# Condylar Bone Quality in Growing Children Is Associated With Genetic Polymorphisms in Genes Involved in Calcium and Phosphate Maintenance

**Authors:** Erika Calvano Küchler, Caio Luiz Bitencourt Reis, Gabriela Fonseca-Souza, Daniel Hemming, Flares Baratto-Filho, Cristiano Miranda de Araujo, Svenja Beisel-Memmert, Juliana Feltrin-Souza, Michelle Nascimento Meger, Bianca Lopes Cavalcante-Leão

PMC · DOI: 10.1155/bmri/9337029 · 2026-01-07

## TL;DR

This study found that genetic variations in genes related to calcium and phosphate regulation are linked to bone quality in growing children's jawbones.

## Contribution

The study identifies specific SNPs in VDBP, SEC23A, and PTH genes associated with condylar bone structure in children.

## Key findings

- The GT and TT genotypes in VDBP (rs4588) showed lower fractal dimensions in condylar bone.
- The GG genotype in SEC23A (rs8018720) and TC genotype in PTH (rs694) showed higher fractal dimensions.
- Fractal analysis of panoramic radiographs revealed associations between SNPs and bone microarchitecture.

## Abstract

Single nucleotide polymorphisms (SNPs) play a crucial role in regulating vitamin D, parathyroid hormone (PTH), and calcitonin concentrations, which are involved in bone health. Some reports suggested that fractal analysis is useful in the morphometric analysis of the mandible trabecular bone in panoramic radiographs. Therefore, we investigated if SNPs in genes that influence vitamin D, calcitonin, and PTH levels are involved in condylar bone quality during the active growing phase of the mandible. Fractal dimension was obtained from the condyle region of interest (ROI) using panoramic radiographs and used to measure the complexity and the microarchitecture of the bone. Fractal dimension using the box‐counting algorithm was then calculated. In order to avoid information bias, a script to automate the commands in the software ImageJ was generated to ensure consistency and minimize the potential for human error during the data analysis process. SNPs in vitamin D receptor (VDR), cytochrome P450 family 27 subfamily B member 1 (CYP27B1), cytochrome P450 family 24 subfamily A member 1 (CYP24A1), vitamin D binding protein (VDBP), SEC23 homolog A (SEC23A), calcitonin receptor (CALCR), and parathyroid hormone (PTH) were analyzed. DNA extracted from saliva was used for genotyping analysis of VDR (rs7975232, rs2228570, and rs1544410), CYP27B1 (rs4646536), CYP24A1 (rs927650), VDBP (rs4588), SEC23A (rs8018720), CALCR (rs1801197), and PTH (rs6256, rs307247, and rs694). A statistical analysis was performed with an alpha error tolerance of 5%. A total of 100 children were included; 50 (50%) were boys and the age ranged from 5 to 14 years old. Fractal dimensions were compared among genotypes. The GT (mean = 1.20 and standard error = 0.03, p = 0.024) and TT genotypes (mean = 1.16 and standard error = 0.06, p = 0.047) in the gene VDBP (rs4588) presented lower fractal dimension. The GG genotype in SEC23A (rs8018720) (mean = 1.34 and standard error = 0.03, p = 0.011) and the TC genotype in PTH (rs694) showed an increased fractal dimension (mean = 1.29 and standard error = 0.03, p = 0.020). In conclusion, SNPs in VDBP, SEC23A, and PTH encoding genes are associated with mandibular condylar trabecular bone structure in children.

## Linked entities

- **Genes:** VDR (vitamin D receptor) [NCBI Gene 7421], CYP27B1 (cytochrome P450 family 27 subfamily B member 1) [NCBI Gene 1594], CYP24A1 (cytochrome P450 family 24 subfamily A member 1) [NCBI Gene 1591], GC (GC vitamin D binding protein) [NCBI Gene 2638], SEC23A (SEC23 homolog A, COPII component) [NCBI Gene 10484], CALCR (calcitonin receptor) [NCBI Gene 799], PTH (parathyroid hormone) [NCBI Gene 5741]

## Full-text entities

- **Genes:** SEC23A (SEC23 homolog A, COPII component) [NCBI Gene 10484] {aka CLSD, hSec23A}, VDR (vitamin D receptor) [NCBI Gene 7421] {aka NR1I1, PPP1R163}, GC (GC vitamin D binding protein) [NCBI Gene 2638] {aka DBP, DBP-maf, DBP/GC, GRD3, Gc-MAF, GcMAF}, CYP24A1 (cytochrome P450 family 24 subfamily A member 1) [NCBI Gene 1591] {aka CP24, CYP24, HCAI, HCINF1, P450-CC24}, PTH (parathyroid hormone) [NCBI Gene 5741] {aka FIH1, PTH1}, CYP27B1 (cytochrome P450 family 27 subfamily B member 1) [NCBI Gene 1594] {aka CP2B, CYP1, CYP1alpha, CYP27B, P450c1, PDDR}, CALCA (calcitonin related polypeptide alpha) [NCBI Gene 796] {aka CALC1, CGRP, CGRP-I, CGRP-alpha, CGRP1, CT}, CALCR (calcitonin receptor) [NCBI Gene 799] {aka CRT, CT-R, CTR, CTR1}
- **Diseases:** Condylar (MESH:C538270)
- **Chemicals:** Phosphate (MESH:D010710), Calcium (MESH:D002118), vitamin D (MESH:D014807)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** rs1801197, rs6256, rs1544410, rs307247, rs694, rs4588, rs8018720, rs4646536, rs7975232, rs927650, rs2228570

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12776005/full.md

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Source: https://tomesphere.com/paper/PMC12776005