Xylene exposure, miR-181b-5p and miR-106b-5p alterations, and type 2 diabetes mellitus: Exploring relationship, mediation, and mechanism
Year: 2026
Type: article
Study design: Observational Study
Abstract: Xylene is a widely encountered volatile organic compound, while little is known about its relationship with type 2 diabetes mellitus (T2DM) as well as possible roles of miR-181b-5p and miR-106b-5p, which are multifunctional microRNAs observed to be implicated in glucose metabolism, and the possible mechanisms. These uncharted territories warrant further investigation. In this case-control study of 138 newly developed T2DM adult patients and 138 matched healthy controls, urinary xylene exposure biomarkers (2-methyl hippuric acid [2MHA]; 3-methyl hippuric acid [3MHA]; 2MHA+3MHA [ΣUXYM]) and plasma miR-181b-5p/miR-106b-5p were measured. Relationships among xylene exposure biomarkers, miR-181b-5p/miR-106b-5p, and T2DM were estimated by generalized linear or logistic models. Potential roles of miR-181b-5p/miR-106b-5p in xylene-T2DM relationship were explored by mediation analyses. Network toxicology and molecular docking were performed to explore the hypothesis-generating pathway linking xylene and T2DM. We observed 2MHA (odds ratio=3.12; 95% confidence interval [CI]: 1.86∼5.24), 3MHA (2.12; 1.45∼3.10), ΣUXYM (2.33; 1.54∼3.54), miR-181b-5p (1.51; 1.25∼1.83), and miR-106b-5p (1.72; 1.42∼2.10) were positively related to T2DM odds. 2MHA was positively related to miR-181b-5p (β=0.40; 95% CI: 0.02∼0.78) and miR-106b-5p (0.56; 0.14∼0.98), which further accounted for 10.25% and 17.75% of the 2MHA-T2DM association, respectively. Peroxisome proliferator-activated receptor (PPAR) signaling pathway was enriched in the xylene-T2DM link, with potential molecular targets (estrogen receptor 1 [ESR1], etc.) identified. Target relationships between miR-181b-5p/miR-106b-5p and PPAR/ESR1 were predicted. Conclusively, exposure of general adults to xylene was positively associated with T2DM, which was partially explained by miR-181b-5p and miR-106b-5p, and PPAR signaling pathway and targets like ESR1 might be involved in the possible mechanisms.
Authors: Qiaoming Liang, Yani Xiong, Zhiying Huo, Sisi Li, Shuhui Wan, Tianyu Zeng, Wei Liu, Feifei Wang, Chundan Luo, Fan Xu, Le Hong, Jiahao Song, Qingfeng Wu, Xiaoting Luo, Minghua Dong, Weihong Chen, Rong Xu, Xiaokang Zhang, Bin Wang
Language: English
Subfield: Cancer Research
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $3,650
OpenAlex ID: W7166463680
