Effects of Novel Antidiabetic Agents on Contrast-Associated Acute Kidney Injury in Diabetic Patients Undergoing

Annunziata Nusca1, Maria Pia Di Bitonto1, Agostino Spanò1

  • 1Research Unit of Cardiac Sciences, Department of Medicine and Surgery, Università Campus Bio-Medico di Roma, Roma, Italy; Cardiology Unit, Fondazione Policlinico Universitario Campus Bio-Medico, Roma, Italy.

PubMed

Insights

Novel antidiabetic agents (NAD) significantly reduce contrast-associated acute kidney injury (CA-AKI) in diabetic patients undergoing PCI. Glucagon-like peptide-1 receptor agonists (GLP-1RAs) and sodium-glucose transporter-2 inhibitors (SGLT2i) showed the greatest renal protection.

Area of Science:

  • Nephrology
  • Cardiology
  • Endocrinology

Background:

  • Contrast-associated acute kidney injury (CA-AKI) is a significant risk following percutaneous coronary revascularization (PCI), particularly in diabetic patients.
  • Existing preventive strategies for CA-AKI are limited, especially for this vulnerable population.

Purpose of the Study:

  • To evaluate the impact of novel antidiabetic agents (NAD) on CA-AKI incidence in diabetic patients undergoing PCI.
  • To compare the efficacy of different classes of NAD, including GLP-1RAs, SGLT2i, and DPP4i, in preventing CA-AKI.

Main Methods:

  • A case-control study involving 293 diabetic patients on NAD undergoing PCI, matched with 293 diabetic patients not on NAD.
  • CA-AKI defined by serum creatinine increase within 48-72 hours post-contrast.
  • Propensity score-adjusted logistic regression analysis to control for confounding factors.

Main Results:

  • NAD use was associated with a significantly lower incidence of CA-AKI (4.1% vs. 8.5%, p=0.023).
  • SGLT2 inhibitors and GLP-1 receptor agonists demonstrated a lower CA-AKI rate compared to DPP-4 inhibitors.
  • NAD therapy was an independent predictor of reduced CA-AKI (OR 0.45-0.48).

Conclusions:

  • This study is the first to examine the combined effect of all three major NAD classes on CA-AKI.
  • NAD, particularly SGLT2i and GLP-1RAs, offers a protective benefit against renal damage in diabetic patients undergoing PCI.
  • The findings support the use of NAD as a preventive strategy for CA-AKI in this patient cohort.

Related Concept Videos

Heart Failure Drugs: Inhibitors of Renin-Angiotensin System01:26

Heart Failure Drugs: Inhibitors of Renin-Angiotensin System

The activation of the sympathetic nervous system and the renin-angiotensin-aldosterone system (RAAS) contributes to cardiac remodeling, and inhibiting the RAAS is a pharmacological target in heart failure management. As a result, neurohumoral modulation is a crucial treatment principle for managing heart failure. This approach involves using medications like ACE inhibitors (ACEIs), angiotensin receptor blockers (ARBs), β-blockers, mineralocorticoid receptor antagonists (MRAs), and neutral...
381
Dipeptidyl Peptidase 4 Inhibitors01:23

Dipeptidyl Peptidase 4 Inhibitors

Dipeptidyl peptidase 4 (DPP-4) is a serine protease widely distributed in the body. It's involved in the inactivation of GLP-1 and GIP hormones, which are crucial for insulin regulation. DPP-4 inhibitors, such as sitagliptin (Januvia), saxagliptin (Onglyza), linagliptin (Tradjenta), alogliptin (Nesina), and vildagliptin (Galvus), help increase the proportion of active GLP-1, enhancing insulin secretion. These inhibitors work by competitively binding to DPP-4. This binding causes a...
165
Antihypertensive Drugs: Direct Renin Inhibitors01:25

Antihypertensive Drugs: Direct Renin Inhibitors

The renin-angiotensin-aldosterone system (RAAS) is an intricate physiological pathway involving numerous enzymes and hormones, including renin, angiotensin-converting enzyme (ACE), angiotensin I and II, and aldosterone. Imbalances within this system increase the production of angiotensin II and aldosterone. Increased angiotensin II levels promote vasoconstriction and blood pressure elevation. Concurrently, higher aldosterone levels stimulate sodium and water reabsorption in the kidneys,...
483
Heart Failure Drugs: Diuretics01:22

Heart Failure Drugs: Diuretics

Heart failure and kidney perfusion are interconnected in a complex way. Reduced renal perfusion and venous congestion are two significant factors that contribute to renal dysfunction in heart failure. The kidneys, primarily responsible for fluid balance in the body, are adversely affected due to compromised cardiac output and increased venous pressure. In response to reduced renal perfusion, the kidneys activate neurohumoral mechanisms to restore balance. However, these mechanisms can be...
338
Antihypertensive Drugs: Angiotensin-Converting Enzyme Inhibitors01:30

Antihypertensive Drugs: Angiotensin-Converting Enzyme Inhibitors

Angiotensin-converting enzyme (ACE), a vital component of the renin-angiotensin-aldosterone system, is abundant in lung endothelial cells. ACE converts the inactive decapeptide, angiotensin I, into the active octapeptide, angiotensin II. This potent vasoconstrictor narrows blood vessels, increasing resistance to blood flow and elevating blood pressure. Angiotensin II also stimulates aldosterone production, encouraging kidney cells to reabsorb more sodium and water from urine, thereby increasing...
470
Oral Hypoglycemic Agents: α-Glucosidase Inhibitors01:19

Oral Hypoglycemic Agents: α-Glucosidase Inhibitors

α-glucosidase inhibitors, including acarbose (Precose), miglitol (Glyset), and voglibose (Voglib) (primarily available in Asia), are drugs that control blood sugar levels by delaying the digestion of starch and disaccharides. They achieve this by inhibiting α-glucosidase enzymes in the intestine, which slow the absorption of carbohydrates in the intestine, which in turn leads to a prolonged release of the glucoregulatory hormone GLP-1 from intestinal L-cells.
Acarbose and miglitol are...
148