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Systemic inflammatory indices and glucose homeostasis in children with obesity: evidence from oral glucose tolerance
1Department of Pediatric Endocrinology, Konya City Hospital, Konya, Türkiye.
Insights
The systemic immune-inflammation index (SII) was unexpectedly higher in children with obesity who had normal blood sugar levels, not those with dysglycemia. These findings suggest SII is not a reliable biomarker for detecting glucose metabolism abnormalities in this population.
Area of Science:
- Pediatric Endocrinology
- Metabolic Health
- Inflammation Biomarkers
Background:
- Chronic low-grade inflammation is linked to metabolic dysfunction in obesity.
- Systemic immune-inflammation index (SII) and pan-immune-inflammation value (PIV) are emerging inflammation biomarkers.
- Limited pediatric data exist on SII/PIV associations with oral glucose tolerance test (OGTT)-defined glucose metabolism.
Purpose of the Study:
- To investigate the association between SII and PIV with glucose metabolism abnormalities in children with obesity.
- To evaluate the utility of SII and PIV as potential biomarkers for dysglycemia in pediatric obesity.
Main Methods:
- Retrospective cross-sectional study of 238 children and adolescents with obesity undergoing OGTT.
- Calculation of SII and PIV from complete blood counts.
- Statistical analysis using ANCOVA adjusted for BMI-SDS, age, sex, and pubertal status.
Main Results:
- BMI-SDS positively correlated with both SII and PIV.
- No significant associations were found between SII/PIV and HbA1c, lipid profile, HOMA-IR, Matsuda index, or insulinogenic index.
- Adjusted SII levels were significantly higher in the normoglycemic group compared to the dysglycemic group (p=0.025).
Conclusions:
- The study found higher SII values in normoglycemic participants, an unexpected result requiring further investigation.
- The findings do not support the use of SII or PIV as diagnostic or screening biomarkers for dysglycemia in children with obesity.
- Neither inflammatory index correlated with OGTT-derived insulin sensitivity or early insulin secretion, limiting their clinical utility.
Abstract:
The systemic immune-inflammation index (SII) and pan-immune-inflammation value (PIV) are emerging biomarkers of chronic low-grade inflammation. This study aimed to evaluate their association with glucose metabolism abnormalities in children with obesity. In this retrospective cross-sectional study, children and adolescents with obesity who underwent an oral glucose tolerance test (OGTT) were included. SII and PIV were calculated from complete blood counts. ANCOVA was used to adjust for body mass index standard deviation score (BMI-SDS), age, sex, and pubertal status, and effect sizes were estimated. A total of 238 participants were analyzed (154 normoglycemic, 84 dysglycemic), most of whom were pubertal (92%). BMI-SDS showed a significant positive correlation with both SII (r = 0.236, p < 0.001) and PIV (r = 0.279, p < 0.001). No significant associations were found between inflammatory indices and metabolic parameters, including HbA1c, lipid profile, HOMA-IR, Matsuda index, or insulinogenic index (p > 0.05). After adjustment for BMI-SDS, age, sex, and pubertal status, SII levels remained significantly higher in the normoglycemic group (679.86 vs. 553.06, p = 0.025), with a small-to-moderate effect size (Cohen's d = 0.341; η2 = 0.021). PIV showed a similar trend without statistical significance.
Conclusion:
Higher SII values were observed in the normoglycemic group; however, the explanation for this unexpected association remains uncertain. The findings do not support the use of SII as a diagnostic or screening biomarker for dysglycemia.
What Is Known:
• Chronic low-grade inflammation contributes to obesity-related metabolic dysfunction. SII and PIV have been associated with metabolic abnormalities, but pediatric data based on OGTT-defined glucose tolerance are limited.
What Is New:
• SII was unexpectedly higher in normoglycemic participants after adjustment, whereas PIV was not independently associated with dysglycemia. Neither index correlated with OGTT-derived insulin sensitivity or early insulin secretion, limiting their clinical utility for detecting dysglycemia.
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