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1.
Sci Rep ; 5: 15318, 2015 Nov 09.
Article in English | MEDLINE | ID: mdl-26549312

ABSTRACT

In this study, we performed a network meta-analysis to compare the outcomes of seven most common surgical procedures to fix DRF, including bridging external fixation, non-bridging external fixation, K-wire fixation, plaster fixation, dorsal plating, volar plating, and dorsal and volar plating. Published studies were retrieved through PubMed, Embase and Cochrane Library databases. The database search terms used were the following keywords and MeSH terms: DRF, bridging external fixation, non-bridging external fixation, K-wire fixation, plaster fixation, dorsal plating, volar plating, and dorsal and volar plating. The network meta-analysis was performed to rank the probabilities of postoperative complication risks for the seven surgical modalities in DRF patients. This network meta-analysis included data obtained from a total of 19 RCTs. Our results revealed that compared to DRF patients treated with bridging external fixation, marked differences in pin-track infection (PTI) rate were found in patients treated with plaster fixation, volar plating, and dorsal and volar plating. Cluster analysis showed that plaster fixation is associated with the lowest probability of postoperative complication in DRF patients. Plaster fixation is associated with the lowest risk for postoperative complications in DRF patients, when compared to six other common DRF surgical methods examined.


Subject(s)
Fracture Fixation, Internal/adverse effects , Postoperative Complications/pathology , Radius Fractures/surgery , Bone Nails/adverse effects , Casts, Surgical/adverse effects , Fracture Fixation, Internal/methods , Humans , Postoperative Complications/epidemiology , Radius Fractures/epidemiology , Radius Fractures/pathology , Risk Factors
2.
Int J Clin Exp Pathol ; 8(3): 2737-45, 2015.
Article in English | MEDLINE | ID: mdl-26045779

ABSTRACT

We aimed to investigate the role of Notch1/Hes signaling pathway in the pathogenesis of abnormal ossification of hip ligament in patients with ankylosing spondylitis (AS). 22 AS patients scheduled for artificial hip arthroplasty were randomly chosen as AS group. As controls, we used 4 patients diagnosed with transcervical fracture who underwent hip replacement surgery. Notch1 and Hes mRNA expressions were detected by real-time fluorescent quantitative polymerase chain reaction (RFQ-PCR). Immunohistochemistry (IHC) was used to detect Notch1 and Hes protein expression. Correlation analyses of Notch-l and Hes with AS-related clinical factors were conducted with spearman's correlation analysis and partial correlation analysis. RFQ-PCR results showed significant differences in Notch1 and Hes mRNA expressions between AS group and the control group (all P<0.05). IHC analysis further indicated positive nuclear signals of Notch1 and Hes protein, indicating functional activation of the Notch1 and Hes pathways. Semi-quantitative IHC showed a higher Notch1 and Hes expression levels in AS group compared to the control group (all P<0.05). Correlation analysis suggested that Hes protein expression was positively associated with the clinical course of the disease in AS patients. In conclusion, Notch1 and Hes overexpression was clearly detected in hip joint ligaments of AS patients, Hes protein expression was associated with the clinical course of AS. Taken together, we suggest that signaling pathways mediated by Notch1-Hes may contribute to ligament ossification of hip joints in AS patients.


Subject(s)
Basic Helix-Loop-Helix Transcription Factors/analysis , Hip Joint/chemistry , Homeodomain Proteins/analysis , Ligaments, Articular/chemistry , Receptor, Notch1/analysis , Signal Transduction , Spondylitis, Ankylosing/metabolism , Adult , Basic Helix-Loop-Helix Transcription Factors/genetics , Case-Control Studies , Female , Hip Joint/pathology , Homeodomain Proteins/genetics , Humans , Immunohistochemistry , Ligaments, Articular/pathology , Male , Middle Aged , Ossification, Heterotopic , RNA, Messenger/genetics , Real-Time Polymerase Chain Reaction , Receptor, Notch1/genetics , Reverse Transcriptase Polymerase Chain Reaction , Spondylitis, Ankylosing/diagnosis , Spondylitis, Ankylosing/genetics
3.
Int J Clin Exp Pathol ; 8(1): 719-26, 2015.
Article in English | MEDLINE | ID: mdl-25755766

ABSTRACT

The present study was designed to evaluate the role of growth differentiation factor-5 (GDF-5) and bone morphogenetic protein type II receptor (BMPR-II) in the development of lumbar intervertebral disc degeneration (IDD). A total of 24 patients with lumbar IDD (experiment group) and 6 patients with lumbar vertebral fracture (control group) were enrolled in the study. Tissue samples of IVD from the experiment group and control group were obtained during lumbar fusion operation, respectively. Fixation and decalcification of IVD tissue were performed, and then HE staining was carried out to observe the morphological changes of the lumbar IVD tissues. The expression of GDF-5 and BMPRII in human lumbar IVD was detected by immunohistochemical staining. HE staining results showed that non- and minimal degeneration was found in 11 cases (score range, 0-3), moderate degeneration in 12 cases (score range, 4-8), and severe degeneration in 7 cases (score range, 9-12). According to the immunohistochemical results, the positive expression rates of GDF-5 and BMPRII in NP were higher than those in AF of the non- and minimal degeneration group, moderate degeneration group and severe degeneration group (all P < 0.05). However, no significant difference in GDF-5 or BMPRII positive expression was observed among the normal, non- and minimal, moderate and severe degeneration groups in neither NP area nor AF area (all P > 0.05). In conclusion, our results showed that GDF-5 and BMPRII expressed both in normal and degenerated IVD tissues, and GDF-5 might have an inhibition effect on degenerated lumbar IVD, suggesting that gene therapy may be a useful approach in producing physiological effects during early- and late-phase of lumbar IDD.


Subject(s)
Bone Morphogenetic Protein Receptors, Type II/biosynthesis , Growth Differentiation Factor 5/biosynthesis , Intervertebral Disc Degeneration/metabolism , Humans , Immunohistochemistry , Lumbar Vertebrae
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