1.Correlation Analysis and Comparison of Adult CE-Chirp ABR Response Threshold and Pure Tone Hearing Threshold
He-Ying CHENG ; Yun-Ge ZHANG ; Yan CHEN ; Sun YIN ; Ming LÜ ; Chun-Xiao LI
Journal of Forensic Medicine 2024;40(1):15-19
		                        		
		                        			
		                        			Objective To study the application of CE-Chirp in the evaluation of hearing impairment in forensic medicine by testing the auditory brainstem response(ABR)in adults using CE-Chirp to ana-lyze the relationship between the V-wave response threshold of CE-Chirp ABR test and the pure tone hearing threshold.Methods Subjects(aged 20-77 with a total of 100 ears)who underwent CE-Chirp ABR test in Changzhou De'an Hospital from January 2018 to June 2019 were selected to obtain the V-wave response threshold,and pure tone air conduction hearing threshold tests were conducted at 0.5,1.0,2.0 and 4.0 kHz,respectively,to obtain pure tone listening threshold.The differences and statistical differences between the average pure tone hearing threshold and V-wave response threshold were compared in different hearing levels and different age groups.The correlation,differences and statistical differences between the two tests at each frequency were analyzed for all subjects.The lin-ear regression equation for estimating pure tone hearing threshold for all subjects CE-Chirp ABR V-wave response threshold was established,and the feasibility of the equation was tested.Results There was no statistical significance in the CE-Chirp ABR response threshold and pure tone hearing threshold dif-ference between different hearing level groups and different age groups(P>0.05).There was a good correlation between adult CE-Chirp ABR V-wave response threshold and pure tone hearing threshold with statistical significance(P<0.05),and linear regression analysis showed a significant linear correla-tion between the two(P<0.05).Conclusion The use of CE-Chirp ABR V-wave response threshold can be used to evaluate subjects'pure tone hearing threshold under certain conditions,and can be used as an audiological test method for forensic hearing impairment assessment.
		                        		
		                        		
		                        		
		                        	
2.Study on Urinary Metabolic Profile in Rats with Deep Venous Thrombosis Based on Pattern Recognition.
Jie CAO ; Xiao Ge LÜ ; Yu LI ; Qian Qian JIN ; Xiao Yun CHU ; Ying Yuan WANG ; Jun Hong SUN
Journal of Forensic Medicine 2018;34(3):228-232
		                        		
		                        			OBJECTIVES:
		                        			To study the urinary metabolic profile in rats with deep venous thrombosis (DVT) based on metabolomics and to screen out small molecular biomarkers for the diagnosis and forensic identification of DVT.
		                        		
		                        			METHODS:
		                        			Inferior vena cava of rats was ligated to construct DVT models. The rats were randomly divided into three groups: DVT, sham, and control groups, 10 in each group. The urine of DVT and sham rats was collected during 24 hours in the metabolic cage at 48 hours after operating, meanwhile, 24 hours urine was collected in control group. The metabolic profile was analyzed by nuclear magnetic resonance. SIMCA-P 14.1 software was used for pattern recognition. The variable importance in projection (VIP) value from orthogonal PLS-DA (OPLS-DA) model combined with Mann-Whitney U test were used to search the different metabolites in the urine.
		                        		
		                        			RESULTS:
		                        			The metabolic profiles of urine from DVT, sham, and control groups had significant differences. The DVT, sham, and control groups could be distinguished by the partial least squares method-discriminant analysis (PLS-DA) model. Compared with the urine of the rats in control groups, the levels of leucine, glutamine, creatine, creatinine and sucrose in the urine of DVT rats were up-regulated, and the levels of 3-hydroxybutyrate, lactate, acetone, α-oxoglutarate, citrate and hippurate were down-regulated.
		                        		
		                        			CONCLUSIONS
		                        			The different metabolites in the urine of DVT rats are expected to become its candidate biomarkers. The results can provide a research basis for the diagnosis, treatment and forensic identification of DVT.
		                        		
		                        		
		                        		
		                        			Animals
		                        			;
		                        		
		                        			Biomarkers/blood*
		                        			;
		                        		
		                        			Discriminant Analysis
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Magnetic Resonance Spectroscopy/methods*
		                        			;
		                        		
		                        			Metabolome
		                        			;
		                        		
		                        			Metabolomics/methods*
		                        			;
		                        		
		                        			Nuclear Magnetic Resonance, Biomolecular/methods*
		                        			;
		                        		
		                        			Rats
		                        			;
		                        		
		                        			Rats, Sprague-Dawley
		                        			;
		                        		
		                        			Urine/chemistry*
		                        			;
		                        		
		                        			Venous Thrombosis/urine*
		                        			
		                        		
		                        	
3.Progress on Post Traumatic Epilepsy and Its Forensic Evaluation.
Yun Ge ZHANG ; Chun Xiao LI ; Guo Fu GUAN ; Ming LÜ ; He Ying CHENG ; Huan CHEN
Journal of Forensic Medicine 2016;32(3):200-203
		                        		
		                        			
		                        			Post traumatic epilepsy (PTE) refers to the epileptic seizures after traumatic brain injury. Organic damage can be found by imaging examination, and abnormal electroencephalogram can be detected via electroencephalogram examination which has the similar location of the brain injury. PTE has the characteristics of low incidence, absence of case reports, and easy to exaggerate the state of illness, which add difficulties to the forensic identification. This paper reviews the status of epidemiology, pathogenesis, clinical treatment and forensic identification for PTE.
		                        		
		                        		
		                        		
		                        			Brain Injuries, Traumatic/physiopathology*
		                        			;
		                        		
		                        			Electroencephalography
		                        			;
		                        		
		                        			Epilepsy
		                        			;
		                        		
		                        			Epilepsy, Post-Traumatic/pathology*
		                        			;
		                        		
		                        			Forensic Pathology
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Incidence
		                        			
		                        		
		                        	
4.Effect of genistein on rat femoral bone metabolic activity in vitro.
Jian ZHOU ; Bao-Feng GE ; Ke-Ming CHEN ; Xiao-Ni MA ; Kui CHENG ; Xiao-Yu GUO ; Xiang LÜ
Acta Pharmaceutica Sinica 2013;48(6):960-964
		                        		
		                        			
		                        			This study is to investigate effects of genistein on rat femoral bone metabolic in vitro. Rat femoral tissues was isolated and randomly divided into two groups including control group and genistein (1 x 10(-5) mol x(-1)) group. Determinations of alkaline phosphatase (ALP) activity, calcium content and osteoprotegerin (OPG), type I-collagen (Collagen-I), RANKL, Runx-2 and bone morphogenetic protein (BMP-2) mRNA expression were done by real-time PCR. The results showed that 1 x 10(-5) mol x L(-1) genistein could increase the activity of ALP and contents of Ca, regulate bone metabolism activity of OPG, RANKL, BMP-2, Collagen-I and Runx-2 mRNA expression level. Genistein can significantly modulate bone metabolism related gene expression level of rat femoral tissue in vitro, and can increase calcium content and the activity of ALP.
		                        		
		                        		
		                        		
		                        			Alkaline Phosphatase
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Animals
		                        			;
		                        		
		                        			Bone Morphogenetic Protein 2
		                        			;
		                        		
		                        			genetics
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Calcium
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Collagen Type I
		                        			;
		                        		
		                        			genetics
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Core Binding Factor Alpha 1 Subunit
		                        			;
		                        		
		                        			genetics
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Enzyme Activation
		                        			;
		                        		
		                        			drug effects
		                        			;
		                        		
		                        			Femur
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Gene Expression Regulation
		                        			;
		                        		
		                        			Genistein
		                        			;
		                        		
		                        			pharmacology
		                        			;
		                        		
		                        			Osteoprotegerin
		                        			;
		                        		
		                        			genetics
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Phytoestrogens
		                        			;
		                        		
		                        			pharmacology
		                        			;
		                        		
		                        			RANK Ligand
		                        			;
		                        		
		                        			genetics
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			RNA, Messenger
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Random Allocation
		                        			;
		                        		
		                        			Rats
		                        			;
		                        		
		                        			Rats, Sprague-Dawley
		                        			;
		                        		
		                        			Real-Time Polymerase Chain Reaction
		                        			
		                        		
		                        	
5.Survey of studies on drug abstinence with acupuncture in recent 10 years.
Xiao-Ge SONG ; Hang LÜ ; Xing-Hui CAI ; Rong-Jun ZHANG
Chinese Acupuncture & Moxibustion 2012;32(7):669-672
		                        		
		                        			
		                        			The effect of acupuncture on substance withdrawl syndromes and craving relapse prevention of the recent 10 years were reviewed as well as its mechanism. The therapeutic effect and the possible mechanism were analyzed on the basis. From the three aspects of anti protracted abstinence symptoms, craving relapse prevention and mechanism of acupuncture, the development tendency and the prospect of application on drug withdrawl with acupuncture were expected. And it is proposed that clinical observation of acupuncture intervention on craving should be developed, the mechanism of acupuncture impact on cognitive behavior, blocking study and memory processing related to drug addiction should be explored, so as to further give play to the advantages of acupuncture on anti-drug addiction.
		                        		
		                        		
		                        		
		                        			Acupuncture Therapy
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Substance-Related Disorders
		                        			;
		                        		
		                        			therapy
		                        			;
		                        		
		                        			Time Factors
		                        			
		                        		
		                        	
6.Comparison of effects of kaempferide and anhydroicaritin on biomineralization of cultured osteoblasts.
Peng SONG ; Juan YAO ; Hui-Ping MA ; Bao-Feng GE ; Ke-Ming CHEN ; Xiao-Yu GUO ; Xiang LÜ
Acta Pharmaceutica Sinica 2012;47(7):890-896
		                        		
		                        			
		                        			This study is to compare the effects of kaempferide and anhydroicaritin on biomineralization of rat osteoblasts (ROB) in vitro. Calvarias were dissected aseptically from newborn SD rats, the osteoblasts were obtained by enzyme digestion and were cultured in MEM containing 10% FBS. The medium was changed every three days, and serial subculture was performed when cells covered with 90% of the dish. Kaempferide and anhydroicaritin were separately added with final concentrations of 1 x 10(-4), 1 x 10(-5), 1 x 10(-6) and 1 x 10(-7) mol x L(-1) under the conditions of osteogenic differentiation. The proliferation was measured by MTT, and the optimal concentration was detected by the ALP activity at the 9th day after osteogenic induction culture. The osteogenic indexes of kaempferide, anhydroicaritin and control group with the optimal concentration were compared. The result showed that the anhydroicaritin at concentration of 1 x 10(-5) mol x L(-1) had significantly promoted the activity of ALP, calcium content and osteocalcin content, increased the number of CFU-F(ALP) and mineralized nodules, enhanced the mRNA level of BMP-2, OSX and Runx-2, which are key genes of osteogenic differentiation, and raised the protein content of collagen-I. However, the kaempferide group had not significantly represented the ability that promoted osteogenic differentiation of ROB. The difference of osteogenic differentiation on ROB between kaempferide and anhydroicaritin was caused by the prenyl group on C-8 of icariin.
		                        		
		                        		
		                        		
		                        			Alkaline Phosphatase
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Animals
		                        			;
		                        		
		                        			Benzopyrans
		                        			;
		                        		
		                        			pharmacology
		                        			;
		                        		
		                        			Bone Morphogenetic Protein 2
		                        			;
		                        		
		                        			genetics
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Calcium
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Cell Proliferation
		                        			;
		                        		
		                        			drug effects
		                        			;
		                        		
		                        			Cells, Cultured
		                        			;
		                        		
		                        			Collagen Type I
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Core Binding Factor Alpha 1 Subunit
		                        			;
		                        		
		                        			genetics
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Kaempferols
		                        			;
		                        		
		                        			pharmacology
		                        			;
		                        		
		                        			Osteoblasts
		                        			;
		                        		
		                        			cytology
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Osteocalcin
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Osteogenesis
		                        			;
		                        		
		                        			drug effects
		                        			;
		                        		
		                        			RNA, Messenger
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Rats
		                        			;
		                        		
		                        			Rats, Sprague-Dawley
		                        			;
		                        		
		                        			Transcription Factors
		                        			;
		                        		
		                        			genetics
		                        			;
		                        		
		                        			metabolism
		                        			
		                        		
		                        	
7.CD30-negative and ALK-positive anaplastic large cell lymphoma: report of a case.
Nan LI ; Dan REN ; Bei-Bei LÜ ; Jian-Lan XIE ; Xiao-Dan ZHENG ; Li-Ping GONG ; Xiao-Ge ZHOU
Chinese Journal of Pathology 2011;40(4):269-270
		                        		
		                        		
		                        		
		                        			Antineoplastic Combined Chemotherapy Protocols
		                        			;
		                        		
		                        			therapeutic use
		                        			;
		                        		
		                        			CD2 Antigens
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Child, Preschool
		                        			;
		                        		
		                        			Chromosome Breakage
		                        			;
		                        		
		                        			Cyclophosphamide
		                        			;
		                        		
		                        			therapeutic use
		                        			;
		                        		
		                        			Doxorubicin
		                        			;
		                        		
		                        			therapeutic use
		                        			;
		                        		
		                        			Female
		                        			;
		                        		
		                        			Follow-Up Studies
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Ki-1 Antigen
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Lymphoma, Large-Cell, Anaplastic
		                        			;
		                        		
		                        			drug therapy
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			pathology
		                        			;
		                        		
		                        			Mucin-1
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Prednisone
		                        			;
		                        		
		                        			therapeutic use
		                        			;
		                        		
		                        			Receptor Protein-Tyrosine Kinases
		                        			;
		                        		
		                        			genetics
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Vincristine
		                        			;
		                        		
		                        			therapeutic use
		                        			
		                        		
		                        	
8.Clinicopathologic features of systemic EBV-positive T/NK-cell lymphoproliferative disease in adults.
Xiao-Dan ZHENG ; Xiao-Ge ZHOU ; Yan JIN ; Jian-Lan XIE ; Xue-Jing WEI ; Shu-Yuan CHEN ; Xue MEI ; Li-Ping GONG ; Bei-Bei LÜ
Chinese Journal of Pathology 2011;40(4):227-234
OBJECTIVETo study the clinicopathologic features, immunophenotype, clonality and Epstein-Barr virus (EBV) status of systemic EBV-positive T/NK-cell lymphoproliferative disease in adults (ASEBV(+)T/NK-LPD).
METHODSTwenty cases of ASEBV(+)T/NK-LPD were analyzed retrospectively with histopathologic review, immunohistochemistry and in-situ hybridization for EBV-encoded RNA (EBER). The follow-up data were collected.
RESULTSThere were altogether 15 males and 5 females. The median age of the patients was 34 years. The average duration from onset of symptoms to diagnosis was 8.7 months. Fever (18/20), hepatosplenomegaly (18/20) and lymphadenopathy (17/20) were the main clinical manifestations. Eleven of the 17 patients died during follow-up, with a mean survival of 2.9 months. Histologically, there was obvious expansion of T zone of the involved lymph nodes, associated with diminished lymphoid follicles. The interfollicular areas were widened and infiltrated by small to median-sized lymphoid cells which showed only mild atypia. Scattered large lymphoid cells were not uncommon. The nodal capsule was thickened in 6 cases. Focal necrosis was seen in 9 cases. Sinus histiocytic proliferation with erythrophagocytosis was observed in 3 cases. In addition, there were mild atypical lymphoid cells infiltrate into the liver, spleen, intestinal mucosa and bone marrow. Immunohistochemical study and in-situ hybridization showed that the EBER-positive cells were of T-cell lineage, with CD3 expression. They were also positive for cytotoxic molecules (granzyme B or TIA-1). Only 1 case was CD56 positive. A predominance of CD8-positive cells was demonstrated in 8 of the 14 cases studied, while CD4-positive cells predominated in the remaining 5 cases. One case showed similar proportion of CD8 and CD4-positive cells. The number of EBER-positive cells ranged from 30 to more than 300 per high-power fields. These EBER-positive cells were of small to large size and located mainly in the expanded T zone and occasionally in the germinal centers. Three of the 7 cases exhibited clonal rearrangement of T-cell receptor gamma gene, while the other 4 cases exhibited polyclonal rearrangement of T-cell receptor gamma gene.
CONCLUSIONSASEBV(+)T/NK-LPD is a systemic disease with a subacute or chronic clinical course. Most patients suffer from relapsing fever, lymphadenopathy and hepatosplenomegaly. The disease is characterized by proliferation of EBV-infected cytotoxic T cells. The T zone of the involved lymph nodes shows expansion by mildly atypical lymphoid cells. The disease is associated with poor clinical outcome and can be life-threatening. The patients often die of multiorgan failure and bleeding.
Adult ; Aged ; CD3 Complex ; metabolism ; Epstein-Barr Virus Infections ; pathology ; Female ; Follow-Up Studies ; Gene Rearrangement, gamma-Chain T-Cell Antigen Receptor ; Granzymes ; metabolism ; Herpesvirus 4, Human ; isolation & purification ; Humans ; Killer Cells, Natural ; pathology ; Lymphoproliferative Disorders ; drug therapy ; genetics ; metabolism ; pathology ; virology ; Male ; Middle Aged ; Poly(A)-Binding Proteins ; metabolism ; RNA, Viral ; metabolism ; Retrospective Studies ; Survival Rate ; T-Cell Intracellular Antigen-1 ; T-Lymphocytes ; pathology ; Young Adult
9.Natural killer cell lymphoma in lymph node: report of a case.
Gang-ping WANG ; Shan-shan WANG ; Xiao-dan ZHENG ; Jian-lan XIE ; Bei-bei LÜ ; Xiao-ge ZHOU
Chinese Journal of Pathology 2010;39(8):561-562
		                        		
		                        		
		                        		
		                        			Adult
		                        			;
		                        		
		                        			CD56 Antigen
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Diagnosis, Differential
		                        			;
		                        		
		                        			Epstein-Barr Virus Infections
		                        			;
		                        		
		                        			Herpesvirus 4, Human
		                        			;
		                        		
		                        			isolation & purification
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Killer Cells, Natural
		                        			;
		                        		
		                        			pathology
		                        			;
		                        		
		                        			Lymph Nodes
		                        			;
		                        		
		                        			pathology
		                        			;
		                        		
		                        			Lymphoma
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			pathology
		                        			;
		                        		
		                        			virology
		                        			;
		                        		
		                        			Lymphoma, Extranodal NK-T-Cell
		                        			;
		                        		
		                        			pathology
		                        			;
		                        		
		                        			Male
		                        			
		                        		
		                        	
10.A randomized, multicenter controlled trial to compare the efficacy of recombinant human parathyroid hormone (1-34) with elcatonin in postmenopausal women with osteoporosis in China.
Xiu-Zhen ZHANG ; Bo WANG ; Jun YANG ; Miao XUAN ; Li-Ge SONG ; Hong LI ; Xiao-Hui GUO ; Xiao-Feng LÜ ; Qing-Yun XUE ; Gang-Yi YANG ; Qiu-He JI ; Jie SHEN ; Zhi-Min LIU ; Cheng-Jiang LI ; Tian-Feng WU ; Xiao-Cui TONG ; Yuan JIA
Chinese Medical Journal 2009;122(24):2933-2938
BACKGROUNDRecombinant human parathyroid hormone (1-34) (rhPTH (1-34)) given by injection is a new seventh class drug of biological products, which is prepared by adopting gene recombination technique. rhPTH (1-34) is mainly used to treat osteoporosis, especially for postmenopausal women. This study compared the clinical efficacy and safety of rhPTH (1-34) with elcatonin for treating postmenopausal women with osteoporosis in 11 urban areas of China.
METHODSTwo hundred and five women with osteoporosis were enrolled in a 6-month, multicenter, randomized, controlled study. They were randomized to receive either rhPTH (1-34) 20 microg (200 U) daily or elcatonin 20 U weekly. Lumbar spine (L1-4) and femoral neck bone mineral density (BMD), as well as biochemical markers of bone turnover were measured. Adverse events were recorded.
RESULTSrhPTH (1-34) increased lumbar BMD significantly more than did elcatonin at 3 months and 6 months (2.38% vs 0.59%, P < 0.05; 5.51% vs 1.55%, P < 0.01), but there were no significant increases of BMD in these two groups at femoral neck. There were larger mean increases in bone markers in the rhPTH (1-34) group than in the elcatonin group at 3 months and 6 months (serum bone-specific alkaline phosphatase (BSAP) 36.79% vs 0.31%; 92.42% vs -0.17%; urinary N-telopeptide/creatinine (NTX/Cr) 48.91% vs -5.32%; 68.82% vs -10.86%). Both treatments were well tolerated and there were no significant differences detected between the two groups in the proportion of any adverse events and any serious adverse events (67.0% vs 59.0%; 0 vs 0).
CONCLUSIONSrhPTH (1-34) has more positive effects on bone formation, as shown by the larger increments of lumbar BMD and bone formation markers, than elcatonin, with only mild adverse events and no significant change in the liver, kidney or hematological indices.
Aged ; Calcitonin ; analogs & derivatives ; pharmacology ; therapeutic use ; Female ; Humans ; Middle Aged ; Osteogenesis ; drug effects ; Osteoporosis, Postmenopausal ; drug therapy ; Parathyroid Hormone ; pharmacology ; therapeutic use ; Recombinant Proteins ; pharmacology ; therapeutic use
            
Result Analysis
Print
Save
E-mail