[The association of renalase single-nucleotide polymorphisms rs2576178 and rs10887800 with hypertension in patients with obstructive sleep apnea].

Objective: To evaluate the associations between the renalase single-nucleotide polymorphisms rs2576178 and rs10887800 and the risk of hypertension in OSA patients. Methods: A total of 3, 570 male OSA subjects diagnosed via standard polysomnography were included in this retrospective study. We recorded anthropometric, genomic, and polysomnographic parameters and blood pressure levels. All subjects were divided into four groups based on quartiles of the apnea-hypopnea index (AHI). The relationships between rs2576178 and rs10887800 and the risk of hypertension were evaluated using the binary logistic regression, and haplotype analysis. Results: In the bottom AHI quartile, rs10887800 was significantly associated with the risk of hypertension according to the dominant model [odds ratio(OR)=0.691, 95% confidence interval (CI)=0.483-0.990, P=0.044] even after adjustment for age, sex, and the body mass index. The G-A haplotype was associated with a co-effect of the two SNPs, namely, the risk of hypertension decreased (OR=0.879, 95%CI=0.784-0.986, P=0.028). Conclusions: We find no association between single rs2576178 or rs10887800 variants with the risk of hypertension in our OSA population. But, the synergistic effect of the two polymorphisms is associated with the risk of hypertension in OSA patients.

A novel near-infrared nanomaterial with high quantum efficiency and its applications in real time in vivo imaging.

Fluorescence imaging signal is severely limited by the quantum efficiency and emission wavelength. To overcome these challenges, novel NIR-emitting K5NdLi2F10 nanoparticles under NIR excitation was introduced as fluorescence imaging probe for the first time. The photostability of K5NdLi2F10 nanoparticles in the water, phosphate buffer saline, fetal bovine serum and living mice was investigated. The fluorescence signal was detected with depths of 3.5 and 2.0 cm in phantom and pork tissue, respectively. Fluorescence spectrum with a significant signal-to-background ratio of 10:1 was captured in living mice. Moreover, clear NIR images were virtualized for the living mice after intravenous injection. The imaging ability of nanoparticles in tumor-beard mice were evaluated, the enrichment of K5NdLi2F10 nanoparticles in tumor site due to the enhanced permeability and retention effect was confirmed. The systematic studies of toxicity, bio-distribution and in-vivo dynamic imaging suggest that these materials give high biocompatibility and low toxicity. These NIR-emitting nanoparticles with high quantum efficiency, high penetration and low toxicity might facilitate tumor identification in deep tissues more sensitively.

Immunopathological study on human cartilage allografts.

The fate of human cartilage allografts and the mechanism of its kinetical development were studied histopathologically and immunohistologically. After transplantation, the grafts underwent necrosis, calcification and were partially invaded by osteoplastic tissue of the host and eventually replaced by bone tissue. Thus, the contour of the transplanted cartilage was kept partially by the living cartilage and the newly-formed osseous tissue. The grafts were surrounded initially by granular tissue and then by scar tissue, in which numerous T cells and a few macrophage infiltrates were noted. In T cells, T4+ lymphocytes predominated but T8+ cells accounted for a small number. B cells were not found within the infiltrates. Most of the infiltrating cells expressed 12 antigens, indicating that the majority of T cells were activated. It was concluded that T lymphocytes mediated cellular immunity played an important role. The chondrocytes of the cartilage did not express HLA I and II antigens before transplantation, but one month later, the living chondrocytes became HLA I and II antigens positive, and the antigen expression became stronger with the elapse of time; this might be induced by lymphokins, especially by interferon produced by the infiltrating lymphocytes. Such an expression of MHC antigens on chondrocytes might contribute to the further enhancement of immunorejection.