-fatal myocardial infarction or non-fatal stroke). Although CV mortality was also reduced, no reduction in HF events were observed.

The SUSTAIN-6 trial enrolled 3,297 patients using similar eligibility criteria and the same primary composite endpoint as LEADER. Although SUSTAIN-6 was not powered for superiority, semaglutide significantly reduced the risk of MACE in a consistent manner.[25] A separate trial examining oral as opposed to injectable semaglutide, PIONEER 6, randomised 3,183 high-risk T2D patients; rates of CV outcomes were similar in either arm of the trial, although both the secondary outcomes of CV and all-cause mortality appeared to be significantly reduced.[25]

The EXSCEL trial enrolled 14,752 subjects, with most having overt CVD, and showed a directionally lower risk of outcomes for exenatide compared with a placebo, but this difference did not reach statistical significance.[26]

Lixisenatide, which was tested in 6,068 patients with acute coronary syndrome in the ELIXA trial, showed no signal for any reduction in MACE.[27]

The HARMONY Outcomes randomised 9,463 participants with CVD, finding albiglutide to be superior to a placebo with respect to MACE.[28] Despite these findings, the drug’s manufacturer has withdrawn it from the worldwide market due to disappointing sales.

Finally, the REWIND trial involving 9,901 patients, most of whom had CV risk factors, but not established CVD, showed that weekly injections of dulaglutide improved CV outcomes in patients with type 2 diabetes regardless of prior CV events, with an overall effect size similar to that observed in other GLP-1 receptor agonist CV outcomes trials.[29]

A recently published meta-analysis included 56,004 participants and pooled data from ELIXA (lixisenatide), LEADER (liraglutide), SUSTAIN-6 (semaglutide), EXSCEL (exenatide), Harmony Outcomes (albiglutide), REWIND (dulaglutide) and PIONEER 6 (oral semaglutide).[30] Overall, GLP-1 receptor agonist treatment reduced MACE by 12% (HR 0.88; 95% CI [0.82–0.94]; p<0.0001), with no evidence of treatment heterogeneity across the subgroups examined. The drug class also appeared to broadly improve renal outcomes, reducing a composite of new-onset macroalbuminuria, decline in the glomerular filtration rate, progression to end-stage kidney disease or death attributable to kidney causes by 17% (HR 0.83; 95% CI [0.78–0.89]; p<0·0001). It should be noted, however, that in contrast to SGLT-2 inhibitors (see below), this renal composite endpoint is driven mainly by a reduction in macroalbuminuria, with no clear effect to decrease the decline in glomerular filtration rates. The authors appropriately concluded that treatment with GLP-1 receptor agonists (as a class) have beneficial effects on CV and, potentially, kidney outcomes in patients with T2D.[30]

Sodium–Glucose Cotransporter 2 Inhibitors

SGLT-2 inhibitors were the first glucose-lowering drug category to show a reduction in MACE among T2D patients at high CV risk. The EMPA-REG OUTCOME trial randomised 7,020 patients with T2D and established CVD to empagliflozin versus a placebo; those receiving empagliflozin had a lower rate of the primary composite three-point MACE than did patients receiving placebo.[31] Notably, the primary driver of this risk reduction was a striking 38% reduction in the risk of CV death. Moreover, the drug was associated with a 35% reduction in the risk of HF hospitalisation. In a prespecified secondary outcome, empaglifozin use was associated with a lower risk of progression of kidney disease, including both macroalbuminuria and ‘harder’ renal outcomes, such as a doubling of the serum creatinine level and initiation of renal replacement therapy.[32]

Following the EMPA-REG OUTCOME were results from the CANVAS program, which integrated findings from two placebo-controlled trials, and included 10,142 subjects with T2D and either known CVD or age >50 years, and at least two additional CV risk factors.[33] The rate of the MACE primary outcome was significantly lower with canagliflozin than with a placebo, and there was also similar evidence of benefit in regard to both HF hospitalisations and in the progression of kidney disease. The MACE benefit appeared to be concentrated among patients with established CVD, although the HF and renal benefits appeared to be shared by even those with CV risk factors alone.

Finally, the DECLARE–TIMI 58 trial randomised a lower-risk population – those with T2D who had or were at risk for atherosclerotic CVD – to receive either dapagliflozin or a placebo.[34] While there were no significant differences in the MACE dual primary outcome, a significant decrease in the risk of the second dual primary outcome, CV death or hospitalisation for HF was observed. Furthermore, as with the prior trials, there was a signal of benefit for various renal outcomes.

The final T2D-CV outcome trial involving an SGLT-2 inhibitor, ertugliflozin, was VERTIS CV, including 8,246 participants with T2D and established CVD. In contrast to the earlier studies, VERTIS CV did not meet its primary efficacy outcome.[35] While ertugliflozin was non-inferior to a placebo for MACE, the HRs for the composite (HR 0.97; 95% CI [0.85–1.11]) and each of its components was statistically neutral. However, HF hospitalisations were less frequent in the active therapy arm (HR 0.70; 95% CI [0.54–0.90]).

Findings from the first three CV outcome trials of SGLT-2 inhibitors were consolidated in a meta-analysis of 34,322 patients that summarised these drugs to have a moderate impact on MACE among patients with established CVD, but striking reductions in HF hospitalisations and progression of kidney disease regardless of the presence of overt CVD or HF at baseline.[36]

Moreover, observational data from large international studies of insurance claims, registries and electronic medical records from a broad T2D population observed in real-world practice have reinforced findings from the clinical trials.[37,38] For example, CVD-REAL compared a propensity-matched cohort of patients receiving other oral medications for T2D. Those receiving SGLT-2 inhibitors had a 51% lower associated risk of all-cause mortality and a 39% lower associated risk of hospitalisation for HF. Comparable results were found in the even larger CVD-REAL 2 study, with a 49% lower risk of all-cause mortality, 36% lower risk of hospitalisation for HF, and lower risks of MI and stroke.

Another real-world data set comes from the EMPRISE study in the US, in which the initiation of empagliflozin was associated with at 50% lower risk of HF hospitalisation compared with patients initiating therapy with sitagliptin (a DPP-4 inhibitor).[39] These findings buttress the benefits of SGLT-2 inhibitors in patients with T2D, as demonstrated in randomised clinical trials.

Finally, since a major benefit of SGLT-2 inhibitors was thought to be in patients with HF, several clinical trials are ongoing to test this hypothesis. The first of these, DAPA-HF, randomised 4,744 patients with left ventricular ejection fraction ≤40% and symptomatic HF to dapagliflozin versus a placebo. The primary outcome was a composite of worsening HF (hospitalisation or an urgent visit resulting in IV therapy for HF) or CV death, occurring significantly less in the dapagliflozin arm (HR 0.74; 95% CI [0.65–0.85]; p<0.001).[40] Importantly, the benefit did not appear to be dependent on whether the patient had diabetes or not. It is anticipated that SGLT-2 inhibitors will play a major role in the treatment of HF in the near future.[41]

Other dedicated HF studies with SGLT-2 inhibitors are underway or soon to report. These include EMPEROR-Reduced, EMPEROR-Preserved and DELIVER.

Prescribing Glucose-lowering Therapies for CVD

Currently, we have robust data demonstrating the benefits of GLP-1 receptor agonists and SGLT-2 inhibitors for patients with T2D and coexisting CV disease. According to the most current T2D treatment guidelines from the American Diabetes Association and the European Association for the Study of Diabetes, metformin is first-line therapy for these patients, mainly due to extensive clinical experience and comparably low cost.[42] Then, additional therapies are added, dictated initially by coexisting CV and/or kidney disease. If atherosclerotic CVD predominates the clinical picture, either a GLP-1 receptor agonist or a SGLT-2 inhibitor shown to improve CV outcomes should be used. If, in contrast, HF or CKD predominate, then a SGLT-2 inhibitor would be favoured, with a GLP-1 receptor agonist used if an SGLT-2 inhibitor were contraindicated; for example, if kidney dysfunction is too advanced. In addition, because the effects on glycaemia are unlikely to be driving the outcomes benefits of these agents, adding either GLP-1 receptor agonists and SGLT-2 inhibitors are now to be considered irrespective of HbA_1c – a radical departure from older glucocentric approaches.

The latest guidelines from the European Society of Cardiology are similar, but go a step further, proposing that for appropriate patients with or at high risk for CVD, beginning with an SGLT-2 inhibitor or a GLP-1 receptor agonist in lieu of metformin may be more prudent.[43] Both American Diabetes Association and the European Association for the Study of Diabetes and European Society of Cardiology guidelines now identify a broader group of patients eligible for CV risk reduction with these newer drug categories, no longer restricting them to those with overt CVD. Both sets of guidelines are reasonable, with the American Diabetes Association and the European Association for the Study of Diabetes consensus report still endorsing metformin as foundation therapy – a concept that is not necessarily any longer evidence-based.

Dosing and clinical considerations for these therapies are shown in Table 2. In cases of equipoise, other distinguishing features of these agents should dictate which one is initiated first. SGLT-2 inhibitors, for example, would seem to be preferred in the setting of HF or mild-to-moderate diabetic kidney disease. The available routes of administration are perhaps among the most evident differences – oral for SGLT-2 inhibitors and subcutaneous for most GLP-1 receptor agonists, although the first oral GLP-1 receptor agonist (semaglutide) recently became available. Cost may also vary substantially based on local market availability, health system or payer formularies and individual health insurance coverage.

Table 2: Prescribing Information for Glucagon-like Peptide-1 Receptor Agonists and Sodium–Glucose Cotransporter 2 Inhibitors (Based on US Labels).

Generic Name	Brand Name	Doses	Schedule	Additional Information
GLP-1R agonists (all injectables except Rybelsus)
Exenatide	Byetta	5, 10 µg	Twice daily	32 G pen needles supplied separately; prefilled, single-use pen
Exenatide extended release	Bydureon	2 mg	Weekly	23 G, hidden needles pre-attached; prefilled autoinjector device
Dulaglutide	Trulicity	0.75, 1.5 mg	Weekly	29 G hidden needles pre-attached; prefilled autoinjector device
Liraglutide	Victoza	0.6, 1.2, 1.8 mg	Daily	Indicated to reduce the risk of MACE in T2D with established CVD; 32-G pen needles supplied separately; prefilled, multi-dose pen
Lixisenatide	Adlyxin	10, 20 µg	Daily	≤8 mm pen needles supplied separately; prefilled, single-use pen
Semaglutide (injection)	Ozempic	0.25, 0.5 mg	Weekly	32 G 4 mm pen needles included; prefilled, single-use pen
Semaglutide (oral)	Rybelsus	3, 7, 14 mg	Daily	Only oral GLP-1RA available
SGLT-2 inhibitors (all oral tablets, most available in fixed-dose combinations with metformin)
Canagliflozin	Invokana	100, 300 mg	Daily	Indicated to reduce risk of MACE in T2D and established CVD; also indicated to reduce risk of progression of kidney disease, CV death and HF hospitalisation in T2D and diabetic kidney disease with macroalbuminuria
Dapagliflozin	Farxiga	5, 10 mg	Daily	Indicated to reduce risk of HF hospitalisation in T2D with established CVD or multiple CV risk factors
Empagliflozin	Jardiance	10, 25 mg	Daily	Indicated to reduce risk of CV death in T2D with established CVD
Ertugliflozin	Steglatro	5, 15 mg	Daily	CV outcomes trial (VERTIS-CV; NCT01986881)

CV = cardiovascular; CVD = cardiovascular disease; GLP-1R = glucagon-like peptide-1 receptor; GLP-1RA = glucagon-like peptide-1 receptor agonist; HF = heart failure; MACE = major adverse cardiovascular events; SGLT-2 = sodium–glucose cotransporter 2; T2D = type 2 diabetes.

Side-effects and Practical Considerations

Most GLP-1 receptor agonists appear to benefit patients in whom atherosclerotic heart disease predominates, but they may be associated with transient nausea and even vomiting, especially when initiating therapy or uptitrating the dose. The subcutaneous route of administration of most GLP-1 receptor agonists dictates that the individual characteristics of each injection pen should also be considered to match patient preferences. Multi-dose pens, for example, are available with liraglutide, semaglutide and exenatide extended release; these agents also use identical needles to insulin pen therapy, and therefore may already be more familiar to insulin users. However, for insulin-naïve patients, the manual dexterity required to attach and remove pen needles for GLP-1 receptor agonist injectable devices before and after use requires direct education.

For clinicians prescribing these therapies, extensive use of the teach-back technique during an office visit, preferably by experienced nurses or diabetes educators, to confirm a patient or caregiver’s ability to safely inject the medication may be necessary. Additionally, separate prescriptions for pen needles must be sent to the outpatient pharmacy if using liraglutide, exenatide and lixisenatide. Only injectable semaglutide contains pen needles in its original packaging. Dulaglitide or exenatide extended release contain built-in needles supplied in an autoinjector pen, which may be favourable for ease of use or patients for whom visible needles may be problematic. Patients must be coached regarding low initial dosing and gradual uptitration to mitigate gastrointestinal side-effects. We avoid these drugs in patients with complex pancreato-biliary disease, prior history of pancreatitis (per label, although no risk has been demonstrated in clinical trials), gastroparesis, prior bariatric surgeries and multiple or significant baseline gastrointestinal symptoms.

An oral formulation of semaglutide recently became available. Because it uses a unique gastric absorption enhancer, this formulation must be taken on an empty stomach with a certain volume of water and with the subsequent avoidance of food or other medications for at least 30 minutes. However, this agent has not yet been demonstrated to reduce CV events.

SGLT-2 inhibitors are also preferred in the context of atherosclerotic CVD, but appear to be particularly beneficial in cases of HF and/or mild-to-moderate kidney disease. They are known to increase the risk of genital mycotic infections, although the latter are usually easily treatable with topical creams. Other considerations include polyuria (which may be specifically problematic in older men with prostatic disease) and the potential for reductions in volume, causing adverse events – those with HF taking loop diuretics may need their dose reduced, particularly if already volume contracted.

Caution is required when prescribing these agents (particularly canagliflozin) to patients with a history of prior amputations, significant peripheral artery disease, or active lower extremity soft tissue ulcers or infections. Rarely, diabetic ketoacidosis may occur (often euglycaemic, which may mask the initial presentation), but more commonly when these agents are used off-label in those with type 1 diabetes and, possibly, in very insulin-deficient, lean and more fragile T2D patients. Practical advice for the safe prescribing of these agents is listed in Table 3.

Table 3: Practical Advice for the Safe Use of Glucagon-Like Peptide-1 Receptor Agonists and Sodium–Glucose Cotransporter 2 Inhibitors.

Class	Recommendations
GLP-1 receptor agonists	Start with lowest dose and titrate slowly Nausea, vomiting and diarrhoea are the most common side-effects; caution patients to eat smaller meals and to eat slowly, stopping when they feel full If starting medication in a diabetes patient, confer with clinician managing the diabetes, so that efforts can be aligned. If already on a sulfonylurea or insulin, consider modest dose reductions (e.g. 25% for sulfonylurea, 20% for insulin if the patient is already tightly controlled, e.g. HbA1c <7% or if patient is already experiencing frequent hypoglycaemic episodes If starting medication in a non-diabetes patient or in a diabetes patient not using a sulfonylurea or insulin, there is essentially no risk of hypoglycaemia Do not use in patients with gastroparesis Do not use in patients with history of medullary carcinoma of the thyroid or multiple endocrine neoplasia, type 2 Do not use in patients with history of pancreatitis Consider other therapies if known biliary disease Consider other therapies following bariatric surgery Consider other therapies if weight loss not desirable Not approved for patients with type 1 diabetes Hold medication temporarily during any acute GI illness or when patient is sick with decreased appetite
SGLT-2 inhibitors	Lower doses appear as effective as higher doses, only advance if additional glucose lowering is needed Patients should be cautioned about likelihood of increased urinary output and frequency, and the need to maintain adequate hydration at all times If starting medication in a diabetes patient, confer with clinician managing the diabetes, so that efforts can be aligned. If already on a sulfonylurea or insulin, consider modest dose reductions (e.g. 25% for sulfonylurea, 20% for insulin if the patient is already tightly controlled, e.g. HbA1c <7% or if patient is already experiencing frequent hypoglycaemic episodes If starting medication in a non-diabetes patient or in a diabetes patient not using sulfonylurea or insulin, there is essentially no risk of hypoglycaemia Consider dose reductions of other diuretics if any signs of volume contraction. Doses of other hypertension medications usually do not need to be reduced Consider other agents in patients with urinary incontinence or men with advanced prostatic disease and troublesome obstructive voiding symptoms Genital mycotic infections are the most common side-effect (especially in woman and uncircumcised men), easily treated with topical agents or systemic antifungals (watch drug–drug interactions if using fluconazole). If recurrent, may need to discontinue therapy Urinary tract infections may occur, but not commonly. However, would not use in patients with history of severe UTIs (pyelonephritis, urosepsis) or those at increased risk (indwelling urinary catheters/stents/ significant stone burden, etc) One SGLT-2 inhibitor (canagliflozin) doubled the risk of lower extremity amputations in one study. Although not reported with other members of this class, consider other therapies if a patient has severe PAD, active foot ulcers and/or prior amputations Do not use in those with advanced kidney disease; eGFR limit depends on specific agent. Most can be used safely down to eGFR of 30 ml/min/1.73m[2], but glucose lowering effect diminishes <45 ml/min/1.73m[2], while other benefits appear to be maintained Avoid in those with hypotension, orthostasis, unexplained syncope or dizziness Not approved for patients with type 1 diabetes or other patients who may be ketosis-prone Hold 3 days prior to major surgical procedures (to avoid ketosis) Hold medication temporarily when ill or hospitalised* (to avoid ketosis)

*Consider the risks/benefits during heart failure admission and may be continued, depending on the clinical circumstances. eGFR = estimated glomerular filtration rate GI = gastrointestinal; GLP-1R = glucagon-like peptide-1 receptor; PAD = peripheral artery disease; SGLT-2 = sodium–glucose cotransporter 2.

Conclusion

The requirement for testing glucose-lowering therapies developed for T2D in large CV outcomes trials has led to the identification of two medication classes conferring CV outcomes benefit –SGLT-2 inhibitors GLP-1 receptor agonists. These findings have shifted our clinical focus from reduction of HbA_1c levels to reducing the risk of MACE, CV death and HF hospitalisations.

The new emphasis on clinical outcomes promotes more patient-centred care over traditional disease-based care, where physicians across several specialties may now collaborate with patients to reduce morbidity and mortality with therapies that were once considered only in the purview of endocrine specialists. Since most patients with CVD and diabetes are seen by cardiologists, this specialty should become engaged in this process – either by discussing evidence-based glucose-lowering therapies with patients and their referring physicians or, potentially, by even taking ownership and prescribing them themselves.

With increasing communication between specialties and a focus on implementation science, such as embedding user-friendly disease treatment algorithms within the electronic health record, we anticipate that the impressive benefits of these therapies seen in clinical trials will translate to widespread clinical benefits for patients in real-world settings.