ArticleHeliyon2025
Pulp stones and kidney stones-related gene: An investigation of single nucleotide polymorphisms in the gene encoding parathyroid hormone.
Article in Heliyon, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
1 citing paper in PubMed.
- Association of Pulp Stones With Single Nucleotide Polymorphisms of Mineralization-Related Genes in Orthodontically Treated Patients: A Cross-Sectional Study.International journal of dentistry · 2026Article
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Authors and funding
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Introduction: Pulp stones (PS), whose origins remain unclear, present a challenge for clinical practice in Endodontics. Similar to other calcifications, a relationship with parathyroid hormone is hypothesized. Purpose: The aim of this study was to investigate the association between the presence of PS and kidney stones (KS) and single nucleotide polymorphisms (SNPs) in the parathyroid hormone ( Methods: This cross-sectional study included adults of both sexes, divided into groups: with PS and without PS. PS diagnosis was based on radiographic evaluation. Saliva samples were collected from all participants, and prior history of KS was recorded. The samples were processed, and genomic DNA was used to genotype the rs694, rs6256, and rs307247 SNPs. The Hardy-Weinberg equilibrium was assessed using the Chi-square test. Genotypic and allelic profiles under additive, dominant, and recessive models were evaluated using a univariate logistic regression model and the Wald test, with analyses conducted in SPSS® version 23.0. Additionally, Fisher's exact test was used to compare the haplotype frequencies. Statistical significance was set at 5 %. Results: The study included 63 patients with PS and 54 without PS, with a mean age of 32.5 years. No statistically significant association was observed between the groups regarding the presence of KS. Allelic and genotypic analyses revealed no significant association (P > 0.05) between the presence of PS and SNPs analyzed in the groups studied. Conclusion: None of the SNPs studied in the gene encoding PTH were associated with PS or KS.
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