Plasma total homocysteine level and bone mineral density - The Hordaland homocysteine study

被引:120
作者
Gjesdal, CG
Vollset, SE
Ueland, PM
Refsum, H
Drevon, CA
Gjessing, HK
Tell, GS
机构
[1] Univ Bergen, Dept Publ Hlth & Primary Hlth Care, N-5018 Bergen, Norway
[2] Univ Bergen, Sect Pharmacol, Inst Med, N-5018 Bergen, Norway
[3] Haukeland Univ Hosp, Dept Rheumatol, Bergen, Norway
[4] Univ Oxford, Dept Pharmacol, Oxford, England
[5] Univ Oslo, Inst Basic Med Sci, Dept Nutr, Oslo, Norway
[6] Norwegian Inst Publ Hlth, Oslo, Norway
关键词
D O I
10.1001/archinte.166.1.88
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Plasma total homocysteine (tHcy) has been associated with hip fracture but not directly with bone mineral density (BMD). We examined the association of hip BMD with levels of plasma tHcy, folate, and vitamin B, and the methylenetetrahydrofolate reductase (MTHFR) 677C -> T and 1298A -> C polymorphisms. Methods: Bone mineral density was measured between 1997 and 2000 in 2268 men and 3070 women, aged 47 to 50 and 71 to 75 years, from the Hordaland Homocysteine Study cohort. Low BMD was defined as BMD in the lowest quintile for each sex and age group. Linear, logistic, and generalized additive regression models were used. Results: Plasma levels of tHcy were inversely related to BMD among middle-aged and elderly women (P <.001) but not among men. The multiple adjusted odds ratio for low BMD among subjects with high ( E 15 mu mol/L [>= 2.02 mg/L]) compared with low (< 9 mu mol/L [< 1.22 mg/L]) tHcy level was 1.96 (95% confidence interval, 1.40-2.75) for women and was not significant for men. Additional adjustments for plasma folate level or intake of calcium and vitamin D did not substantially alter the results. Plasma folate level was associated with BMD in women only. We observed no association between BMD and vitamin B-12 level or the MTHFR polymorphisms. Conclusions: Elevated tHcy and low folate levels were associated with reduced BMD in women but not in men. These findings suggest that tHcy may be a potential modifiable risk factor for osteoporosis in women.
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页码:88 / 94
页数:7
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