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Feasibility of Serum Pentosidine Level as a Potential Risk Factor for Osteoporotic Vertebral Compression Fracture

STUDY DESIGN: Feasibility study. PURPOSE: To evaluate the feasibility of using serum pentosidine level as a potential marker for osteoporotic vertebral compression fracture (OVCF). OVERVIEW OF LITERATURE: A review of previous studies suggests a negative correlation between serum pentosidine concentr...

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Detalles Bibliográficos
Autores principales: Choi, Dong-Hyuk, Lee, Sang-Min, Lim, Sung-An, Choi, Yong-Soo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Spine Surgery 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6284123/
https://www.ncbi.nlm.nih.gov/pubmed/30322258
http://dx.doi.org/10.31616/asj.2018.12.6.992
Descripción
Sumario:STUDY DESIGN: Feasibility study. PURPOSE: To evaluate the feasibility of using serum pentosidine level as a potential marker for osteoporotic vertebral compression fracture (OVCF). OVERVIEW OF LITERATURE: A review of previous studies suggests a negative correlation between serum pentosidine concentration and bone strength. However, it is unclear whether serum pentosidine level might be a potential marker of OVCF in Koreans. METHODS: Forty patients who underwent bone mineral density examination were included in this study, and their serum pentosidine levels were prospectively analyzed. Serum pentosidine level was evaluated using enzyme-linked immunosorbent assay. Among all the patients, 11 with OVCF were assigned to the vertebral fracture group and 29 who did not have vertebral fracture were included in the non-fracture group. In addition, we used the Fracture Risk Assessment (FRAX) tool Korean version for assessing the 10-year probability of fracture. RESULTS: There was a statistically significant difference in the mean serum pentosidine level (p=0.04) of the vertebral fracture group (110.8 ng/mL) and the non-fracture group (64.3 ng/mL). Logistic regression analyses showed that serum pentosidine was significantly associated with OVCF. The vertebral fracture group had significantly higher 10-year probability of major osteoporotic fracture as per FRAX than the non-fracture group. There was a positive correlation between pentosidine level and FRAX results (r=0.35, p=0.02). CONCLUSIONS: These results suggest that increased serum pentosidine level could be a potential marker for OVCF.