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Sensor-augmented pump and Down syndrome: a new tool in tricky patients. 传感器增强泵和唐氏综合症:棘手患者的新工具。
Pub Date : 2014-06-01 DOI: 10.1590/0004-2730000002948
Andrea E Scaramuzza, Valentina Comaschi, Matteo Ferrari, Gian Vincenzo Zuccotti
W e read with great interest the paper by Piccini and cols. (1) published in the July issue of this Journal. Some years ago, we published the first report ever (to the best of our knowledge) of successful treatment of a girl with Down syndrome, Hashimoto’s thyroiditis and celiac disease with continuous subcutaneous insulin infusion (2). Since then, her glycemic control was kept constant and, most of the time, in the target range (HbA1c in 2009: 7.75 ± 0.21%; HbA1c in 2010: 7.35 ± 0.19%; HbA1c in 2011: 7.42 ± 0.30%). At the end of 2011, sensor-augmented pump was initiated (Animas® VibeTM, West Chester, PA, USA) because of both a quite high glycemic variability and the parents’ request, and her HbA1c kept improving (HbA1c in 2012: 7.30 ± 0.20%; HbA1c in 2013: 7.10 ± 0.28%). CSII has been recognized as effective and safe in pediatric (3) and in adult patients (4), not only in the short run, but even after many years (5). In patients with Down syndrome and type 1 diabetes, glycemic control may sometimes be particularly tricky (6,7). In our patient, as well as in the one of Piccini and cols. (1), CSII was a safe and effective way to manage diabetes. For a successful CSII therapy in a patient with Down syndrome, whose mental function may be impaired, the collaboration of a highly motivated and compliant family is essential, as well as a skilled multidisciplinary diabetes team (8). Given all of this, pump increased the patient’s and family’s flexibility, as we had previously reported (2). The significant improvement in the glycemic control observed, and the high level of acceptance of CSII therapy observed in both our case and in that of Piccini and cols. is worth the effort of the patient’s family and of the diabetes team in ensuring that the patient has a flexible life. Perhaps CSII therapy might be taken into account when considering insulin therapy in patients with Down’s syndrome.
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引用次数: 0
Fasting ghrelin but not PYY(3-36) is associated with insulin-resistance independently of body weight in Wistar rats. 在Wistar大鼠中,空腹饥饿素(ghrelin)而非PYY(3-36)与独立于体重的胰岛素抵抗相关。
Pub Date : 2014-06-01 DOI: 10.1590/0004-2730000002927
Luciana da Conceição Antunes, Manoela Neves da Jornada, Jessica Lorenzzi Elkfury, Kelly Carraro Foletto, Marcello Casaccia Bertoluci

Objective: The objective of this study was to evaluate the association between insulin-resistance and fasting levels of ghrelin and PYY in Wistar rats.

Materials and methods: A total of 25 male Wistar rats, weighing 200-300 g, was included in this study. The animals were maintained in cages with a 12/12h light-dark cycle and fed standard chow and water ad libitum. After 12-h overnight fasting, ghrelin, PYY, insulin and glucose values were determined. Insulin resistance was assessed by means of the HOMA-IR, which was ranked and the median was used as a cut-off value to categorize insulin-resistance. HOMA-IR values equal and above 2.62 were considered insulin-resistant (IR) while values below 2.62 were considered insulin sensitive (IS). Differences between means were determined using the Student t-test. Multiple regression and Pearson's correlation test were used to evaluate the association between variables.

Results: HOMA-IR median IQ range values for IS and IR groups were, respectively, 1.56 (0.89 - 2.16) vs. [4.06 (3.50 - 4.61); p < 0.001]. The IR group presented increased levels of fasting ghrelin, PYY and insulin respectively: [50.35 (25.99 - 74.71) pg/mL vs. 12.33 (8.77 - 15.89) pg/mL; p = 0.001]; [54.38 (37.50 - 71.26) pg/mL vs. 33.17 (22.34 - 43.99) pg/mL; p = 0.016]; [18.04 (14.48 - 21.60) uU/mL vs. 7.09 (4.83 - 9.35) uU/mL; p = 0.001]. Ghrelin, but not PYY, correlated linearly and positively with HOMA-IR: ghrelin vs. HOMA-IR (r = 0.52; p = 0.008), and PYY vs. HOMA-IR (r = 0.22; p = 0.200). This correlation was independent of body weight.

Conclusion: Fasting ghrelin and PYY serum levels are increased in lean, relatively insulin resistant Wistar rats, and this increase is independent of weight.

目的:本研究的目的是评估胰岛素抵抗与Wistar大鼠空腹胃饥饿素和PYY水平之间的关系。材料与方法:选取雄性Wistar大鼠25只,体重200-300 g。饲养于12/12h明暗循环的笼中,随意饲喂标准饲料和水。禁食12小时后,测定胃饥饿素、PYY、胰岛素和葡萄糖值。通过HOMA-IR评估胰岛素抵抗,对其进行排名,并使用中位数作为胰岛素抵抗分类的临界值。HOMA-IR等于或大于2.62被认为是胰岛素抵抗(IR),低于2.62被认为是胰岛素敏感(IS)。均值之间的差异使用学生t检验确定。采用多元回归和Pearson相关检验评价变量间的相关性。结果:IS组和IR组的HOMA-IR中位IQ范围值分别为1.56(0.89 ~ 2.16)和4.06 (3.50 ~ 4.61);P < 0.001]。IR组空腹胃饥饿素、PYY和胰岛素水平分别升高:[50.35 (25.99 - 74.71)pg/mL vs. 12.33 (8.77 - 15.89) pg/mL;P = 0.001];[54.38 (37.50 ~ 71.26) pg/mL vs. 33.17 (22.34 ~ 43.99) pg/mL;P = 0.016];[18.04 (14.48 ~ 21.60) uU/mL vs. 7.09 (4.83 ~ 9.35) uU/mL;P = 0.001]。Ghrelin与HOMA-IR呈线性正相关,而PYY与HOMA-IR无关(r = 0.52;p = 0.008), PYY vs. HOMA-IR (r = 0.22;P = 0.200)。这种相关性与体重无关。结论:在瘦弱、相对胰岛素抵抗的Wistar大鼠中,空腹胃饥饿素和PYY血清水平升高,且这种升高与体重无关。
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引用次数: 3
[Intestinal microbiota and cardiometabolic risk: mechanisms and diet modulation]. 肠道微生物群和心脏代谢风险:机制和饮食调节。
Pub Date : 2014-06-01 DOI: 10.1590/0004-2730000002940
Ana Carolina Franco de Moraes, Isis Tande da Silva, Bianca de Almeida-Pititto, Sandra Roberta G Ferreira

The gut microbiota obtained after birth is composed of a large range of bacteria that play different roles in the human host, such as nutrient uptake, protection against pathogens and immune modulation. The intestinal bacterial content is not completely known, but it is influenced by internal, and mainly by external factors, which modulate its composition and function. Studies indicate that the gut microbiota differs in lean and obese individuals, and in individuals with different food habits. There is evidence that the relationship between diet, inflammation, insulin resistance, and cardiometabolic risk are, in part, mediated by the composition of intestinal bacteria. Knowledge about the gut microbiota may result in different strategies to manipulate bacterial populations and promote health. This review discusses the relevance of understanding the role of dietary factors or patterns in the composition of the microbiota, as well as pathophysiological mechanisms of chronic metabolic diseases, and the potential of prebiotics and probiotics on the cardiometabolic risk profile.

出生后获得的肠道微生物群由大量细菌组成,这些细菌在人类宿主中发挥着不同的作用,如营养摄取、对病原体的保护和免疫调节。肠道细菌含量尚不完全清楚,但它受内部因素的影响,主要受外部因素的影响,这些因素调节了其组成和功能。研究表明,在瘦人和肥胖者以及不同饮食习惯的个体中,肠道微生物群是不同的。有证据表明,饮食、炎症、胰岛素抵抗和心脏代谢风险之间的关系在一定程度上是由肠道细菌的组成介导的。对肠道微生物群的了解可能会导致不同的策略来控制细菌数量和促进健康。这篇综述讨论了理解饮食因素或模式在微生物群组成中的作用的相关性,以及慢性代谢性疾病的病理生理机制,以及益生元和益生菌对心脏代谢风险的潜在影响。
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引用次数: 37
[Accuracy of body fat and waist circumference in predicting metabolic abnormalities indicating cardiovascular risk in adolescents]. [体脂和腰围在预测青少年心血管风险代谢异常中的准确性]。
Pub Date : 2014-06-01 DOI: 10.1590/0004-2730000002865
Milena Miranda de Moraes, Gloria Valeria da Veiga

Objective: To evaluate the performance of percent body fat (%BF) and waist circumference (WC) in predicting metabolic abnormalities indicating cardiovascular risk in adolescents.

Subjects and methods: Cross-sectional study with a probabilistic sample of 573 adolescents aged 12 to 19 years from state public schools in Niterói, RJ. The Receiver Operating Characteristic Curve was used to evaluate the accuracy of WC and %BF in predicting alterations in blood pressure, lipid profile, and blood glucose.

Results: The best %BF cutoff points were 21% for boys, and 23% for girls, with sensitivity (SE) and specificity (SP) of approximately 60%. The best WC cutoff points were 71 cm for boys, and 66 cm for girls (SE: 55% to 70%; SP: 55% to 78%).

Conclusion: Even the best cutoff points misidentified high proportions of adolescents with metabolic abnormalities. Caution is recommended in the use of these indicators for cardiovascular risk screening in this age group.

目的:评价体脂率(%BF)和腰围(WC)在预测青少年心血管危险代谢异常中的作用。对象和方法:横断面研究与概率抽样573名12至19岁的青少年在Niterói, RJ公立学校。采用受试者工作特征曲线(Receiver Operating Characteristic Curve)评价WC和%BF预测血压、血脂和血糖变化的准确性。结果:最佳BF分界点为男孩21%,女孩23%,敏感性(SE)和特异性(SP)约为60%。最佳WC分界点为男生71 cm,女生66 cm (SE: 55% ~ 70%;标普:55%至78%)。结论:即使是最好的分界点也误判了高比例的青少年代谢异常。建议谨慎使用这些指标在这一年龄组进行心血管风险筛查。
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引用次数: 9
TSH reference range in older adults: a Brazilian study. 老年人TSH参考范围:一项巴西研究。
Pub Date : 2014-06-01 DOI: 10.1590/0004-2730000003065
Pedro Weslley Rosario, Maria Regina Calsolari

Objective: To establish serum TSH reference values for a population of Brazilian elderly, and to compare them to those found in the adult population.

Subjects and methods: Healthy volunteers aged 70 to 85 years, without known thyroid disease or risk factors for thyroid dysfunction, who did not use any medication that could potentially interfere with TSH, were selected. Subjects with goiter, palpable thyroid nodules, anti-thyroperoxidase antibodies, or altered free T4 were excluded. The sample consisted of 360 older adults (180 per sex).

Results: TSH values corresponding to the 2.5th and 97.5th percentile of the sample were 0.2 and 4.62 mIU/L, respectively. TSH > 2.5 mIU/L was seen in 25.26% of the volunteers, > 3 mIU/L in 15.26%, and > 4 mIU/L in 6.1% of them. TSH values were slightly higher than those previously reported for adults (18-60 years).

Conclusion: This study suggests an upper limit for normal TSH of approximately 4.6 mIU/L for the Brazilian elderly population.

目的:建立巴西老年人血清TSH参考值,并将其与成人人群进行比较。受试者和方法:选择年龄在70 - 85岁之间、无已知甲状腺疾病或甲状腺功能障碍危险因素、未使用任何可能干扰TSH的药物的健康志愿者。排除甲状腺肿、可触及甲状腺结节、抗甲状腺过氧化物酶抗体或游离T4改变的受试者。样本包括360名老年人(男女各180人)。结果:样品第2.5和97.5百分位对应的TSH值分别为0.2和4.62 mIU/L。TSH > 2.5 mIU/L的占25.26%,> 3 mIU/L的占15.26%,> 4 mIU/L的占6.1%。TSH值略高于先前报道的成人(18-60岁)。结论:本研究表明,巴西老年人正常TSH上限约为4.6 mIU/L。
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引用次数: 9
The rs1893217 (T/C) polymorphism in PTPN2 gene is not associated with type 1 diabetes mellitus in subjects from Southern Brazil. PTPN2基因rs1893217 (T/C)多态性与巴西南部受试者的1型糖尿病无关。
Pub Date : 2014-06-01 DOI: 10.1590/0004-2730000003050
Jakeline Rheinheimer, Fernanda dos Santos de Oliveira, Luís Henrique Canani, Daisy Crispim

Objective: To evaluate the association of the PTPN2 rs1893217 polymorphism with T1DM and/or its clinical and laboratory characteristics in a Caucasian population from Southern Brazil.

Subjects and methods: Four hundred and eighty six patients with T1DM and 484 non-diabetic subjects were included in the study. Genotyping of the PTPN2 rs1893217 was performed by real-time PCR.

Results: Genotype frequencies did not differ between T1DM patients and non-diabetic subjects (P = 0.265). The C allele was observed in 14.5% of the T1DM sample and 12.2% of the non-diabetic group (P = 0.152). Moreover, the frequencies of this variant did not differ statistically between T1DM patients and non-diabetic subjects when assuming recessive, dominant, or additive inheritance models. The clinical and laboratory characteristics of T1DM patients did not differ significantly among the three genotypes of the rs1893217 polymorphism, either.

Conclusion: The PTPN2 rs1893217 polymorphism is not significantly associated with T1DM in Caucasian subjects from Southern Brazil.

目的:评估PTPN2 rs1893217多态性与巴西南部高加索人群T1DM和/或其临床和实验室特征的关系。对象和方法:纳入486例T1DM患者和484例非糖尿病患者。采用实时荧光定量PCR对PTPN2 rs1893217进行基因分型。结果:基因型频率在T1DM患者和非糖尿病患者之间没有差异(P = 0.265)。14.5%的T1DM组和12.2%的非糖尿病组存在C等位基因(P = 0.152)。此外,当采用隐性、显性或加性遗传模型时,该变异的频率在T1DM患者和非糖尿病患者之间没有统计学差异。rs1893217多态性的三种基因型在T1DM患者的临床和实验室特征上也没有显著差异。结论:PTPN2 rs1893217多态性与巴西南部高加索人群T1DM无显著相关性。
{"title":"The rs1893217 (T/C) polymorphism in PTPN2 gene is not associated with type 1 diabetes mellitus in subjects from Southern Brazil.","authors":"Jakeline Rheinheimer,&nbsp;Fernanda dos Santos de Oliveira,&nbsp;Luís Henrique Canani,&nbsp;Daisy Crispim","doi":"10.1590/0004-2730000003050","DOIUrl":"https://doi.org/10.1590/0004-2730000003050","url":null,"abstract":"<p><strong>Objective: </strong>To evaluate the association of the PTPN2 rs1893217 polymorphism with T1DM and/or its clinical and laboratory characteristics in a Caucasian population from Southern Brazil.</p><p><strong>Subjects and methods: </strong>Four hundred and eighty six patients with T1DM and 484 non-diabetic subjects were included in the study. Genotyping of the PTPN2 rs1893217 was performed by real-time PCR.</p><p><strong>Results: </strong>Genotype frequencies did not differ between T1DM patients and non-diabetic subjects (P = 0.265). The C allele was observed in 14.5% of the T1DM sample and 12.2% of the non-diabetic group (P = 0.152). Moreover, the frequencies of this variant did not differ statistically between T1DM patients and non-diabetic subjects when assuming recessive, dominant, or additive inheritance models. The clinical and laboratory characteristics of T1DM patients did not differ significantly among the three genotypes of the rs1893217 polymorphism, either.</p><p><strong>Conclusion: </strong>The PTPN2 rs1893217 polymorphism is not significantly associated with T1DM in Caucasian subjects from Southern Brazil.</p>","PeriodicalId":8395,"journal":{"name":"Arquivos brasileiros de endocrinologia e metabologia","volume":"58 4","pages":"382-8"},"PeriodicalIF":0.0,"publicationDate":"2014-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1590/0004-2730000003050","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32432041","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: 6
[The importance of memory bias in obtaining age of menarche by recall method in Brazilian adolescents]. [记忆偏差在巴西青少年回忆法获得月经初潮年龄中的重要性]。
Pub Date : 2014-06-01 DOI: 10.1590/0004-2730000003080
Silvia Diez Castilho, Luciana Bertoldi Nucci, Samanta Ramos Assuino, Lucca Ortolan Hansen

Objective: To compare the age at menarche obtained by recall method according to the time elapsed since the event, in order to verify the importance of the recall bias.

Subjects and methods: Were evaluated 1,671 girls (7-18 years) at schools in Campinas-SP regarding the occurrence of menarche by the status quo method (menarche: yes or no) and the recall method (date of menarche, for those who mentioned it). The age at menarche obtained by the status quo method was calculated by logit, which considers the whole group, and the age obtained by the recall method was calculated as the average of the mentioned age at menarche. In this group, the age at menarche was obtained by the difference between the date of the event and the date of birth. Girls who reported menarche (883, 52.8%) were divided into four groups according to the time elapsed since the event. To analyze the results, we used ANOVA and logistic regression for the analysis, with a significance level of 0.05.

Results: The age at menarche calculated by logit was 12.14 y/o (95% CI 12.08 to 12.20). Mean ages obtained by recall were: for those who experienced menarche within the previous year 12.26 y/o (±1.14), between > 1-2 years before, 12.29 y (±1.22); between > 2-3 years before, 12.23 y/o (±1.27); and more than 3 years before, 11.55y/o (±1.24), p < 0.001.

Conclusion: The age at menarche obtained by the recall method was similar for girls who menstruated within the previous 3 years (and approaches the age calculated by logit); when more than 3 years have passed, the recall bias was significant.

目的:根据事件发生后的时间,比较回忆法获得的初潮年龄,以验证回忆偏倚的重要性。对象和方法:采用现状法(月经初潮:有或没有)和回忆法(月经初潮日期,提及者)对坎皮纳斯- sp学校1671名7-18岁女生月经初潮发生情况进行评估。现状法得到的初潮年龄采用logit计算,考虑整个群体,召回法得到的初潮年龄计算为上述初潮年龄的平均值。在这一组中,月经初潮的年龄是通过事件发生日期和出生日期之间的差异来获得的。报告月经初潮的女生(883,52.8%)根据月经初潮发生的时间分为四组。对结果进行分析,我们采用方差分析和逻辑回归进行分析,显著性水平为0.05。结果:经logit计算月经初潮年龄为12.14 y/o (95% CI 12.08 ~ 12.20)。回忆得到的平均年龄为:前一年初潮者12.26 y/o(±1.14),前1-2年者12.29 y(±1.22);> 2-3年前,12.23 y/o(±1.27);与3年前相比,11.55y/o(±1.24),p < 0.001。结论:前3年内来过月经的女生,用召回法得到的月经初潮年龄相近(且接近logit法计算的年龄);当时间超过3年时,回忆偏差显著。
{"title":"[The importance of memory bias in obtaining age of menarche by recall method in Brazilian adolescents].","authors":"Silvia Diez Castilho,&nbsp;Luciana Bertoldi Nucci,&nbsp;Samanta Ramos Assuino,&nbsp;Lucca Ortolan Hansen","doi":"10.1590/0004-2730000003080","DOIUrl":"https://doi.org/10.1590/0004-2730000003080","url":null,"abstract":"<p><strong>Objective: </strong>To compare the age at menarche obtained by recall method according to the time elapsed since the event, in order to verify the importance of the recall bias.</p><p><strong>Subjects and methods: </strong>Were evaluated 1,671 girls (7-18 years) at schools in Campinas-SP regarding the occurrence of menarche by the status quo method (menarche: yes or no) and the recall method (date of menarche, for those who mentioned it). The age at menarche obtained by the status quo method was calculated by logit, which considers the whole group, and the age obtained by the recall method was calculated as the average of the mentioned age at menarche. In this group, the age at menarche was obtained by the difference between the date of the event and the date of birth. Girls who reported menarche (883, 52.8%) were divided into four groups according to the time elapsed since the event. To analyze the results, we used ANOVA and logistic regression for the analysis, with a significance level of 0.05.</p><p><strong>Results: </strong>The age at menarche calculated by logit was 12.14 y/o (95% CI 12.08 to 12.20). Mean ages obtained by recall were: for those who experienced menarche within the previous year 12.26 y/o (±1.14), between > 1-2 years before, 12.29 y (±1.22); between > 2-3 years before, 12.23 y/o (±1.27); and more than 3 years before, 11.55y/o (±1.24), p < 0.001.</p><p><strong>Conclusion: </strong>The age at menarche obtained by the recall method was similar for girls who menstruated within the previous 3 years (and approaches the age calculated by logit); when more than 3 years have passed, the recall bias was significant.</p>","PeriodicalId":8395,"journal":{"name":"Arquivos brasileiros de endocrinologia e metabologia","volume":"58 4","pages":"394-7"},"PeriodicalIF":0.0,"publicationDate":"2014-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1590/0004-2730000003080","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32432043","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: 9
An uncommon case of Marine-Lenhart syndrome. 罕见的海洋-伦哈特综合征病例。
Pub Date : 2014-06-01 DOI: 10.1590/0004-2730000003173
Giuseppe Giuffrida, Salvatore Giovinazzo, Rosaria Certo, Teresa Manuela Vicchio, Sergio Baldari, Alfredo Campennì, Rosaria Maddalena Ruggeri

The term Marine-Lenhart syndrome describes the association between Graves' disease and autonomously functioning thyroid nodules (AFTN), such as toxic adenoma or toxic multinodular goiter. The two diseases may coexist or may be present at different moments in the same patient. In the literature, there are many reports on the development of Graves' disease after radioiodine treatment for AFTN, but very little information may be found on the occurrence of AFTN after radioiodine therapy for Graves' disease. We describe here the case of a female patient with Graves' disease who was successfully treated with radioiodine for Graves' disease, returning to normal thyroid function. Three years later, biochemical analysis and ultrasound examination identified a thyroid nodule that progressively increased in size. The 99mTc-pertechnetate scintigraphy showed avid uptake in the right lobule, which corresponded to a nodular lesion consistent with AFTN.

术语Marine-Lenhart综合征描述了Graves病与自主功能甲状腺结节(AFTN)之间的关系,如中毒性腺瘤或中毒性多结节性甲状腺肿。这两种疾病可能同时存在,也可能在同一病人的不同时刻出现。文献中有很多关于放射性碘治疗Graves病后发生AFTN的报道,但关于放射性碘治疗Graves病后发生AFTN的报道很少。我们在此描述一例女性格雷夫斯病患者,她成功地用放射性碘治疗格雷夫斯病,恢复了正常的甲状腺功能。三年后,生化分析和超声检查发现甲状腺结节逐渐增大。99mtc高显像显示右侧小叶摄取旺盛,与AFTN相一致的结节状病变。
{"title":"An uncommon case of Marine-Lenhart syndrome.","authors":"Giuseppe Giuffrida,&nbsp;Salvatore Giovinazzo,&nbsp;Rosaria Certo,&nbsp;Teresa Manuela Vicchio,&nbsp;Sergio Baldari,&nbsp;Alfredo Campennì,&nbsp;Rosaria Maddalena Ruggeri","doi":"10.1590/0004-2730000003173","DOIUrl":"https://doi.org/10.1590/0004-2730000003173","url":null,"abstract":"<p><p>The term Marine-Lenhart syndrome describes the association between Graves' disease and autonomously functioning thyroid nodules (AFTN), such as toxic adenoma or toxic multinodular goiter. The two diseases may coexist or may be present at different moments in the same patient. In the literature, there are many reports on the development of Graves' disease after radioiodine treatment for AFTN, but very little information may be found on the occurrence of AFTN after radioiodine therapy for Graves' disease. We describe here the case of a female patient with Graves' disease who was successfully treated with radioiodine for Graves' disease, returning to normal thyroid function. Three years later, biochemical analysis and ultrasound examination identified a thyroid nodule that progressively increased in size. The 99mTc-pertechnetate scintigraphy showed avid uptake in the right lobule, which corresponded to a nodular lesion consistent with AFTN.</p>","PeriodicalId":8395,"journal":{"name":"Arquivos brasileiros de endocrinologia e metabologia","volume":"58 4","pages":"398-401"},"PeriodicalIF":0.0,"publicationDate":"2014-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1590/0004-2730000003173","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32432044","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: 10
Malignant solitary fibrous tumor of the thyroid: a case-report and review of the literature. 甲状腺恶性孤立性纤维性肿瘤1例报告及文献复习。
Pub Date : 2014-06-01 DOI: 10.1590/0004-2730000003230
Wellington Alves Filho, Renata Regina da Graça Lorencetti Mahmoud, Daniel Marin Ramos, Vergilius José Furtado de Araujo-Filho, Patricia Picciarelli de Lima, Claudio Roberto Cernea, Lenine Garcia Brandão

Solitary fibrous tumor (SFT) is an uncommon spindle-cell neoplasm that most often involves the pleura, rarely occurring in extra-thoracic locations. Twenty-six cases of SFT arising in the thyroid gland have been described. We report a case of a 60-year-old woman presenting an 8-month history of enlargement of the neck associated with dysphagia. The patient underwent a right hemithyroidectomy and SFT of the thyroid was diagnosed. Immunohistochemistry showed positivity for CD34 marker, and the high number of mitoses and the presence of cellular atypia suggested that the tumor was malignant. To our knowledge, this is the second case of malignant SFT of the thyroid gland ever reported. Due to the rarity of these tumors, the indication of adjuvant therapy and prognosis are uncertain. Long-term follow-up after surgical resection seems to be advisable.

孤立性纤维性肿瘤(SFT)是一种罕见的梭形细胞肿瘤,最常累及胸膜,很少发生在胸外部位。本文报道了26例发生于甲状腺的SFT。我们报告一个60岁的妇女的情况下,提出了8个月的历史的颈部扩大与吞咽困难。患者接受了右甲状腺切除术和甲状腺SFT诊断。免疫组化CD34标记物阳性,有丝分裂数高,细胞异型性提示肿瘤为恶性。据我们所知,这是甲状腺恶性SFT的第二例报道。由于这些肿瘤的罕见性,辅助治疗的适应症和预后不确定。手术切除后长期随访似乎是可取的。
{"title":"Malignant solitary fibrous tumor of the thyroid: a case-report and review of the literature.","authors":"Wellington Alves Filho,&nbsp;Renata Regina da Graça Lorencetti Mahmoud,&nbsp;Daniel Marin Ramos,&nbsp;Vergilius José Furtado de Araujo-Filho,&nbsp;Patricia Picciarelli de Lima,&nbsp;Claudio Roberto Cernea,&nbsp;Lenine Garcia Brandão","doi":"10.1590/0004-2730000003230","DOIUrl":"https://doi.org/10.1590/0004-2730000003230","url":null,"abstract":"<p><p>Solitary fibrous tumor (SFT) is an uncommon spindle-cell neoplasm that most often involves the pleura, rarely occurring in extra-thoracic locations. Twenty-six cases of SFT arising in the thyroid gland have been described. We report a case of a 60-year-old woman presenting an 8-month history of enlargement of the neck associated with dysphagia. The patient underwent a right hemithyroidectomy and SFT of the thyroid was diagnosed. Immunohistochemistry showed positivity for CD34 marker, and the high number of mitoses and the presence of cellular atypia suggested that the tumor was malignant. To our knowledge, this is the second case of malignant SFT of the thyroid gland ever reported. Due to the rarity of these tumors, the indication of adjuvant therapy and prognosis are uncertain. Long-term follow-up after surgical resection seems to be advisable. </p>","PeriodicalId":8395,"journal":{"name":"Arquivos brasileiros de endocrinologia e metabologia","volume":"58 4","pages":"402-6"},"PeriodicalIF":0.0,"publicationDate":"2014-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1590/0004-2730000003230","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32429858","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: 9
Hypercholesterolemic diet induces hepatic steatosis and alterations in mRNA expression of NADPH oxidase in rat livers. 高胆固醇饮食诱导大鼠肝脏脂肪变性和NADPH氧化酶mRNA表达的改变。
Pub Date : 2014-04-01 DOI: 10.1590/0004-2730000002831
Isabel Cristina Mallosto Emerich de Abreu, Joyce Ferreira da Costa Guerra, Renata Rebeca Pereira, Maísa Silva, Wanderson Geraldo de Lima, Marcelo Eustáquio Silva, Maria Lúcia Pedrosa

Objective: This study aimed to determine whether a hypercholesterolemic diet induces hepatic steatosis, alterations in mRNA expression of NADPH oxidase subunits, and antioxidant defenses.

Materials and methods: Fischer rats were divided into two groups of eight animals according to the treatment, control (C) and hypercholesterolemic diet (H). Those in group C were fed a standard diet (AIN-93M), and those of the group H were fed a hypercholesterolemic diet (25% soybean oil and 1% cholesterol).

Results: The hypercholesterolemic diet did not affect body weight, but resulted in the accumulation of lipids in the liver, increased serum activities of aminotransferases and cholesterol levels. Biomarker of lipid peroxidation (TBARS) and mRNA expression of NADPH oxidase subunits p22(phox) and p47(phox) were increased in the liver of animals in group H. Besides, the activity and expression of antioxidant enzymes were altered.

Conclusion: The results show increased mRNA expression of NADPH oxidase subunits and changes in antioxidant enzyme activities in diet-induced hepatic steatosis.

目的:本研究旨在确定高胆固醇饮食是否会导致肝脂肪变性、NADPH氧化酶亚基mRNA表达的改变和抗氧化防御。材料与方法:将Fischer大鼠按对照组(C)和高胆固醇血症饲粮(H)分为两组,每组8只,C组饲喂标准饲粮(AIN-93M), H组饲喂高胆固醇血症饲粮(25%大豆油+ 1%胆固醇)。结果:高胆固醇饮食不影响体重,但导致肝脏脂质堆积,血清转氨酶活性和胆固醇水平升高。h组动物肝脏脂质过氧化生物标志物(TBARS)和NADPH氧化酶亚基p22(phox)、p47(phox) mRNA表达量升高,抗氧化酶活性和表达发生改变。结论:饮食诱导的肝脂肪变性中NADPH氧化酶亚基mRNA表达增加,抗氧化酶活性发生变化。
{"title":"Hypercholesterolemic diet induces hepatic steatosis and alterations in mRNA expression of NADPH oxidase in rat livers.","authors":"Isabel Cristina Mallosto Emerich de Abreu,&nbsp;Joyce Ferreira da Costa Guerra,&nbsp;Renata Rebeca Pereira,&nbsp;Maísa Silva,&nbsp;Wanderson Geraldo de Lima,&nbsp;Marcelo Eustáquio Silva,&nbsp;Maria Lúcia Pedrosa","doi":"10.1590/0004-2730000002831","DOIUrl":"https://doi.org/10.1590/0004-2730000002831","url":null,"abstract":"<p><strong>Objective: </strong>This study aimed to determine whether a hypercholesterolemic diet induces hepatic steatosis, alterations in mRNA expression of NADPH oxidase subunits, and antioxidant defenses.</p><p><strong>Materials and methods: </strong>Fischer rats were divided into two groups of eight animals according to the treatment, control (C) and hypercholesterolemic diet (H). Those in group C were fed a standard diet (AIN-93M), and those of the group H were fed a hypercholesterolemic diet (25% soybean oil and 1% cholesterol).</p><p><strong>Results: </strong>The hypercholesterolemic diet did not affect body weight, but resulted in the accumulation of lipids in the liver, increased serum activities of aminotransferases and cholesterol levels. Biomarker of lipid peroxidation (TBARS) and mRNA expression of NADPH oxidase subunits p22(phox) and p47(phox) were increased in the liver of animals in group H. Besides, the activity and expression of antioxidant enzymes were altered.</p><p><strong>Conclusion: </strong>The results show increased mRNA expression of NADPH oxidase subunits and changes in antioxidant enzyme activities in diet-induced hepatic steatosis.</p>","PeriodicalId":8395,"journal":{"name":"Arquivos brasileiros de endocrinologia e metabologia","volume":"58 3","pages":"251-9"},"PeriodicalIF":0.0,"publicationDate":"2014-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1590/0004-2730000002831","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32370001","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: 29
期刊
Arquivos brasileiros de endocrinologia e metabologia
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