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The Role of Adipose Tissue Vasculature in Energy Balance 脂肪组织血管系统在能量平衡中的作用
Pub Date : 2011-12-01 DOI: 10.6065/JKSPE.2011.16.3.139
Hyun Ju Kim, Sang‐Hyun Choi, B. Chun, Dong Hoon Kim
Received: 8 December, 2011, Accepted: 12 December, 2011 Address for correspondence: Dong-Hoon Kim, M.D., Ph.D. Department of Pharmacology, Korea University College of Medicine, 126-1, 5-ga Anam-dong, Seongbuk-gu, Seoul 136-705, Korea Tel: +82.2-920-6237, Fax: +82.2-927-0824 E-mail: LDHKIM@korea.ac.kr 질병의심각성을고려해볼때 이에대처할방법은절대적으 , 로 부족하다 4) 특히 체내에서 에너지균형 . , (energy balance) 을조절하는신경내분비계기전(neuroendocrine mechanism) 의강력한방어기전으로장기투여목적의치료제로사용할 수있는비만치료제는극히드물다 5, 6) 미국과유럽의경우 . 년에 과 년에 가 각각 장기 2010 sibutramine 2008 rimonabant 투여시유발되는남용과부작용으로인하여승인이취소되 었으며 현재승인된비만치료제는 인 , lipase inhibitor orlistat 이유일하다 4, . 에너지균형은 에너지섭취 와 에너지소비 (energy intake) 가두축을이루어상호작용함으로써엄 (energy expenditure) 격하게 유지되고있다 체중 의증가는에너지 . (body weight) 균형 조절기전이 손상되어 지속적인 에너지섭취의 증가 또 는에너지소비의감소가초래되어유발된다 5, 6) 렙틴저항성 . 은 손상된 에너지균형 조절기전의 주원인 (leptin resistance) 에너지균형에 미치는 흰지방조직 내 혈관의 역할
2011年12月12日,2011年12月12日Address for correspondence:Dong-Hoon Kim, m.d., Ph.D. Department of Pharmacology, Korea University College of Medicine, 126- 1,5 -ga Anam- Dong, Seongbuk-gu, Seoul 136-705, Korea Tel: +82.2-920-6237, Fax: +82.2-927-0824 E-mail:LDHKIM@korea.ac.kr考虑到疾病疑似症状的觉醒,应对方法是绝对的,不足4)特别是在体内能量平衡。,调节(energy balance)的神经内分泌系统机制(neuroendocrine mechanism)的强力的韩医期前,能够作为长期治疗目的的肥胖治疗剂极少,5,6)美国和欧洲。年和年分别因服用2010 sibutramine 2008 rimonabant引起的滥用过度作用而取消了认可,目前认可的肥胖治疗药物只有磷、lipase inhibitor orlistat 4。能量平衡是由能量摄取和能量消耗(energy intake)组成双轴相互作用来维持的。体重的增加是能量。(body weight)平衡调节机制受损,导致持续能量摄取增加,又导致能源消费减少,从而导致发病5,6)胰岛素抵抗性。白脂肪组织内血管对能量平衡的作用(leptin resistance)
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引用次数: 3
Body Composition Analysis in Newly Diagnosed Diabetic Adolescent Girls 新诊断糖尿病少女的身体成分分析
Pub Date : 2011-12-01 DOI: 10.6065/JKSPE.2011.16.3.172
Yong Hyuk Kim, M. Song, Sochung Chung
Purpose: The objective of this study was to determine the type differences of diabetes by analyzing the growth status and body composition of newly diagnosed diabetic adolescent girls. Methods: The study included 6 type 1 diabetic adolescent girls (age 11.7 ± 1.9 years) and 6 type 2 diabetic adole- scent girls (age 14.4 ± 2.6 years). The height, weight and body composition of fat mass and fat-free mass were measured in each patient. Body mass index (BMI), fat mass index (FMI), fat free mass index (FFMI) and percent body fat (PBF) were calculated and each component was plotted on a body composition chart. Results: Type 2 diabetic adolescent girls seemed to be taller and heavier compared to type 1 diabetic girls, but the differences in height and weight z-score were not significant. BMI, FFMI, FMI, PBF were also higher in type 2 diabetic girls. The body composition chart revealed that type 2 diabetic girls had significantly higher FMI and PBF. In type 1 diabetic girls, FFMI was lower compared to type 2 diabetic girls. The BMI difference between diabetes types was explained with the difference in FFMI as well as FMI. Conclusion: The components of body composition differ according to diabetes type in adolescent girls. Measuring the body composition of diabetic girls might help to promote growth and adequate FFM gain during childhood. In diabetes control, diet and exercise should be emphasized along with insulin treatment.
目的:本研究旨在通过分析初诊糖尿病少女的生长状况和身体组成来确定糖尿病的类型差异。方法:选取6例1型糖尿病少女(11.7±1.9岁)和6例2型糖尿病少女(14.4±2.6岁)为研究对象。测量每位患者的身高、体重、体成分、脂肪量和无脂肪量。计算身体质量指数(BMI)、脂肪质量指数(FMI)、无脂肪质量指数(FFMI)和体脂百分比(PBF),并将各组成部分绘制在身体成分图上。结果:2型糖尿病少女比1型糖尿病少女似乎更高、更重,但身高、体重z-score差异不显著。2型糖尿病女孩的BMI、FFMI、FMI、PBF也较高。身体成分图显示,2型糖尿病女孩的FMI和PBF明显较高。在1型糖尿病女孩中,FFMI低于2型糖尿病女孩。不同糖尿病类型之间的BMI差异可以用FFMI和FMI的差异来解释。结论:不同糖尿病类型的少女体成分存在差异。测量糖尿病女孩的身体成分可能有助于促进生长和在儿童时期获得足够的FFM。在控制糖尿病时,应在胰岛素治疗的同时强调饮食和运动。
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引用次数: 3
Assessment of Bone Age During Pubertal Age 青春期骨龄的评估
Pub Date : 2011-12-01 DOI: 10.6065/JKSPE.2011.16.3.135
Duk-Hee Kim
Received: 5 November, 2011, Accepted: 5 November, 2011 Address for correspondence: Duk Hee Kim M.D. Department of Pediatrics, Sowha Children's Hospital 224-32, Seogyel-dong, Yongsan-gu, Seoul 140-829, Korea Tel: +82.2-705-9112, Fax: +82.2-705-9000 E-mail: dhkim345@naver.com 여아 세 남아 세가 된다 사춘기동안 앉은 키 13 , 15 . (sitting 는척추와머리높이로여아에서 남아에서 height) 7.5 cm, 8.5 성장된다 하지 는 여아 남아 cm . (lower extremities) 7 cm, 8 성장된다 사춘기시작은신장치와앉은키를 개월간격 cm . 6 으로측정하여성장속도증가여부를찾아낼수있다 신장 . 이 여아에서 남아 되면 6 cm/year, 8 cm/year peak height 에도달하게된다 velocity 6-7) 또한성장속도가증가될때성 . 성숙도 가 단계가된다 이러한 (sexual maturation rate, SMR) 2 . 시기의 는여아 세 남아 세가된다 BA 11 , 13 .
2011年5月5日,Accepted: 5月5日,2011年Address for correspondence:Duk Hee Kim m.d. Department of Pediatrics, Sowha Children's Hospital 224-32, Seogyel-dong, Yongsan-gu, Seoul 140-829, Korea Tel: +82.2-705-9112, Fax: +82.2-705-9000 E-mail:dhkim345@naver.com女孩变成男孩,青春期期间坐着的身高13,15。(sitting是脊椎和头部的高度,从女婴到男婴的height)长7.5厘米,从男婴长8.5厘米。(lower extremities) 7厘米,成长8厘米青春期开始隐身装置和坐高间隔1个月cm。用6测定,可找出增长速度是否增加。velocity 6-7)在成长速度增加时也可达到6厘米/year, 8厘米/year peak height。成熟度达到阶段(sexual maturation rate, SMR) 2。时期是女婴和男婴。BA 11,13。
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引用次数: 5
A Case of Thyrotoxic Periodic Paralysis in Adolescent with Graves' Disease 青少年Graves病伴甲状腺毒性周期性麻痹1例
Pub Date : 2011-12-01 DOI: 10.6065/JKSPE.2011.16.3.196
Ki Won Oh, J. Jeong, J. Kim
Thyrotoxic periodic paralysis (TPP) is a rare complication of hyperthyroidism characterized by recurrent paralysis of skeletal muscle and hypokalemia caused by a massive intracellular shift of potassium. TPP mainly affects young male patients of Asian descent. We describe a case of TPP in a 14-year-old girl who presented with palpitation and intermittent weakness of the lower extremities especially after physical exercises. The patient showed sinus tachycardia, proximal weakness of both legs and a severe hypokalemia. Thyroid function tests showed hyperthy- roidism, and thyroid scan revealed diffusely enlarged goiter consistent with Graves' disease. After the management with antithyroid drug, beta-adrenergic blocker and potassium supplementation for TPP, she has remained euthyroid state and symptom free on the follow-up. TPP should be considered in children with acute paralysis of skeletal muscle and hypokalemia, also thyroid function should be evaluated.
甲状腺毒性周期性麻痹(TPP)是一种罕见的甲状腺机能亢进并发症,以骨骼肌反复麻痹和细胞内大量钾离子转移引起的低钾血症为特征。TPP主要影响年轻男性亚裔患者。我们描述了一个14岁女孩的TPP病例,她表现为心悸和间歇性下肢无力,特别是在体育锻炼后。患者表现为窦性心动过速,两腿近端无力和严重的低血钾。甲状腺功能检查显示甲状腺功能亢进,甲状腺扫描显示弥漫性甲状腺肿大,符合格雷夫斯病。经抗甲状腺药物、β -肾上腺素受体阻滞剂及补钾治疗后,患者甲状腺功能正常,随访无症状。急性骨骼肌麻痹和低钾血症的儿童应考虑TPP,并应评估甲状腺功能。
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引用次数: 3
A Case of Idiopathic Hypomagnesemia with Hypocalcemia Presenting as Generalized Tonic-Clonic Seizure 特发性低镁血症伴低钙血症表现为全身性强直阵挛性发作1例
Pub Date : 2011-12-01 DOI: 10.6065/JKSPE.2011.16.3.193
Seul Lee, A. Kwon, H. Chae, Ho-Seong Kim
Hypomagnesemia may arise from various disorders such as renal magnesium wasting, familial hypomagnesemia, inadequate intake and increased gastrointestinal loss. Hypomagnesemia and hypocalcemia were found in a month- old female patient with generalized tonic-clonic seizure. Twenty-four hour urine collection samples were used to assess renal magnesium wasting; fractional excretion of 24-hr urine magnesium was less than 1.45%, i.e., within the normal limits. The patient had no history of chronic diarrhea or failure to thrive, which supports the conclusion that intake was adequate. She had no family history of hypocalcemia, hypomagnesemia, or seizures. Here, we report a case of idiopathic hypomagnesemia.
低镁血症可由多种疾病引起,如肾性镁消耗、家族性低镁血症、摄入不足和胃肠道损失增加。低镁血症和低钙血症是发现在一个月大的女性全身性强直阵挛发作。24小时尿液收集样本用于评估肾镁的损耗;24小时尿镁排泄量小于1.45%,在正常范围内。该患者无慢性腹泻史,也没有发育不良史,这支持了摄入充足的结论。无低钙、低镁、癫痫家族史。在此,我们报告一例特发性低镁血症。
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引用次数: 0
The Relationship between Initial Body Mass Index and Body Mass Index after One Year of Gonadotropin-Releasing Hormone Agonist Therapy in Idiopathic True Precocious Puberty Girls 特发性真性性早熟女童促性腺激素释放激素激动剂治疗1年后初始体重指数与体重指数的关系
Pub Date : 2011-12-01 DOI: 10.6065/JKSPE.2011.16.3.165
J. Yoon, M. Kang, S. Y. Kim, J. Seo, S. Yang, Y. Lee, Jieun Lee, H. Chung, C. Shin
The Relationship between Initial Body Mass Index and Body Mass Index after One Year of Gonadotropin-Releasing Hormone Agonist Therapy in Idiopathic True Precocious Puberty Girls Ju Young Yoon, M.D., Min Jae Kang, M.D., Se Young Kim, M.D., Ji Young Seo, M.D., Sei Won Yang, M.D., Young Ah Lee, M.D., Ji Eun Lee, M.D., Hye Rim Chung, M.D and Choong Ho Shin, M.D. Department of Pediatrics , Seoul National University College of Medicine, Seoul, Department of Pediatrics, Bundang Jesaeng General Hospital, Seongnam, Department of Pediatrics, Eulji University School of Medicine, Seoul, Department of Pediatrics, Seoul National University Bundang Hospital, Seongnam, Korea
特发性真性性早熟女童接受促性腺激素释放激素激动剂治疗一年后初始体重指数与体重指数的关系尹珠英,医学博士,姜敏在,医学博士,金世英,医学博士,徐智英,医学博士,杨世媛,医学博士,李英娥,医学博士,李智恩,医学博士,郑慧琳,医学博士,申忠浩,医学博士,首尔国立大学医学院儿科学系,首尔,儿科学系,城南市盆唐济生综合医院、乙支大学医学院儿科、首尔大学城南市盆唐医院儿科
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引用次数: 5
Pamidronate Treatment in 9-Year-Old Boy Diagnosed with Gorham Disease 帕米膦酸钠治疗9岁男童戈勒姆病
Pub Date : 2011-12-01 DOI: 10.6065/JKSPE.2011.16.3.189
J. Yoon, Jieun Lee, Seung Wan Park, M. Kang, Y. Lee, S. Yang, K. Park, C. Shin
병은뼈에서의비정상적인혈관증식으로인한골 Gorham 용해를 특징으로하는질환이다 주 증상은골 소실로 인한 . 골절이나유미흉 혈흉등이있으며 주된침범부위는상악 , , 골 어깨뼈 늑골 골반뼈등이다 , , , 1) 등 . Heffez 2) 은 병 Gorham 의진단기준으로 생검소견상혈관종성조직소견 비 1) , 2) 정형세포가없을것 신생골형성이나이영양성석회화가 , 3) 없을것 진행되는국소성골용해소견 비증식성 비궤 , 4) , 5) , 양성병변 내부장기의침범이없을것 방사선학적으 , 6) , 7) 로골용해소견이보일것 유전적인대사이상 면역학적 , 8) , 이상 악성종양이나 감염이 없을 것 등을 제시하였다 , . Gor병은현재까지약 예가보고된드문질환으로 발병 ham 200 원인과그기전은밝혀져있지않으며적립된치료법도없다. 이에저자들은 세에 병으로진단받은남아에서파 9 Gorham 미드로네이트 치료 후 성공적으로 질병 활동성이 안정화되
病是骨头上非正常血管增殖导致骨Gorham溶解的特征。主要症状是骨消失引起的。有骨折,幽美胸,血胸等,主要侵犯部位是上岳,骨肩胛骨,肋骨,骨盆骨等,,,1)等。heffez 2)为gorham病的诊断标准,生得节俭犬관종声调职见识比1)、2)情况不会有细胞新生骨形成和李英石灰培养画家、3)不会进行的局部圣骨溶解到非增殖性别比仪轨,4),5),良性病变激起내부장기不会侵犯放射线学籍、六)、7)溶解露骨意见이보일免疫遗传人大之间上学籍,8)没有异常恶性肿瘤或感染。Gor病是目前为止药科报告的罕见疾病,发病ham 200的原因和之前还没有查明,也没有积累的治疗方法。因此,作者在三岁时被诊断为疾病的南部治疗了帕9 Gorham中针后,成功地稳定了疾病的活动性
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引用次数: 2
A Single-Arm, Phase III Study to Assess Efficacy and Safety after 6-Month-Treatment of Eutropin™ Inj. (Recombinant Human Growth Hormone) in Prepubertal Children with Short Stature due to Small for Gestational Age 一项评估Eutropin™注射液治疗6个月后疗效和安全性的单臂III期研究(重组人生长激素)在胎龄小导致身材矮小的青春期前儿童中的应用
Pub Date : 2011-12-01 DOI: 10.6065/JKSPE.2011.16.3.157
Kee Hyoung Lee, B. Lee, C. Ko, D. Jin, S. Yang, H. Yoo, W. Chung, Duk-Hee Kim, Byung-Kyu Suh
Department of Pediatrics, Korea University Hospital, Department of Pediatrics, The Catholic University St. Mary s Hospital, Seoul, ’ Department of Pediatrics, Kyungpook National University Hospital, Daegu, Department of Pediatrics, Samsung Medical Center, Department of Pediatrics, Seoul National University Children's Hospital, Department of Pediatrics, Asan Medical Center, Seoul, Department of Pediatrics, Inje University Busan Paik Hospital, Busan, Department of Pediatrics, Severance Hospital, Department of Pediatrics, The Catholic University Seoul St. Mary s Hospital, Seoul, Korea ’
高丽大学医院儿科、汉城天主教大学圣母医院儿科、大邱庆北大学医院儿科、三星首尔医院儿科、汉城大学儿童医院儿科、汉城峨山医院儿科、仁济大学釜山白医院儿科、釜山Severance医院儿科、天主教大学首尔圣母医院儿科
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引用次数: 6
Pamidronate Therapy in Children and Adolescents with Secondary Osteoporosis 帕米膦酸钠治疗儿童和青少年继发性骨质疏松症
Pub Date : 2011-12-01 DOI: 10.6065/JKSPE.2011.16.3.178
Jieun Lee, J. Yoon, Y. Lee, J. Lim, C. Shin, S. Yang
Purpose: The aim of this study was to evaluate the efficacy of pamidronate therapy in children and adolescents with secondary osteoporosis. Methods: Nine patients (7 males, 2 females, 13.2 ± 2.5 years, 10.1-17.4 years) with secondary osteoporosis who had a history of severe bone pain and/or fracture were enrolled. Intravenous pamidronate 1.5 mg/kg (0.5 mg/kg for 3 consecutive days) was given every 6 to 8 weeks for 0.86 ± 0.15 years (6 or 8 cycles). Bone mineral density (BMD) in lumbar spine and femoral neck and their Z-scores were measured before treatment, after the fourth and last cycle (sixth or eighth cycle). Results: Underlying diseases were as follows; neurofibromatosis type 1 (n = 2), epilepsy with/without cerebral palsy (N=2), autoimmune disease treated with steroid (n = 2), hematologic malignancy (n = 3). Bone pain was relieved in most of the patients after the first cycle of treatment, and no more fracture occurred thereafter. There was a significant increase in BMD Z-score of the lumbar spine and femoral neck after the last cycle of therapy, compared to baseline values (from -3.91 ± 1.79 to 1.86 ± 1.18, in L1-4 and -3.71 ± 1.83 to -2.53 ± 1.77 for femoral neck; P = 0.008 and 0.011, respectively). However, there was no significant change in BMD Z-scores between the fourth cycle and the last cycle. Fever developed in 7 out of 9 patients (77.8%), which was relieved by antipyretics. Total serum levels of calcium and phosphorus were significantly decreased (calcium, P = 0.008; phosphorus, P = 0.015) after pamidronate therapy, and three of them experienced symptomatic hypocalcemia during the first cycle. The growth velocity was normal during follow-up periods (mean, 4.47 ± 1.69 years; range, 1.05 to 6.77 years). Conclusion: In conclusion, pamidronate can be administered to the patients with secondary osteoporosis, relieving the symptoms and signs effectively and safely. However, its side effects should be monitored during treatment.
目的:本研究的目的是评估帕米膦酸盐治疗继发性骨质疏松症的儿童和青少年的疗效。方法:9例继发性骨质疏松患者(男性7例,女性2例,年龄13.2±2.5岁,10.1 ~ 17.4岁)均有严重骨痛和/或骨折病史。帕米膦酸酯静脉注射1.5 mg/kg (0.5 mg/kg,连续3天),每6 ~ 8周一次,共0.86±0.15年(6或8个周期)。治疗前、第4周期、最后1周期(第6、8周期)后测定腰椎、股骨颈骨密度(BMD)及z评分。结果:基础疾病如下;1型神经纤维瘤病(n =2),癫痫伴/不伴脑瘫(n =2),类固醇治疗自身免疫性疾病(n =2),血液系统恶性肿瘤(n = 3)。大多数患者在第一个周期治疗后骨痛减轻,此后不再发生骨折。与基线值相比,最后一个治疗周期后腰椎和股骨颈的BMD z -评分显著增加(L1-4组从-3.91±1.79增加到1.86±1.18,股骨颈从-3.71±1.83增加到-2.53±1.77;P分别= 0.008和0.011)。然而,在第四个周期和最后一个周期之间,BMD z -评分没有显著变化。9例患者中有7例(77.8%)出现发热,经退烧药缓解。血清总钙、磷水平显著降低(钙,P = 0.008;P = 0.015),其中3例在第一个周期出现症状性低钙血症。随访期间生长速度正常(平均4.47±1.69年;范围:1.05至6.77年)。结论:帕米膦酸钠可有效、安全地缓解继发性骨质疏松症患者的症状和体征。然而,在治疗过程中应监测其副作用。
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引用次数: 4
Pituitary Hyperplasia Secondary to Hypothyroidism Caused by Hashimoto's Thyroiditis in a Female Adolescent 青春期女性桥本甲状腺炎致甲状腺功能减退继发垂体增生一例
Pub Date : 2011-12-01 DOI: 10.6065/JKSPE.2011.16.3.185
Jeoung Suk Kim, Min Sun Kim, Sun Jun Kim, G. Chung, P. Hwang, Dae-Yeol Lee
Pituitary enlargement secondary to primary hypothyroidism is a known but uncommon occurrence and is difficult to distinguish on computed tomography (CT) and magnetic resonance imaging (MRI) from primary pituitary tumor. The lack of thyroxine feedback found in uncontrolled primary hypothyroidism leads to elevated levels of thyrotropin-releasing hormone (TRH), which causes both pituitary thyrotroph and lactotroph hyperplasia, increasing the secretion of both thyroidstimulating hormone (TSH) and prolactin. With long-standing hypothyroidism, thyrotroph hyperplasia can result in expansion of the sella turcica and enlargement of the pituitary gland. Pituitary hyperplasia usually regresses following adequate treatment with hormone replacement over a period of a few months. We herein report a case of pituitary hyperplasia associated with hypothyroidism in a short statured female adolescent without the typical clinical features associated with hypothy-
继发于原发性甲状腺功能减退的垂体肿大是一种已知但不常见的情况,很难在计算机断层扫描(CT)和磁共振成像(MRI)上与原发性垂体瘤区分开来。未控制的原发性甲状腺功能减退缺乏甲状腺素反馈,导致促甲状腺素释放激素(TRH)水平升高,导致垂体促甲状腺和乳营养增生,增加促甲状腺激素(TSH)和催乳素的分泌。长期甲状腺功能减退,甲状腺增生可导致蝶鞍扩张和垂体肿大。经过几个月的激素替代治疗后,垂体增生通常会消退。我们在此报告一例垂体增生合并甲状腺功能减退的矮小女性青少年,没有典型的与甲状腺功能减退相关的临床特征
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引用次数: 1
期刊
Journal of Korean Society of Pediatric Endocrinology
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