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Urinary Pentosidine levels negatively associates with trabecular bone scores in patients with type 2 diabetes mellitus
  • Choi, Y. J. ;
  • Ock, S. Y. ;
  • Jin, Y. ;
  • Lee, J. S. ;
  • Kim, S. H. ;
  • Chung, Y. S.
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Publication Year
2018-04-01
Publisher
Springer London
Citation
Osteoporosis International, Vol.29, pp.907-915
Keyword
Bone qualityPentosidineTrabecular bone scoreType 2 diabetes mellitusVertebral fracture
Mesh Keyword
Absorptiometry, PhotonAgedArginineBiomarkersBone DensityCancellous BoneCase-Control StudiesDiabetes Mellitus, Type 2FemaleHumansLumbar VertebraeLysineMaleMiddle AgedOsteoporotic FracturesSpinal Fractures
All Science Classification Codes (ASJC)
Endocrinology, Diabetes and Metabolism
Abstract
Summary: Pentosidine levels were higher in diabetic patients with vertebral fractures. Trabecular bone scores were negatively associated with pentosidine levels in diabetic patients only. Our results provide further evidence that AGEs are associated with the pathogenesis of bone fragility in patients with T2DM. Introduction: Type 2 diabetes mellitus (T2DM) is associated with fracture risk. Pentosidine, an advanced glycation end product (AGE), is associated with prevalent vertebral fractures (VFs) in patients with T2DM. Trabecular bone score (TBS) has been proposed as an index of bone microarchitecture associated with bone quality. This study evaluated the associations of urine pentosidine and TBS in T2DM and non-T2DM groups. Methods: A total of 112 T2DM patients and 62 non-T2DM subjects were enrolled. TBS was calculated using TBS insight® software (version 2.1). Pentosidine levels were measured using high-performance liquid chromatography method. We compared the BMD, TBS, and pentosidine levels between those with and without VFs with or without adjustment for age and sex. The association with TBS, lumbar spine BMD, and pentosidine levels were also evaluated in both T2DM and non-T2DM groups. Results: Pentosidine levels were significantly higher in T2DM patients with VFs. TBSs were significantly lower in patients with T2DM and VFs. In non-diabetic patients, there were no significant differences in TBS and pentosidine levels for those with and without VFs after adjustment for age and sex. Pentosidine levels were negatively associated with TBS only in patients with T2DM. In multivariate stepwise regression analysis, pentosidine levels were significantly associated with TBS in patients with T2DM. Conclusions: TBS and pentosidine could be used as a method to assess bone quality to identify T2DM patients at risk of VFs. Our results also provide further evidence that AGEs are associated with the pathogenesis of bone fragility in patients with T2DM.
Language
eng
URI
https://dspace.ajou.ac.kr/dev/handle/2018.oak/30065
DOI
https://doi.org/10.1007/s00198-017-4359-7
Fulltext

Type
Article
Funding
Acknowledgements This research was partly supported by the Korea Health Technology R&D Project (HI16C0992), through the Korea Health Industry Development Institute (KHIDI), which is funded by the Ministry of Health and Welfare, Republic of Korea (So Hee Kim). The authors are grateful to the technologist, Byung Joo Lee, for his assistance with the analyses of trabecular bone score. The authors are also grateful to professor Yunhwan Lee for his advice on the statistical analyses.
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Kim, So Hee김소희
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