Related Experiment Video
Updated: May 3, 2026

A Simple Pit Assay Protocol to Visualize and Quantify Osteoclastic Resorption In Vitro
Published on: June 16, 2022
Circulating undercarboxylated osteocalcin and gingival crevicular fluid tumour necrosis factor-α in children
Khady Kâ1, Marie-Claude Rousseau, Simon D Tran
1Faculty of Dentistry, McGill University, Montreal, QC, Canada; Epidemiology and Biostatistics Unit, INRS-Armand-Frappier Institute, Laval, QC, Canada.
Insights
Undercarboxylated osteocalcin (ucOC), a bone formation marker, is linked to reduced gingival inflammation (GCF TNF-α) in children. This suggests early childhood links between bone health and gum disease markers.
Area of Science:
- Pediatric Endocrinology
- Periodontology
- Biochemistry
Background:
- Osteocalcin, a bone formation protein, shows a negative association with adult periodontal disease.
- The relationship between osteocalcin and periodontal disease in children remains largely unexplored.
Purpose of the Study:
- To investigate the association between plasma undercarboxylated osteocalcin (ucOC) and gingival crevicular fluid tumor necrosis factor-alpha (GCF TNF-α) in children.
- To assess ucOC as a potential indicator of gingival inflammation in pediatric populations.
Main Methods:
- Cross-sectional analysis of 120 Caucasian children aged 8-10 years from the Quebec Adipose and Lifestyle InvesTigation in Youth cohort.
- Measurement of plasma ucOC and GCF TNF-α levels using enzyme-linked immunosorbent assay.
- Linear regression analyses adjusted for various covariates including age, obesity, and physical activity.
Main Results:
- A statistically significant negative association was found between ucOC and GCF TNF-α levels.
- Each 1-ng/ml increase in ucOC was associated with a 0.96% decrease in GCF TNF-α (95% CI: -1.69, -0.23).
Conclusions:
- A negative association between a bone formation marker (ucOC) and a gingival inflammation marker (GCF TNF-α) is evident in childhood.
- Findings suggest potential early links between bone metabolism and periodontal health in at-risk pediatric populations.
Background:
Osteocalcin, a protein secreted by osteoblasts during bone formation, is negatively associated with adult periodontal disease. Little is known about this association in children.
Aim:
To examine the extent to which plasma undercarboxylated osteocalcin (ucOC) is associated with gingival crevicular fluid tumour necrosis factor-alpha (GCF TNF-α) - a potential marker of gingival inflammation - in children.
Methods:
We used data from the Quebec Adipose and Lifestyle InvesTigation in Youth cohort, an ongoing longitudinal study on the natural history of obesity among Caucasian children with a family history of obesity in Quebec, Canada. This cross-sectional analysis from the baseline visit includes 120 children aged 8-10 years. Plasma ucOC and GCF TNF-α levels were determined by enzyme-linked immunosorbent assay. Linear regression analyses, adjusting for age, gender, family income, sexual maturity stage, daily physical activity, obesity, and fasting glucose were conducted, with TNF-α level as the dependent variable.
Results:
A 1-ng/ml increase in ucOC was associated with a 0.96% decrease (95% confidence interval (CI): -1.69, -0.23) in GCF TNF-α level.
Conclusion:
A negative association between a marker of bone formation and a marker of gingival inflammation was observed as early as childhood among Caucasian children with a family history of obesity.
Related Concept Videos
Synthesis and Functions of Calcitonin
The exact mechanisms by which calcitonin operates in calcium homeostasis remain elusive, but its significance is evident in several vital...
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...
Osteoclasts in Bone Remodeling
TGF - β Signaling Pathway
Regulation of Hematopoietic Stem Cells

