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Association between Large Neutral Amino Acids and Brain Integrity in Middle-Aged Adults at Metabolic Risk.
Youn, Cherry; Caillaud, Marie L; Li, Yanrong; Gallagher, Isabelle A; Strasser, Barbara; Fuchs, Dietmar; Tanaka, Hirofumi; Haley, Andreana P.
Afiliação
  • Youn C; Department of Psychology, The University of Texas at Austin, Austin, Texas, USA.
  • Caillaud ML; Department of Psychology, The University of Texas at Austin, Austin, Texas, USA.
  • Li Y; Department of Psychology, The University of Texas at Austin, Austin, Texas, USA.
  • Gallagher IA; Department of Psychology, The University of Texas at Austin, Austin, Texas, USA.
  • Strasser B; Medical Faculty, Sigmund Freud Private University Vienna, Vienna, Austria.
  • Fuchs D; Institute of Biological Chemistry, Biocentre, Medical University of Innsbruck, Innsbruck, Austria.
  • Tanaka H; Department of Kinesiology and Health Education, The University of Texas at Austin, Austin, Texas, USA.
  • Haley AP; Department of Psychology, The University of Texas at Austin, Austin, Texas, USA.
Res Sq ; 2024 Feb 16.
Article em En | MEDLINE | ID: mdl-38410466
ABSTRACT
This investigation delves into the interplay between large neutral amino acids (LNAA) and metabolic syndrome (MetS) in midlife adults, examining their collective influence on brain structure and cognitive function. While LNAA, such as tryptophan and phenylalanine, are known to bolster cognition in youth, our study hypothesizes a reversal of these benefits in older adults with MetS, potentially signaling premature cognitive aging. Eighty participants between 40-61 years underwent MetS component quantification, LNAA measurement via high-performance liquid chromatography, and brain imaging to evaluate white matter hyperintensity (WMH) volume and medial temporal lobe (MTL) cortical thickness. Our linear regression analysis, adjusting for sex, age, and education, revealed that phenylalanine levels moderated the relationship between MetS and WMH volume (F(6, 69) = 3.134, p < 0.05, R2 = 0.214), suggesting that MetS's cognitive impact may be partly due to phenylalanine catabolism byproducts. However, LNAA metabolites did not significantly modulate the MetS-MTL cortical thickness relationship. The findings suggest that LNAA metabolic dysregulation, marked by elevated levels in the presence of MetS, could correlate with brain structural compromises, particularly in the form of MTL cortical thinning and increased WMH load, detectable in midlife. This nuanced understanding of LNAA's role in cognitive health amid cardiovascular risk factors is pivotal, proposing a potential biomarker for early intervention. Further research is crucial to elucidate the longitudinal influence of LNAA and MetS on brain health, thereby informing strategies to mitigate cognitive decline.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article