Genetically predicted major depression causally increases the risk of temporomandibular joint disorders.

Objective: Observational studies have reported that mental disorders are comorbid with temporomandibular joint disorder (TMD). However, the causal relationship remains uncertain. To clarify the causal relationship between three common mental illnesses and TMD, we conduct this Mendelian Randomization (MR) study. Methods: The large-scale genome-wide association studies data of major depression, bipolar disorder and schizophrenia were retrieved from the Psychiatric Genomics Consortium. The summary data of TMD was obtained from the Finn-Gen consortium, including 211,023 subjects of European descent (5,668 cases and 205,355 controls). The main approach utilized was inverse variance weighting (IVW) to evaluate the causal association between the three mental disorders and TMD. Five sensitivity analyses including MR-Egger, Maximum Likelihood, Weighted median, MR. RAPS and MR-PRESSO were used as supplements. We conducted heterogeneity tests and pleiotropic tests to ensure the robustness. Results: As shown by the IVW method, genetically determined major depression was associated with a 1.65-fold risk of TMD (95% CI = 1.10-2.47, p < 0.05). The direction and effect size remained consistent with sensitivity analyses. The odds ratios (ORs) were 1.51 (95% CI = 0.24-9.41, p > 0.05) for MR-Egger, 1.60 (95% CI = 0.98-2.61, p > 0.05) for Weighted median, 1.68 (95% CI = 1.19-2.38, p < 0.05) for Maximum likelihood, 1.56 (95% CI = 1.05-2.33, p < 0.05) for MR. RAPS, and 1.65 (95% CI = 1.10-2.47, p < 0.05) for MR-PRESSO, respectively. No pleiotropy was observed (both P for MR-Egger intercept and Global test >0.05). In addition, the IVW method identified no significant correlation between bipolar disorder, schizophrenia and TMD. Conclusion: Genetic evidence supports a causal relationship between major depression and TMD, instead of bipolar disorder and schizophrenia. These findings emphasize the importance of assessing a patient's depressive status in clinical settings.

[Expression of vascular endothelial growth factor in periodontal tissues during orthodontic tooth movement and its role in bone remodeling].

PURPOSE: To investigate the expression of VEGF in periodontal tissues and its role in bone remodeling during orthodontic tooth movement in rats. METHODS: Rat model of tooth movement was established, and 30 rats in the experimental group were divided into 5 groups, 6 rats in each group. At 2 days, 4 days, 7 days, 14 days and 20 days, the rats were sacrificed to make periodontal tissue slice. The morphological changes of periodontal tissue were observed under H-E staining, and the expression of VEGF was semi-quantitatively analyzed by immunohistochemistry. The data were analyzed using SPSS21.0 software package. RESULTS: Expression of VEGF in normal rat periodontal tissues was very weak or without positive expression; 2 days after tooth movement, VEGF expression in periodontal tissues began to increase from seventh to fourteenth days; on the fourteenth day, the expression reached a peak; after twentieth day, the expression of VEGF decreased slightly, but still higher than the control group. The expression of VEGF was mainly found in the cytoplasm of vascular endothelial cells, osteoblasts, fibroblasts, and osteoclasts. CONCLUSIONS: Expression of VEGF may play an important role in the early remodeling of periodontal tissues during orthodontic tooth movement.

A Ferroelectric Ceramic/Polymer Composite-Based Capacitive Electrode Array for In Vivo Recordings.

A new implantable capacitive electrode array for electrocorticography signal recording is developed with ferroelectric ceramic/polymer composite. This ultrathin and electrically safe capacitive electrode array is capable of attaching to the biological tissue conformably. The barium titanate/polyimide (BaTiO3 /PI) nanocomposite with high dielectric constant is successfully synthesized and employed as the ultrathin dielectric layer of the capacitive BaTiO3 /PI electrode array. The performance of the capacitive BaTiO3 /PI electrode array is evaluated by electrical characterization and 3D finite-element modeling. In vivo, neural experiments on the visual cortex of rats show the reliability of the capacitive BaTiO3 /PI electrode array. This work shows the potentials of capacitive BaTiO3 /PI electrode array in the field of brain/computer interfaces.

Boronic acid functionalized core-satellite composite nanoparticles for advanced enrichment of glycopeptides and glycoproteins.

A core-satellite-structured composite material has been successfully synthesized for capturing glycosylated peptides or proteins. This novel hybrid material is composed of a silica-coated ferrite "core" and numerous "satellites" of gold nanoparticles with lots of "anchors". The anchor, 3-aminophenylboronic acid, designed for capturing target molecules, is highly specific toward glycosylated species. The long organic chains bridging the gold surface and the anchors could reduce the steric hindrance among the bound molecules and suppress nonspecific bindings. Due to the excellent structure of the current material, the trap-and-release enrichment of glycosylated samples is quite simple, specific, and effective. Indeed, the composite nanoparticles could be used for enriching glycosylated peptides and proteins with very low concentrations, and the enriched samples can be easily separated from bulk solution by a magnet. By using this strategy, the recovery of glycopeptides and glycoproteins after enrichment were found to be 85.9 and 71.6% separately, whereas the adsorption capacity of the composite nanoparticles was proven to be more than 79 mg of glycoproteins per gram of the material. Moreover, the new composite nanoparticles were applied to enrich glycosylated proteins from human colorectal cancer tissues for identification of N-glycosylation sites. In all, 194 unique glycosylation sites mapped to 155 different glycoproteins have been identified, of which 165 sites (85.1%) were newly identified.