绝经后高血压危险因素的Meta分析

背景 流行病学研究表明,绝经后女性的高血压患病率高于老年男性。近年来,有关绝经后高血压的临床表现、病理特征、发病机制、治疗方法等受到越来越多的关注,但由于受到研究设计、样本量、人群特征、资源不足等因素的影响,其危险因素的研究结果不一致且缺乏全面报道。目的 运用系统评价方式探讨女性绝经后高血压的危险因素,为更好地预防和管理绝经后高血压提供循证证据。方法 于2022年1—5月,计算机检索中国知网、万方数据知识服务平台、中国生物医学文献服务系统、PubMed、EmBase、the Cochrane Library、Web of Science电子数据库,获取与绝经后高血压危险因素相关的队列及病例对照研究。检索时限为建库起至2022-05-20。由2名研究者独立根据纳入和排除标准筛选文献、提取资料,采用纽卡斯尔-渥太华量表（NOS）对所提取的文献进行偏倚风险评估,将得分≥6分（高质量）的文献纳入研究,最后采用RevMan 5.3对其进行Meta分析。结果 共纳入10篇文献,5篇为队列研究,5篇为病例对照研究,共涉及16个危险因素,总样本量为34 864,且均为高质量文献。Meta分析结果显示,...     

基于十年随访的心血管代谢性危险因素聚集与社区≥55岁人群全因死亡风险关系的队列研究

背景 心血管代谢性危险因素聚集（CRFC）是老年人常见的健康问题,目前相关研究主要集中在流行病学分布特征的描述,有关CRFC与人群全因死亡风险的研究鲜有报道。目的 探讨CRFC与社区≥55岁人群全因死亡风险的关系,为开展≥55岁人群社区保健提供参考。方法 于2011年9—11月采用典型抽样法选取宁夏回族自治区吴忠市和银川市5个社区的1 046名≥55岁人群作为研究对象,对其开展一般情况问卷调查、体格检查、超声检查、实验室检查和CRFC评价[纳入中心性肥胖、高胆固醇血症、高三酰甘油血症、高低密度脂蛋白血症、低高密度脂蛋白血症、高血压、糖尿病、高尿酸血症、非酒精性脂肪性肝病（NAFLD）共计9项心血管代谢性危险因素后,控制一般情况变量,通过构建多因素Cox比例风险回归模型,估计各个心血管代谢性危险因素的回归系数β,以回归系数β为权重将所有心血管代谢性危险因素的评分相加得出心血管代谢危险因素危险总评分],将心血管代谢危险因素危险总评分按照四分位数分为三组：P75组;分别于2017年,2019年和2021年通过面访和死因监测系统搜索的方式完成随访。采...     

脂质比值与代谢综合征的关联及预测价值评价：基于多阶段横断面研究

背景 随着代谢性疾病发病率的上升,代谢综合征(MS)的预防与控制引起广泛的关注。而脂质比值是重要的筛查指标之一,与MS之间的关系成为热点研究话题。目的 基于贵州省多阶段横断面研究人群分析三酰甘油/高密度脂蛋白胆固醇(TG/HDL-C)、总胆固醇/HDL-C(TC/HDL-C)、低密度脂蛋白胆固醇/HDL-C(LDL-C/HDL-C)及非高密度脂蛋白胆固醇(non-HDL-C)与MS发病风险的关联及预测价值评价。方法 回顾性选取贵州省参与2010年全国疾病监测地区慢性病及危险因素调查、2013年中国慢性病及其危险因素监测、2015年中国成人慢性病与营养监测和2018年中国成人慢性病与营养监测的21 727例自然人群为研究对象,收集研究对象的基线资料,根据是否患有MS将研究对象分为MS组(n=4 981)和非MS组(n=16 746)。绘制受试者工作特征曲线(ROC曲线)分别评价男性和女性TG/HDL-C、TC/HDL-C、LDL-C/HDL-C和non-HDL-C对MS的预测价值。通过Delong检验比较脂质比值预测MS发生的ROC曲线下面积(AUC)的差异。采用多因素Logistic回...     

The GABA hypothesis of kindling: Recent assay studies

The GABA (gamma-aminobutyric acid) hypothesis of kindling suggests that the permanent changes caused by the kindling procedure result from a loss of GABA-mediated inhibition. Pharmacological studies have generally supported this hypothesis: GABA-complex antagonists accelerate (or stimulate) kindling, whereas GABA-complex agonists retard (or reverse) it. Assay studies, however, have presented an inconsistent picture. Earlier studies found no GABAergic brain changes after kindling, whereas recent studies have reported postkindling changes in a number of GABA-related parameters. The crucial difference seems to be that earlier studies assayed GABA parameters in "whole tissue," whereas recent studies have concentrated on "synaptic" GABA. As indicated by recent studies, when the "metabolic pool" is excluded, kindled subjects show a variety of persistent abnormalities in the GABA system. These data are generally consistent with the GABA hypothesis of kindling.     

Application of adjunct techniques in cytologic material in the diagnosis of rhabdomyosarcoma: case report and review of the literature

A 4(1/2)-yr-old female presented with right-sided pleural effusion and a retroperitoneal mass. Cytologic analysis of the pleural fluid yielded malignant small round blue cells, which were noncohesive, 3-4 times the size of lymphocytes. The malignant cells had hyperchromatic, pleomorphic nuclei with moderate amounts of vacuolated cytoplasm. A few fiber-shaped cells were also seen. Immunostains for desmin, muscle-specific actin were positive; ultrastructural findings of thick and thin actin-myosin filaments confirmed the diagnosis of embryonal rhabdomyosarcoma. This case illustrates the importance of performing appropriate immunohistochemical stains and ultrastructural studies on cytological material to arrive at a definitive diagnosis.     

儿童智商与父母智商的相关性

目的：通过对儿童智商（IQ）与父母亲IQ和IQ分项相关研究，探讨儿童IQ和父母亲IQ的深层关系。方法：在合肥市某中学、小学和幼儿园，分别按年龄和性别分层，随机抽取4-14岁健康儿童206名及其父母作为研究对象，应用韦氏智力量表（成人和儿童）测定儿童和其父母的IQ，填写自编的影响儿童智力发育因素调查问卷。最后在考虑儿童的年龄、性别、克托莱指数（Quetelet index）和是否独生子女等可能混杂因素下将儿童的总IQ、语言IQ和操作IQ与其父母的总IQ、语言IQ、操作IQ和IQ分项进行多元逐步回归分析。结果：按F〉2．0标准，儿童总IQ与父母亲总IQ成正相关（偏相关系数分别为0．50和0．22）；儿童语言IQ与母亲算术、母亲知识、父亲算术、父亲拼物成正相关（偏相关系数0.23-0．37）；儿童操作IQ和母亲积木图案、母亲拼物和父亲拼物成正相关（偏相关系数0．31-0．50）。结论：父母亲的总IQ和父母IQ分项中的算术、拼物、积木图案和知识等对儿童总IQ、语言IQ和操作IQ影响最大。     

注意缺陷多动障碍儿童视觉保持及运动研究

目的探讨注意缺陷多动障碍(attentiondeficithyperactivitydisorder,ADHD)儿童的视觉机能特征。方法采用本顿视觉保持测验(Bentonvisualretentiontest,BVRT)、连线测验(TrailMakingTest,TMT)及符号-数字模式测验(Symbol-DigitModalitiesTest,SDMT)3种方法,分别测试50例ADHD儿童和50例正常儿童的视知觉、视觉记忆、视空间结构、视觉运动注意和视觉扫描等。结果①ADHD组BVRT三种测验方试C、D、E正确分总分(4.9±2.0)低于对照组(7.7±1.4)(t总=8.00,P<0.01),而失误分总分(6.9±3.9)高于对照组(2.5±1.7)(t总=12.1,P<0.01)。②ADHD组完成A型TMT时间较对照组延长(94.6±51.2/56.9±23.7,t=4.61,P<0.05),所犯错误次数与对照组相比差异有显著性(0.3±0.8/0.1±0.3,Hc=4.46,P<0.05);ADHD组完成B型TMT时间较对照组延长(228.0±142.1/120.1±43.8,t=5.14,P<0.05),所犯错误次数较对照组明显增多(6.0±5.5/2.1±3.4,Hc=22.96,P<0.01)。③ADHD组SDMT得分低于对照组(65.2±29.3/97.9±18.8,t=6.65,P<0.01)。结论ADHD儿童存在视知觉、视觉记忆、视空间结构、视觉运动注意以及视觉扫描等视觉机能方面缺陷。     

胃癌患者生活质量问卷(QLQ-STO22)中文版的制定

目的:将QLQ-STO22引入国内,并评价其可行性、信度和效度。方法:以2003年6月1日至12 月31日在某市三家医院入院治疗的胃癌患者为研究对象。调查内容主要包括一般状况、简明病情调查表及QLQ-STO22。结果:重复测量前后比较,STO22量表各个维度的ICC 值均大于0.75;Cronbaeh'a 系数为0.80; 量表的分半信度系数分别为0.78。表明量表的重测信度、分半信度和内部一致性良好。对STO22量表的各个维度做因子分析,得到3个因子,它们分别能解释总体方差的72.8%,各公共因子在相应项目上的因子载荷均>0. 5,表明该量表具有较满意的结构效度。结论:QLQ-STO22中文版具有较好的信度和效度。     

Serological studies of monoclonal RH1(D) antibodies with RH1(D) variants

In this paper we chose to emphasize three aspects of our work. First we underlined that “low grade and high grade” D weak red blood cells studied at the DNA level could, when monoclonal antibodies were used, give patterns of positive and negative reactions like partial RH1(D) cells. Secondly, we showed the importance of the technical conditions of the study which are essential for establishing a pattern of reactivity defining an epitope. It appears that the use of papain treated cells at room temperature can be misleading for the definition of epitope especially with IgM antibodies. Lastly we pointed out the interest of Rh variant cells, defined at the gene level, to study the expression of RH1(D) epitopes on the external part of the membrane.     

Editorial: Genetics of Brain Function and Cognition

There is overwhelming evidence for the existence of substantial genetic influences on individual differences in general and specific cognitive abilities, especially in adults. The actual localization and identification of genes underlying variation in cognitive abilities and intelligence has only just started, however. Successes are currently limited to neurological mutations with rather severe cognitive effects. The current approaches to trace genes responsible for variation in the normal ranges of cognitive ability consist of large scale linkage and association studies. These are hampered by the usual problems of low statistical power to detect quantitative trait loci (QTLs) of small effect. One strategy to boost the power of genomic searches is to employ endophenotypes of cognition derived from the booming field of cognitive neuroscienceThis special issue of Behavior Genetics reports on one of the first genome-wide association studies for general IQ. A second paper summarizes candidate genes for cognition, based on animal studies. A series of papers then introduces two additional levels of analysis in the black box between genes and cognitive ability: (1) behavioral measures of information-processing speed (inspection time, reaction time, rapid naming) and working memory capacity (performance on on single or dual tasks of verbal and spatio-visual working memory), and (2) electrophyiosological derived measures of brain function (e.g., event-related potentials). The obvious way to assess the reliability and validity of these endophenotypes and their usefulness in the search for cognitive ability genes is through the examination of their genetic architecture in twin family studies. Papers in this special issue show that much of the association between intelligence and speed-of-information processing/brain function is due to a common gene or set of genes, and thereby demonstrate the usefulness of considering these measures in gene-hunting studies for IQ.