Heart failure therapy in diabetic patients-comparison with the recent ESC/EASD guideline

All subjects recruited within the German Heart Failure Network are characterized by an extensive standardizes baseline data set including information on socio-demographics, physical examination, heart failure aetiology and classification, cardiovascular risk factors, comorbidities, medication, ECG, echocardiography, coronary angiography, routine laboratory, and quality of life [9]. In all studies, a uniform baseline data set was obtained. All diagnostic procedures were performed in accordance with pre-specified Standard Operating Procedures. All individual studies were approved by local ethics committees.

For the current analysis, all patients from prospective follow-up studies with a diagnosis of heart failure were eligible.

In all patients echocardiography was performed according to guidelines of the American Society of Echocardiography (ASE) current at the time of data collection, including targeted M-Mode and Doppler techniques. All examinations were performed by physicians experienced in the technique and a pre-specified standard operation procedure regarding echocardiography was given. Preferable, the left ventricular ejection fraction was determined using the Simpson's model of discs. If patient's constitution did not allow sufficient appliance of the Simpson's method, visual estimation of LVEF was permitted too. Patients were classified as having SHF or HFNEF by echocardiographically determined left ventricular ejection fraction using a cut-off of 50%. Glomerular filtration rate was calculated by MDRD formula [10].

Data are presented as mean+/-SD or percentages. Estimates of percent of patients receiving a certain substance class are provided with 95% confidence intervals (CI).

Data were analysed by analysis of variance (quantitative) and logistic regression (frequencies), both including interaction terms for diabetes and left ventricular function. A two-tailed p < 0.05 was considered statistical significant. SPSS 15 (SPSS Inc., Chicago, IL) was used for analysis.

All individual studies were approved by local ethics committees. The authors had full access to and take full responsibility for the integrity of the data.

3304 patients with heart failure from nine different sub-studies were included into this analysis. In the total sample, 711 patients (22%, 353 women) had preserved ejection fraction and 2593 patients (78%, 653 women) had SHF. 2310 patients (70%) were free of diabetes, 622 (19%) had mild diabetes (treated by diet or oral anti-hyperglycemic drugs) and 372 (11%) had severe diabetes (insulin-dependent treatment). Baseline characteristics of the study cohort are also displayed in table 1, showing significant differences for most variables according to presence of diabetes or SHF. Except for the SF-36 score, no significant interaction of effects of diabetes and ejection fraction was seen on all baseline variables.

Overall, a high percentage of patients received the class I recommended therapy (i.e., angiotensin converting enzyme inhibitors [ACEi] or angiotensin-2 receptor-1 blocker [ARB] and beta-blockers). However, differences were observed between HFNEF and SHF patients. Blood pressure control in HFNEF was poorer than in SHF, and was poorer in patients with diabetes than in patients without diabetes (see table 1). There were also differences how guideline-recommended substance classes were applied in SHF and HFNEF for three important sub-groups: Patients free of diabetes, patients with mild diabetes and patients with severe diabetes [7]. As displayed in figure 1 around 90% of patients with SHF received ACEi or ARB (panel A) and beta-blockers (panel B) and neither the presence nor the severity affected the treatment with these substance classes (p = 0.409 and p = 0.724, respectively). By contrast, the intake of diuretics (figure 2, panel A) increased with the presence and severity of diabetes (p < 0.001, respectively) and a reduction in aldosterone receptor blocker usage with diabetes (Figure 2, panel B) was observed (p < 0.001).

As shown in figure 1, in HFNEF fewer patients received ACEi/ARB therapy than in SHF (p < 0.001). However, in contrast to SHF, both presence and the severity of diabetes were associated with a higher intake frequency of these substance classes (p < 0.001). A similar pattern was seen for beta-blockers (figure 1): The intake in HFNEF was reduced, but increased with the presence and severity of diabetes (p = 0.014). The presence of CAD was associated with a higher intake frequency of beta-blockers in HFNEF, but not in SHF. Comparable to SHF, diuretic therapy (figure 2) increased with the presence and severity of diabetes (p < 0.001). As also shown in figure 2, aldosterone receptor blockers were administered with lower frequency in HFNEF (p < 0.001); this association was unaffected by the presence and severity of diabetes (p = 0.198).

We investigated in detail the associations between renal dysfunction and the intake frequency of aldosterone receptor blockers, since hyperkalemia due to spironolactone poses a relevant risk in heart failure therapy [11]. Glomerular filtration rate was lower in SHF than in HFNEF and lower in diabetic than in non-diabetic patients and was lower in diabetic SHF than in diabetics HFNEF patients (see table 1). Figure 3 shows the treatment frequency of aldosterone receptor blockers stratified by preserved or reduced renal function and type of heart failure. In SHF, the percentage of patients receiving aldosterone receptor blockers decreased with the presence and severity of diabetes. Interestingly, this tendency was similar in patients with reduced and preserved renal function. Moreover, serum potassium levels were not different in patients without and with diabetes (p = 0.756 for HFNEF, p = 0.162 for SHF).

In the whole sample, the intake of ACEi/ARB was independently associated with the presence of diabetes, hypertension and renal dysfunction. In contrast, the intake of beta-blockers was associated with the presence of coronary artery disease and hypertension.

The percentage of patients with SHF receiving ACEi/ARB and betablockers was close to 90% and, hence, much higher than reported in previous surveys (e. g., the EuroHeart Survey) [12]. The large proportion of university centres and the exclusive recruitment in cardiology clinics may be an explanation [13]. An additional possibility is that slowly but steadily we reach a better implementation of guidelines in Germany.

There are very few, if any, clinical trials on heart failure treatment available that specifically address heart failure with the comorbidity diabetes. Therefore, recent recommendations carry a low level of evidence (level C) and are derived from subgroup analyses of patients suffering from diabetes in large heart failure trials [7]. In patients with SHF, the use of ACEi/ARB, beta-blockers and aldosterone antagonists have been shown to reduce morbidity and mortality (for review, see [1]). Aldosterone antagonists reduce mortality in heart failure patients with reduced ejection fraction and are of benefit in patients with systolic heart failure and recent myocardial infarction, with or without concomitant diabetes [14‐16].

For HFNEF, there is yet no evidence-based drug-specific mortality reducing therapy available. Three trials investigated the use of ACEi and ARBs in HFNEF patients and failed to show a reduction in mortality [17‐19]. Other treatment strategies, e.g. aldosterone receptor blockade, are currently investigated in clinical trials. Tight blood pressure control is the only recommendation supported by evidence in HFNEF, thus one would expect that this only recommendation would be strictly followed. However, our study shows that blood pressure control in HFNEF was inferior to SHF, the difference of about 15 mmHg in systolic blood pressure is partly explained by less pharmacotherapy.

The lack of evidence for heart failure treatment in HFNEF might explain the lower use of ACEi/ARBs, beta-blockers and aldosterone receptor blockers in patients with HFNEF. In contrast, data from the CHARM trial which was the largest trial to include patients with both SHF and HFNEF, showed that the presence of diabetes was of greater harm in HFNEF than in SHF patients [20]. It is unknown whether a more aggressive antihypertensive therapy develops benefit in patients with HFNEF, but it has been shown that diastolic dysfunction, a relevant pathophysiology in HFNEF, is improved by lowering blood pressure [21]. We were recently able to show that diastolic dysfunction is impaired along the whole diabetic continuum [22]. Furthermore, diastolic dysfunction, which is believed to be the responsible mechanism for the development of heart failure in the majority of patients with HFNEF, is known to be found more frequent in diabetic patients [23]. This increase in frequency of diastolic dysfunction in diabetes mellitus is thereby independent of renal function and can also be found under effective glycaemic control [24, 25]. Given the proposed association of diabetes mellitus and blood pressure control with diastolic dysfunction, we argue for an improvement of antihypertensive therapy and of glycaemic control in patients with HFNEF. However, the hypothesis that strict blood pressure and glycaemic control is beneficial in diabetic HFNEF patients should be tested in a prospective randomised trial.

The use of ACEi/ARB or spironolactone may cause hyperkalemia, especially in patients with impaired renal function. A large population-based study from Ontario showed an increased incidence of hyperkalemia and subsequent mortality after the publication of the RALES trial and the rate of hyperkalemia in real-world is thought to be much higher than in clinical trials for various reasons (e. g. less frequent assessment of electrolytes and renal function, higher dosage of medication) [11, 26, 27]. In heart failure patients, diabetes has been shown to be an independent risk factor for the development of hyperkalemia and severe hyperkalemia (associated with hospitalization or death) [28, 29]. Even with impaired renal function, however, heart failure patients with diabetes will benefit from ARB therapy and aldosterone receptor blockade, similarly to patients without diabetes [28, 29]. Our data from a clinical practice setting suggest that the presence of the heart failure comorbidity diabetes restrains doctors from prescribing evidence-based therapy in heart failure patients - possibly in fear of side-effects, although these side-effects can be easily monitored by simple blood tests. As a consequence, we suggest that diabetic heart failure patients should receive appropriate doses of ACEi/ARB and/or aldosterone receptor blockers under a tight control of potassium and renal function markers, rather than withholding these potentially life-saving drugs. Moreover, future heart failure trials should focus on common comorbidities in heart failure populations (diabetes, impaired renal function, high age).