TY - JOUR
T1 - Metabolomics-based profiles predictive of low bone mass in menopausal women
AU - Miyamoto, Takeshi
AU - Hirayama, Akiyoshi
AU - Sato, Yuiko
AU - Koboyashi, Tami
AU - Katsuyama, Eri
AU - Kanagawa, Hiroya
AU - Fujie, Atsuhiro
AU - Morita, Mayu
AU - Watanabe, Ryuichi
AU - Tando, Toshimi
AU - Miyamoto, Kana
AU - Tsuji, Takashi
AU - Funayama, Atsushi
AU - Soga, Tomoyoshi
AU - Tomita, Masaru
AU - Nakamura, Masaya
AU - Matsumoto, Morio
N1 - Funding Information:
We thank S. Ikeda, F. Shoji and N. Yamaguchi for technical assistance. T. Miyamoto was supported by a Grant-in-Aid from the Ministry of Education, Culture, Sports, Science and Technology of Japan, and a grant from the Japan Agency for Medical Research and Development. K. Miyamoto and Y. Sato were supported by a grant-in-aid for Scientific Research in Japan. This study was supported in part by a research grant from Eli Lilly Japan K.K .
Publisher Copyright:
© 2018 The Authors
PY - 2018/12
Y1 - 2018/12
N2 - 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.
AB - 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.
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U2 - 10.1016/j.bonr.2018.06.004
DO - 10.1016/j.bonr.2018.06.004
M3 - Article
AN - SCOPUS:85048828187
SN - 2352-1872
VL - 9
SP - 11
EP - 18
JO - Bone Reports
JF - Bone Reports
ER -