# Multi-dimensional roles of sodium-glucose cotransporter 2 inhibitors: beyond hypoglycemic and cardiorenal protection

**Authors:** Siyu Li, Yaqi Wang, Quan Gong

PMC · DOI: 10.3389/fendo.2025.1641699 · 2025-09-29

## TL;DR

This paper reviews how SGLT2 inhibitors offer benefits beyond blood sugar control, including protection for the heart, kidneys, and other organs.

## Contribution

The paper highlights the diverse, multi-organ protective effects of SGLT2 inhibitors and summarizes recent findings on their mechanisms.

## Key findings

- SGLT2 inhibitors improve obesity, insulin resistance, and other metabolic disorders.
- They provide benefits for cardiovascular and kidney diseases beyond their initial hypoglycemic use.
- SGLT2 inhibitors may protect the liver, brain, and islet β cells, and influence immune and tumor functions.

## Abstract

Sodium glucose cotransporter-2 inhibitors (SGLT2i) have been found to have a range of benefits, including improving obesity and insulin resistance, hyperuricemia, hypertension, hyperlipidemia, and other metabolic disorders. Initially used for the hypoglycemic effects, they are now found to benefit atherosclerotic cardiovascular disease and chronic kidney disease. Additionally, SGLT2i has been found to have multiple functions, such as improving liver metabolism, affecting brain function, protecting islet β cell function, anti-tumor, and affecting immune system function. This review provides an overview of the protective effects of SGLT2i on different organs and tissues, as well as the potential mechanisms underlying the functional improvement induced by SGLT2i in recent years.

## Linked entities

- **Proteins:** SLC5A2 (solute carrier family 5 member 2)
- **Diseases:** obesity (MONDO:0011122), hyperuricemia (MONDO:0002144), hyperlipidemia (MONDO:0021187), atherosclerotic cardiovascular disease (MONDO:1060134), chronic kidney disease (MONDO:0005300)

## Full-text entities

- **Diseases:** hypertension (MESH:D006973), insulin resistance (MESH:D007333), hyperlipidemia (MESH:D006949), cardiovascular disease (MESH:D002318), chronic kidney disease (MESH:D051436), obesity (MESH:D009765), tumor (MESH:D009369), atherosclerotic (MESH:D050197), metabolic disorders (MESH:D008659), hyperuricemia (MESH:D033461)
- **Chemicals:** sodium-glucose cotransporter 2 inhibitors (-)

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12515626/full.md

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Source: https://tomesphere.com/paper/PMC12515626