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1.
Clin Endocrinol (Oxf) ; 54(5): 583-92, 2001 May.
Artigo em Inglês | MEDLINE | ID: mdl-11380488

RESUMO

OBJECTIVE AND BACKGROUND: Old people in residential care are at the highest risk of any group for hip fracture. This may relate to their high prevalence of hyperparathyroidism. There are few data, however, on relationships with serum parathyroid hormone (PTH) in these individuals. This study therefore examined complex associations with serum PTH in nursing home and hostel residents. DESIGN: Cross-sectional analysis. PATIENTS: One hundred and forty-three nursing home and hostel residents of median age 84 years. MEASUREMENTS: Serum PTH, 25-hydroxyvitamin D (25OHD), 1,25-dihydroxyvitamin D (1,25-(OH)2D), plasma creatinine, phosphate, calcium, albumin, Bsm-1 vitamin D receptor genotype, age, weight and use of frusemide or thiazide. RESULTS: The statistical models determined accounted for half the interindividual variation in serum PTH. Heavier weight was associated with both the prevalence of secondary hyperparathyroidism and the serum concentration of PTH. Novel interactions with serum PTH were identified between: weight and 25OHD; 25OHD and phosphate; and phosphate and thiazide diuretic use. Plasma phosphate was associated with PTH independently of calcium and 1,25-(OH)2D. There was no independent association between PTH and nuclear vitamin D receptor genotype. CONCLUSIONS: Heavier weight is associated with both the prevalence and severity of secondary hyperparathyroidism and consistent with animal models of secondary hyperparathyroidism, phosphate may relate to serum PTH independently of 1,25-(OH)2D or calcium.


Assuntos
Peso Corporal , Instituição de Longa Permanência para Idosos , Hiperparatireoidismo Secundário/diagnóstico , Institucionalização , Casas de Saúde , Hormônio Paratireóideo/sangue , Idoso , Idoso de 80 Anos ou mais , Benzotiadiazinas , Estudos Transversais , Diuréticos , Feminino , Furosemida/uso terapêutico , Genótipo , Fraturas do Quadril/etiologia , Humanos , Hidroxicolecalciferóis/sangue , Hiperparatireoidismo Secundário/complicações , Modelos Lineares , Masculino , Fosfatos/sangue , Receptores de Calcitriol/genética , Fatores de Risco , Inibidores de Simportadores de Cloreto de Sódio/uso terapêutico
2.
Am J Physiol ; 275(1): C278-84, 1998 07.
Artigo em Inglês | MEDLINE | ID: mdl-9688859

RESUMO

Adhesion to novel basement membrane component BM180 in the presence of laminin-1 promotes stimulus-secretion coupling in lacrimal acinar cells [G. W. Laurie, J. D. Glass, R. A. Ogle, C. M. Stone, J. R. Sluss, and L. Chen. Am. J. Physiol. 270 (Cell Physiol. 39): C1743-C1750, 1996]. The identity of the active laminin-1 site and the possibility that other promoters of coupling are present in the acinar cell microenvironment were probed by use of different substrates, media, neutralizing antibodies and cell numbers. Regulated peroxidase secretion was unaffected by basement membrane coat concentration and was detectable at reduced levels in serum-free medium. Anti-laminin-1 antibodies, particularly against sites in the beta1 and gamma1 chains, but not alpha1 chains, partially suppressed regulated secretion, as did an anti-collagen IV antibody. Without effect were RGD peptide and antibodies against entactin, the beta1-integrin subunit, and several growth factors. Increasing cell number in serum-free medium revealed an unknown, serum-maskable, secretion-enhancing activity with a remarkable specificity for regulated secretion. Stimulus-secretion coupling, therefore, appears to be modulated by several extracellular factors whose relative contributions remain to be determined.


Assuntos
Anticorpos/farmacologia , Colágeno/fisiologia , Substâncias de Crescimento/imunologia , Aparelho Lacrimal/metabolismo , Laminina/fisiologia , Peroxidases/metabolismo , Animais , Atropina/farmacologia , Membrana Basal/fisiologia , Carbacol/farmacologia , Células Cultivadas , Colágeno/imunologia , Meios de Cultura Livres de Soro , Aparelho Lacrimal/citologia , Aparelho Lacrimal/efeitos dos fármacos , Laminina/imunologia , Masculino , Ratos , Ratos Sprague-Dawley , Lágrimas/metabolismo , Peptídeo Intestinal Vasoativo/farmacologia
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