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1.
Arch Endocrinol Metab ; 61(6): 600-607, 2017 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-29412385

RESUMEN

OBJECTIVE: Selenium (Se) supplementation has been used to help prevent the progression of Graves' ophthalmopathy (GO) and autoimmune thyroid diseases (AITD) patients. We investigated Se serum and selenoprotein P (SePP) levels in Graves' disease (GD) with and without GO, Hashimoto's thyroiditis (HT) patients and in 27 control individuals (C). SUBJECTS AND METHODS: We studied 54 female and 19 male patients: 19 with GD without GO, 21 GD with GO, 14 with HT and 19 with HT+LT4. Se values were measured using graphite furnace atomic absorption spectrophotometry. Serum SePP levels were measured by ELISA. RESULTS: Median Se levels were similar among all groups; GD patients: 54.2 (46.5-61.1 µg/L), GO: 53.6 (43.5-60.0 µg/L), HT: 51.9 (44.6-58.5 µg/L), HT+LT4 54.4 (44-63.4) and C group patients: 56.0 (52.4-61.5 µg/L); P = 0.48. However, serum SePP was lower in GO patients: 0.30 (0.15-1.05 µg/mL) and in HT patients: 0.35 (0.2-1.17 µg/mL) compared to C group patients: 1.00 (0.564.21 µg/mL) as well as to GD patients: 1.19 (0.62-2.5 µg/mL) and HT+LT4 patients: 0.7 (0,25-1.95); P = 0.002. Linear regression analysis showed a significant relationship between SePP and TPOAb values (r = 0.445, R2 = 0.293; P < 0.0001). Multiple regression analysis found no independent variables related to Se or SePP. CONCLUSION: A serum Se concentration was lower than in some other countries, but not significantly among AITD patients. The low serum SePP levels in GO and HT patients seems to express inflammatory reactions with a subsequent increase in Se-dependent protein consumption remains unclear.


Asunto(s)
Enfermedad de Graves/sangre , Enfermedad de Hashimoto/sangre , Selenio/sangre , Selenoproteína P/sangre , Adulto , Anciano , Biomarcadores/sangre , Estudios de Casos y Controles , Estudios Transversales , Progresión de la Enfermedad , Femenino , Oftalmopatía de Graves/sangre , Humanos , Masculino , Persona de Mediana Edad , Espectrofotometría Atómica
2.
Magnes Res ; 28(4): 136-45, 2015 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-26878253

RESUMEN

PURPOSE: Magnesium is an important electrolyte for very many cell functions and its deficiency may lead to a wide spectrum of diseases. We report a clinical case of hypomagnesemia resulting from the chronic use of a proton pump inhibitor (PPI). PPIs are drugs widely used in medical practice, and a growing number of cases of PPIs causing hypomagnesemia have been described. Our aim was to monitor the clinical and electrolyte findings during recovery from hypomagnesemia caused by long-term PPI use. RESULTS: A 65-year old female who had been using omeprazole for 10 years, presented with arrhythmia and paresthesia of the lower and upper limbs that had been attributed to severe hypomagnesemia, hypocalcemia, and hypoparathyroidism. Her laboratory tests revealed the following results: magnesium 0.6 mg/dL (NR: 1.5 to 2.5 mg/dL), calcium 7.3 mg/dL (NR: 8.5 to 10.2 mg/dL), parathyroid hormone (PTH) 13.3 pg/mL (NR: 15 to 65 pg/mL), and low urinary calcium and magnesium excretion. Her electrocardiogram disclosed typical, prolonged QT interval, ST depression, and U waves. We discuss the differential diagnoses, pathophysiology, and reversibility of symptoms after effective treatment of the hypomagnesemia. CONCLUSION: this report emphasizes that even if long-term PPI users appear largely asymptomatic, life-threatening arrhythmias can present very suddenly. Long-term PPI users should be monitored for otherwise unexplained hypomagnesemia, hypocalcemia, functional hypoparathyroidism and associated symptoms.


Asunto(s)
Magnesio/sangre , Enfermedades Metabólicas/inducido químicamente , Omeprazol/efectos adversos , Inhibidores de la Bomba de Protones/efectos adversos , Anciano , Arritmias Cardíacas/sangre , Arritmias Cardíacas/inducido químicamente , Biomarcadores/sangre , Diagnóstico Diferencial , Regulación hacia Abajo , Electrocardiografía , Femenino , Humanos , Hipocalcemia/sangre , Hipocalcemia/inducido químicamente , Hipoparatiroidismo/sangre , Hipoparatiroidismo/inducido químicamente , Enfermedades Metabólicas/sangre , Enfermedades Metabólicas/diagnóstico , Enfermedades Metabólicas/terapia , Parestesia/sangre , Parestesia/inducido químicamente , Valor Predictivo de las Pruebas , Factores de Riesgo , Resultado del Tratamiento
3.
Arch. endocrinol. metab. (Online) ; 61(6): 600-607, Dec. 2017. tab, graf
Artículo en Inglés | LILACS | ID: biblio-887610

RESUMEN

ABSTRACT Objective: Selenium (Se) supplementation has been used to help prevent the progression of Graves' ophthalmopathy (GO) and autoimmune thyroid diseases (AITD) patients. We investigated Se serum and selenoprotein P (SePP) levels in Graves' disease (GD) with and without GO, Hashimoto's thyroiditis (HT) patients and in 27 control individuals (C). Subjects and methods: We studied 54 female and 19 male patients: 19 with GD without GO, 21 GD with GO, 14 with HT and 19 with HT+LT4. Se values were measured using graphite furnace atomic absorption spectrophotometry. Serum SePP levels were measured by ELISA. Results: Median Se levels were similar among all groups; GD patients: 54.2 (46.5-61.1 μg/L), GO: 53.6 (43.5-60.0 μg/L), HT: 51.9 (44.6-58.5 μg/L), HT+LT4 54.4 (44-63.4) and C group patients: 56.0 (52.4-61.5 μg/L); P = 0.48. However, serum SePP was lower in GO patients: 0.30 (0.15-1.05 μg/mL) and in HT patients: 0.35 (0.2-1.17 μg/mL) compared to C group patients: 1.00 (0.564.21 μg/mL) as well as to GD patients: 1.19 (0.62-2.5 μg/mL) and HT+LT4 patients: 0.7 (0,25-1.95); P = 0.002. Linear regression analysis showed a significant relationship between SePP and TPOAb values (r = 0.445, R2 = 0.293; P < 0.0001). Multiple regression analysis found no independent variables related to Se or SePP. Conclusion: A serum Se concentration was lower than in some other countries, but not significantly among AITD patients. The low serum SePP levels in GO and HT patients seems to express inflammatory reactions with a subsequent increase in Se-dependent protein consumption remains unclear.


Asunto(s)
Humanos , Masculino , Femenino , Adulto , Persona de Mediana Edad , Anciano , Selenio/sangre , Enfermedad de Graves/sangre , Enfermedad de Hashimoto/sangre , Selenoproteína P/sangre , Espectrofotometría Atómica , Biomarcadores/sangre , Estudios de Casos y Controles , Estudios Transversales , Progresión de la Enfermedad , Oftalmopatía de Graves/sangre
4.
Säo Paulo; s.n; 1998. 64 p. ilus, tab.
Tesis en Portugués | LILACS | ID: lil-204974

RESUMEN

Os defeitos da reposiçäo do hormônio do crescimento (GH) nos níveis séricosrmônios tirpoidianos säo controversos. Para melhor estudar estes efeitos e procurar definir seus mecanismos, estudamos 20 pacientes (17M/3F, 9-18,5 anos) com diagnóstico de deficiência de GH (DGH), clinicamente em eutiroidismo e com dosagem de tiroxina livre (T4 livre) normal, no período sem reposiçäo de GH (antes de iniciar a terapêutica ou após suspensäo de 30 a 60 dias) e com reposiçäo de GH(0,5-7 anos). Em l2pacientes que näo receberam reposiçäo de tiroxina os níveis basais do hormônio tiroestimulante (TSH) estavam normais ou discretamente elevados (Grupo A) e em 8 que recebiam tiroxina (2,7 a 3,7 µg/Kg/dia) os níveis de TSH estavam suprimidos (Grupo B). As doses de reposiçäo de tiroxina foram mantidas constantes durante o estudo. Os níveis séricos de T4 Livre, triiodotironina total (T3 Total), T3 reverso (rT3) e do TSH basal e após estímulo com TRH foram determinados por imunoensaios específicos, sendo que as amostras do mesmo paciente foram dosadas sempre no mesmo ensaio. A secreçäo estimulada do TSH pelo TRH foi expressa como àra sob a curva (ASC). A anàlise estatística foi realizada pelo teste t pareado ou näo, e pelo teste de Wilcoxon dependendo da normalidade na distribuiçäo das amostras. O nível de significância adotado foi de 0.05. Os resultados säo expressos com média ñ DP


Asunto(s)
Hormona del Crecimiento , Hormona del Crecimiento/deficiencia , Hipopituitarismo , Hipotiroidismo
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