Related Experiment Video
Updated: Feb 19, 2026

Skeletal Phenotype Analysis of a Conditional Stat3 Deletion Mouse Model
Published on: July 3, 2020
A Study of the Relationship Between Cystatin C and Metabolic Bone Disease in Preterm Infants
Sabriye Korkut1, Şeyma Memur1, Hülya Halis1
1Erciyes University Faculty of Medicine, Department of Neonatology, Kayseri, Turkey
Insights
Serum Cystatin C (CysC) levels in preterm infants are not affected by osteopenia of prematurity (OP). This finding supports the safe use of CysC as a renal insufficiency marker in these vulnerable infants.
Area of Science:
- Neonatology
- Pediatric Nephrology
- Biochemistry
Background:
- Cystatin C (CysC) is a widely recognized biomarker for assessing kidney function in premature infants.
- Osteopenia of prematurity (OP) is a common complication in preterm infants, potentially impacting various physiological markers.
- The reliability of CysC in infants with OP requires specific investigation.
Purpose of the Study:
- To evaluate serum CysC levels in preterm infants diagnosed with osteopenia of prematurity (OP).
- To determine if OP influences the accuracy and safety of using CysC as a marker for renal insufficiency in preterm neonates.
Main Methods:
- A cohort of 50 preterm infants (gestational age ≤32 weeks) was studied.
- Serum levels of calcium, phosphorus, alkaline phosphatase, and CysC were measured at nine weeks postnatal.
- Bone mineral density was assessed using quantitative ultrasonography; OP was defined by a Z score of <-2.
Main Results:
- Mean serum CysC levels were 1.50±0.19 mg/L at nine weeks postnatal.
- No significant correlation was observed between CysC levels and bone density parameters (speed of sound, Z scores) or serum levels of calcium, phosphorus, and alkaline phosphatase.
- Serum CysC levels did not differ significantly between infants with and without OP.
Conclusions:
- The presence of osteopenia of prematurity does not compromise the validity of Cystatin C as a marker for renal insufficiency in preterm infants.
- CysC remains a safe and reliable biomarker for monitoring kidney function in preterm neonates, irrespective of OP status.
Objective:
Cystatin C (CysC) is commonly used as a marker of renal failure in premature infants. The aim of this study was to investigate serum CysC levels in osteopenia of prematurity (OP) and determine whether CysC could be safely used as a marker of renal insufficiency in infants with OP.
Methods:
Subjects were 50 preterm infants (≤32 gestational weeks). Calcium (Ca), phosphorus (P) and alkaline phosphatase (ALP) serum levels were measured in postnatal week nine, and bone density was measured concurrently by quantitative ultrasonography. Patients with a Z score of <-2 were considered to have OP.
Results:
The mean serum CysC levels in preterm infants in postnatal week nine were 1.50±0.19 mg/L. Serum CysC levels were not correlated with speed of sound values, Z scores, serum Ca, P or ALP levels. Serum CysC levels were not significantly different between infants with OP [1.50 (1.35-1.61) mg/L] and in infants without OP [1.58 (1.28-1.70) mg/L].
Conclusion:
The presence of OP does not affect the safety of CysC as a marker of renal insufficiency in preterm infants.
Related Concept Videos
Urinary Tract Calculi I: Introduction
Bone Disorders
Bone deposition is also affected by the levels of sex hormones like estrogen and testosterone that promote osteoblast activity and bone matrix synthesis. When the level of these hormones decreases due to aging, it causes a reduction in bone deposition. As a result, bone resorption by osteoclasts...
Inborn Errors of Metabolism
Overview of Protein Metabolism
Amino acids play various roles in the body once they are absorbed into cells. They are restructured...
Hormones and Bone Tissue
Hormones That Influence Osteoblasts and/or Maintain the Matrix
Several hormones are necessary for controlling bone growth and maintaining the bone matrix. The pituitary gland secretes growth hormone (GH), which, as its name implies, controls bone growth. This happens in several ways: first, it triggers chondrocyte...
Cystic Fibrosis: Pathogenesis
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...

