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Endokrynologia, diabetologia i choroby przemiany materii wieku rozwojowego : organ Polskiego Towarzystwa Endokrynologow Dzieciecych最新文献

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[Normalisation of contralateral adrenal function after long-term mitotane therapy in a girl after surgical treatment of adrenocortical carcinoma]. [1例女孩肾上腺皮质癌术后长期米托坦治疗后对侧肾上腺功能恢复正常]。
Agnieszka Lecka, Maria Ginalska-Malinowska

The main method of treatment of adrenocortical tumours is surgery. The efficacy of the mitotane therapy is still controversial with many serious side effects of the therapy. Moreover, patients receiving mitotane should be carefully monitored for adrenal insufficiency and usually require long-term hormone replacement therapy. We present a rare case of normalisation of the contralateral adrenal function after long-term mitotane therapy as a post-surgical treatment of the adrenocortical tumour.

治疗肾上腺皮质肿瘤的主要方法是手术。米托坦治疗的疗效仍有争议,治疗有许多严重的副作用。此外,接受米托坦治疗的患者应仔细监测肾上腺功能不全,通常需要长期激素替代治疗。我们提出了一个罕见的情况下,长期米托坦治疗后,对侧肾上腺功能的正常化作为一个术后治疗肾上腺皮质肿瘤。
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引用次数: 0
[Physical fitness of short-statured boys as related to percentile norms for calendar or growth age]. [矮个子男孩的身体健康与日历或生长年龄的百分位数标准的关系]。
Katarzyna Milde, Paweł Tomaszewski, Edyta Sienkiewicz-Dianzenza, Dariusz Nowicki, Andrzej Wiśniewski, Romuald Stupnicki

Objectives: To assess the physical fitness of short-statured boys aged 7 - 20 years by applying fitness norms established for the Polish population in relation to calendar or growth age.

Material and methods: The results of EUROFIT fitness tests recorded in 3517 short-statured (below percentile 10 for body height) boys, aged 7-20 years, selected from a large (n=37 000) representative male cohort, were analysed.

Results: Individual results were confronted with the respective percentile norms related to calendar age (CA) or growth age (GA), since body height deficiency at given CA could have affected the results of fitness tests expected for that CA. The percentages of subjects below, the percentile 3 or above percentile 97 for given fitness test and CA or GA for the Polish population, were determined. No differences between the percentages computed for CA and GA were noted in case of the following tests: sit-and-reach (SAR) and bent-arm hang (BAH). Significant differences in percentages for both percentiles were found for the following tests: standing broad jump (SBJ), endurance shuttle run (ESR), handgrip (HGR) and plate tapping (PLT). In case of sit-ups (SUP) significant differences in percentages between CA and GA norms were found below the percentile 3, and in case of shuttle run (SHR) and flamingo balance (FLB) -- above percentile 97.

Summary and conclusions: Fitness tests were classified into two categories according to the differences between the results related to norms for calendar or growth age: those independent of whether CA or GA norms were applied (SAR and BAH), and those susceptible to the kind of norm (SBJ, HGR, PLT, SHR, FLB and SUP). The results of tests from the latter category should thus be evaluated by confronting them with the norms established for the growth age, and not calendar age.

目的:通过应用与日历或生长年龄相关的波兰人口健康标准,评估7 - 20岁矮小男孩的身体健康状况。材料和方法:对3517名7-20岁的矮小(身高低于百分位数10)男孩的EUROFIT体能测试结果进行分析,这些男孩来自一个大型(n= 37000)有代表性的男性队列。结果:个体结果面对与日历年龄(CA)或生长年龄(GA)相关的各自的百分位数规范,因为给定CA的身高不足可能会影响该CA的预期健康测试结果。确定了给定健康测试和波兰人口CA或GA的百分位数低于,百分位数3或高于97的受试者百分比。在以下测试中,CA和GA的计算百分比没有差异:坐与伸(SAR)和弯臂悬挂(BAH)。立定跳远(SBJ)、耐力穿梭跑(ESR)、握拍(HGR)和轻拍(PLT)的百分位数百分比均有显著差异。在仰卧起坐(SUP)的情况下,CA和GA规范之间的百分比差异显着低于百分位数3,而在穿梭跑(SHR)和火烈鸟平衡(FLB)的情况下-高于百分位数97。摘要与结论:根据与日历或生长年龄规范相关的结果差异,将适应度检验分为两类:独立于CA或GA规范的(SAR和BAH)和受规范类型影响的(SBJ、HGR、PLT、SHR、FLB和SUP)。因此,对后一类试验的结果进行评价时,应对照生长年龄而不是日历年龄所确定的标准。
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引用次数: 0
[Fibrous dysplasia of bone in a 12-year old girl]. [一名12岁女孩的骨纤维发育不良]。
Jolanta Bieniasz, Anna Maj, Anna Noczyńska

Fibrous dysplasia of bone is a rare congenital bone disease, usually coming out before the age of 30. It is 2.5% of all bone tumours and 7.5 % of benign tumours of bones. The authors present a case of a 12-years old girl with fibrous dysplasia of bone admitted to the Department with hyperparathyroidism suspicion. Pathological changes were localized in the orbital cavity and sinuses. The diagnosis was established on the basis of the clinical course, imaging and histopathological examinations. The therapy with pamidronian acid was applied.

骨纤维发育不良是一种罕见的先天性骨病,通常出现在30岁之前。它占所有骨肿瘤的2.5%和骨骼良性肿瘤的7.5%。作者提出的情况下,一个12岁的女孩与骨纤维发育不良入院的部门与甲状旁腺功能亢进的怀疑。病变局限于眶腔和鼻窦。诊断依据临床病程、影像学及组织病理学检查。应用帕米膦酸治疗。
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引用次数: 0
[Assessment of the dietary habits of short girls and boys]. [矮个子女孩和男孩的饮食习惯评估]。
Edyta Suliga

Background: The problem of body height deficiency, being the effect of undernutrition of children in developing countries, is widely described in the literature, whereas very little attention is devoted to the estimation of the nourishment of children and adolescents with a simple body height deficiency in developed countries.

Aim of the study: The purpose of the study was to estimate the nourishment of short-height girls and boys, with special regard to the realisation of the norms of daily demand for basic nutrients.

Material and methods: The investigation included 60 subjects in two age groups: 10.5 and 13.5 years old. The body height of the investigated children was below 10 centile in relation to the development norms for a given age and gender. Estimations of nourishment were made with the use of an interview about the consumption in the last 24 hours.

Results: In 22% of the investigated, energy intake was found to be lower than 75% of the daily demand. The percentage of the realisation of the norm for mineral components amounted on average to: 38.6-56.7% for calcium; 49.2-77.4% for iron; 50.1-93.2% and 45.9-72.2% for zinc and copper, respectively. Hypovitaminosis was relatively much less marked in comparison with the deficiency of mineral components. A lower consumption of animal protein and vitamin C was noted among adolescents from rural areas.

Conclusion: Among short girls and boys a frequent occurrence of deficiency of energy and mineral components (calcium, zinc, copper and iron) was found. The irregularly balanced diet could be the cause of a smaller body height in relation to peers among a considerable percentage of the investigated adolescents.

背景:身高不足的问题是发展中国家儿童营养不良的影响,在文献中得到了广泛的描述,而在发达国家,对单纯身高不足的儿童和青少年的营养估计却很少受到关注。研究目的:本研究的目的是估计身高不高的女孩和男孩的营养状况,特别考虑到实现基本营养物质的日常需求规范。材料与方法:调查对象60名,分为10.5岁和13.5岁两个年龄组。被调查儿童的身高与特定年龄和性别的发育标准相比低于10百分位。对营养的估计是通过对过去24小时内的消费进行采访来完成的。结果:22%的被调查者的能量摄入低于每日需求量的75%。矿物质含量达标比例平均为:钙38.6-56.7%;铁含量49.2-77.4%;锌和铜分别为50.1-93.2%和45.9-72.2%。与矿物质成分缺乏相比,维生素缺乏症相对不那么明显。农村地区的青少年动物蛋白和维生素C的摄入量较低。结论:矮个子女孩和男孩经常出现能量和矿物质成分缺乏症(钙、锌、铜、铁)。在相当一部分被调查的青少年中,不规律的均衡饮食可能是导致他们相对于同龄人身高偏小的原因。
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引用次数: 0
[Cytofluorometric analysis of chosen markers of apoptosis CD95/CD95L (Fas/FasL) in thyroid tissues from young patients with Graves' disease and Hashimoto's thyroiditis]. [格雷夫斯病和桥本甲状腺炎年轻患者甲状腺组织中CD95/CD95L (Fas/FasL)凋亡标记物的细胞荧光分析]。
Artur Bossowski, Anna Stasiak-Barmuta, Barbara Czarnocka, Mirosława Urban, Anna Łyczkowska, Marek Niedziela, Krzysztof Bardadin, Jolanta Czerwińska, Jacek Dadan, Marek Baltaziak

Background: Apoptosis, one of the forms of programmed cell death, is a physiologic process of cell death that is central to normal development and occurs in response to a variety of physiologic and pathophysiologic stimuli. In the thyroid, abnormal apoptotic activity may be involved in a variety of diseases such as Hashimoto thyroiditis and Graves disease. The aim of this study was to estimate the expression of chosen apoptotic molecules CD95 (Fas) and CD95L (FasL) on the surface of thyroid follicular cells in application of mouse monoclonal antibodies #64 which recognized B antigen regions of thyroid peroxidase (TPO) and infiltrating inflammatory cells.

Material and methods: The investigation was performed on thyroid cells isolated from surgically treated thyroid tissues of 15 patients with Graves' disease (GD), 15 patients with a nontoxic multinodular goiter (NTMG) and 15 aspirates obtained by FNAB from patients with Hashimoto thyroiditis (HT). The thyrocytes were identified by an indirect method: in the first stage we added mouse monoclonal autoantibodies specific for TPO (mAb #64) regions and in the second stage we conjugated this complex with rabbit anti-mouse antibodies IgG (Fab')2 with FITC. In the next step the cellular suspension was completed with suitably well-chosen two-colour monoclonal antibodies marked (PE or PerCP) (Becton Dickinson) directed against suitable apoptotic (Fas/FasL) molecules. All investigations were performed by flow cytometry using Coulter EPICS XL apparatus.

Results: The percentages of thyroid cells were estimated with expression of region B antigenic TPO in reference to individual apoptotic molecules. The analysis of Fas and FasL expression in thyroid tissues revealed significantly increased percentage of intrathyroidal T cells with CD95+ (p<0.005, p<0.001), CD95L+ (p<0.02, p<0.01) and both CD95/CD95L (ns, p<0.05) expression in comparison to percentages of T cells in patients with HT and NTMG. In addition, on the surface of thyroid follicular cells in patients with GD (p<0.01, p<0.01) and NTMG (p<0.001, p<0.004) we observed a lower percentage of thyrocytes with CD95 and CD95L molecules than in cases with HT. The expression of both apoptotic molecules on thyroid cells was higher (18%) in patients with HT in comparison to the percentages of positive cells in patients with GD (p<0.02, p<0.002) and NTMG, 8% and 1%, respectively.

Conclusions: We conclude that alterations in the expression of death receptors and their ligands on the surface of thyroid follicular cells may play a role in the regulation of apoptosis in thyroid autoimmune disorders.

背景:细胞凋亡是细胞程序性死亡的一种形式,是细胞死亡的一个生理过程,对正常发育至关重要,是对各种生理和病理生理刺激的反应。在甲状腺,异常凋亡活动可能涉及多种疾病,如桥本甲状腺炎和格雷夫斯病。本研究的目的是利用识别甲状腺过氧化物酶(TPO) B抗原区和浸润性炎症细胞的小鼠单克隆抗体#64,研究选定的凋亡分子CD95 (Fas)和CD95L (FasL)在甲状腺滤泡细胞表面的表达。材料和方法:研究从15例格雷夫斯病(GD)、15例无毒多结节性甲状腺肿(NTMG)和15例桥本甲状腺炎(HT)患者的FNAB抽吸物中分离的甲状腺细胞。通过间接方法鉴定甲状腺细胞:在第一阶段,我们加入了TPO区域特异性的小鼠单克隆自身抗体(mAb #64),在第二阶段,我们将该复合物与兔抗小鼠抗体IgG (Fab’)2结合FITC。在下一步,细胞悬浮液用适当选择的双色单克隆抗体标记(PE或PerCP) (Becton Dickinson)完成,针对合适的凋亡(Fas/FasL)分子。所有研究均采用Coulter EPICS XL流式细胞仪进行。结果:以B区抗原TPO的表达为参考,估计甲状腺细胞凋亡百分比。Fas和FasL在甲状腺组织中的表达分析显示,CD95+的甲状腺内T细胞比例显著增加(结论:甲状腺滤泡细胞表面死亡受体及其配体表达的改变可能在甲状腺自身免疫性疾病的凋亡调控中起作用。
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引用次数: 0
[The frequency of CTLA-4 gene polymorphism at position 49 exon 1 in children with Hashimoto's thyroiditis]. [桥本甲状腺炎患儿外显子1 49位CTLA-4基因多态性的频率]。
Anna Kucharska, Alicja Wiśniewska, Barbara Rymkiewicz-Kluczyńska

Introduction: The cytotoxic T lymphocyte antigen-4 (CTLA-4) is a molecule present on T cells that plays a critical role in the down regulation of antigen-activated immune responses. Its gene polymorphism is a strong candidate gene for conferring susceptibility to thyroid autoimmunity. THE AIM of the study was to analyse the frequency of CTLA-4 exon 1 polymorphism (A49G) in children with Hashimoto's thyroiditis.

Material and methods: Blood samples from 68 children were analysed: 30 with Hashimoto's thyroiditis and 38 healthy, age-matched controls, mean age: 13.6 years. CTLA-4 exon 1 polymorphism (A49G) was defined by the PCR method and single-strand conformational polymorphism analysis and confirmed by using BbvI enzyme. Statistical analysis was performed using the t- test and Chi-square test.

Results: Polymorphism analysis showed that statistically significant more patients with Hashimoto's thyroiditis were homozygous for G (Ala), and G allele frequency was significant higher than in the control group.

Conclusion: The results confirmed the association between CTLA-4 exon 1 polymorphism (A49G) and Hashimoto's thyroiditis in polish children.

细胞毒性T淋巴细胞抗原-4 (CTLA-4)是存在于T细胞上的一种分子,在下调抗原激活免疫反应中起关键作用。其基因多态性是一个强有力的候选基因赋予甲状腺自身免疫易感性。该研究的目的是分析CTLA-4外显子1多态性(A49G)在桥本甲状腺炎儿童中的频率。材料和方法:分析了68名儿童的血液样本:30名患有桥本甲状腺炎,38名健康,年龄匹配的对照组,平均年龄:13.6岁。采用PCR法和单链构象多态性分析确定CTLA-4外显子1多态性(A49G),并用BbvI酶进行验证。采用t检验和卡方检验进行统计学分析。结果:多态分析显示,桥本甲状腺炎患者G (Ala)纯合子发生率显著高于对照组,且G等位基因频率显著高于对照组。结论:CTLA-4外显子1多态性(A49G)与波兰儿童桥本甲状腺炎存在相关性。
{"title":"[The frequency of CTLA-4 gene polymorphism at position 49 exon 1 in children with Hashimoto's thyroiditis].","authors":"Anna Kucharska,&nbsp;Alicja Wiśniewska,&nbsp;Barbara Rymkiewicz-Kluczyńska","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Introduction: </strong>The cytotoxic T lymphocyte antigen-4 (CTLA-4) is a molecule present on T cells that plays a critical role in the down regulation of antigen-activated immune responses. Its gene polymorphism is a strong candidate gene for conferring susceptibility to thyroid autoimmunity. THE AIM of the study was to analyse the frequency of CTLA-4 exon 1 polymorphism (A49G) in children with Hashimoto's thyroiditis.</p><p><strong>Material and methods: </strong>Blood samples from 68 children were analysed: 30 with Hashimoto's thyroiditis and 38 healthy, age-matched controls, mean age: 13.6 years. CTLA-4 exon 1 polymorphism (A49G) was defined by the PCR method and single-strand conformational polymorphism analysis and confirmed by using BbvI enzyme. Statistical analysis was performed using the t- test and Chi-square test.</p><p><strong>Results: </strong>Polymorphism analysis showed that statistically significant more patients with Hashimoto's thyroiditis were homozygous for G (Ala), and G allele frequency was significant higher than in the control group.</p><p><strong>Conclusion: </strong>The results confirmed the association between CTLA-4 exon 1 polymorphism (A49G) and Hashimoto's thyroiditis in polish children.</p>","PeriodicalId":11550,"journal":{"name":"Endokrynologia, diabetologia i choroby przemiany materii wieku rozwojowego : organ Polskiego Towarzystwa Endokrynologow Dzieciecych","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2006-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"26291824","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Obesity related complications in children and adolescents]. [儿童和青少年肥胖相关并发症]。
Piotr Fichna, Bogda Skowrońska

The epidemic of obesity concerns also children and adolescents. Excess weight increases the risk of metabolic complications, diabetes type 2, hypertension, cardiovascular disease, pulmonary and musculoskeletal disorders, psychosocial problems. Simple obesity leads to secondary endocrine disturbances. Long lasting insulin resistance and proinflammatory state induced by cytokines, which are produced in adipose tissue, play the main role in the development of obesity associated complications. Many disturbances can be reversed at the early stage, if even small weight loss is achieved.

肥胖的流行也关系到儿童和青少年。体重过重会增加代谢并发症、2型糖尿病、高血压、心血管疾病、肺部和肌肉骨骼疾病、社会心理问题的风险。单纯性肥胖可导致继发性内分泌紊乱。脂肪组织产生的细胞因子诱导的长期胰岛素抵抗和促炎状态在肥胖相关并发症的发生中起主要作用。许多干扰可以在早期阶段逆转,即使是很小的体重减轻。
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引用次数: 0
[Is arterial hypertension a significant problem in children and adolescents with type 1 diabetes?]. 动脉高血压是儿童和青少年1型糖尿病患者的一个重要问题吗?
Renata Wasikowa, Aleksander Basiak

In the last two decades the problem of arterial hypertension in patients in the developmental age gained an increasing interest. The frequency of arterial hypertension in children was estimated at the level of 1-5% of the population. It was demonstrated that hypertension is observed in patients with type 1 diabetes over two-three times more frequently than in the general population. Arterial hypertension is a significant risk factor for cardio-vascular complications. The coexistence of diabetes type 1 and arterial hypertension predisposes to ischemic heart disease, stroke and premature death. Normal range of arterial tension for children was established during the Task Force on Blood Pressure Control study in children. Models depending on age and sex were created. Measurements above the 95 percentile for age and sex were referred to as significant hypertension and above the 97 percentile as heavy hypertension. For the development of arterial hypertension in patients with type 1 diabetes, which is the dominant type in children and adolescents, apart from the genetic predisposition, the coexistence of nephropathy is important. In children and adolescents almost exclusively secondary nephrogenic hypertension is observed, which develops usually 2 years after microproteinuria. Seldom in children and adolescents with type 1 diabetes essential hypertension or hypertension of other causes, as for example contraction of the nephrotic artery, may be observed. A particular form of arterial hypertension is lack of pressure decrease during the night, with a maintenance of the normal rhythm during the day. Recently the state called "pre-hypertension", considered as a precursor of hypertension and a predictor of excessive cardiovascular risk, has gained increasing interest. The pharmacological therapy of arterial hypertension in patients with diabetes type 1 may be taylored individually, depending on the degree and form of diabetes, and also on its late complications. In case of an unfavourable course dialysis may be considered and transplantation of the kidney, as hemodialysis in children with type 1 diabetes is connected with frequent complications. It is crucial to consider the transplantation of the kidney at early stages, when the creatinine level is above 5 mg/dl. It has been proved that the results of transplantation in patients with diabetes are similar to those in patients without diabetes.

在过去的二十年中,在发育年龄的患者中动脉高血压的问题得到了越来越多的关注。据估计,儿童患动脉高血压的频率约占总人口的1-5%。研究表明,高血压在1型糖尿病患者中出现的频率是一般人群的2 - 3倍。动脉高血压是心血管并发症的重要危险因素。1型糖尿病和动脉高血压共存,易患缺血性心脏病、中风和过早死亡。儿童动脉张力的正常范围是在儿童血压控制研究工作组期间确定的。根据年龄和性别建立了模型。年龄和性别超过95%的测量值被称为显著高血压,超过97%的测量值被称为重度高血压。1型糖尿病是儿童和青少年的主要类型,对于1型糖尿病患者动脉高血压的发展,除了遗传易感性外,肾病的共存是重要的。在儿童和青少年中几乎完全观察到继发性肾源性高血压,通常在微量蛋白尿后2年发生。在患有1型糖尿病的儿童和青少年中,原发性高血压或其他原因的高血压,如肾病动脉收缩,可能很少观察到。动脉高血压的一种特殊形式是夜间血压不降,白天维持正常节律。最近,被称为“高血压前期”的状态,被认为是高血压的前兆和心血管疾病风险过高的预测因子,引起了越来越多的关注。1型糖尿病患者动脉高血压的药物治疗可以根据糖尿病的程度和形式以及晚期并发症进行个体化治疗。在不利的情况下,可以考虑透析和肾脏移植,因为1型糖尿病儿童的血液透析与频繁的并发症有关。当肌酐水平高于5 mg/dl时,在早期阶段考虑肾移植是至关重要的。已经证明,糖尿病患者的移植结果与非糖尿病患者相似。
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引用次数: 0
[Declared attitudes of girls with Turner's syndrome towards physical education classes]. [特纳综合症女孩对体育课的公开态度]。
Edyta Sienkiewicz-Dianzenza, Katarzyna Milde, Mirosława Frac

Objectives: To learn the attitudes and opinions of girls with Turner's syndrome about physical education classes and to determine the level of physical activity of those girls by applying the MVPA (moderate-to-vigorous physical activity) index.

Material and methods: A group of 36 girls with Turner's syndrome, aged 10-19 years, participants of a summer camp at the sea shore in 2004, were subjected to a questionnaire study. The resulting MVPA index served as an indicator of the degree of physical activity.

Results: About one-fourth of girls were chronically disqualified by physicians from physical education (PE) classes, 69% declared they "liked" or "liked very much" PE classes, but only 29% stated that the degree of difficulty of PE activities matched the abilities of schoolchildren. Mean MVPA value in those girls amounted to 3.5 days a week and only 19% of girls met the recommended level of 5 or more days a week.

Summary and conclusions: The girls with Turner's syndrome had good opinions of their PE teachers but the participation of those girls in physical activities was unsatisfactory. The teachers ought to seek efficient ways to motivate schoolchildren for increasing their physical activities and their participation in various forms of sport and leisure activities.

目的:了解特纳综合征女生对体育课的态度和看法,并应用MVPA (moderate- vigorous physical activity)指数确定特纳综合征女生的体育活动水平。材料与方法:对2004年参加海边夏令营的36名10-19岁特纳氏综合征女孩进行问卷调查。由此得出的MVPA指数作为身体活动程度的指标。结果:大约四分之一的女孩被医生长期取消了体育课的资格,69%的女孩表示她们“喜欢”或“非常喜欢”体育课,但只有29%的女孩表示体育活动的难度与学龄儿童的能力相匹配。这些女孩的平均MVPA值为每周3.5天,只有19%的女孩达到每周5天或更多的建议水平。总结与结论:特纳综合征女生对体育老师的评价较高,但参与体育活动的情况不理想。教师应该寻找有效的方法来激励学生增加他们的体育活动和参与各种形式的体育和休闲活动。
{"title":"[Declared attitudes of girls with Turner's syndrome towards physical education classes].","authors":"Edyta Sienkiewicz-Dianzenza,&nbsp;Katarzyna Milde,&nbsp;Mirosława Frac","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Objectives: </strong>To learn the attitudes and opinions of girls with Turner's syndrome about physical education classes and to determine the level of physical activity of those girls by applying the MVPA (moderate-to-vigorous physical activity) index.</p><p><strong>Material and methods: </strong>A group of 36 girls with Turner's syndrome, aged 10-19 years, participants of a summer camp at the sea shore in 2004, were subjected to a questionnaire study. The resulting MVPA index served as an indicator of the degree of physical activity.</p><p><strong>Results: </strong>About one-fourth of girls were chronically disqualified by physicians from physical education (PE) classes, 69% declared they \"liked\" or \"liked very much\" PE classes, but only 29% stated that the degree of difficulty of PE activities matched the abilities of schoolchildren. Mean MVPA value in those girls amounted to 3.5 days a week and only 19% of girls met the recommended level of 5 or more days a week.</p><p><strong>Summary and conclusions: </strong>The girls with Turner's syndrome had good opinions of their PE teachers but the participation of those girls in physical activities was unsatisfactory. The teachers ought to seek efficient ways to motivate schoolchildren for increasing their physical activities and their participation in various forms of sport and leisure activities.</p>","PeriodicalId":11550,"journal":{"name":"Endokrynologia, diabetologia i choroby przemiany materii wieku rozwojowego : organ Polskiego Towarzystwa Endokrynologow Dzieciecych","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2006-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"26122764","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Selected matrix metalloproteinases (MMP-2, MMP-9) in obese children and adolescents]. [选择基质金属蛋白酶(MMP-2, MMP-9)在肥胖儿童和青少年]。
Barbara Głowińska-Olszewska, Mirosława Urban, Bozena Florys

Introduction: In the last years it has been proved that matrix metalloproteinases participate in the development of all stages of atherosclerotic process. It has been suggested that plasma levels of metalloproteinases can be a novel, inflammatory marker of atherosclerosis. THE AIM OF THE STUDY was to evaluate plasma levels of selected matrix metalloproteinases (MMP-2 and MMP-9) in obese children and adolescents.

Material and methods: We studied 45 children and adolescents with simple obesity aged 15+/-1.8 years. The control group comprised 28 healthy, slim children aged 14.5 years. The obese children were studied according to coexistence of hypertension, hyperlipidemia, positive family history of cardiovascular diseases and insulin resistance. Levels of matrix metalloproteinases were assessed by use of ready ELISA kits (R&D Systems).

Results: MMP-9 level in the study group equaled 553.5+/-311 ng/ml and was significantly higher compared to the control group: 400.4+/-204 ng/ml, p=0.02. MMP-2 level in the study group was significantly lower compared to the control group: 211+/-37 ng/ml vs. 258+/-56 ng/ml, p<0,0001. In obese children with coexisting hypertension we found higher levels of MMP-9 when compared to children with obesity only: 635+/-308 ng/ml vs. 450+/-289 ng/ml (p=0,04), MMP-2 levels remained similar in both groups.

Conclusions: Different levels of plasma matrix metalloproteinases in obese and hypertensive children compared to healthy, slim controls can indicate an altered metabolism of the extracellular matrix (ECM) of vessels and heart muscle. Changed metabolism of ECM may be of significant importance in enhancing the atherosclerotic process in this young patients.

近年来,已经证明基质金属蛋白酶参与动脉粥样硬化过程的各个阶段的发展。有研究表明,血浆金属蛋白酶水平可能是动脉粥样硬化的一种新的炎症标志物。该研究的目的是评估肥胖儿童和青少年中选定的基质金属蛋白酶(MMP-2和MMP-9)的血浆水平。材料和方法:我们研究了45例15+/-1.8岁的单纯性肥胖儿童和青少年。对照组由28名14.5岁的健康、苗条的儿童组成。根据高血压、高脂血症、心血管疾病家族史和胰岛素抵抗的共存情况对肥胖儿童进行调查。使用现成的ELISA试剂盒(R&D Systems)评估基质金属蛋白酶水平。结果:研究组MMP-9水平为553.5+/-311 ng/ml,显著高于对照组400.4+/-204 ng/ml, p=0.02。研究组的MMP-2水平明显低于对照组,分别为211+/-37 ng/ml和258+/-56 ng/ml。结论:肥胖和高血压儿童与健康、苗条的对照组相比,血浆基质金属蛋白酶水平的不同可能表明血管和心肌细胞外基质(ECM)代谢的改变。ECM代谢的改变可能在促进这名年轻患者的动脉粥样硬化过程中具有重要意义。
{"title":"[Selected matrix metalloproteinases (MMP-2, MMP-9) in obese children and adolescents].","authors":"Barbara Głowińska-Olszewska,&nbsp;Mirosława Urban,&nbsp;Bozena Florys","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Introduction: </strong>In the last years it has been proved that matrix metalloproteinases participate in the development of all stages of atherosclerotic process. It has been suggested that plasma levels of metalloproteinases can be a novel, inflammatory marker of atherosclerosis. THE AIM OF THE STUDY was to evaluate plasma levels of selected matrix metalloproteinases (MMP-2 and MMP-9) in obese children and adolescents.</p><p><strong>Material and methods: </strong>We studied 45 children and adolescents with simple obesity aged 15+/-1.8 years. The control group comprised 28 healthy, slim children aged 14.5 years. The obese children were studied according to coexistence of hypertension, hyperlipidemia, positive family history of cardiovascular diseases and insulin resistance. Levels of matrix metalloproteinases were assessed by use of ready ELISA kits (R&D Systems).</p><p><strong>Results: </strong>MMP-9 level in the study group equaled 553.5+/-311 ng/ml and was significantly higher compared to the control group: 400.4+/-204 ng/ml, p=0.02. MMP-2 level in the study group was significantly lower compared to the control group: 211+/-37 ng/ml vs. 258+/-56 ng/ml, p<0,0001. In obese children with coexisting hypertension we found higher levels of MMP-9 when compared to children with obesity only: 635+/-308 ng/ml vs. 450+/-289 ng/ml (p=0,04), MMP-2 levels remained similar in both groups.</p><p><strong>Conclusions: </strong>Different levels of plasma matrix metalloproteinases in obese and hypertensive children compared to healthy, slim controls can indicate an altered metabolism of the extracellular matrix (ECM) of vessels and heart muscle. Changed metabolism of ECM may be of significant importance in enhancing the atherosclerotic process in this young patients.</p>","PeriodicalId":11550,"journal":{"name":"Endokrynologia, diabetologia i choroby przemiany materii wieku rozwojowego : organ Polskiego Towarzystwa Endokrynologow Dzieciecych","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2006-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"26291783","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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Endokrynologia, diabetologia i choroby przemiany materii wieku rozwojowego : organ Polskiego Towarzystwa Endokrynologow Dzieciecych
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