21 results on '"Weizhe Shi"'
Search Results
2. Novel de novo TRPV4 mutation identified in a Chinese family with metatropic dysplasia inhibits chondrogenic differentiation
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Ping Wei, Weizhe Shi, Tianying Nong, Caixia Xian, Xia Li, Zhaohui Li, Xin Li, Jianping Wu, Liyuan Shang, Fulong Xu, Yibo Xu, Hongwen Xu, and Mingwei Zhu
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Medicine (General) ,R5-920 ,Genetics ,QH426-470 - Published
- 2024
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3. A novel compound heterozygous variation in the FKBP10 gene causes Bruck syndrome without congenital contractures: A case report
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Liyuan Shang, Weizhe Shi, Yibo Xu, Tianying Nong, Xia Li, Zhaohui Li, Yanhan Liu, Jingchun Li, Ya-Ping Tang, Mingwei Zhu, and Hongwen Xu
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Bruck syndrome ,Osteogenesis imperfecta ,Whole-exome sequencing ,FKBP10 ,Case report ,Science (General) ,Q1-390 ,Social sciences (General) ,H1-99 - Abstract
Background: Bruck syndrome (BS) is an extremely rare autosomal-recessive connective tissue disorder mainly characterized by bone fragility, congenital joint contracture, and spinal deformity. It is also considered as a rare form of osteogenesis imperfecta (OI) due to features of osteopenia and fragility fractures. Its two forms, BS1 and BS2, are caused by pathogenic variations in FKBP10 and PLOD2, respectively. Objective: We aimed to improve the clinical understanding of BS by presenting a case from China and to identify the genetic variants that led to this case. Methods: OI was suspected in a Chinese boy with a history of recurrent long bone fractures, lumbar kyphosis, and dentinogenesis imperfecta (DI). Whole-exome sequencing (WES) was performed to identify pathogenic variations. Sanger sequencing was used to confirm the results of the WES. In silico analysis was used to predict the pathogenicity of genetic variants. Results: WES and Sanger sequencing revealed a compound heterozygous variation in the FKBP10 gene (NM_021939, c.23dupG in exon 1, and c.825dupC in exon 5). Both variants resulted in a frameshift and premature stop codon. Of these two variants, c.23dupG has not been previously reported. The patient's parents were heterozygous carriers of one variant. In addition, zoledronic acid treatment improved the vertebral deformity and bone mineral density (BMD) significantly in this patient. Conclusions: A novel compound heterozygous variation of FKBP10, c.23dupG/c.825dupC, was identified in a patient with moderately severe OI. Based on these findings, the patient was diagnosed with BS1 without congenital joint contractures or OI type XI. This study expands the spectrum of FKBP10 genetic variants that cause BS and OI.
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- 2024
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4. Radiographic features of congenital thumb duplication type C2 of Wu et al. classification: new subtypes and surgical strategies
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JianPing Wu, WeiZhe Shi, Hai Zhao, JingChun Li, YiQiang Li, Kai Hong, Zhe Yuan, MingWei Zhu, YuanZhong Liu, Federico Canavese, and HongWen Xu
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congenital thumb duplication ,Wu et al. classification ,anatomy ,interphalangeal joint alignment ,surgery ,Pediatrics ,RJ1-570 - Abstract
ObjectiveThis study aimed (i) to evaluate the radiographic characteristics of patients with congenital thumb duplication (CTD) type C2 according to the classification of Wu et al., (ii) to describe the various subtypes of type C2 CTD, and (iii) to propose a classification system that allows the identification of different surgical strategies based on the radiographic anatomy of this specific subtype of duplication.MethodsWe retrospectively reviewed 92 patients (92 thumbs) with type C2 CTD according to the Wu et al. classification in our institution between August 2015 and April 2021. All CTDs were classified according to the interphalangeal joint alignment of the main thumb at the posteroanterior radiograph of the thumb before operation: type I (no deviation), type II (ulnar deviation), and type III (radial deviation).ResultsAll CTDs (n = 92) could be classified according to the proposed classification system: 76 (82.6%) were type I, 10 (10.9%) were type II, and six were type III (6.5%). According to the Kim system of subtype classification, there were 55 (59.8%) type 1, 24 (26.1%) type 2, and 13 (14.1%) type 3 cases.ConclusionsThe suggested classification completes the Wu et al. system and has the potential to guide surgical treatment in children with type C2 CTD.Level of evidenceIII.
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- 2024
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5. Epidemiological characteristics and distribution of congenital thumb duplication in south China: An analysis of 2,300 thumbs in 2,108 children
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JianPing Wu, WeiZhe Shi, XueMei Lin, JingChun Li, Zhe Yuan, Mingwei Zhu, YuanZhong Liu, YiQiang Li, Federico Canavese, and HongWen Xu
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thumb duplication ,epidemiology ,classification ,anatomy ,morphology ,associated anomaly ,Pediatrics ,RJ1-570 - Abstract
ObjectiveThe objective of this study was to evaluate epidemiological and anatomical characteristics of children with congenital thumb duplication (CTD).MethodsWe retrospectively reviewed 2108 children with CTD. Data regarding sex, age at the surgery, laterality, uni- or bilateral involvement, and dominant side were retrieved from the medical charts. Plain radiographs were used to classify all CTD according to Wassel-Flatt, Rotterdam and Chung classification systems and to evaluate the patho-anatomy of the duplication as well as the presence of associated anomaly.ResultsA total of 796 girls and 1,312 boys with CTD (n = 2,300 thumbs) met the inclusion criteria. The male to female and unilateral to bilateral ratio were 1.6:1 and 10:1, respectively. Associated anomaly was found in 238/2108 patients (11.3%), and the middle phalanx deformity of the 5th finger was the most common one. A dominant thumb, larger and more developed, was on the ulnar side in 2270/2,300 cases (98.7%).According to the Wassel-Flatt classification, type IV (40.2%) was the most common deformity and the extra thumb was connected to the main thumb by a joint in most cases (437/780); overall, 15.7% of thumbs (n = 360) did not fit the Wassel-Flatt classification.According to the Rotterdam classification, type IV (51.3%) was the most common form; in most cases (363/1180) the thumb was hypoplastic or floating. Overall, 3/2,300 thumbs (0.1%) could not be classified according to Rotterdam classification.According to the Chung classification, type A was the most common subtype (44.1%); in most cases (716/1015) the duplication was at the level of the metacarpal bone. Overall, 2/2,300 thumbs (0.1%) did not fit the Chung classification.ConclusionsIn patients from southern China, CTD shows male and right-sided predominance with ulnar-dominant thumb. Abnormalities of the middle phalanx of the 5th finger are more frequent in patients with associated anomaly. The development of a simple and comprehensive classification system is needed to guide treatment and to adequately assess the epidemiological characteristics of patients with CTD in order to facilitate comparison between different patients' populations.Level of evidenceIII
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- 2022
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6. Identification of a novel TBX5 mutation in a Chinese family with rare symptoms of Holt–Oram syndrome
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Xia Li, Weizhe Shi, Xuejiao Ding, Jingchun Li, Yiqiang Li, Jianping Wu, Zhe Yuan, Tianying Nong, Hongwen Xu, and Mingwei Zhu
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Holt–Oram syndrome ,Common atrium ,Whole exome sequencing ,TBX5 ,Novel mutation ,Science (General) ,Q1-390 ,Social sciences (General) ,H1-99 - Abstract
Holt–Oram syndrome (HOS) is a rare autosomal dominant disorder characterized by skeletal abnormalities of the upper limbs and often cardiac malformations. We investigated a Chinese family with clinical features suggestive of HOS. Clinical examinations revealed that both the proband and his father had anomalies in the upper limbs and heart. The proband had a rare common atrium. Whole exome sequencing detected a novel small–insertion mutation (c.680_681insCTGAGAATAAT; p.Ile227fs∗) in TBX5 gene, the known disease gene for HOS. The mutation cosegregated with HOS phenotypes in the family and was predicted to cause frameshift, resulting in a truncated protein. In this study, we described a rare HOS case with common atrium. A novel small–insertion in TBX5 coding sequence was identified and speculated to be the disease–causing genetic variant in the family. Our finding expands the clinical feature spectrum and genetic aetiology spectrum of HOS.
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- 2022
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7. Expression and significance of related genes in the early stage of post-traumatic heterotopic ossification in a rat model of Achilles tenotomy
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Du Yu, Jinyong Ju, Feng Xue, Yong Zhao, Weizhe Shi, and Haijun Xiao
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Orthopedic surgery ,RD701-811 - Published
- 2021
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8. To Angulate or Not to Angulate the Ulna during the Progressive Distraction Period Performed with a Monolateral External Fixator in Paediatric Patients with a Chronic Monteggia Fracture?
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Yanhan Liu, Hai Zhao, Hongwen Xu, Weizhe Shi, Jingchun Li, Yiqiang Li, and Federico Canavese
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chronic Monteggia fracture ,ulna osteotomy ,distraction ,angulation ,children ,Medicine (General) ,R5-920 - Abstract
Background and Objectives: The purpose of this study was to compare the clinical and radiographic evolution of chronic Monteggia fractures (CMFs) treated by ulnar osteotomy and monolateral external fixators (MEFs) with or without angulation of the ulna during the distraction period. Materials and Methods: This retrospective study evaluated 20 children (14 boys and 6 girls) with CMFs. According to the strategy of ulnar lengthening, two groups of patients were identified: patients undergoing gradual lengthening with (Group A, n = 11) or without ulna angulation (Group B, n = 9). The mean age at the time of surgery was 7.7 years old (range, 5.4–12.9). The mean time from initial trauma to surgery was 26.3 months (range, 1–96), and the mean follow-up was 24.6 months (range, 5.5–45.4). Clinical outcomes were evaluated by Kim et al.’s Elbow Performance Score, while radiographic outcomes were assessed on plain radiographs. Results: Age at surgery, sex, laterality, time between trauma and surgery, and time of follow up in the two groups of patients showed no significant differences. The radial head was successfully reduced in 9 of 9 and 10 of 11 patients in Groups B and A, respectively (p = 1.00). The mean time to achieve radial head reduction was shorter in Group B (18.1 ± 5.3 days) than in Group A (39.2 ± 18.7 days; p = 0.004). The mean angulation of the ulna at the end of treatment was significantly lower in Group B (0.6° ± 1.1°) than in Group A (25.9° ± 6.3°; p < 0.0001). The average ulnar lengthening at the end of treatment in Group B (14.1 ± 5.8 mm) was, on average, 7.7 mm less than that in Group A (21.8 ± 9.7 mm; p = 0.05). The Kim et al. Elbow Performance Score at the last follow-up visit was comparable between the two groups of patients (p = 1.00). Conclusions: A shorter time to achieve radial head reduction and less deformity of the ulna can be expected in paediatric patients with CMFs undergoing intraoperative restoration of ulnar alignment and gradual lengthening without angulation postoperatively.
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- 2022
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9. A novel mutation in ext2 caused hereditary multiple exostoses through reducing the synthesis of heparan sulfate
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Caixia Xian, Mingwei Zhu, Tianying Nong, Yiqiang Li, Xingmei Xie, Xia Li, Jiangui Li, Jingchun Li, Jianping Wu, Weizhe Shi, Ping Wei, Hongwen Xu, and Ya-ping Tang
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Osteochondroma ,hereditary ,EXT1 ,EXT2 ,heparan sulfate ,Genetics ,QH426-470 - Abstract
Abstract Hereditary multiple exostoses (HME) is a rare skeletal disorder characterized by the formation of multiple benign cartilage-capped tumors, usually in the metaphyseal region of the long bones. Over 70% of HME cases arise from monoallelic mutations in either of the two genes encoding the heparan sulfate (HS) synthesis enzymes, ext1 and ext2. To identify more HME-associated mutations, genomic DNA from members of five independent consanguineous families with HME was sequenced with whole exome sequencing (WES). A novel heterozygous splice site mutation (c.1173+2T>A) in ext2 was detected in all three affected members of family V. Further study showed that the novel mutation caused exon 7 of ext2 mRNA to be skipped during splicing and caused a frameshift after the codon for Arg360, which results in the appearance of new 43 codons, followed by a termination codon. Although the resulting truncated protein was still localized to the Golgi, similar to the full-length EXT2, its HS synthesis activity decreased by 40%. In this study, a novel splice site mutation in ext2 was identified and suggested to be a pathogenic mutation of HME, which may expand the genetic etiology spectrum of HME and may be helpful for clinical genetic counseling and prenatal diagnosis.
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- 2021
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10. Closed reduction and percutaneous pinning versus open reduction and internal fixation for Jakob type 3 lateral condyle fractures in children
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Yanhan Liu, Weizhe Shi, Hai Zhao, Yiqiang Li, Jingchun Li, Fuxin Xun, Federico Canavese, and Hongwen Xu
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Fracture Fixation, Internal ,Fractures, Bone ,Open Fracture Reduction ,Treatment Outcome ,Humans ,Orthopedics and Sports Medicine ,Surgery ,Child ,Bone and Bones ,Fracture Fixation, Intramedullary ,Retrospective Studies - Abstract
The management of type 3 lateral condyle fractures (LCFs) remains controversial. The main goal of this study was to evaluate the feasibility of closed reduction and percutaneous pinning (CRPP) in patients with type 3 LCFs and to assess the outcome of such injuries according to the type of treatment, CRPP, or open reduction and internal fixation (ORIF).This is a retrospective review of prospectively enrolled children with type 3 LCF managed by CRPP or ORIF between 2018 and 2021. All patients were followed for at least 12 months. Patients were divided into two groups according to the type of treatment, CRPP or ORIF. Demographic characteristics were recorded for all patients. Standard radiographs were used to identify, evaluate, and classify each fracture and to detect the presence of other concomitant bone lesions. The clinical outcome was assessed according to the Hardacre et al. criteria.Seventy-eight children with type 3 LCF were included; 42 were treated by CRPP (53.8%) and 36 by ORIF (46.2%); the mean follow-up time was 17.7 months (range, 12.3-40.9). The baseline characteristics did not differ between the two groups of patients. Overall, successful CRPP could be achieved in 39 out of 42 patients (92.9%). The mean surgical time was 63.4 and 84.5 min in patients treated by CRPP and ORIF, respectively (p = 0.01). Fluoroscopy time was significantly shorter in patients managed by ORIF than in those treated by CRPP (12 versus 40 s, respectively; p 0.001). Clinical outcome according to the Hardacre et al. criteria was excellent in 37 out of 39 (94.4%) and in 35 out of 36 patients (97.2%) treated by CRPP and ORIF, respectively (p = 0.09).CRPP management of paediatric type 3 LCF has clinical and radiographic outcomes similar to ORIF; if satisfactory reduction cannot be achieved by CRPP, conversion to ORIF should be considered.
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- 2022
11. Ulnar osteotomy and monolateral external fixator for the treatment of chronic Monteggia fractures in children: comparison between gradual and acute radial head reduction.
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Yanhan Liu, Weizhe Shi, Yiqiang Li, Kai Hong, Jingchun Li, Fuxin Xun, Canavese, Federico, and Hongwen Xu
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- 2023
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12. Effects of posterior hemivertebra resection and short segment fusion on the evolution of sagittal balance in children with congenital scoliosis
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HongWen Xu, FuXing Xun, Fulong Xu, Feng Liang, Weizhe Shi, YiQiang Li, and Federico Canavese
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medicine.medical_specialty ,Hemivertebra ,Lumbar Vertebrae ,business.industry ,Sagittal balance ,Thoracic Vertebrae ,Surgery ,Resection ,Spinal Fusion ,Lumbar ,Scoliosis ,Short segment ,Pediatrics, Perinatology and Child Health ,Lordosis ,medicine ,Humans ,Sagittal alignment ,Orthopedics and Sports Medicine ,Kyphosis ,Child ,Lumbar lordosis ,business ,Congenital scoliosis ,Retrospective Studies - Abstract
There is a paucity of data describing sagittal alignment changes in children with congenital scoliosis (CS) treated by hemivertebra (HV) resection. This study aimed to evaluate the effects of posterior HV resection on spine sagittal alignment in children with CS. This is a retrospective analysis of 31 children with CS (mean age at surgery: 49.61 ± 10.21 months; range, 39-72; mean follow-up time: 5.16 ± 1.21 years; range: 3-7) treated at our Institution. Only patients with single thoracic or single lumbar, fully segmented HV managed by posterior HV resection and two segments fusion with four screws and two robs were included. According to the anatomical location of the HV, patients were divided into two groups: thoracic (group A) and lumbar (group B). Thoracic kyphosis (T1-T12; TK) and lumbar lordosis (L1-S1; LL) were measured pre- and postoperatively at 6 months interval. Postoperative TK and LL were 30.3 ± 11.47 and 28.8 ± 9.47, and were 31.98 ± 9.66 and 46.7 ± 11.37 at the last follow-up visit, respectively. The incidence of thoracic hypokyphosis in group B was 53.3%, and it was significantly higher compared to group A (12.5%, P = 0.04). During follow-up, TK changes were comparable between the two groups of patients while LL improved in all patients 6 months after surgery, and continued to improve thereafter. Posterior HV resection and short segment fusion have limited impact on the evolution of TK; in particular, children with lumbar HV were more likely to be hypokyphotic preoperatively, but less likely postoperatively with an increase in LL and a stabilization of TK.
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- 2021
13. Modified Radiographic Classification System for Congenital Thumb Duplication: An Analysis of 2,300 Thumbs in 2,108 Children
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JianPing Wu, WeiZhe Shi, XueMei Lin, JingChun Li, Kai Hong, YuanZhong Liu, YiQiang Li, Federico Canavese, and HongWen Xu
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Orthopedics and Sports Medicine ,Surgery - Abstract
The objectives of this study were to (1) evaluate the radiographic characteristics of children with congenital thumb duplication (CTD) seen in our institution between August 2015 and April 2021; (2) introduce a modified radiographic classification system (MCS) capable of including all cases of CTD based on their radiographic pathoanatomy; and (3) evaluate the inter- and intrarater reliability of the new classification system.We retrospectively reviewed 2,108 patients with 2,300 CTDs. The MCS is based on the Wassel-Flatt and Chung et al classification systems and includes specific subtypes from the Rotterdam and modified Wassel-Flatt classifications. The MCS is characterized by 4 groups according to the anatomical morphology of the duplication: A (joint), B (epiphysis), C (bone), and D (soft tissues). Each group includes 4 subtypes according to the location of the CTD, with subtypes 1-3 extending from the distal phalanx to the metacarpal or interphalangeal joints, then to the carpometacarpal joint, and with subtype 4 only including the triphalangia of the main thumb.Among the 2,300 fingers, 360 (15.7%), 2 (0.1%), and 3 (0.1%) CTDs could not be classified according to the Wassel-Flatt, Chung et al, and Rotterdam classifications, respectively. According to the MCS, the 2 most common forms of CTD were A2 (680/2,300; 29.6%) and D2 (308/2,300; 13.4%). All cases could be classified according to this classification system. The MCS showed excellent intrarater (0.875) and interrater (0.851) reliability relative to the Wassel-Flatt (0.863 and 0.820, respectively), Chung et al (0.793 and 0.822, respectively), and Rotterdam (0.873 and 0.836, respectively) systems.The MCS is a potential radiographic classification for CTD that enables the classification of all patients and has excellent inter- and intrarater reliability.Existing classification systems do not allow classification of the full spectrum of CTD and are not always related to surgery, and some existing systems are complex, with many categories that are rarely encountered, or are difficult to use widely in clinical practice.
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- 2022
14. A novel mutation in ext2 caused hereditary multiple exostoses through reducing the synthesis of heparan sulfate
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Caixia Xian, HongWen Xu, Mingwei Zhu, Weizhe Shi, YiQiang Li, Xingmei Xie, Jiangui Li, Xia Li, Jianping Wu, Ya-Ping Tang, Ping Wei, JingChun Li, and Tianying Nong
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0106 biological sciences ,0301 basic medicine ,Osteochondroma ,Hereditary multiple exostoses ,QH426-470 ,Biology ,01 natural sciences ,Frameshift mutation ,03 medical and health sciences ,chemistry.chemical_compound ,Exon ,Skeletal disorder ,Genetics ,medicine ,Molecular Biology ,Exome sequencing ,Splice site mutation ,EXT2 ,Heparan sulfate ,EXT1 ,medicine.disease ,Stop codon ,030104 developmental biology ,chemistry ,Human and Medical Genetics ,heparan sulfate ,hereditary ,010606 plant biology & botany - Abstract
Hereditary multiple exostoses (HME) is a rare skeletal disorder characterized by the formation of multiple benign cartilage-capped tumors, usually in the metaphyseal region of the long bones. Over 70% of HME cases arise from monoallelic mutations in either of the two genes encoding the heparan sulfate (HS) synthesis enzymes, ext1 and ext2. To identify more HME-associated mutations, genomic DNA from members of five independent consanguineous families with HME was sequenced with whole exome sequencing (WES). A novel heterozygous splice site mutation (c.1173+2T>A) in ext2 was detected in all three affected members of family V. Further study showed that the novel mutation caused exon 7 of ext2 mRNA to be skipped during splicing and caused a frameshift after the codon for Arg360, which results in the appearance of new 43 codons, followed by a termination codon. Although the resulting truncated protein was still localized to the Golgi, similar to the full-length EXT2, its HS synthesis activity decreased by 40%. In this study, a novel splice site mutation in ext2 was identified and suggested to be a pathogenic mutation of HME, which may expand the genetic etiology spectrum of HME and may be helpful for clinical genetic counseling and prenatal diagnosis.
- Published
- 2020
15. Inhibition of Nf-ҝb prevents trauma-induced heterotopic ossification in rat model
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Du Yu, Yong Zhao, Feng Xue, Mingmang Pan, Weizhe Shi, Jinyong Ju, Haijun Xiao, and Guo Tang
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Male ,medicine.medical_specialty ,medicine.medical_treatment ,0206 medical engineering ,Rat model ,Tenotomy ,Urology ,H&E stain ,Inflammation ,02 engineering and technology ,Biochemistry ,Rats, Sprague-Dawley ,Pathogenesis ,03 medical and health sciences ,Rheumatology ,Western blot ,medicine ,Animals ,Orthopedics and Sports Medicine ,Molecular Biology ,030304 developmental biology ,0303 health sciences ,medicine.diagnostic_test ,business.industry ,Ossification, Heterotopic ,NF-kappa B ,Cell Biology ,medicine.disease ,020601 biomedical engineering ,Tendon ,Disease Models, Animal ,medicine.anatomical_structure ,Wounds and Injuries ,Heterotopic ossification ,medicine.symptom ,business ,Signal Transduction - Abstract
Background. To find a better prophylactic regimen, the pathogenesis of acquired heterotopic ossification (AHO) must be more understood. To date, AHO formation is largely thought to be related to inflammation, which is activated by trauma, resulting in AHO by up-regulation of pro-osteogenic genes. Methods. Brain-traumatic/burn/tenotomy model is firstly used in experiment. At first, 44 rats were randomly divided into two groups: E group and C group. Two rats in every group were euthanized during second, third, fourth, sixth, eighth, tenth weeks for collecting tendon. The remaining rats survived until tenth week for X-Ray radiation examination to confirm the size of AHO.Then, 124 rats were randomly divided into four group: P group, L group, M group, H group. The three rats of every group were euthanized during every week of the first seven weeks for collecting tendon to detect P65 protein. The remaining rats survived until tenth week for X-Ray examination to confirm the size of AHO. Results. The success rate of Brain-traumatic/Burn/Tenotomy model is 100%. Difference of P65 expression in E group and in C group are statistically significant,and that in E group is higher.Pharmacologic inhibition of Nf-ҝb signaling pathway limits AHO formation, and that The bone formation content of M group is decreased. Conclusion. Brain-traumatic/Burn/Tenotomy model is highly reliable.Results indicate that the Nf-ҝb /p65 signaling response occurs in the forming process of AHO. PDTC limits formation of AHO. The most effective concentration is 6mg/ml for local injection.
- Published
- 2018
16. Fetuin A is down-regulated in rats during heterotopic ossification after Achilles tenotomy
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Feng Xue, J Wu, Haijun Xiao, and Weizhe Shi
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0301 basic medicine ,Male ,medicine.medical_specialty ,Histology ,alpha-2-HS-Glycoprotein ,Down-Regulation ,Enzyme-Linked Immunosorbent Assay ,Ectopic bone formation ,Achilles Tendon ,Polymerase Chain Reaction ,03 medical and health sciences ,Internal medicine ,medicine ,Animals ,Humans ,RNA, Messenger ,Histological examination ,Achilles tendon ,business.industry ,Ossification, Heterotopic ,General Medicine ,medicine.disease ,Fetuin ,Immunohistochemistry ,Surgery ,Rats ,Medical Laboratory Technology ,Disease Models, Animal ,030104 developmental biology ,Endocrinology ,medicine.anatomical_structure ,Tenotomy ,Mrna level ,Heterotopic ossification ,Achilles tenotomy ,business - Abstract
We investigated the role of fetuin A during heterotopic ossification (HO) in rats following Achilles tenotomy. We performed a right midpoint Achilles tenotomy on 24 rats. At 5 and 10 h after surgery, we investigated the formation of ectopic bone using X-ray and histological examination. We evaluated the mRNA level of fetuin A using real-time PCR. Presence of fetuin A in the Achilles tendon was assessed by immunohistochemical staining. We also measured the serum concentration of fetuin A using enzyme linked immunosorbent assay (ELISA). The expression of fetuin A was significantly decreased in both the liver and Achilles tendon during HO. ELISA showed a small amount of fetuin A in blood throughout the development of HO. Immunohistochemical staining showed that fetuin A was abundant in the ectopic bone. Fetuin A appears to be involved in the formation of ectopic bone induced by Achilles tenotomy, and a deficiency of fetuin A plays a role in the development of HO.
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- 2016
17. [EFFECTIVENESS OF SURGICAL TREATMENT FOR SENILE CHRONIC SHOULDER DISLOCATION]
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Du, Yu, Haijun, Xiao, Weizhe, Shi, and Jinyong, Ju
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Male ,Fractures, Bone ,Shoulder ,Rotation ,Recurrence ,Shoulder Joint ,Shoulder Dislocation ,Humans ,Female ,Range of Motion, Articular ,Bone Plates ,Aged - Abstract
To investigate the surgical treatment and effectiveness of senile chronic shoulder dislocation.Between October 2011 and April 2014, 7 elderly patients with chronic shoulder dislocation were treated. There were 2 males and 5 females with an average age of 74 years (range, 61-83 years). The causes of injuries were falling injury in 6 patients and traffic accident injury in 1 patient. The interval between injury and confirmed diagnosis was 4-12 weeks (mean, 6.7 weeks). Preoperative apprehension test and Dugas sign of the shoulder joint were positive. Before operation, the forward elevation, abduction, and external rotation were (50.7±8.4), (44.5±3.3), and (35.8±4.8), respectively; and internal rotation reached T6, T11, L4 in 1 case and reached T10, T12 in 2 cases separately. The Constant-Murley score and Neer score were 51.2±8.3 and 45.4±7.3, respectively.All the incisions healed by first intention, and no complication of fracture or neurovascular injuries occurred. Seven patients were followed up 12-18 months (mean, 16 months), and no re-dislocation happened. At last follow-up, apprehension test and Dugas sign of the shoulder joint were negative. The forward elevation, abduction, and external rotation were significantly improved to (117.5±13.1), (72.0±4.6), and (39.0±3.4)° (t= -33.746, P=0.000; t= -30.614, P=0.000; t= -2.802, P=0.031); and internal rotation reached T6, T10, T12, and L3 in 1 case respectively, and L3 in 3 cases, showing no significant difference when compared with preoperative values (Z= -1.732, P=0.083). The Constant-Murley score and Neer score were significantly improved to 85.4±4.3 and 84.0±4.8 when compared with preoperative score (t= -21.016, P=0.000; t= -29.518, P=0.000).Surgical treatment of senile chronic shoulder dislocation can improve the range of motion and function of the shoulder joint obviously.
- Published
- 2016
18. [Dynamic changes of matrix metalloproteinase 9 in heterotopic ossification of rat model]
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Weizhe, Shi, Haijun, Xiao, Feng, Xue, and Jiang, Wu
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Male ,Reverse Transcriptase Polymerase Chain Reaction ,Ossification, Heterotopic ,Enzyme-Linked Immunosorbent Assay ,Achilles Tendon ,Collagen Type I ,Rats ,Rats, Sprague-Dawley ,Disease Models, Animal ,Cartilage ,Matrix Metalloproteinase 9 ,Tendon Injuries ,Animals ,RNA, Messenger - Abstract
To explore the value of matrix metalloproteinase 9 (MMP-9) in predicting the occurrence of heterotopic ossification by observing the expression of MMP-9 in heterotopic ossification of the early trauma rat model.A total of 132 male Sprague Dawley rats, aged 4-5 weeks, weighing (135.0 ± 6.5) g, were randomly divided into experimental group and control group (n = 66). In experimental group, the Achilles tendon was cut off and clamped to prepare heterotopic ossification model; in control group, only Achilles tendon was exposed by making a incision. The general condition of the rats was observed after operation; at 2, 3, 4, 5, 6, 7, and 8 days after operation, the Achilles tendon tissue was harvested for gross observation, histological observation, and immunohistochemical staining observation; the serum and Achilles tendon tissue were harvested to detect the expressions of MMP-9 protein and mRNA by ELISA and RT-PCR. The X-ray films at 5 and 10 weeks and histological examination at 10 weeks after operation were used to observe heterotopic ossification.All rats survived to the end of the experiment. The Achilles tendon had no significant change in control group at each time point, showing normal tendon structure. In experimental group, the hardness of Achilles tendon tissue gradually increased with the time; there were a large number of irregular connective tissue and cartilage cells; and immunohistochemical staining for MMP-9 was positive results. The MMP-9 protein and mRNA expression levels of experimental group were significantly higher than those of the control group at each time point (P0.05). MMP-9 protein and mRNA expression levels of experimental group showed an increasing tendency (P0.05). According to the results of X-ray films and histological observation, heterotopic ossification occurred at 10 weeks after operation in experimental group, but no heterotopic ossification was observed in control group.In early heterotopic ossification of rat Achilles tendon, the expression of MMP-9 increases significantly, indicating that it has reference significance in predicting heterotopic ossification.
- Published
- 2014
19. A Ka-band axial ratio bandwidth enhanced circularly polarized LTCC patch antenna with truncated artificial magnetic conductor
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Hao Wang, Weizhe Shi, Baolin Cao, Jing Dai, Yong Huang, and Dan Li
- Subjects
Physics ,Patch antenna ,Microstrip antenna ,Optics ,business.industry ,Plane (geometry) ,Axial ratio bandwidth ,Ka band ,Antenna (radio) ,business ,Circular polarization ,Conductor - Abstract
In this paper, a novel method to enhance axial ratio bandwidth of circularly polarized (CP) patch antenna using artificial magnetic conductor (AMC) structures with LTCC technology at Ka-band is proposed. In order to improve the axial ratio bandwidth, the traditional PEC plane is replaced by an AMC plane. The AMC is composed of periodic square unit cells with truncated opposite corners. The AMC structure and the antenna are simulated using a full-wave solver and the results show a 10 dB return loss bandwidth of 30% and a 3 dB axial ratio bandwidth of 12.7%, and gain is around 7.5 dB within this band, which compared with the traditional corner-cut square circular polarization patch antenna, the axial ratio bandwidth of proposed antenna increased by 9.5%.
- Published
- 2014
20. Low-loss LTCC-based gap waveguide feeding network for W-band application
- Author
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Weizhe Shi, Hao Wang, Dan Li, Baolin Cao, and Yong Huang
- Subjects
Waveguide (electromagnetism) ,Materials science ,Transmission (telecommunications) ,W band ,business.industry ,Transmission line ,Electronic engineering ,Optoelectronics ,Insertion loss ,Dielectric loss ,business ,Microstrip ,Power (physics) - Abstract
In this paper, a novel low-loss gap waveguide (GWG) transmission line with Low Temperature Co-Fired Ceramic (LTCC) technology for W-band is presented. To illustrate the low-loss characteristics of the proposed line, microstrip line (MSL) and laminated waveguide (LWG) are also designed with LTCC, and the corresponding measured values of insertion loss are given. From the measured results, the value of the dielectric loss tangent is extracted. As an example, two kinds of eight-way power dividers are shown, which are composed of LWG and GWG, respectively. Simulated results of transmission and reflection coefficients are presented. Comparison of two power dividers has shown the low-loss superiority of the new design.
- Published
- 2014
21. [Effects of selective and non-selective cyclooxygenase 2 inhibitors on heterotopic ossification in rat model with Achilles tenotomy]
- Author
-
Jiang, Wu, Haijun, Xiao, Feng, Xue, Weizhe, Shi, and Hang, Zhao
- Subjects
Male ,Sulfonamides ,Cyclooxygenase 2 Inhibitors ,Ossification, Heterotopic ,Indomethacin ,Bone Morphogenetic Protein 2 ,Achilles Tendon ,Immunohistochemistry ,Rats ,Rats, Sprague-Dawley ,Disease Models, Animal ,Random Allocation ,Tenotomy ,Celecoxib ,Cyclooxygenase 2 ,Animals ,Pyrazoles - Abstract
To compare the efficacy of selective cyclooxygenase 2 (COX2) inhibitor and non-selective COX2 inhibitor drugs in prevention of heterotopic ossification in rats model so as to provide reference for clinical drugs selection of heterotopic ossification prevention.Fifty male Sprague Dawley rats, 6 to 8 weeks old, weight (190.0 +/- 8.5) g, were selected; the right Achilles tendon was cut off to induce ectopic bone formation. The rats were randomly divided into 5 groups (n = 10): on the 1st day after modeling, celecoxib was given in groups A [2 mg/(kg x d)] and B [10 mg/(kg x d)], indomethacin in groups C [(2 mg/(kg x d) and D [10 mg/(kg x d)], and 2 mL of saline in group E for 10 weeks. The general condition of rats was observed after operation. At 5 and 10 weeks after operation, X-ray films of the right lower limb were taken to observe new bone formation. At 10 weeks after operation, the right Achilles tendon tissue was harvested for histological observation. Based on X-ray and histological results, heterotopic ossification was assessed. Immunohistochemical staining was used to evaluate COX2 and bone morphogenetic protein 2 (BMP-2) expression levels in local Achilles tendon.During the experiment, 5 rats died (2 in group B, 1 in group C, and 2 in group D), the other rats survived to the end of the experiment. General observation of Achilles tendon tissue showed that the tendon tissue volume of group B was the smallest, with soft texture and no cartilage-like tissue; the tendon tissue volume of group E was the biggest, with hard texture and cartilage-like tissue. The incidence of heterotopic ossification was 80.0% (8/10), 25.0% (2/8), 88.9% (8/9), 50.0% (4/8), and 100% (10/10) in groups A-E respectively at 10 weeks after operation; significant differences were found between groups B, D and group E (P = 0.002, P = 0.023) and between groups B and C (P = 0.015), but no significant difference was found among the other groups (P0.05). COX2 expression level in groups B and D was significantly lower than that in group E (P0.05 ), but no significant difference was found among the other groups (P0.05); BMP-2 expression level in group B was significantly lower than that in groups A, C, and E (P0.05), but no significant difference was found among the other groups (P0.05).Celecoxib at a dose of 10 mg/(kg x d) can effectively reduce the incidence of heterotopic ossification in rats.
- Published
- 2014
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