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A Randomized Controlled Study of Effects of Dietary Magnesium Oxide Supplementation on Bone Mineral Content in Healthy Girls

Departments of Pediatrics (T.O.C., M.C.D., J.D.) and Internal Medicine (G.B., J.D., K.F.P., D.B.), Center for Biomedical Informatics (D.C.), and the General Clinical Research Center (J.D.), Yale University School of Medicine, New Haven, Connecticut 06250; The Cooperative Studies Program Coordinating Center (J.H.Z.), Veterans Affairs Connecticut Healthcare System, West Haven, Connecticut 06516; and Department of Nutrition (L.T.), Yale-New Haven Hospital, New Haven, Connecticut 06510

Address all correspondence and requests for reprints to: Thomas O. Carpenter, M.D., Yale University School of Medicine, P.O. Box 208064; 333 Cedar Street, New Haven, Connecticut 06520-8064. E-mail: thomas.carpenter{at}yale.edu.

Context: The role of magnesium (Mg) as a determinant of bone mass has not been extensively explored. Limited studies suggest that dietary Mg intake and bone mineral density are correlated in adults, but no data from interventional studies in children and adolescents are available.

Objective: We sought to determine whether Mg supplementation in periadolescent girls enhances accrual of bone mass.

Design: We carried out a prospective, placebo-controlled, randomized, one-year double-blind trial of Mg supplementation.

Setting: The study was conducted in the Clinical Research Centers at Yale University School of Medicine.

Patients or Other Participants: Healthy 8- to 14-yr-old Caucasian girls were recruited from community pediatricians’ offices. Dietary diaries from over 120 volunteers were analyzed, and those with dietary Mg intake of less than 220 mg/d were invited to participate in the intervention.

Intervention: Magnesium (300 mg elemental Mg per day in two divided doses) or placebo was given orally for 12 months.

Main Outcome Measure: The primary outcome measure was interval change in bone mineral content (BMC) of the total hip, femoral neck, Ward’s area, and lumbar spine (L1–L4) after 12 months of Mg supplementation.

Results: Significantly increased accrual (P = 0.05) in integrated hip BMC occurred in the Mg-supplemented vs. placebo group. Trends for a positive Mg effect were evident in the pre- and early puberty and in mid-late puberty. Lumbar spinal BMC accrual was slightly (but not significantly) greater in the Mg-treated group. Compliance was excellent; 73% of capsules were ingested as inferred by pill counts. Serum mineral levels, calciotropic hormones, and bone markers were similar between groups.

Conclusions: Oral Mg oxide capsules are safe and well tolerated. A positive effect of Mg supplementation on integrated hip BMC was evident in this small cohort.