# Effects of metformin on arterial elasticity and pro-inflammatory markers in black diabetes patients

**Authors:** Tsakani L. Rasakanya, Elzbieta Osuch

PMC · DOI: 10.4102/hsag.v29i0.2419 · Health SA Gesondheid · 2024-06-14

## TL;DR

This study found that metformin, alone or with glimepiride, did not improve arterial elasticity or reduce inflammation in Black South African patients with type 2 diabetes.

## Contribution

The study provides new evidence on metformin's effects on arterial elasticity and inflammation in a specific demographic group.

## Key findings

- Metformin alone or with glimepiride did not significantly improve arterial elasticity markers like PWV and Aix.
- IL-1β levels initially increased but later decreased, though other pro-inflammatory markers remained unchanged.
- No significant reduction in pro-inflammatory cytokines was observed in either treatment group.

## Abstract

Pro-inflammatory markers are linked with the development and progression of type 2 diabetes mellitus and arterial stiffening. Pulse Wave Velocity (PWV) and Augmentation Index (Aix) are non-invasive standard markers of arterial elasticity and predictors of cardiovascular mortality and morbidity.

To investigate the effects of metformin alone and in combination with glimepiride on arterial elasticity, pro-inflammatory cytokines in black type 2 diabetes mellitus patients.

Participants were enrolled from Sefako Makgatho Health Sciences University community, Gauteng, South Africa.

PWV and Aix were measured using the AtCor SphygmoCor® system (AtCor Medical, Inc., Sydney, Australia). Cytokines levels were measured using Multiplexing with Bio-Plex Pro™ human inflammation panel I assay. Treatment naïve type 2 diabetes participants were divided into two groups: metformin (M) (n = 10) and metformin glimepiride (MS) (n = 14). The study participants were followed up at 4 and 8 months after treatment initiation.

In the M and MS, IL-1β increased significantly at four months (58.19 ± 0.03 pg/ml, 58.35 ± 0.30 pg/ml) when compared to baseline (33.05 ± 18.56 pg/ml, 34.79 ± 18.77 pg/ml) then decreased significantly at eight months (29.25 ± 11.64 pg/ml, 32.54 ± 14.26 pg/ml) when compared to four months (58.19 ± 0.03 pg/ml, 58.35 ± 0.3 pg/ml) (p < 0.05). There were no significant changes in PWV, Aix, IL-1ra, IL-2, IL-6, IL-8, TNF-α and hs-CRP levels at both treatment intervals.

Metformin alone or in combination with glimepiride did not improve arterial elasticity and did not reduce pro-inflammatory cytokines levels in T2DM black South African patients.

The context-based knowledge generated by the current study is expected to enhance the continuum of care for T2DM patients.

## Linked entities

- **Proteins:** IL1B (interleukin 1 beta), IL1R1 (interleukin 1 receptor type 1), IL2 (interleukin 2), IL6 (interleukin 6), CXCL8 (C-X-C motif chemokine ligand 8), TNF (tumor necrosis factor)
- **Chemicals:** metformin (PubChem CID 4091), glimepiride (PubChem CID 3476)
- **Diseases:** type 2 diabetes mellitus (MONDO:0005148)

## Full-text entities

- **Genes:** CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL1RN (interleukin 1 receptor antagonist) [NCBI Gene 3557] {aka CRMO2, DIRA, ICIL-1RA, IL-1RN, IL-1ra, IL-1ra3}, IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}
- **Diseases:** inflammation (MESH:D007249), arterial stiffening (MESH:D012078), type 2 diabetes (MESH:D003924), M (MESH:C566367), diabetes (MESH:D003920), MS (MESH:D009103)
- **Chemicals:** glimepiride (MESH:C057619), Metformin (MESH:D008687)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

33 references — full list in the complete paper: https://tomesphere.com/paper/PMC11220136/full.md

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Source: https://tomesphere.com/paper/PMC11220136