School of Biological Sciences, University of Adelaide, Adelaide, SA, Australia.
Adelaide Dental School, University of Adelaide, Adelaide, SA, Australia.
BMC Oral Health. 2023 Jan 11;23(1):15. doi: 10.1186/s12903-022-02625-0.
Hyperlipidaemia may play a significant role in the interrelationship between type 1 diabetes (T1D) and periodontal disease. A potential mechanism that links these three aspects together is the oral microbiota. We wanted to determine if there is an association between hyperlipidaemia, periodontal disease, and the oral microbiota of children with T1D, as this has not yet been explored.
In a post-hoc, cross-sectional study using 16S rRNA gene sequencing, we explored links between oral bacterial diversity and composition of gingival swab samples from 72 children with T1D to periodontal risk factors and hyperlipidaemia status of first-degree relatives. While multiple periodontal risk factors were assessed, we used periodontal pocket depth of 3 mm to characterise periodontal risk. As periodontal pocket depth confounded the analysis of familial history of hyperlipidaemia, a multivariate analyses were performed (i.e., no periodontal risk markers in children with or without a family history of hyperlipidaemia were compared to counterparts who did not have periodontal risk markers) to examine linkages between these factors and diversity and composition of the microbiome.
In participants with no periodontitis risk, children with a family history of dyslipidemia had different bacterial diversity and composition compared to those without a familar hisitory. In contrast, such differences did not exist in the children with periodontal risk, whether or not they had a family history of hyperlipidaemia. Co-occurrence networks showed that these differences in children with no periodontists risk were linked to the presence of fewer oral microbial networks, but more microbes linked to mature plaque structures. In contrast, children with periodontal risk markers, regardless of family history of hyperlipidaemia, contained co-occurrence networks that were associated with microbes linked to periodontal disease.
In children diagnosed with T1D, our findings support an association between oral microbiota and two different exposure variables: familial history of hyperlipidaemia and periodontal risk factors.
高脂血症可能在 1 型糖尿病(T1D)与牙周病之间的相互关系中起重要作用。将这三个方面联系在一起的一个潜在机制是口腔微生物群。我们想确定 T1D 儿童的高脂血症、牙周病和口腔微生物群之间是否存在关联,因为这尚未得到探索。
在使用 16S rRNA 基因测序的事后横断面研究中,我们探讨了 72 名 T1D 儿童的牙龈拭子样本中口腔细菌多样性与牙周病危险因素和一级亲属高脂血症状况之间的关系。虽然评估了多种牙周病危险因素,但我们使用牙周袋深度 3mm 来描述牙周病危险因素。由于牙周袋深度会混淆对家族性高脂血症病史的分析,因此进行了多变量分析(即,比较有或没有家族性高脂血症病史的儿童与没有牙周病危险因素的儿童),以检查这些因素与微生物组多样性和组成之间的联系。
在无牙周病危险因素的参与者中,有家族性血脂异常病史的儿童与无家族性血脂异常病史的儿童相比,其细菌多样性和组成存在差异。相比之下,在有或没有牙周病危险因素的儿童中,这种差异并不存在。共生网络显示,这些无牙周病危险因素的儿童之间的差异与较少的口腔微生物网络存在相关,但与成熟斑块结构相关的微生物较多。相比之下,无论是否有家族性高脂血症病史,具有牙周病危险因素的儿童的共生网络与与牙周病相关的微生物相关。
在诊断为 T1D 的儿童中,我们的研究结果支持口腔微生物群与两个不同的暴露变量之间的关联:家族性高脂血症病史和牙周病危险因素。