# The relationship between remote diffusion-weighted imaging lesions and the triglyceride-glucose index and clinical outcomes in patients with intracerebral hemorrhage

**Authors:** Lu Wang, Yu Gu, Guoliang Jiang, Chunyan Lei, Potao Zhang, Wen Jiang, Xinglong Yang, Ansong Jin, Qionghua Deng

PMC · DOI: 10.3389/fneur.2025.1562361 · Frontiers in Neurology · 2025-07-21

## TL;DR

This study explores how remote brain lesions and blood markers relate to outcomes in patients with brain hemorrhage.

## Contribution

Identifies fasting glucose and hematoma location as predictors of DWI lesions in ICH patients.

## Key findings

- 46 out of 245 ICH patients had distal DWI lesions.
- High fasting glucose and hematoma site predict DWI lesions.
- Older age and higher NIHSS scores predict poor outcomes.

## Abstract

This study aimed to observe the relationship between the presence of distal diffusion-weighted imaging (DWI) lesions and triglyceride-glucose (TyG) index and clinical outcome after intracerebral hemorrhage (ICH), and identify the risk factors for DWI lesions in ICH patients.

ICH patients at the First Affiliated Hospital of Kunming Medical University were retrospectively collected. Demographic data, laboratory examination, and imaging data of the patients were collected. The patients were divided into two groups based on the presence or absence of distal DWI lesions as determined by magnetic resonance imaging (MRI). Multivariate logistic regression analysis was used to evaluate the risk factors for DWI lesions and clinical outcomes.

Among 245 ICH patients included in this study, 46 (18.78%) had DWI lesions and 199 (81.22%) did not. We found that the occurrence probability of DWI lesions reached the maximum in the range Q2 of the TyG index. ICH patients with DWI lesions had a similar frequency of death or disability at 90 days compared with patients without DWI lesions. Multivariate logistic regression analysis showed that high fasting glucose (p = 0.039) and hematoma site (p = 0.048) were significant predictors of DWI lesions after ICH. The old age (p < 0.001), higher National Institutes of Health Stroke Scale (NIHSS) score (p < 0.001), and midline shift (p = 0.034) were independent predictors of poor functional outcome at 3 months.

There was no definitive correlation between the TyG index and distal DWI lesions in our study. The elevated high fasting glucose levels and hematoma site were significant predictors for DWI lesions after ICH.

## Linked entities

- **Diseases:** intracerebral hemorrhage (MONDO:0013792)

## Full-text entities

- **Genes:** INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** dyslipidemia (MESH:D050171), blood loss (MESH:D016063), cerebral venous thrombosis (MESH:D020767), hypertension (MESH:D006973), Hematoma (MESH:D006406), coronary artery disease (MESH:D003324), infarctions (MESH:D007238), neuroinflammation (MESH:D000090862), DWI (MESH:C564543), NIHSS (MESH:C538175), ischemia (MESH:D007511), bleeding (MESH:D006470), diabetes (MESH:D003920), thrombosis (MESH:D013927), midline shift (MESH:D020178), intraventricular hemorrhage (MESH:D000074042), EPVS (MESH:D054973), atherosclerosis (MESH:D050197), endothelial dysfunction (MESH:D014652), vascular malformation (MESH:D054079), brain atrophy (MESH:C566985), pulse disease (MESH:D004194), atrial fibrillation (MESH:D001281), Hyperglycemia (MESH:D006943), cerebrovascular disease (MESH:D002561), hyperlipidemia (MESH:D006949), cardiovascular and cerebrovascular diseases (MESH:D002318), moyamoya disease (MESH:D009072), aneurysm (MESH:D000783), cardiac emboli (MESH:D020766), death (MESH:D003643), lacunar infarction (MESH:D059409), WMH (MESH:D056784), midline (MESH:C538667), cavernous hemangioma (MESH:D006392), blood coagulation (MESH:D001778), carotid plaque (MESH:D016893), inflammation (MESH:D007249), malignancy (MESH:D009369), subarachnoid hemorrhage (MESH:D013345), metabolic abnormality (MESH:D008659), ICH (MESH:D002543), IR (MESH:D007333), Stroke (MESH:D020521), coronary heart disease (MESH:D003327), cerebral infarction (MESH:D002544)
- **Chemicals:** blood glucose (MESH:D001786), TyG (-), glucose (MESH:D005947), catecholamine (MESH:D002395), triglyceride (MESH:D014280), lipid (MESH:D008055), cortisol (MESH:D006854)
- **Species:** 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/PMC12318738/full.md

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12318738/full.md

## References

44 references — full list in the complete paper: https://tomesphere.com/paper/PMC12318738/full.md

---
Source: https://tomesphere.com/paper/PMC12318738