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1.
Rev. Assoc. Med. Bras. (1992) ; 65(1): 51-55, Jan. 2019. tab, graf
Artigo em Inglês | LILACS | ID: biblio-985012

RESUMO

SUMMARY OBJECTIVE Vitamin D deficiency is not only associated with bone metabolism but also with diabetes mellitus. We aimed to study the possible association between serum vitamin D concentration and HbA1c level in patients with type 2 diabetes mellitus (T2DM) in this retrospective report. METHODS Patients with T2DM were enrolled to the study either in regulated or non-regulated T2DM groups, according to HbA1c levels. An HbA1c level of <8% was considered as relatively controlled and others were considered as poorly controlled T2DM. RESULTS Serum vitamin D levels in poorly controlled T2DM subjects (9.4 (4.9-34) ng/ml) were significantly lower than that of the relatively well regulated T2DM patients (13.5 (3.4-36) ng/ml) (p=0.03). Vitamin D was strongly and inversely correlated with HbA1c levels (r= -0.295, p=0.005). CONCLUSION Whatever the cause or result of the diabetes mellitus, it is clear that lower vitamin D is strongly associated with worse diabetic regulation in T2DM subjects. Randomized controlled larger studies, which research the relation between diabetic regulation and vitamin D status, are needed to claim whether it could be a therapeutic target in future in diabetic subjects.


RESUMO CONTEXTO E OBJETIVO A deficiência de vitamina D não é apenas associada ao metabolismo ósseo, mas também ao diabetes mellitus. Procurou-se estudar a possível associação entre os níveis de concentração do soro de vitamina D e de HbA1c em pacientes com diabetes mellitus tipo 2 neste relatório retrospectivo. MÉTODOS Os pacientes com diabetes mellitus tipo 2 foram inscritos no estudo em regulada ou não regulada de acordo com os grupos de níveis de HbA1c DM2. HbA1c nível de <8% caracterizava DM2 controlada e HbA1c > 8% DM2 descontrolada. RESULTADOS Os níveis de vitamina D no soro em indivíduos com DM2 mal regulados (9,4 (4,9 a 34) ng/ml) foram significativamente menores do que o do bem regulado em doentes DM2 (13,5 (3,4-36) ng/ml) (p = 0,03). A vitamina D foi forte e inversamente correlacionada com os níveis de HbA1c (p = 0,005). CONCLUSÃO Seja qual for a causa ou o resultado do diabetes mellitus, é claro que níveis baixos de vitamina D são fortemente associados com pior regulação em indivíduos diabéticos com DM2. Maiores estudos randomizados e controlados que pesquisam a relação entre o status de vitamina D e a regulação em diabéticos são necessários para molusco se é, no futuro, poderia ser um alvo terapêutico em indivíduos diabéticos.


Assuntos
Humanos , Masculino , Feminino , Adulto , Idoso , Idoso de 80 Anos ou mais , Vitamina D/sangue , Deficiência de Vitamina D/metabolismo , Diabetes Mellitus Tipo 2/sangue , Deficiência de Vitamina D/complicações , Índice de Massa Corporal , Estudos Retrospectivos , Fatores de Risco , Diabetes Mellitus Tipo 2/complicações , Pessoa de Meia-Idade
2.
Arch. argent. pediatr ; 115(2): 133-139, abr. 2017. tab
Artigo em Inglês, Espanhol | LILACS, BINACIS | ID: biblio-838339

RESUMO

Introducción. La dislipidemia es una de las mayores complicaciones de la obesidad; la deficiencia de vitamina D y la resistencia a la insulina son complicaciones metabólicas que se presentan en niños obesos con dislipidemia. Objetivo. Determinar si la deficiencia de vitamina D y la resistencia a la insulina son factores de riesgo de dislipidemia en niños obesos. Materiales y métodos. Este estudio se llevó a cabo en el Departamento de Pediatría del Hospital Universitario y de Investigación Bagcilar en Estambul, Turquía, entre 2014 y 2015. Se incluyeron en el estudio pacientes obesos de 8 a 14 años de edad. Se midió la concentración sérica de triglicéridos, colesterol total, colesterol de las LDL, colesterol de las HDL, glucemia en ayunas, insulina, alanina aminotransferasa y vitamina D; también se hicieron ecografías hepáticas. La resistencia a la insulina se calculó utilizando el índice de la evaluación del modelo homeostático (HOMA-IR). Resultados. Se incluyeron en el estudio 108 niños obesos, de los cuales 39 (36,11%) padecían dislipidemia. Los valores promedio de glucemia en ayunas (88,74 ± 7,58 frente a 95,31 ± 6,82; p= 0,0001), insulina (14,71 ± 12,44 frente a 24,39 ± 15,02; p= 0,0001) y alanina aminotransferasa (23,45 ± 11,18 frente a 30,4 ± 18,95; p= 0,018) fueron significativamente más altos en los niños con dislipidemia. En los niños obesos con dislipidemia, la tasa promedio de esteatosis hepática y el índice HOMA-IR fueron más altos: 28 niños (71,9%) tuvieron esteatosis hepática y 37 (94,87%), presentaron resistencia a la insulina; las concentraciones de vitamina D fueron <20 ng/ml en el 69,3% de los niños. La deficiencia de vitamina D fue notablemente más frecuente (p= 0,033). El análisis de regresión multivariante confirmó que el aumento del índice HOMA-IR (p= 0,015) y el bajo nivel de vitamina D (p= 0,04) fueron factores importantes de riesgo de dislipidemia. Conclusión. En los niños obesos de nuestra región se observanbajas concentraciones de vitamina D y aumento del índice HOMA-IR, ambos factores de riesgo significativos para la dislipidemia.


Introduction. Dyslipidemia is one of the major complications of obesity; vitamin D deficiency and insulin resistance are attending metabolic complications in dyslipidemic obese children. Objective. To determine if vitamin D deficiency and insulin resistance are risk factors for dyslipidemia in obese children. Materials and Methods. This study was conducted in the Department of Pediatrics at Bagcilar Training and Research Hospital in Istanbul, Turkey between 2014 and 2015. Obese patients whose age range was 8-14 were included in the study. The serum triglyceride, total cholesterol, low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, fasting glucose, insulin, alanine aminotransferase, vitamin D levels were measured; a liver ultrasonography was performed. Homeostatic model assessment (HOMA-IR), was used to calculate insulin resistance. Results. 108 obese children were included; 39 (36.11%) had dyslipidemia. The average fasting blood glucose (88.74 ± 7.58 vs. 95.31 ± 6.82; p= 0.0001), insulin level (14.71 ± 12.44 vs. 24.39 ± 15.02; p= 0.0001) and alanine aminotransferase level (23.45 ± 11.18 vs. 30.4 ± 18.95; p= 0.018) were significantly higher in the children with dyslipidemia. In the dyslipidemic obese children, the average hepatosteatosis rate and HOMA-IR level were higher; 28 (71.9%) had hepatosteatosis, 37 (94.87%) had insulin resistance; the vitamin D levels were <20 ng/ml in 69.3%. Vitamin D deficiency was significantly more common (p= 0.033). The multivariate regression analysis confirmed that the increase in the HOMA-IR level (p= 0.015) and the low vitamin D level (p= 0.04) were important risk factors for dyslipidemia. Conclusion. Obese children in our region exhibit low vitamin D and increased HOMA-IR levels, which are efficient risk factors of dyslipidemia.


Assuntos
Humanos , Criança , Adolescente , Deficiência de Vitamina D/complicações , Deficiência de Vitamina D/metabolismo , Resistência à Insulina , Dislipidemias/etiologia , Obesidade Infantil/complicações , Obesidade Infantil/metabolismo , Turquia , Fatores de Risco , Dislipidemias/epidemiologia
3.
Int. j. med. surg. sci. (Print) ; 3(3): 933-941, sept. 2016.
Artigo em Espanhol | LILACS | ID: biblio-1087613

RESUMO

La vitamina D clásicamente ha sido relacionada con el metabolismo óseo, sin embargo ejerce diversas funciones en varios tejidos del organismo que poseen el receptor para vitamina D (VCR) yson susceptibles a su efecto. La disminución de vitamina D también se ha asociado a patologías "no clásicas"como hipertensión, síndrome metabólico, resistencia a insulina, diabetes, desarrollo de algunos canceres,alteraciones pulmonares, autoinmunidad e infertilidad, entre otras. También se ha asociado la deficiencia materna de vitamina D en la génesis de patologías postnatales. Además, muchas de estas patologías se producirían por alteraciones moleculares, principalmente relacionadas con su metabolismo y con polimorfismos del receptor VCR. La vitamina D se considerara una hormona, puede ser sintetizada en la piel a partir 7-dehidrocolesterol mediante radiación ultravioleta B. Su metabolismo es complejo e implica la interacción de diversos factores en su incorporación y formación final de calcitriol, su forma activa. Para ejercer su efecto requiere de la activación del receptor VDR en la célula blanco, el cual a su vez activa secuencias de genes específicos con funciones diversas, a través de secuencias promotoras del ADN denominadas elementos de respuesta de vitamina D (VDRE). Muchos tejidos presentan el receptor VDR y enzimas necesarias para su metabolismo, por lo cual el espectro de acción de la vitamina D es muy amplio, así como la variedad de patologías que produce. Esta revisión de vitamina D, está centrada principalmente en los aspectos moleculares de su metabolismo y su rol en la génesis de enfermedades "no clásicas", producto de su disminución o alteración de su metabolismo.


Vitamin D has traditionally been associated with bone metabolism, however it exerts different functions in various tissues of the body that possess the vitamin D (VCR) receptor and they are susceptible to its effect. Decreased vitamin D has also been associated with "nonclassical" diseases such as hypertension, metabolic syndrome, insulin resistance, diabetes, development of some cancers, lung disorders,autoimmunity and infertility, among others. Maternal vitamin D deficiency has been associated in the genesis of postnatal diseases. Further, many of these pathologies are produced by molecular alterations, mainly related to metabolism and receptor polymorphisms VCR. Vitamin D is considered a hormone, can be synthesized in the skin from 7-dehydrocholesterol by ultraviolet radiation B. The metabolism is complex and involves the interaction of several factors in its incorporation and final formation of calcitriol, the active form. To produce its effect requires activation of VDR receptor on the target cell, which activates specific gene sequences with different functions, through DNA promoter sequences in identified vitamin D response elements (VDRE).Many tissues have the VDR receptor and enzymes necessary for metabolism, so the spectrum of vitamin Daction is very broad in the variety of pathologies produced. This review of vitamin D focuses primarily on the molecular aspects of its metabolism and its role in the genesis of "nonclassical", diseases, product of its reduction or alteration of metabolic diseases.


Assuntos
Humanos , Vitamina D/metabolismo , Deficiência de Vitamina D/metabolismo , Receptores de Calcitriol/deficiência , Sistema Imunitário/metabolismo , Deficiência de Vitamina D/complicações , Doença/etiologia , Redes e Vias Metabólicas , Hormônios/metabolismo
4.
Annals of Laboratory Medicine ; : 98-103, 2014.
Artigo em Inglês | WPRIM | ID: wpr-158565

RESUMO

BACKGROUND: Vitamin D deficiency and a high mean platelet volume (MPV) are related to cardiovascular disease. We investigated whether vitamin D deficiency is associated with high MPV. METHODS: This study included 434 patients without chronic disease who were not taking vitamin D or calcium supplements. Vitamin D was measured by chemiluminescent microparticle immunoassay on the Architect-I2000 system (Abbott Diagnostics, USA), and MPV was measured on the Cell-Dyn Ruby analyzer (Abbott Diagnostics). Patients were divided into Groups 1 (138 [men/women, 46/92]), 2 (148 [men/women, 54/94]), and 3 (148 [men/women, 50/98]) according to vitamin D levels of 20 ng/mL, respectively. RESULTS: The vitamin D level in Group 1 (7.7+/-1.9 ng/mL) was lower than that in Group 2 (15.1+/-1.6 ng/mL, P<0.001) and Group 3 (25.6+/-6.3 ng/mL, P<0.001). The MPV in Group 3 (7.5+/-1.0 fL) was lower than that in Group 1 (8.1+/-1.1 fL, P<0.001) and Group 2 (7.9+/-1.0 fL, P=0.009). Linear regression analysis showed that low levels of vitamin D (beta=-0.109, P=0.019) was independently associated with increased MPV. CONCLUSIONS: There was a strong association between a low vitamin D level and a high MPV; therefore, vitamin D deficiency may be associated with increased MPV.


Assuntos
Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Adulto Jovem , Fatores Etários , Glicemia/análise , Plaquetas/citologia , Tamanho Celular , Imunoensaio , Medições Luminescentes , Vitamina D/análise , Deficiência de Vitamina D/metabolismo
7.
Rev. méd. Chile ; 132(12): 1527-1531, dez. 2004. tab
Artigo em Espanhol | LILACS | ID: lil-394453

RESUMO

Pseudohypoparathyroidism is characterized by a resistance to parathormone, with variable phenotypical and biochemical manifestations. Its diagnosis is difficult. We report a 28 years old male presenting with a hypokalemic periodic paralysis. His serum PTH was elevated to 1,343 and 1,101 pg/ml with concomitant hypocalcemia of 7.9 and 6.7 mg/dl. Twenty four hour urinary calcium and serum 25 hydroxy vitamin D were normal. Bone mineral density was normal. The patient was managed with calcitriol in doses of 1 to 2 µg/d, associated to calcium 2 g/day. Serum calcium levels and PTH normalized after two months and six months of treatment respectively.


Assuntos
Adulto , Humanos , Masculino , Pseudo-Hipoparatireoidismo/diagnóstico , Deficiência de Vitamina D/diagnóstico , Monofosfato de Adenosina/urina , Cálcio/sangue , Diagnóstico Diferencial , Hipocalcemia/metabolismo , Paralisia Periódica Hipopotassêmica/metabolismo , Hormônio Paratireóideo/sangue , Pseudo-Hipoparatireoidismo/classificação , Pseudo-Hipoparatireoidismo/metabolismo , Deficiência de Vitamina D/metabolismo
8.
Ceylon Med J ; 1999 Sep; 44(3): 149
Artigo em Inglês | IMSEAR | ID: sea-49032
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