1.Quality of Life in Elderly with Cardiovascular Diseases in A Community in Beijing
Ling TIAN ; Qing LIN ; Di CHEN
Chinese Journal of Rehabilitation Theory and Practice 2010;16(5):423-424
ObjectiveTo investigate the quality of life (QOL) of old patients with cardiovascular diseases in community. Methods100 old patients with cardiovascular diseases in Xiluoyuan, Beijing were investigated with WHOQOL-BREF. ResultsThe QOL-BREF scores in the dimensions of physical health, psychology, social relationships, and environment were (53.21±11.50), (53.27±15.99), (54.29±14.41) and (57.65±15.30) respectively. There was not significant difference between self-rating scores and scores in four dimensions of QOL-BREF (P>0.05). There was not significant difference of QOL-BREF scores in four dimensions between male and female, nor the ones whether complicated with diabetes (P>0.05). The incidence of satisfaction was 31% for QOL, 23% for health, and 62% for the healthy system as self-report. ConclusionThe QOL of the patients is related to diseases.
2.The correlation of distal latency and esophageal motility under esophageal high resolution manometry in gastroesophageal reflux disease
Di CHEN ; Hui WANG ; Ling ZHANG ; Han LIN ; Duowu ZOU
Chinese Journal of Digestive Endoscopy 2014;31(6):304-307
Objective To investigate the relationship between esophageal motility and distal latency (DL) in gastroesophageal reflux disease (GERD) using high resolution manometry (HRM).Methods A total of 51 GERD patients underwent HRM and 24 h-esophageal pH monitoring.According to the HRM topography (characterized as either break peristalsis or normal esophageal movement),all GERD patients were divided into two groups:hypomotility group (n =28) and normal group (n =23).Fourteen non-GERD controls were enrolled.The monitoring results were analyzed.Results The HRM DL of 28 esophageal hypomotility patients(54.9%,28/51) were the longest (7.27 ± 1.44) s.Patients with normal peristalsis also had longer latency (6.70 ± 1.41)s than the non-GERD controls (5.86 ± 0.96)s.All the differences were statistically significant (P < 0.01).DCI of hypotensive peristalsis patients (712.49 ± 703.10) mmHg · s · cm was lower compared with the other groups [(1 285.85 ± 850.83) mmHg · s · cm,(1 109.74 ± 611.70) mmHg · s · cm] (P <0.O1).Other indicators such as LES pressure,CFV and IBP showed no significant differences among groups (P > 0.05).Conclusion Esophageal manometry of GERD patients indicates that esophageal hypomotility is accompanied with prolonged DL.Because DL of all GERD sufferers are extended,esophageal dysmotility has great implications for GERD's development.
3.The changes of serum IL-17 in children with Kawasaki disease
Yunyan LI ; Ling WU ; Tianrui MA ; Yuanling CHEN ; Yazhen DI
Journal of Clinical Pediatrics 2013;(8):741-743
Objectives To explore the change of interleukin-17 (IL-17) in Kawasaki disease (KD). Methods Fourty KD pediatric patients, among them 12 patients with echocardiographic abnormalities in acute phase, 25 age-matched non-KD patients were enrolled. The level of serum IL-17 was measured by enzyme linked immunosorbent assay in acute and convalescent phase of KD patients and non-KD patients. At the same time, C-reactive protein (CRP), globulin, albumin were detected. Results In acute phase of KD patients, the level of serum IL-17 were signiifcantly higher than that in convalescent phase of KD patients and non-KD patients (P<0.05). The level of serum IL-17 was no signiifcant differences in convalescent phase of KD patients and non-KD patients (P>0.05). In acute phase of KD patients with echocardiography abnormalities, the level of serum IL-17 was signiifcantly higher than that with non-echocardiography abnormalities (P<0.05). The level of serum IL-17 in acute phase of KD patients were positively correlated with CRP and globulin (r=0.750, 0.750, P<0.05), and negatively correlated with albumin (r=-0.779, P<0.05). Conclusions IL-17 may be involved in KD immune pathogenesis. Serum IL-17 is one of the activity index of KD, which associ-ated with cardiovascular damages.
4.The effects of infrasound on the ultrastructure of the rat pallium
Di TANG ; Jingzao CHEN ; Ling LI ; Jing LIU
Chinese Journal of Physical Medicine and Rehabilitation 2003;0(05):-
Objective To further investigate the threshold value and the dose-effect relationship of infrasound on the rat pallium, and to observe the effects on the pallium's ultrastructure. Methods Rats were exposed to 16 Hz, 90 dB infrasound for 2 hours daily. With a transmission electron microscope, changes in the ultrastructure of the cortex of the rats' parietal lobes were observed 2 hours, 3 days and 7 days after the treatment. Results There were no changes in the ultrastructure of the pallium in rats which had been exposed for 7 days or 14 days. Denaturation appeared when the rats had been exposed for 21 days, 28 days or 35 days. Denaturation become more serious as the exposure time increased beyond 21 days. Denaturation and damage gradually returned to normal with time after exposure. Conclusion 16 Hz, 90 dB infrasound exposure over an extended time may cause denaturation and other changes in the ultrastructure of the pallium in rats. Such changes can return to normal with time.
5.Appropriate compatibility of propofol and sevoflurane for posterior lumbar interbody fusion of patients with mild cognitive impairment
Yimeng CHEN ; Haiyun WANG ; Hongbai WANG ; Ping LI ; Di GUO ; Tang LI ; Qiu QU ; Ling CHEN
The Journal of Clinical Anesthesiology 2017;33(7):637-641
Objective To investigate the appropriate compatibility of appropriate compatibility of sevoflurane and propofol for patients with mild cognitive impairment (MCI) undergoing posterior lumbar interbody fusion in order to protect their cognitive function.Methods Eighty patients, 41 males, 39 females, aged 65-75 years, BMI 17-26 kg/m2, ASA physical status Ⅰ or Ⅱ, scheduled to undergo elective posterior lumbar interbody fusion, were to be scored according to Montreal cognitive assessment (MoCA), mini mental state examination (MMSE), dementia scale (CDR) and daily living ability scale (ADL) to identify patients with MCI before the surgery.They were randomly assigned to 4 groups (n=20 each) using a random number table: TCI propofol 2.0-2.5 μg/ml group (group P), TCI propofol 1.2 μg/ml+sevoflurane 0.6 MAC group (group PS1), TCI propofol 0.6 μg/ml+sevoflurane 0.9 MAC group (group PS2), 1.0-1.5 MAC sevoflurane group (group S).MoCA and MMSE were used to evaluate the cognitive function of patients 1 d before the operation (T0), after patients become wide-awake (T1), 3 d and 7 d after operation (T2 and T3).Apolipoprotein J (ApoJ) concentration related to cognitive function in blood samples, which were drawn at T0-T3 would be measured with ELISA method.Results Compared with T0, the scores of MMSE and MoCA in four groups decreased significantly (P<0.05) at T1, the scores of MMSE and MoCA in group S decreased significantly (P<0.05) at T2;compared with T1, the score of MMSE in the four groups increased significantly at T2, T3 (P<0.05).The scores of MMSE at T1, T3 in group S decreased significantly compared with groups P, PS1 and PS2 (P<0.05).The scores of MoCA at T2, T3 in group S decreased significantly compared with groups P, PS1 and PS2 (P<0.05).Compared with T0, the concentration of plasma ApoJ in the four groups increased significantly at T1 (P<0.05).Compared with T1, the concentration of plasma ApoJ in the four groups decreased significantly at T2 and T3 (P<0.05).Compared with group PS1, the concentration of plasma ApoJ at T1, T3 increased significantly in groups S and group PS2 (P<0.05).Conclusion TCI propofol 1.2 μg/ml combined with 0.6 MAC sevoflurane group is the appropriate compatibility of sevoflurane and propofol for patients with MCI undergoing posterior lumbar interbody fusion,because it has less negative influence on cognitive function and lower concentration of plasma ApoJ.
6.Study on anti-hyperlipidemia mechanism of high frequency herb pairs by molecular docking method.
Lu-di JIANG ; Yu-su HE ; Xi CHEN ; Ou TAO ; Gong-Yu LI ; Yan-ling ZHANG
China Journal of Chinese Materia Medica 2015;40(12):2413-2419
Traditional Chinese medicine (TCM) has definitely clinical effect in treating hyperlipidemia, but the action mechanism still need to be explored. Based on consulting Chinese Pharmacopoeia (2010), all the lipid-lowering Chinese patent medicines were analyzed by associated rules data mining method to explore high frequency herb pairs. The top three couplet medicines with high support degree were Puerariae Lobatae Radix-Crataegi Fructus, Salviae Miltiorrhizae Radix et Rhizoma-Crataegi Fructus, and Polygoni Multiflori Radix-Crataegi Fructus. The 20 main ingredients were selected from the herb pairs and docked with 3 key hyperlipidemia targets, namely 3-hydroxy-3-methylglutaryl coenzyme A reductase (HMG-CoA reductase), peroxisome proliferator activated receptor-α (PPAR-α ) and niemann-pick C1 like 1 (NPC1L1) to further discuss the molecular mechanism of the high frequency herb pairs, by using the docking program, LibDock. To construct evaluation rules for the ingredients of herb pairs, the root-mean-square deviation (RMSD) value between computed and initial complexes was first calculated to validate the fitness of LibDock models. Then, the key residues were also confirmed by analyzing the interactions of those 3 proteins and corresponding marketed drugs. The docking results showed that hyperin, puerarin, salvianolic acid A and polydatin can interact with two targets, and the other five compounds may be potent for at least one of the three targets. In this study, the multi-target effect of high frequency herb pairs for lipid-lowering was discussed on the molecular level, which can help further researching new multi-target anti-hyperlipidemia drug.
Asteraceae
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chemistry
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Drugs, Chinese Herbal
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chemistry
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metabolism
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Humans
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Hydroxymethylglutaryl CoA Reductases
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chemistry
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genetics
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metabolism
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Hyperlipidemias
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drug therapy
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enzymology
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genetics
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metabolism
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Hypolipidemic Agents
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chemistry
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metabolism
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Membrane Proteins
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chemistry
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genetics
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metabolism
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Molecular Docking Simulation
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PPAR alpha
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chemistry
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genetics
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metabolism
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Protein Binding
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Pueraria
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chemistry
8.Investigation on the correlation between incidence rate of high uric acid and biochemical indicators of organ lesions among hospitalized children
Ling WU ; Yazhen DI ; Yuanling CHEN ; Shiling ZHONG ; Lei HE ; Nan SUN
Chinese Journal of Rheumatology 2014;18(9):632-636
Objective To explore the correlation between the distribution of uric acid (UA) level and the biochemical indicators which reflect the degree of organ lesions among hospitalized children.Methods Patients who were hospitalized to the Department of Pediatrics and received the blood UA test from June 2012 to October 2013 were included,23 217 cases in total.The biochemical analyzer-Japan's Olympus AU 2700 was used to detect blood biochemistry; and uricase-peroxidase coupling method was used to detect blood UA.Among these patients,2 099 cases whose UA level exceeded the normal level.Then the patients' gender,age,primary diagnosis and UA level were recorded; and the distribution of their UA level was described.The Chi-square or Fisher test was used to assess the incidence rate.At the same time,each blood biochemical indicators of the patients with high UA level were recorded ; and the relationships between the blood UA of the 1 650 patients with complete records and each blood biochemical indicator were analyzed with Pearson correlation analysis.Results The incidence rate of hyperuricemia among the hospitalized children was 9.04%(2 099/23 217).In particular,the incidence rate among boys and girls was 6.5t%(890/13 657) and 12.65% (1 209/9 560) respectively (x2 =256.9,P<0.05).The incidence rate of hyperuricemiin different diseases was as follows:in the critical illness 36.93% (113/306),neonatal disease 20.34% (922/4 533),urinary system diseases 12.08% (47/389),circulatory system diseases 11.67% (21/180),nervous system diseases 11.05%(112/1 014),digestive diseases 10.50%(190/1 810),infectious diseases 10.18%(120/1 179),blood diseases 7.58% (55/726),endocrine system diseases 5.74% (17/296),autoimmune diseases 4.24% (48/1 131),respiratory diseases 3.90% (454/11 653) respectively (x2=1423.0,P<0.05).The incidence of hyperuricemia at younger than one month was 18.31%(929/5 075),younger than one year old was 4.22% (359/8 501),younger than six years old was 10.68%(600/5 618),younger than 15 years old was 5.24% (211/4 023) respectively (x2=858.5,P<0.05).Blood UA was positively correlated to urea nitrogen,creatinine,lacticdehydrogenase,α-hydroxy-butyrate dehydrogenase,creatine kinase and creatine kinase-MB (r=0.426,0.44,0.324,0.367,0.413,0.431,P<0.05).Blood UA was not correlated to fructosamine,blood glucose,triglycerides,total cholesterol,low-density lipoprotein and high density lipoprotein.Conclusion The incidence of hyper-uricemia among hospitalized children is high; and the incidence among children with severe diseases and newborn babies is high; followed by in children with urinary system and circulatory system diseases.The blood UA level is closely related to the blood biochemical indicators which reflect the lesions of heart and kidney.
9.Application of WHO standards in diagnose and classification of MDS
Hong CHENG ; Wei DU ; Ming JIANG ; Jianping HAO ; Shuang CHEN ; Di ZHONG ; Yuqing MA ; Ling LI
Journal of Leukemia & Lymphoma 2012;21(5):297-299
ObjectiveTo diagnose and classify 249 patients with myelodysplastic syndrome (MDS) according to the WHO standards.MethodsAccording to the WHO standards,cell morphology,cytogenetics,immune phenotype and bone marrow pathologic biopsy in 249 cases of MDS were analyzed.ResultsGreat shape and oval cell of mature erythrocyte could be observed in all MDS patients peripheral blood. The incidence of immature erythrocyte,immature granulocyte,pelger-like abnormal nucleus and neutrophils cells without granular increased with subtypes progressing.These abnormal characteristics and proportion tended to more apparent with MDS subtypes progressing.With the dynamic follow-up,we found the rate of MDS transition to AL increased with subtypes progressing(P<0.05 ).The immune phenotype analysis of 148 patients was undertook and found that the trend to express myeloid specific antigen (CD33) increased gradually with subtypes progressing The chromosome inspection in 138 patients was undertook and found that 53 patients (38.7 % with abnormal karyotype,mainly in 20q- and +8;16 cases with complex abnormal karyotype (28 %), two patients in 5q-. 180 patients were underwent bone marrow biopsy at the same time and found that 19 patients with abnormal morphology;42 patients with bone marrow fibrosis.ConclusionsCombining with multiple index to detect the MDS contributes to the classification and diagnosis more accuratcly and long-term follow-up helps to judgment the prognosis.
10.Significance of dysplasia and cytogenetic changes on the diagnosis and typing of myelodysplastic syndrome
Ling LI ; Ming JIANG ; Hong CHENG ; Shuang CHEN ; Jianping HAO ; Di ZHONG ; Bingzhao WEN
Journal of Leukemia & Lymphoma 2012;21(7):408-411
Objective To explore the significance of dysplasia and cytogenetic changes to the diagnosis and typing of myelodysplastic syndrome (MDS).Methods The dysplasia performance of each series in every isoforms was observed by the bone marrow aspiration and peripheral blood smear to the 132 patients with MDS. At the same time do the chromosome karyotype was analizad combined with morbidness cells and chromosome karyotype abnormal analysis associated with MDS subtype. Resuits Acorrding to the dysplasia ≥0.10, the totle detection rate of granulocyte series, erythrocyte series and megakaryocytic was 43.4 %.The morbidness granulocyte and megalokaryocyte ≥0.10was mainly in RCMD (P < 0.01); morbidness erythrocytes≥0.10 mainly in RA + RARS (P < 0.01). the totle detection rate of chromosome karyotype abnormal in MDS was 44.0 %.The detection rate in RA and RARS was lower than other isoforms,but showed no statistically significant (P > 0.05).the relationships of dysplasia and chromosome karyotype abnormal with the isoforms of MDS:in RA group,50.0 %(3/6) patients had karyotype abnormal simultaneous the detection of morbidness cells≥0.10, 76.0 %(19/25) in RCMD group and 60.9 %(14/23) in RAEB group (P < 0.01).Conclusion Theve is relationships between the patients with chromosome karyotype abnormal and dysplasia ≥0.10 and the isoforms of MDS. Closely monitoring the hemopoiesis and cytogenetic changes is significance to diagnose MDS.