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Identification of a novel biomarker for sarcopenia diagnosis using serum metabolomic analysis: a pilot study.
Shida, Takashi; Yoshida, Yasuko; Ohta, Takahisa; Kojima, Narumi; Osuka, Yosuke; Takekoshi, Kazuhiro; Sasai, Hiroyuki.
Afiliação
  • Shida T; Research Team for Promoting Independence and Mental Health, Tokyo Metropolitan Institute for Geriatrics and Gerontology, Tokyo, Japan. t_shida@tmig.or.jp.
  • Yoshida Y; Niigata University of Pharmacy and Medical and Life Sciences Faculty of Medical Technology Department of Medical Technology, Niigata, Japan.
  • Ohta T; Research Team for Promoting Independence and Mental Health, Tokyo Metropolitan Institute for Geriatrics and Gerontology, Tokyo, Japan.
  • Kojima N; Research Team for Promoting Independence and Mental Health, Tokyo Metropolitan Institute for Geriatrics and Gerontology, Tokyo, Japan.
  • Osuka Y; Department of Frailty Research, Center for Gerontology and Social Science, National Center for Geriatrics and Gerontology, Research Institute, Aichi, Japan.
  • Takekoshi K; Faculty of Medicine, University of Tsukuba, Ibaraki, Japan.
  • Sasai H; Research Team for Promoting Independence and Mental Health, Tokyo Metropolitan Institute for Geriatrics and Gerontology, Tokyo, Japan.
Eur Geriatr Med ; 15(2): 571-577, 2024 Apr.
Article em En | MEDLINE | ID: mdl-38214867
ABSTRACT

PURPOSE:

This pilot study compared serum metabolites in participants with and without sarcopenia.

METHODS:

Metabolomic techniques were applied to identify serum metabolites and novel biomarkers specific to patients with sarcopenia. In accordance with AWGS2019 criteria, sarcopenia was defined as low muscle mass plus either low muscle strength/low physical function, and severe sarcopenia was defined as low muscle mass, low muscle strength, and low physical function all together.

RESULTS:

The sarcopenia group had higher hypoxanthine, galactose, and mannose levels but lower triethanolamine and homogentisic acid levels than the non-sarcopenia group. The severe sarcopenia group had lower levels of alpha-tocopherol than the mild and moderate sarcopenia groups.

CONCLUSION:

This study is the first to identify hypoxanthine as a potential biomarker for sarcopenia in humans and provides new insights into the pathophysiology of sarcopenia. Furthermore, the identified metabolites may be useful for the early detection of sarcopenia.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sarcopenia Tipo de estudo: Diagnostic_studies / Prognostic_studies / Screening_studies Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sarcopenia Tipo de estudo: Diagnostic_studies / Prognostic_studies / Screening_studies Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article