Mark K Britton, Greg Jensen, Richard Ae Edden, Nicolaas Aj Puts, Sara A Nolin, Stacy Suzanne Merritt, Roxanne F Rezaei, Megan Forbes, Keyanni Joy Johnson, Pradyumna K Bharadwaj, Mary Kathryn Franchetti, David A Raichlen, Cortney J Jessup, G Alex Hishaw, Emily J Van Etten, Aaron T Gudmundson, Saipavitra Murali-Manohar, Hannah Cowart, Theodore P Trouard, David S Geldmacher, Virginia G Wadley, Noam Alperin, Bonnie E Levin, Tatjana Rundek, Kristina M Visscher, Adam J Woods, Gene E Alexander, Ronald A Cohen, Eric C Porges
{"title":"\"Surviving and Thriving\": evidence for cortical GABA stabilization in cognitively-intact oldest-old adults.","authors":"Mark K Britton, Greg Jensen, Richard Ae Edden, Nicolaas Aj Puts, Sara A Nolin, Stacy Suzanne Merritt, Roxanne F Rezaei, Megan Forbes, Keyanni Joy Johnson, Pradyumna K Bharadwaj, Mary Kathryn Franchetti, David A Raichlen, Cortney J Jessup, G Alex Hishaw, Emily J Van Etten, Aaron T Gudmundson, Saipavitra Murali-Manohar, Hannah Cowart, Theodore P Trouard, David S Geldmacher, Virginia G Wadley, Noam Alperin, Bonnie E Levin, Tatjana Rundek, Kristina M Visscher, Adam J Woods, Gene E Alexander, Ronald A Cohen, Eric C Porges","doi":"10.1038/s41398-025-03302-w","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":23278,"journal":{"name":"Translational Psychiatry","volume":"15 1","pages":"79"},"PeriodicalIF":5.8000,"publicationDate":"2025-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11906729/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Translational Psychiatry","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1038/s41398-025-03302-w","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PSYCHIATRY","Score":null,"Total":0}
引用次数: 0
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.
期刊介绍:
Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.