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Updated: Sep 11, 2025

Assessment of Child Anthropometry in a Large Epidemiologic Study
Published on: February 2, 2017
Elevated serum phoenixin levels in boys with central precocious puberty are positively correlated with BMI
Tao Xie1,2,3, Wei Qin1,2,3, Dan Zeng1
1Department of Pediatrics, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Insights
Phoenixin (PNX) levels are elevated in boys with central precocious puberty (CPP) and correlate with BMI. PNX aids in CPP diagnosis and monitoring treatment effectiveness.
Area of Science:
- Endocrinology
- Pediatric Endocrinology
- Reproductive Biology
Background:
- Central precocious puberty (CPP) involves early onset of puberty in children.
- Phoenixin (PNX) is a peptide hormone with potential roles in reproductive function.
- Factors influencing PNX levels in CPP require further investigation.
Purpose of the Study:
- To investigate serum phoenixin (PNX) levels in boys with CPP.
- To evaluate the diagnostic and therapeutic relevance of PNX in CPP.
- To identify factors influencing PNX expression in CPP.
Main Methods:
- Serum PNX-14 and PNX-20 levels were measured in 43 boys with CPP and 48 controls using ELISA.
- Correlations with luteinizing hormone (LH), testosterone, and BMI were analyzed.
- Receiver operating characteristic (ROC) analysis assessed diagnostic performance; 12 boys were followed post-treatment.
Main Results:
- Serum PNX-20 and PNX-14 levels were significantly higher in boys with CPP compared to controls.
- Higher PNX levels were observed in overweight/obese CPP patients.
- PNX levels correlated positively with LH, testosterone, and BMI; PNX-14 associated with LH, PNX-20 with BMI.
Conclusions:
- PNX is linked to pubertal progression and BMI in boys with CPP.
- PNX demonstrates moderate diagnostic value, particularly PNX-20, as an adjunct marker.
- PNX-20 levels decreased after treatment, suggesting its utility in monitoring therapy.
Objective:
This study investigated changes in serum phoenixin (PNX) levels in boys with central precocious puberty (CPP), aiming to evaluate its diagnostic and therapeutic relevance and identify factors influencing its expression.
Method:
Serum samples were collected from 43 boys with CPP and 48 age-matched prepubertal controls. Participants were further divided into overweight/obese and normal-weight subgroups based on body mass index (BMI). Levels of phoenixin-14 (PNX-14) and phoenixin-20 (PNX-20) were measured using enzyme-linked immunosorbent assay (ELISA). Correlations with luteinizing hormone (LH), testosterone, and BMI were analyzed. Multiple linear regression identified independent influencing factors, and receiver operating characteristic (ROC) analysis assessed the diagnostic performance of PNX. Twelve CPP boys were followed for 6 months after gonadotropin-releasing hormone analog (GnRHa) treatment.
Results:
PNX-20 and PNX-14 levels were significantly higher in the CPP group than in controls (P = 0.001). Among subgroups, the overweight/obese CPP group exhibited the highest levels. Both PNX forms were positively correlated with baseline LH, testosterone, and BMI; PNX-14 was most strongly associated with LH, and PNX-20 with BMI. ROC analysis showed moderate diagnostic value for PNX-14 (AUC: 0.710) and PNX-20 (AUC: 0.696), with a combined AUC of 0.718. Following treatment, levels of PNX-20, LH, follicle-stimulating hormone (FSH), and testosterone significantly declined, while PNX-14 remained unchanged.
Conclusions:
PNX is associated with pubertal progression and BMI in boys with CPP. While not suitable as a standalone diagnostic marker, PNX - especially PNX-20 - may serve as a useful adjunct for diagnosis and treatment monitoring.
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