Please use this identifier to cite or link to this item:
http://hdl.handle.net/10553/50202
DC Field | Value | Language |
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dc.contributor.author | Henríquez, Manuel Sosa | en_US |
dc.contributor.author | Ramírez, Armando Torres | en_US |
dc.contributor.author | Domínguez Cabrera, Casimira | en_US |
dc.contributor.author | Salido, Eduardo | en_US |
dc.contributor.author | Saavedra Santana, Pedro | en_US |
dc.contributor.author | Barrios, Ysamar | en_US |
dc.contributor.author | Limiñana Cañal, Jose Maria | en_US |
dc.contributor.author | León, Pedro Betancor | en_US |
dc.date.accessioned | 2018-11-24T14:10:37Z | - |
dc.date.available | 2018-11-24T14:10:37Z | - |
dc.date.issued | 1998 | en_US |
dc.identifier.issn | 0025-7753 | en_US |
dc.identifier.uri | http://hdl.handle.net/10553/50202 | - |
dc.description.abstract | BACKGROUND: Genetic factors conditionate an important part of bone mass, The role of vitamin D receptor polymorphism (VDR) as genetic marker of osteoporosis is a matter of discussion. We have studied the possible influence of VDR on bone remodelling, calciotropic hormones, on the presence of osteoporosis and osteoporotic bone fractures.PATIENTS, CONTROL POPULATION AND METHODS: A case-control study. We have studied a total of 127 postmenopausal canarian women from Canary Islands, Spain; 66 healthy controls and 61 with the diagnosis of osteoporosis, which was made by clinical, radiological and densitometric criteria. 17 osteoporotic women have had a fracture: Colles, hip or vertebral (spinal deformity index) fracture. VDR were determined by PCR directed to demonstrate the presence (b) or ausence (B) of a restriction target for Bsml in intron 7. We analized some biochemical markers of bone remodelling: serum levels of alkaline phosphatase, tartrate resistant acid phosphatase and urine ratios of calcium/creatinin and hydroxyproline/creatinin. We also determined calciotropic hormones: parathyroid hormone and calcitonin. Bone mass was measured by DEXA and TC.RESULTS: There were no significant differences in either biochemical bone remodelling markers or in bone mass between the three genotypes: bb, Bb and BE, either in controls or in osteoporotic women with the exception of alkaline phosphatase which had a significative increase compared to control in women with unfavorable alleles distribution (bB and BE). Distribution of genotypes was similar between controls and osteoporotic women, with or without fractures.CONCLUSIONS: In canarian women, VDR genotype is not associated with changes in biochemical markers of bone remodelling or in bone mass or with the presence of osteoporosis or osteoporotic fractures. | en_US |
dc.language | eng | en_US |
dc.relation.ispartof | Medicina Clínica | en_US |
dc.source | Medicina Clinica[ISSN 0025-7753],v. 110, p. 646-650 | en_US |
dc.subject | 32 Ciencias médicas | en_US |
dc.subject | 3201 Ciencias clínicas | en_US |
dc.subject.other | Bone-Mineral Density | en_US |
dc.subject.other | Postmenopausal Women | en_US |
dc.subject.other | Premenopausal Women | en_US |
dc.subject.other | Computed-Tomography | en_US |
dc.subject.other | Mass | en_US |
dc.subject.other | Alleles | en_US |
dc.subject.other | Genotype | en_US |
dc.subject.other | Association | en_US |
dc.subject.other | Spine | en_US |
dc.subject.other | Determinants | en_US |
dc.title | Vitamin D receptor genetic polymorphysm and osteoporosis | en_US |
dc.type | info:eu-repo/semantics/Article | en_US |
dc.type | Article | en_US |
dc.identifier.scopus | 0032537271 | - |
dc.identifier.isi | 000074113000002 | - |
dc.contributor.authorscopusid | 7003438915 | - |
dc.contributor.authorscopusid | 7401734920 | - |
dc.contributor.authorscopusid | 57206303997 | - |
dc.contributor.authorscopusid | 57206303997 | - |
dc.contributor.authorscopusid | 14023538500 | - |
dc.contributor.authorscopusid | 35854556500 | - |
dc.contributor.authorscopusid | 6701386278 | - |
dc.contributor.authorscopusid | 7004386478 | - |
dc.contributor.authorscopusid | 7006146272 | - |
dc.description.lastpage | 650 | en_US |
dc.description.firstpage | 646 | en_US |
dc.relation.volume | 110 | en_US |
dc.investigacion | Ciencias de la Salud | en_US |
dc.type2 | Artículo | en_US |
dc.contributor.daisngid | 34942777 | - |
dc.contributor.daisngid | 1285492 | - |
dc.contributor.daisngid | 4297253 | - |
dc.contributor.daisngid | 61141 | - |
dc.contributor.daisngid | 1515062 | - |
dc.contributor.daisngid | 21687494 | - |
dc.contributor.daisngid | 2555805 | - |
dc.contributor.daisngid | 1657471 | - |
dc.description.numberofpages | 5 | en_US |
dc.utils.revision | Sí | en_US |
dc.contributor.wosstandard | WOS:Henriquez, MS | - |
dc.contributor.wosstandard | WOS:Ramirez, AT | - |
dc.contributor.wosstandard | WOS:Cabrera, CD | - |
dc.contributor.wosstandard | WOS:Salido, E | - |
dc.contributor.wosstandard | WOS:Santana, PS | - |
dc.contributor.wosstandard | WOS:Barrios, Y | - |
dc.contributor.wosstandard | WOS:Canal, JML | - |
dc.contributor.wosstandard | WOS:Leon, PB | - |
dc.date.coverdate | Mayo 1998 | en_US |
dc.identifier.ulpgc | Sí | en_US |
dc.contributor.buulpgc | BU-MED | en_US |
dc.description.jcr | 0,789 | - |
dc.description.jcrq | Q2 | - |
dc.description.scie | SCIE | - |
item.grantfulltext | none | - |
item.fulltext | Sin texto completo | - |
crisitem.author.dept | GIR SIANI: Ingeniería biomédica aplicada a estimulación neural y sensorial | - |
crisitem.author.dept | IU Sistemas Inteligentes y Aplicaciones Numéricas | - |
crisitem.author.dept | GIR Estadística | - |
crisitem.author.dept | Departamento de Matemáticas | - |
crisitem.author.orcid | 0000-0001-6845-2933 | - |
crisitem.author.orcid | 0000-0003-1681-7165 | - |
crisitem.author.parentorg | IU Sistemas Inteligentes y Aplicaciones Numéricas | - |
crisitem.author.parentorg | Departamento de Matemáticas | - |
crisitem.author.fullName | Sosa Henríquez,Manuel José | - |
crisitem.author.fullName | Domínguez Cabrera, Casimira | - |
crisitem.author.fullName | Saavedra Santana, Pedro | - |
crisitem.author.fullName | Limiñana Cañal, Jose Maria | - |
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