Sodium-Glucose Cotransporter-2 Inhibitors Could Help Delay Renal Impairment in Patients with Type 2 Diabetes: A

Gyunam Park1, Byungha Choi1,2, Soyoung Kang1,3

  • 1Department of Pharmacy and Yonsei Institute of Pharmaceutical Sciences, Yonsei University, Incheon 21983, Korea.

Journal of Clinical Medicine
|September 23, 2022
PubMed

Insights

Sodium-glucose cotransporter-2 (SGLT2) inhibitors demonstrated superior renoprotective effects compared to dipeptidyl peptidase-4 (DPP-4) inhibitors in type 2 diabetes mellitus patients. SGLT2 inhibitors significantly reduced renal events and slowed estimated glomerular filtration rate decline.

Area of Science:

  • Nephrology
  • Endocrinology
  • Pharmacology

Background:

  • Type 2 diabetes mellitus (T2DM) is a leading cause of chronic kidney disease.
  • Both sodium-glucose cotransporter-2 (SGLT2) inhibitors and dipeptidyl peptidase-4 (DPP-4) inhibitors are used to manage T2DM.
  • Comparative data on their long-term renoprotective effects are crucial.

Purpose of the Study:

  • To compare the renoprotective efficacy of SGLT2 inhibitors versus DPP-4 inhibitors in T2DM patients.
  • To evaluate the impact of these drug classes on renal function decline and serum uric acid levels.

Main Methods:

  • Retrospective cohort study utilizing electronic medical records.
  • Inclusion of 2396 T2DM patients, with 1198 in each treatment group (SGLT2 inhibitors vs. DPP-4 inhibitors).
  • Primary outcome: first occurrence of estimated glomerular filtration rate (eGFR) <45 mL/min/1.73 m2; secondary analysis of eGFR and serum uric acid (SUA) changes.

Main Results:

  • Significantly lower rate of renal events in the SGLT2 inhibitors group (HR, 0.46; p = 0.0007).
  • Slower annual mean eGFR decline in the SGLT2 inhibitors group (0.86 mL/min/1.73 m2/year; p < 0.0001).
  • Lower mean serum uric acid levels observed with SGLT2 inhibitors.

Conclusions:

  • SGLT2 inhibitors exhibit superior renoprotective properties compared to DPP-4 inhibitors in T2DM.
  • These findings suggest SGLT2 inhibitors can delay the progression of renal impairment in T2DM patients.
  • The reduction in eGFR decline and SUA levels highlights a potential mechanism for renoprotection.

Related Concept Videos

Oral Hypoglycemic Agents: Biguanides and Glitazones01:26

Oral Hypoglycemic Agents: Biguanides and Glitazones

Biguanides, particularly metformin (Glucophage), are insulin sensitizers that enhance glucose uptake, thereby reducing insulin resistance. Unlike sulfonylureas, metformin doesn't prompt insulin secretion, which helps to curb hypoglycemia risk. Metformin is beneficial in treating conditions like polycystic ovary syndrome due to its insulin-resistance reduction capability. The drug's primary action involves curtailing hepatic gluconeogenesis, a significant contributor to high blood...
270
Oral Hypoglycemic Agents: Glinides01:06

Oral Hypoglycemic Agents: Glinides

Repaglinide (Prandin) and Nateglinide (Starlix), known as glinides, are oral insulin secretagogues that stimulate insulin release from pancreatic β cells by closing the ATP-sensitive potassium channels (KATP channel). Repaglinide controls insulin release from pancreatic β cells by managing potassium efflux. It shares two binding sites with sulfonylureas and also has a unique site, indicating overlapping mechanisms of action. With a rapid onset and a 4-7 hour duration, it effectively...
230
Diabetes Mellitus: Type 2 and Gestational01:22

Diabetes Mellitus: Type 2 and Gestational

Type 2 diabetes, characterized by insulin resistance, arises when the insulin receptors on cells lose responsiveness to insulin, diminishing the cell's capacity to take up glucose, resulting in elevated blood glucose levels. To receive a diagnosis of Type 2 diabetes, a series of blood glucose tests are necessary to assess whether the blood glucose falls within normal parameters. If the result is out of the normal range, a patient may be diagnosed as prediabetic or diabetic, depending on the...
2.7K
Oral Hypoglycemic Agents: &#945;-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...
240
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...
235
Glucose Transporters01:27

Glucose Transporters

Glucose transporters facilitate the transport of glucose across the cell membrane. In addition to glucose, some glucose transporters can also aid the movement of other hexoses such as fructose, mannose, and galactose.
Facilitated diffusion-glucose transporters (GLUTs) are encoded by the solute-linked carrier (SLC) family 2, subfamily A gene family, or SLC2A. The 14 GLUT protein members are distributed into three classes:
24.0K