Serum tyrosine is associated with better cognition in Lewy body dementia
•Amino acids’ (AAs) neuroactivity are linked to dementia.•Effect of circulating AAs on cognitive prognosis in dementia subgroups is unknown.•Longitudinal follow-up and linear-mixed effects model stratified by diagnosis.•Tyrosine associated with cognition in Lewy body dementia but not Alzheimer'...
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Veröffentlicht in: | Brain research 2021-08, Vol.1765, p.147481-147481, Article 147481 |
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Sprache: | eng |
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Zusammenfassung: | •Amino acids’ (AAs) neuroactivity are linked to dementia.•Effect of circulating AAs on cognitive prognosis in dementia subgroups is unknown.•Longitudinal follow-up and linear-mixed effects model stratified by diagnosis.•Tyrosine associated with cognition in Lewy body dementia but not Alzheimer's.•Tyrosine availability and catecholamine synthesis may effect cognitive performance.
Amino acids’ neuroactivity, and roles in excitotoxity and oxidative stress are linked to dementia. We aimed to investigate whether circulating amino acid concentrations were associated with cognitive decline in patients with mild Alzheimer’s disease (AD) and Lewy body dementia (LBD). Baseline serum amino acid concentrations were measured in 89 patients with AD and 65 with LBD (13 with Parkinson’s disease dementia and 52 with dementia with Lewy bodies). The Mini-Mental State Examination (MMSE) was administered at baseline and annually for five years. Associations between baseline amino acid concentrations and longitudinal MMSE score were assessed using a linear-mixed effects model stratified by diagnosis with adjustment for multiple comparisons. The results of the study indicated that serum tyrosine was positively associated with MMSE performance during the five-year follow-up period in patients with LBD (q-value = 0.012), but not AD. In conclusion, higher baseline serum concentrations of tyrosine, the precursor amino acid in dopamine and norepinephrine synthesis, was associated with better cognitive performance in patients with LBD, but not AD, throughout the 5-year follow-up period. |
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ISSN: | 0006-8993 1872-6240 1872-6240 |
DOI: | 10.1016/j.brainres.2021.147481 |