1.Prediction of high risk of thrombus by haemodynamics changes in left atrial appendage using transesophageal echocardiography
Fanxia MENG ; Ming CHEN ; Jingping SUN ; Yun DONG
Chinese Journal of Ultrasonography 2014;23(6):473-479
Objective To study the left atrial appendage (LAA) function and haemodynamics by transesophageal echocardiography,and predict high risk of thrombosis.Methods Eighty-nine consecutive patients were studied using transesophageal echocardiography.According to with spontaneous echo contrast (SEC) or not,all patients were divided into SEC group (n =17) and non-SEC group (n-=72).LAA emptying peak flow velocity (LAA-EV),filling peak flow velocity (LAA-FV) were measured by pulsed Doppler.The middle segment of the LAA medial wall systolic peak velocity (LAA-TSV) and diastolic peak velocity (LAA-TDV) were obtained by tissue Doppler imaging.LAA color Doppler and M-mode color Doppler images were acquired and derived the LAA emptying flow propagation velocity (LAA-EPV).Results LAA-EV,LAA-FV,LAA-TSV,LAA-TDV,LAA-EPV of SEC group were lower than those of non-SEC group (P <0.05).LAA M-mode color Doppler had four characteristic patterns,N pattern (normal pattern) which flow eject from LAA apical to LAA orifice,R pattern (reverse pattern) which flow eject from LAA orifice to LAA apical,V pattern (vertical pattern) vertical signals seen in systole and without efficient flow,S pattern (stasis pattern) almost no flow signal.V,R and S patterns may indicate high risk of SEC and thrombosis.LAA-EPV had strong correlation with LAA-EV (r =0.742,P <0.001),and moderate correlation with LAA-TSV (r =0.462,P <0.01),LAA-EV had strong correlation with LAA-TSV (r =0.600,P <0.01).Conclusions LAA dysfunction would result in hypokinetic LAA wall motion and reduced blood flow velocity.Emptying abnormalities of LAA might be the important reasons for blood stasis and thrombus formation.Emptying characteristic low patterns of V,R and S might be novel methods to predict high risk of thrombus.
2.Preliminary application of diastolic inflow inside left ventricle using color singular value
Ming CHEN ; Yi LIU ; Aiyu MIAO ; Shenglin LIU ; Bo ZHANG ; Jialiang ZHENG ; Jinkang HUANG ; Yuhui ZHANG ; Jianhua ZHENG ; Jing MA ; Fanxia MENG
Chinese Journal of Ultrasonography 2010;19(5):374-377
Objective To develop a new method for describe features of inflow of left ventricle(LV) from color Doppler image by color singular value,and evaluat the value of color singular value in assessment of diastolic dysfunction. Methods Patients with diastolic dysfunction of LV including myocardial infarction (n = 37), angina( n = 35), cardiomyopathy( n = 45) and hypertension ( n =46) were selected and 30 healthy cases as control. CV and AV from color singular value of LV inflow was displayed and calculated automatically by an analyzing system developed in our laboratory. Results Compared with that of control (CV:2.40 0.22 and AV: -0.25 0.05), the absolute value of CV(1.67-1.90 in average)and AV( - 0. 11~-0. 20 in average) from color singular value were decreased significantly( P <0. 001) in groupsof myocardial infarction, angina, cardiomyopathy and hypertension. Conclusions Singular value can be applied to detect color differences in LV inflow from color Doppler signals. Changes of singular value within the diastolic inflow under pathological conditions may reflect the diastolic dysfunction of LV.
3.Conserved arginine residue in the membrane-spanning domain of HIV-1 gp41 is required for efficient membrane fusion.
Yufei LONG ; Fanxia MENG ; Naoyuki KONDO ; Aikichi IWAMOTO ; Zene MATSUDA
Protein & Cell 2011;2(5):369-376
Despite the high mutation rate of HIV-1, the amino acid sequences of the membrane-spanning domain (MSD) of HIV-1 gp41 are well conserved. Arginine residues are rarely found in single membrane-spanning domains, yet an arginine residue, R(696) (the numbering is based on that of HXB2), is highly conserved in HIV-1 gp41. To examine the role of R(696), it was mutated to K, A, I, L, D, E, N, and Q. Most of these substitutions did not affect the expression, processing or surface distribution of the envelope protein (Env). However, a syncytia formation assay showed that the substitution of R(696) with amino acid residues other than K, a naturally observed mutation in the gp41 MSD, decreased fusion activity. Substitution with hydrophobic amino acid residues (A, I, and L) resulted in a modest decrease, while substitution with D or E, potentially negatively-charged residues, almost abolished the syncytia formation. All the fusion-defective mutants showed slower kinetics with the cell-based dual split protein (DSP) assay that scores the degree of membrane fusion based on pore formation between fusing cells. Interestingly, the D and E substitutions did show some fusion activity in the DSP assays, suggesting that proteins containing D or E substitutions retained some fusion pore-forming capability. However, nascent pores failed to develop, due probably to impaired activity in the pore enlargement process. Our data show the importance of this conserved arginine residue for efficient membrane fusion.
Amino Acid Substitution
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Animals
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Arginine
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chemistry
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metabolism
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Cell Line
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Cercopithecus aethiops
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HIV Envelope Protein gp41
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chemistry
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metabolism
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HIV-1
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metabolism
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Humans
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Kinetics
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Membrane Fusion
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physiology
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Mutation
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Protein Structure, Tertiary
4.Analysis of Clinical Features of 13 Cases with Late-Onset Pompe Disease
Fang JI ; Fangping HE ; Yi LI ; Jie NI ; Lihua YU ; Fanxia MENG ; Haiyan CHEN ; Qing KE
JOURNAL OF RARE DISEASES 2024;3(3):318-325
To investigate the clinical features and genetic characteristics of patients with late-onset Pompe disease(LOPD). A total of 13 patients diagnosed with LOPD in the First Affiliated Hospital of Zhejiang University School of Medicine from September 2020 to December 2023 were selected, and all patients were subjected to clinical investigation, GAA activity detection and Among the 13 patients, 7 were males and 6 were females; 5 were family patients and 8 were sporadic patients; and the median age of onset was 17 years(8-52 years), the median age of presentation was 24 years(10-52 years), and the median age of diagnosis was 31 years(14-58 years). In terms of the first symptoms, 10 patients presented with limb weakness and 3 patients presented with dyspnea. The average serum creatine kinase level was 552 U/L(55-1084 U/L), and the serum creatine kinase level was normal in one patient. All patients had scoliosis and different degrees of restrictive ventilatory dysfunction. Neuroelectrophysiological examinations of 9 patients showed myogenic damage, and 8 of them had muscle tonic discharge. The mean value of GAA activity was 0.3 μmol/(L·h)[0.17-0.5 μmol/(L·h)]. A total of 13 mutations were detected in LOPD is a rare disease that tends to delay diagnosis. Proximal limb weakness, decreased respiratory function, mild-to-moderate elevation of creatine kinase, scoliosis, and clinical inferior tonic discharge on electromyography are high-risk images of LOPD. c.2238G > C(p.W746C)is a hotspot mutation, and the discovery of five new mutations enriches the