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基于代谢组学的绝经后女性低骨量预测特征。

Metabolomics-based profiles predictive of low bone mass in menopausal women.

作者信息

Miyamoto Takeshi, Hirayama Akiyoshi, Sato Yuiko, Koboyashi Tami, Katsuyama Eri, Kanagawa Hiroya, Fujie Atsuhiro, Morita Mayu, Watanabe Ryuichi, Tando Toshimi, Miyamoto Kana, Tsuji Takashi, Funayama Atsushi, Soga Tomoyoshi, Tomita Masaru, Nakamura Masaya, Matsumoto Morio

机构信息

Department of Orthopedic Surgery, Keio University School of Medicine, 35 Shinano-machi, Shinjuku-ku, Tokyo 160-8582, Japan.

Department of Advanced Therapy for Musculoskeletal Disorders, Keio University School of Medicine, 35 Shinano-machi, Shinjuku-ku, Tokyo 160-8582, Japan.

出版信息

Bone Rep. 2018 Jun 18;9:11-18. doi: 10.1016/j.bonr.2018.06.004. eCollection 2018 Dec.

Abstract

Osteoporosis is a skeletal disorder characterized by compromised bone strength and increased risk of fracture. Low bone mass and/or pre-existing bone fragility fractures serve as diagnostic criteria in deciding when to start medication for osteoporosis. Although osteoporosis is a metabolic disorder, metabolic markers to predict reduced bone mass are unknown. Here, we show serum metabolomics profiles of women grouped as pre-menopausal with normal bone mineral density (BMD) (normal estrogen and normal BMD; NN), post-menopausal with normal BMD (low estrogen and normal BMD; LN) or post-menopausal with low BMD (low estrogen and low BMD; LL) using comprehensive metabolomics analysis. To do so, we enrolled healthy volunteer and osteoporosis patient female subjects, surveyed them with a questionnaire, measured their BMD, and then undertook a comprehensive metabolomics analysis of sera of the three groups named above. We identified 24 metabolites whose levels differed significantly between NN/LN and NN/LL groups, as well as 18 or 10 metabolites whose levels differed significantly between NN/LN and LN/LL, or LN/LL and NN/LN groups, respectively. Our data shows metabolomics changes represent useful markers to predict estrogen deficiency and/or bone loss.

摘要

骨质疏松症是一种以骨强度受损和骨折风险增加为特征的骨骼疾病。低骨量和/或既往存在的脆性骨折是决定何时开始骨质疏松症药物治疗的诊断标准。尽管骨质疏松症是一种代谢性疾病,但预测骨量减少的代谢标志物尚不清楚。在此,我们使用综合代谢组学分析展示了分为绝经前骨密度正常(正常雌激素和正常骨密度;NN)、绝经后骨密度正常(低雌激素和正常骨密度;LN)或绝经后骨密度低(低雌激素和低骨密度;LL)的女性血清代谢组学谱。为此,我们招募了健康志愿者和骨质疏松症患者女性受试者,用问卷对她们进行调查,测量她们的骨密度,然后对上述三组的血清进行综合代谢组学分析。我们鉴定出24种在NN/LN和NN/LL组之间水平有显著差异的代谢物,以及分别在NN/LN和LN/LL组之间,或LN/LL和NN/LN组之间水平有显著差异的18种或10种代谢物。我们的数据表明,代谢组学变化代表了预测雌激素缺乏和/或骨质流失的有用标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdb4/6019687/a66fb332bd78/gr1.jpg

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