“Surviving and Thriving”: evidence for cortical GABA stabilization in cognitively-intact oldest-old adults

Age-related alterations in GABAergic function, including depletion of cortical GABA concentrations, is likely associated with declining cognitive performance in normative aging. However, the extent to which GABAergic function is perturbed in the highest-functioning stratum of the oldest-old (85+) population is unknown. For the first time, we report the stability of cortical GABA in this population. We extend our previously-reported Individual Participant Data Meta-Analysis of GABA levels across the lifespan, integrating four large cross-sectional datasets sampling cognitively-intact oldest-old adults. Within our lifespan model, the slope of age-related GABA differences in cognitively-intact oldest-old adults flattens after roughly age 80; within oldest-old adults only, inclusion of age does not improve the fit of models predicting GABA. We interpret these findings as an effect of survivorship: inclusion in the study required intact cognition, and too great a reduction of GABA levels may not be compatible with neurophysiological function needed for intact cognition. This work contributes to a growing body of evidence suggesting that successful cognitive aging may require intact GABAergic function, as well as further characterizing successful aging amongst oldest-old adults and emphasizing GABA as a potential target for interventions to prolong cognitive health in aging.

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Publication Details

Journal
Translational Psychiatry
Published
2025-03-13
DOI
https://doi.org/10.1038/s41398-025-03302-w
Citations
3
Primary Topic
Neuroscience and Neuropharmacology Research
Type
article
Field-Weighted Citation Impact
2.73

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article

“Surviving and Thriving”: evidence for cortical GABA stabilization in cognitively-intact oldest-old adults

Cortney J. Jessup, Emily J. Van Etten, Adam J. Woods, Noam Alperin et al.
3 citations
Translational Psychiatry
Neuroscience and Neuropharmacology Research
2.73
article

“Surviving and Thriving”: evidence for cortical GABA stabilization in cognitively-intact oldest-old adults

Cortney J. Jessup, Emily J. Van Etten, Adam J. Woods, Noam Alperin, Keyanni Joy Johnson, Megan A. Forbes, Aaron T. Gudmundson, Tatjana Rundek, Greg Jensen, Ronald A. Cohen, Kristina Visscher, David A. Raichlen, Sara A. Nolin, Mary Kathryn Franchetti, Pradyumna K. Bharadwaj, Hannah Cowart, Saipavitra Murali‐Manohar, David Geldmacher, Eric C. Porges, Nicolaas A.J. Puts, Mark K. Britton, Roxanne F Rezaei, Bonnie Levin, Theodore P. Trouard, Virginia G. Wadley, Richard AE Edden, Gene E. Alexander, Georg A. Hishaw, Sharon L. Merritt
article en
3 citations

Abstract

Age-related alterations in GABAergic function, including depletion of cortical GABA concentrations, is likely associated with declining cognitive performance in normative aging. However, the extent to which GABAergic function is perturbed in the highest-functioning stratum of the oldest-old (85+) population is unknown. For the first time, we report the stability of cortical GABA in this population. We extend our previously-reported Individual Participant Data Meta-Analysis of GABA levels across the lifespan, integrating four large cross-sectional datasets sampling cognitively-intact oldest-old adults. Within our lifespan model, the slope of age-related GABA differences in cognitively-intact oldest-old adults flattens after roughly age 80; within oldest-old adults only, inclusion of age does not improve the fit of models predicting GABA. We interpret these findings as an effect of survivorship: inclusion in the study required intact cognition, and too great a reduction of GABA levels may not be compatible with neurophysiological function needed for intact cognition. This work contributes to a growing body of evidence suggesting that successful cognitive aging may require intact GABAergic function, as well as further characterizing successful aging amongst oldest-old adults and emphasizing GABA as a potential target for interventions to prolong cognitive health in aging.

Translational PsychiatryVol. 15(1)
University of Southern California (US), Kennedy Krieger Institute (US), University of Arizona (US), Johns Hopkins University (US), University of Miami (US), Medical University of South Carolina (US), The University of Texas at Dallas (US), King's College London (GB), University of Florida Health (US), VA Boston Healthcare System (US), University of Alabama at Birmingham (US), University of Florida (US), Reed College (US), Florida College (US)
National Institute on Alcohol Abuse and Alcoholism, National Institute on Aging, National Institute of Diabetes and Digestive and Kidney Diseases, National Institute of Biomedical Imaging and Bioengineering
Reduced inequalities
Openalex Percentile: Top 11%
Neuroscience and Neuropharmacology Research
2.73
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