# Elevated inflammation supra-additively promotes the progression from prediabetes to diabetes: a prospective cohort study

**Authors:** Yulong Lan, Dan Wu, Huancong Zheng, Xiong Ding, Hui Zhou, Kuangyi Wu, Weiqiang Wu, Zegui Huang, Xianxuan Wang, Wei Wang, Shouling Wu, Youren Chen

PMC · DOI: 10.7189/jogh.15.04318 · Journal of Global Health · 2025-10-24

## TL;DR

This study finds that high inflammation levels, along with prediabetes, significantly increase the risk of developing diabetes, especially in younger adults.

## Contribution

The study reveals a synergistic effect of inflammation and prediabetes in accelerating diabetes progression, with age-specific differences.

## Key findings

- Elevated inflammation and impaired fasting glucose jointly increase diabetes risk more than their individual effects.
- The interaction effect is stronger in individuals under 60 years old compared to those aged 60 and above.

## Abstract

Factors impacting on the conversion of prediabetes to diabetes or normoglycemia remain unclear. This study aimed to investigate the role of subclinical inflammation, assessed by high-sensitivity C-reactive protein (hsCRP), in the progression to diabetes from prediabetes, assessed by impaired fasting glucose (IFG).

Time-to-event survival analyses were conducted among 82 475 participants without diabetes from Kailuan Study (a real-life prospective cohort in China) to access the isolated and joint effect of hsCRP and IFG on diabetes risk, and quantify their relative contribution to incident diabetes.

Over a median 11-year follow-up, 14 215 diabetes cases were recorded. IFG and hsCRP independently and jointly increased diabetes risk. Diabetes incidence was higher in those with elevated inflammation (hsCRP≥2 mg/L: 90.45 vs. 66.76 per 1000 person-years). The joint effect risk (hazard ratios (HR) = 4.96; 95% confidence interval (CI) = 4.66–5.28) exceeded the sum of individual risks (HR = 4.29; 95% CI = 4.09–4.49 for IFG and HR = 1.11; 95% CI = 1.06–1.16 for elevated inflammation), with a relative excess risk due to interaction of 0.56 (95% CI = 0.23–0.89). Attributable proportions were 83.08% for IFG, 2.78% for hsCRP, and 14.14% for their interaction. The joint risks and the additive interaction were significant in both men and women, and were more pronounced among individuals aged <60 years than those aged ≥60 years.

Elevated inflammation synergistically amplifies diabetes risk in prediabetes among Chinese adults, particularly in those <60 years.

## Linked entities

- **Diseases:** diabetes (MONDO:0005015), prediabetes (MONDO:0006920)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** IFG (MESH:D007003), Diabetes (MESH:D003920), prediabetes (MESH:D011236), inflammation (MESH:D007249)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12550539/full.md

## References

51 references — full list in the complete paper: https://tomesphere.com/paper/PMC12550539/full.md

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Source: https://tomesphere.com/paper/PMC12550539