TY - JOUR
T1 - Alzheimer's Imaging Consortium
AU - Hazelton, Jessica L.
AU - Migeot, Joaquín
AU - Gonzalez-Gomez, Raul
AU - Altschuler, Florencia
AU - Duran-Aniotz, Claudia
AU - Wen, Olivia
AU - Rial, Dante Sebastián Galván
AU - Barttfeld, Pablo
AU - Medel, Vicente
AU - Campo, Cecilia Gonzalez
AU - Laguardia, Ana Maria Castro
AU - Hernandez, Hernan
AU - Gonzalez-Silva, Carolina
AU - Castaner, Olga
AU - Hu, Kun
AU - Li, Peng
AU - Behrens, María Isabel
AU - Bruno, Martin Alejandro
AU - Cardona, Juan
AU - Custodio, Nilton
AU - Santamaria-Garcia, Hernando
AU - Garcia, Adolfo M.
AU - Godoy, Maria Eugenia
AU - Alberto Ávila Funes, José
AU - Maito, Marcelo Adrian
AU - Matallana, Diana L.
AU - Miller, Bruce L.
AU - Lopera, Francisco
AU - de Oliveira, Maira Okada
AU - Pina-Escudero, Stefanie
AU - Possin, Katherine L.
AU - de Paula, Elisa
AU - Resende, França
AU - Reyes, Pablo A.
AU - Slachevsky, Andrea
AU - Sosa, Ana Luisa
AU - Takada, Leonel Tadao
AU - Yokoyama, Jennifer S.
AU - Ibanez, Agustin
N1 - Publisher Copyright:
© 2025 The Alzheimer's Association. Alzheimer's & Dementia published by Wiley Periodicals LLC on behalf of Alzheimer's Association.
PY - 2025/12/1
Y1 - 2025/12/1
N2 - BACKGROUND: Cardiovascular risk factors, such diabetes, hypertension, blood pressure, obesity, and smoking, are linked with allostatic-interoception - the continuous monitoring of internal bodily states in anticipation of environmental demands. These risk factors are associated with dementia risk. How these factors affect brain networks vulnerable to neurodegeneration and involved in allostatic-interoception, such as the Allostatic-Interoceptive Network (AIN), is unknown. We investigated the relationship between cardiovascular risk and AIN structure and function in frontotemporal lobar degeneration (FTLD) and Alzheimer's disease (AD). METHOD: We recruited 1501 participants (304 with FTLD, 512 with AD, and 685 healthy controls) from the Multi-Partner Consortium to Expand Dementia Research in Latin America (ReDLat)(Figure 1). A cardiovascular risk score was calculated based on: age, sex, diabetes, hypertension, systolic blood pressure, body mass index, and smoking status. Cardiovascular risk was associated with gray matter integrity and functional connectivity in age- and sex-matched patient-control groups focusing on predefined regions of interest within the AIN. RESULT: Higher cardiovascular risk was associated with reduced structural integrity and functional connectivity within the AIN in both FTLD and AD. In FTLD patients, extensive structural (Figure 2) and functional connectivity disruptions (Figure 3) were observed throughout the AIN. In AD patients, structural reductions in the AIN were prominent (Figure 2), with functional connectivity restricted to the hippocampus, parahippocampal gyrus, and orbitofrontal regions (Figure 3). CONCLUSION: Cardiovascular risk factors appear to adversely impact the AIN structure and function, with disease-specific patterns of vulnerability. Our results underscore the importance of integrating cardiovascular health into models of neurodegenerative disease and managing cardiovascular health to support brain integrity in dementia. Future work is needed to uncover longitudinal effects of cardiovascular risk in dementia and to determine if cardiovascular risk factors exacerbate neurodegenerative processes.
AB - BACKGROUND: Cardiovascular risk factors, such diabetes, hypertension, blood pressure, obesity, and smoking, are linked with allostatic-interoception - the continuous monitoring of internal bodily states in anticipation of environmental demands. These risk factors are associated with dementia risk. How these factors affect brain networks vulnerable to neurodegeneration and involved in allostatic-interoception, such as the Allostatic-Interoceptive Network (AIN), is unknown. We investigated the relationship between cardiovascular risk and AIN structure and function in frontotemporal lobar degeneration (FTLD) and Alzheimer's disease (AD). METHOD: We recruited 1501 participants (304 with FTLD, 512 with AD, and 685 healthy controls) from the Multi-Partner Consortium to Expand Dementia Research in Latin America (ReDLat)(Figure 1). A cardiovascular risk score was calculated based on: age, sex, diabetes, hypertension, systolic blood pressure, body mass index, and smoking status. Cardiovascular risk was associated with gray matter integrity and functional connectivity in age- and sex-matched patient-control groups focusing on predefined regions of interest within the AIN. RESULT: Higher cardiovascular risk was associated with reduced structural integrity and functional connectivity within the AIN in both FTLD and AD. In FTLD patients, extensive structural (Figure 2) and functional connectivity disruptions (Figure 3) were observed throughout the AIN. In AD patients, structural reductions in the AIN were prominent (Figure 2), with functional connectivity restricted to the hippocampus, parahippocampal gyrus, and orbitofrontal regions (Figure 3). CONCLUSION: Cardiovascular risk factors appear to adversely impact the AIN structure and function, with disease-specific patterns of vulnerability. Our results underscore the importance of integrating cardiovascular health into models of neurodegenerative disease and managing cardiovascular health to support brain integrity in dementia. Future work is needed to uncover longitudinal effects of cardiovascular risk in dementia and to determine if cardiovascular risk factors exacerbate neurodegenerative processes.
UR - https://www.scopus.com/pages/publications/105025739441
U2 - 10.1002/alz70862_109908
DO - 10.1002/alz70862_109908
M3 - Article
C2 - 41434205
AN - SCOPUS:105025739441
SN - 1552-5260
VL - 21
SP - e109908
JO - Alzheimer's and Dementia
JF - Alzheimer's and Dementia
ER -