One carbon metabolism and bone homeostasis and remodeling: A review of experimental research and population studies

被引:11
作者
Feigerlova, Eva [1 ,2 ]
Demarquet, Lea [1 ,2 ,3 ]
Gueant, Jean-Louis [1 ,2 ]
机构
[1] Univ Lorraine, Fac Med, INSERM U954, Nutr Genet & Exposit Risques Environm, Vandoeuvre Les Nancy, France
[2] Reg Univ Hosp Ctr Nancy, Vandoeuvre Les Nancy, France
[3] Reg Univ Hosp Ctr Nancy, Div Endocrinol, Vandoeuvre Les Nancy, France
关键词
Bone; One carbon metabolism; Homocysteine; Folate; Vitamin B12; PLASMA HOMOCYSTEINE CONCENTRATION; FOLIC-ACID SUPPLEMENTATION; COLLAGEN CROSS-LINKING; MINERAL DENSITY; TURNOVER MARKERS; FRACTURE RISK; LYSYL OXIDASE; HIP FRACTURE; B-VITAMINS; METHYLENETETRAHYDROFOLATE REDUCTASE;
D O I
10.1016/j.biochi.2016.04.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
.Homocysteine (HCY) is a degradation product of the methionine pathway. The B vitamins, in particular vitamin B12 and folate, are the primary nutritional determinant of HCY levels and therefore their deficiencies result in hyperhomocysteinaemia (HHCY). Prevalence of hyperhomocysteinemia (HHCY) and related dietary deficiencies in B vitamins and folate increase with age and have been related to osteoporosis and abnormal development of epiphyseal cartilage and bone in rodents. Here we provide a review of experimental and population studies. The negative effects of HHCY and/or B vitamins and folate deficiencies on bone formation and remodeling are documented by cell models, including primary osteoblasts, osteoclast and bone progenitor cells as well as by animal and human studies. However, underlying pathophysiological mechanisms are complex and remain poorly understood. Whether these associations are the direct consequences of impaired one carbon metabolism is not clarified and more studies are still needed to translate these findings to human population. To date, the evidence is limited and somewhat conflicting, however further trials in groups most vulnerable to impaired one carbon metabolism are required. (C) 2016 Published by Elsevier B.V.
引用
收藏
页码:115 / 123
页数:9
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