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1.
Clin Nephrol ; 77(6): 445-53, 2012 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-22595386

RESUMO

AIMS: Patients with nephrotic range proteinuria are known to have an increased risk of cardiovascular disease partly due to possessing the atherogenic lipoprotein phenotype. The aim of this study was to examine the effect of high dose omega-3 fatty acids on atherogenic triglyceride rich lipoproteins in patients with nephrotic range proteinuria, comparing their effect on lipoprotein profiles in age and sex matched controls. METHODS: 17 patients with nephrotic range proteinuria and 17 age and sex matched controls were studied. Fasting lipids and lipoproteins were measured before and after 8 weeks treatment with 4 g daily of omega-3 fatty acids (Omacor®). RESULTS: In patients with proteinuria treatment reduced plasma triglyceride by a mean of 0.45 mmol/l (95%CI 0.16 - 0.74, p = 0.005) and plasma very low density lipoprotein cholesterol by a mean of 0.38 (95%CI 0.01 - 0.75, p = 0.04). LDL III concentration fell from 178.8 mg/dl (61.6 - 231.0) to 96.1 mg/dl (49.3 - 204.5), p = 0.05. In patients treatment altered the LDL profile so that LDLIII which was the major subfraction present at baseline was reduced from 49.9% to 29.8% (p = 0.01). Remnant lipoproteins (RLP) also fell with a mean reduction of 3.5 mg/dl in RLP-Cholesterol (95%CI 0.1 - 6.9, p = 0.05) and 12.4 mg/dl in RLP-triglyceride (95%CI 2.6 - 22.2, p = 0.03). There was however a 0.6 mmol/l rise in LDL-C (p = 0.06) in the patients. Treatment did not alter HDL-C. CONCLUSION: In patients with nephrotic range proteinuria, omega-3 fatty acids reduced triglyceride rich lipoproteins, LDL III and remnant lipoproteins. A tendency to an increase in LDL-C was observed but this was offset by an alteration in the distribution of the LDL profile towards lighter, larger LDL particles. We propose that treatment with omega-3 fatty acids in conjunction with a statin may be the ideal therapy in these patients.


Assuntos
Aterosclerose/tratamento farmacológico , Suplementos Nutricionais , Ácidos Docosa-Hexaenoicos/uso terapêutico , Ácido Eicosapentaenoico/uso terapêutico , Hipolipemiantes/uso terapêutico , Lipoproteínas/sangue , Nefrose/tratamento farmacológico , Proteinúria/tratamento farmacológico , Idoso , Aterosclerose/sangue , Aterosclerose/complicações , Biomarcadores/sangue , Combinação de Medicamentos , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Nefrose/sangue , Nefrose/complicações , Fenótipo , Proteinúria/sangue , Proteinúria/complicações , Escócia , Fatores de Tempo , Resultado do Tratamento
2.
BMJ Case Rep ; 20152015 Jul 08.
Artigo em Inglês | MEDLINE | ID: mdl-26156834

RESUMO

The case of a patient with clinical symptoms, laboratory and imaging findings of hypoparathyroidism, sensorineural deafness, renal dysplasia HDR, or Barakat syndrome (hypoparathyroidism, deafness, renal dysplasia), and vitamin D deficiency, is presented. A Caucasian man aged 51 years with a history of chronic hypocalcaemia since childhood, was admitted with hypertonia of the body and extremities, and loss of consciousness. On admission, he was found to have severe hypocalcaemia, hyperphosphataemia, severe hypoparathyroidism, low serum magnesium and mild renal insufficiency. Calcium gluconate was administered intravenously supplemented with magnesium, and the patient recovered consciousness while clinical and laboratory findings improved. Evaluation revealed left renal aplasia and sensorineural deafness affecting both ears. Vitamin D deficiency was also present. He was given calcium and vitamin D supplements orally, and the hypocalcaemia was corrected. This case is described as it is an extremely rare case of HDR syndrome with concurrent vitamin D deficiency.


Assuntos
Perda Auditiva Neurossensorial/etiologia , Hipoparatireoidismo/etiologia , Nefrose/diagnóstico , Insuficiência Renal/etiologia , Deficiência de Vitamina D/complicações , Gluconato de Cálcio/administração & dosagem , Hidratação , Perda Auditiva Neurossensorial/complicações , Perda Auditiva Neurossensorial/diagnóstico , Perda Auditiva Neurossensorial/tratamento farmacológico , Humanos , Hipoparatireoidismo/complicações , Hipoparatireoidismo/diagnóstico , Hipoparatireoidismo/tratamento farmacológico , Rim/anormalidades , Masculino , Pessoa de Meia-Idade , Nefrose/complicações , Nefrose/tratamento farmacológico , Insuficiência Renal/diagnóstico , Resultado do Tratamento , Vitamina D/administração & dosagem , Deficiência de Vitamina D/diagnóstico , Deficiência de Vitamina D/tratamento farmacológico , Vitaminas/administração & dosagem
3.
J Pediatr ; 118(5): 703-7, 1991 May.
Artigo em Inglês | MEDLINE | ID: mdl-2019923

RESUMO

To determine the effect of intranasal administration of salmon calcitonin on glucocorticoid-induced osteoporosis in children with nephrosis, we gave 100 U of calcitonin intranasally on alternate days with 1 alpha-hydroxyvitamin D3 to five children, 8 to 12 years of age, with frequently relapsing nephrosis. Four patients with osteoporosis, 10 to 14 years of age, were treated only with 1 alpha-hydroxyvitamin D3 and served as control subjects. Both groups were treated with an almost equal amount of glucocorticoids previously and during this study period. Bone mineral content of the spine was measured by a quantitative computed tomographic technique. The bone mineral content was preserved in both cortical and spongeous areas of the vertebrae during the 16-month period in the calcitonin-treated group but was decreased significantly in the control group. Urinary hydroxyproline and calcium excretion decreased significantly in the calcitonin-treated group. The serum calcium and phosphorus concentrations and the parathyroid function did not change significantly in either group. We conclude that calcitonin suppressed bone resorption and might be useful for the long-term treatment of osteoporosis, in combination with 1 alpha-hydroxyvitamin D3, in children with nephrosis requiring long-term glucocorticoid therapy.


Assuntos
Calcitonina/administração & dosagem , Glucocorticoides/efeitos adversos , Nefrose/complicações , Osteoporose/prevenção & controle , Administração Intranasal , Aerossóis , Densidade Óssea , Criança , Quimioterapia Combinada , Glucocorticoides/administração & dosagem , Humanos , Hidroxicolecalciferóis/administração & dosagem , Nefrose/tratamento farmacológico , Nefrose/metabolismo , Osteoporose/induzido quimicamente , Osteoporose/metabolismo , Recidiva , Coluna Vertebral/diagnóstico por imagem , Tomografia Computadorizada por Raios X
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