Journal Article DZNE-2023-00080

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Midlife occupational cognitive requirements protect cognitive function in old age by increasing cognitive reserve.

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2022
Frontiers Research Foundation Lausanne

Frontiers in psychology 13, 957308 () [10.3389/fpsyg.2022.957308]

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Abstract: Several lifestyle factors promote protection against Alzheimer's disease (AD) throughout a person's lifespan. Although such protective effects have been described for occupational cognitive requirements (OCR) in midlife, it is currently unknown whether they are conveyed by brain maintenance (BM), brain reserve (BR), or cognitive reserve (CR) or a combination of them.We systematically derived hypotheses for these resilience concepts and tested them in the population-based AgeCoDe cohort and memory clinic-based AD high-risk DELCODE study. The OCR score (OCRS) was measured using job activities based on the O*NET occupational classification system. Four sets of analyses were conducted: (1) the interaction of OCR and APOE-ε4 with regard to cognitive decline (N = 2,369, AgeCoDe), (2) association with differentially shaped retrospective trajectories before the onset of dementia of the Alzheimer's type (DAT; N = 474, AgeCoDe), (3) cross-sectional interaction of the OCR and cerebrospinal fluid (CSF) AD biomarkers and brain structural measures regarding memory function (N = 873, DELCODE), and (4) cross-sectional and longitudinal association of OCR with CSF AD biomarkers and brain structural measures (N = 873, DELCODE).Regarding (1), higher OCRS was associated with a reduced association of APOE-ε4 with cognitive decline (mean follow-up = 6.03 years), consistent with CR and BR. Regarding (2), high OCRS was associated with a later onset but subsequently stronger cognitive decline in individuals converting to DAT, consistent with CR. Regarding (3), higher OCRS was associated with a weaker association of the CSF Aβ42/40 ratio and hippocampal volume with memory function, consistent with CR. Regarding (4), OCR was not associated with the levels or changes in CSF AD biomarkers (mean follow-up = 2.61 years). We found a cross-sectional, age-independent association of OCRS with some MRI markers, but no association with 1-year-change. OCR was not associated with the intracranial volume. These results are not completely consistent with those of BR or BM.Our results support the link between OCR and CR. Promoting and seeking complex and stimulating work conditions in midlife could therefore contribute to increased resistance to pathologies in old age and might complement prevention measures aimed at reducing pathology.

Keyword(s): Alzheimer's disease ; brain maintenance ; brain reserve ; cognitive reserve ; mid-life cognitive demands ; occupation

Classification:

Contributing Institute(s):
  1. Neuropsychology (AG Wagner)
  2. Psychosocial Epidemiology and Public Health (AG Rodriguez)
  3. Interdisciplinary Dementia Research (AG Endres)
  4. Vascular Pathology (AG Dirnagl)
  5. Translational Neuropsychiatry (AG Priller)
  6. Patient Studies Bonn (Patient Studies Bonn)
  7. Patient Studies (AG Klockgether)
  8. Translational Dementia Research (Bonn) (AG Schneider)
  9. Epigenetics and Systems Medicine in Neurodegenerative Diseases (AG Fischer)
  10. Molecular biomarkers for predictive diagnostics of neurodegenerative diseases (AG Wiltfang)
  11. Cooperation Unit for Applied Prevention Research (KAP) (KAP)
  12. Clinical Neurophysiology and Memory (AG Düzel)
  13. Vascular Cognitive Impairment & Post-Stroke Dementia (AG Dichgans)
  14. Clinical Dementia Research (Rostock /Greifswald) (AG Teipel)
  15. Interventional Trials and Biomarkers in Neurodegenerative Diseases (Biomarker)
  16. Clinical Alzheimer’s Disease Research (AG Jessen)
  17. Clinical Research Platform (CRP) (Clinical Research Platform (CRP))
  18. Molecular Neurobiology (AG Simons)
  19. Parkinson Genetics (AG Gasser)
  20. Delcode (Delcode)
Research Program(s):
  1. 353 - Clinical and Health Care Research (POF4-353) (POF4-353)
  2. 352 - Disease Mechanisms (POF4-352) (POF4-352)
  3. 351 - Brain Function (POF4-351) (POF4-351)
Experiment(s):
  1. Longitudinal Cognitive Impairment and Dementia Study

Appears in the scientific report 2022
Database coverage:
Medline ; Creative Commons Attribution CC BY (No Version) ; DOAJ ; OpenAccess ; Article Processing Charges ; Clarivate Analytics Master Journal List ; Current Contents - Clinical Medicine ; Current Contents - Social and Behavioral Sciences ; DOAJ Seal ; Essential Science Indicators ; Fees ; IF < 5 ; JCR ; SCOPUS ; Social Sciences Citation Index
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The record appears in these collections:
Institute Collections > BN DZNE > BN DZNE-Clinical Research Platform (CRP)
Institute Collections > MD DZNE > MD DZNE-Applied Prevention Research
Institute Collections > BN DZNE > BN DZNE-Clinical Research (Bonn)
Institute Collections > BN DZNE > BN DZNE-Patient Studies (Bonn)
Document types > Articles > Journal Article
Institute Collections > ROS DZNE > ROS DZNE-AG Rodriguez
Institute Collections > GÖ DZNE > GÖ DZNE-AG Wiltfang
Institute Collections > BN DZNE > BN DZNE-AG Schneider
Institute Collections > GÖ DZNE > GÖ DZNE-AG Fischer
Institute Collections > ROS DZNE > ROS DZNE-AG Teipel
Institute Collections > TÜ DZNE > TÜ DZNE-AG Gasser
Institute Collections > BN DZNE > BN DZNE-AG Jessen
Institute Collections > MD DZNE > MD DZNE-AG Düzel
Institute Collections > BN DZNE > BN DZNE-AG Wagner
Institute Collections > BN DZNE > BN DZNE-Biomarker
Institute Collections > M DZNE > M DZNE-AG Dichgans
Institute Collections > B DZNE > B DZNE-AG Priller
Institute Collections > B DZNE > B DZNE-AG Dirnagl
Institute Collections > M DZNE > M DZNE-AG Simons
Institute Collections > B DZNE > B DZNE-AG Endres
Institute Collections > M DZNE > M DZNE-Delcode
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 Record created 2023-01-03, last modified 2024-08-26


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