1.The Application Value of Improved Intermittent Compression Strain Elastography in Improving Stability of Breast Elastography and Ability to Distinguish Benign and Malignant Nodules
Qingwen KANG ; Daozhong HUANG ; Ying ZHAO
Acta Medicinae Universitatis Scientiae et Technologiae Huazhong 2023;52(6):858-862
Objective To investigate the application value of improved intermittent compression strain elastography in im-proving the image stability of breast elastography and the identification ability of benign and malignant nodules.Methods In all,113 patients(138 breast lesions)were recruited in this study,who accepted high frequency color Doppler ultrasound,im-proved intermittent compression strain elastography(IICSE)and nonintermittent compression strain elastography(NCSE)one week ahead of the surgery.By comparing the first three times of IICSE and NCSE,the same elastic result rate was obtained,and the receiver operating characteristic(ROC)curve of IICSE and NCSE elastic score was drawn to identify benign and malignant breast lesions,and the area under the curve(AUC)was calculated,and those with larger AUC area were selected to adjust the classification of BI-RADS.To compare the difference of diagnosis of benign and malignant breast lesions of different BI-RADS classification by high-frequency color ultrasound and high-frequency color ultrasound combined with IICSE,and the difference of the composition ratio of nodules classified by different BI-RADS.Results The consistency rate of elastic results obtained by IICSE was higher than that of NCSE(90.6%vs.34.8%,P<0.05).ROC curve showed that the area under the curve(AUC)of IICSE was greater than that of NCSE(0.865 vs.0.636,P<0.05).Comparing the results before and after high-frequency color ultrasound combined with IICSE,the number of BI-RADS type 3 and type 5 nodules increased significantly,while the number of BI-RADS type 4 nodules decreased(both P<0.05).Conclusion IICSE improves low stability of conventional elastic ima-ging.At the same time,IICSE reduces the number of patients who need further examination,reducing overuse of medical re-sources.
2.Study of left atrial diameters and prothrombotic state in senile patients with hypertension and atrial fibrillation
Qingwen ZHANG ; Yide MIAO ; Liping KANG ; Lin SU ; Wei LI
Chinese Journal of Geriatrics 2012;31(3):182-184
Objective To explore the relationship between left atrial diameters (LAD) and prothrombotic state in senile patients with hypertension (HT) and atrial fibrillation (AF). Mcthods Totally 105 patients with cssential hypertension were divided into 65 patients with atrial fibrillation and 40 cases without atrial fibrillation,and then patients with atrial fibrillation were subgrouped into paroxysmal and persistent atrial fibrillation groups.30 healthy people without hypertension and atrial fibrillation were used as control group.LAD was determined by M type ultrasound cardiogram.Fibrinogen (Fg),D-Dimer(D-Dimer),von willebrand (vwF) and haematocrit (HCT) were also measured as prothrombotic state and compared among the groups. Results In groups of HT with AF versus HT without AF versus control,LAD[(43.56 ± 6.72) mm vs.(36.28 ± 5.83) mm vs.(31.63±4.32)mm],Fg[(4.24±0.59)g/L vs.(3.09 ±0.49)g/L vs.(2.80± 0.46)g/L],D-Dimer [(0.43±0.13)mg/L vs.(0.28±0.]0)mg/L vs.(0.18±0.08)mg/L],vwF[(290.44±29.02)% vs.(101.32±21.36)% vs.(84.15±20.26) %],HCT[(0.46±±0.07)vs.(0.37±0.05)vs.(0.34±0.03)]were significantly higher in HT patients with atrial fibrillation than those without atrial fibrillation and control ( all P< 0.05),and there were differences in LAD and D-Dimet (P<<0.05),but not in Fg,vwF and HCT (all P>0.05) between patients without atrial fibrillation and control.LAD[(46.75±7.32)mm vs.(40.82±6.21)mm],Fg [(4.68±0.65)g/L vs.(3.85±0.53)g/L],D-Dimer [(0.48±0.16)mg/L vs.(0.40±0.12)mg/L],vwF [(384.96±29.75)% vs.(209.43±28.63)%] and HCT [(0.49±0.08)vs.(0.43±0.06)] in persistent atrial fibrillation group were increased than those in paroxysmal atrial fibrillation group ( P < 0.05 ).Fg ( r =0.683 ),D-Dimer ( r =0.735 ),vwF ( r=0.763) and HCT(r=0.759)were corrclated with LAD (all P<0.01). Conclusions Increased LADmight he one of the elevated risks of atrial fibrillation and a higher prothrombotic state is increasing with larger LAD in senile hypertension.
3.Long-term and stable expression of transgene mediated by piggyBac transposon in gynecological malignant tumor cells
Yu KANG ; Qingwen SUN ; Wenbo YU ; Mingjun CHENG ; Xiaoyan ZHANG ; Xin WU ; Chunmei CHEN ; Yufang ZHENG ; Congjian XU
Chinese Journal of Obstetrics and Gynecology 2010;45(4):292-297
Objective To investigate the expression of exogenous gene transferred by piggyBac (PB) transposon in various gynecological malignant cell lines and reveal its potential application of gene therapy in gynecological cancer.Methods Amplified herpes simplex virus thymidine kinase (HSV-tk) gene coding region by PCR and integrated it into PB expression vector, PB[Act-RFP]DS, for reconstructing PB[Act-RFP, HSV-tk]DS (pPB/TK).By using different transfection reagents: FuGENE HD, jetPEI, lipofectamine 2000, pPB/TK together with helper plasmid Act-PBase were cotransfected into four mostly common gynecological malignant tumor cell lines HeLa, JEG-3, SKOV3 and HEC-1B.The mRFP1 report gene expressions was observed and detected by fluorescence microscope and flow cytometry to analyze transfection efficiency.The expressions of HSV-tk and mRFP1 gene were detected by reverse transcription PCR (RT-PCR).The cytotoxic effect of various concentration of pro-drug ganciclovir (GCV) for transfected cells was detected by methyl thiazole tetrazolium assay.The transfected cells were positive sorted by flow cytometry and limiting diluted to obtain the stable transfected cell line.The insertion sites of foreign gene tranferred by PB transposon in genome were analyzed by inverse PCR.Results (1) Double digests analysis and sequences test demonstrated that pPB/TK vector was reconstructed successfully.(2) Using three different transfective reagents, PB trausposon transferred HSV-tk gene and mRFP1 gene into HeLa, HEC-1 B, SKOV3 and JEG-3 cell efficiently, and the transfection efficiency of pPB/TK for the same cell was different by using different transfective reagents; in Hela cell, the transfection efficiency of FuGENE HD [(78.7 ± 9.2) %]was higher than that of lipofectamine 2000 [(54.1 ± 11.4) %]and jetPEI [(46.5 ± 7.4) %, all P < 0.05] ; using the same transfective reagent, the transfection efficiency of pPB/TK was also different on various cell lines, using FuGENE HD, the transfeetion efficiency of pPB/TK on HeLa, JEG-3 and SKOV3 cell was (78.7 ± 9.2) %, (74.4 ± 8.9) % and (83.2 ± 9.7) % respectively, which all were higher than that on HEC-1B [(39.5 ± 8.7) %, P < 0.05] .(3) RT-PCR showed that there were the mRNA expression of HSV-tk and mRFP1 in all cell lines.(4) 50% inhibitory concentration of GCV for transfected cells, HeLa, JEG-3, SKOV3 and HEC-1B, was 1.29, 3.35, 0.09 and 13.28 μg/ml respectively.Inhibitory effect of GCV (10 μg/ml) on SKOV3 transfected with pPB/TK was (86 ± 9) %, which was superior to that transfected with pORF-HSVtk alone [(52 ± 12)%, P < 0.05] .(5) The insertion sites of PB transposon in the target cells genome were located at TTAA sites, mRFP1 expression still could be detected in three months after transfected.Conclusions PB transposon could transfer exogenous gene into various gynecological malignant cells, which could integrated into genome and obtain a long-term and stable expression.It is expected that PB transposon may supply a more efficient and safer transgene technology platform for gene therapy in gynecological cancer.
4.Molecular etiology of 573 patients with nonsyndromic hearing loss in 5 provinces of northwest region of China.
Qingwen ZHU ; Xin LIU ; Dongyi HAN ; Dongyang KANG ; Xin ZHANG ; Zhengce JIN ; Mei LI ; Pu DAI
Journal of Clinical Otorhinolaryngology Head and Neck Surgery 2007;21(10):460-462
OBJECTIVE:
To analyze the prevalence of an A-to-G mutation at nucleotide 1555 of the mitochondrial genome in patients with nonsyndromic hearing impairment (NSHI) of northwest region of China.
METHOD:
A standardized program of epidemiological design, administrative support, sample collection and mutation screening for mtDNA 12SrRNA A1555G were used performed to study the general condition and the molecular etiology of patients with severe to profound hearing loss from 5 provinces of northwest region of China.
RESULT:
Five-hundred-seventy-three cases with severe profound hearing loss from 5 provinces were collected and 31 cases were found to carry mtDNA 12SrRNA A1555G mutation.
CONCLUSION
Among the patients with severe to profound hearing loss from 5 provinces of northwest region, there was a high proportion of hereditary hearing impairment caused by mtDNA 12SrRNA A1555G mutation. Screening and testing for this mutation are effective methods to prevent ototoxicity in A1555G carriers and their maternal family members.
Adolescent
;
Adult
;
Child
;
Child, Preschool
;
China
;
epidemiology
;
DNA Mutational Analysis
;
DNA, Mitochondrial
;
genetics
;
Female
;
Hearing Loss
;
epidemiology
;
genetics
;
Humans
;
Male
;
RNA, Ribosomal
;
genetics
;
Young Adult
5.Genotypic and phenotypic analysis of SLC26A4 gene in deaf patients of Chifeng area by whole gene sequencing strategy
Yongyi YUAN ; Pu DAI ; Deliang HUANG ; Xiuhui ZHU ; Qingwen ZHU ; Dongyang KANG ; Lixian LIU ; Guochun TENG
Chinese Archives of Otolaryngology-Head and Neck Surgery 2006;0(05):-
OBJECTIVE To investigate the genetic causes of deaf patients in a special educational school of Chifeng city, Inner Mongolia by SLC26A4 whole gene sequencing. This study focused on analyzing mutations of coding sequence of SLC26A4 gene and their relevant phenotype. METHODS DNA were extracted from peripheral blood of 134 deaf patients of Chifeng special educational school and 100 normal hearing controls in Northern China. SLC26A4 gene mutation was analyzed by direct sequencing for its 20 coding exons. All individuals found with SLC26A4 mutation were given temporal bone CT scan, and those with confirmed enlarged vestibular aqueduct and/or other malformation of inner ear were then given further ultrasound scan of thyroid and thyroid hormone assays. RESULTS The sequencing results revealed 32 cases carried SLC26A4 mutation. Twenty-nine cases underwent temporal bone CT scan. Twentycases were confirmed to have malformation of inner ear by CT scan (eighteen were EVA, one was EVA and other inner ear malformation and one was Mondini Syndrome). The shape and function of thyroid were confirmed to be normal by ultrasound scan of thyroid and thyroid hormone assays in nineteen of these 20 patients except one who had cystoid change in the right side of thyroid. Twelve types of novel variants of SLC26A4 gene were found. CONCLUSION Byscreening SLC26A4 gene coupled with temporal bone CT scan ,we could determine genetic cause related to this gene up to 14.93 % of deaf patients in special educational school of Chifeng city. SLC26A4 is another common gene besides GJB2 that cause deafness in this area. The discovery of novel variants of SLC26A4 gene makes the mutational and polymorphic spectrum more plentiful in Chinese population.
6.Image segmentation based on "catalyst" segmentation method
Zhuang KANG ; Xiaogang DENG ; Qingwen LV
Chinese Medical Equipment Journal 2003;0(11):-
Objective To propose a novel method for image segmentation based on"catalyst" segmentation method.Methods Feeler image was imported into segmentation algorithm as the"catalyst",and whether the candidate nodes should stop segmentation or not was decided according to whether the catalyst appeared in the segmentation result.Results Image segmentation based on "catalyst" segmentation method could judge the right class number for segmented images.Conclusions Primary experiments shows that "catalyst" segmentation method is simple and useful.

Result Analysis
Print
Save
E-mail