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101.
BACKGROUND AND OBJECTIVES: We have previously reported that high rat urinary allergen (RUA) exposure was not associated with increased risk of rat allergy in long-term-exposed laboratory animal (LA) workers. We aimed to assess whether strong allergen-specific IgG4 responses could explain the absence of a dose response in these subjects. We investigated whether IgG4 was associated with allergen exposure and prevalence of sensitization or respiratory symptoms to rats. The longitudinal relation between IgG4 and rat allergy was studied using data obtained during 2 years of follow-up. METHODS: Five hundred and twenty-nine LA workers answered a questionnaire on respiratory symptoms and occupational history and participated in skin prick testing. Blood samples were analysed for specific IgG4 and IgE to RUA. Exposure to RUA was estimated based on personal air samples. The relation between IgG4 and newly occurring sensitization or rat allergy was studied in workers who were not sensitized or did not report respiratory symptoms to rats. RESULTS: IgG4 titres were higher in atopic than in non-atopic subjects, and increased with higher allergen exposure. Titres were highest in subjects who were sensitized and reported respiratory symptoms to rats when compared with those who were not (geometric mean [geometric standard deviation] = 202 [5.7] vs. 8.4 [18.3] AU). The association between IgG4 and sensitization or symptomatic rat allergy was independent of estimated allergen exposure. IgG4 was a strong predictor of newly occurring sensitization and symptomatic rat allergy during follow-up in atopic and rat-sensitized subjects. CONCLUSION: High exposure to RUA is associated with a strong allergen-specific IgG4 antibody response. High anti-RUA IgG4 is a strong predictor of prevalent and incident sensitization and symptomatic rat allergy in atopic and rat-sensitized subjects. IgG4 can therefore not explain the absence of a dose response between allergen exposure and allergy in long-term-exposed workers. We consider anti-RUA IgG4 to be a marker that combines aspects of exposure and susceptibility.  相似文献   
102.
Quantitative cerebral blood flow (CBF) values can be obtained from dynamic susceptibility contrast (DSC) MR perfusion studies using the standard singular value decomposition (sSVD) deconvolution algorithm. Reports in the literature from simulation and in vivo studies suggest that CBF estimates obtained using sSVD deconvolution depend on the arterial-tissue delay (ATD). By contrast, Fourier transform (FT) deconvolution produces CBF estimates that are independent of ATD. The diagnostic reliability of quantitative CBF measurements to define areas of normal tissue flow and tissue at risk is brought into doubt by such gross sensitivity to the specifics of the deconvolution approach. This variation of CBF values with ATD is shown to be an artifact associated with the current implementation of the sSVD deconvolution algorithm. A reformulated version of the SVD deconvolution algorithm (rSVD) is presented and compared to the standard SVD algorithm through simulation and patient case studies.  相似文献   
103.
The purpose of this study was to examine motor learning and retention given extensive practice in two fundamentally different movement sequences. One sequence was a memory-driven task (performing a series of whole body positions from memory) and the other a context-driven task (buttoning). Practice took place over 3 weeks, with performance measured weekly; retention was measured weekly for 3 weeks after practice. There were 7 people with Parkinson's disease (PD) and 7 age-matched neurologically healthy people who participated in this study. Both groups improved performance on both tasks with practice, with the majority of the change for the PD group occurring between 1 and 2 weeks of practice. Although those with PD did not necessarily perform as well as age-matched controls, they learned both sequences in a manner similar to age-matched controls, and exhibited retention across the 3-week retention interval. If people with PD are given sufficient practice they can learn and retain both memory-based and context-driven movement sequences as well as age-matched controls. The results provide support for maintaining physical activity and for intervention through movement therapy.  相似文献   
104.
We calculated how long to wait before repeating bone mineral density (BMD) measurements to reassess fracture risk. Correlation results from serial measurements of 495 postmenopausal Japanese-American women were used to estimate 95% confidence intervals (CI) for future BMD. After 7 years of follow-up, BMD correlations with the initial measurement ranged between 0.81 and 0.94, depending on age group and measurement site. In this analysis, the period between measurements was defined as the time required for the lower 95% CI to fall below the BMD value corresponding to doubling of fracture risk. Progressive bone loss causes fracture risk to double after 10 years, on average. However, the 95% CIs indicate that a second BMD measurement will detect risk doubling after only 2 or 3 years for some women. For untreated, early postmenopausal women, the period between measurements was approximately 2–5 years for the radius and 4–6 years for the calcaneus, depending on the initial BMD level. The period was approximately 1 year longer for women age 60 and older. Treatments that halve the bone loss rate would increase the period by 1–3 years. In the absence of a second measurement of BMD, the CI will continue to expand with time, corresponding to a wider range in risk between individuals, and a greater proportion of women will be at increased fracture risk. Obtaining a second BMD measurement pinpoints the patient's status within the precision of the measurement. We conclude that repeated BMD measurements will provide a more accurate estimate of fracture risk than a single, baseline measurement.  相似文献   
105.
Fetal diagnosis has vastly improved over the last decade. Ultrasound has become the imaging modality of choice. As real-time equipment has improved technologically, the ability to deduce subtle abnormalities has greatly increased. The fetal genitourinary tract may be evaluated for renal dysplasias, anomalies, or obstruction. Points of obstruction and, at times, the exact cause of obstruction may be deduced. Abnormalities of the ureter, bladder, urethra, scrotum, or reproductive system can be detected.  相似文献   
106.
The crystal structure of a tripeptide, tryptophanyl-glycyl-glycine dihydrate (C15H18N4O4·2H2O, molecular weight = 354) has been determined. The crystals are orthorhombic, space group P212121 with a= 7.875 (1) A,b= 9.009(1), c= 24.307(1) and Z = 4. The final R-index is 0.058 for 1488 reflections ((sin θ/λ≤ 0.6 A?1) with I < 2σ(I). The molecule exists as a zwitterion, with terminal NH+3 and COO? groups. The peptide units are trans and nearly perpendicular to the plane of the carboxyl group. The backbone torsion angles are: ψ1= 132.7°, ω1= 174.2°, φ2 88.2°, ψ= 8.6°, ω2 - 179.8°, φ= - 85.2°, ψ31, = - 178.1°, ψ32 5.0°. For the sidechain of tryptophan, χ1= - 171.6°, χ2 101.0°.  相似文献   
107.
BACKGROUND: It is established that the A3 domain in von Willebrand factor (VWF) contains the major collagen-binding site. However, there are conflicting reports describing the capacity of the A1 domain to interact with collagen types I and III. METHODS: In this study, we have used recombinant VWF-A1 polypeptides, as well as conformation-specific monoclonal antibodies (mAb), to analyze the A1-collagen interaction. RESULTS: The A1 domain bound to collagen with K(d) approximately 8.0 nm and this binding was blocked by the mAb 6G1, which blocks the interaction between ristocetin and VWF. In addition, collagen-bound A1 protein was able to support flow-dependent adhesion of platelets, demonstrating that the binding sites for collagen and glycoprotein (GP)Ib are different. Analysis with two conformation-specific mAb demonstrated that the structure of the A1 domain changed as a result of the binding to collagen. In contrast, the antibodies failed to detect conformational change in the G1324S mutant (type 2M von Willebrand disease). Thus, direct binding to collagen induces a change in the structural conformation within the VWF-A1 domain, and the G1324S substitution prevents this conformational change. CONCLUSION: This study has shown that the isolated A1 domain can simultaneously bind to collagen and platelet GPIb, supporting platelet adhesion under high-flow conditions. In addition, this study has used mAb to demonstrate that the binding of the isolated A1 domain or full-length VWF to collagen is accompanied by a conformational change in A1 domain.  相似文献   
108.
目的 评价国产流行性感冒(简称流感)病毒裂解疫苗的安全性和免疫效果.方法 选择6岁~、16岁~和>60岁3个年龄段人群共606名,每个年龄段人群按数字表法随机分入试验组(共213名)、对照组1(共195名)和对照组2(共198名),分别接种国产流感疫苗和2种进口流感疫苗,比较三组人群接种后副反应发牛率、抗体阳转率、保护率及几何平均滴度(GMT)增长倍数的差异.率的比较采用X2检验,几何平均滴度(GMT)增长倍数采用方差分析,P<0.05为差异有统计学意义.结果 试验组、对照组1、对照组2副反应发生率分别为3.76%(8/213)、4.10%(8/195)和3.54%(7/198),差异无统计学意义(X2=0.87,P=0.93).3个组H1N1、H3N2和B(亚)型血凝抑制(H1)抗体总阳转率分别为89.2%(190/213)、63.4%(135/213)、86.4%(184/213),88.7%(173/195)、61.5%(120/195)、87.2%(170/195),87.9%(174/198)、61.6%(122/198)、84.8%(168/198),各(亚)型抗体总阳转率差异无统计学意义(X2H1N1=0.94,PH1N1=0.63;X2H1N2=0.94,PH3N2=0.63;X2B=0.75,PB=0.69);3个组H1N1、H3N2及B型H1抗体平均增长倍数分别为10.7、7.3、8.4倍,10.5、6.3、8.3倍,10.2、7.1、8.8倍,各(亚)型H1抗体GMT增长倍数差异无统计学意义(FH1N1=0.35,PH1N1=0.70;FH3N2=2.22,PH3N2=0.11;FB=1.51,PB=0.35);3个组H1N1、H3N2及B型H1抗体保护率分别为100%(213/213)、70.0%(149/213)、95.3%(203/213),100%(195/195)、66.7%(130/195)、97.9%(191/195),99.5%(197/198)、66.2%(131/198)、96.5%(191/198),各(亚)型抗体保护率差异无统计学意义(X2H1N1=2.04,PH1N1=0.36;X2H3N2=0.74,PH3N2=0.69;X2B=0.42,PB=0.82).结论 国产裂解流感疫苗具有良好的安全性和免疫效果,可用于群体性接种.  相似文献   
109.
目的 了解上海地区学生午餐营养及供应链状况,为改善学生午餐营养状况,保障食品供应安全提供参考。方法 分析上海市学生午餐的营养、卫生、供应链、加工工艺等状况,采用定期抽检的方法,应用SNHAS对营养素、食品安全、感官进行综合评价。结果 各单位样本综合评价均合格,其中热量、蛋白质、脂肪均能达到或超过DRIs供给量的要求,但矿物质中Ca(仅为AI的32%)、视黄醇当量(仅为AI的57%)供给量较低。对供应链及卫生状况的分析表明,大型企业对各个环节控制严格,产品质量较好,但也存在保存时间过长等问题。结论 应进一步完善供应体系,建立高效的质量控制体系,推广营养配膳系统。  相似文献   
110.
An 8-year longitudinal study of elderly people has provided data concerning age-associated impairment (AAMI). In 1985 a random sample of 146 persons aged 65 years or more, living in their own homes, were assessed using the Guild Memory Test the Mini–Mental State Examination (MMSE) and other ratings. After excluding 21% of the sample because they scored less than 24 on the MMSE, and another 34% who fulfilled other exclusion criteria, some 48% of the remainder (22% of the total sample) clearly fulfilled NIMH criteria for AAMI and a further 36% (16% of the total sample) were recorded as forgetful. The NIMH criteria are appropriate for certain research purposes but not in assessing prevalence of memory disorders. Follow–up interviews were conducted after 2, 4, 6 and 8 years. The mortality rate and development of dementia among those fulfilling criteria for AAMI appeared similar to the other non-demented groups of subjects; the mortality rate of those with MMSE scores below 24 was significantly higher. Guild test results at 2-yearly intervals showed considerable changes; half of those scoring least well who were retested showed improvement.  相似文献   
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