Purificacion Rey-Sanchez
University of Extremadura
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Featured researches published by Purificacion Rey-Sanchez.
Human Psychopharmacology-clinical and Experimental | 2009
Purificacion Rey-Sanchez; Jesus M. Lavado-Garcia; Maria L. Canal-Macias; María A Gómez-Zubeldia; Raul Roncero-Martin; Juan D. Pedrera-Zamorano
To determine bone mass using quantitative phalangeal bone ultrasound in institutionalized schizophrenic patients under chronic treatment with antipsychotic drugs.
Nutrients | 2012
Julian F. Calderon-Garcia; Jose M. Moran; Raul Roncero-Martin; Purificacion Rey-Sanchez; Francisco J. Rodriguez-Velasco; Juan D. Pedrera-Zamorano
The moderate consumption of fish is recommended for a healthy diet and is also a feature of the Mediterranean diet. Fish is a major food group in diets throughout the world, and studies show that fish consumption is associated with a lower risk of a number of conditions. Spain has one of the highest annual per capita consumptions of fish worldwide. As fish is a source of high quality protein; n-3 polyunsaturated fatty acids; vitamins, such as A and D; and minerals, such as selenium, calcium, iodine, magnesium, copper and zinc, nutrients that have positive effects on bone characteristics, it has been proposed that its consumption could improve bone health. In this cross-sectional study, we have investigated the relationship between dietary habits and nutrient intake of 151 Spanish premenopausal women and analyzed the association of fish consumption on bone mass measured by quantitative ultrasound of the phalanges. A higher (P < 0.05) bone mass and vitamin D intake (P < 0.05) was observed in the group with a fish intake of 5–7 servings/week. We conclude that increased fish consumption is helpful in maintaining an adequate bone mass in Spanish premenopausal women.
International Journal of Molecular Sciences | 2012
Jose M. Moran; Raul Roncero-Martin; Francisco J. Rodriguez-Velasco; Julian F. Calderon-Garcia; Purificacion Rey-Sanchez; Vicente Vera; Maria L. Canal-Macias; Juan D. Pedrera-Zamorano
Curcumin (diferuloylmethane) is found in the rhizomes of the turmeric plant (Curcuma longa L.) and has been used for centuries as a dietary spice and as a traditional Indian medicine used to treat different conditions. At the cellular level, curcumin modulates important molecular targets: transcription factors, enzymes, cell cycle proteins, cytokines, receptors and cell surface adhesion molecules. Because many of the curcumin targets mentioned above participate in the regulation of bone remodeling, curcumin may affect the skeletal system. Nitric oxide (NO) is a gaseous molecule generated from l-arginine during the catalization of nitric oxide synthase (NOS), and it plays crucial roles in catalization and in the nervous, cardiovascular and immune systems. Human osteoblasts have been shown to express NOS isoforms, and the exact mechanism(s) by which NO regulates bone formation remain unclear. Curcumin has been widely described to inhibit inducible nitric oxide synthase expression and nitric oxide production, at least in part via direct interference in NF-κB activation. In the present study, after exposure of human osteoblast-like cells (MG-63), we have observed that curcumin abrogated inducible NOS expression and decreased NO levels, inhibiting also cell prolifieration. This effect was prevented by the NO donor sodium nitroprusside. Under osteogenic conditions, curcumin also decreased the level of mineralization. Our results indicate that NO plays a role in the osteoblastic profile of MG-63 cells.
Nutrients | 2013
Jose M. Moran; Luis Gonzalez Lopez-Arza; Jesus M. Lavado-Garcia; Maria Pedrera-Canal; Purificacion Rey-Sanchez; Francisco J. Rodriguez-Velasco; Pilar Fernandez; Juan D. Pedrera-Zamorano
We aim to evaluate whether calcium and vitamin D intake is associated with 25-hydroxyvitamin D (25-OH-Vitamin D3) and parathyroid hormone (PTH) serum concentrations or is associated with either the phalangeal dual energy X-ray absorptiometry (pDXA) or the quantitative bone ultrasound (QUS) in independent elderly men. Serum PTH and 25-OH-Vitamin D3 were measured in 195 healthy elderly men (mean age: 73.31 ± 5.10 year). Food intake was quantified using a dietetic scale. Participants with 25-OH-Vitamin D3 levels ≥ 30 ng/mL (75 nmol/L) and a calcium intake of 800–1200 mg/day exhibited the lowest PTH levels (41.49 ± 16.72 ng/mL). The highest PTH levels (75.60 ± 14.16 ng/mL) were observed in the <30 ng/mL group 25-OH-Vitamin D3 with a calcium intake >1200 mg/day. No significant differences in the serum PTH levels based on the serum 25-OH-Vitamin D3 levels were observed among participants with a calcium intake of 800–1200 mg/day. Serum PTH was inversely correlated with serum 25-OH-Vitamin D3 in the entire patient sample (r = −0.288, p = 0.019). No differences in any of the three densitometry techniques were observed between any of the age groups in the 800–1200 mg/day and >1200 mg/day calcium intake groups. PTH levels correlate negatively with serum 25-OH-Vitamin D3 levels, and neither calcium nor vitamin D intake exert a strong influence on either of the two parameters.
American Journal of Human Biology | 2015
Juan D. Pedrera-Zamorano; Raul Roncero-Martin; Jesus M. Lavado-Garcia; Julian F. Calderon-Garcia; Purificacion Rey-Sanchez; Vicente Vera; Mariana Martinez; Jose M. Moran
This study provides updated data on body composition in adult Spanish women.
International Scholarly Research Notices | 2014
Jose M. Moran; Francisco J. Rodriguez-Velasco; Raul Roncero-Martin; Purificacion Rey-Sanchez; Mariana Martinez; Juan D. Pedrera-Zamorano
The objective of this study was to identify, through a systematic review of the literature, Vitamin D receptor gene (VDR) polymorphisms related to osteoporosis and their effects on bone mineral density (BMD). The articles dated between January 2000 and December 2011 in the Scielo and PubMed databases were reviewed. A total of 23 articles that studied the association between the BsmI, ApaI, FokI, and TaqI polymorphisms and bone mineral density in postmenopausal women were selected. We found systematic studies/meta-analysis (level E-I) and case-control/cohort (level E-IV) studies. No definite conclusions can be made regarding the association of BsmI, ApaI, FokI, and TaqI polymorphisms with BMD among postmenopausal women. Larger and more rigorous analytical studies with consideration of gene-gene/environment interactions are needed to further dissect the mechanisms by which VDR alleles influence BMD.
Archives of Medical Science | 2015
Juan D. Pedrera-Zamorano; Raul Roncero-Martin; Julian F. Calderon-Garcia; Mercedes Santos-Vivas; Vicente Vera; Mariana Martínez-Álvarez; Purificacion Rey-Sanchez
Introduction The results of studies examining the influence of subclinical hypothyroidism (SCH) and levothyroxine (L-T4) replacement therapy on bone have generated considerable interest but also controversy. The present research aims to evaluate the effects of L-T4 treatment on different skeletal sites in women. Material and methods A group of 45 premenopausal (mean age: 43.62 ±6.65 years) and 180 postmenopausal (mean age: 59.51 ±7.90 years) women with SCH who were undergoing L-T4 replacement therapy for at least 6 months were compared to 58 pre- and 180 postmenopausal women with SCH (untreated) matched for age. The mean doses of L-T4 were 90.88 ±42.59 µg/day in the premenopausal women and 86.35 ±34.11 µg/day in the postmenopausal women. Bone measurements were obtained using quantitative bone ultrasound (QUS) for the phalanx, dual-energy X-ray absorptiometry (DXA) for the lumbar spine and hip, and peripheral quantitative computed tomography (pQCT) for the non-dominant distal forearm. Results No differences were observed between patients and untreated controls in these bone measurements except in the bone mineral density (BMD) of the spine (p = 0.0214) in postmenopausal women, which was greater in treated women than in untreated controls. Conclusions Our results indicate that adequate metabolic control through replacement treatment with L-T4 in pre- and postmenopausal women does not affect bone mass.
Journal of Bone and Mineral Metabolism | 2011
Purificacion Rey-Sanchez; Jesus M. Lavado-Garcia; Maria L. Canal-Macias; María Trinidad Rodríguez-Domínguez; Jose Luis Bote-Mohedano; Juan D. Pedrera-Zamorano
17th European Congress of Endocrinology | 2015
Jose M. Moran; Maria Pedrera-Canal; Jesus M. Lavado-Garcia; Raul Roncero-Martin; Purificacion Rey-Sanchez; Julian F. Calderon-Garcia; Juan D. Pedrera-Zamorano
European Calcified Tissue Society Congress 2014 | 2014
Jose M. Moran; L Canal-Macias Maria; Raul Roncero; Jesus M. Lavado-Garcia; Julian F. Calderon-Garcia; Purificacion Rey-Sanchez; Juan D. Pedrera-Zamorano