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重度幼儿龋患儿与非重度幼儿龋患儿人类白细胞抗原-DR和人类白细胞抗原-DQ的评估及相关性:一项随机临床试验

Estimation and Correlation of Human Leukocyte Antigen-DR and Human Leukocyte Antigen-DQ in Children with and without Severe-early Childhood Caries: A Randomized Clinical Trial.

作者信息

Thimmegowda Umapathy, Dhamnekar Pradnya

机构信息

Department of Pediatric and Preventive Dentistry, RajaRajeswari Dental College and Hospital, Bengaluru, Karnataka, India.

出版信息

Int J Clin Pediatr Dent. 2024 Dec;17(12):1346-1351. doi: 10.5005/jp-journals-10005-3011.

DOI:10.5005/jp-journals-10005-3011
PMID:39867115
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11760412/
Abstract

BACKGROUND/AIM: Early childhood caries (ECC) is a prevalent dental disease, influenced by genetic and environmental factors. Human leukocyte antigens (HLA) have been suggested as a predisposing factor. This study aims to estimate and correlate HLA-DR and HLA-DQ activity in the saliva of caries-active and caries-free children, potentially aiding disease diagnosis and prevention.

MATERIALS AND METHODS

A comparative study was performed on 50 children, divided into two groups: caries-active and caries-free, consisting of 25 children each, aged 3-6 years. Unstimulated saliva samples were collected and subjected to enzyme-linked immunosorbent assay (ELISA) for analysis. HLA-DR and HLA-DQ levels will be estimated and correlated with caries score, age, and gender.

RESULTS

HLA-DR level was 33.032 ± 2.869 pg/mL in the caries-active group and 5.288 ± 0.960 pg/mL in the caries-free group, and was statistically significant at < 0.001. HLA-DQ isotype level was 5.603 ± 1.264 ng/L in the caries-active group and 4.596 ± 0.748 ng/L in the caries-free group, and was statistically significant at < 0.001. HLA-DR level showed a statistically significant positive moderate correlation with caries score ( < 0.001), whereas HLA-DQ levels demonstrated a positive very weak correlation with caries score and were not statistically significant. HLA-DQ was statistically significant at < 0.001 when compared between genders in the caries-active group.

CONCLUSION

Results suggest a substantial correlation between HLA-DR level and the severity of dental caries, and an increase in HLA-DR may be linked to an increase in caries severity. Thus, HLA-DR detection as a molecular biomarker for early diagnosis of ECC may be recommended.

HOW TO CITE THIS ARTICLE

Thimmegowda U, Dhamnekar P. Estimation and Correlation of Human Leukocyte Antigen-DR and Human Leukocyte Antigen-DQ in Children with and without Severe-early Childhood Caries: A Randomized Clinical Trial. Int J Clin Pediatr Dent 2024;17(12):1346-1351.

摘要

背景/目的:幼儿龋(ECC)是一种常见的牙科疾病,受遗传和环境因素影响。人类白细胞抗原(HLA)被认为是一个易感因素。本研究旨在评估患龋活跃与无龋儿童唾液中的HLA - DR和HLA - DQ活性,并进行相关性分析,可能有助于疾病的诊断和预防。

材料与方法

对50名3至6岁儿童进行了一项对比研究,分为两组:患龋活跃组和无龋组,每组25名儿童。收集未刺激的唾液样本,采用酶联免疫吸附测定(ELISA)进行分析。评估HLA - DR和HLA - DQ水平,并与龋病评分、年龄和性别进行相关性分析。

结果

患龋活跃组的HLA - DR水平为33.032±2.869 pg/mL,无龋组为5.288±0.960 pg/mL,差异有统计学意义(<0.001)。患龋活跃组的HLA - DQ同种型水平为5.603±1.264 ng/L,无龋组为4.596±0.748 ng/L,差异有统计学意义(<0.001)。HLA - DR水平与龋病评分呈显著正中度相关(<0.001),而HLA - DQ水平与龋病评分呈正非常弱相关,且无统计学意义。在患龋活跃组中,HLA - DQ在性别间比较差异有统计学意义(<0.001)。

结论

结果表明HLA - DR水平与龋齿严重程度之间存在显著相关性,HLA - DR的升高可能与龋病严重程度增加有关。因此,推荐检测HLA - DR作为ECC早期诊断的分子生物标志物。

如何引用本文

Thimmegowda U, Dhamnekar P. Estimation and Correlation of Human Leukocyte Antigen - DR and Human Leukocyte Antigen - DQ in Children with and without Severe - early Childhood Caries: A Randomized Clinical Trial. Int J Clin Pediatr Dent 2024;17(12):1346 - 1351.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe38/11760412/c0e039524577/ijcpd-17-1346-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe38/11760412/ce75745be765/ijcpd-17-1346-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe38/11760412/e70ee7937b32/ijcpd-17-1346-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe38/11760412/1639059cb371/ijcpd-17-1346-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe38/11760412/39a41791bfce/ijcpd-17-1346-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe38/11760412/c0e039524577/ijcpd-17-1346-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe38/11760412/ce75745be765/ijcpd-17-1346-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe38/11760412/e70ee7937b32/ijcpd-17-1346-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe38/11760412/1639059cb371/ijcpd-17-1346-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe38/11760412/39a41791bfce/ijcpd-17-1346-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe38/11760412/c0e039524577/ijcpd-17-1346-g005.jpg

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