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Table of Content

    30 August 2017, Volume 32 Issue 8
    Orginal Article
    Comparison on thromboelastography and conventional coagulation tests for evaluating blood coagulation function in elderly patients with asymptomatic cerebral infarction
    LU Jing, ZOU Zhuoru, ZHUANG Guihua
    2017, 32(8):  663-667.  DOI: 10.3969/j.issn.1673-8640.2017.08.001
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    Objective To investigate the commonness and difference between thromboelastography (TEG) and conventional coagulation tests for evaluating blood coagulation function in elderly patients with asymptomatic cerebral infarction (ACI). Methods A total of 86 elderly patients with acute ACI (ACI group) and 90 healthy subjects (healthy control group) were enrolled. The 2 groups were determined by TEG and conventional coagulation tests simultaneously. After treatment for 4 weeks,TEG and conventional coagulation tests were performed as well in the 2 groups. Results The correlation analysis showed that reaction time (R)had positive correlations with prothrombin time(PT) and prothrombin time-international normalized ratio (PT-INR),and had a negative correlation with fibrinogen (Fib). Maximum clot strength(MA) was positively correlated with Fib,synthesize coagulation index(CI) was negatively correlated with PT and PT-INR,and CI was positively correlated with Fib. In ACI group,R,clotting time(K),PT,PT-INR and activated partial thromboplastin time (APTT) were lower than those in healthy control group,while angle(α),MA,CI and Fib were higher (P<0.05). After treatment,R,K,PT-INR and APTT were increased,and α,MA,CI and Fib were decreased (P<0.05). However, compared with healthy control group,after treatment,R,K,PT and PT-INR were still lower,and α,MA,CI and Fib were still higher than those in healthy control group (P<0.05). In ACI group, the Kappa values of TEG with conventional coagulation tests before and after treatment were 0.072 and 0.124 (P>0.05),and χ2 were 13.40 and 7.60 (P<0.01). In addition,the results of TEG showed that the platelet hypercoagulabilities before and after treatment were 4.65% and 10.46% in ACI group,the enzymatic hypercoagulabilities were 23.26% and 25.58% ,and the platelet and enzymatic hypercoagulabilities were 40.70% and 15.12%. Conclusions There is a correlation between some indicators of TEG and conventional coagulation tests. Conventional coagulation tests have a certain efficiency on the determination of blood coagulation function in elderly patients with ACI,but the sensitivity is poor compared with TEG. As a sensitive and comprehensive determination of blood coagulation function,TEG is useful for the early determination and clinical treatment of ACI for elderly patients.

    Platelet parameters and bone marrow megakaryocyte count and classification in May-Hegglin anomaly
    GAO Feng, ZHANG Hongjie, LIU Ruifang, LI Li, YANG Lei, LIU Liguo, YAN Guoyan
    2017, 32(8):  668-670.  DOI: 10.3969/j.issn.1673-8640.2017.08.002
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    Objective To evaluate the roles of platelet (PLT)parameters and bone marrow megakaryocyte count and classification in May-Hegglin anomaly(MHA)and primary immune thrombocytopenia(ITP). Methods A total of 88 patients with acute and chronic primary ITP were enrolled,there were 15 patients with MHA,and 40 healthy subjects were enrolled as control group. They were classified into 4 groups,and megakaryocyte count and classification and 4 parameters of PLT [PLT count,plateletcrit(PCT),mean platelet volume(MPV)and platelet volume distribution width(PDW)] were determined. Results PDW and MPV were higher in MHA group than those in acute and chronic primary ITP group and control group(P<0.05). There was statistical significance for megakaryocyte count and classification in MHA group compared with those in acute and chronic primary ITP group (P<0.05),and there was no statistical significance compared with control group (P>0.05). Conclusions MPV and PDW play roles in the diagnosis of MHA. Megakaryocyte count and classification can identify MHA and acute and chronic primary ITP.

    Clinical application of plasma cell-free deoxyribonucleic acid levels and its integrity in breast cancer
    GU Yifeng, ZHU Zili, ZHANG Jinye, ZHANG Min, ZHANG Xiaoxia, ZHU Jiwen
    2017, 32(8):  671-676.  DOI: 10.3969/j.issn.1673-8640.2017.08.003
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    Objective To investigate the roles of plasma cell-free deoxyribonucleic acid(cfDNA)levels and its integrity in the diagnosis and prognosis of breast cancer. Methods Plasma samples were collected from 106 patients newly diagnosed as breast cancer,72 breast benign disease patients and 301 healthy subjects. Plasma cfDNA was extracted,and then 100 bp and 241 bp human telomerase reverse transcriptases(hTERT)were quantified by real-time fluorescence quantitation polymerase chain reaction(PCR). The cfDNA integrity was calculated,and the difference among the 3 groups and the relationship with tumor burden were analyzed. The sensitivities and specificities of 100 bp and 241 bp hTERT levels and cfDNA integrity for the diagnosis of breast cancer were evaluated by receiver operating characteristic(ROC)curve. Results The levels of 100 bp and 241 bp hTERT in breast cancer patients were higher than those in breast benign disease patients and healthy subjects(P<0.001). The integrity of cfDNA was related to lymph node metastasis(P<0.01). The areas under ROC curves (AUC)of 100 bp and 241 bp hTERT levels and cfDNA integrity were 0.693,0.792 and 0.865. The sensitivities were 73.3%,68.0% and 66.7%,and the specificities were 68%,80% and 92%,respectively. Conclusions The determinations of cfDNA levels and its integrity have certain clinical significance in the diagnosis and treatment of breast cancer,which could be as tumor biomarkers for the diagnosis and prognosis of breast cancer.

    Correlation of the changes of serum alpha2-Heremans-Schmid glycoprotein levels with metabolic syndrome
    JI Hongbing, JU Huixiang, SUN Mingzhong, CHEN Hongmei, HAN Yuqing, ZHOU Zhongwei
    2017, 32(8):  677-680.  DOI: 10.3969/j.issn.1673-8640.2017.08.004
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    Objective To investigate the correlation of the changes of serum alpha2-Heremans-Schmid glycoprotein(AHSG)levels with metabolic syndrome(MS). Methods A total of 726 subjects were enrolled. Their clinical data [waist circumference, blood pressure,body mass index(BMI), fasting plasma glucose(FPG), total cholesterol (TC), triglyceride(TG),high-density lipoprotein cholesterol(HDL-C),low-density lipoprotein cholesterol(LDL-C),C-reactive protein(CRP),homeostasis model assessment for insulin resistance(HOMA-IR)and free fatty acid(FFA)] were collected,and serum levels of AHSG were determined by enzyme-linked immunosorbent assay. A total of 211 of 726 subjects were identified with MS,according to the revision of the Adult Treatment Panel Ⅲ of the National Cholesterol Education Program(NCEP-ATP Ⅲ)in 2005. The parameters were compared between MS and non-MS groups. The relation between AHSG and parameters was analyzed by Pearson correlation analysis and multiple linear regression analysis. The quartiles of AHSG and the relative risk of MS were evaluated by Logistic regression analysis,and receiver operating characteristic(ROC)curve was used to assess the role of AHSG for the diagnosis of MS. Results Serum AHSG level was higher in MS group than that in non-MS group(P<0.05),and there was statistical significance for the other parameters between the 2 groups(P<0.05,P<0.01). AHSG was positively correlated with waist circumference,FPG,TG,LDL-C,CRP,HOMA-IR and FFA(r=0.094,0.133,0.107,0.078,0.088,0.126 and 0.119,P<0.05),and was correlated independently with waist circumference, CRP and HOMA-IR(β=0.088, 0.083 and 0.091, P=0.022, 0.033 and 0.014). The risk of MS increased with increasing quartiles of AHSG in Logistic regression analysis(P<0.01). ROC curve showed that the area under the curve was 0.709,and the cut-off value was 285.3 μg/mL. The sensitivity was 70.5%,and the specificity was 73.8%. Conclusions Increased AHSG level is one of risk factors for MS,and it plays a role for predicting the incidence of MS.

    Establishment of reference intervals for renal function parameters in middle and late pregnancy
    XU Liyuan, YING Chunmei
    2017, 32(8):  682-685.  DOI: 10.3969/j.issn.1673-8640.2017.08.005
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    Objective To investigate the renal function parameters [urea,creatinine(Cr),uric acid(UA),urea/Cr ratio and UA/Cr ratio] during healthy pregnancy,and to establish the reference intervals for renal function parameters in middle and late pregnancy. Methods The levels of urea,Cr and UA were determined in 4 000 healthy pregnant women(pregnancy group)and 4 000 healthy women of childbearing age(healthy control group). For pregnancy group,urea,Cr and UA levels were determined at 14-20,24-28 and 37-40 gestational weeks.The reference intervals in middle and late pregnancy were defined as the 2.5th percentile (P2.5)- the 97.5th percentile (P97.5). Results The levels of urea and Cr in pregnancy group were lower than those in healthy control group(P<0.05),and the levels of UA at 14-20 and 24-28 gestational weeks were lower than those in healthy control group(P<0.05). The levels of UA in 37-40 gestational weeks were higher than those in healthy control group(P<0.05).Compared with healthy control group,serum urea/Cr ratio in pregnancy group decreased to various degrees at 14-20 and 24-28 gestational weeks(P<0.05),and then increased at 37-40 gestational weeks(P>0.05).Serum UA/Cr ratio in pregnancy group decreased at 14-20 gestational weeks,and then increased with the progression of gestational weeks(P<0.05).The reference intervals of renal function parameters at 14-20,24-28 and 37-40 gestational weeks were 1.8-3.9,1.7-3.8,1.7-5.0 mmol/L for urea,33-53,32-54,31-60 μmol/L for Cr,141-269,127-352,161-457 μmol/L for UA,43.66-92.71,39.97-97.37,36.44-124.04 for urea/Cr ratio,and 3.15-6.25,3.17-8.55,3.18-11.20 for UA/Cr ratio. Conclusions There are different degrees of physiological changes of renal function in pregnant women with the progression of pregnancy,so it should establish the reference intervals of renal function parameters in middle and late pregnancy.

    Complement 1q determination for autoimmune diseases
    TAN Liming, DING Yaodong, CHEN Juanjuan, LI Hua, JIANG Yongqing, WAN Yani, WANG Liyun, WANG Tian
    2017, 32(8):  686-690.  DOI: 10.3969/j.issn.1673-8640.2017.08.006
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    Objective To evaluate the role of complement (C)1q determination for autoimmune diseases(AID). Methods A total of 203 AID patients [86 cases of autoimmune thyroid disease(AITD),56 cases of systemic lupus erythematosus(SLE),32 cases of rheumatoid arthritis(RA)and 29 cases of other connective tissue diseases] and 100 healthy subjects(healthy control group)were enrolled from the Second Affiliated Hospital of Nanchang University from May 2014 to September 2015. Using transmission turbidimetry,turbidimetric immunoassay,indirect immunofluorescence(IIF)and linear immunoblot assay(LIA),C1q, C-reactive protein(CRP),antinuclear antibody(ANA),anti-double-stranded DNA(ds-DNA)antibody and anti-Sm antibody were determined respectively. Results Compared with healthy control group, C1q level in SLE group was decreased(P<0.05),and that in RA group was increased(P<0.05). The level of C1q decreased with the increasing of ANA titer degrees(P<0.05). The C1q levels in anti-ds-DNA antibody positive and anti-Sm antibody positive group were lower than those in anti-ds-DNA antibody negative and anti-Sm antibody negative group (P<0.05). CRP levels in AID groups were increased(P<0.01). The correlation coefficient between C1q and CRP was >0.300(P<0.05). Regression equation showed that the range of cut-off values(COV)was 167.42-198.37 mg/L. For C1q and autoantibodies,the abnormal rate(C1q<COV)was higher in ANA positive group than that in ANA negative group,that in ANA positive with anti-ds-DNA positive group was higher than those of other autoantibody distribution types,and that in ANA positive with anti-Sm antibody positive or with anti-Sm and anti-ds-DNA antibodies positive increased. The abnormal rate(C1q>COV)in ANA negative group was 67.2%. Conclusions For patients with AID,C1q has moderate correlation with CRP,the abnormal rate of C1q has correlations with some autoantibody distribution types and the status of patients' illness.

    Correlation between serum interleukin 19 level and diabetic nephropathy
    LI Li, HU Juanyu, YU Zhengqing, MENG Hai
    2017, 32(8):  691-694.  DOI: 10.3969/j.issn.1673-8640.2017.08.007
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    Objective To investigate the correlation between serum interleukin 19(IL-19)level and diabetic nephropathy. Methods A total of 200 patients with type 2 diabetes mellitus(T2DM)were enrolled,and they were classified into non-albuminuria nephropathy group(102 cases),micro-albuminuria nephropathy group(72 cases)and macro-albuminuria nephropathy group(26 cases)according to urinary albumin excretion(UAE). A total of 50 healthy subjects were enrolled. Serum IL-19 level,high-sensitivity C-reactive protein(hs-CRP),cystatin C(Cys C),glycated hemoglobin A1c(HbA1c)and UAE were determined. Results Compared with healthy control group,serum IL-19 levels in micro-albuminuria nephropathy and macro-albuminuria nephropathy groups were higher(P<0.05). Serum IL-19 level was positively correlated with hs-CRP, Cys C, UAE and HbA1cr=0.623, 0.611, 0.591 and 0.526,P<0.01). Conclusions Serum IL-19 level is increased in patients with diabetic nephropathy. It might be involved in the development of diabetic nephropathy.

    Human papillomavirus infection in Shanghai Songjiang
    HUANG Luyao, XU Yanyan, LOU Xiaoli, CAO Hui, XIA Wanbao, HOU Yanqiang
    2017, 32(8):  695-699.  DOI: 10.3969/j.issn.1673-8640.2017.08.008
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    Objective To investigate human papillomavirus(HPV)infection and subtype distribution in Shanghai Songjiang,to analyze HPV pathogenicity on cervical cells,and to provide a reference for the control and prevention of cervical cancer. Methods A total of 5 039 female outpatients' cervical secretion samples from Shanghai Songjiang Central Hospital were collected from February 1st to March 31st in 2016. HPV genotyping was performed,and the subtype distribution in different ages was analyzed. HPV pathogenicity on cervical cells was evaluated. Results There were 1 140 positive samples,including 798 cases of single infection and 342 cases of multiple infection,and the infection rate was 22.6%. The infection rates were 29.5% in < 20-year-old group,21.0% in 21-30-year-old group,21.7% in 31-40-year-old group,21.7% in 41-50-year-old group,30.0% in 51-60-year-old group and 28.8% in >60-year-old group(P=0.000 161). The top 5 subtypes were type 16(17.0%), 52(14.6%), 58(12.8%), 54(8.2%)and 51(8.2%). The proportion of lesion ≥ atypical squamous cells of undetermined significance (ASCUS)in high-risk HPV group(HPV type 16 and 18)was higher than those in low-risk HPV group(other subtypes,except HPV type 16 and 18)and negative control group(P<0.05). Conclusions HPV infection rate in 51-60-year-old group is the highest in Shanghai Songjiang. HPV type 16 or 18 is more likely to cause cervical cell lesion. HPV screening for high-risk population is helpful for the prevention and treatment of cervical cancer.

    Relationship between human papillomavirus infection and the severity of cervical lesions
    YAN Xiaohui, LIN Jinduan
    2017, 32(8):  700-703.  DOI: 10.3969/j.issn.1673-8640.2017.08.009
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    Objective To study the infection characteristics of human papillomavirus(HPV)in cervical cells from different lesion tissues,and to investigate the relationship between HPV infection and the severity of cervical lesions. Methods A total of 53 cases of normal or mild inflammation,79 cases of cervical intraepithelial neoplasia(CIN)Ⅰ,42 cases of CIN Ⅱ,87 cases of CIN Ⅲ,or 54 cases of invasive cervical cancer(ICC)were determined for 23 HPV genotypes by multiplex polymerase chain reaction(PCR)-reverse dot blotting(RDB). The infection characteristics of HPV and the severity of cervical lesions were evaluated,and the relationship between different HPV genotypes and the severity of cervical lesions were investigated as well. Results HPV infection and the severity of cervical lesions had correlation(r =0.500),and the determination rate of HPV increased as the severity of cervical lesions increased(χ2=43.322,P<0.05). The determination rates of HPV with different grades of cervical lesions had statistical significance(P<0.01),except CIN Ⅲ and ICC groups(χ2=0.003,P>0.05). Multiple HPV infections were related with the severity of cervical lesions(r =0.496,P<0.05). The determination rate of multiple HPV increased as the severity of cervical lesions increased,except ICC group(P<0.01). The determination rate and the proportion of high-risk HPV infection were increased with the severity of cervical lesions. Different HPV genotypes had statistical significance on cervical lesions(χ2=46.775,P<0.05). The top 5 HPV genotypes to cervical lesions were type 16,18, 31,33 and 58. Conclusions The severity of cervical lesions is correlated with HPVgenotypes and multiple HPV infections. The proportions of HPV genotypes among different cervical lesion grades are different. With the severity of cervical lesions increased,the determination rate of high-risk HPV infection and its proportion are increased.

    Application on Feulgen-EA staining fixative
    HUANG Rongxiang, YU Lanlan, ZHU Chenyan, HE Wenbo, MA Liang, NIE Kun, ZHANG Jing
    2017, 32(8):  704-708.  DOI: 10.3969/j.issn.1673-8640.2017.08.010
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    Objective To investigate Feulgen-EA staining fixative primarily. Methods By image analysis,cells were scanned after fixation by 5 fixatives [glacial acetic acid(acetic acid),AF,improved AF,Clarke and Bohm-Sprenger],nucleus integrated optical density(IOD),coefficient of variation(CV)and area were compared,and suitable DNA fixative was obtained. The influence of temperature on fixation was evaluated. The effect of cytoplasmic staining was compared by EA staining. Results DNA fixation may choose appropriately AF or Bohm-Sprenger fixed-liquid reaction for 30 min. When temperature was too low,it may influence on DNA fixation,and the effect of EA to cytoplasmic staining was good. Conclusions AF and Bohm-Sprenger fixatives are suitable for Feulgen-EA double staining.

    Primary study on the reference method for hemoglobin determination
    XU Lei, WANG Qing, ZHU Peichao, MIAO Yingbo, SONG Ying
    2017, 32(8):  709-712.  DOI: 10.3969/j.issn.1673-8640.2017.08.011
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    Objective To investigate the reference method for hemoglobin(Hb)determination,and to provide a reference for trueness verification of Hb determination. Methods According to the requirements of the International Council for Standardization in Haematology(ICSH),UV-2550 spectrophotometer was used for Hb reference materials with low,medium and high levels being labeled by Japanese Reference Material Institute for Clinical Chemistry Standards and 2 trueness verification samples in the first External Quality Assessment of Shanghai Clinical Laboratory 2016. The precision,accuracy and comparability were analyzed. Results The total precision(CV)of the 5 samples using the reference method for Hb determination was <0.5%. The accuracy of Hb reference materials with 3 levels met the certification of reference materials. The bias of Hb determination total means (x?) determined by 615 clinical laboratories and Hb determination values by hematological analyzers with different brands was <2.7%,compared to reference method assignments. Conclusions The precision and accuracy of reference method for Hb determination by UV-2550 spectrophotometer meet related requirements. The level of Hb can be delivered well to routine hematological analyzers.

    Stability of alanine aminotransferase trueness control samples
    OU Yuanzhu, YU Xiaoxuan, TANG Liping, JU Yi, WANG Meijuan, LIU Wenbin, JIN Zhonggan
    2017, 32(8):  713-717.  DOI: 10.3969/j.issn.1673-8640.2017.08.012
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    Objective To investigate the status of alanine aminotransferase(ALT)trueness verification in Shanghai and the application of stabilizer betaine in trueness control samples,so as to optimize trueness verification. Methods A total of 4 trueness control samples(ALT-A,ALT-B,ALT-C and ALT-D)undergoing centrifugation and filtration processing were delivered to clinical laboratories under cold chain. ALT-B and ALT-D were added stabilizer betaine,and the trueness control samples were determined for 3 d. The trueness control samples were assigned using the International Federation of Clinical Chemistry and Laboratory Medicine(IFCC)primary reference method,obtaining target values. The bias of each trueness control sample's mean and target value in each laboratory was calculated,and the allowable bias judgment standard was ≤6%. Stability experiment for 3 d at -20℃of trueness control samples was performed by synchronizing method,and the stabilities of 4 trueness control samples in all laboratories were analyzed. Results At -20 ℃ for 3 d,ALT-B and ALT-D had good stabilities (the activities at the 3 rd day were 99.1% and 100.0% of initial value). ALT-A and ALT-C were unstable(the activities at the 3 rd day were 96.7% and 94.9% of initial value),which were the same as those for trueness control samples in all laboratories.Among 74 laboratories,there were 23.0%(17 cases) of ALT-A and 33.8%(25 cases) of ALT-C in the range of allowable bias,while there were 66.2%(49 cases) of ALT-B and ALT-D in the range of allowable bias. There were 65.8% (27 cases)of ALT-B and 63.4%(26 cases)of ALT-D in the range of allowable bias in 41 Level 3 hospitals,and there were 66.7%(22 cases)of ALT-B and 69.7%(23 cases)of ALT-D in the range of allowable bias in 33 Level 2 hospitals. There were 59.5%(44 cases)of ALT-B and ALT-D in the range of allowable bias,of which 61.0%(25 cases) in Level 3 hospitals and 57.6%(19 cases) in Level 2 hospitals. Conclusions There is no difference for bias between Level 3 and Level 2 hospitals. ALT trueness control samples with no stabilizer can not meet the needs of trueness verification,and ALT trueness control samples adding stabilizer betaine can satisfy the needs of trueness verification.

    Comparison of homogeneous enzyme immunoassay and latex-enhanced immunoturbidimetric assay for the determination of cholyglycine
    LIANG Yunlai, LIAO Jingzhong, WANG Kun, XIE Xulin, YI Bin
    2017, 32(8):  718-721.  DOI: 10.3969/j.issn.1673-8640.2017.08.013
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    Objective To compare homogeneous enzyme immunoassay and latex-enhanced immuno-turbidimetric assay for the determination of cholyglycine(CG),and to provide a reference for selecting appropriate method. Methods The positive rates,precisions and linear ranges of the 2 methods were compared,and then 248 samples were determined by the 2 methods for statistical analysis. Results The positive rates of homogeneous enzyme immunoassay and latex-enhanced immunoturbidimetric assay were 53.23% and 51.21%,and the positive coincidence rate was 97.58%. The coefficients of variation (CV)of within-run precision for high-value serum were 1.13% and 2.65%,and those for low-value serum were 3.52% and 7.51%,respectively. In linear evaluation,the linear regression equation of homogeneous enzyme immunoassay was Y=1.068 2X+0.421 6(r =0.995 7),and the linear regression equation of latex-enhanced immunoturbidimetric assay was Y=1.016 1X+0.875 2(r =0.997 7). The relationship between the 2 methods was Y=1.156X+0.543 [coefficient of determination(R2)=0.98]. Conclusions The results of the 2 methods have high consistency,and they have good accuracy,stability and reliability,which meet clinical determination requirements. However,the stability of homogeneous enzyme immunoassay is better than that of latex-enhanced immunoturbidimetric assay.

    Xpert MTB/RIF assay for the rapid determination of Mycobacterium tuberculosis and rifampin resistance
    XU Dongfang, WANG Qing
    2017, 32(8):  722-726.  DOI: 10.3969/j.issn.1673-8640.2017.08.014
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    Objective To investigate Xpert MTB/RIF assay for the rapid determination of Mycobacterium tuberculosis (MTB) and rifampin resistance. Methods A total of 616 sputum or bronchoalveolar lavage fluid (BALF) samples from patients with pulmonary tuberculosis and suspected with pulmonary tuberculosis in Anhui Provincial Chest Hospital were collected from April 2015 to December 2015.Diagnostic performance of Xpert MTB/RIF assay,liquid culturing and acid-fast staining smear microscopy was evaluated,according to gold standard for statistical analysis. Results The sensitivities for MTB determination were 39.61%(225/568),36.44%(207/568)and 17.78%(101/568)for Xpert MTB/RIF assay,liquid culturing and acid-fast staining smear microscopy. There was a consistency for sensitivities between Xpert MTB/RIF assay and liquid culturing(χ2=1.21,P>0.05),and the sensitivity of Xpert MTB/RIF assay was higher than that of acid-fast staining smear microscopy(χ2=66.15,P<0.05). For rifampin resistance determinatin,the rifampin resistance rate by Xpert MTB/RIF assay was 19.40%(39/201),the sensitivity and specificity were 94.59% (35/37) and 97.56% (160/164) , and there was no statistical significance compared with liquid culturing(χ2= 0.167,P>0.05). All cultures being positive for rifampin resistance gene were performed for sequencing as the gold standard of rpoB resistance gene determination. For Xpert MTB / RIF assay,the main rifampin resistance locus was Probe E(58.98%,23/39). S531L and L533P were main in sequencing(62.16%,23/37). The 2 methods had the same mutation locus (χ2=0.081,P>0.05). Conclusions Xpert MTB/RIF assay can be used for the rapid determination of MTB and rifampin resistance.

    Preparation and performance of recombinant human cystatin C quality control material
    LI Jiangfeng, FENG Minyi, QIAN Wei, ZHAO Xiaoni, CHEN Zitong, JIAO Liyuan, WANG Jihua, CAI Lei
    2017, 32(8):  733-737.  DOI: 10.3969/j.issn.1673-8640.2017.08.017
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    Objective To prepare cystatin C(Cys C) quality control material by using recombinant human Cys C protein expressed in Escherichia coli BL21 as basic material. Methods By gene engineering method,recombinant human Cys C protein was expressed through pCold1 and BL21. Freeze drying was performed after purification. Results Inclusion bodies of recombinant human Cys C protein was expressed successfully. After renaturation by dialysis method,soluble recombinant human Cys C protein with immunological activity had been prepared. Cys C quality control material was prepared by using the recombinant human Cys C protein and determined by HITACHI and ROCHE analysis systems. Cys C quality control was suitable for the 2 analysis systems. Conclusions Cys C quality control material prepared by recombinant human Cys C protein has good stability and reliability,it could be used in various analysis platforms of in vitro diagnosis.

    Research progress of myeloperoxidase in cardiovascular diseases
    BO Lei, SHAN Jigang, ZHAO Zhiwen
    2017, 32(8):  738-743.  DOI: 10.3969/j.issn.1673-8640.2017.08.018
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    Myeloperoxidase(MPO)which exists in myeloid cells(mainly in neutrophils and monocytes),is an enzyme derived of leukocytes that catalyzes the formation of numerous reactive oxidant species. Besides innate in defense function,current knowledge has been proved the contribution of these oxidants to tissue injury during inflammation,and MPO plays an important role in the initiation,propagation and acute complications of atherosclerotic process. Growing researches demonstrate the action of MPO as central participant of the link in nitric oxide,lipid metabolism and acute coronary syndrome. This review focuses on the research progress of MPO in cardiovascular diseases.