首页 > 最新文献

Pediatric endocrinology reviews : PER最新文献

英文 中文
Decision Support Systems for Insulin Treatment Adjustment in People with Type 1 Diabetes. 1型糖尿病患者胰岛素治疗调整的决策支持系统
4区 医学 Q2 Medicine Pub Date : 2020-03-01 DOI: 10.17458/per.vol17.2020.n.insulintreatmenttype1diabetes
Revital Nimri

For people with type 1 diabetes, achieving optimal glycemic control requires use of intensive insulin therapy. To achieve this goal individuals are required to become proficient in accurately determining the appropriate amount of insulin needed to address a variety of situations throughout the day while considering numerous influencing factors. They also need to perform multiple tasks a day such as counting carbohydrates to accurately determine the required premeal bolus. There is also a need to periodically adjust insulin dosing as insulin sensitivity varies considerably over time. Sophisticated advanced technologies are being used by growing numbers of individuals to manage diabetes. However, despite innovations in glucose monitoring technologies and new insulin formulations, many of these individuals are not achieving their glycemic goals. The new technologies provide ample amount of valuable diabetes related data that may complicate even further the insulin dosing decision making for people with diabetes as well as for the health care providers. Mobile health, digital tools and decision support systems can help to increase accurate, timely insulin dosing and insulin titration and holds the potential to improve glycemic control to a wide range of individuals with diabetes. The emerging mobile toolbox for insulin dosing adjustments that will be reviewed in this paper includes insulin management Apps; diverse range of Apps to guide insulin adjustments such as in times of physical activity and eating; data management systems which enable visualization and analysis of insulin and glucose data of various devices; real-time alarms and glucose prediction Apps that help to prevent hypoglycemia and hyperglycemia events; various bolus calculators for meal time dosing; sophisticated decision support algorithms for people using insulin pump, multiple insulin injections and closed loop systems for real-time and retrospective insulin dosing adjustments.

对于1型糖尿病患者,达到最佳血糖控制需要使用强化胰岛素治疗。为了实现这一目标,个人需要在考虑众多影响因素的情况下,准确地确定一天中各种情况所需的适当胰岛素量。他们还需要在一天内完成多项任务,比如计算碳水化合物以准确确定所需的餐前剂量。也需要定期调整胰岛素剂量,因为胰岛素敏感性随时间变化很大。越来越多的个人正在使用复杂的先进技术来控制糖尿病。然而,尽管血糖监测技术和新的胰岛素配方不断创新,这些人中的许多人并没有达到他们的血糖目标。新技术提供了大量有价值的糖尿病相关数据,这些数据可能会使糖尿病患者以及医疗保健提供者的胰岛素剂量决策进一步复杂化。移动医疗、数字工具和决策支持系统可以帮助增加准确、及时的胰岛素剂量和胰岛素滴定,并有可能改善广泛的糖尿病患者的血糖控制。本文将回顾的用于胰岛素剂量调整的新兴移动工具箱包括胰岛素管理应用程序;各种各样的应用程序来指导胰岛素调整,比如在体育活动和饮食的时候;数据管理系统,可以对各种设备的胰岛素和葡萄糖数据进行可视化和分析;帮助预防低血糖和高血糖事件的实时警报和血糖预测应用程序;用于用餐时间给药的各种剂量计算器;为使用胰岛素泵的人提供复杂的决策支持算法,多次胰岛素注射和闭环系统,用于实时和回顾性胰岛素剂量调整。
{"title":"Decision Support Systems for Insulin Treatment Adjustment in People with Type 1 Diabetes.","authors":"Revital Nimri","doi":"10.17458/per.vol17.2020.n.insulintreatmenttype1diabetes","DOIUrl":"https://doi.org/10.17458/per.vol17.2020.n.insulintreatmenttype1diabetes","url":null,"abstract":"<p><p>For people with type 1 diabetes, achieving optimal glycemic control requires use of intensive insulin therapy. To achieve this goal individuals are required to become proficient in accurately determining the appropriate amount of insulin needed to address a variety of situations throughout the day while considering numerous influencing factors. They also need to perform multiple tasks a day such as counting carbohydrates to accurately determine the required premeal bolus. There is also a need to periodically adjust insulin dosing as insulin sensitivity varies considerably over time. Sophisticated advanced technologies are being used by growing numbers of individuals to manage diabetes. However, despite innovations in glucose monitoring technologies and new insulin formulations, many of these individuals are not achieving their glycemic goals. The new technologies provide ample amount of valuable diabetes related data that may complicate even further the insulin dosing decision making for people with diabetes as well as for the health care providers. Mobile health, digital tools and decision support systems can help to increase accurate, timely insulin dosing and insulin titration and holds the potential to improve glycemic control to a wide range of individuals with diabetes. The emerging mobile toolbox for insulin dosing adjustments that will be reviewed in this paper includes insulin management Apps; diverse range of Apps to guide insulin adjustments such as in times of physical activity and eating; data management systems which enable visualization and analysis of insulin and glucose data of various devices; real-time alarms and glucose prediction Apps that help to prevent hypoglycemia and hyperglycemia events; various bolus calculators for meal time dosing; sophisticated decision support algorithms for people using insulin pump, multiple insulin injections and closed loop systems for real-time and retrospective insulin dosing adjustments.</p>","PeriodicalId":19827,"journal":{"name":"Pediatric endocrinology reviews : PER","volume":"17 Suppl 1","pages":"170-182"},"PeriodicalIF":0.0,"publicationDate":"2020-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37768708","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
History of Insulin Treatment in Children and Adolescents with Diabetes in Japan. 日本儿童和青少年糖尿病胰岛素治疗史
4区 医学 Q2 Medicine Pub Date : 2020-03-01 DOI: 10.17458/per.vol17.2020.u.insulintreatchildadolescentjapan
Tatsuhiko Urakami

For the increasing number of type 1 diabetes in Japan, after 1960, a greater supply of insulin was required, accordingly the availability of insulin gradually improved, The National Health Insurance approved self-injections of insulin at home in 1981. Afterwards, intensive insulin treatment with short-acting insulin and intermediate-acting insulin became widely used. Recombinant rapid-acting insulin analog was introduced in 1986 and long-acting insulin analog was introduced in 2003. In recent years, basal-bolus insulin regimens using these insulin analogs have become popular in children and adolescents with type 1 diabetes in Japan, which can improve the metabolic state and quality of life. This also will contribute to prevent the occurrence and progression of micro- and macro-vascular complications later in life.

1960年以后,日本的1型糖尿病患者越来越多,需要更多的胰岛素供应,因此胰岛素的供应逐渐改善,国民健康保险于1981年批准在家中自行注射胰岛素。此后,短效胰岛素和中效胰岛素的强化胰岛素治疗得到广泛应用。重组速效胰岛素类似物于1986年推出,长效胰岛素类似物于2003年推出。近年来,使用这些胰岛素类似物的基础胰岛素方案在日本的1型糖尿病儿童和青少年中很受欢迎,可以改善代谢状态和生活质量。这也将有助于预防生命后期微血管和大血管并发症的发生和发展。
{"title":"History of Insulin Treatment in Children and Adolescents with Diabetes in Japan.","authors":"Tatsuhiko Urakami","doi":"10.17458/per.vol17.2020.u.insulintreatchildadolescentjapan","DOIUrl":"https://doi.org/10.17458/per.vol17.2020.u.insulintreatchildadolescentjapan","url":null,"abstract":"<p><p>For the increasing number of type 1 diabetes in Japan, after 1960, a greater supply of insulin was required, accordingly the availability of insulin gradually improved, The National Health Insurance approved self-injections of insulin at home in 1981. Afterwards, intensive insulin treatment with short-acting insulin and intermediate-acting insulin became widely used. Recombinant rapid-acting insulin analog was introduced in 1986 and long-acting insulin analog was introduced in 2003. In recent years, basal-bolus insulin regimens using these insulin analogs have become popular in children and adolescents with type 1 diabetes in Japan, which can improve the metabolic state and quality of life. This also will contribute to prevent the occurrence and progression of micro- and macro-vascular complications later in life.</p>","PeriodicalId":19827,"journal":{"name":"Pediatric endocrinology reviews : PER","volume":"17 Suppl 1","pages":"220-221"},"PeriodicalIF":0.0,"publicationDate":"2020-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37768713","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Update on Worldwide Trends in Occurrence of Childhood Type 1 Diabetes in 2020. 2020年全球儿童1型糖尿病发生趋势的最新进展
4区 医学 Q2 Medicine Pub Date : 2020-03-01 DOI: 10.17458/per.vol17.2020.tol.epidemiologychildtype1diabetes
Jaakko Tuomilehto, Graham D Ogle, Nicolai A Lund-Blix, Lars C Stene

Epidemiological data on pediatric type 1 diabetes (T1D), mainly incidence, have become increasingly available since the second half of the 20th century. Comparative incidence data across populations were only obtained since the 1980s. The 2019 IDF Atlas provides T1D incidence, prevalence and mortality estimates for children < 15 years for all 211 countries, but actual data were available for only 94 countries (only 3 low-income). The estimated prevalent cases were 600,900 and incident cases 98,200. Incidence remains highest in Finland (60/100,000/ year), Sardinia and Sweden, followed by Kuwait, some other northern European countries, Saudi Arabia, Algeria, Australia, New Zealand, USA and Canada. The lowest incidence is seen across East and South-East Asia. Globally, the average increase in incidence has been 3-4%/year over past decades, being steeper in low-incidence countries. Although T1D mortality has drastically decreased, there is still a higher risk compared with the non-diabetic population, especially in people with diabetic nephropathy.

自20世纪下半叶以来,儿童1型糖尿病(T1D)的流行病学数据(主要是发病率)越来越多。从20世纪80年代以来才获得了人群间发病率的比较数据。2019年IDF地图集提供了所有211个国家15岁以下儿童的T1D发病率、患病率和死亡率估计数,但只有94个国家(只有3个低收入国家)可获得实际数据。估计流行病例为60 900例,意外病例为98 200例。芬兰、撒丁岛和瑞典的发病率仍然最高(60/10万/年),其次是科威特、一些其他北欧国家、沙特阿拉伯、阿尔及利亚、澳大利亚、新西兰、美国和加拿大。东亚和东南亚的发病率最低。在过去几十年中,全球发病率的平均增长率为每年3-4%,在低发病率国家更为陡峭。虽然T1D的死亡率急剧下降,但与非糖尿病人群相比,其风险仍然较高,尤其是糖尿病肾病患者。
{"title":"Update on Worldwide Trends in Occurrence of Childhood Type 1 Diabetes in 2020.","authors":"Jaakko Tuomilehto,&nbsp;Graham D Ogle,&nbsp;Nicolai A Lund-Blix,&nbsp;Lars C Stene","doi":"10.17458/per.vol17.2020.tol.epidemiologychildtype1diabetes","DOIUrl":"https://doi.org/10.17458/per.vol17.2020.tol.epidemiologychildtype1diabetes","url":null,"abstract":"<p><p>Epidemiological data on pediatric type 1 diabetes (T1D), mainly incidence, have become increasingly available since the second half of the 20th century. Comparative incidence data across populations were only obtained since the 1980s. The 2019 IDF Atlas provides T1D incidence, prevalence and mortality estimates for children < 15 years for all 211 countries, but actual data were available for only 94 countries (only 3 low-income). The estimated prevalent cases were 600,900 and incident cases 98,200. Incidence remains highest in Finland (60/100,000/ year), Sardinia and Sweden, followed by Kuwait, some other northern European countries, Saudi Arabia, Algeria, Australia, New Zealand, USA and Canada. The lowest incidence is seen across East and South-East Asia. Globally, the average increase in incidence has been 3-4%/year over past decades, being steeper in low-incidence countries. Although T1D mortality has drastically decreased, there is still a higher risk compared with the non-diabetic population, especially in people with diabetic nephropathy.</p>","PeriodicalId":19827,"journal":{"name":"Pediatric endocrinology reviews : PER","volume":"17 Suppl 1","pages":"198-209"},"PeriodicalIF":0.0,"publicationDate":"2020-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37768711","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 53
Eli Lilly and Company Insulins - A Century of Innovation. 礼来公司胰岛素-一个世纪的创新。
4区 医学 Q2 Medicine Pub Date : 2020-03-01 DOI: 10.17458/per.vol17.2020.jjh.elilillycompanyinsulin
J K Malone, J H Jr Anderson, H A Wolpert, L L Ilag, B H Frank, M R De Felippis, C D Paavola, A L Orr, J M Beals

Eli Lilly and Company has played a pivotal role in the development of insulin products since its discovery in 1921. Through their dedication to pharmaceutical innovation, Josiah K. Lilly Sr. and George HA Clowes, in close collaborations with the University of Toronto, made insulin commercially available in 1923. Other innovations include the development and commercialization of the first biosynthetic human insulin, a rapid-acting insulin analog and analog mixtures. Lilly has advanced the field of knowledge with significant efforts toward developing a hepatic preferential basal insulin. Other important insulin projects include the first concentrated rapid-acting insulin analog, clinical studies supporting the use of highly concentrated human insulin, and an advanced clinical development program for an ultra-rapid insulin analog. Lilly's commitment to people affected with diabetes remains strong and will continue into the future through collaborative research, innovative product development and investing in advanced technologies.

自1921年发现胰岛素产品以来,礼来公司在胰岛素产品的开发中发挥了关键作用。通过他们对制药创新的奉献,Josiah K. Lilly和George HA Clowes与多伦多大学密切合作,于1923年将胰岛素商业化。其他创新包括首个生物合成人胰岛素的开发和商业化,这是一种速效胰岛素类似物和类似物混合物。礼来公司在开发肝脏优先型基础胰岛素方面做出了重大努力,推动了知识领域的发展。其他重要的胰岛素项目包括首个浓缩速效胰岛素类似物,支持使用高浓度人胰岛素的临床研究,以及超快速胰岛素类似物的高级临床开发项目。礼来对糖尿病患者的承诺依然坚定,并将通过合作研究、创新产品开发和对先进技术的投资,在未来继续下去。
{"title":"Eli Lilly and Company Insulins - A Century of Innovation.","authors":"J K Malone,&nbsp;J H Jr Anderson,&nbsp;H A Wolpert,&nbsp;L L Ilag,&nbsp;B H Frank,&nbsp;M R De Felippis,&nbsp;C D Paavola,&nbsp;A L Orr,&nbsp;J M Beals","doi":"10.17458/per.vol17.2020.jjh.elilillycompanyinsulin","DOIUrl":"https://doi.org/10.17458/per.vol17.2020.jjh.elilillycompanyinsulin","url":null,"abstract":"<p><p>Eli Lilly and Company has played a pivotal role in the development of insulin products since its discovery in 1921. Through their dedication to pharmaceutical innovation, Josiah K. Lilly Sr. and George HA Clowes, in close collaborations with the University of Toronto, made insulin commercially available in 1923. Other innovations include the development and commercialization of the first biosynthetic human insulin, a rapid-acting insulin analog and analog mixtures. Lilly has advanced the field of knowledge with significant efforts toward developing a hepatic preferential basal insulin. Other important insulin projects include the first concentrated rapid-acting insulin analog, clinical studies supporting the use of highly concentrated human insulin, and an advanced clinical development program for an ultra-rapid insulin analog. Lilly's commitment to people affected with diabetes remains strong and will continue into the future through collaborative research, innovative product development and investing in advanced technologies.</p>","PeriodicalId":19827,"journal":{"name":"Pediatric endocrinology reviews : PER","volume":"17 Suppl 1","pages":"138-160"},"PeriodicalIF":0.0,"publicationDate":"2020-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37768242","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 5
The Discovery and Structure of Human Insulin. 人胰岛素的发现及其结构。
4区 医学 Q2 Medicine Pub Date : 2020-03-01 DOI: 10.17458/per.vol17.2020.zfs.discoverystructureinsulin
Chelsea Zimmerman, Gregory Forlenza, Desmond Schatz

The isolation and purification of insulin nearly 100 years ago has been one of the most ground-breaking discoveries in the history of medicine. Subsequent determination of the specific structure of human insulin has permitted further developments and modifications of the formulations of insulin to allow improved quality of care and quality of life for patients with diabetes. In this paper, we will review insulin structure and biosynthesis, treatment and prognosis of type 1 diabetes prior to insulin therapy, experimentation leading to the discovery of insulin, and the first patients to be treated with insulin.

近100年前,胰岛素的分离和纯化是医学史上最具突破性的发现之一。随后对人胰岛素具体结构的确定使胰岛素配方的进一步发展和修改成为可能,从而提高糖尿病患者的护理质量和生活质量。本文将对胰岛素的结构和生物合成、胰岛素治疗前1型糖尿病的治疗和预后、胰岛素发现的实验以及第一批接受胰岛素治疗的患者进行综述。
{"title":"The Discovery and Structure of Human Insulin.","authors":"Chelsea Zimmerman,&nbsp;Gregory Forlenza,&nbsp;Desmond Schatz","doi":"10.17458/per.vol17.2020.zfs.discoverystructureinsulin","DOIUrl":"https://doi.org/10.17458/per.vol17.2020.zfs.discoverystructureinsulin","url":null,"abstract":"<p><p>The isolation and purification of insulin nearly 100 years ago has been one of the most ground-breaking discoveries in the history of medicine. Subsequent determination of the specific structure of human insulin has permitted further developments and modifications of the formulations of insulin to allow improved quality of care and quality of life for patients with diabetes. In this paper, we will review insulin structure and biosynthesis, treatment and prognosis of type 1 diabetes prior to insulin therapy, experimentation leading to the discovery of insulin, and the first patients to be treated with insulin.</p>","PeriodicalId":19827,"journal":{"name":"Pediatric endocrinology reviews : PER","volume":"17 Suppl 1","pages":"131-137"},"PeriodicalIF":0.0,"publicationDate":"2020-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37767894","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Insulin: A Growth Hormone and Potential Oncogene. 胰岛素:生长激素和潜在的致癌基因。
4区 医学 Q2 Medicine Pub Date : 2020-03-01 DOI: 10.17458/per.vol17.2020.lw.insulinghpotentialoncogene
Zvi Laron, Haim Werner

Both in vitro and in vivo experimental studies proved that insulin has an important anabolic role. This physiological function of insulin is reflected in its well documented involvement in protein metabolism and in acceleration of cell proliferation. Support for a growth promoting action of insulin is further provided by clinical studies that revealed that children with hypoinsulinemia have a decreased growth rate whereas, on the other hand, children with hyperinsulinemia have an accelerated growth. While it was initially assumed that the growth activities of insulin are facilitated via cross-talk with the closely related insulin-like growth factor-1 receptor (IGF-1R), it is now clear that the vast majority of these activities are mediated via direct interaction with the insulin receptor (IR). The present article provides an overview of the growth and proliferative actions of insulin, with an emphasis on a number of pathological conditions, including cancer.

体外和体内实验研究均证明胰岛素具有重要的合成代谢作用。胰岛素的这种生理功能反映在其充分记录的参与蛋白质代谢和加速细胞增殖。临床研究进一步支持胰岛素促进生长的作用,表明低胰岛素血症儿童的生长速度下降,而另一方面,高胰岛素血症儿童的生长速度加快。虽然最初认为胰岛素的生长活性是通过与密切相关的胰岛素样生长因子-1受体(IGF-1R)的串扰促进的,但现在很清楚,绝大多数这些活性是通过与胰岛素受体(IR)的直接相互作用介导的。本文概述了胰岛素的生长和增殖作用,重点介绍了一些病理条件,包括癌症。
{"title":"Insulin: A Growth Hormone and Potential Oncogene.","authors":"Zvi Laron,&nbsp;Haim Werner","doi":"10.17458/per.vol17.2020.lw.insulinghpotentialoncogene","DOIUrl":"https://doi.org/10.17458/per.vol17.2020.lw.insulinghpotentialoncogene","url":null,"abstract":"<p><p>Both in vitro and in vivo experimental studies proved that insulin has an important anabolic role. This physiological function of insulin is reflected in its well documented involvement in protein metabolism and in acceleration of cell proliferation. Support for a growth promoting action of insulin is further provided by clinical studies that revealed that children with hypoinsulinemia have a decreased growth rate whereas, on the other hand, children with hyperinsulinemia have an accelerated growth. While it was initially assumed that the growth activities of insulin are facilitated via cross-talk with the closely related insulin-like growth factor-1 receptor (IGF-1R), it is now clear that the vast majority of these activities are mediated via direct interaction with the insulin receptor (IR). The present article provides an overview of the growth and proliferative actions of insulin, with an emphasis on a number of pathological conditions, including cancer.</p>","PeriodicalId":19827,"journal":{"name":"Pediatric endocrinology reviews : PER","volume":"17 Suppl 1","pages":"191-197"},"PeriodicalIF":0.0,"publicationDate":"2020-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37768710","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 5
Precocious puberty. 性早熟。
4区 医学 Q2 Medicine Pub Date : 2020-02-07 DOI: 10.32388/hyqwd0
A. Papathanasiou, C. Hadjiathanasiou
The term precocious puberty encompasses a group of heterogeneous conditions that range from variants of normal to slowly progressive and rapidly progressive maturation of both sexes. It is defined as the appearance of secondary sex characteristics before the age of 8 in girls and 9 in boys. The clinician who is evaluating a child with precocious puberty should be aware of the normal events of puberty, the ages at which pubertal milestones are achieved and the tempo of pubertal progression. The mechanisms involved in the onset and progression of normal puberty are briefly discussed in this article. The diverse etiology of precocious puberty, the diagnostic evaluation of the patient including clinical, laboratory and radiological investigation as well as problems associated with precocious puberty and indications for treatment and treatment modalities are further discussed in the article.
“性早熟”一词包含了一组不同的情况,从正常的变异到两性缓慢渐进和迅速渐进的成熟。它被定义为女孩在8岁之前,男孩在9岁之前出现第二性征。评估性早熟儿童的临床医生应该了解青春期的正常事件,达到青春期里程碑的年龄和青春期发展的速度。本文简要讨论了正常青春期发生和发展的机制。本文将进一步讨论性早熟的多种病因,包括临床、实验室和影像学检查在内的对患者的诊断评价,以及与性早熟有关的问题和治疗的适应症和治疗方式。
{"title":"Precocious puberty.","authors":"A. Papathanasiou, C. Hadjiathanasiou","doi":"10.32388/hyqwd0","DOIUrl":"https://doi.org/10.32388/hyqwd0","url":null,"abstract":"The term precocious puberty encompasses a group of heterogeneous conditions that range from variants of normal to slowly progressive and rapidly progressive maturation of both sexes. It is defined as the appearance of secondary sex characteristics before the age of 8 in girls and 9 in boys. The clinician who is evaluating a child with precocious puberty should be aware of the normal events of puberty, the ages at which pubertal milestones are achieved and the tempo of pubertal progression. The mechanisms involved in the onset and progression of normal puberty are briefly discussed in this article. The diverse etiology of precocious puberty, the diagnostic evaluation of the patient including clinical, laboratory and radiological investigation as well as problems associated with precocious puberty and indications for treatment and treatment modalities are further discussed in the article.","PeriodicalId":19827,"journal":{"name":"Pediatric endocrinology reviews : PER","volume":"133 1","pages":"182-7"},"PeriodicalIF":0.0,"publicationDate":"2020-02-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"81745978","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Primary School Performance of Girls with Turner Syndrome: A Transcultural Assessment. 特纳综合症女童小学表现的跨文化评估。
4区 医学 Q2 Medicine Pub Date : 2019-12-01 DOI: 10.17458/per.vol17.2019.lhs.gilrsturnersyndrome
J. Lebl, R. Hamza, J. Stoklasova, J. Zapletalová, S. Koloušková, O. Souček, B. Obermannová, M. Šnajderová, S. Amaratunga, Z. Šumník, M. Pavlíková, S. Pruhova
OBJECTIVESWe analyzed primary school performance of girls with Turner syndrome (TS) in two distinct countries to ascertain if the cognitive phenotype of TS causes selective learning difficulties.METHODSThe cohort comprised of 44 Czech and 50 Egyptian girls with TS who attended public schools. School reports from grades 1 to 9 were obtained retrospectively from Czech participants with TS. Only recent school reports were obtained from Egyptian participants. Two controls per participant were requested - biological sisters and/or female classmates. The results were converted into a 5-point scale (1-excellent; 5-unsatisfactory).RESULTSAnalysis of longitudinal Czech data displayed a strong time component in both subjects and controls. Showing better points in lower grades with its gradual worsening as the education complexity increased. In contrast, there was a strong statistically significant difference between groups in Mathematics (p=0.0041, p=0.0205 after Bonferroni correction) and this difference increased over time. The points for Mathematics did not differ in grades 1+2 (0.05 difference in mean grade between the two groups), however, they differed by 0.28 in grades 6+7 and by 0.32 in grades 8+9. While slightly different in character (cross-sectional vs. longitudinal), the Egyptian cohort data confirmed our findings, showing no difference in general school performance but having similar trends in Mathematics (grades 1+2: 0.11, grades 6+7: 0.54, grades 8+9: 0.68; p=0.0058, p=0.029 after Bonferroni correction).CONCLUSIONExcluding results in Mathematics, which showed pronounced worsening in relation to age in comparison with unaffected controls, girls with TS performed similarly to their controls.
目的分析两个不同国家特纳综合征(TS)女童的小学表现,以确定TS的认知表型是否会导致选择性学习困难。方法该队列包括44名捷克和50名埃及公立学校的TS女孩。从一年级到九年级的学校报告回顾性地从患有TS的捷克参与者那里获得,仅从埃及参与者那里获得最近的学校报告。每个参与者被要求做两个对照——亲生姐妹和/或女同学。结果被转换成5分制(1-优秀;5-unsatisfactory)。结果捷克纵向数据分析显示受试者和对照组均存在较强的时间成分。随着教育复杂性的增加,低年级的分数越高,分数越差。相比之下,数学组间差异有统计学意义(p=0.0041,经Bonferroni校正后p=0.0205),且随着时间的推移,差异增加。1+2年级的数学分数没有差异(两组的平均分数相差0.05),然而,6+7年级的数学分数相差0.28,8+9年级的数学分数相差0.32。虽然在特征上略有不同(横断面与纵向),但埃及队列数据证实了我们的发现,显示一般学校表现没有差异,但在数学方面有相似的趋势(1+2年级:0.11,6+7年级:0.54,8+9年级:0.68;p=0.0058,经Bonferroni校正后p=0.029)。结论:与未受影响的对照组相比,数学成绩与年龄相关,数学成绩明显恶化,排除数学成绩外,TS女孩的表现与对照组相似。
{"title":"Primary School Performance of Girls with Turner Syndrome: A Transcultural Assessment.","authors":"J. Lebl, R. Hamza, J. Stoklasova, J. Zapletalová, S. Koloušková, O. Souček, B. Obermannová, M. Šnajderová, S. Amaratunga, Z. Šumník, M. Pavlíková, S. Pruhova","doi":"10.17458/per.vol17.2019.lhs.gilrsturnersyndrome","DOIUrl":"https://doi.org/10.17458/per.vol17.2019.lhs.gilrsturnersyndrome","url":null,"abstract":"OBJECTIVES\u0000We analyzed primary school performance of girls with Turner syndrome (TS) in two distinct countries to ascertain if the cognitive phenotype of TS causes selective learning difficulties.\u0000\u0000\u0000METHODS\u0000The cohort comprised of 44 Czech and 50 Egyptian girls with TS who attended public schools. School reports from grades 1 to 9 were obtained retrospectively from Czech participants with TS. Only recent school reports were obtained from Egyptian participants. Two controls per participant were requested - biological sisters and/or female classmates. The results were converted into a 5-point scale (1-excellent; 5-unsatisfactory).\u0000\u0000\u0000RESULTS\u0000Analysis of longitudinal Czech data displayed a strong time component in both subjects and controls. Showing better points in lower grades with its gradual worsening as the education complexity increased. In contrast, there was a strong statistically significant difference between groups in Mathematics (p=0.0041, p=0.0205 after Bonferroni correction) and this difference increased over time. The points for Mathematics did not differ in grades 1+2 (0.05 difference in mean grade between the two groups), however, they differed by 0.28 in grades 6+7 and by 0.32 in grades 8+9. While slightly different in character (cross-sectional vs. longitudinal), the Egyptian cohort data confirmed our findings, showing no difference in general school performance but having similar trends in Mathematics (grades 1+2: 0.11, grades 6+7: 0.54, grades 8+9: 0.68; p=0.0058, p=0.029 after Bonferroni correction).\u0000\u0000\u0000CONCLUSION\u0000Excluding results in Mathematics, which showed pronounced worsening in relation to age in comparison with unaffected controls, girls with TS performed similarly to their controls.","PeriodicalId":19827,"journal":{"name":"Pediatric endocrinology reviews : PER","volume":"29 10","pages":"117-124"},"PeriodicalIF":0.0,"publicationDate":"2019-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"72470620","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Pediatric Cushing Syndrome; an Overview. 儿童库欣综合征;概述。
4区 医学 Q2 Medicine Pub Date : 2019-12-01 DOI: 10.17458/per.vol17.2019.ts.pediatriccushingsyndrome
C. Tatsi, C. Stratakis
Endogenous Cushing syndrome (CS) is a rare entity in the pediatric population. Patients usually present with height deceleration and continuous weight gain, along with other classic stigmata of CS, such as acne, striae, hirsutism and others. The diagnosis of CS involves documentation of abnormal cortisol secretion with measurement of urinary free cortisol and midnight serum or salivary cortisol, and the use of the 1mg dexamethasone suppression test. After confirmation of CS, localization of the source of hypercortisolemia, involves differentiation of ACTH-dependent versus ACTH-independent causes of CS. Surgical resection of the identified source of CS is the preferred method of treatment whenever possible.
内源性库欣综合征(CS)在儿科人群中是一种罕见的疾病。患者通常表现为身高下降,体重持续增加,并伴有其他典型的CS的柱头,如痤疮,条纹,多毛等。CS的诊断包括通过测量尿游离皮质醇和午夜血清或唾液皮质醇来记录异常皮质醇分泌,并使用1mg地塞米松抑制试验。CS确诊后,高皮质血症来源的定位涉及到CS的acth依赖型和acth非依赖型病因的分化。手术切除已确定的CS来源是治疗的首选方法,只要可能。
{"title":"Pediatric Cushing Syndrome; an Overview.","authors":"C. Tatsi, C. Stratakis","doi":"10.17458/per.vol17.2019.ts.pediatriccushingsyndrome","DOIUrl":"https://doi.org/10.17458/per.vol17.2019.ts.pediatriccushingsyndrome","url":null,"abstract":"Endogenous Cushing syndrome (CS) is a rare entity in the pediatric population. Patients usually present with height deceleration and continuous weight gain, along with other classic stigmata of CS, such as acne, striae, hirsutism and others. The diagnosis of CS involves documentation of abnormal cortisol secretion with measurement of urinary free cortisol and midnight serum or salivary cortisol, and the use of the 1mg dexamethasone suppression test. After confirmation of CS, localization of the source of hypercortisolemia, involves differentiation of ACTH-dependent versus ACTH-independent causes of CS. Surgical resection of the identified source of CS is the preferred method of treatment whenever possible.","PeriodicalId":19827,"journal":{"name":"Pediatric endocrinology reviews : PER","volume":"36 1","pages":"100-109"},"PeriodicalIF":0.0,"publicationDate":"2019-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80936361","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
For Debate: Programing of the Autoimmune Diabetogenic Response in the Thymus during Fetal and Perinatal Life. 辩论:胎儿和围产期胸腺自身免疫性糖尿病反应的编程。
4区 医学 Q2 Medicine Pub Date : 2019-12-01 DOI: 10.17458/per.vol17.2019.gh.fd.autoimmunediabetogenicthymus
V. Geenen, D. Hober
T he presentation of self-peptides in the thymus is responsible both for negative selection of selfreactive T cells emerging during stochastic TCR recombination in fetal life, as well as positive selection of self-specific regulatory thymic T (tTreg) cells during and after perinatal life. The combination of these two sequential processes programs central self-tolerance, a fundamental property of the adaptive immune system. A defect in intrathymic self-presentation, either genetic or acquired, is the earliest event in the pathogenesis of autoimmunity already during fetal development. This defect is necessary but not sufficient for the appearance of a classical autoimmune disease like type 1 diabetes (T1D). Environmental factors are required for activation of the diabetogenic autoimmune response that targets insulin-secreting β cells in pancreatic Langerhans’ islets. Based on epidemiological studies, viral infections have been suspected for a long time to be one of those environmental factors. In this Debate article, we present a series of experimental data that support the hypothesis that, following vertical transplacental transfer, viruses might infect the fetal thymus and disturb already in utero central self-tolerance orchestrated by this organ. “It is with logic that we prove but it is with intuition that we discover.” Henri Poincaré (1854-1912) Ref: Ped. Endocrinol. Rev. 2019;17(2):00-00 doi:
胸腺中自我肽的呈现既负责胎儿生命中随机TCR重组过程中出现的自我反应性T细胞的负选择,也负责围产期和之后自我特异性调节性胸腺T (tTreg)细胞的正选择。这两个连续的过程的结合决定了自我耐受性,这是适应性免疫系统的基本特性。胸腺内自我表现的缺陷,无论是遗传的还是获得的,都是胎儿发育过程中自身免疫发病的最早事件。这种缺陷是典型的自身免疫性疾病如1型糖尿病(T1D)出现的必要条件,但不是充分条件。环境因素是激活糖尿病源性自身免疫反应所必需的,其目标是胰腺朗格汉斯胰岛中胰岛素分泌β细胞。根据流行病学研究,病毒感染长期以来一直被怀疑是这些环境因素之一。在这篇辩论文章中,我们提出了一系列的实验数据来支持这一假设,即在垂直胎盘移植后,病毒可能会感染胎儿胸腺,并干扰已经在子宫内由该器官协调的中央自我耐受性。“我们用逻辑来证明,但用直觉来发现。”亨利·庞加莱(1854-1912)性。Rev. 2019;17(2):00-00 doi:
{"title":"For Debate: Programing of the Autoimmune Diabetogenic Response in the Thymus during Fetal and Perinatal Life.","authors":"V. Geenen, D. Hober","doi":"10.17458/per.vol17.2019.gh.fd.autoimmunediabetogenicthymus","DOIUrl":"https://doi.org/10.17458/per.vol17.2019.gh.fd.autoimmunediabetogenicthymus","url":null,"abstract":"T he presentation of self-peptides in the thymus is responsible both for negative selection of selfreactive T cells emerging during stochastic TCR recombination in fetal life, as well as positive selection of self-specific regulatory thymic T (tTreg) cells during and after perinatal life. The combination of these two sequential processes programs central self-tolerance, a fundamental property of the adaptive immune system. A defect in intrathymic self-presentation, either genetic or acquired, is the earliest event in the pathogenesis of autoimmunity already during fetal development. This defect is necessary but not sufficient for the appearance of a classical autoimmune disease like type 1 diabetes (T1D). Environmental factors are required for activation of the diabetogenic autoimmune response that targets insulin-secreting β cells in pancreatic Langerhans’ islets. Based on epidemiological studies, viral infections have been suspected for a long time to be one of those environmental factors. In this Debate article, we present a series of experimental data that support the hypothesis that, following vertical transplacental transfer, viruses might infect the fetal thymus and disturb already in utero central self-tolerance orchestrated by this organ. “It is with logic that we prove but it is with intuition that we discover.” Henri Poincaré (1854-1912) Ref: Ped. Endocrinol. Rev. 2019;17(2):00-00 doi:","PeriodicalId":19827,"journal":{"name":"Pediatric endocrinology reviews : PER","volume":"65 1","pages":"78-83"},"PeriodicalIF":0.0,"publicationDate":"2019-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83938172","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
期刊
Pediatric endocrinology reviews : PER
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1