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    15 January 2020, Volume 48 Issue 1 Previous Issue    Next Issue

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    The mechanism of PM2.5 induced lung epithelial cell BEAS-2B injury based on RNA-sequencing
    HU Ling-juan, HE Xiang, ZHANG Lei, RAN Qin, LI Guo-ping
    2020, 48 (1):  1-7.  doi: 10.11958/20192370
    Abstract ( 822 )   PDF (1129KB) ( 5390 )  
    Objective To investigate the effect of PM2.5 on gene expressions of lung epithelial cell BEAS-2B and explore the signaling pathway. Methods BEAS-2B cells were divided into control group (PBS treatment) and experimental group (PM2.5 treatment). Total RNA of each group was extracted 24h after RNA-sequencing. After quality control, the sequence was compared with the reference genome. The mapped data (reads) were used for the assembly of subsequent transcripts, and the expression quantity calculation was obtained. And the results were analyzed in the following terms: NR, Swiss-Prot, Pfam, COG (Evolutionary genealogy of genes), GO (Gene Ontology), KEGG (Kyoto Encyclopedia of genes and genes) annotations in the six major databases. Differential expression genes (DEGs) were screened by DESeq2. Then, bioinformatics analysis was used to analyze the biological functions of DEGs, including GO and KEGG databases, and five key genes (FOSB, FOSL1, MUC5AC, CSF2 and IL-6) were detected by qRT-PCR for verification. Results The transcriptome data were compared between PM2.5 group and control group, and a total of 961 differentially expressed genes were obtained. Among them 453 genes were up-expressed and 508 genes were down-expressed. Through functional analysis of GO and KEGG, it was found that these differentially expressed genes were mainly involved in the regulation of protein phosphorylation, immune system process, positive regulation of signal transduction and apoptosis pathways. And they were significantly enriched in the IL-17 signaling pathway. qRT-PCR results showed that the relative expressions of key genes (FOSB, FOSL1 and IL-6) were significantly up-regulated in PM2.5 treatment group (P<0.05), which was consistent with the results of RNA-seq. Conclusion It is possible that PM2.5 aggravates inflammatory response in beas-2b cells through regulating the key genes of the "IL-17 signaling pathway and promotes apoptosis.
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    Transcriptional upregulation of EGFR by Wnt signaling pathway to promote gefitinib resistance in non-small cell lung cancer
    WANG Qian, LI Xie-meng-dan, LUO Kai, ZHENG Guo-pei, ZHANG Zhi-jie, LU Min-ying, DONG Jing, JIA Xiao-ting, HE Zhi-min
    2020, 48 (1):  8-13.  doi: 10.11958/20192340
    Abstract ( 763 )   PDF (717KB) ( 4267 )  
    Objective To investigate the effect of Wnt signaling pathway and epidermal growth factor receptor (EGFR) on gefitinib resistance of non-small cell lung cancer (NSCLC) and its mechanism. Methods EGFR expressions in parental cells and gefitinib-resistant HCC827 / R cells were detected by qRT-PCR and Western blot assay. Immunohistochemical (IHC) staining was used to detect the expressions of EGFR in NSCLC tissues before and after drug resistance. Activation status of Wnt signaling pathway in cells were detected by luciferase assay. TCF/LEF transcription factor binding sites on the EGFR promoter region were predicted in the Jaspar database. The regulation of transcription factors on gene expression was detected by Chip and luciferase assays. Functional blockade assay was used to detect whether Wnt signaling pathway/EGFR pathway mediated gefitinib resistance. Results Compared with the parental cells, the expression of EGFR in HCC827/R cells was significantly increased at mRNA and protein levels (P<0.05). The results of IHC showed that high expressions of EGFR in NSCLC tissue samples after drug resistance were detected in 2 of 3 paired NSCLC tissue samples before and after gefitinib resistance. Luciferase results showed that Wnt/β-catenin signaling pathway was abnormally activated in resistant HCC827/R cells compared with that of parental cells (P<0.05). Bioinformatics analysis predicted that there were TCF3/ TCF4 sites, which were downstream transcription factors of the Wnt/β-catenin signaling pathway, the binding site located on the promoter region of EGFR gene (- 1476~ - 1468), and Chip and Luciferase experiments confirmed that EGFR gene expression could be up-regulated by Wnt/β - catenin signaling pathway (P<0.05). The results of functional blockade experiments showed that when Wnt3a was used to stimulate parental HCC827 cells while knocking down EGFR, the inhibition rate of 3.13 μM gefitinib on cells was restored compared with that of Wnt3a alone (P<0.05). Conclusion Wnt/ β-catenin signaling pathway up-regulates EGFR expression to promote gefitinib resistance in NSCLC, which provides the new experimental evidence for improving the therapeutic effect of gefitinib targeted therapy on NSCLC.
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    The effect of upregulating miR-223 by Notch pathway to inhibit the expression of FBXW7 on the biology of colorectal cancer HCT116 cells
    LIU Zhi-xin, DUAN Ju-feng, MA Teng, YANG Jing, TAN Hua-bing, LIU Long
    2020, 48 (1):  14-18.  doi: 10.11958/20192099
    Abstract ( 606 )   PDF (410KB) ( 4332 )  
    Abstract: Objective To investigate the effects of microRNAs (miRNAs) on the proliferation and apoptosis of colorectal cancer HCT116 cells and its mechanism. Methods The FBXW7 mRNA and protein levels were detected by realtime quantitative PCR and Western blot assay in 20 clinical specimens. After predicted by TargetScan tool, verified by quantitative PCR and luciferase activity assay, the miRNAs combined with FBXW7 were identified. The FBXW7 mRNA and protein levels were detected after transient transfection of miR-223 and its control miCtr and inhibitor (inhibitor) into HCT116 cells. CCK-8 and flow cytometry were used respectively to detect the cell viability and apoptosis rate. In addition, the level of miR-223 and the number of apoptosis were detected after down-regulating the expression of Notch3 by siRNA. Results The FBXW7 mRNA and protein levels were lower in colorectal tumor tissues than those in adjacent tissues (P< 0.05). It was predicted and confirmed that miR-223 and miR-25 could specifically bind to FBXW7 gene. After transfection of miR-223 in HCT116 cells, the FBXW7 mRNA and protein levels were down-regulated (P<0.01), the cell viability was increased (P<0.05) and the number of apoptotic cells was decreased (P<0.01). After down-regulation of Notch3 pathway, miR-223 mRNA levels decreased (P<0.001), FBXW7 mRNA levels increased (P<0.01) and apoptotic cells decreased (P< 0.05). Conclusion Notch pathway upregulates the miR-223 level, which inhibits the expression of FBXW7 and eventually promotes the proliferation and inhibits its apoptosis of colon cancer cell line HCT116.
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    The molecular mechanism of inhibiting effect of miR-149 on the metastasis of human colonic carcinoma cells
    LIU Xiao-zhu, LI Yin-feng
    2020, 48 (1):  19-24.  doi: 10.11958/20192289
    Abstract ( 696 )   PDF (739KB) ( 5767 )  
    Objective To investigate the regulation and function of miR-149 in human colorectal cancer cell lines. Methods miR-149 expression patterns were detected in SW620 and LS174T cell lines using quantitative real-time fluorescence PCR (q-PCR) method. And then, the target gene of miR-149 was explored via luciferase reporter assay. The expressions of STAT3 and p-STAT3 mRNA and proteins in CRC cells were detected by q-PCR and Western blot assay, respectively. miR-149 mimics and pEGFP/STAT3 vector were transfected or co-transformation into CRC cells. CRC cells were divided into miR-NC group, miR-149 mimics group and miR-149 mimics + pEGFP / STAT3 group. Proliferation, migration, invasion and apoptosis were determined by CCK-8 assay, wound-healing assay, transwell assay and flow cytometry, respectively. Results miR-149 expression was down-regulated in SW620 and LS174T cell lines compared to that of the normal colon epithelial cell FHC detected using q-PCR methods (P<0.01). Then, STAT3 was identified as a direct target gene of miR-149 in CRC cells by luciferase reporter assay. Further studies indicated that the introduction of miR-149 was able to down-regulate the mRNA and proteins expression of STAT3 and p-STAT3, suppress cell proliferation, migration and invasion, and promote apoptosis of CRC cells (P<0.01). However, the over-expression of STAT3 could decrease the inhibiting effect of miR-149 on the proliferation,migration and invasion of CRC cells. Conclusion miR-149 can inhibit proliferation, invasion and migration and promote apoptosis of CRC cells via targeting STAT3.
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    Expression and significance of connexin-43 in guinea pig model of diabetic cystopathy
    LI Peng, QIAN Biao, SHEN Mao-lei, ZHAO Guo-li, WANG Qin-zhang
    2020, 48 (1):  25-29.  doi: 10.11958/20191779
    Abstract ( 508 )   PDF (524KB) ( 4836 )  
    Objective To investigate the expression of connexin43 (Cx43) in diabetic cystopathy (DCP) and study its significance. Methods Fifty guinea pigs were randomly divided into DCP group (n=30), sodium citrate group (n=10) and blank control group (n=10). Diabetic model was established by intraperitoneal injection of streptozotocin in DCP group. Diabetic bladder guinea pigs were screened by urodynamics test. The sodium group was intraperitoneally injected with sodium citrate solution, and the blank control group was injected intraperitoneally with normal saline. The location and distribution of Cx43 in the three groups of bladder detrusor were observed by immunohistochemical staining, and expressions of Cx43 proteins were detected by Western blot assay. Results Immunohistochemical staining showed that the intensity of Cx43-specific staining was significantly lower in DCP group than that in the other two groups. There was no significant difference in the positive staining intensity between sodium citrate group and blank control group. Western blot analysis showed that the expression of Cx43 protein was significantly lower in bladder tissue of DCP group (0.52±0.02) than that of blank control group (0.68±0.02) and sodium citrate group (0.70±0.03, P<0.01). There was no significant difference in the expression of Cx43 protein in the bladder tissue between the sodium citrate group and blank control group (P>0.01). Conclusion The decreased expression of Cx43 in detrusor tissue plays an important role in the formation of diabetic bladder and may be a new starting point for studying the pathogenesis of diabetic bladder.
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    Correlation between protein carbonylation and the heart failure cachexia in rats
    KONG Wen-wen, ZHANG Xin
    2020, 48 (1):  30-33.  doi: 10.11958/20191937
    Abstract ( 586 )   PDF (434KB) ( 4188 )  
    Objective To investigate whether protein carbonylation was involved in the development of heart failure cachexia in rats. Methods Ninety 12-month-old clean male Sprague-Dawley rats were randomly divided into three groups: isoproterenol (ISO) group, hydralazine (HYD) + ISO group and control group, 30 in each group. Rats in the ISO group and the HYD+ISO group were injected with isoproterenol, the rats in the HYD+ISO group were orally administered with hydralazine, and the rats of control group were injected with normal saline. After 6 weeks, the rat modelling success rate was evaluated based on the echocardiogram and body weight changes. The serum levels of total albumin, triglyceride, cholesterol and blood glucose concentrations in rats were detected by automatic biochemical analyzer. The serum concentration of brain natriuretic peptide (BNP) was detected by ELISA kit. UV spectrophotometer was used to detect protein carbonyl concentration. The immunohistochemistry was used to detect the expression of protein carbonyl. Results In the control group, HYD+ISO group and ISO group, the serum levels of total albumin and blood glucose decreased in turn, and the serum levels of triglyceride, cholesterol, BNP, protein carbonyl in myocardium and skeletal muscle increased in turn (P<0.05). Conclusion In the rat model of heart failure cachexia caused by ISO, protein carbonylation is elevated. HYD can inhibit the formation of protein carbonylation in rats with heart failure cachexia, which may prevent the occurrence and development of heart failure cachexia.
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    The relationship between PPAR gamma activation and pyroptosis in the early stage of cerebral ischemia-reperfusion in rats
    LIU Hai-ying, FENG Zi-ren, SUN Hui, MENG Ai-guo, ZHAO Jun-jian, ZHANG Wen-ting
    2020, 48 (1):  34-37.  doi: 10.11958/20192153
    Abstract ( 763 )   PDF (538KB) ( 4086 )  
    Objective To investigate the relationship between peroxisome proliferator activated receptor γ (PPARγ) activation and pyroptosis in rat model of cerebral ischemia-reperfusion injury. Methods Forty male SD rats of SPF were randomly divided into sham operation group, MCAO model group, pioglitazone group and pioglitazone+GW9662 group, 10 rats for each group. Neurological deficits were measured by Zea-Longa score, and infarct sizes were measured by TTC staining. The expressions of PPARγ, caspase-1, Gasdermin D (GSDMD), interleukin (IL) - 1β and IL-18 in ischemic penumbra were observed by Western blot assay. Results The expression level of PPARγ protein was significantly lower 24- h after cerebral ischemia-reperfusion injury in MCAO group than that of sham group (P<0.05). The values of caspase-1, GSDMD, IL-1β and IL-18 were significantly higher in MCAO group than those in sham operation group (P<0.05). Meanwhile, the neurological deficits and infarct sizes were significantly higher in MCAO group than those of sham operation group (P<0.01). The level of PPARγ was significantly increased in PGZ group compared with that of MCAO group (P< 0.05), while the caspase-1, GSDMD, IL-1β and IL-18 decreased (P<0.05). And neurological deficits and infarct sizes decreased significantly (P<0.01). However, in PGZ+GW9662 group, the effect of PPARγ was reversed. Conclusion At the early stage of rat cerebral ischemia/reperfusion, the activation of PPARγ inhibits the pyroptosis to reduce neuron injury.
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    The role and mechanism of Akt-Kv4.3-CaMKII in aerobic exercise inhibited pressure overload-induced cardiac hypertrophy
    GE Guang-quan, ZHAO Feng, CHEN Dao-hu, SHI Zhen-su, CHEN Ze-lun, WANG Tian-guang, HE Shu-wu, WEI Yi-zhen
    2020, 48 (1):  38-44.  doi: 10.11958/20190267
    Abstract ( 624 )   PDF (703KB) ( 4711 )  
    Objective To investigate the role and mechanism of serine / threonine kinase (Akt) - ion channel Kv4.3 (Kv4.3) - calmodulin-dependent protein kinase Ⅱ (CaMK Ⅱ) signaling pathway in aerobic exercise inhibited pressure overload-induced cardiac hypertrophy. Methods Sixty mice were divided into five groups: Sham group, transverse aortic constriction (TAC) group, SHAM+ aerobic exercise (E) group, TAC + E group and TAC+ E + AKt inhibitor perifosine (Peri) group. Transthoracic echocardiography was used to assess the cardiac function and extent of myocardial hypertrophy. The cross-sectional area of myocardial cells was measured by WGA staining. The mRNA expression of ANP was detected by RTqPCR. The protein expression levels of ANP, p-AKt, Kv4.3 and p-CaMKⅡ were detected by Western-blot assay. Results Compared with Sham group, the cardiac function of mice was deteriorated in TAC group (P<0.01), and the extent of cardiac hypertrophy was increased (P<0.01). After aerobic exercise training, the cardiac function was improved in TAC + E group, and the level of myocardial hypertrophy was alleviated compared with TAC group (P<0.01). Western-blot assay showed that the expressions of p-AKT and Kv4.3 were down-regulated, p-CaMKⅡ was up-regulated in TAC group than those in Sham group (P<0.01). However, the expressions of p-AKT and Kv4.3 were higher, p-CaMKⅡ was lower in TAC+E group than those in TAC mice (P<0.01). Furthermore, pretreatment with the AKT inhibitor perifosine, deteriorated cardiac function, augmented myocardial hypertrophy and ANP, increased cross-sectional area were observed in TAC+E+Peri group compared with those of TAC+E group (P<0.01). Meanwhile, the downregulation of p-AKT、Kv4.3 and upregulation p-CaMKⅡ were detected in the TAC+E+Peri group compared with the TAC+E group. Conclusion Aerobic exercise training can inhibit pressure overload-induced cardiac hypertrophy by regulating Akt-Kv4.3-CaMKⅡ.
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    The role of postmastectomy radiotherapy after neoadjuvant chemotherapy in pathologically node-positive, stage T1-2N1M0 breast cancer patients with ypN0
    CHENG Hong-lian, WANG Meng, YU Yue, CAO Xu-chen
    2020, 48 (1):  45-50.  doi: 10.11958/20191490
    Abstract ( 1131 )   PDF (481KB) ( 4409 )  
    Objective To investigate the effect of postmastectomy radiotherapy (PMRT) in patients with pathologically node-positive, stage T1-2N1M0 breast cancer after neoadjuvant chemotherapy (NAC) and mastectomy with ypN0. Methods A total of 187 pathologically node-positive, stage T1-2N1M0 breast cancer patients treated with NAC and modified radical mastectomy with and without PMRT who achieved ypN0 were retrospectively analyzed in our institution from 2003 to 2013. Patients all received fine needle aspiration biopsy (FNAB) of axillary nodes before NAC. Patients were divided into PMRT group (n=81) and NO PMRT group (n=106) according to whether they received postoperative radiotherapy for breast cancer. Statistical analyses were conducted using Chi-square test, Fisher exact test, Kaplan-Meier method, log-rank test and Cox proportional hazards regression model. Results DFS and DMFS were significantly improved in the PMRT group (P<0.05), but there was no significant difference between the LRFFS and OS groups (P>0.05). The prognosis of DMFS and DFS was better in patients with earlier pathological T stage, PMRT and age ≥ 40 years after NAC (P<0.05). Patients with soft tissue involvement showed a poor prognosis (P<0.05). Conclusion Patients with pathologically node-positive, stage T1-2N1M0 breast cancer, completed nodal response to NAC and received following modified radical mastectomy with ALND show comparatively good prognosis. PMRT could increase DFS and DMFS but have a marginal effect on LRR or OS in this study.
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    Application of infection biomarkers in early diagnosis of multiple resistant bacteria bloodstream infection
    XIA Fei, HU Guang-xu, LIAO Ya-ling, XU Xin, CHEN Min, DU Ming
    2020, 48 (1):  50-54.  doi: 10.11958/20190785
    Abstract ( 780 )   PDF (427KB) ( 4013 )  
    Objective To evaluate the role of bacterial infection related inflammatory biomarkers in identifying multi-drug resistant (MDR) bloodstream infections (BSIs) confirmed by blood culture (BC) and predicting pathogen types. Methods A retrospective analysis was conducted on 852 MDR infection patients in the Third People’s Hospital of Hubei Province, while 526 patients with concurrent laboratory test results including blood culture, routine blood tests, C reaction protein (CRP), procalcitonin (PCT) and serum pancreatic amyloid (SAA). The differences of the above indicators were analyzed in negative blood culture and positive blood culture groups, and the diagnostic value for the bloodstream infections was also evaluated. Results In 526 patients, there were 108 BSIs cases, including 42 cases (38.9%) were infected with Gram-positive bacteria and 66 cases (61.1%) were infected with Gran-negative bacteria. MRSA (23 cases), ESBL-positive Escherichia coli (39 cases) and ESBL-positive klebsiella pneumoniae (20 cases) were the major pathogens in BSIs. In BC positive cases, there were significant differences in CRP, PCT, SAA and NEU between Gram-negative bacteria group and Gram-positive bacteria group (Z=2.448, 5.647, 3.368, 4.905, all P<0.05). Within cases of Gram-positive bacteria, there was statistical significance in CRP (H=19.021, P<0.001), with the highest level of MRSA (114.35 mg/L). Within cases of Gram-negative bacteria, both CRP and PCT showed statistical significance (H=19.369, 15.013, P<0.01), with the highest level in ESBL-positive escherichia coli (164.60 mg/L, 97.42-217.50; 7.361 µg/L, 3.51-9.95). The area under the receiver operating characteristic curves (ROC-AUCs) of CRP, PCT, SAA, WBC and NEU for discriminating positive MDR-BC from MDR-BC negative cases were 0.778, 0.728, 0.658, 0.578, and 0.645, with statistical significance in CRP and PCT (P< 0.01). For discriminating Gram-negative bacteria BC, AUCs of CRP and PCT were 0.692 and 0.883 with statistical significance (P<0.01). Conclusion CRP is more applicable for the early diagnosis of BSI compared with PCT. After confirming BSI, PCT is suitable for discriminating Gram-negative bacteria infection. Therefore, the combination of PCT and CRP may help medical staff to judge the BSI and type the possible pathogens, and to rationally use drugs
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    The expression of inflammatory cytokines and its relationship with high sensitivity C-reactive protein and erythrocyte edimentation rate in knee osteoarthritis
    LIU Jian-hua , ZHAO Hai-yong, WEN Fang, ZHAO Yan-yan, YOU Yang, DING Hong-mei
    2020, 48 (1):  55-58.  doi: 10.11958/20192074
    Abstract ( 714 )   PDF (350KB) ( 4763 )  
    Objective To investigate the expression of interleukin (IL)-1β, tumor necrosis factor (TNF)-α and IL-6 and their correlation with high sensitivity C-reactive protein (hs-CRP) and erythrocyte sedimentation rate (ESR) in patients with knee osteoarthritis (KOA). Methods Serum samples were obtained from 85 patients with KOA and 80 healthy controls (HC). Joint fluid samples were obtained from 25 patients with KOA. The levels of IL-1β, TNF-α and IL-6 in serum and joint fluid were measured by enzyme-linked immnuosorbent assay (ELISA). The serum levels of hs-CRP were measured by Latex immunoturbidimetry assay. Serum levels of ESR were measured by automatic ESR monitor. The correlations between IL-1β, TNF-α, IL-6, hs-CRP and ESR were evaluated using Pearson correlation test. Results Serum levels of IL-1β, TNF-α and IL-6 were significantly higher in KOA group compared with those of HC group (all P<0.01). Moreover, the levels of IL-1β, TNF-α and IL-6 increased with the increase of clinical severity. The levels of IL-1β, TNF-α and IL-6 were significantly higher in joint fluid than those in serum (all P<0.05). The levels of hs-CRP and ESR were higher in KOA group than those of HC group (all P<0.01). The serum levels of IL-1β, TNF-α and IL-6 were positively correlated with hsCRP (r=0.489, 0.426 and 0.389, respectively) and ESR (r=0.348, 0.423 and 0.394, respectively). The levels of IL-1β, TNF- α and IL-6 in joint fluid were positively correlated with serum levels of hs-CRP (r=0.547, 0.644 and 0.511, respectively) and ESR (r=0.564, 0.579 and 0.589, respectively). Conclusion Our data show that the detection of inflammatory cytokines and hs-CRP, ESR can be used as potential biomarkers for early diagnosis, disease evaluation and prognosis assessment of KOA.
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    A comparative study of gestational weeks and pregnancy outcomes between SLCPV and selective RFA in patients with twin transfusion syndrome
    FANG You-zhen, CHEN Man, LUO Qing-qing, ZHANG Dong-dong
    2020, 48 (1):  59-63.  doi: 10.11958/20191789
    Abstract ( 716 )   PDF (399KB) ( 3990 )  
    Objective To compare the gestational weeks and pregnancy outcomes after selective laser coagulation of placental vessels (SLCPV) and selective radiofrequency ablation (RFA) in twin transfusion syndrome. Methods Eighty patients with twin transfusion syndrome admitted to our hospital from January 2015 to January 2018 were selected in this study. According to the surgical method, the patients were divided into SLCPV group and RFA group. SLCPV group was treated with SLCPV, and RFA group was treated with selective RFA fetal reduction. The gestational weeks, fetal status and pregnancy outcomes were observed in the two groups, and the therapeutic effects were compared between the two methods. Results The mean operation time was (28.74±4.59) min in SLCPV group, and which was significantly longer than that of RFA group (16.27 ± 3.94) min (P<0.05). The incidence of maternal complications was 10.00% in SLCPV group, and no significant maternal complications were found in RFA group (P>0.05). There were no significance in maternal complications between groups (P=0.116). The delivery rate was 90.00% (36/40) in SLCPV group and 100.00 (40/40) in RFA group (P>0.05). The average gestational weeks of delivery were (30.15 ± 2.41) in SLCPV group, which were significantly shorter than those of RAF group (32.85±2.53, P<0.05). There were no significant differences in the incidences of gestational diabetes mellitus (GDM) and pregnancy induced hypertension (HDCP) between the two groups (P>0.05). There was no significant difference in the overall survival rate between the two groups (P>0.05). The total survival rate of at least one fetus was 75.0% in SLCPV group, which was significantly lower than that of RFA group (P<0.05). The body mass and Apgar score were significantly higher in RFA group than those in SLCPV group (P<0.05). Conclusion SLCPV and selective RFA abortion can achieve better therapeutic effect for twin transfusion syndrome patients. However, RFA can better ensure the delivery and survival at least one fetus, and patients can obtain longer gestational weeks of delivery, which is a recommended treatment option.
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    Construction and verification of risk assessment model for cardio-cerebrovascular diseases in type 2 diabetes mellitus
    MENG Xiang-ying, ZHOU Yong, WANG Yi, ZHAO Qian, CHEN Feng, SHI Yong-quan, TANG Wei
    2020, 48 (1):  63-67.  doi: 10.11958/20192347
    Abstract ( 763 )   PDF (430KB) ( 5141 )  
    Objective To establish a risk assessment model of cardio-cerebrovascular events in type 2 diabetes mellitus (T2DM) patients. Methods The study was conducted retrospectively to analysis 2 175 T2DM patients from diabetes mellitus management database. A total of 26 risk factor variables were chosen. The independent risk factors for the incidence of cardiovascular and cerebrovascular diseases of T2DM were evaluated by univariate and multivariate Cox regression analysis, and to construct a predictive incidence risk score model of cardio-cerebral vascular disease for T2DM. Results The median follow-up duration was 5.1 years in the model group. A total of 145 cases were diagnosed as the occurrence of cardio-cerebrovascular events at the end of follow-up. The cardio-cerebrovascular risk model for T2DM patients was 0.059×age (years)+0.936×smoking (yes=1)+0.006×glycosylated hemoglobin (%)+0.380×duration of diabetes (years)+0.048×body mass index (kg/m2)+0.009×systolic blood pressure (mmHg)+0.807×atrial fibrillation (yes=1)+0.175× non-high-density lipoprotein cholesterol (mmol/L)-0.034×log glomerular filtration rate(mL/min). The predictive probability of cardio-cerebrovascular disease in T2DM patients for five years was P ∧ = 1 - 0.928exp(∑i p= 1βi χi - 12.736 ). The goodness-of-fit result for the risk assessment model in the validation group was HL χ2=1.49, P=0.81, and the area under ROC curve was 0.798 and 95%CI was 0.759-0.818. Conclusion A simple risk assessment model on the occurrence of cardiocerebrovascular events with T2DM patients is established, which will not only contribute to monitor the risk of cardiocerebrovascular incidents of T2DM patients, but help to provide basis for clinical treatment.
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    The correlation between the growth arrest-specific protein 6 and other inflammatory factors in patients with severe preeclampsia
    LIU Li, ZHANG Jing-rui, CHEN Ying
    2020, 48 (1):  68-70.  doi: 10.11958/20191951
    Abstract ( 764 )   PDF (317KB) ( 4239 )  
    Objective To investigate the correlation between the serum level of growth arrest-specific protein 6 (GAS6) and other inflammatory factors in patients with severe preeclampsia. Methods A total of 133 cases of pregnant women hospitalized in our hospital were retrospectively chosen from January to October of 2018. Patients were divided into two groups. The case group included 77 cases of patients with severe preeclampsia. The control group included 56 healthy pregnant women. The serum levels of GAS6, interleukin 6 (IL-6), IL-10 and IL-18 were measured by enzyme-linked immune sorbent assay. C reactive protein (CRP) was measured by biochemical analyzer. The correlation of the above indexes were analyzed in two groups of patients. Results The systolic blood pressure and diastolic blood pressure were higher in the severe preeclampsia group than those of the control group, and the gestational age was less in the severe preeclampsia group than that of the control group. The serum levels of GAS6 and IL-10 were significantly lower in the severe preeclampsia group than those in the control group (P<0.05), while the levels of IL-6 and IL-18 were higher than those in the control group (P<0 05). The serum GAS6 level was negatively correlated with IL-6. Conclusion In severe preeclampsia patients, the serum GAS6 is involved in inflammatory reaction and plays the role of anti-inflammatory factors. The serum level of GAS6 is related with the severity of inflammatory reaction.
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    Research progress of chimeric antigen receptor T cell immunotherapy in B-cell non-Hodgkin lymphoma
    ZHAO Pei-qi, ZHANG Hui-lai
    2020, 48 (1):  71-75.  doi: 10.11958/20191721
    Abstract ( 685 )   PDF (354KB) ( 4545 )  
    Abstract: Non-Hodgkin lymphoma (NHL) is the most common hematological malignancy, and the prognosis of patients with relapse and refractory is poor. Chimeric antigen receptor T-cell immunotherapy (CAR-T) is a new immunotherapy method in recent years, which has made many breakthroughs in the treatment of malignant tumors, especially hematological tumors. In particular, there is hope for patients with relapsed and refractory B-cell NHL. At present, Food and Drug Administration (FDA) has approved two CAR-T cell therapy tisagenlecleucel and axicabtagene ciloleucel. Several other products are still in clinical trials. This article reviews the structure of CAR-T and its efficacy, safety and research trends in common B-cell NHL
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    Advances in the indications of unicompartmental knee arthroplasty
    LI Bing, LIU Tian-sheng, WANG Lei, BU Yan-min, LI Xiao-hui, ZHANG Xiao-fei, LIU Jun
    2020, 48 (1):  76-80.  doi: 10.11958/20192330
    Abstract ( 871 )   PDF (350KB) ( 4816 )  
    Abstract: Unicompartmental knee arthroplasty (UKA) is one of the surgical treatments for single-compartment knee osteoarthritis (OA), which can provide symptomatic relief and promote knee function. However, the traditional operation indications of UKA are strict, including requirements of demographic characteristics, knee joint function and radiological measurement. With the development of implant design and surgical technique, the indications and contraindications of UKA keeps are changing. Some contraindications are break through, and the range of indications are expanded. Therefore, the current review focuses on the indications of UKA from the aspects of age, body mass index (BMI), anterior cruciate ligament (ACL) function and patella-femoral joint arthritis (PFO) to provide reference for clinical treatment.
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