Published online Sep 9, 2024. doi: 10.5409/wjcp.v13.i3.94721
Revised: June 28, 2024
Accepted: July 10, 2024
Published online: September 9, 2024
Processing time: 159 Days and 7.6 Hours
Insulin resistance and obesity present significant challenges in pediatric populations. Selenoprotein P1 (SEPP1) serves as a biomarker for assessing sele
To ascertain SEPP1 blood levels in children and adolescents diagnosed with obesity and to assess its correlation with insulin resistance and adiposity indices.
170 children participated in this study, including 85 diagnosed with obesity and an equal number of healthy counterparts matched for age and sex. Each participant underwent a comprehensive medical evaluation, encompassing a detailed medical history, clinical examination, and anthropometric measurements like waist circumference and waist-to-height ratio. Furthermore, routine blood tests were conducted, including serum SEPP1, visceral adiposity index (VAI), and Homeostatic Model Assessment of Insulin Resistance (HOMA-IR) level.
Our findings revealed significantly lower serum SEPP1 levels in children with obesity compared to their healthy peers. Moreover, notable negative correlations were observed between serum SEPP1 levels and body mass index, VAI, and HOMA-IR.
The study suggests that SEPP1 could serve as a valuable predictor for insulin resistance among children and adolescents diagnosed with obesity. This highlights the potential utility of SEPP1 in pediatric metabolic health assessment and warrants further investigation.
Core Tip: This study investigates the association between serum Selenoprotein P1 (SEPP1) levels and insulin resistance in pediatric obesity. Conducted on 170 children, the study reveals significantly lower SEPP1 levels in obese children compared to healthy peers, with notable negative correlations between SEPP1 levels and adiposity indices such as body mass index, visceral adiposity index, and Homeostatic Model Assessment of Insulin Resistance. The findings suggest SEPP1's potential as a predictor for insulin resistance in pediatric obesity, highlighting its utility in metabolic health assessment. However, further research is needed to determine the temporal relationship between SEPP1 levels and insulin resistance onset in pediatric obesity, emphasizing the importance of continued investigation in this area for clinical practice.