Chronic exposure of the skin to sunlight causes damage to the underlying connective tissue with a loss of elasticity and firmness. Silicon (Si) was suggested to have an important function in the formation and maintena...Chronic exposure of the skin to sunlight causes damage to the underlying connective tissue with a loss of elasticity and firmness. Silicon (Si) was suggested to have an important function in the formation and maintenance of connective tissue. Choline- stabilized orthosilicic acid (“ ch- OSA” ) is a bioavailable form of silicon which was found to increase the hydroxyproline concentration in the dermis of animals. The effect of ch- OSA on skin, nails and hair was investigated in a randomized, double blind, placebo- controlled study. Fifty women with photodamaged facial skin were administered orally during 20 weeks, 10 mg Si/day in the form of ch- OSA pellets (n=25) or a placebo (n=25). Noninvasive methods were used to evaluate skin microrelief (forearm), hydration (forearm) andmechanical anisotropy (forehead). Volunteers evaluated on a virtual analog scale (VAS, “ none=0, severe=3” ) brittleness of hair and nails. The serum Si concentration was significantly higher after a 20- week supplementation in subjects with ch- OSA compared to the placebo group. Skin roughness parameters increased in the placebo group (Rt: + 8% ; Rm: + 11% ; Rz: + 6% ) but decreased in the ch- OSA group (Rt: - 16% ; Rm: - 19% ; Rz: - 8% ). The change in roughness from baseline was significantly different between ch- OSA and placebo groups for Rt and Rm. The difference in longitudinal and lateral shear propagation time increased after 20 weeks in the placebo group but decreased in the ch- OSA group suggesting improvement in isotropy of the skin. VAS scores for nail and hair brittleness were significantly lower after 20 weeks in the ch- OSA group compared to baseline scores. Oral intake of ch- OSA during the 20 weeks results in a significant positive effect on skin surface and skin mechanical properties, and on brittleness of hair and nails.展开更多
文摘Chronic exposure of the skin to sunlight causes damage to the underlying connective tissue with a loss of elasticity and firmness. Silicon (Si) was suggested to have an important function in the formation and maintenance of connective tissue. Choline- stabilized orthosilicic acid (“ ch- OSA” ) is a bioavailable form of silicon which was found to increase the hydroxyproline concentration in the dermis of animals. The effect of ch- OSA on skin, nails and hair was investigated in a randomized, double blind, placebo- controlled study. Fifty women with photodamaged facial skin were administered orally during 20 weeks, 10 mg Si/day in the form of ch- OSA pellets (n=25) or a placebo (n=25). Noninvasive methods were used to evaluate skin microrelief (forearm), hydration (forearm) andmechanical anisotropy (forehead). Volunteers evaluated on a virtual analog scale (VAS, “ none=0, severe=3” ) brittleness of hair and nails. The serum Si concentration was significantly higher after a 20- week supplementation in subjects with ch- OSA compared to the placebo group. Skin roughness parameters increased in the placebo group (Rt: + 8% ; Rm: + 11% ; Rz: + 6% ) but decreased in the ch- OSA group (Rt: - 16% ; Rm: - 19% ; Rz: - 8% ). The change in roughness from baseline was significantly different between ch- OSA and placebo groups for Rt and Rm. The difference in longitudinal and lateral shear propagation time increased after 20 weeks in the placebo group but decreased in the ch- OSA group suggesting improvement in isotropy of the skin. VAS scores for nail and hair brittleness were significantly lower after 20 weeks in the ch- OSA group compared to baseline scores. Oral intake of ch- OSA during the 20 weeks results in a significant positive effect on skin surface and skin mechanical properties, and on brittleness of hair and nails.
