TY - JOUR
T1 - Gene–Environment Interplay in Physical, Psychological, and Cognitive Domains in Mid to Late Adulthood
T2 - Is APOE a Variability Gene?
AU - Reynolds, Chandra A.
AU - Gatz, Margaret
AU - Christensen, Kaare
AU - Christiansen, Lene
AU - Dahl Aslan, Anna K.
AU - Kaprio, Jaakko
AU - Korhonen, Tellervo
AU - Kremen, William S.
AU - Krueger, Robert
AU - McGue, Matt
AU - Neiderhiser, Jenae M.
AU - Pedersen, Nancy L.
N1 - Publisher Copyright:
© 2015, Springer Science+Business Media New York.
PY - 2016/1/1
Y1 - 2016/1/1
N2 - Despite emerging interest in gene–environment interaction (GxE) effects, there is a dearth of studies evaluating its potential relevance apart from specific hypothesized environments and biometrical variance trends. Using a monozygotic within-pair approach, we evaluated evidence of G×E for body mass index (BMI), depressive symptoms, and cognition (verbal, spatial, attention, working memory, perceptual speed) in twin studies from four countries. We also evaluated whether APOE is a ‘variability gene’ across these measures and whether it partly represents the ‘G’ in G×E effects. In all three domains, G×E effects were pervasive across country and gender, with small-to-moderate effects. Age-cohort trends were generally stable for BMI and depressive symptoms; however, they were variable—with both increasing and decreasing age-cohort trends—for different cognitive measures. Results also suggested that APOE may represent a ‘variability gene’ for depressive symptoms and spatial reasoning, but not for BMI or other cognitive measures. Hence, additional genes are salient beyond APOE.
AB - Despite emerging interest in gene–environment interaction (GxE) effects, there is a dearth of studies evaluating its potential relevance apart from specific hypothesized environments and biometrical variance trends. Using a monozygotic within-pair approach, we evaluated evidence of G×E for body mass index (BMI), depressive symptoms, and cognition (verbal, spatial, attention, working memory, perceptual speed) in twin studies from four countries. We also evaluated whether APOE is a ‘variability gene’ across these measures and whether it partly represents the ‘G’ in G×E effects. In all three domains, G×E effects were pervasive across country and gender, with small-to-moderate effects. Age-cohort trends were generally stable for BMI and depressive symptoms; however, they were variable—with both increasing and decreasing age-cohort trends—for different cognitive measures. Results also suggested that APOE may represent a ‘variability gene’ for depressive symptoms and spatial reasoning, but not for BMI or other cognitive measures. Hence, additional genes are salient beyond APOE.
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U2 - 10.1007/s10519-015-9761-3
DO - 10.1007/s10519-015-9761-3
M3 - Article
C2 - 26538244
AN - SCOPUS:84958166807
SN - 0001-8244
VL - 46
SP - 4
EP - 19
JO - Behavior Genetics
JF - Behavior Genetics
IS - 1
ER -