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Intramuscular short-chain acylcarnitines in elderly people are decreased in (pre-)frail females, but not in males
MD. van der Hoek, AG. Nieuwenhuizen, O. Kuda, P. Bos, V. Paluchová, L. Verschuren, AM. van den Hoek, R. Kleemann, NJGM. Veeger, FR. van der Leij, J. Keijer
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
32672378
DOI
10.1096/fj.202000493r
Knihovny.cz E-resources
- MeSH
- Walking physiology MeSH
- Carnitine analogs & derivatives blood chemistry metabolism MeSH
- Frailty metabolism physiopathology MeSH
- Frail Elderly MeSH
- Humans MeSH
- Cross-Sectional Studies MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Sex Factors MeSH
- Hand Strength physiology MeSH
- Aging metabolism physiology MeSH
- Muscles metabolism MeSH
- Physical Fitness physiology MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
This study tested the hypothesis that in human aging, a decreased intramuscular acylcarnitine status is associated with (pre-)frailty, reduced physical performance, and altered mitochondrial function. We used a cross-sectional study design with well-matched fit and (pre-)frail old males and females, using young males and females as healthy controls. Frailty was assessed according to the Fried criteria and physical performance was determined by 400 m walk test, short physical performance battery and handgrip strength. Muscle and plasma acylcarnitine status, and muscle mitochondrial gene expression was analyzed. Results showed that intramuscular total carnitine levels and short-chain acylcarnitine levels were lower in (pre-)frail old females compared to fit old females and young females, whereas no differences were observed in males. The low intramuscular short-chain acylcarnitine levels in females correlated with low physical performance, even after correction for muscle mass (%), and were accompanied with lowered expression of genes involved in mitochondrial energy production and functionality. It is, therefore, concluded that in (pre-)frail old females, intramuscular total carnitine levels and short-chain acylcarnitine levels are decreased, and this decrease is associated with reduced physical performance and low expression of a wide range of genes critical for mitochondrial function. The results stress the importance of taking sex differences into account in aging research.
Human and Animal Physiology Wageningen University Wageningen the Netherlands
Institute of Physiology Czech Academy of Sciences Prague Czech Republic
MCL Academy Medical Centre Leeuwarden Leeuwarden the Netherlands
RIC AFL Inholland University of Applied Sciences Delft and Amsterdam the Netherlands
References provided by Crossref.org
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- $a This study tested the hypothesis that in human aging, a decreased intramuscular acylcarnitine status is associated with (pre-)frailty, reduced physical performance, and altered mitochondrial function. We used a cross-sectional study design with well-matched fit and (pre-)frail old males and females, using young males and females as healthy controls. Frailty was assessed according to the Fried criteria and physical performance was determined by 400 m walk test, short physical performance battery and handgrip strength. Muscle and plasma acylcarnitine status, and muscle mitochondrial gene expression was analyzed. Results showed that intramuscular total carnitine levels and short-chain acylcarnitine levels were lower in (pre-)frail old females compared to fit old females and young females, whereas no differences were observed in males. The low intramuscular short-chain acylcarnitine levels in females correlated with low physical performance, even after correction for muscle mass (%), and were accompanied with lowered expression of genes involved in mitochondrial energy production and functionality. It is, therefore, concluded that in (pre-)frail old females, intramuscular total carnitine levels and short-chain acylcarnitine levels are decreased, and this decrease is associated with reduced physical performance and low expression of a wide range of genes critical for mitochondrial function. The results stress the importance of taking sex differences into account in aging research.
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