# Sudomotor dysfunction reflects early atherosclerosis risk in adults with type 1 diabetes

**Authors:** Dariusz Naskręt, Agnieszka Gandecka-Pempera, Michał Kulecki, Aleksandra Araszkiewicz, Dorota Zozulińska-Ziółkiewicz

PMC · DOI: 10.1038/s41598-026-36292-w · Scientific Reports · 2026-01-16

## TL;DR

This study shows that early nerve dysfunction in type 1 diabetes is linked to increased risk of atherosclerosis and vascular aging.

## Contribution

The study introduces sudomotor function testing as a potential non-invasive tool for assessing cardiovascular risk in type 1 diabetes.

## Key findings

- Participants with sudomotor dysfunction had significantly thicker carotid intima-media and higher vascular age.
- Reduced sudomotor function remained significantly associated with vascular age after adjusting for key factors.
- Sudomotor dysfunction is linked to early signs of atherosclerosis in adults with type 1 diabetes.

## Abstract

Adults with type 1 diabetes (T1D) are at increased risk of premature atherosclerosis. Sudomotor dysfunction (SMD), an early manifestation of diabetic neuropathy, may contribute to vascular injury. This cross-sectional study assessed the relationship between sudomotor function (SMF), carotid intima-media thickness (cIMT), and vascular age (VA) in T1D. The study included 299 adults with T1D (137 men), aged 34 (IQR: 25–44) years, disease duration 16 (IQR: 11–25) years, and HbA1c of 7.7 (IQR: 7.0–8.7)%. Sudomotor function was measured with the SUDOSCAN device; abnormal function was defined as Feet ESC < 70 µS (SMD). cIMT was assessed with carotid ultrasound, and VA was derived from cIMT values. Participants with SMD had thicker cIMT [0.56 (IQR: 0.5–0.67) vs 0.54 (0.48–0.52), p = 0.04] and higher VA [48 (36–70) vs 42 (32–58), p = 0.04]. We found a negative correlation between Feet ESC and cIMT (Rs = − 0.22, p < 0.001). In a multiple linear regression model adjusted for sex, HbA1c, BMI, and creatinine, reduced Feet ESC remained significantly associated with VA (β = 0.13, p = 0.03), R2 = 0.065. SMD is associated with increased cIMT and VA in adults with T1D. SMF assessment by SUDOSCAN may represent a rapid, non-invasive tool to identify individuals at higher cardiovascular risk.

## Linked entities

- **Diseases:** type 1 diabetes (MONDO:0005147), atherosclerosis (MONDO:0005311)

## Full-text entities

- **Genes:** CIMT (Carotid intimal medial thickness) [NCBI Gene 404677], CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** Diabetic Retinopathy (MESH:D003930), Small-fiber neuropathy (MESH:D000071075), impaired sudomotor function (MESH:D003072), death (MESH:D003643), CVD (MESH:D002318), Complications (MESH:D008107), Hypoxia (MESH:D000860), SMF (MESH:D003291), peripheral arterial disease (MESH:D058729), metabolic dysregulation (MESH:D021081), Diabetes (MESH:D003920), insulin deficiency (MESH:D007333), T1D (MESH:D003922), vascular complications (MESH:D003925), atherosclerosis (MESH:D050197), dyslipidemia (MESH:D050171), CAN (MESH:D006331), neurovascular complication (MESH:D013901), chronic inflammation (MESH:D007249), VA (MESH:D057772), ESC (MESH:D012871), microangiopathy (MESH:D014652), microvascular injury (MESH:D017566), hyperglycemia (MESH:D006943), mental and neurological disorder (MESH:D001523), HT (MESH:D006973), Microvascular complications (OMIM:603933), infection (MESH:D007239), hyperlipidemia (MESH:D006949), DPN (MESH:D010523), DKD (MESH:D003928), foot ulceration (MESH:D016523), T2D (MESH:D003924), diabetic neuropathy (MESH:D003929), autonomic neuropathy (MESH:D009422), Peripheral nerve degeneration (MESH:D009410), ketoacidosis (MESH:D007662)
- **Chemicals:** TG (MESH:D013866), triglycerides (MESH:D014280), insulin (MESH:D007328), chloride (MESH:D002712), glycemia (MESH:D001786), cholesterol (MESH:D002784), AGEs (MESH:D017127), lipid (MESH:D008055), creatinine (MESH:D003404), nitric oxide (MESH:D009569), ESC (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

1 references — full list in the complete paper: https://tomesphere.com/paper/PMC12881360/full.md

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Source: https://tomesphere.com/paper/PMC12881360