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Lowering homocysteine with B vitamins has no effect on biomarkers of bone turnover in older persons: a 2-y randomized controlled trial
Oleh:
Green, Timothy J.
;
McMahon, Jennifer A
;
Skeaff, C. Murray
;
Williams, Sheila M.
;
Whiting, Susan J.
Jenis:
Article from Journal - ilmiah internasional
Dalam koleksi:
The American Journal of Clinical Nutrition vol. 85 no. 02 (Feb. 2007)
,
page 460.
Ketersediaan
Perpustakaan FK
Nomor Panggil:
A07.K.2007.01
Non-tandon:
1 (dapat dipinjam: 0)
Tandon:
tidak ada
Lihat Detail Induk
Isi artikel
Background: In recent prospective studies, higher homocysteine concentrations were shown to be a risk factor for osteoporotic fractures in older persons. Supplements containing folate and vitamins B-12 and B-6 lower homocysteine concentrations. Objective: The objective of the study was to determine in healthy older persons whether lowering homocysteine with B vitamins affects plasma biomarkers of bone turnover. Design: Healthy older persons (n = 276; aged 65 y) were randomly assigned to receive either a daily supplement containing folate (1 mg), vitamin B-12 (500 µg), and vitamin B-6 (10 mg) or a placebo for 2 y. Of these participants, we selected 135 with baseline homocysteine concentrations >15.0 µmol/L, and we measured serum bone-specific alkaline phosphatase, a marker of bone formation, and bone-derived collagen fragments, a marker of bone resorption, at baseline and 2 y later. Results: At 2 y, plasma homocysteine concentrations were 5.2 µmol/L (95% CI: 3.9, 6.6 µmol/L; P < 0.001) lower in the vitamin than in the placebo group. No significant differences were found in either serum bone-specific alkaline phosphatase (–0.3 µg/L; 95% CI: –2.8, 2.1 µg/L; P = 0.79) or bone-derived collagen fragments (–0.0 µg/L; 95% CI: –0.1, 0.1 µg/L; P = 0.76) between the vitamin and placebo groups, respectively, with 2 y of supplementation. Conclusion: Supplementation with folate and vitamins B-6 and B-12 lowered plasma homocysteine but had no beneficial effect on bone turnover at the end of 2 y, as assessed by biomarkers of bone formation and resorption.
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