Kun Zhu1,2, Wendy H Oddy3, Patrick Holt4, Wendy Chan She Ping-Delfos5, Jenny Mountain6, Stephen Lye7, Craig Pennell8, Prue H Hart4, John P Walsh9,2. 1. Department of Endocrinology and Diabetes, Sir Charles Gairdner Hospital, Perth, Australia; Schools of kun.zhu@uwa.edu.au. 2. Medicine and Pharmacology. 3. Menzies Institute for Medical Research, University of Tasmania, Hobart, Australia. 4. Telethon Kids Institute, Perth, Australia. 5. University of Notre Dame, Perth, Australia; and. 6. Population Health, and. 7. Samuel Lunenfeld Research Institute, Mount Sinai Hospital, Toronto, Canada. 8. Women's and Infants' Health, University of Western Australia, Perth, Australia. 9. Department of Endocrinology and Diabetes, Sir Charles Gairdner Hospital, Perth, Australia; Schools of.
Abstract
Background: To our knowledge, there are few longitudinal studies of vitamin D status from childhood to early adulthood, and it is uncertain whether vitamin D predicts peak bone mass in young adults. Objectives: The purpose of this longitudinal study was to evaluate the long-term stability of vitamin D status from ages 6 to 20 y in healthy individuals and to study associations between serum 25-hydroxyvitamin D [25(OH)D] at different developmental stages and bone mass measured at age 20 y.Design: Participants were offspring of the Western Australian Pregnancy Cohort (Raine) study. Serum 25(OH)D was assessed at ages 6, 14, 17, and 20 y, and whole-body bone mineral content (BMC) and bone mineral density (BMD) were measured at age 20 y through the use of dual-energy X-ray absorptiometry (DXA). Our analysis included 821 participants (385 females) who had ≥3 serum 25(OH)D measures and DXA data. We used latent class growth analysis and identified 4 vitamin D status trajectories: consistently lower (n = 259), decreasing (n = 125), increasing (n = 138), and consistently higher (n = 299). Results: There were significant correlations between serum 25(OH)D concentrations at different time points in both sexes (r = 0.346-0.560, P < 0.001), with stronger correlations at adjacent time points. In males, but not in females, serum 25(OH)D at ages 6, 17, and 20 y was positively associated with total-body BMC and BMD at age 20 y [covariate-adjusted increments of 40.7-53.9 g and 14.7-18.6 mg/cm2, respectively, per 25 nmol/L 25(OH)D]; when 25(OH)D at all 4 ages was included in the same model, the concentration at age 6 y remained significant. Males in the "consistently higher" trajectory had 3.2-3.4% higher total body BMC and BMD than those who were in the "consistently lower" trajectory, accounting for age and anthropometric and lifestyle factors.Conclusions: Within both sexes, there are moderate associations between vitamin D status measured in prepuberty, adolescence, and early adulthood. Vitamin D status in childhood is a significant predictor of peak bone mass in male but not female subjects.
Background: To our knowledge, there are few longitudinal studies of vitamin D status from childhood to early adulthood, and it is uncertain whether vitamin D predicts peak bone mass in young adults. Objectives: The purpose of this longitudinal study was to evaluate the long-term stability of vitamin D status from ages 6 to 20 y in healthy individuals and to study associations between serum 25-hydroxyvitamin D [25(OH)D] at different developmental stages and bone mass measured at age 20 y.Design: Participants were offspring of the Western Australian Pregnancy Cohort (Raine) study. Serum 25(OH)D was assessed at ages 6, 14, 17, and 20 y, and whole-body bone mineral content (BMC) and bone mineral density (BMD) were measured at age 20 y through the use of dual-energy X-ray absorptiometry (DXA). Our analysis included 821 participants (385 females) who had ≥3 serum 25(OH)D measures and DXA data. We used latent class growth analysis and identified 4 vitamin D status trajectories: consistently lower (n = 259), decreasing (n = 125), increasing (n = 138), and consistently higher (n = 299). Results: There were significant correlations between serum 25(OH)D concentrations at different time points in both sexes (r = 0.346-0.560, P < 0.001), with stronger correlations at adjacent time points. In males, but not in females, serum 25(OH)D at ages 6, 17, and 20 y was positively associated with total-body BMC and BMD at age 20 y [covariate-adjusted increments of 40.7-53.9 g and 14.7-18.6 mg/cm2, respectively, per 25 nmol/L 25(OH)D]; when 25(OH)D at all 4 ages was included in the same model, the concentration at age 6 y remained significant. Males in the "consistently higher" trajectory had 3.2-3.4% higher total body BMC and BMD than those who were in the "consistently lower" trajectory, accounting for age and anthropometric and lifestyle factors.Conclusions: Within both sexes, there are moderate associations between vitamin D status measured in prepuberty, adolescence, and early adulthood. Vitamin D status in childhood is a significant predictor of peak bone mass in male but not female subjects.
Authors: Gareth Lingham; Seyhan Yazar; Robyn M Lucas; John P Walsh; Kun Zhu; Michael Hunter; Ee Mun Lim; Brian R Cooke; David A Mackey Journal: Transl Vis Sci Technol Date: 2019-01-22 Impact factor: 3.283
Authors: Joo-Hyun Jeong; Jill Korsiak; Eszter Papp; Joy Shi; Alison D Gernand; Abdullah Al Mahmud; Daniel E Roth Journal: Curr Dev Nutr Date: 2019-10-07
Authors: Daniel E Roth; Steven A Abrams; John Aloia; Gilles Bergeron; Megan W Bourassa; Kenneth H Brown; Mona S Calvo; Kevin D Cashman; Gerald Combs; Luz María De-Regil; Maria Elena Jefferds; Kerry S Jones; Hallie Kapner; Adrian R Martineau; Lynnette M Neufeld; Rosemary L Schleicher; Tom D Thacher; Susan J Whiting Journal: Ann N Y Acad Sci Date: 2018-09-18 Impact factor: 5.691
Authors: Kun Zhu; Wendy H Oddy; Patrick Holt; Wendy Chan She Ping-Delfos; Joanne McVeigh; Leon Straker; Trevor A Mori; Stephen Lye; Craig Pennell; John P Walsh Journal: J Endocr Soc Date: 2019-01-21