# Effects of Sodium Glucose Cotransporter 2 (SGLT2) Inhibitors on Lipid Profiles in Type 2 Diabetes: A Systematic Review

**Authors:** Mushrega Abdalla, Mudathir Elyas Suleiman Khamees, Ahmed-Lamin Gehani, Abubaker Ibrahim Mohammed Ibrahim, Muntassir Y Yousif, Noor Kheir, Safa Mohammed Qasem Alqasem, Asim Ahmed

PMC · DOI: 10.7759/cureus.102618 · Cureus · 2026-01-30

## TL;DR

This paper reviews how SGLT2 inhibitors affect lipid levels in people with type 2 diabetes, finding mostly neutral to slightly positive effects on cholesterol and triglycerides.

## Contribution

The study systematically evaluates the lipid effects of SGLT2 inhibitors, highlighting inconsistencies in advanced lipid measures and the need for standardized reporting.

## Key findings

- SGLT2 inhibitors show a neutral effect on LDL cholesterol in type 2 diabetes patients.
- They tend to favorably affect HDL cholesterol and triglycerides in some settings.
- Results on advanced lipid markers remain inconsistent across studies.

## Abstract

Sodium glucose cotransporter 2 (SGLT2) inhibitors provide cardiometabolic benefits in adults with type 2 diabetes mellitus, yet their effects on lipid metabolism are reported inconsistently across clinical trials and mechanistic studies and may vary with background statin therapy and differences in lipid measurement and reporting. We conducted a systematic review to evaluate the impact of SGLT2 inhibitors on conventional lipid parameters first and selected advanced lipid markers second in adults with type 2 diabetes. We searched multiple databases using predefined eligibility criteria and extracted data in duplicate. We assessed the risk of bias using design-appropriate tools and synthesized findings qualitatively because heterogeneity limited quantitative pooling. Overall, evidence across included studies suggests that SGLT2 inhibitors are essentially neutral with respect to low-density lipoprotein cholesterol (LDL-C), with generally favorable directions for high-density lipoprotein cholesterol (HDL-C) and triglycerides in some study settings. At the same time, findings on qualitative lipoprotein remodeling and advanced lipid phenotypes remain heterogeneous. These results support a lipid neutral to mildly favorable profile on standard lipid panels and emphasize the need for standardized reporting of advanced lipid measures and longer follow-up to clarify clinical relevance.

## Linked entities

- **Diseases:** type 2 diabetes mellitus (MONDO:0005148), type 2 diabetes (MONDO:0005148)

## Full-text entities

- **Genes:** GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, SLC5A2 (solute carrier family 5 member 2) [NCBI Gene 6524] {aka SGLT2}, APOB (apolipoprotein B) [NCBI Gene 338] {aka FCHL2, FLDB, LDLCQ4, apoB-100, apoB-48}, ANGPTL3 (angiopoietin like 3) [NCBI Gene 27329] {aka ANG-5, ANGPT5, ANL3, FHBL2}, JPH3 (junctophilin 3) [NCBI Gene 57338] {aka CAGL237, HDL2, JP-3, JP3, TNRC22}
- **Diseases:** insulin resistance (MESH:D007333), diabetes (MESH:D003920), cardiovascular and renal complications (MESH:D002318), NAFLD (MESH:D065626), Atherogenic (MESH:D050197), atherogenic dyslipidemia (MESH:D050171), metabolic syndrome (MESH:D024821), hyperglycemia (MESH:D006943), renal and hepatic fibrosis (MESH:D005355), Liver disease (MESH:D008107), TC (OMIM:275350), metabolic dysfunction (MESH:D008659), diabetic kidney disease (MESH:D003928), nephropathy (MESH:D007674), obese (MESH:D009765), Heart failure (MESH:D006333), Type 2 Diabetes (MESH:D003924)
- **Chemicals:** fatty acid (MESH:D005227), Dapagliflozin (MESH:C529054), Triglycerides (MESH:D014280), sitagliptin (MESH:D000068900), TC (MESH:D013667), campesterol (MESH:C021273), TG (MESH:D013866), inhibitors (-), vildagliptin (MESH:D000077597), cholesterol (MESH:D002784), voglibose (MESH:C102817), glucose (MESH:D005947), ertugliflozin (MESH:C570288), Empagliflozin (MESH:C570240), luseogliflozin (MESH:C549343), Lipid (MESH:D008055), ipragliflozin (MESH:C572941), canagliflozin (MESH:D000068896)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

49 references — full list in the complete paper: https://tomesphere.com/paper/PMC12949959/full.md

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Source: https://tomesphere.com/paper/PMC12949959