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Diagnostic criteria, prevalence, and clinical outcomes of pediatric sarcopenia: A scoping review.
Inoue, Tatsuro; Wakabayashi, Hidetaka; Kawase, Fumiya; Kokura, Yoji; Takamasu, Tetsuya; Fujiwara, Dai; Maeda, Keisuke.
Afiliação
  • Inoue T; Department of Physical Therapy, Niigata University of Health and Welfare, Niigata, Japan. Electronic address: tatsuro-inoue@nuhw.ac.jp.
  • Wakabayashi H; Department of Rehabilitation Medicine, Tokyo Women's Medical University Hospital, Tokyo 162-8666, Japan.
  • Kawase F; Department of Nutrition, Asuke Hospital Aichi Prefectural Welfare Federation of Agricultural Cooperatives, Aichi, Japan. Electronic address: fumi.kawase@gmail.com.
  • Kokura Y; Department of Nutritional Management, Keiju Hatogaoka Integrated Facility for Medical and Long-term Care, Hosu, Japan. Electronic address: yojikokura@hotmail.com.
  • Takamasu T; Department of Community Health Promotion, Kanagawa Children's Medical Center, Yokohama, Kanagawa, Japan. Electronic address: takamasu.0122r@kanagawa-pho.jp.
  • Fujiwara D; Department of Rehabilitation Medicine, Saka General Hospital, Shiogama, 985-8506, Japan. Electronic address: dai.fujiwara3901@gmail.com.
  • Maeda K; Nutrition Therapy Support Center, Aichi Medical University Hospital, Aichi, Japan. Electronic address: kskmaeda1701@gmail.com.
Clin Nutr ; 43(8): 1825-1843, 2024 Aug.
Article em En | MEDLINE | ID: mdl-38959660
ABSTRACT
BACKGROUND &

AIMS:

Sarcopenia, characterized by loss of muscle mass and decreased muscle strength, significantly affects adults but also influences pediatric health. However, definitions for low muscle mass, decreased strength, and sarcopenia in children are less established, impacting interventions for improving health outcomes. The objective of this scoping review is synthesize the existing literature on the diagnostic criteria, prevalence and clinical outcomes of sarcopenia.

METHODS:

A scoping review, following the PRISMA extension for scoping reviews, examined pediatric sarcopenia literature until June 2023. The literature search was performed using MEDLINE and the Cochrane Central Register of Controlled Trials with the last search conducted on June 30, 2023. Criteria included studies on aged 0-20 years, covering healthy subjects, acutely ill patients, and chronic disease cases excluding specific conditions like neuromuscular diseases or prematurity.

RESULTS:

Initial search found 503 studies, finally, we included 56 studies. Most studies diagnosed sarcopenia using skeletal muscle mass indicators like total psoas muscle area from Computed Tomography or Magnetic Resonance Imaging. Around half of the longitudinal studies highlighted sarcopenia as a risk factor for various clinical outcomes, predominantly in hospitalized patients. However, cutoff values for sarcopenia indicators lacked consistency, with studies employing diverse percentile-based measurements or z-scores.

CONCLUSION:

Pediatric sarcopenia diagnosis primarily relies on skeletal muscle mass, with identified links to future clinical outcomes in specific conditions. The lack of standardized cutoffs for sarcopenia indicators underscores the necessity for age, gender, and race-specific cutoff values derived from studies establishing reference values for muscle mass and strength across diverse pediatric populations.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sarcopenia Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sarcopenia Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Ano de publicação: 2024 Tipo de documento: Article