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1.
Medicina (Kaunas) ; 59(6)2023 Jun 20.
Artículo en Inglés | MEDLINE | ID: mdl-37374383

RESUMEN

Background and Objectives: Osteoporosis is characterized by low bone mass and high bone fragility. Findings regarding the association of coffee and tea intake with osteoporosis have been inconsistent. We conducted this meta-analysis to investigate whether coffee and tea intake is associated with low bone mineral density (BMD) and high hip fracture risk. Materials and Methods: PubMed, MEDLINE, and Embase were searched for relevant studies published before 2022. Studies on the effects of coffee/tea intake on hip fracture/BMD were included in our meta-analysis, whereas those focusing on specific disease groups and those with no relevant coffee/tea intake data were excluded. We assessed mean difference (MD; for BMD) and pooled hazard ratio (HR; for hip fracture) values with 95% confidence interval (CI) values. The cohort was divided into high- and low-intake groups considering the thresholds of 1 and 2 cups/day for tea and coffee, respectively. Results: Our meta-analysis included 20 studies comprising 508,312 individuals. The pooled MD was 0.020 for coffee (95% CI, -0.003 to 0.044) and 0.039 for tea (95% CI, -0.012 to 0.09), whereas the pooled HR was 1.008 for coffee (95% CI, 0.760 to 1.337) and 0.93 for tea (95% CI, 0.84 to 1.03). Conclusions: Our meta-analysis results suggest that daily coffee or tea consumption is not associated with BMD or hip fracture risk.


Asunto(s)
Fracturas de Cadera , Osteoporosis , Humanos , Densidad Ósea , Café/efectos adversos , Té/efectos adversos , Factores de Riesgo
2.
Anal Sci ; 31(12): 1297-302, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-26656821

RESUMEN

Honokiol is a potential candidate for the treatment of intervertebral disc (IVD) degeneration. In this study, we develop in vitro and in vivo methods to detect the distribution of honokiol in intervertebral discs using high-performance liquid chromatography. A rat tail disc was used for both experimental models. For the in vivo animal experiment, blood samples and tail discs were collected at 15, 30, 60, 120 and 240 min after honokiol administration (30 mg/kg, i.v.). The analyte was separated by a mobile phase of methanol and 10 mM NaH2PO4 buffer at pH 2.8 (78:22, v/v) and pumped through a reversed-phase analytical column (250 × 4.6 mm, particle size 5 µm) at room temperature. The in vitro experimental results demonstrated that honokiol diffused into the intervertebral disc and was concentration-dependent. The active concentration is obtained for the therapeutic level at 15 and 30 min after honokiol administration in the in vivo model.


Asunto(s)
Antiinflamatorios/farmacocinética , Compuestos de Bifenilo/farmacocinética , Medicamentos Herbarios Chinos/farmacocinética , Disco Intervertebral/metabolismo , Lignanos/farmacocinética , Acetofenonas/administración & dosificación , Acetofenonas/sangre , Acetofenonas/farmacocinética , Animales , Antiinflamatorios/administración & dosificación , Antiinflamatorios/sangre , Compuestos de Bifenilo/administración & dosificación , Compuestos de Bifenilo/sangre , Cromatografía Líquida de Alta Presión , Relación Dosis-Respuesta a Droga , Medicamentos Herbarios Chinos/administración & dosificación , Técnicas In Vitro , Inyecciones Intravenosas , Lignanos/administración & dosificación , Lignanos/sangre , Masculino , Estructura Molecular , Permeabilidad , Ratas Sprague-Dawley , Factores de Tiempo , Distribución Tisular
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