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Forschungsstelle
BASPO
Projektnummer
FG04-004
Projekttitel
Leistungsfähigkeit bei Eu- bzw. Hyperglykämie

Texte zu diesem Projekt

 DeutschFranzösischItalienischEnglisch
Schlüsselwörter
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Kurzbeschreibung
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Projektziele
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Abstract
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Erfasste Texte


KategorieText
Schlüsselwörter
(Deutsch)
Leistungsfähigkeit
Hyperglykämie
Kurzbeschreibung
(Deutsch)
Spezifizierung nur auf begründete Rückfragen hin
Projektziele
(Deutsch)
Spezifizierung nur auf begründete Rückfragen hin
Abstract
(Deutsch)

Background: Circumstantial evidence suggests that an increase in plasma glucose availability

improves exercise capacity in subjects with type 1 diabetes mellitus. The aim of this study

was to assess exercise capacity in eu- and hyperglycaemic conditions in subjects with type 1

diabetes.

 

Methods: Eight moderately trained male subjects with type 1 diabetes on continuous

subcutaneous insulin infusion were studied. Using identical insulin infusion rates, the patients

were randomly allocated to perform two stepwise ergometer tests in a eu- and hyperglycaemic

clamp condition. The primary endpoint was the peak power output, secondary endpoints

comprised the rate of perceived exertion, lactate levels, heart rate, and respiratory exchange

ratio.

 

Results: Eu- and hyperglycaemic clamp conditions were at a plasma glucose concentration of

5.3±0.6 mmol/l and 12.4±2.1 mmol/l, respectively (mean ± SD), and remained stable

throughout the physical exercise. Insulin levels were similar in both condition.

Hyperglycaemia did not result in a significant increase in the peak power output compared to

euglycaemia (mean paired difference of 4.96 W, 95% CI -11.3 to 21.2, p=0.49).

Hyperglycaemia did not significantly impact on the secondary endpoints compared to

euglycaemia. Sensitivity analyses confirmed these results.

 

Conclusions: In subjects with type 1 diabetes exercise capacity is not influenced by

hyperglycaemia. Comparable levels of lactate and similar respiratory exchange ratio suggest

that an increase in extracellular glucose availability did not translate into increased

intracellular glucose oxidation.