1.A research on the aortic distensibility in patients with coronary artery disease
Zhen LI ; Guilin LU ; Zhong WANG ; Liping LUO ; Jinjia WU ; Feng TAN ; Yinjun TIAN ; Juncang DUAN
Journal of Medical Postgraduates 2003;0(06):-
0.05].Sao and Eao was significantly different between CHD group and the control group,but Aao has not significant different.③Sao positively correlated with ascending aortic distensibility coefficient(D)(r=0.73,P=0.03),and negatively correlated with aortic stiffness(?)(r=-0.68,P=0.03).Conclusion:Elastic properties of the aorta can directly be assessed by measuring the movements in the upper wall of the aorta with DTI.Reduced aortic S-velocity is significantly correlated with Ascending aortic distensibility coefficient(D) and stiffness index beta(?),which are important factors in assessing the changes of the aortic distensibility.
2.Echocardiographic interpretation for 2015 ESC/ERS guidelines for the pulmonary hypertension and discussion on the translations of pulmonary hypertension and pulmonary arterial hypertension
Zhen WANG ; Lijun YUAN ; Yunyou DUAN ; Tiesheng CAO ; Ying HOU ; Tian ZHOU ; Yang FENG ; Xueying ZHOU
Chinese Journal of Ultrasonography 2017;26(5):454-457
3.Radiological Analysis of Thoracolumbar Junctional Degenerative Kyphosis in Patients with Lumbar Degenerative Kyphosis
Liu CHEN?JUN ; Zhu ZHEN?QI ; Wang KAI?FENG ; Duan SHUO ; Xu SHUAI ; Liu HAI?YING
Chinese Medical Journal 2017;(21):2535-2540
Background: Thoracolumbar junction (TLJ) is the transitional area between the lower thoracic spine and the upper lumbar spine. Vertebral compression fractures and proximal junctional kyphosis following spine surgery often occur in this area. Therefore, the study of development and mechanisms of thoracolumbar junctional degeneration is important for planning surgical management. This study aimed to review radiological parameters of thoracolumbar junctional degenerative kyphosis (TLJDK) in patients with lumbar degenerative kyphosis and to analyze compensatory mechanisms of sagittal balance. Methods: From January 2016 to March 2017, patients with lumbar degenerative kyphosis were enrolled in this radiographic study. Patients were divided into two groups according to thoracolumbar junctional angle (TLJA): the non?TLJDK (NTLJDK) group (TLJA <10°) and the TLJDK group (TLJA≥10°). Complete spinopelvic radiographic parameters were analyzed and compared between two groups. Pearson or Spearman correlation coefficients and independent two?sample t?test or Mann?Whitney U?test were used. Results: Atotal of 77 patients with symptomatic sagittal imbalance due to lumbar degenerative kyphosis were enrolled in this study. There were 34 patients in NTLJDK group (TLJA <10°) and 43 patients in TLJDK group (TLJA ≥10°). The median angle of lumbar lordosis (LL) in the NTLJDK or TLJDK groups was 23.40° (18.50°, 29.48°) or 19.50° (13.30°, 24.55°), respectively. The median TLJAs in all patients and both groups were ?11.20° (?14.60°, ?4.80°), ?3.70° (?7.53°, ?1.73°), and ?14.30° (?17.45°, ?13.00°), respectively. In the NTLJDK group, LLwas correlated with thoracic kyphosis (TK; r = ?0.400, P = 0.019), sacral slope (SS; r = 0.681, P < 0.001), and C7?sagittal vertical axis (r = ?0.402, P = 0.018). In the TLJDK group, LL was correlated with TK (r = ?0.345, P = 0.024), SS (r = 0.595, P < 0.001), and pelvic tilt (r = ?0.363, P = 0.017). There were significant differences in LL, TLJA, TK, SS, and pelvic incidence (PI) between two groups. Conclusions:Although TLJDK is common in patients with lumbar degenerative kyphosis, it might be generated by special characteristics of morphology and biomechanics of the TLJ. To maintain sagittal balance, pelvis back tilt might be more important in patients with TLJDK, whereas thoracic curve changes might be more important in patients without TLJDK.
4.Pharmacokinetics of armodafinil tablets in Chinese healthy volunteers
Li ZHANG ; Li-Wei LANG ; Zhen-Zhen ZHU ; Zhen CHEN ; Feng DUAN ; Zhen-Man WEI
The Chinese Journal of Clinical Pharmacology 2017;33(14):1321-1323
Objective To study the single dose oral administration of armodafinil in Chinese healthy volunteers.Methods This was a single center,opened,randomized,three-way crossover study.Twelve healthy Chinese volunteers received armodafinil 100,200,400 mg,oral administration,respectively.The plasma concentrations were determined by LC-MS/MS.Pharmacokinetic parameters were obtained using DAS 2.1.1 program.Results The main pharmacokinetic parameters of armodafinil of 100,200,400 mg dose groups were as follows:t1/2 were (11.96 ± 1.37),(12.66 ± 1.56),(13.13 ± 1.05) h,tmax were (2.41 ±1.43),(2.50 ± 1.28),(3.00 ± 1.37) h,Cmax were (3117 ±715.8),(5952 ± 1183),(11522 ± 2821) μg · L-1.AUC0-t were (535.49±126.21) ×102,(1081.53 ±241.91) ×102,(2268.71 ±564.30) × 102 h μg L-1,AUC0-∞ were (553.66 ± 124.27) × 102,(1105.26±250.90) × 102,(2293.59 ±565.52) × 102 h · μg · L-1.Conclusion Armodafinil 100,200,400 mg were safe in Chinese healthy volunteers.
5.Therapeutic effect of low dose interleukin-2 on experimental autoimmune encephalo-myelitis in mice
Zhen WANG ; Hai-Feng DUAN ; Xin-Tong FAN ; Chun-Yang XU ; Jin-Feng LI ; Shan-Shan WANG ; Yun-Liang WANG ; Chu-Tse WU
Military Medical Sciences 2017;41(12):968-972,977
Objective To investigate the therapeutic effect of interleukin-2(IL-2)on experimental autoimmune encephalomyelitis(EAE)mice.Methods After establishment of the EAE(experimental autoimmune encephalomyelitis) mouse models with MOG35-55 polypeptides,the mice were grouped according to the neurological function score and divided into control group,EAE group and low dose IL-2 treatment group.A double blind method was used to evaluate the neuro-logical impairment in mice.On the 29th day,pathological experiments were carried out in the mice's brain and spinal cord, hematoxylin-eosin staining was used to evaluate the scoring of inflammatory cell infiltration and luxol fast blue staining was used to evaluate the scoring of demyelinating.The proportion of regulatory T cells(Treg)and NK cells(natural killer cell, NK)was detected by flow cytometry,and the immunohistochemical method was used to detect the expressions of glial fibril -lary acidic protein(GFAP)and myelin basic protein(MBP)in the spinal cord.Results Compared with the EAE group, the neurological function score, the inflammatory cell infiltration score and the demyelinating score of the low dose IL-2 treatment group were reduced.The proportion of Treg cells in the low dose IL-2 treatment group was significantly higher than that in the EAE group,and the proportion of NK cells in the low dose IL-2 treatment group was slightly higher than that in the EAE group The expression of GFAP and MBP was detected by immunohistochemistry.The expression level of GFAP in low dose IL-2 treatment group was significantly lower than that in the EAE group,while the expression level of MBP was higher than that in the EAE group.Conclusion Low dose IL-2 has significant therapeutic effect on EAE mice.
6.Interventional treatment of dural arteriovenous fistula
Xiao-Ping LIU ; Qiang RAO ; Xi-Feng LI ; Xu-Ying HE ; Chuan-Zhi DUAN ; Zhen-Yong LI
Chinese Journal of Neuromedicine 2011;10(1):63-65
Objective To explore the clinical skills and curative efficacy of endovascular embolization on dural arteriovenous fistula (DAVF). Methods A total of 50 patients with DAVF,admitted to our hospital from 2000 to 2009, underwent endovascular embolization with different materials through a microcatheter under DSA. After embolization, imaging examination was applied and clinical manifestations were noted during the clinical follow-up to evaluate the clinical efficacies.Results Immediate postoperative angiography indicated that the fistulas were totally occluded in 43patients, occluded evidently in 6 and occluded partially in 1. The 6-84 months follow-up found that clinical symptoms of 34 patients disappeared, 6 alleviated evidently, 7 relapsed, and 3 worsened; no complications were noted. Conclusion The endovascular embolization for DAVF is effective; and choosing the right embolic approach and material and improving the technology are the keys of successful treatment.
7.PhaseⅠclinical tolerance study of Picika oral solution in healthy volunteers
Feng DUAN ; Jing-Feng BI ; Ben-Chao CHEN ; Zhen-Zhen ZHU ; Bin SUN ; Zhen CHEN ; Yu ZHANG ; Yan-Yan CHU ; Li ZHANG ; Min WANG ; Wen-Shu LI ; Cheng JIN ; Zhen-Man WEI
The Chinese Journal of Clinical Pharmacology 2014;(10):912-914
Objective To study the tolerability and safety of single and multiple doses of Picika oral solution in healthy volunteers.Methods A single center, randomized, single -blind, placebo -controlled, dose -escalation study was designed.50 patients were given single dose, and 10 cases were given multiple doses.All of them had half male and fe-male.Single -dose group: 20 mL(4 subjects), 40 mL(6 subjects), 60 mL(10 subjects; 2 using placebo), 90 mL(10 subjects; 2 using place-bo), 120 mL (10 subjects ; 2 using placebo), 160 mL (10 subjects; 2 using placebo); multiple doses group: 10 subjects(2 using placebo), 40 mL? times-1 , tid, continuous medication for 10 days.Results Of the sixty healthy subjects enrolled , 58 finally completed the trial, and two shed.One case (female) of adverse event in single -dose 160 mL group was reported: her ctivated partial thromboplastin time (APTT) was ab-normal with clinical significance.It may not be associated with the medi-cation.In multiple doses group, one case of abdominal pain (female) was reported, may not be associated with the medication.Conclusion Single and multiple doses of Picika oral solution are safe and well tolera -ted in healthy subjects.
8.Effect of diet on the pharmacokinetic of Picika oral solution in healthy human
Feng DUAN ; Zhen-Zhen ZHU ; Jing-Feng BI ; Ben-Chao CHEN ; Zhen CHEN ; Li ZHANG ; Hui JI ; Li-Wei LANG ; Min WANG ; Zhen-Man WEI
The Chinese Journal of Clinical Pharmacology 2016;(3):227-229
Objective To study the influence of diet on the pharmacoki-netic of Picika oral solution in healthy subjects.Methods This study taken random , before and after self-control design.Twelve subjects were randomly divided into 2 groups, each group was 6 cases, then they were given Picika oral solution 60 mL respectively before and after meal.Before and after administration , blood and urine samples were collected at different points , the plasma and urine concentration was measured and pharmacokinetic parameters were calculated.Results Before and after administration of Picika oral solution 60 mL, the drug pharmacokinetic parameters of active ingredients -CKL-A03 were listed as follows:t1/2 was ( 126.13 ± 74.04 ) , ( 104.81 ± 68.44 ) min; tmax were (53.75 ±10.03 ) and (58.75 ±11.89 ) min;Cmax were (3.06 ±0.86 ) and ( 3.81 ±2.82 )μg· L-1; AUC0-t were ( 268.81 ±84.25 ) and (355.03 ±177.82 )μg· L-1 · min in plasma respectively.t1/2 was (1.14 ± 0.12 ), ( 1.24 ± 0.16 ) h in the urine respectively.Conclusion Diet may affect the absorption and eliminate speed of the drug.
9.Pharmacokinetics of single dose of Picika oral solution in Chinese healthy volunteers
Zhen-Zhen ZHU ; Feng DUAN ; Jing-Feng BI ; Zhen CHEN ; Min WANG ; Li ZHANG ; Hui JI ; Li-Wei LANG ; Ben-Chao CHEN ; Zhen-Man WEI
The Chinese Journal of Clinical Pharmacology 2016;(3):230-234
Objective To evaluate the pharmacokinetic changes of Picika oral solution in healthy subjects after single dose.Methods This study taken random , three cross experiment design , 12 subjects were randomly divided into 6 groups, each group was 2 cases, then they were respec-tively given single oral doseof Picika oral solution (60, 90, 120 mL) in each cycle.Before and after administration , biological samples were col-lected for detection of blood drug concentration and urine drug concentra-tion, furthermore, calculation of blood and urine drug pharmacokinetic parameters.Results After single oral dose of 60, 90, 120 mL Picika oral solution, the main pharmacokinetic parameters of plasma CKL -A03, Cmax were (3.08 ±0.92), (3.63 ±0.75), (4.29 ±1.00)μg· L-1, tmax were (57.50 ±17.90 ), (52.50 ±20.73 ), (56.25 ±19.32 ) min, t1/2 were (197.51 ±106.35 ), (233.86 ±196.75 ), (141.34 ±65.16 ) min, AUC0-t were ( 383.28 ± 86.42 ) , ( 479.00 ± 136.25 ) , (540.59 ±102.87)μg · L-1 · min, AUC0-∞ were (710.06 ±233.03 ), (916.59 ±378.62 ), (782.65 ±130.40 )μg· L-1 · min, respectively. The main pharmacokinetic parameters of urine CKL -A03, t1/2 were (1.29 ±0.33), (1.23 ±0.20), (1.11 ±0.11) h, total urine discharge rates were (0.28 ±0.22)%, (0.20 ±0.11)%, (0.18 ±0.09)%, urine discharge amount were (74486.02 ±57923.42 ), (80015.14 ±43379.01 ), (93017.33 ±46658.61 ) mg.Conclusion The maximum oral absorption amount of Picika oral solution is possible 90 mL.And there is no apparent proportional relationship between the total urine discharge rate , urine discharge amount and the increased doses.
10.The clinical significance of petrosal vein in operation of cerebellopontine angle tumor
Jian XI ; Xian-Rui YUAN ; Xue-Jun LI ; Xing-Jun JIANG ; Feng-Hua CHEN ; Zhen-Yan LI ; Ming-Yu ZHANG ; Ze-feng PENG ; Zhi-quan YANG ; Wei-xi JIANG ; Duan-wu LUO ;
Chinese Journal of Microsurgery 2000;0(03):-
Objective To discuss the clinical significance of petrosal vein in operation of cerebel- lopontine angle(CPA)tumor.Methods From Dec.2004 to Mar.2006,33 patients with tumor in CPA were operated,the petrosal vein were protected well in 31 cases and failed to protect in 2 cases.Results No hemorrhagic infarction observed in 31 cases with well protection of petrosal vein.Two cases with petrosal vein damage occured with vein infarction and hemorrhagic edema.One was dead and the other was recovered well after decompression of posterior cranial fossa.Conclusion Petrosal vein should be well protected in the tumor operation of CPA area,the decompression of posterior cranial fossa should be considered if petrosal vein failed to protect.