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Herrmann, M; Wildemann, B; Claes, L; Klohs, S; Ohnmacht, M; Taban-Shomal, O; Hübner, U; Pexa, A; Umanskaya, N; Herrmann, W.
Experimental hyperhomocysteinemia reduces bone quality in rats.
Clin Chem. 2007; 53(8):1455-1461 Doi: 10.1373/clinchem.2007.086272 [OPEN ACCESS]
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Abstract:
Recently, hyperhomocysteinemia (HHCY) has been suggested as a new risk factor for osteoporosis. This study investigated if HHCY is a causal osteoporotic factor in vivo. We used 3 groups of rats: a control group (n = 20), a moderate HHCY group (induced by a 2.4% methionine-enriched diet, n = 10), and an intermediate HHCY group (induced by a 2% homocystine-enriched diet, n = 10). We measured bone fragility [maximum force of an axial compression test (F(max))], bone area as percentage of total area (BAr/TAr, histomorphometry), and biochemical bone turnover markers [osteocalcin (OC) and collagen I C-terminal crosslaps (CTx)]. Compared with controls, 3 months of moderate or intermediate HHCY increased mean (SD) bone fragility at the femoral neck by 18% (6%) in methionine-fed (P = 0.001) and 36% (13%) in homocystine-fed rats (P <0.001). Mean (SD) BAr/TAr at the distal femur in methionine and homocystine groups was decreased by 45% (21%; P = 0.001) and 93% (9%; P = 0.001), respectively. At the femoral neck, BAr/TAr was decreased by 19% (11%; P <0.001) and 55% (19%; P <0.001). At the lumbar spine, the reduction of BAr/TAr was 17% (23%; P = 0.099) and 44% (19%; P <0.001). Plasma OC (bone formation marker) was decreased by 23% (20%; P = 0.006) and 34% (21%; P <0.001). Plasma CTx (bone resorption marker) did not differ between groups. Bone quality is consistently decreased in the presence of increased circulating homocysteine. The results provide evidence that HHCY is a causal osteoporotic factor.
Find related publications in this database (using NLM MeSH Indexing)
Animals -
Biomarkers - blood
Compressive Strength -
Female -
Femoral Fractures - etiology
Femoral Fractures - pathology
Femoral Fractures - physiopathology
Femur - metabolism
Femur - pathology
Femur - physiopathology
Fractures, Compression - etiology
Fractures, Compression - pathology
Fractures, Compression - physiopathology
Hyperhomocysteinemia - complications
Hyperhomocysteinemia - metabolism
Hyperhomocysteinemia - pathology
Hyperhomocysteinemia - physiopathology
Osteogenesis -
Osteoporosis - etiology
Rats -
Rats, Wistar -
Risk Factors -

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