中学生生活事件与抑郁的关系

目的：探讨中学生具体生活事件和抑郁状况的关系。方法：采用青少年生活事件量表和中学生抑郁量表对558名中学生进行问卷调查。结果：除个别生活事件项目外，青少年生活事件量表中的多数项目均与中学生抑郁呈显著正相关；生活事件与抑郁的回归分析表明，学习负担重，受人歧视冷遇，不喜欢上学，家庭经济困难，与同学或好友发生纠纷，升学压力，被盗或丢失东西，考试失败或不理想，受批评或处分，生活习惯明显变化，恋爱不顺利或失恋，被罚款等12类生活事件进入了对抑郁的回归方程，对抑郁的预测作用较大。结论：中学生生活事件与其抑郁存在广泛的正相关关系。12项生活事件对中学生抑郁有较大的预测作用。     

中小学教师心理控制源、应付方式与自我和谐的关系

目的考察中小学教师自我和谐、心理控制源、应付方式的状况及其关系。方法使用自我和谐量表、内控性、有势力的他人及机遇量表、应付方式问卷对200名中小学教师进行调查。结果①教师整体上倾向内控,使用最多的应付方式是解决问题,最少的是自责;②任教地点、职务、职称、学历不同的教师自我和谐、应付方式有显著差异,年龄、教龄、任班主任年限、自评心理健康水平、生活压力、工作满意度与心理控制源、应付方式、自我和谐的不同维度相关显著;③机遇和幻想对自我和谐有正向预测作用,内控、解决问题、求助对自我和谐有负向预测作用。结论自我和谐可以作为衡量心理健康水平的一个标志,中小学教师心理控制源与应付方式对自我和谐有重要影响。     

Cloning and characterization of the cDNA encoding the HA protein of a hemagglutination-defective measles virus strain

cDNA clones corresponding to the mRNA for the hemagglutinin of the hemagglutination-defective strain AK-1 of measles virus were isolated and characterized. Compared with the prototype Edmonstron strain, 60 nucleotide substitutions that resulted in 18 amino acid changes were detected. An additional potential N-linked glycosylation site was added by point mutation, which was supported by the observation that the hemagglutinin of the AK-1 strain was stained more heavily after NaDodSO₄PAGE and periodic acid-Schiff (PAS) staining than the Edmonston strain. Computer-assisted analysis revealed that three reverse turns in the secondary structure had disappeared in the hemagglutinin of the AK-1 strain. Moreover, one of these structural changes occurred in the closely glycosylated region at amino acid residues 168–240, which appeared to be a biologically important functional domain. The isoelectric point calculated from the predicted amino acid sequence became about 1 pH unit more basic in the AK-1 strain than the Edmonston strain. This present study is the first sequence analysis of the hemagglutinin gene in a hemagglutination-defective strain of the measles virus.     

Nkx2.5‐negative myocardium of the posterior heart field and its correlation with podoplanin expression in cells from the developing cardiac pacemaking and conduction system

Recent advances in the study of cardiac development have shown the relevance of addition of myocardium to the primary myocardial heart tube. In wild‐type mouse embryos (E9.5–15.5), we have studied the myocardium at the venous pole of the heart using immunohistochemistry and 3D reconstructions of expression patterns of MLC‐2a, Nkx2.5, and podoplanin, a novel coelomic and myocardial marker. Podoplanin‐positive coelomic epithelium was continuous with adjacent podoplanin‐ and MLC‐2a‐positive myocardium that formed a conspicuous band along the left cardinal vein extending through the base of the atrial septum to the posterior myocardium of the atrioventricular canal, the atrioventricular nodal region, and the His‐Purkinje system. Later on, podoplanin expression was also found in the myocardium surrounding the pulmonary vein. On the right side, podoplanin‐positive cells were seen along the right cardinal vein, which during development persisted in the sinoatrial node and part of the venous valves. In the MLC‐2a‐ and podoplanin‐positive myocardium, Nkx2.5 expression was absent in the sinoatrial node and the wall of the cardinal veins. There was a mosaic positivity in the wall of the common pulmonary vein and the atrioventricular conduction system as opposed to the overall Nkx2.5 expression seen in the chamber myocardium. We conclude that we have found podoplanin as a marker that links a novel Nkx2.5‐negative sinus venosus myocardial area, which we refer to as the posterior heart field, with the cardiac conduction system. Anat Rec, 290:115–122, 2007. © 2006 Wiley‐Liss, Inc.     

Operative morbidity and reproductive outcome in secondary myomectomy: a prospective cohort study

BACKGROUND: This prospective study was designed to evaluate the operative morbidity and reproductive outcome in patients who had secondary myomectomy for recurrent symptomatic uterine fibroids. METHODS: A total of 58 women were subjected to a secondary myomectomy via the abdominal route. The operative morbidity such as blood loss, presence of adhesions and febrile index were estimated and the pregnancy outcome over a 2-4 year period of follow-up. RESULTS: The mean age and standard deviation (+/- SD) of the women was 35 (+/- 2.4) years. Nineteen patients (33%) had a postoperative temperature vertical line 100 degrees F and the estimated blood loss ranged from 159-2500 ml (median 700 ml). Seven patients (12%) required blood transfusion and one had a hysterectomy due to haemorrhage. Nine women (15.5%) became pregnant but only five (56%) had live births. Those with successful pregnancies tended to be younger with a mean age of 31.8 (+/- 2.6) years versus 35 (+/- 1.8) years, (P = 0.08, non-significant) and had fewer uterine leiomyomata; median with range values, 2 (1-6) versus 7 (6-15). The variables which best predicted the postoperative likelihood of pregnancy were; age, presence of tubal adhesions and the number of uterine fibroids. CONCLUSION: This prospective study showed a high operative morbidity and a poor fertility outcome after a repeat myomectomy. The factors affecting successful outcome in a logistic regression model were age, tubal adhesions and number of uterine fibroids.     

内蒙古中学生神经衰弱患病情况调查

目的 :调查研究内蒙古不同民族中学生神经衰弱患病情况。方法 :采用随机整群抽样法 ,对内蒙古八所中学六个民族的中学生进行调查 ,以CCMD -2 -R中神经衰弱标准作最后医学诊断 ,所得数据进行卡方检验。结果 :总患病率为 2 3 5 % ,城市学生患病率高于乡村学生 ,高中生患病率高于初中生 ,均有显著差异 (P <0 0 5 ) ;男女生之间患病率无显著性差异。回族学生患病率最低 ,鄂伦春族学生患病率最高 ,汉族与回族学生之间患病率无显著差异 ,而与蒙古族、鄂温克族、鄂伦春族、达斡尔族之间患病率有显著差异(P <0 0 5 )。结论 :内蒙古中学生神经衰弱患病率较高 ,对来自于城市生、高中生应作为重点防治对象 ,关注少数民族学生的心理健康状况     

大脑中动脉供血区脑缺血后同侧丘脑继发性损害的MR实验研究

本文应用磁共振(magnetic resonance,MR)成像在体观察大脑中动脉(middle cerebral artery,MCA)供血区脑缺血后同侧丘脑的信号变化。结果显示:(1)通过MRA(magnetic resonance angiography)可以观测到单侧MCA的闭塞与血流再通,而供应丘脑的大脑后动脉信号无变化;(2)脑缺血后1d MR T2WI(T2weighted imaging)显示单侧MCA供血区原发病灶呈高信号,3d、7d时此原发病灶信号增高程度有所降低,至14d信号强度再次明显增高;(3)脑缺血后1d和3d时双侧丘脑T2信号无差别,7d和14d时脑缺血同侧丘脑T2信号减低,T2值降低;(4)MCA供血区脑缺血后原发病灶和同侧丘脑T2值的变化不同步。上述结果证实MR能够在活体显示MCA供血区脑缺血后同侧丘脑的继发性损害。     

Genetic alterations in primary and secondary hyperparathyroidism

Hyperparathyroidism refers to a term representing a wide spectrum of parathyroid disorders that are characterized by the increased production of parathyroid hormone. Hyperparathyroidism was once thought to be tare but is now more commonly recognized, aifecting 1 in 500 women over 40 years of age. Yet the interpretation of parathyroid pathology is still controversial and confusing. Over the past 10 years, genetic changes ( ret and menin genes) involved in the pathogenesis of MEN 2 and MEN 1 have been discovered in succession. Different mutations of the calcium-sensing receptor gene have been identified in neonatal severe hyperparathyroidism and familial hypocalciuric hypercal-cemia, respectively. The HRPT 2 gene responsible for the development of heredltaty hyperparathyroidism and jaw tumors has been localized on the 1q21–31 locus. Several genetic alterations have also been characterized in primary and secondary hyperparathyroidism. Different genetic alterations appear to involve the development of different types of hyperparathyroidism. These novel advances give us new insights into the pathogenesis of hyperparathyroidism and allow better differentiation between the different types of parathyroid disorders.     

DNA sequence analysis of the apocytochrome b gene of Podospora anserina: a new family of intronic open reading frame

Summary The 5,969 by (base pair) DNA sequence of the apocytochrome b mitochondrial (mt) gene of race A Podospora anserina was located in a 8.5 Kbp region. This gene contained a 2,499 by subgroup IB and a 1,306 by subgroup ID intron as well as a 990 bp subgroup IB intron which is present in race A but not race s. The large subgroup IB intron and the race A specific IB intron both contained potential alternate splice sites which brought their open reading frames into phase with their upstream exon sequences. All three introns were compared with regard to their secondary structures and open reading frames to the other 30 group I introns in Podospora anserina, as well as to other fungal introns. We detected a new family of intronic ORFs comprising seven P. anserina introns, several N. crassa introns, as well as the T4td bacteriophage intron. Sequence similarities to intron-encoded endonucleases were noteworthy. The DNA sequences reported here and in the accompanying paper complete the analysis of race s and race A mitochondrial DNA.     

303例闭经患者的病因学分析

目的分析统计女性闭经的病因。方法收集2016年1月至2019年6月云南省第一人民医院妇科门诊闭经患者303例,通过病史、查体、抽血查性激素六项、甲状腺功能、空腹血糖等指标、影像学评估及对原发性闭经患者行染色体检查,确定闭经原因并进行统计分析。结果303例患者中,原发性闭经36例(11.89%),继发性闭经267例(88.11%)。导致原发性闭经最常见的疾病为苗勒管发育不全综合征(Mayer-Rokitansky-Kuster-Hauser syndrome,MRKH综合征),36例患者中有7例是MRKH综合征患者,多囊卵巢综合征(polycystic ovarian syndrome,PCOS)是次要原因,有5例患者为PCOS。在继发性闭经中,Asherman综合征和PCOS是最主要的致病原因,分别占29.96%和29.59%。36例原发性闭经患者中,正常核型46,XX患者24例,占原发性闭经患者总数的66.67%。结论闭经患者最常见病因是PCOS和Asherman综合征。