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Effect of hyperinsulinemia during hemodialysis on the insulin-like growth factor system and inflammatory biomarkers: a randomized open-label crossover study
by
Christiansen, Jens S
, Ivarsen, Per
, Reinhard, Mark
, Frystyk, Jan
, Jespersen, Bente
, Flyvbjerg, Allan
, Bjerre, Mette
in
Adult
/ Aged
/ Analysis
/ Biological markers
/ Biomarkers - blood
/ Blood Glucose - metabolism
/ Computer software industry
/ Cross-Over Studies
/ Dextrose
/ Dialysis and Transplantation
/ Female
/ Glucose
/ Glucose - administration & dosage
/ Hemodialysis
/ Humans
/ Hyperinsulinism - blood
/ Hyperinsulinism - chemically induced
/ Inflammation Mediators - blood
/ Insulin
/ Insulin - administration & dosage
/ Insulin - blood
/ Insulin-Like Growth Factor I - metabolism
/ Insulin-like growth factors
/ Interleukins
/ Internal Medicine
/ Male
/ Medical research
/ Medicine
/ Medicine & Public Health
/ Middle Aged
/ Nephrology
/ Protein binding
/ Proteins
/ Renal Dialysis - trends
/ Research Article
/ Studies
2013
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Effect of hyperinsulinemia during hemodialysis on the insulin-like growth factor system and inflammatory biomarkers: a randomized open-label crossover study
by
Christiansen, Jens S
, Ivarsen, Per
, Reinhard, Mark
, Frystyk, Jan
, Jespersen, Bente
, Flyvbjerg, Allan
, Bjerre, Mette
in
Adult
/ Aged
/ Analysis
/ Biological markers
/ Biomarkers - blood
/ Blood Glucose - metabolism
/ Computer software industry
/ Cross-Over Studies
/ Dextrose
/ Dialysis and Transplantation
/ Female
/ Glucose
/ Glucose - administration & dosage
/ Hemodialysis
/ Humans
/ Hyperinsulinism - blood
/ Hyperinsulinism - chemically induced
/ Inflammation Mediators - blood
/ Insulin
/ Insulin - administration & dosage
/ Insulin - blood
/ Insulin-Like Growth Factor I - metabolism
/ Insulin-like growth factors
/ Interleukins
/ Internal Medicine
/ Male
/ Medical research
/ Medicine
/ Medicine & Public Health
/ Middle Aged
/ Nephrology
/ Protein binding
/ Proteins
/ Renal Dialysis - trends
/ Research Article
/ Studies
2013
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Effect of hyperinsulinemia during hemodialysis on the insulin-like growth factor system and inflammatory biomarkers: a randomized open-label crossover study
by
Christiansen, Jens S
, Ivarsen, Per
, Reinhard, Mark
, Frystyk, Jan
, Jespersen, Bente
, Flyvbjerg, Allan
, Bjerre, Mette
in
Adult
/ Aged
/ Analysis
/ Biological markers
/ Biomarkers - blood
/ Blood Glucose - metabolism
/ Computer software industry
/ Cross-Over Studies
/ Dextrose
/ Dialysis and Transplantation
/ Female
/ Glucose
/ Glucose - administration & dosage
/ Hemodialysis
/ Humans
/ Hyperinsulinism - blood
/ Hyperinsulinism - chemically induced
/ Inflammation Mediators - blood
/ Insulin
/ Insulin - administration & dosage
/ Insulin - blood
/ Insulin-Like Growth Factor I - metabolism
/ Insulin-like growth factors
/ Interleukins
/ Internal Medicine
/ Male
/ Medical research
/ Medicine
/ Medicine & Public Health
/ Middle Aged
/ Nephrology
/ Protein binding
/ Proteins
/ Renal Dialysis - trends
/ Research Article
/ Studies
2013
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Effect of hyperinsulinemia during hemodialysis on the insulin-like growth factor system and inflammatory biomarkers: a randomized open-label crossover study
Journal Article
Effect of hyperinsulinemia during hemodialysis on the insulin-like growth factor system and inflammatory biomarkers: a randomized open-label crossover study
2013
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Overview
Background
A marked reduction in serum levels of bioactive insulin-like growth factor-I (IGF-I) has been observed in fasting hemodialysis (HD) patients during a 4-h HD session. The aim of the present study was to investigate the beneficial effect of hyperinsulinemia during HD on bioactive IGF-I and inflammatory biomarkers.
Methods
In a randomized cross-over study, 11 non-diabetic HD patients received a standardised HD session with either: 1) no treatment, 2) glucose infusion (10% glucose, 2.5 mL/kg/h), or 3) glucose-insulin infusion (10% glucose added 30 IU NovoRapid® per litre, 2.5 mL/kg/h). Each experiment consisted of three periods: pre-HD (−120 to 0 min), HD (0 to 240 min), and post-HD (240 to 360 min). A meal was served at baseline (−120 min); infusions were administered from baseline to 240 min. The primary outcome was change in bioactive IGF-I during the experiment. Secondary outcomes were changes in high-sensitivity C-reactive protein, interleukin-1β, interleukin-6, and tumor necrosis factor α. Comparisons were performed using mixed-model analysis of variance for repeated measures.
Results
From baseline to the end of study, no significant differences were observed in the changes in either serum bioactive IGF-I or total IGF-I between study days. Overall, serum bioactive IGF-I levels rose above baseline at 120 to 300 min with a maximum increase of 20% at 120 min (95% confidence interval (CI), 9 to 31%; p < 0.001), whereas total IGF-I levels rose above baseline at 180 to 300 min with a maximum increase of 5% at 240 min (95% CI, 2 to 9%; p = 0.004). A significant difference was observed in the changes in serum IGF-binding protein-1 (IGFBP-1) between study days (p = 0.008), but differences were only significant in the post-HD period. From baseline to the end of HD, no significant difference was observed in the changes in serum IGFBP-1 levels between study days, and in this time period overall serum IGFBP-1 levels were below baseline at all time points with a maximum decrease of 51% at 180 min (95% CI, 45 to 57%; p < 0.001). None of the investigated inflammatory biomarkers showed any differences in the changes over time between study days.
Conclusions
Postprandial insulin secretion stimulated the IGF-system during HD with no further effect of adding glucose or glucose-insulin infusion. Hyperinsulinemia during HD had no effect on biomarkers of inflammation.
Trial registration
ClinicalTrials.gov registry:
NCT01209403
Publisher
BioMed Central,BioMed Central Ltd,Springer Nature B.V
Subject
/ Aged
/ Analysis
/ Dextrose
/ Dialysis and Transplantation
/ Female
/ Glucose
/ Glucose - administration & dosage
/ Humans
/ Hyperinsulinism - chemically induced
/ Inflammation Mediators - blood
/ Insulin
/ Insulin - administration & dosage
/ Insulin-Like Growth Factor I - metabolism
/ Male
/ Medicine
/ Proteins
/ Studies
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