Review of SGLT2i for the Treatment of Renal Complications: Experience in Patients with and Without T2D.

The management of type 2 diabetes (T2D) involves decreasing plasma glucose levels and reducing cardiovascular and microvascular complications. Diabetic kidney disease (DKD), defined as presence of albuminuria, impaired glomerular filtration, or both, is an insidious microvascular complication of diabetes that generates a substantial personal and clinical burden. The progressive reduction in renal function and increased albuminuria results in an increase of cardiovascular events. Thus, patients with DKD require exhaustive control of the associated cardiovascular risk factors. People with diabetes and renal impairment have fewer options of antidiabetic drugs because of contraindications, adverse effects, or altered pharmacokinetics. Sodium-glucose cotransporter type 2 inhibitors (SGLT2i) reduce blood glucose concentrations by blocking the uptake of sodium and glucose in the proximal tubule and promoting glycosuria, and these agents now have an important role in the management of T2D. The results of several cardiovascular outcomes trials suggested that SGLT2i are associated with improvements in renal endpoints in addition to their reduction in cardiovascular events and mortality, which represents a major advance in the care of this population. The dedicated kidney outcomes trials have confirmed the renoprotective action of SGLT2i across different glomerular filtration and albuminuria values, even in patients with non-diabetic chronic kidney disease. Notably, this improvement in kidney function may indirectly benefit cardiac function through multifaceted interorgan cross talk, which can break the cardiorenal vicious circle linked to T2D. In this article, we briefly review the different mechanisms of action that may explain the renal beneficial effects of SGLT2i and disclose the results of the key renal outcome trials and the subsequent update of related clinical guidelines.

Key Summary Points

Introduction

The kidneys are involved in regulating glucose homeostasis, and glucose reabsorption through sodium–glucose cotransporters located in the proximal tubules is one of their tasks [1]. The management of type 2 diabetes (T2D) involves decreasing plasma glucose levels and reducing macrovascular and microvascular complications, including chronic kidney disease (CKD). There have been limited treatment options beyond glycemic control and antihypertensive agents to slow kidney disease progression in these patients. In fact, since the development of renin–angiotensin–aldosterone system (RAAS) inhibitors, such as angiotensin-converting enzyme (ACE) inhibitors and angiotensin receptor blockers (ARBs), almost 20 years ago, no new treatments have become available. Moreover, people with diabetes and CKD may have fewer options of antidiabetic drugs because of contraindications, adverse effects, or altered pharmacokinetics.

Sodium–glucose cotransporter type 2 inhibitors (SGLT2i) are the newest drug class for the management of hyperglycemia in T2D, as they lower blood glucose concentrations by blocking the uptake of sodium and glucose in the proximal tubule and promote glycosuria [2]. In patients with impaired kidney function, the filtered glucose load is reduced and their effectiveness may be blunted [3]. Thus, these agents were initially approved for use as glucose-lowering drugs for people with T2D and (nearly) preserved kidney function. However, the results of several cardiovascular outcomes trials (CVOTs) suggested that SGLT2i are associated with improvements in renal endpoints apart from their reduction in cardiovascular events and mortality [4-6], which represents a major advance in the care of this population. On the basis of the findings of CVOTs, dedicated kidney outcomes trials (such as DAPA-CKD and CREDENCE) have been conducted, confirming the renoprotective benefit of SGLT2i across different glomerular filtration and albuminuria values [7, 8]. Herein, we briefly review the different mechanisms of action that may explain the renal beneficial effects of SGLT2i and disclose the results of the key renal outcome trials and the subsequent update of related clinical guidelines. This article is based on previously conducted studies and does not contain any studies with human participants or animals performed by any of the authors.

CKD and T2D: Dance Partners in CV Disease

The burden of diabetes and hypertension, both considered as leading drivers of CKD, has increased significantly over recent decades. Diabetic kidney disease (DKD), defined as presence of albuminuria, impaired glomerular filtration, or both, is an insidious microvascular complication of diabetes that develops in approximately 40% of patients with T2D and accounts for more than 50% of new patients beginning renal replacement therapy [9, 10]. Apart from genetic susceptibility, the pathogenic mechanisms that contribute to DKD involve metabolic, hemodynamic, profibrotic, and inflammatory factors, which ultimately lead to the development of end-stage kidney disease (ESKD) [11]. As per chronic hyperglycemia, a classic study that followed patients with T2D during 11 years demonstrated a strong association between glycemic control and the incidence of CKD, regardless previous traditional risk factors for CKD and even in the absence of albuminuria and retinopathy [12]. Together with hypertension and hyperglycemia, other risk factors for DKD are older age, early-onset diabetes, and the presence of albuminuria [13, 14] and diabetic retinopathy [15].

Patients with DKD may initially exhibit glomerular hyperfiltration, a process that leads to a progressive reduction in estimated glomerular filtration rate (eGFR) and increased albuminuria, which results in an increase of cardiovascular events [16]. Despite optimal preventive and treatment strategies, classically based on lifestyle modification, reduction of blood glucose levels, lipid levels, and blood pressure and the use of RAAS inhibitors, patients with T2D remain at high risk of developing/worsening renal and cardiovascular complications [17-19]. According to the Global Burden of Disease Study 2017, almost 7% of the total cardiovascular disease burden can be attributed to impaired kidney function [20]. Indeed, patients with DKD seem to concentrate most of the excess of all-cause and cardiovascular mortality risk among patients with T2D, with a sixfold higher risk for mortality associated with albuminuria and 15-fold higher risk with the combination of albuminuria and decreased GFR [21]. Micro- and macroalbuminuria are associated with higher risks of incident ischemic stroke, myocardial infarction, and all-cause mortality in patients with T2D without previous cardiovascular disease [22], whereas reduction of albuminuria (owing to better blood pressure or glycemic control) is associated with significantly less all-cause mortality [23]. All this evidence indicates that patients with DKD require exhaustive control of the associated cardiovascular risk factors and that albuminuria may be considered as a relevant target for therapy.

Mechanisms of SGLT2i Effects on Renal Condition

The characteristic ischemic nephropathy associated with T2D is initially provoked by chronic hyperglycemia. This stimulates SGLT2 expression and activity leading to an increase in proximal tubular glucose and sodium reabsorption and reduced sodium uptake at the juxtaglomerular macula densa, blunting the tubuloglomerular feedback (TGF), and dysregulating vasoactive substances. All these processes enhance preglomerular dilatation, postglomerular constriction, intraglomerular capillary pressure, and finally lead to hyperfiltration [24]. SGLT2i can correct TGF/intraglomerular hemodynamics by preventing sodium reabsorption, which partially explains the renoprotective effect of these agents. Enhanced natriuresis and osmotic diuresis contribute to decrease systolic and diastolic blood pressure by an average of 5 and 2 mmHg, respectively [25], and provoke contraction in plasma volume, reduced sympathetic tone and arterial stiffness, thus improving cardiac perfusion [26, 27]. Moreover, the lower glomerular hyperfiltration translates into the reduction of albuminuria, contributing to minimize the progression of kidney disease [28, 29].

Apart from the activation of the TGF, other mechanisms for the beneficial effects of SGLT2i on kidney function have been proposed (Table 1): induction of ketone body production and an elevation in hematocrit concentration, which can contribute to the beneficial effect of these agents on cardiovascular outcomes [30]; lowering of serum uric acid concentrations by inducing renal uric acid excretion [31]; reduction of inflammatory and fibrotic mediators induced by hyperglycemia in proximal tubular cells [32, 33]; stimulation of autophagy, which is essential for homeostasis of podocytes, tubular cells, mesangial and glomerular endothelial cells [34]; and amelioration of renal hypoxia by decreasing renal oxygen demand and increasing oxygen supply [35]. Several clinical trials are ongoing to further explore the impact and mechanism of action of SGLT2i on renoprotection (Table 2), and eventually will be able to identify the subgroups of patients most likely to benefit from them, even among individuals with CKD but without diabetes.

Table 1

Effects of SGLT2i on kidney function

Mechanism	Effect
Correct TGF/intraglomerular hemodynamics	Reduce hyperfiltration and reduction of albuminuria [22]
Induction of ketone body production	Elevation in hematocrit concentration [28]
Elevation of renal acid uric excretion	Lower serum uric acid concentrations [29]
Reduction of inflammatory and fibrotic mediators induced by hyperglycemia in proximal tubular cells	Reversal of molecular processes related to inflammation, extracellular matrix deregulation, and fibrosis [30, 31]
Correct hyperglycemia-induced decreased AMPK activity and autophagic flux reduction	Stimulation of autophagy and homeostasis of renal cells [32]
Decrease in renal oxygen demand and increase in oxygen supply	Ameliorate renal hypoxia [33]

AMPK AMP-activated protein kinase, SGLT2i sodium glucose cotransporter 2 inhibitors, TGF tubuloglomerular feedback

Table 2

Clinical trials evaluating the renal effects of SGLT2i

Drug	Enrollment	Phase	Conditions	Endpoints	Identification
Dapagliflozin	10	2	Cystinuria	Change in cystine stone size over time (1 year and 3 months)	NCT05058859
Dapagliflozin	36	1	CKD, diabetes	Change in serum klotho levels at 12 and 24 weeks	NCT05033054
Dapagliflozin	87,727	NA	CKD	Relative hazard of the composite of end-stage renal disease or all-cause mortality	NCT04882813
Dapagliflozin	10	2	Cystinuria	Change in cysteine level in freshly voided urine	NCT04818034
Dapagliflozin	1722	1	Left cardiac catheterization, PCI, AKI	Incidence of AKI	NCT04806633
Dapagliflozin	32	2	CKD	GFR 24-h urinary protein excretion	NCT04794517
Dapagliflozin	2500	2–3	ESKD	Composite of cardiovascular death, myocardial infarction, or ischemic stroke	NCT04764097
Dapagliflozin	17	4	T2D, impaired renal function	Change in 24-h sodium excretion	NCT04620590
Dapagliflozin	60	4	Diabetic nephropathy	Decrease in proteinuria	NCT03573102
Dapagliflozin (+ AZD9977)	540	2	Heart failure, CKD	Percentage change in UACR from baseline at 12 weeks	NCT04595370
Dapagliflozin (+ zibotentan)	660	2	CKD	Change in UACR from baseline to week 12	NCT04724837
Empagliflozin	40	4	T2D, CAD, AKI	Serum creatinine values in pre-specified periods NGAL values in pre-specified periods	NCT05037695
Empagliflozin	45	NA	CKD stage 3	Urinary excretion of adenosine and markers of osteocyte function and glomerular damage	NCT04961931
Empagliflozin	800	NA	Kidney protection against contrast in diabetic kidney	SGLT2i proves protective effect	NCT04806633
Empagliflozin	144	4	T2D, CAD, CABG, AKI	Development of post-CABG AKI	NCT04523064
Empagliflozin	172	4	Hyponatremia	Change in average daily AUC for serum sodium concentration	NCT04447911
Empagliflozin	6609	3	CKD	Time to first occurrence of relevant kidney disease progression or cardiovascular death	NCT03594110
Empagliflozin (+ linagliptin)	66	4	T2D	Changes in GFR at 8 and 16 weeks	NCT03433248
Empagliflozin (+ semaglutide)	80	4	T2D, albuminuria	Change from randomization to week 52 in albuminuria	NCT04061200
Ertugliflozin	40	4	T2D	Renal oxygenation	NCT04027530
SGLT2i	70	4	Diabetic nephropathy	Change in urinary albuminuria from baseline to week 12	NCT04127084

AKI acute kidney injury, AUC area under the curve, CABG coronary artery bypass grafting, CAD coronary artery disease, CKD chronic kidney disease, ESKD end-stage kidney disease, GFR glomerular filtration rate, PCI percutaneous coronary intervention, T2D type 2 diabetes, UACR urine albumin-to-creatinine ratio

Benefits of SGLT2i on Renal Function Beyond Their Glycemic Control

The Canagliflozin and Renal Events in Diabetes with Established Nephropathy Clinical Evaluation (CREDENCE) was the first dedicated renal outcomes trial that assessed a primary cardiorenal composite endpoint in people with impaired kidney function [7]. The study population differed from previous CVOTs, as the enrolment was restricted to participants with T2D and CKD with macroalbuminuria (baseline eGFR 30 to < 90 mL/min/1.73 m2; urine albumin-to-creatinine ratio [UACR] 300 to < 5000 mg/g) that were receiving an ACE inhibitor or ARB. A total of 4401 patients were randomized, of whom 2202 received a daily dose of 100 mg of canagliflozin and 2199 received a placebo. After a mean follow-up of 2.62 years, the primary outcome (composite of ESKD, defined as the need of dialysis, kidney transplantation, or a sustained eGFR below 15 mL/min/1.73 m2, doubling of serum creatinine, or renal or cardiovascular death) was 30% lower in the canagliflozin group than in the placebo group, with event rates of 43.2 and 61.2 per 1000 patient-years, respectively [7]. Consistent effects were observed for each of the components of the primary composite endpoint, and for the secondary renal, cardiovascular, and mortality endpoints (Table 3). A subgroup analysis showed that canagliflozin reduced the risk of advancing renal disease to kidney failure in subjects with eGFR above and below 30 mL/min/1.73 m2, without differences in the rates of renal adverse events [36], supporting the use and continuation of SGLT2i until initiation of dialysis or kidney transplantation.

Table 3

Summary of the renal outcomes trials with SGLT2i

	CREDENCE(Canagliflozin)	DAPA-CKD(Dapagliflozin)	SCORED*(Sotagliflozin)
Sample	4401	4304	10,584
Follow-up (years)	2.6	2.4	4.2
Study population	T2D + CKD	CKD ± T2D	T2D + CKD
Established CV disease	50.4%	37.4%	31% (HF)
eGFR for inclusion (mL/min/1.73 m2)	30–90	25–75	25–60
Mean eGFR (mL/min/1.73 m2)	56.2	43.1	44.5 (median)
Median UACR (mg/g)	927	949	74
Baseline UACR subgroup (mg/g)
< 30	31 (0.7%)	NA	3709 (35.0%)
30–300	496 (11.3%)	NA	3589 (33.9%)
> 300	3874 (88.0%)	NA	3286 (31.0%)
> 1000	2053 (46.6%)	2079 (48.3%)	NA
Primary outcome (HR [95% CI])	Composite of ESKD, doubling serum creatinine, or death from renal or CV disease: 0.70 (0.59–0.82), p = 0.00001	Composite of sustained ≥ 50% eGFR decline, ESKD, renal death or CV death: 0.61 (0.51–0.72), p < 0.001 NNT 19	Deaths from CV causes, hospitalizations for HF, and urgent visits for HF: 0.74 (0.63–0.88), p < 0.001
Renal secondary outcomes (HR [95% CI])	ESKD, doubling serum creatinine, or renal death: 0.66 (0.53–0.81), p < 0.001 Dialysis, kidney transplantation, or renal death: 0.72 (0.54–0.97), NA for p value	≥ 50% eGFR decline, ESKD, renal death: 0.56 (0.45–0.68), p < 0.001	≥ 50% eGFR decline, long-term dialysis, renal transplantation, or eGFR < 15 mL/min/1.73 m2: 0.71 (0.46–1.08), NA for p value
CV secondary outcomes (HR [95% CI])	CV death of hospitalization for HF: 0.69 (0.57–0.83), p < 0.001 CV death, MI, or stroke: 0.80 (0.67–0.95), p = 0.01 Hospitalization for HF: 0.61 (0.47–0.80), p < 0.001	CV death or hospitalization for HF: 0.71 (0.55–0.92), p = 0.009	Hospitalizations and urgent visits for HF: 0.67 (0.55–0.82), p < 0.001 CV death: 0.90 (0.73–1.12), p = 0.35
All-cause mortality (HR [95% CI])	0.83 (0.68–1.02), NA for p value	0.69 (0.53–0.88), p = 0.004	0.99 (0.83–1.18), NA for p value

*The trial ended early because of loss of funding

CI confidence interval, CV cardiovascular, eGFR estimated glomerular filtration rate, ESKD end-stage renal disease, HF heart failure, HR hazard ratio, MI myocardial infarction, NA not applicable, NNT number needed to treat; UACR, urine albumin-to-creatinine ratio

In the CVOT evaluating dapagliflozin (DECLARE-TIMI 58), approximately 13.1% of the participants had CKD (defined as eGFR < 60 mL/min/1.73 m2, UACR > 300 mg/g, or both) at baseline [6]. In the whole patient sample, dapagliflozin treatment was associated with a significantly lower risk (− 47%) of the renal composite of decline in eGFR of ≥ 40% to less than 60 mL/min/1.73 m2, ESKD or renal death, compared with placebo [28]. To further confirm this benefit, the Dapagliflozin and Prevention of Adverse outcomes in CKD (DAPA-CKD) trial investigated the safety and renal outcomes of dapagliflozin in patients with CKD, the majority of them (97%) already receiving RAAS blockers as background renoprotective therapy. Unlike CREDENCE, the DAPA-CKD trial also included people without T2D, to explore whether the benefits of SGLT2i may extend to patients with non-DKD [8]. A total of 4304 patients with CKD were enrolled, 2906 (68%) of them with T2D. Dapagliflozin demonstrated a clear reduction (− 39% lower risk) in primary composite outcome events (sustained decline in the eGFR of ≥ 50%, ESKD, or death from renal or cardiovascular causes), regardless of the presence of diabetes. Additionally, dapagliflozin reduced all three secondary endpoints compared with placebo: decline in eGFR of ≥ 50%, ESKD, or death from renal causes (− 44%), hospitalization for heart failure or cardiovascular death (− 29%), and all-cause mortality (− 31%) (Table 3). There were no significant differences in the primary endpoint between patients with diabetes and without [37], indicating that the renal benefit associated with dapagliflozin is at least similar in patients with non-DKD, such as chronic glomerulonephritides, ischemic or hypertensive CKD, or CKD of other or unknown cause. The baseline glycemic status (normoglycemic, prediabetes, or T2D) of DAPA-CKD trial participants did not modify the effect of dapagliflozin on the primary composite endpoint [38], and recent sub-analyses have shown that dapagliflozin significantly reduced albuminuria [39], slowed long-term eGFR decline [40], and reduced the risk of abrupt declines in kidney function [41]. In addition to this, and in a similar fashion to DAPA-HF, dapagliflozin treatment in DAPA-CKD led to a numerical reduction in the cases of new T2D onset, which reaches statistical significance when pooled with DAPA-HF data (33% relative risk reduction) [42].

The ongoing EMPA-KIDNEY trial of empagliflozin in patients with CKD has a similar design to DAPA-CKD and will further evaluate renal outcomes and CV mortality with SGLT2i in patients with and without T2D (NCT03594110).

Regarding other renal outcomes trials with dapagliflozin, the DELIGHT study recruited patients with T2D and impaired renal function (UACR ≥ 30 mg/g and eGFR 25–75 mL/min/1.73 m2) to assess the albuminuria-lowering effect of dapagliflozin with and without the dipeptidyl peptidase 4 inhibitor saxagliptin. At week 24, patients treated with dapagliflozin showed a decrease in UACR (− 21%), which was even deeper for the combination of dapagliflozin and saxagliptin (− 38.0%), compared with placebo [43].

Sotagliflozin is a dual SGLT2i that also blocks SGLT1, expressed on small intestine, heart, and brain, apart from the renal proximal tubule [44]. The Sotagliflozin on Cardiovascular and Renal Events in Patients with Type 2 Diabetes and Moderate Renal Impairment Who Are at Cardiovascular Risk (SCORED) trial included patients with T2D and CKD (eGFR 25–60 mL/min/1.73 m2), with or without albuminuria, that were followed for a median of 16 months. Sotagliflozin reduced (− 26%) the composite outcome of cardiovascular death, hospitalization for heart failure, and urgent heart failure, whereas the renal composite outcome was not different in the group treated with sotagliflozin versus placebo [45] (Table 3). However, the trial was prematurely interrupted because of loss of funding, and it was not adequately powered for detecting changes in secondary outcomes, precluding any conclusion regarding a possible renal benefit from the study.

Several meta-analyses have concluded that SGLT2i reduce the risk of renal-related outcomes in patients with T2D, irrespective of the presence or absence of previous renal disease, with a reduction ranging from − 39% to − 33% [46-49], and one of them calculated the pooled number needed to treat (NNT) to be 20 [49]. Moreover, SGLT2i significantly reduce the annual decline in eGFR slope versus placebo, achieving a mean treatment difference of 1.35 mL/min/1.73 m2/year [50]. “Real world” data from large databases are consistent with the results observed in the clinical trials, demonstrating an important reduction (− 51%) in the composite renal outcome of substantial loss of eGFR and ESKD with SGLT2i [51].

Current Recommendations for Treatment of Renal Complications with SGLT2i

Owing to the robust renoprotective effects demonstrated by SGLT2i in the DAPA-CKD trial, in addition to the previous results of CVOTs, dapagliflozin is the first SGLT2i approved by the European Medicines Agency (EMA) for the treatment of CKD regardless of diabetes status (https://www.ema.europa.eu/en/medicines/human/EPAR/forxiga). This news has also led to a modification of Forxiga SmPC, allowing the therapy to be started in patients with eGFR above 25 mL/min/1.73 m2 for all the approved indications (T2D, heart failure, and CKD). The US prescribing information for canagliflozin, although not in Europe, included a new indication to reduce the risk of ESKD and worsening of kidney function, cardiovascular death, and hospitalization for heart failure in patients with T2D and CKD, allowing the initiation in people with eGFR of ≥ 30 mL/min/1.73 m2 and continuation of treatment in those who reach eGFR < 30 mL/min/1.73 m2 and albuminuria > 300 mg/day until initiation of dialysis or kidney transplantation (https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/204042s036lbl.pdf). These changes have broadened the patients eligible for SGLT2i treatment to ameliorate the progression of CKD.

Additionally, the most relevant professional societies have updated their guidelines and recommendations regarding the use of these agents in people with CKD (Fig. 1). The American Diabetes Association (ADA) guidelines state: “For patients with type 2 diabetes and diabetic kidney disease, use of a SGLT2i in patients with an eGFR ≥ 25 mL/min/1.73 m2 and urinary albumin ≥ 300 mg/g creatinine is recommended to reduce kidney disease progression and cardiovascular events.” The ADA further recommends additional use of SGLT2i in these patients for cardiovascular risk reduction when eGFR and UACR are ≥ 25 mL/min/1.73 m2 or ≥ 300 mg/g, respectively [52].

Fig. 1

Pharmacological recommendations to reduce kidney and cardiovascular risks in patients with CKD and T2D. ACEi angiotensin-converting enzyme inhibitor, ADA American Diabetes Association, ARB angiotensin receptor blocker, CV cardiovascular, EASD European Association for the Study of Diabetes, eGFR estimated glomerular filtration rate, ESC European Society of Cardiology, GLP-1 RA glucagon-like peptide 1 receptors agonist, KDIGO Kidney Disease: Improving Global Outcomes, UACR urine albumin-to-creatinine ratio

The European Society of Cardiology, in collaboration with the European Association for the Study of Diabetes, have updated their guidelines to recommend SGLT2i as first-line therapy for the prevention and management of CKD (eGFR 30 to < 90 mL/min/1.73 m2) in patients with T2D and albuminuric kidney disease [53]. The Kidney Disease: Improving Global Outcomes (KDIGO) guidelines recommend the use of metformin in combination with SGLT2i (with GFR ≥ 30 mL/min/1.73 m2) as first-line antihyperglycemic therapy for patients with T2D and CKD. In patients on treatment that have a drop in GFR below 30 mL/min/1.73 m2, the SGLT2i can be continued until initiation of kidney replacement therapy [54]. Finally, a Scientific Statement from the American Heart Association advocated the use of SGLT2i in patients with earlier stages of CKD and postponement of glucagon-like peptide 1 receptors agonists (GLP-1 RAs) in more advanced CKD because there is more experience with these agents in patients with severe CKD [55].

Changing Paradigm: The Cardiorenal and Metabolic Continuum

As stated above, SGLT2i are changing the clinical management of T2D thanks to the evidence supporting their renal and cardiovascular protection, which share common risk factors and pathogenic mechanisms [56]. These agents have demonstrated benefits in different clinical scenarios: patients with T2D with and without established cardiovascular disease [6], patients with T2D with CKD [57], patients with CKD with and without T2D [8], patients with heart failure with and without T2D [58], etc. Indeed, the populations included in the trials of dapagliflozin cover a wide range of diabetic patient profiles, going from those in the earlier stages of the cardiorenal continuum (DECLARE-TIMI 58) to those at more advanced stages (DAPA-CKD and DAPA-HF). Thus, the benefits of SGLT2i are present from the beginning and extend to the advancing disease (Fig. 2).

Fig. 2

Across the cardiorenal continuum and its SGLT2 inhibitors clinical trials

Adapted from Fontes-Carvalho et al. [56]

In general, all these trials showed a significant reduction in heart failure hospitalization and a reduction in the composite renal outcome. SGLT2i induce significant natriuresis, enhanced by the combination with loop diuretics, which results in an improvement in blood volume. The diuretic effect facilitates a better management of volume status in patients with heart failure and may contribute to the long-term decrease of heart failure events reported with these agents [59]. Moreover, an improved kidney function itself may indirectly benefit cardiac function through multifaceted interorgan cross talk, breaking the cardiorenal vicious circle [56]. Some authors have defined the cardiorenal disease in patients with T2D as the development of heart failure and CKD, and suggested a novel outcome, major adverse renal and cardiac events (MARCE), to be evaluated in future clinical trials [60, 61].

Patients with T2D suffer multiple comorbid conditions and usually receive several treatments such as antihypertensive agents, diuretics, insulin, or other glucose-lowering medications. The number of therapy choices to be combined is higher early in the course of diabetes, before the development of serious comorbidities, including renal function impairment. Although the glucose-lowering effect of these drugs decreases as glomerular filtration worsens, SGLT2i can be prescribed for patients with renal impairment for organ protection. Moreover, the likelihood of response to treatment is greater with shorter T2D duration [62].

Conclusions

The dedicated kidney outcomes trials of SGLT2i (such as DAPA-CKD and CREDECE) have confirmed the renoprotective benefit of these drugs across different glomerular filtration rates and albuminuria values. SGLT2i can correct TGF/intraglomerular hemodynamics by preventing sodium reabsorption, whereas other mechanisms such as ketone body production, lowering of serum uric acid concentrations, and increasing oxygen supply can contribute to their beneficial effects on cardiovascular outcomes. Accordingly, the most relevant professional societies have updated their guidelines and recommendations regarding the use of these agents in people with CKD. Diabetes is normally addressed by multiple specialists including endocrinologists, cardiologists, and nephrologists, as well as primary care providers. The multidisciplinary team should select the therapeutic strategy on the basis of the target organ of protection and patients’ comorbidities and profile, going beyond glycemic control and ensuring that patients are able to benefit from the metabolic, cardiovascular, and kidney protection associated with SGLT2i.

The management of type 2 diabetes (T2D) involves decreasing plasma glucose levels and reducing macrovascular and microvascular complications, including chronic kidney disease (CKD).

Sodium–glucose cotransporter type 2 inhibitors (SGLT2i) lower blood glucose concentrations by blocking the uptake of sodium and glucose in the renal proximal tubule and promoting glycosuria.

In addition to the metabolic and cardiovascular benefits, SGLT2i have also demonstrated renoprotective effects across different glomerular filtration and albuminuria values in patients with and without T2D.

SGLT2i are changing the clinical management of T2D owing to their renal and cardiovascular protection. This can benefit patients with early stages of disease and also those with established cardiovascular and/or renal disease, and even patients without diabetes.