1.A case-control study on the risk factors of hand, foot and mouth disease in children in Tianjin.
Wen-Ti XU ; Lu GAO ; Ying ZHANG
Chinese Journal of Epidemiology 2009;30(1):100-101
Animals
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Case-Control Studies
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Child
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Child, Preschool
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China
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epidemiology
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Female
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Foot-and-Mouth Disease
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epidemiology
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Humans
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Infant
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Infant, Newborn
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Male
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Risk Factors
2.Study on risk factors and serologic status among brucellosis inapparent infection farmers in Tianjin, 2007.
Ying ZHANG ; Wen-Ti XU ; Jie-Ying YIN
Chinese Journal of Epidemiology 2008;29(9):949-950
Adult
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Brucellosis
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epidemiology
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Case-Control Studies
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China
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epidemiology
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Female
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Humans
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Male
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Occupational Exposure
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Risk Factors
4.A review of the epidemiology and economic burden of herpes zoster and postherpetic neuralgia
Tianjin Medical Journal 2018;46(5):552-556
Herpes zoster is a kind of acute viral infection caused by varicella zoster virus.The postherpetic neuralgia is the main complication of herpes zoster.Herpes zoster and postherpetic neuralgia cause huge disease burden and economic burden in the world. In this paper, we reviewed the epidemiological characters and economic burden of herpes zoster and postherpetic neuralgia based on the latest studies,and provided a new research direction for prevention and treatment for our country.
5.Genetic characterization of measles virus caused the measles outbreak in Xinjiang.
Mai-mai-ti MIJITI ; Hui-ling WANG ; Song-tao XU ; Nai-ying MAO ; Wen-bo XU ; Yan ZHANG
Chinese Journal of Experimental and Clinical Virology 2010;24(5):337-339
OBJECTIVETo analyze the genetic characterizations of wild type measles viruses caused the measles outbreak in Xinjiang.
METHODSVero/Slam cell were used for measles viruses isolation from the specimens collected from measles outbreaks patients. Fragment of 676 nucleotide acids of the carboxylend of nucleoprotein gene were amplified using reverse transcription-polymerase chain reaction (RT-PCR) method and then the PCR products were directly sequenced and analyzed. Phylogenetic tree was constructed based on 450 nucleotide acids of the N-terminus of nucleoprotein gene, and homological analysis was performed at nucleotide acid level.
RESULTS11 measles viruses were sequenced and all belonged to H1a subgenotype. The nucleotide difference was 0-0.2% between 11 Xinjiang isolates. And the nucleotide difference was 2.2%-2.4% between Xinjiang isolates and H1 genotype reference strain.
CONCLUSIONThe Measles viruses causing the measles outbreak in Xinjiang were H1a subgenotype.
China ; epidemiology ; Disease Outbreaks ; Humans ; Measles ; epidemiology ; virology ; Measles virus ; classification ; genetics ; isolation & purification ; Molecular Sequence Data ; Nucleoproteins ; genetics ; Phylogeny ; Viral Proteins ; genetics
7.Thyroid nodular diseases in the population indergoing medical examination and the analysis of its relative factors in Dalian City,Liaoning Province
Xiao-fang, PAN ; Xi-yan, SUN ; Xiao-dong, JIA ; Feng, XU ; Ti, ZHAO ; Ting, JIANG ; Zheng-nan, GAO ; Xiao-hong, GAO ; Xiao-Feng, LI ; Wen-fei, QIN ; Xi-zhuo, SUN
Chinese Journal of Endemiology 2009;28(5):568-571
Objective To investigate the characteristics about the prevalence of thyroid nodules detected on color Doppler uhrasonography(US) in people residing in Dalian City who undergo regular physical examinations, as well as its relative factors. Methods All thyroid sonographic and questionair procedures were performed in the 6020 people above 18-year-old living in the four districts of Dalian City for at least 5 years, who were examined at the department of health medical center of Dalian Municipal Central Hospital from May 2006 to March 2007. Urinary iodine concentration was measured in 2039 healthy adults selected by age layers in our study population. Moreover, urinary iodine concentrations were determined in 220 children aged 8-10 years old who were randomly chosen from four communities (55 children per elementary school from each community). The analysis of logistic regression was conducted for the risk factors linked to thyroid nodules. Results The prevalence of thyroid nodules in the 6020 adults was 38.5%(2319/6020), in which nodules sized between 0.3 and up to 0.5 cm were found in 17.1% (1030/6020), and those above 0.5 cm in 21.4% (1289/6020). Ultrsonography revealed solitary nodules in 17.2% (1036/6020), multinodular goiter in 21.3% (1283/6020). Fifty-four point nine percent (1272/2319) thyroid nodules showed solid internal echographic structures, 30.2%(701/2319) mixed and 14.9%(346/2319). The thyroid nodule detected rate in female individuals was 46.1% (1102/2393), among whom multinodular goiter [59.1% (651/1102)] was more than solitary nodules[40.9(451/1102)] in female; while only 33.6%(1217/3627) of male were detected to have thyroid nodule, there was a difference between the genders (χ2=95,079,P<0.01). The mediam urinary iodine concentration(MUI) was 184.32 μg/L in children and 216.75 μg/L in the health adults, moreover, it was 216.55 μg/L and 217.00 μg/L in the people with thyroid nodules and those without nodules without a significant difference (P>0.05). The rate of thyroid nodules gradually increased with age(χ2=344.998, P<0.01). The occurance of thyroid nodules was significant associated with gender and age(P<0.01). Conclusions The nutritional iodine intake in the four communities of Dalian City are adequate. The prevalence of thyroid incidentalomas is relatively high in this group of people receiving medical examination.
8.The Detection of Clonal IgH Gene Rearrangement in Bone Marrow and Peripheral Blood from B-NHL Patients and Its Clinic Significance
Zhen-Ling LI ; Ti SHEN ; Xiao-Neng LI ; Jie CHEN ; Shu-Jie WANG ; Shao-Hua XU ; Chang-Wen GE ; Yong-Ji WU
Journal of Experimental Hematology 2001;9(2):135-138
To evaluate the significance of bone marrow (BM) and peripheral blood (PB) cells with clonal gene rearrangement of the third complementary determining region of immunoglobulin heavy chain (IgHCDR3) in the diagnosis, clinical staging, determination of treatment effects and prediction of relapse in B-NHL, clonal IgH gene rearrangement of BM from 46 and PB from 38 cases with B-NHL were tested by semi-nested polymerase chain reaction (SnPCR) and polyacrylamide gel electrophoresis before treatment, and ten of them were tested in complete remission after treatment. Results showed that this method was applicable to detecting one clonal IgHCDR3 gene rearrangement positive cell from up to 1 000 normal cells. Specificity of detection was 97%. Clonal IgHCDR3 rearrangement was shown in all 3 cases of BM and 2 of PB specimens with morphologic involvement. The clonal IgHCDR3 was detected in 65.1% of the BM and 44.4% of the PB without morphologic involvement in untreated patients with B-NHL, independent of Ann Arbor staging and systemic symptoms. In 10 cases of B-NHL with clonal IgHCDR3 rearrangement in diagnostic tissues, the molecular marker became negative in 7 patients who entered and remained in complete remission. Two cases relapsed in whom clonal IgHCDR3 rearrangements were detected in serial samples of BM or PB after autologous PBSCT. One patient in whom clonal IgHCDR3 rearrangement was detected at 10 months post-PBSCT remained in complete remission up to now. It was concluded that clonal IgHCDR3 gene rearrangements were found in BM and PB from B-NHL patients without morphologic abnormality. Persistence of molecular marker-positive may be associated with relapse for patients in complete remission, and the patients without clonal IgHCDR3 rearrangement will be in continuous complete remission. Little is known about a few patient who was a long-term disease-free survivor despite the presence of PCR-IgH rearrangement in the marrow.
9.Analysis of etiology of four pandemic influenza A (H1N1) virus outbreaks in Shandong province, in 2009.
Zhong LI ; Ti LIU ; Yi LIN ; Sheng-Yang ZHANG ; Jun LIU ; Wen-Guo JIANG ; Xian-Jun WANG ; Ai-Qiang XU ; Zhen-Qiang BI
Chinese Journal of Preventive Medicine 2010;44(12):1069-1074
OBJECTIVETo isolate and identify the influenza virus that caused four influenza-like-illness outbreaks in Jining city of Shandong Province in 2009 and analyze the genetic characteristics of hemagglutinin (HA) and neuraminidase (NA) gene, the variation of these genes were studied.
METHODS34 nasopharyngeal swabs from fever patients of four influenza-like-illness outbreaks were collected and diagnosed by real time quantitative RT-PCR method. The positive samples were incubated and cultured for virus. HA and NA genes of isolated pandemic influenza A (H1N1) virus were sequenced, the homology analysis was done with DNAStar software and the genetic evolution and amino acid substitutions were performed with Mega 4.0 software. The sequences were compared with WHO recommended vaccine virus, native reference virus.
RESULTSSeventeen of 34 nasopharyngeal swabs were positive, 11 pandemic influenza A (H1N1) viruses were isolated and HA and NA genes of 7 strains were sequenced. Phylogenetic analysis for hemagglutinin and neuraminidase gene of Shandong outbreak strains showed that there were 98.4% - 99.6% and 99.2% - 100.0% sequence identity. Compared with WHO-recommended vaccine strain, the reference virus in mainland China strain, eleven amino acids were changed for HA protein, including position 38, 40, 56, 90, 100, 145, 172, 173, 220, 303 and 338, and 38, 40, 303 of HA protein were located in the antigenic determination C cluster, 172, 173 in the D cluster, 56 in the E cluster, site 40 of HA protein were glycosylated. In NA protein, seven amino acids were changed, including position 80, 106, 241, 248, 351, 369 and 386, site 40 of NA protein were glycosylated. No mutations of 275 in NA protein were found.
CONCLUSIONThe HA and NA genes of the epidemic strains showed high homology, some mutations in the HA and NA proteins were found, the antigenic site and glycosylation site of some strains were changed during the epidemic process.
China ; epidemiology ; Disease Outbreaks ; Glycosylation ; Hemagglutinin Glycoproteins, Influenza Virus ; genetics ; Humans ; Influenza A Virus, H1N1 Subtype ; classification ; genetics ; isolation & purification ; Influenza, Human ; epidemiology ; virology ; Neuraminidase ; genetics
10.Dairy Consumption and Associations with Nutritional Status of Chinese Children and Adolescents.
Pei Pei XU ; Ti Ti YANG ; Juan XU ; Li LI ; Wei CAO ; Qian GAN ; Xiao Qi HU ; Hui PAN ; Wen Hua ZHAO ; Qian ZHANG
Biomedical and Environmental Sciences 2019;32(6):393-405
OBJECTIVE:
This study aimed to describe frequency and quantity of total dairy consumption of Chinese children and adolescents and explore the associations between dairy consumption and nutrition status, including stunting, wasting, overweight, and obesity.
METHODS:
Participants included 28,250 children and adolescents aged 6-17 years old. A food frequency questionnaire (FFQ) including 100 kinds of food was used to collect information about frequency and quantity of dairy consumption. Determination of stunting was with a height cutoff value for age and gender, and determination for wasting, overweight, and obesity was with BMI for age and gender.
RESULTS:
Of the total sample, 36.1% of children aged 6-17 reported consuming dairy food more than once per day (⪖ 1/day). The average total dairy intake of all the participants was 126.7 g/day. For boys, dairy consumption had an inverse correlation with stunting and wasting after controlling for confounders. For girls, dairy consumption was negatively associated with stunting and obesity after controlling for confounders as above.
CONCLUSION
Dairy consumption in Chinese children and adolescents was relatively lower than that in developed countries, and was negatively associated with stunting and wasting for boys and with stunting and obesity for girls.
Adolescent
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Child
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China
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epidemiology
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Dairy Products
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statistics & numerical data
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Female
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Growth Disorders
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epidemiology
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Humans
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Male
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Nutrition Surveys
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Nutritional Status
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Pediatric Obesity
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epidemiology
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Wasting Syndrome
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epidemiology