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1.
Zhongguo Gu Shang ; 37(2): 153-8, 2024 Feb 25.
Article in Chinese | MEDLINE | ID: mdl-38425066

ABSTRACT

OBJECTIVE: To explore the potential value of three-dimensional fast spin echo(3D-SPACE) combined with multilayer spiral CT (MSCT) in the diagnosis of knee cruciate ligament injury, to provide a new direction for the optimization of subsequent clinical diagnosis. METHODS: A total of 120 patients with knee cruciate ligament injury were treated from April 2020 to April 2021, aged from 21 to 68 with an average of(41.52±4.13) years old. For all patients, separate MSCT scanner scans, 3D-SPACE sequence scans alone and 3D-SPACE sequence combined with MSCT scans were used. The injury and classification of the anterior and posterior cruciate ligament of the knee were compared, the length of the anterior-medial bundle and posterolateral bundle and its angle of the knee with the horizontal plane were observed, the diagnostic value of 3 diagnostic methods in knee cruciate ligament injury were determined. RESULTS: There was no significant difference between the 3D-SPACE sequence scan alone and the MSCT test alone on the total diagnostic rate and grading total diagnostic rate(P>0.05). The total diagnostic rate and grading total diagnostic rate of 3D-SPACE scan combined with MSCT were significantly higher than those of 3D-SPACE scan or MSCT alone(P<0.05). The 3D-SPACE sequence scan alone and the MSCT detection alone had no significant difference in the measurement values related to the anterior and posterior cruciate ligaments of the knee joint(P>0.05). 3D-SPACE sequence scanning combined with MSCT detection on the knee joint anterior and posterior cruciate ligament related measurements were significantly higher than the 3D-SPACE sequence scan or MSCT detection alone(P<0.05). The area under the ROC curve estimated by 3D-SPACE sequence scanning combined with MSCT was 0.960, which was significantly higher than that of 3D-SPACE sequence scanning and MSCT alone evaluating the area under the ROC curve line of 0.756 and 0.795. The combined 3D-SPACE sequence scanning and 3D-SPACE sequence scanning MSCT analysis and prediction models were statistically different(Z=2.236, P<0.05), and MSCT alone and 3D-SPACE sequence scanning combined with MSCT analysis and prediction models were statistically different(Z=2.653, P<0.05). CONCLUSION: The application of 3D-SPACE sequence combined with MSCT scanning for knee cruciate ligament injury can improve the diagnosis rate of patients with knee cruciate ligament injury.It can be used as a diagnostic tool for patients with knee cruciate ligament injury and is worthy of clinical application.


Subject(s)
Anterior Cruciate Ligament Injuries , Knee Injuries , Posterior Cruciate Ligament , Soft Tissue Injuries , Humans , Adult , Middle Aged , Magnetic Resonance Imaging/methods , Arthroscopy , Knee Injuries/diagnostic imaging , Knee Joint/diagnostic imaging , Posterior Cruciate Ligament/injuries , Tomography, Spiral Computed , Anterior Cruciate Ligament Injuries/diagnostic imaging
2.
Infect Agent Cancer ; 15(1): 70, 2020 Nov 23.
Article in English | MEDLINE | ID: mdl-33292429

ABSTRACT

BACKGROUND: To explore the value of alpha fetoprotein (AFP) and protein induced by vitamin K absence or antagonist-II (PIVKA-II) in diagnosis of HBV-related hepatocellular carcinoma (HCC) and their relationship with vascular invasion, tumor differentiation and size. METHODS: A total of 433 participants were enrolled in this study including 266 cases with HBV-related HCC, 87 cases with HBV DNA positive benign liver disease and 80 healthy individuals. Then we explored the correlation between AFP, PIVKA-II serum level and several pathological features such as vascular invasion, tumor differentiation and size. The value of these two markers used singly or jointly in diagnosing HBV-related HCC was evaluated by receiver operating characteristic (ROC) curve. The ROC curve was also plotted to identify AFP, PIVKA-II serum cut-off values that would best distinguish HBV-related HCC patients with and without vascular invasion. RESULTS: The level of AFP and PIVKA-II in HBV-related HCC group was significantly higher (Z was 7.428, 11.243 respectively, all P < 0.01). When AFP and PIVKA-II were used as the individual tumor marker, the areas under the ROC curve (AUC) of HBV-related HCC diagnosis were 0.765 (95% CI, 0.713 ~ 0.8170) for AFP, 0.901 (95% CI, 0.868 ~ 0.935) for PIVKA-II, and 0.917 (95% CI, 0.886 ~ 0.948) for AFP and PIVKA-II simultaneously. The serum levels of AFP and PIVKA-II were positively correlated with tumor differentiation and size. High AFP and PIVKA-II expression was significantly associated with the presence of vascular invasion (P was 0.007 and 0.014 respectively). The AFP level > 64.4 ng/ml or PIVKA-II level > 957.61mAU/ml was the best critical value to predict the presence of vascular invasion. CONCLUSION: Our results validate that AFP and PIVKA-II play a significant role in the diagnosis of HBV-related HCC. The diagnostic value of AFP and PIVKA-II combined detection or single assay of PIVKA-II is higher than that of separate assay of AFP. Moreover, their concentration has important clinical value in judging tumor size, tumor cell differentiation and vascular invasion.

3.
Asia Ocean J Nucl Med Biol ; 7(1): 84-88, 2019.
Article in English | MEDLINE | ID: mdl-30705914

ABSTRACT

Granulocyte colony-stimulating factor (G-CSF) is a hematopoietic cytokine which controls the differentiation and growth of hematopoietic cells in the bone marrow. We report a severe aplastic anemia (SAA) patient with false-negative 99mTc sodium phytate bone marrow imaging findings under concurrent G-CSF therapy. The first bone marrow imaging showed a normal bone marrow activity. However, the bone marrow biopsy pathology report revealed a lack of hematopoietic cells. Furthermore, the complete blood count indicated severe pancytopenia resulting in the diagnosis of aplastic anemia (AA). A second marrow scan implemented after the stoppage of G-CSF showed an abnormal bone marrow activity, which matched the pathology reports. Accordingly, the concurrent administration of G-CSF was considered as the cause of false-negative bone marrow imaging findings obtained in the first scan. Consequently, it should be kept in mind that a 99mTc sodium phytate bone marrow scintigraphy during the concurrent administration of G-CSF may lead to the achievement of false negative results because it induces changes in bone marrow mimicking a normal marrow scan in patients with AA.

4.
Clin Nucl Med ; 40(5): 423-6, 2015 May.
Article in English | MEDLINE | ID: mdl-25706786

ABSTRACT

Primary hyperplasia of parathyroid is uncommon and rarely documented in literatures. We report an 18-year-old female patient with hyperparathyroidism due to unifocal primary hyperplasia of parathyroid glands. Dual-phase Tc-MIBI imaging was performed for this patient. We found remarkably increased MIBI uptake in the hyperplastic lesion in early imaging and no extinction of the uptake in delayed imaging. These results suggest that the dual-phase Tc-MIBI imaging is useful in localizing the hyperfunctioning lesions of primary hyperplasia of parathyroid glands.


Subject(s)
Parathyroid Glands/diagnostic imaging , Radiopharmaceuticals , Technetium Tc 99m Sestamibi , Adolescent , Female , Humans , Hyperplasia/diagnostic imaging , Parathyroid Glands/pathology , Radionuclide Imaging
5.
ScientificWorldJournal ; 2014: 256256, 2014.
Article in English | MEDLINE | ID: mdl-24901015

ABSTRACT

PURPOSE: To investigate the clinical value of (99)Tc(m)-MDP SPECT for the diagnosis of unilateral condylar hyperplasia (UCH). METHODS: One hundred forty-nine patients who underwent mandibular (99)Tc(m)-MDP SPECT between January 2009 and December 2012 were studied, including 105 cases that were clinically suspected of UCH and 44 comparable cases without UCH as a control group. RESULTS: Increased bone activity was observed in the affected condyles for all UCH patients. In the UCH group, the relative percentage uptake on the affected side was 59% (SD ± 4.3%), significantly higher than the 41% (SD ± 4.1%) uptake on the contralateral side (P<0.001). Similarly, the condyle/skull ratio was significantly higher for the affected side (1.66 ± 0.63) than for the contralateral side (1.34 ± 0.34, P < 0.01. No significant difference was found in the control group between the left and right condyles. Values for the sensitivity (95%), specificity (61%), positive (84.4%) and negative (84.6%) predictive values, and accuracy (84.5%) for (99)Tc(m)-MDP SPECT in the diagnosis of UCH were calculated. However, for the hyperplastic condyle, no correlation was observed between the thickness of each cartilage layer and the relative uptake in the SPECT image. CONCLUSION: (99)Tc(m)-MDP SPECT is accurate for diagnosing UCH and can provide a reference for treatment options.


Subject(s)
Bone and Bones/diagnostic imaging , Hyperplasia/diagnosis , Hyperplasia/pathology , Mandibular Condyle/pathology , Radionuclide Imaging/methods , Tomography, Emission-Computed, Single-Photon/methods , Adolescent , Adult , Female , Humans , Male , Young Adult
6.
Clin Lab ; 60(5): 821-5, 2014.
Article in English | MEDLINE | ID: mdl-24839826

ABSTRACT

BACKGROUND: Killer cell immunoglobulin-like receptors (KIRs) are expressed on natural killer (NK) cells and T cells and organized in highly polymorphic families. Genetic diversity is an important characteristic of KIR genes. The aim of the study was to investigate the influence of KIR genotypes and halotypes on the risk of pulmonary tuberculosis (PTB). METHODS: A sequence specific primer polymerase chain reaction (SSP-PCR) was employed to amplify the KIR genes and pseudogenes in 139 pulmonary tuberculosis (PTB) patients and 30 healthy controls. The innovative point of our study was the subdivision of the patient group according to sputum smear test (positive and negative). KIR genotype and haplotype frequencies were compared between the PTB group and the control group by Chi-square test, and p < 0.05 was regarded as statistically significant. RESULTS: The genotype AH and FZ14 may be associated with the clearance of Mycobacterium. In addition, haplotype B may be the susceptive haplotype that facilitated the clearance of Mycobacterium and haplotype A may be protective haplotype of PTB. CONCLUSIONS: Therefore, the diversity of genotypes and haplotypes induced an inflammatory reaction that resulted in continuous infection.


Subject(s)
Genetic Predisposition to Disease , Genotype , Haplotypes , Receptors, KIR/genetics , Tuberculosis, Pulmonary/genetics , Case-Control Studies , Gene Frequency , Humans , Inflammation/genetics , Inflammation/microbiology , Inflammation/pathology , Tuberculosis, Pulmonary/pathology
7.
Oncol Lett ; 6(6): 1729-1732, 2013 Dec.
Article in English | MEDLINE | ID: mdl-24273606

ABSTRACT

99mTcO4- thyroid imaging is often used to detect thyroid diseases that are confined to the neck. However, this examination is not frequently used to detect metastatic lesions of thyroid cancer in the whole body, while 131I imaging is often used to detect the metastases of differentiated thyroid cancers. The present study performed 99mTcO4- thyroid imaging for a 69-year-old patient with a thyroid nodule and incidentally identified a lesion with abnormally increased 99mTcO4- uptake in the chest of the patient. Furthermore, a whole-body scan was performed for this patient and multiple lesions with increased 99mTcO4- uptake were identified. The results confirmed that these lesions were follicular thyroid cancer and the metastatic lesions were distributed in numerous locations. The results revealed that analysis of the whole body is significant when regional lesions with abnormally increased 99mTcO4- uptake outside of thyroid tissues are identified by routine 99mTcO4- thyroid imaging.

8.
Oncol Lett ; 5(1): 391-397, 2013 Jan.
Article in English | MEDLINE | ID: mdl-23255956

ABSTRACT

The purpose of the present study was to investigate the distribution characteristics of bone metastases in breast and prostate carcinomas. Bone scintigraphies were performed in 504 cancer patients. We studied the correlation between the distribution and total number of metastatic bone lesions, and compared the distribution of metastatic bone lesions between breast and prostate carcinomas. In the early stage, the distribution in the thoracic vertebrae, lumbar vertebrae and pelvis of the metastatic lesions of the prostate carcinoma (81.0%, 47/58) was significantly higher than that of the breast carcinoma (41.7%, 63/151; χ(2)=27.6, P=0.000). The distribution of the lesions in the thoracic skeleton in the cases of the breast carcinoma (65.6%, 99/151) was significantly higher than that of the prostate carcinoma (27.6%, 16/58; χ(2)=24.8, P=0.000); however, the distributions in the advanced cases were not markedly different. The differences in the proportions of the metastatic lesions in the lumbar vertebrae (χ(2)=56.1, P=0.000) and ribs (χ(2)=39.1, P=0.000) in the cases of the prostate carcinoma, and in the sternum (χ(2)=31.2, P=0.000), skull (χ(2)=26.5, P=0.000) and femur (χ(2)=13.6, P=0.001) in the cases of the breast carcinoma were significant. Between the breast and prostate carcinomas, the differences in the proportions of the metastatic lesions of certain bones were also significant. In cases with few bone metastases, the proportion of sternum metastases of patients with breast carcinoma (17.9%) was significantly higher than that of patients with prostate carcinoma (1.7%; χ(2)=12.7, P=0.000); the proportion of metastases in the lumbar vertebrae of prostate carcinoma (39.7%) was significantly higher than that of breast carcinoma (13.9%; χ(2)=15.4, P=0.000); the proportion of rib metastases of breast carcinoma (27.2%) was significantly higher than that of prostate carcinoma (8.6%; χ(2)=9.6, P=0.002). In cases with extensive bone metastases, the proportions of metastatic lesions in the sternum and lumbar vertebrae in breast and prostate carcinomas were not significantly different (P>0.05). In conclusion, the distribution of bone metastases is correlated with the total number of metastatic bone lesions in breast and prostate carcinoma patients, and has different characteristics in different lesions.

9.
Zhonghua Yu Fang Yi Xue Za Zhi ; 46(10): 898-902, 2012 Oct.
Article in Chinese | MEDLINE | ID: mdl-23363863

ABSTRACT

OBJECTIVE: To explore the spatial and temporal characteristics of measles patients younger than 1 year old in Shandong province. METHODS: A total of 5309 cases of measles, whose patients were younger than 1 year old in Shandong province between year 1999 and 2008 were collected. The epidemic features of measles were described, and the annual infant incidence was calculated. Software ArcGIS9.3 was applied to draw the spatial map of the disease, and the software GeoDa0.95i-beta was adopted to analyze the spatial autocorrelation. RESULTS: The incidence among infants younger than 1 year old reported in Shandong province rose from 23.45/100 000 (206 cases) in 1999 to 269.60/100 000 (2791 cases) in 2008.5309 cases covered all month-aged infants under 1 year old, except 12 months old. Most patients (3494 cases) aged between 6 - 9 months old; especially the infants around 8 months old, accounting for 20.7% (1100/5309). The epidemic peak was between March and May, accounting for 45.5% (2414/5309). The spatial and temporal distribution features showed an up and down temporal trend and an increase from east to west in spatial trend. The global Moran's I values of measles incidence among infants in Shandong province were 0.346, 0.150, 0.396, 0.213, 0.477, 0.354 and 0.331 in year 1999, 2001 - 2002, 2005 - 2008 (P < 0.01) and 0.076 in year 2004 (P < 0.05). The local spatial autocorrelation analysis showed that southwest and northwest districts of Shandong were highly clustered districts of measles. CONCLUSION: In Shandong, the measles incidence among infants younger than 1 year old rose obviously; especially the infants aged between 6-9 months age. The epidemic peak was between March and May. A positive spatial correlation was found, the disease showed a distinct regional distribution feature, and a cluster district was found.


Subject(s)
Geography , Measles/epidemiology , China/epidemiology , Humans , Incidence , Infant , Infant, Newborn , Space-Time Clustering
10.
Zhonghua Zhong Liu Za Zhi ; 32(5): 382-6, 2010 May.
Article in Chinese | MEDLINE | ID: mdl-20723439

ABSTRACT

OBJECTIVE: To explore the image characteristics of bone metastasis of primary lung carcinoma. METHODS: Whole-body bone imaging ((99)Tc(m)-MDP) was performed in 258 patients with pathologically proven lung carcinoma. The rate of bone metastasis, distribution of the metastatic lesions and their characteristics were analyzed. RESULTS: Among the 258 cases, 142 patients developed bone metastasis. The overall rate of bone metastasis was 55.0%. The metastases located in axial skeleton were 49.6%, appendicular skeleton 36.0%, trunk bones of the axial skeleton 48.4%, and appendicular girdle skeleton 31.4%. Ribs, thoracic vertebrae, ilium and lumbar vertebrae had a higher rate of bone metastasis, higher than 20%, respectively. 1252 lesions were detected including 406 at the left side of the body, 387 in the axial skeleton and 459 at the right side of the body. There was no significant difference in terms of number of lesions between left side and right side (chi(2) = 3.3, P = 0.072). 1224 bone metastatic foci (97.8%) were presented as strong radioactive, 26 (2.1%) mixed lesion, and 2 (0.2%) low radioactive. According to the shape of the lesions, there were 810 punctate lesions (71.5%), 159 (14.0%) lump form, 108 (9.5%) strip form and 56 (4.9%) lamellar form. The accumulative bone metastasis rate was 28.7% for the patients with one to three lesions. The metastasis rate decreased gradually with the increasing number of metastatic lesions. CONCLUSION: Bone metastasis is very common in patients with lung cancer. Most bone metastases are characterized by strong radioactive and earlier punctate form, often occurs in the trunk bones of axial skeleton or appendicular girdles. The distribution of earlier metastases has not obvious regularity, and advanced bone metastases are often concurrent, multiple and multiform, widely and randomly distributed in the body.


Subject(s)
Bone Neoplasms/diagnostic imaging , Bone Neoplasms/secondary , Technetium Tc 99m Medronate , Tomography, Emission-Computed, Single-Photon , Whole Body Imaging , Adenocarcinoma/diagnostic imaging , Adenocarcinoma/pathology , Adenocarcinoma of Lung , Adult , Aged , Aged, 80 and over , Bone and Bones/diagnostic imaging , Bone and Bones/pathology , Female , Humans , Lung Neoplasms/diagnostic imaging , Lung Neoplasms/pathology , Male , Middle Aged , Radiopharmaceuticals
12.
Bing Du Xue Bao ; 26(6): 471-6, 2010 Nov.
Article in Chinese | MEDLINE | ID: mdl-21344752

ABSTRACT

Analyze the genetic characteristics of sixteen strains of wild-type rubella viruses derived from Vero cells, Rk13 cells or Vero/slam cells, and isolated from throat samples in Shandong province during 2000-2007. The 1107 nucleotide sequence of nucleoprotein (E1) gene of these isolates were amplified by RT-PCR, and the PCR products were directly sequenced. Comparing with the gene tree that was constructed based on the 739 gene sequences of the WHO reference strains, twelve isolated strains belonged to 1E genotype, one strain belonged to 1F genotype, three strains belonged to 2A genotype. The first strain belonged to 1E genotype was isolated in Shandong province in 2001, then genotype 1E became dominant genotype of wild rubella viruses circulated. The 1E genotype circulated from 2006-2007 was different compared with that circulated from 2001 to 2002, but no significant deviation in temporal and geographic distribution was found. The strain belonged to Genotype 1F was only isolated during 2000 to 2001. The three strains of 2A genotype of rubella viruses were similar to rubella viruses vaccine strain (BRDII). The most nucleotide mutation of rubella viruses among the sixteen strains were nonsense mutation, and the amino acid sequences were highly conservative with no change in important antigen sites. Alike the previous reports, there was the same amino acid mutation in protein E1 at the site of 338 in all of the 1E genotype rubella viruses isolated during 2001- 2007 in Shandong (Leu338 --> Phe338).


Subject(s)
Rubella virus/genetics , Rubella virus/isolation & purification , Rubella/epidemiology , Rubella/virology , Animals , China/epidemiology , Chlorocebus aethiops , Humans , Molecular Epidemiology , Molecular Sequence Data , Phylogeny , Rubella virus/classification , Vero Cells , Viral Proteins/genetics
13.
Croat Med J ; 50(2): 117-23, 2009 Apr.
Article in English | MEDLINE | ID: mdl-19399944

ABSTRACT

AIM: To analyze the association of estrogen receptor alpha (OR alpha) gene polymorphisms with cytokine genes expression in patients with systemic lupus erythematosus (SLE) and controls. METHODS: Genomic DNA was extracted and polymorphisms of XbaI, Ukrainian (XX, Xx, or xx genotype) and PvuII (PP, Pp, or pp) in intron 1 of OR alpha gene were detected by polymerase chain reaction-restriction fragment length polymorphisms (PCR-RFLP) method. The messenger RNA (mRNA) levels of interleukin (IL)-10, IL-4, interferon (IFN)-gamma, and IL-2 were assessed by semiquantitative reverse transcription polymerase chain reaction (RT-PCR). RESULTS: In patients with SLE with PpXx genotype, IL-10 and IL-4 mRNA expression was higher (P < 0.001 and P = 0.013, respectively), while in patients with SLE with Ppxx genotype IFN-gamma and IL-2 mRNA expression was lower than in controls (P < 0.001). There was no significant difference in mRNA expression of 4 cytokines among controls with various genotypes. CONCLUSION: OR alpha gene polymorphism may be associated with the expression of IL-10, IL-4, IL-2, and IFN-gamma in patients with SLE.


Subject(s)
Cytokines/genetics , Estrogen Receptor alpha/genetics , Lupus Erythematosus, Systemic/genetics , Polymorphism, Genetic , Adult , Case-Control Studies , Cytokines/metabolism , Disease Progression , Estrogen Receptor alpha/metabolism , Female , Gene Expression Regulation , Genetic Predisposition to Disease , Genotype , Humans , Lupus Erythematosus, Systemic/physiopathology , Polymerase Chain Reaction , Polymorphism, Restriction Fragment Length , Probability , Prognosis , RNA, Messenger/analysis , Reference Values , Risk Factors , Sensitivity and Specificity , Severity of Illness Index , Statistics, Nonparametric , Young Adult
14.
Zhongguo Yi Miao He Mian Yi ; 15(1): 8-13, 2009 Feb.
Article in Chinese | MEDLINE | ID: mdl-20077668

ABSTRACT

OBJECTIVE: To analyze genetic characteristics of mumps virus in China from 2006 to 2008. METHODS: In the study, the fragments containing 316 nucleotides of SH genes from 7 mumps virus isolates in China from 2007 to 2008 were amplified by RT-PCR method, the PCR products were directly sequenced and analyzed with other 7 mumps virus sequences in China in 2006 and WHO mumps reference strains downloaded from Genbank together. RESULTS: The results of homology and phylogenetic analyses based on 316 nucleotides showed that all 14 Chinese mumps virus strains in 2006-2008 belong to a distinguish branch of F genotype, but there were some differences between these 14 mumps virus strains. The mumps virus sequences in different provinces or different years showed dispersed distributions in phylogenetic tree, which was no obvious tendency of the distribution for years and geography. Otherwise, with the analyses of genetic distance between and within mumps virus strains groups in 2006, 2007 and 2008, it was found that the mumps sequences in 2006-2008 were no obvious regular variation, which were similar with the results of homology and phylogenetic analyses. CONCLUSION: It suggested that F genotype of mumps virus was the predominant genotype in 2006-2008, and the mumps prevailed in recent years was mainly caused by F genotype mumps viruses with multi-transmission routes. However, the mumps viruses circulated during 2006 to 2008 were different from those in 1995,these mumps virus occured genetics evolution in some extent during 14-year period from to 2008. Furthermore, comparing with other genotype mumps strains from other countries, there were 5 shared nucleotides mutations (C(Nt65),C(Nt105), G(Nt137), C(Nt192), C(Nt239)) in SH gene in all Chinese F genotype mumps viruses. However, these mutations were not found in the other genotype of mumps virus.


Subject(s)
Mumps virus/genetics , Mumps/virology , China , Genotype , Molecular Sequence Data , Mumps virus/classification , Mumps virus/isolation & purification , Phylogeny , Viral Proteins/genetics
15.
Zhongguo Yi Miao He Mian Yi ; 15(1): 14-8, 2009 Feb.
Article in Chinese | MEDLINE | ID: mdl-20077669

ABSTRACT

OBJECTIVE: A SYBR Green real-time RT-PCR assay was developed to detect mumps virus gene rapidly. METHODS: The primers were selected based on SH gene of mumps virus, the assay was optimized in reactive system and condition to improve the sensitivity and specificity. The SH gene of 5 mumps virus isolates were detected and genotyped using this assay. RESULTS: A SYBR Green real-time RT-PCR assay had good sensitivity and specificity. There was no cross reaction with other respiratory virus. The detection limit of the assay was 10 TCID50. The sensitivity of the two assays, RT-PCR and real-time RT-PCR, was not different. Compared with traditional RT-PCR, real-time RT-PCR saved half detection time. The products of SYBR Green real-time RT-PCR were directly sequenced and genotyped. CONCLUSIONS: SYBR Green real-time RT-PCR was a rapid, specific and sensitive method for the detection of mumps virus and genotyping.


Subject(s)
Mumps virus/isolation & purification , Mumps/virology , Reverse Transcriptase Polymerase Chain Reaction/methods , Viral Proteins/genetics , Benzothiazoles , Diamines , Humans , Molecular Sequence Data , Mumps virus/classification , Mumps virus/genetics , Mumps virus/metabolism , Organic Chemicals/metabolism , Phylogeny , Quinolines , Sensitivity and Specificity
16.
Zhonghua Liu Xing Bing Xue Za Zhi ; 26(11): 861-3, 2005 Nov.
Article in Chinese | MEDLINE | ID: mdl-16676605

ABSTRACT

OBJECTIVE: To analyze the changing of age patterns among rubella patients after implementing rubella vaccine immunization to children in Shandong province since 1995. METHODS: Epidemiologic data on rubella through surveillance system for suspected measles from 1999 to 2004 and data on rubella vaccination were used and analyzed. RESULTS: The annual average incidence rate of rubella from 1999 to 2004 had been 0.59 per 100 thousands population while 81.17% of cases were concentrated during the outbreaks. 77.77% of the cases were school children between 7-15 years old and 7.93% of the cases were under 7 years old. The age-median of cases were 10.37, 11.66, 11.41, 12.81, 14.28 and 13.96 years old from 1999 to 2004, respectively. The estimated coverage of rubella vaccine for pre-school children was about 60% but only 20% were for school children. CONCLUSION: The peak age of cases moved from youth towards adolescence which indicated that women with child-bearing age might have been under risk of developing the congenital rubella syndrome (CRS). It is necessary to carry out screening test of rubella antibody and vaccination to women with child-bearing age and the immunization strategy should be established to guide the control of rubella and CRS.


Subject(s)
Rubella/epidemiology , Rubella/prevention & control , Vaccination/statistics & numerical data , Viral Vaccines/immunology , Adolescent , Adult , Age Distribution , Child , Child, Preschool , China/epidemiology , Disease Outbreaks , Humans , Immunization Schedule , Infant , Infant, Newborn , Rubella/complications , Young Adult
17.
Zhonghua Liu Xing Bing Xue Za Zhi ; 25(5): 417-20, 2004 May.
Article in Chinese | MEDLINE | ID: mdl-15231169

ABSTRACT

OBJECTIVE: To study the incidence of cases with rash and fever illness (RFIs) after measles vaccine (MV) inoculation. METHODS: During 1999 to 2002, 150 RFIs cases reported by the special measles surveillance system in Shandong province, China, were investigated and analyzed epidemiologically. RESULTS: 7 674 690 ml MV were distributed during 1999 to 2002 and the annual average incidence of RFIs cases after MV inoculation was 0.20/10 000 ml (0.2 ml per dose). There was significant difference of incidences each year (chi(2) = 10.13, P < 0.05). All RFIs cases were sporadically distributed without epidemiological links. Clinical symptoms showed that 88.67% of the 150 RFIs cases having > 38.5 degrees C fever and 75.33% of all cases appeared typical rash after 4 to 11 days (the medium was 8 days) after MV inoculation. The order of rash onset among RFIs cases was consistent with that of regular measles cases caused by wild virus. 68.67% of the RFIs cases had first MV inoculation and 94.71% were 8 to 12 month-olds. IgM sera antibody test from RFIs cases were rubella negative and 45.65% positive for measles. CONCLUSION: RFIs due to allergic reaction or measles vaccine virus infection might occur after MV inoculation. There seemed to be a correlation between RFIs incidence and the doses of MV. Measles virus genotype analysis needs to be carried out to confirm if the onset of some RFIs cases is aetiologically associated to MV vaccine virus infection.


Subject(s)
Exanthema/etiology , Fever/etiology , Measles Vaccine/adverse effects , Measles/prevention & control , Exanthema/virology , Fever/virology , Humans , Measles virus/immunology , Polymerase Chain Reaction , Vaccination
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