TY - JOUR
T1 - Association of dietary and nutritional factors with cognitive decline, dementia, and depressive symptomatology in older individuals according to a neurogenesis-centred biological susceptibility to brain ageing
AU - Du Preez, Andrea
AU - Lefèvre-Arbogast, Sophie
AU - González-Domínguez, Raúl
AU - Houghton, Vikki
AU - de Lucia, Chiara
AU - Lee, Hyunah
AU - Low, Dorrain Y
AU - Helmer, Catherine
AU - Féart, Catherine
AU - Delcourt, Cécile
AU - Proust-Lima, Cécile
AU - Pallàs, Mercè
AU - Sánchez-Pla, Alex
AU - Urpi-Sardà, Mireia
AU - Ruigrok, Silvie R
AU - Altendorfer, Barbara
AU - Aigner, Ludwig
AU - Lucassen, Paul J
AU - Korosi, Aniko
AU - Manach, Claudine
AU - Andres-Lacueva, Cristina
AU - Samieri, Cécilia
AU - Thuret, Sandrine
N1 - Altendorfer, Aigner: Institute of Molecular Regenerative Medicine, Spinal Cord Injury and Tissue Regeneration Center Salzburg, Paracelsus Medical
University, Salzburg 5020, Austria
PY - 2024/5/11
Y1 - 2024/5/11
N2 - Hippocampal neurogenesis (HN) occurs throughout the life course and is important for memory and mood. Declining with age, HN plays a pivotal role in cognitive decline (CD), dementia, and late-life depression, such that altered HN could represent a neurobiological susceptibility to these conditions. Pertinently, dietary patterns (e.g., Mediterranean diet) and/or individual nutrients (e.g., vitamin D, omega 3) can modify HN, but also modify risk for CD, dementia, and depression. Therefore, the interaction between diet/nutrition and HN may alter risk trajectories for these ageing-related brain conditions. Using a subsample (n = 371) of the Three-City cohort-where older adults provided information on diet and blood biobanking at baseline and were assessed for CD, dementia, and depressive symptomatology across 12 years-we tested for interactions between food consumption, nutrient intake, and nutritional biomarker concentrations and neurogenesis-centred susceptibility status (defined by baseline readouts of hippocampal progenitor cell integrity, cell death, and differentiation) on CD, Alzheimer's disease (AD), vascular and other dementias (VoD), and depressive symptomatology, using multivariable-adjusted logistic regression models. Increased plasma lycopene concentrations (OR [95% CI] = 1.07 [1.01, 1.14]), higher red meat (OR [95% CI] = 1.10 [1.03, 1.19]), and lower poultry consumption (OR [95% CI] = 0.93 [0.87, 0.99]) were associated with an increased risk for AD in individuals with a neurogenesis-centred susceptibility. Increased vitamin D consumption (OR [95% CI] = 1.05 [1.01, 1.11]) and plasma gamma-tocopherol concentrations (OR [95% CI] = 1.08 [1.01, 1.18]) were associated with increased risk for VoD and depressive symptomatology, respectively, but only in susceptible individuals. This research highlights an important role for diet/nutrition in modifying dementia and depression risk in individuals with a neurogenesis-centred susceptibility.
AB - Hippocampal neurogenesis (HN) occurs throughout the life course and is important for memory and mood. Declining with age, HN plays a pivotal role in cognitive decline (CD), dementia, and late-life depression, such that altered HN could represent a neurobiological susceptibility to these conditions. Pertinently, dietary patterns (e.g., Mediterranean diet) and/or individual nutrients (e.g., vitamin D, omega 3) can modify HN, but also modify risk for CD, dementia, and depression. Therefore, the interaction between diet/nutrition and HN may alter risk trajectories for these ageing-related brain conditions. Using a subsample (n = 371) of the Three-City cohort-where older adults provided information on diet and blood biobanking at baseline and were assessed for CD, dementia, and depressive symptomatology across 12 years-we tested for interactions between food consumption, nutrient intake, and nutritional biomarker concentrations and neurogenesis-centred susceptibility status (defined by baseline readouts of hippocampal progenitor cell integrity, cell death, and differentiation) on CD, Alzheimer's disease (AD), vascular and other dementias (VoD), and depressive symptomatology, using multivariable-adjusted logistic regression models. Increased plasma lycopene concentrations (OR [95% CI] = 1.07 [1.01, 1.14]), higher red meat (OR [95% CI] = 1.10 [1.03, 1.19]), and lower poultry consumption (OR [95% CI] = 0.93 [0.87, 0.99]) were associated with an increased risk for AD in individuals with a neurogenesis-centred susceptibility. Increased vitamin D consumption (OR [95% CI] = 1.05 [1.01, 1.11]) and plasma gamma-tocopherol concentrations (OR [95% CI] = 1.08 [1.01, 1.18]) were associated with increased risk for VoD and depressive symptomatology, respectively, but only in susceptible individuals. This research highlights an important role for diet/nutrition in modifying dementia and depression risk in individuals with a neurogenesis-centred susceptibility.
KW - Humans
KW - Neurogenesis
KW - Aged
KW - Male
KW - Female
KW - Depression/psychology
KW - Cognitive Dysfunction/blood
KW - Dementia/psychology
KW - Nutritional Status
KW - Risk Factors
KW - Hippocampus/metabolism
KW - Aging/psychology
KW - Aged, 80 and over
KW - Cognition
KW - Age Factors
KW - Diet/adverse effects
KW - Cognitive Aging/psychology
KW - Biomarkers/blood
U2 - 10.1093/ageing/afae042
DO - 10.1093/ageing/afae042
M3 - Original Article
C2 - 38745492
SN - 0002-0729
VL - 53
SP - ii47-ii59
JO - Age and Ageing
JF - Age and Ageing
IS - Suppl 2
ER -