1.Economic Growth, Health Input and Investment Benefits: Empirical Study Based on FAVAR Model
Chinese Health Economics 2017;36(6):79-81
Objective:To make full use of existing variables set,study on the dynamic connection between economic growth,health input and investment benefits.Methods:Using Factor Augmented VAR(FAVAR) to draw common factors and perform VAR estimation with the variables sets.Results:The impact of economic growth on health output had two sides.Increasing health input would significantly stimulate health output and economic growth.The increase of health level would promote economic growth in short time and hamper in the long run.Conclusion:The government should increase health input and consider the health loss brought by economic growth.It should prevent the not rich but old risk with the pursuit of health benefit.
2.Analysis of reasons for unqualified blood specimens in coagulation test in tumor patients and its countermeasures
Li MA ; Xiaoqin MA ; Li YANG
International Journal of Laboratory Medicine 2015;(18):2694-2696
Objective To analyze reasons for the generation of unqualified blood specimens in coagulation test in tumor patients and to develop countermeasures ,so as to ensure the quality of samples prior to analysis .Methods Blood specimens received from outpatients in Tumor Hospital of Yunnan Province in 2012(40 253 specimens) ,2013(46 756 specimens) and first quarter of 2014 (14 566 specimens)were retrospectively analysed .Unqualified rate was used to describe situation of unqualified specimens ,and the distribution and changes of unqualified specimens were compared among the three years .Results The unqualified rate of blood specimens in coagulation test in 2012 and 2013 was 0 .57% and 0 .96% ,respectively .Reasons for unqualified blood specimens in 2012 was ,in order ,specimens agglutination ,insufficient amount of specimen ,excessive amount of specimen ,wrong container ,no specimen .Reasons for unqualified blood specimens in 2013 was ,in order ,specimens agglutination ,insufficient amount of specimen , excessive amount of specimen ,bar code error ,contaminated specimen ,wrong container ,no specimen ,hematocrit≥55% ,repeated in‐spection .Conclusion Coagulation test requires high quality specimen and quality assurance prior to analysis is particularly impor‐tant .The clinical laboratories should strengthen the links between the nursing and clinical departments ,timely communicate and feedback situation of unqualified specimens ,find the cause together and develop and implement effective improvement measures ,in order to ensure the quality of specimens on the steps before analysis .
3.Analysis of College students' Vocational Values
Jun MA ; Xiao-Li YANG ;
Chinese Journal of Medical Education Research 2006;0(10):-
The article analyses the actualities and causes of present-day college students'vocational values.Then it elaborates how to guide college students to have correct vocational values.Teaching college students' vocational values is a comprehensive work over a long period of time.
4.Study of the activated state of TH1/TH2 cytokines on ankylosing sondylitis
Chinese Journal of Immunology 2000;0(08):-
Objective:To investigate the activated state of TH1/TH2 cytokines and T lymphocytes and to explore the pathogenesis of ankylosing sondylitis.Methods:Cytokine levels of Th1(IFN-?、TNF-?、IL-2)and Th2(IL-10、IL-5、IL-4) in plasma, percentages of CD3 +、CD4 +、CD8 + T cells、B cells(CD19 +) NK cells(CD16 +56 +)and CD3 +HLA-DR +、CD4 +HLA-DR +、CD8 +HLA-DR + T cells in peripheral blood lymphocytes were detected by Flow Cytometry.Results:In patients with AS ,plasma levels of TNF-?、IL-2 were significantly lower than that of healthy controls. IL-10 were significantly higher than that of healthy controls. In AS patients, percentages of CD3 +and CD8 + T cell from peripheral blood lymphocytes were significantly lower than that of healthy controls. Percentages of CD8 +HLA-DR + T cell were significantly lower than that of healthy controls. CD4 +HLA-DR +T cell was significantly highter than that of healthy controls.Conclusion:In patients with AS , lower levels of TNF-?、 IL-2 and higher level IL-10 at plasma indicate an inclination between TH1 and TH2, such as an impaired TH1 cytokine profile and an activated TH2 cytokine profile, especially in TNF-?.
6.Removing TMS-induced artifacts from EEG
Yang WANG ; Manfang MA ; Yingjie LI
International Journal of Biomedical Engineering 2011;34(6):362-366
The combination of transcranial magnetic stimulation and electroencephalogram (TMS-EEG) is an effective means for understanding the network of brain functions.The development of TMS-EEG,however,has been hampered by strong TMS-induced artifacts in the electrode leads.This article first introduces the TMS technology and expounds the causes of TMS-induced artifacts.According to the source of the artifact,the study reviews the artifact removing methods reported in the recent ten years regarding TMS discharge,muscle artifacts and auditory artifacts and residual artifacts.Perspectives of the related techniques are introduced at the end of the article.It is expectable that there will be a great breakthrough not only on the TMS theory but also in clinical research due to the attractive prospect in application and high research value of TMS.TMS-induced artifacts will be well solved at that time.
7.Effects of Botulinum Toxin Type A on Proliferation, Apoptosis and ERK/MAPK Signaling Pathway of Hypertrophic Scar Fibroblasts
Li SHEN ; Yang YU ; Shaolin MA
Journal of Medical Research 2017;46(7):26-29,74
Objective To investigate the effects of botulinum toxin type A on the proliferation,apoptosis and ERK/MAPK signaling pathway of human hypertrophic scar fibroblasts in vitro.Methods Fibroblasts were isolated from human hypertrophic scar and cultured by tissue explant method.The cells were divided into control and botulinum toxin type A groups.The botulinum toxin group A was cultured in DMEM medium containing 0.4U/L botulinum toxin type A.The control group was cultured with DMEM alone.Cell proliferation was measured by CCK8 kit at days 1,3,5 and 7 and compared within groups.Apoptosis of fibroblasts was detected by flow cytometry which treated with botulinum toxin and control group.Western blot was used to detect the relative expression of collagen Ⅰ,p-ERK1/2 and total ERK protein in fibroblasts of control,botulinum toxin type A and U0126 groups.Results Botulinum toxin type A could significantly inhibit the proliferation of fibroblasts,the number of cells was only 68.9% in the control group at 7th days.The apoptotic rate of botulinum toxin type A was 35.9%,which was significantly higher than that of the control group.ERK 1/2 protein expression in the three groups was not significantly different (P > 0.05),while p-ERK 1/2 expression in the control group was still significantly higher,but the p-EKR 1/2 in botulinum toxin type A and U0126 group was significantly inhibited.Collagen Ⅰ was highly expressed in the control group,which was significantly higher than that in the botulinum toxin type A and U0126 groups (P < 0.05).Conclusion Botulinum toxin type A can inhibit the ERK/MAPK signaling pathway and increased fibroblasts apoptosis,decreased proliferation activity and collagen Ⅰ secretion.
8.Change of Cyclic Nucleotide in Brain of Rats induced by Acute Stress
Wentao MA ; Laiqi YANG ; Shuya LI
Chinese Mental Health Journal 1988;0(06):-
Objective: To study the change of cyclic nucleotide in brain of rats induced by acute stress Method: The concentration of cAMP and cGMP in frontal lob, hippcampus, midbrain and hypothalamus were measured in 1 and 3 hours after stress respectively Results:The concentration of cGMP in hippcampus and hypothalamus were significantly higher than that of control group at 1 hour after stress (P
10.Preliminary study on xenografts of oral lichen planus tissue into SCID mice
Linglan YANG ; Ping YE ; Li MA
Journal of Practical Stomatology 1996;0(02):-
Objective:To establish an animal model of oral lichen planus (OLP). Methods:Human non-erosive OLP lesion tissue was surgically transplanted into dorsal hypoderm or tongue abdomen in 10 severe combined immunodeficiency (SCID) mice, thereafter, growth and possible alterations of histopathological characteristics of the xenografts were observed for 2 weeks. Results:All the xenografts transplanted into dorsal hypoderm or tongue abdomen healed well.Partial liquefaction and subepithelial lymphocytes diffuse infiltration were observed in epithelial basement membrane in the first week after transplantation. During the subsequent week, the degenerated moiety was hardly to be seen, and the number of subepithelial lymphocytes was gradually decreased. Conclusions:The epithelia of OLP xenografts grow well in SCID mice but can not keep its histopathological features.