Volume 16, Issue S4 e045741
BIOMARKERS
Free Access

Brain beta-amyloid in twin pairs discordant for episodic memory performance

Neuroimaging: Imaging genetics

Noora Lindgren

Noora Lindgren

University of Turku, Turku, Finland

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Tomi Karjalainen

Tomi Karjalainen

Turku PET Centre, University of Turku, Turku, Finland

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Laura L. Ekblad

Laura L. Ekblad

Amsterdam UMC, Amsterdam, Netherlands

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Semi Helin

Semi Helin

University of Turku, Turku, Finland

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Mira Karrasch

Mira Karrasch

Åbo Akademi University, Turku, Finland

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Jarmo Teuho

Jarmo Teuho

Turku PET Centre, University of Turku, Turku, Finland

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Jouni Tuisku

Jouni Tuisku

University of Turku, Turku, Finland

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Jaakko Kaprio

Jaakko Kaprio

University of Helsinki, Helsinki, Finland

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Juha O. Rinne

Juha O. Rinne

Turku University Hospital, Turku, Finland

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Eero Vuoksimaa

Corresponding Author

Eero Vuoksimaa

University of Helsinki, Helsinki, Finland

Correspondence

Eero Vuoksimaa, University of Helsinki, Helsinki, Finland.

Email: [email protected]

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First published: 07 December 2020

Abstract

Background

β-amyloid pathology (Aβ) and episodic memory (EM) impairment are biological and cognitive hallmarks of Alzheimer’s disease (AD). However, most studies on the Aβ–EM association have been conducted in unrelated individuals and cannot tell if this relationship is confounded by shared genetic and/or environmental effects. We investigated if cortical amyloid pathology-EM relationship is evident within twin pairs: a design that controls for shared genetic (fully in monozygotic [MZ] and partly in dizygotic [DZ] pairs) and environmental effects.

Method

We studied 45 same-sex (mean [SD] age = 72.9 [4.0] years; 18 women pairs) twin pairs. EM discordance was based on a mean of two verbal delayed free recall measures: Logical Memory and Word List Learning from CERAD-NB. We also studied within-pair differences in 3 continuous EM scores (verbal immediate free recall [VerIFR], verbal delayed free recall [VerDFR], and visual delayed free recall [VisDFR]) in relation to within-pair differences in cortical amyloid pathology. Cortical amyloid pathology in AD signature regions was measured with carbon-11-labelled Pittsburgh compound B ([11C]PiB) and quantified as standardized uptake value ratio (SUVR) with cerebellar cortex as a reference region.

Result

A total of 42 pairs were discordant for EM (23DZ/19MZ). Twins with poorer EM had higher cortical [11C]PiB SUVR compared to their co-twins (1.44 vs 1.36), but this difference was not statistically significant (mean intra-pair difference of 6% / 0.08 SUVR units [95%CI: -0.05; 0.20], P=0.23). Using continuous scores within all pairs, co-twins with higher SUVR had poorer EM scores (Ps< 0.006): VerIFR (r= -0.42), VerDFR (r= -0.41) and VisDFR (r= -0.46). In DZs, within-pair differences in EM scores were significantly related to within-pair differences in SUVR with correlations ranging from -0.42 to -0.51 (Ps< 0.05, N=24). In MZs, non-significant within-twin pair correlations ranged from -0.31 to -0.36, (Ps= 0.11 – 0.16, N=21).

Conclusion

By using case-control twin design we showed that within twin pairs, a co-twin with higher amyloid pathology had poorer episodic memory. Results suggest that amyloid-EM relationship is evident when controlling for shared environmental and genetic effects, but studies with larger samples of MZ and DZ twins in different stages of AD continuum are warranted.