Systemic inflammation in relation to exceptional memory in the Long Life Family Study (LLFS)
Ruhee Patel1, Stephanie Cosentino1, Esther Zhiwei Zheng1
1Cognitive Neuroscience Division, Taub Institute for Research on Alzheimer's Disease and the Aging Brain, Gertrude H. Sergievsky Center, Department of Neurology, Columbia University Medical Center, New York, NY, 10032, USA.
Long-lived families with exceptional memory (EM) showed higher baseline monocyte counts, particularly in men. Systemic inflammation did not differ significantly in its trajectory over time between EM and non-EM families.
Area of Science:
- Gerontology
- Immunology
- Genetics
Background:
- Familial aggregation of healthy aging phenotypes, including exceptional memory (EM), has been observed in long-lived individuals.
- Systemic inflammation is implicated in aging and cognitive function.
Purpose of the Study:
- To investigate differences in systemic inflammation status and trajectory between long-lived families with and without exceptional memory (EM).
Main Methods:
- Analysis of 4333 participants from the Long Life Family Study (LLFS), classifying families as EM or non-EM.
- Measurement of inflammatory biomarkers including white blood cell counts, C-reactive protein, and interleukin-6.
- Generalized linear models used to assess cross-sectional and longitudinal differences in biomarkers between EM and non-EM families.
Main Results:
- EM families exhibited marginally higher monocyte counts at baseline, especially in men.
- Monocyte counts increased over time in both EM and non-EM families.
- Lymphocyte and platelet counts decreased over time in non-EM families but not in EM families.
- No significant differences in the rate of biomarker change over time were found between EM and non-EM families.
Conclusions:
- Higher baseline monocyte counts in EM families suggest a potential pathway for EM development, particularly in men.
- While baseline inflammation markers differ, the trajectory of systemic inflammation over time does not distinguish between EM and non-EM families in long-lived populations.
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