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Updated: May 24, 2026

Evaluation of Cerebral Blood Flow Autoregulation in the Rat Using Laser Doppler Flowmetry
Published on: January 19, 2020
Microvascular autoregulation in children and adolescents with type 1 diabetes mellitus
O Schlager1, A Hammer, A Willfort-Ehringer
1Department of Medicine II, Division of Angiology, Medical University of Vienna, Währinger Gürtel 18-20, 1090 Vienna, Austria.
Insights
Postocclusive reactive hyperaemia (PORH) testing reveals impaired microvascular autoregulation in children with type 1 diabetes. This suggests potential early changes in blood vessel function in young patients with diabetes.
Area of Science:
- Pediatric Endocrinology
- Vascular Physiology
- Diabetes Research
Background:
- Microvascular dysfunction is an early complication of type 1 diabetes mellitus.
- Assessing microvascular autoregulation in children with type 1 diabetes is crucial for understanding disease progression.
Purpose of the Study:
- To investigate if microvascular autoregulation is impaired in children with type 1 diabetes.
- To determine if postocclusive reactive hyperaemia (PORH) can non-invasively detect these impairments.
Main Methods:
- Assessed microvascular autoregulation using PORH with laser Doppler fluxmetry in 58 children with type 1 diabetes and 58 healthy controls.
- Measured baseline perfusion, biological zero, peak perfusion, time to peak, and recovery time.
Main Results:
- Children with type 1 diabetes exhibited higher peak perfusion (1.7 ± 0.93 AU vs 1.29 ± 0.46 AU; p = 0.004) and lower biological zero (0.14 ± 0.04 AU vs 0.19 ± 0.04 AU; p < 0.0001) compared to controls.
- No significant differences were found in baseline perfusion, time to peak, or recovery time.
Conclusions:
- PORH effectively identifies impaired microvascular autoregulation in children with type 1 diabetes.
- Elevated peak perfusion may indicate reduced vasoconstrictive capacity in arteriolar smooth muscle cells in this population.
Aims/Hypothesis:
Deterioration of microvascular function may have an early onset in individuals with type 1 diabetes mellitus. We hypothesised that microvascular autoregulation is impaired in children with type 1 diabetes and can be detected non-invasively by postocclusive reactive hyperaemia (PORH).
Methods:
Microvascular autoregulation was assessed in 58 children with type 1 diabetes and 58 age- and sex-matched healthy controls by PORH using laser Doppler fluxmetry. Baseline perfusion, biological zero (defined as a 'no flow' laser Doppler signal during suprasystolic occlusion), peak perfusion following occlusion, time to peak and recovery time (time until baseline perfusion is resumed) were recorded and compared between the groups.
Results:
Peak perfusion was higher in children with type 1 diabetes than in healthy controls (1.7 ± 0.93 AU [arbitrary units] vs 1.29 ± 0.46 AU; p = 0.004), and biological zero was lower in children with type 1 diabetes vs controls (0.14 ± 0.04 AU vs 0.19 ± 0.04 AU; p < 0.0001). No differences were seen between the groups in baseline perfusion, time to peak during PORH and recovery time following PORH.
Conclusions/Interpretation:
PORH reveals impaired microvascular autoregulation in children with type 1 diabetes. The higher peak perfusion might reflect a decline in the vasoconstrictive ability of arteriolar smooth muscle cells upstream of capillary beds in children with type 1 diabetes.
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