# Effect of Direct-Acting Antiviral Therapy on Glycemic Control in Patients with Chronic Hepatitis C and Type 2 Diabetes: A Systematic Review and Meta-Analysis

**Authors:** Jing-Hong Hu, Ming-Ling Chang, Ming-Shyan Lin, Tung-Jung Huang, Yung-Yu Hsieh

PMC · DOI: 10.3390/v18020239 · Viruses · 2026-02-13

## TL;DR

Treating hepatitis C with DAAs improves blood sugar control in patients with type 2 diabetes, but results vary widely.

## Contribution

This study quantifies the impact of DAA therapy on glycemic control in T2DM patients with HCV.

## Key findings

- DAA therapy led to a significant average 0.45% reduction in HbA1c after SVR.
- The effect was highly variable across studies, with heterogeneity at 97.8%.
- HCV appears to be a modifiable factor contributing to chronic hyperglycemia.

## Abstract

The eradication of hepatitis C virus (HCV) with interferon-free direct-acting antivirals (DAAs) has transformed the management of chronic HCV infection. Chronic HCV infection is associated with an increased risk of type 2 diabetes mellitus (T2DM) and poor glycemic control. However, the magnitude and consistency of improvement in glycated hemoglobin (HbA1c) after DAA-induced sustained virologic response (SVR) in patients with established T2DM remain unclear. We conducted a systematic review and meta-analysis of six cohort studies comprising 2805 patients. Overall, DAA therapy was associated with a significant reduction in HbA1c after SVR, with a pooled random-effect mean difference of −0.45% (95% CI −0.74% to −0.16%; I2 = 97.8%). This effect is highly heterogeneous but suggests that HCV may be a modifiable contributor to chronic hyperglycemia. These findings highlight the need for close glucose monitoring and individualized adjustment of antidiabetic therapy after SVR to optimize metabolic outcomes.

## Linked entities

- **Diseases:** type 2 diabetes mellitus (MONDO:0005148), T2DM (MONDO:0005148)

## Full-text entities

- **Genes:** INSR (insulin receptor) [NCBI Gene 3643] {aka CD220, HHF5}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IARS1 (isoleucyl-tRNA synthetase 1) [NCBI Gene 3376] {aka GRIDHH, IARS, ILERS, ILRS, IRS, PRO0785}, DPP4 (dipeptidyl peptidase 4) [NCBI Gene 1803] {aka ADABP, ADCP2, CD26, DPPIV, TP103}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** hypoglycemic (MESH:C000721848), metabolic dysregulation (MESH:D021081), metabolic defects (MESH:D008659), obesity (MESH:D009765), hepatic steatosis (MESH:D005234), Chronic HCV infection (MESH:D019698), liver fibrosis (MESH:D008103), diabetes (MESH:D003920), cirrhosis (MESH:D005355), hyperglycemia (MESH:D006943), metabolic disturbances (MESH:D024821), injury to (MESH:D014947), MASLD (MESH:D008107), inflammation (MESH:D007249), hepatocellular carcinoma (MESH:D006528), type 1 diabetes (MESH:D003922), hepatic injury (MESH:D056486), beta-cell dysfunction (MESH:D007340), hepatic decompensation (MESH:D006333), renal disease (MESH:D007674), T2DM (MESH:D003924), mixed cryoglobulinemia (MESH:C565141), IR (MESH:D007333), infected (MESH:D007239), Hypoglycemia (MESH:D007003), cardiovascular complications (MESH:D002318), HCV infection (MESH:D006526)
- **Chemicals:** cholesterol (MESH:D002784), sulfonylureas (MESH:D013453), metformin (MESH:D008687), TG (MESH:D014280), simeprevir (MESH:D000069616), Glucose (MESH:D005947), daclatasvir (MESH:C549273), ledipasvir (MESH:C586541), lipid (MESH:D008055), paritaprevir (MESH:C585405), DAA (-)
- **Species:** Hepatitis B virus (no rank) [taxon 10407], HCV [taxon 11103], Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12945286/full.md

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12945286/full.md

## References

17 references — full list in the complete paper: https://tomesphere.com/paper/PMC12945286/full.md

---
Source: https://tomesphere.com/paper/PMC12945286