1. Current status of body mass index and related influencing factors in the elderly aged 65 years and older in 8 longevity areas in China
Yingjian ZHANG ; Yuebin LYU ; Jinhui ZHOU ; Feng ZHAO ; Yingli QU ; Ling LIU ; Yingchun LIU ; Jiaonan WANG ; Zhaojin CAO ; Shiman RUAN ; Xiaoming SHI
Chinese Journal of Epidemiology 2020;41(1):25-30
Objective:
To understand the current status of BMI of the elderly and related factors in longevity areas in China, and provide scientific evidence for the control of BMI level in elderly population.
Methods:
Data used in this study were obtained from Healthy Aging and Biomarkers Cohort Study, a sub-cohort of the Chinese Longitudinal Healthy Longevity Survey. A total of 2 825 elderly in 8 longevity areas in China were surveyed and measured in 2017. The BMI levels of 2 217 elderly aged 65 years and older were calculated and in follow up. The ordered classification logistic regression model was used to analyze the influencd factors for the BMI in the elderly.
Results:
The BMI of the elderly in 8 longevity areas in China was (22.36±3.87) kg/m2, and it was (22.76±3.58) kg/m2 for males and (21.75±3.98) kg/m2 for females. The BMI levels were normal in 1 165 elderly persons. The prevalence of underweight, overweight and obesity were 15.8
2.Effect of miR-191 on the proliferation of malignant meningioma cell through EGR1/TP53 signaling pathway
Shuangjun PAN ; Yupei YANG ; Yong HOU ; Shanping RUAN ; Jie WANG ; Jianfeng WANG ; Xiaoming HU ; Yizheng ZANG
Chinese Journal of Endocrine Surgery 2018;12(6):497-501,521
Objective To study the influence of miR-191 expression on the proliferation of human malignant meningioma cell line IOMM-Lee in vitro and to explore its mechanism.Methods The expression of miR-191 in malignant meningioma tissue,the adjacent normal tissues and human Malignant meningioma cell lines IOMM-Lee and CH157-MN was tested by Realtime PCR.miR-191 inhibitor was transfected in IOMM-Lee cells and MTT assay was employed to detect the cell viability.Bioinformatics prediction software was used in miR-191 target gene predictive analysis and verified by luciferase reporter system.The effect of EGR1 siRNA on the proliferation of IOMM-Lee cells was observed.Prorein interaction database was used to analyze which proteins could interact with EGR1.The effect of inhibition of EGR1 expression on TP53 protein expression was detected.The influence of inhibition of miR-191 expression on EGR1and TP53 expression was observed.Result The expression of miR-191 in malignant meningioma tissue (0.933±0.144) was higher than that in the adjacent normal tissue (0.459±0.104,P<0.05).The expressiong of miR-191 in humam malignant meningioma cell line IOMM-Lee (1.25±0.07) was higher than that in CH157-MN cell line (0.50±0.14,P<0.05).The cell proliferation capability was significantly decreased in miR-191 inhibitor group [(0.53±0.02) vs (0.74±0.01),P<0.05].EGR1 was identified and validated to be a target gene of miR-191.Inhibition of EGR1 gene can promote OMM-Lee cell proliferation (0.83±0.02,0.71 ±0.01,P<0.05).EGR 1 could positively regulate TP53 protein expression [(13 758.17±57.22) vs (10 239.00±71.30),P<0.001.miR-191 Inhibition could increase EGR1 [(14 663.00±80.08) vs (11 184.33±153.90),P<0.001] and TP53 expression [(15 206.17±102.08) vs(11 400.17±97.00),P<0.001].Conclusion Downregulation of miR-191 can inhibit the proliferation of IOMM-Lee cell,which may be related to the upregulation of EGR1/TP53 signaling pathway.
3. A long-term follow-up study of 82 children with acute myeloid leukemia
Min RUAN ; Benquan QI ; Fang LIU ; Tianfeng LIU ; Xiaoming LIU ; Xiaojuan CHEN ; Wenyu YANG ; Ye GUO ; Li ZHANG ; Yao ZOU ; Yumei CHEN ; Xiaofan ZHU
Chinese Journal of Pediatrics 2018;56(10):730-734
Objective:
To investigate the efficacy and the prognostic factors of Chinese Academy of Medical Sciences 2005 (CAMS-2005) regimen in the treatment of pediatric acute myeloid leukemia (AML).
Methods:
Eighty-eight cases of newly-diagnosed AML patients, who were treated with the CAMS-2005 regimen from April 2005 to July 2009, were enrolled in this case observational study. Clinical characteristics, long-term prognosis and prognostic factors were analyzed retrospectively. Overall survival (OS) and event free survival (EFS) rates were estimated by the Kaplan-Meier method. Rates of survival between the groups were compared by the Log-rank test. Prognostic factors were evaluated by COX regression analysis.
Results:
A total of 82 cases were enrolled in this study, including 34 core binding factor(CBF)-AML patients and 48 non-CBF-AML patients. There were 45 males and 37 females. The median age at diagnosis was 8.0 (0.7-16.0) years. During the induction therapy, 3 patients (4%) developed treatment-related early-death, while 63 patients (77%) achieved complete remission (CR) and 53 patients (65%) achieved CR after 1 course. Twenty-one patients (33%) had relapsed disease. The CR rates of CBF-AML patients and non-CBF-AML patients were 91% (31/34) and 67% (32/48) (χ2=5.410,
4. Study on autophagy in nucleated red blood cells in patients with myelodysplastic syndromes
Liyan YANG ; Huaquan WANG ; Rong FU ; Wen QU ; Erbao RUAN ; Xiaoming WANG ; Guojin WANG ; Yuhong WU ; Hong LIU ; Jia SONG ; Jing GUAN ; Limin XING ; Lijuan LI ; Huijuan JIANG ; Hui LIU ; Yihao WANG ; Chunyan LIU ; Wei ZHANG ; Zonghong SHAO
Chinese Journal of Hematology 2017;38(5):432-436
Objective:
To investigate the change of autophagy level of bone marrow nucleated red blood cell (RBC) in patients with myelodysplastic syndromes (MDS) .
Methods:
Fifty-four MDS patients and thirty-three controls were enrolled in this study. The mitophagy were observed by transmission electron microscopy (TEM) . The level of autophagy-associated protein LC3B in GlycoA+ nucleated RBC was measured by flow cytometry. The expressions of ULK1 and mTOR mRNA in GlycoA+ nucleated RBC were measured by real-time PCR. The expression of the mitochondrial outer membrane protein TOM20 in GlycoA+ nucleated RBC was detected by Western blot.
Results:
Autophagosomes or autolysosomes were scarcely observed by TEM in MDS patients. The expression of LC3B in GlycoA+ nucleated RBC in high-risk MDS patients (0.22±0.12) was significantly lower than that in normal controls (0.43±0.22,
5. Heterogeneity and clonal evolution in pediatric ETV6-RUNX1+ acute lymphoblastic leukemia by quantitative multigene fluorescence in situ hybridization
Li ZHANG ; Linping HU ; Xiaoming LIU ; Ye GUO ; Wenyu YANG ; Jiayuan ZHANG ; Fang LIU ; Tianfeng LIU ; Shuchun WANG ; Xiaojuan CHEN ; Min RUAN ; Benquan QI ; Lixian CHANG ; Yumei CHEN ; Yao ZOU ; Xiaofan ZHU
Chinese Journal of Hematology 2017;38(7):586-591
Objective:
To evaluate heterogeneity and clonal evolution in pediatric ETV6-RUNX1+ acute lymphoblastic leukemia (ALL) in China.
Methods:
Totally 48 children (<14 years) with newly diagnosed ETV6-RUNX1+ ALL in Institute of Hematology and Blood Disease Hospital, CAMS and PUMC, from February 2006 to June 2011 were included. The copy number variations were analyzed by quantitative multigene fluorescence in situ hybridization (QM-FISH) in 48 patients. Non-normal distribution of measurement data were shown with Median (range) , count data were shown with percent (%) . Overall survival and event-free survival were estimated by the Kaplan-Meier method and compared with the log-rank test.
Results:
Forty-eight patients were tested by QM-FISH. Of 48 patients, 70.8% harbored one clone, 18.8% two subclones, and 10.4% three or more subclones. The clone heterogeneity was detected by two different models: the linear succession model and the branching evolution model. ETV6-RUNX1+ ALL relapse evolved from an ancestral clone or a new clone. The patients relapsed from a new clone got the worse outcome.
Conclusion
The clone evolution was detected in pediatric ETV6-RUNX1+ ALL in China. QM-FISH might be helpful to evaluate the outcome of relapsed patients. A new clone was associated with a poorer outcome.
6. Characteristic and function of peripheral blood mononuclear cells-induced macrophages in patients with myelodysplastic syndrome
Yu HAN ; Huaquan WANG ; Rong FU ; Wen QU ; Erbao RUAN ; Xiaoming WANG ; Guojin WANG ; Yuhong WU ; Hong LIU ; Jia SONG ; Jing GUAN ; Limin XING ; Lijuan LI ; Huijuan JIANG ; Hui LIU ; Yihao WANG ; Chunyan LIU ; Wei ZHANG ; Zonghong SHAO
Chinese Journal of Hematology 2017;38(8):706-709
Objective:
To explore characteristic and function of peripheral blood mononuclear cells (PBMNC) -induced macrophages in patients with myelodysplastic syndrome (MDS) to couple with its progression.
Methods:
A total of 24 MDS patients (11 low-risk patients and 13 high-risk group patients) referred to Department of Hematology of Tianjin Medical University General Hospital and normal controls were enrolled from September 2014 to December 2015. PBMNC was stimulated with GM-CSF to transform to macrophages. The morphology of macrophages was observed by microscope. The quantity of macrophages, CD206 and SIRPα on surface of macrophages were detected by flow cytometry. The phagocytic function of macrophages was analyzed by fluorescence microscopy and flow cytometry.
Results:
The morphology of macrophages from MDS patients was abnormal. The percentage of transformed macrophages was (5.17±3.47) % in patients with MDS, which was lower than that in controls significantly[ (66.18±13.43) %,
7.Significance of ikaros family zinc finger 1 deletion in pediatric B-acute lymphoblastic leukemia without reproducible cytogenetic abnormalities.
Xiaoming LIU ; Li ZHANG ; Yao ZOU ; Lixian CHANG ; Wei WEI ; Min RUAN ; Yumei CHEN ; Wenyu YANG ; Xiaojuan CHEN ; Ye GUO ; Shuchun WANG ; Tianfeng LIU ; Jiayuan ZHANG ; Fang LIU ; Benquan QI ; Wenbin AN ; Xiaofan ZHU
Chinese Journal of Pediatrics 2016;54(2):126-130
OBJECTIVETo identify ikaros family zinc finger1 (IKZF1) deletion in patients with pediatric B cells-acute lymphoblastic leukemia (B-ALL) without reproducible chromosomal abnomalities and further investigate its value in this part of patients' pathogenesis and prognosis.
METHODThe study was approved by the institutional review board of the authors' hospital and informed consent was obtained from the patients and/or their legal guardians. Data of 96 children with B-ALL patients without reproducible cytogenetic abnormalities whose bone marrows specimens were enough for DNA extraction for the detection were retrospectively selected. All the patients were diagnosed and systematically treated according to CCLG-ALL2008 in our hospital from April 2008 to April 2013. The 96 patients were divided into two groups according to the result of IKZF1's detection by multiplex ligation-dependent probe amplification (MLPA): The cases that with any of eight exons of IKZF1 deleted were entered into"Group with IKZF1 deletion"otherwise entered"Group without IKZF1 deletion". Disease free survival (DFS), event-free survival (EFS) and overall survival (OS) were compared between the two groups.
RESULTNineteen out of 96 B-ALL patients without reproducible cytogenetic abnormalities had IKZF1 deletion (20%). Three of 19 patients with IKZF1 deletions of the whole gene; ten of 19 patients with IKZF1 deletions of exon 1; 4 of 19 patients with IKZF1 deletions of exons 4-7; one of 19 patients with IKZF1 deletions of exons 2-7 and one of 19 patients with IKZF1 deletions of exons 1-6. Whose white blood cell (WBC) ≥ 50 × 10(9)/L inIKZF1 diletion group was more than whthout IKZF1 deletion group(42% vs. 13%, P=0.004). Patients with IKZF1 deletions had a lower 3-year DFS (0.67 ± 0.13 vs. 0.93 ± 0.04, P=0.001); EFS (0.67 ± 0.13 vs. 0.90 ± 0.04, P = 0.012) and OS(0.79 ± 0.09 vs. 0.96 ± 0.02, P=0.010) compared to those without IKZF1 deletions. Excluding the influence of sex, age, WBC count at diagnosis, cerebrospinal fluid state and prednisone response IKZF1 deletion still affected the patients' DFS, EFS and OS ( P<0.05 for all comparisons).
CONCLUSIONSome of pediatric B-cell precursor ALL without reproducible cytogenetic abnormalities had been detected to have IKZF1 deletion; IKZF1 deletion is an independent poor prognostic factor in these patients.
Child ; Chromosome Aberrations ; Disease-Free Survival ; Exons ; Gene Deletion ; Humans ; Ikaros Transcription Factor ; genetics ; Multiplex Polymerase Chain Reaction ; Precursor B-Cell Lymphoblastic Leukemia-Lymphoma ; genetics ; Prognosis ; Zinc Fingers
8.The impact of long- and short-time blood pressure variability on glomerular filtration rate in elderly population.
Yang WANG ; Xiaoming ZHENG ; Shasha AN ; Zhifang LI ; Wenyan ZHANG ; Chunhui LI ; Hualing ZHAO ; Lu SONG ; Shuohua CHEN ; Yao ZHENG ; Chunyu RUAN ; Shouling WU
Chinese Journal of Cardiology 2016;44(1):60-67
OBJECTIVETo investigate the impact of long-time and short-time blood pressure variability (BPV) on glomerular filtration rate (eGFR) in elderly population.
METHODSA total of 2 464 participants aged of ≥60 years old without history of stroke and coronary heart disease were selected with random sampling method from the individuals underwent health check up in Tangshan Kailuan Hospital, Kailuan Linxi Hospital, Kailuan Zhaogezhuang Hospital between 2006 and 2013. The study participants were asked to join a face-to-face interview every two years. Long-time BPV was defined as the standard deviation of all SBP values at the baseline visit and following visits, short-time BPV was defined as the standard deviation of day time blood pressure and night time blood pressure which was derived from 24 hours ambulatory blood pressure monitoring. Multivariate linear regression models were used to test the impact of long- and short-time BPV on eGFR.
RESULTSThe study included 3 participants groups including the long-time SBPV group (2 279 participants), the short-time SBPV group (1 636 participants) and the long- plus short-time SBPV group (1 632 participants). Participants were further sub grouped by median value (NO.1
CONCLUSIONThe higher day time SBPV is associated with reduced eGFR in the elderly population.Clinical Trail Registry Chinese Clinical Trial Registry, ChiCTR-TNC-11001489.
Aged ; Blood Pressure ; Blood Pressure Monitoring, Ambulatory ; Coronary Disease ; Glomerular Filtration Rate ; Humans ; Time Factors
9.Copy number variations in pediatric ETV6/RUNX1 positive acute lymphoblastic leukemia.
Yao ZOU ; Li ZHANG ; Xiaoming LIU ; Ye GUO ; Wenyu YANG ; Jiayuan ZHANG ; Fang LIU ; Tianfeng LIU ; Shuchun WANG ; Xiaojuan CHEN ; Min RUAN ; Benquan QI ; Lixian CHANG ; Yumei CHEN ; Xiaofan ZHU
Chinese Journal of Pediatrics 2016;54(3):209-213
OBJECTIVETo evaluate the copy number variations (CNVs) in pediatric ETV6/RUNX1 gene positive acute lymphoblastic leukemia(ALL) and its correlation with clinical features and prognosis.
METHODTotally 141 children (<14 years of age) with newly diagnosed ETV6/RUNX1 positive ALL in Institute of Hematology and Blood Diseases Hospital, were included from January 2006 to November 2012. The CNVs were analyzed by multiplex ligation-dependent probe amplification (MLPA). The survival rate between the patients with CNVs were explored. Overall survival (OS) and event-free survival (EFS) were estimated by the Kaplan-Meier method and compared with the log-rank test.
RESULTAmong the 141 cases, 55.3% (n=78) were boys and 44.7% (n=63) were girls and the median age was 4 (1-13) years. The estimated 5-year DFS rate for the patients was (84±4)%. The estimated 5-year OS rate for the patients was (85±4)%. Ninety-five patients were tested MLPA. CNVs were detected in 73 cases (76.8%). CNVs of genes EBF1(15.8%), CDKN2A/2B(18.9%), PAX5(21.1%), ETV6(54.8%), BTG1(10.5%) were detected in more than 10% of the patients. Among the 95 patients, EBF1 deletions were found in 9 patients and EBF1 amplifications were found in 6 patients; 5-year recurrence-free survival (RFS) was statistically significant among 3 groups (χ(2)=9.809, P=0.007) . PAX5 deletions were found in 13 patients and PAX5 amplifications were found in 7 patients; the difference in 5-year RFS was statistically significant between 3 groups(χ(2)=7.622, P=0.022). ETV6 deletions were found in 39 patients and ETV6 amplifications were found in 13 patients; the difference in 5-year RFS was statistically significant among the 3 groups (χ(2)=11.045, P=0.004).
CONCLUSIONThe CNVs had prognostic relevance in ETV6/RUNX1 positive ALL.
Adolescent ; Child ; Core Binding Factor Alpha 2 Subunit ; DNA Copy Number Variations ; Disease-Free Survival ; Humans ; Multiplex Polymerase Chain Reaction ; Precursor Cell Lymphoblastic Leukemia-Lymphoma ; Prognosis ; Proto-Oncogene Proteins c-ets ; Repressor Proteins ; Survival Rate
10.Application of transparent film dressing in fistula nursing of patients with PCN
Meiyan WANG ; Xiangni WANG ; Jiying SUN ; Ruixia RUAN ; Jianrui NIU ; Xiaoming LIU ; Yonghong WU
Chinese Journal of Modern Nursing 2016;22(32):4721-4724
Objective To evaluate the clinical application effect of transparent film dressing in fistula nursing of patients with percutanueous nephrostomy (PCN).Methods By using before-after self control study method,40 patients with pelvic tumor that caused by postrenal renal failure,and needed long-term fistula remained after PCN surgery were selected as the research object.Conventional sterile gauze and tape were used to nurse the fistula before intervention and transparent film dressing was used after intervention.Results Patents always worried about trachea cannula exodus and infection before intervention.After intervention,the comfort degree of their daily life (like showering,sleeping and daily activities) was obviously higher than that before intervention (P<0.01).The incidence of renal fistula local adverse effect after intervention is relatively low.And the difference was statistically significant (P< 0.01).Before intervention,the tape was loosing in (5.47 ± 1.48) days,there were three cases of accidental trachea cannula exodus;and after intervention,transparent film dressing hemmed in (14.22±1.99) days,and no accidental trachea cannula exodus occurred (P<0.01);and no hyper-sensitive cases happened with the transparent film dressing.Conclusions The transparent film dressing has the advantages of stable viscosity,waterproofing,fungi-proofing,breathability and hypoallergenic,etc.It can well protect and fix the fistula,and it is suitable for nursing care of patients with long-term renal fistula.

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