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Working Memory Training in Amnestic and Non-amnestic Patients With Mild Cognitive Impairment: Preliminary Findings From Genotype Variants on Training Effects.


ABSTRACT: Working memory training (WMT) effects may be modulated by mild cognitive impairment (MCI) subtypes, and variations in APOE-epsilon (APOE-?) and LMX1A genotypes. Sixty-one individuals (41 men/20 women, mean age 66 years) diagnosed with MCI (31 amnestic/30 non-amnestic) and genotyped for APOE-? and LMX1A completed 4 weeks/20-25 sessions of WMT. Cognitive functions were assessed before, 4 weeks and 16 weeks after WMT. Except for Processing Speed, the non-amnestic MCI group (naMCI) outperformed the amnestic MCI (aMCI) group in all cognitive domains across all time-points. At 4 weeks, working memory function improved in both groups (p < 0.0001), but at 16 weeks the effects only remained in the naMCI group. Better performance was found after training for the naMCI patients with LMX1A-AA genotype and for the APOE-?4 carriers. Only the naMCI-APOE-?4 group showed improved Executive Function at 16 weeks. WMT improved working memory and some non-trained cognitive functions in individuals with MCI. The naMCI group had greater training gain than aMCI group, especially in those with LMX1A-AA genotype and among APOE-?4-carriers. Further research with larger sample sizes for the subgroups and longer follow-up evaluations is warranted.

SUBMITTER: Hernes SS 

PROVIDER: S-EPMC7917210 | biostudies-literature | 2021

REPOSITORIES: biostudies-literature

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Working Memory Training in Amnestic and Non-amnestic Patients With Mild Cognitive Impairment: Preliminary Findings From Genotype Variants on Training Effects.

Hernes Susanne S SS   Flak Marianne M MM   Løhaugen Gro C C GCC   Skranes Jon J   Hol Haakon R HR   Madsen Bengt-Ove BO   Knapskog Anne-Brita AB   Engvig Andreas A   Pripp Are A   Ulstein Ingun I   Lona Trine T   Zhang Xin X   Chang Linda L  

Frontiers in aging neuroscience 20210215


Working memory training (WMT) effects may be modulated by mild cognitive impairment (MCI) subtypes, and variations in <i>APOE</i>-epsilon (<i>APOE</i>-ε) and <i>LMX1A</i> genotypes. Sixty-one individuals (41 men/20 women, mean age 66 years) diagnosed with MCI (31 amnestic/30 non-amnestic) and genotyped for <i>APOE</i>-ε and <i>LMX1A</i> completed 4 weeks/20-25 sessions of WMT. Cognitive functions were assessed before, 4 weeks and 16 weeks after WMT. Except for Processing Speed, the non-amnestic  ...[more]

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