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Soluble receptor for advanced glycation end products as a potential biomarker to predict weight loss and improvement of insulin sensitivity by a very low calorie diet of obese human subjects.

Cytokine
June 1, 2015
Imke Hagen et al. (8 authors)
Clinical TrialJournal ArticleHuman StudyClinical
Study Details

Study Goal

The researchers aimed to determine whether serum sRAGE levels are related to weight loss and insulin resistance improvement in obese subjects following a very low-calorie diet (VLCD).

Results Summary

Lower baseline sRAGE levels were significantly associated with greater BMI reduction and improved insulin resistance. Changes in sRAGE levels during the intervention correlated with changes in BMI, suggesting sRAGE as a potential biomarker for predicting dietary intervention outcomes.

Population

22 severely obese subjects (median BMI: 44.5 kg/m²).

Effective Dosage

800 kcal/day (VLCD phase).

Duration

6 months (12 weeks VLCD, 12 weeks weight maintenance).

Interactions

None mentioned

Extracted Claims (7)
InterventionDirectionEndpointPopulationDosageImpactClaim #
very low calorie diet (VLCD)
decrease
body weight
22 severe obese subjects
21.7kg
reduction
#1
very low calorie diet (VLCD)
decrease
insulin resistance
22 severe obese subjects
-
significant improvement
#2
-
decrease
sRAGE serum levels
22 severe obese subjects
-
significantly inversely related
#3
-
decrease
sRAGE serum levels
22 severe obese subjects
-
significantly inversely related
#4
-
decrease
sRAGE serum levels at baseline
study subjects with greater reduction of BMI
-
significantly lower
#5
-
decrease
HOMA reduction
subjects with lower sRAGE serum levels at baseline
-
significantly greater
#6
very low calorie diet (VLCD)
decrease
changes of sRAGE serum levels
22 severe obese subjects
-
significantly correlated
#7
Abstract

INTRODUCTION: Obesity is associated with low-grade systemic inflammation which is thought to trigger the development of comorbidities such as type 2 diabetes. The soluble receptor for advanced glycation end products (sRAGE) belongs to the innate immune system and has been linked to obesity, recently. The aim of the present study was to examine whether serum sRAGE concentrations are related to the grade of weight loss and improvement of insulin resistance due to a very low calorie diet (VLCD). METHODS: 22 severe obese subjects (Median Body Mass Index (BMI): 44.5kg/m(2)) were included in a dietary intervention study of 6month, consisting of a very low calorie formula diet phase (VLCD: 800kcal/d) for 12 weeks and a following 12 week weight maintenance phase. Fasting glucose, fasting insulin, adiponectin, leptin and sRAGE were determined from sera. Insulin sensitivity was estimated by Homeostasis Model Assessment (HOMA) index and leptin-to-adiponectin-ratio (LAR). RESULTS: Mean body weight reduction by VLCD accounted to 21.7kg with a significant improvement of insulin resistance. At baseline, sRAGE serum levels were significantly inversely related to BMI (rS=-0.642, p=0.001) and HOMA (rS=-0.419, p=0.041). Of interest, sRAGE serum levels at baseline were significantly lower in study subjects with greater reduction of BMI (p=0.017). In addition, a significantly greater HOMA reduction was observed in subjects with lower sRAGE serum levels at baseline (p=0.006). Finally, correlation analysis revealed, that changes of sRAGE serum levels were significantly correlated to changes of BMI (rS=-0.650, p=0.022) during intervention. CONCLUSION: Anti-inflammatory sRAGE might be a potential future biomarker to predict weight loss and improvement of insulin resistance by a VLCD whereby lower baseline sRAGE serum levels indicate a better outcome of the dietary intervention.

Medical Subject Headings (MeSH)
AnthropometryBiomarkersBody Mass IndexCaloric RestrictionFemaleHumansInsulinInsulin ResistanceMaleMiddle AgedObesityReceptor for Advanced Glycation End ProductsSolubilityWeight Loss
Study Links
Quality Scores
SafetyNot Assessed
Efficacy75/10
Quality70/10
Citation Metrics
Total Citations28
Citations/Year2.8
Relative Citation Ratio1.12
NIH Percentile54.3%
Research Impact Scores
APT Score0.50
Weight Score1.65
Normalized Score0.64