Lifetime Socioeconomic Status, Cognitive Decline, and Brain Characteristics

被引:1
|
作者
Krueger, Kristin R. [1 ]
Desai, Pankaja [1 ]
Beck, Todd [1 ]
Barnes, Lisa L. [2 ]
Bond, Jerenda [1 ]
Decarli, Charles [3 ]
Aggarwal, Neelum T. [2 ]
Evans, Denis A. [1 ]
Rajan, Kumar B. [1 ,3 ]
机构
[1] Rush Univ, Rush Inst Hlth Aging, Med Ctr, Triangle Off Bldg,1700 W Van Buren,Ste 245, Chicago, IL 60612 USA
[2] Rush Univ, Rush Alzheimers Dis Ctr, Med Ctr, Chicago, IL USA
[3] Univ Calif Davis, Dept Neurol, Davis, CA USA
基金
美国国家卫生研究院;
关键词
SEGMENTATION; ASSOCIATION; COMMUNITY; EDUCATION;
D O I
10.1001/jamanetworkopen.2024.61208
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IMPORTANCESocioeconomic status (SES) has an important association with cognitive function and structural brain indices. Identifying the nature of this association will guide strategies for improving health equity. OBJECTIVETo test the longitudinal associations of SES with cognitive decline and brain characteristics and to examine whether these associations differ between Black and White individuals. DESIGN, SETTING, AND PARTICIPANTSParticipants aged 65 years old or older were recruited for this population-based cohort study from 4 communities on the south side of Chicago, Illinois. At-home interviews were conducted between 1993 and 2012. The data were analyzed in April 2024. MAIN OUTCOMES AND MEASURESOutcome measures were level and change in global cognition and 4 individual tests. Three magnetic resonance imaging (MRI) measures of the brain included total brain volume, hippocampal volumes, and white matter hyperintensities (WMH). Childhood SES was assessed using parental education levels, father's occupation, and childhood finance rating. Adulthood SES was assessed using the participants' education, occupation, and income. Lifetime SES was assessed on the basis of the mother's education, childhood SES, and participants' occupation and income. RESULTSOf the 7303 participants (mean [SD] age, 72.3 [6.3] years; 4573 female participants [63%]), 4581 (63%) were non-Hispanic Black, and 2722 (37%) were non-Hispanic White. SES was higher for White individuals compared with Black individuals in childhood, adulthood, and across the lifespan. Higher lifetime SES was associated with better global cognitive functioning at baseline (estimate, 0.337; 95% CI, 0.317 to 0.357; P < .001) but not with decline over time (estimate, 0.003; 95% CI, -0.001 to 0.006; P = .10). Higher lifetime SES was associated with a better baseline score on the Mini-Mental State Examination (estimate, 0.281; 95% CI, 0.261 to 0.302; P < .001) and a slower decline for all participants (estimate, 0.012; 95% CI, 0.008 to 0.016; P < .001). In a subset of 933 participants who underwent MRI, there was an association between lifetime SES and healthier brain structures, as measured by total brain volume (estimate, 3.18; 95% CI, 0.20 to 6.17; P = .04) and WMH burden (estimate, -0.11; 95% CI, -0.21 to -0.01; P = .03). CONCLUSIONS AND RELEVANCEIn this cohort study, SES, mainly in adulthood, was associated with a person's cognitive status and brain structure, resulting in a discrepancy in cognitive status over time. These findings point to a need for interventions that improve SES throughout the lifespan, particularly for Black individuals, who had lower SES than White individuals.
引用
收藏
页数:13
相关论文
共 50 条
  • [41] Development of Iron Status Measures during Youth: Associations with Sex, Neighborhood Socioeconomic Status, Cognitive Performance, and Brain Structure
    Larsen, Bart
    Baller, Erica B.
    Boucher, Alexander A.
    Calkins, Monica E.
    Laney, Nina
    Moore, Tyler M.
    Roalf, David R.
    Ruparel, Kosha
    Gur, Ruben C.
    Gur, Raquel E.
    Georgieff, Michael K.
    Satterthwaite, Theodore
    AMERICAN JOURNAL OF CLINICAL NUTRITION, 2023, 118 (01): : 121 - 131
  • [42] Association of Lifetime Intellectual Enrichment With Cognitive Decline in the Older Population
    Vemuri, Prashanthi
    Lesnick, Timothy G.
    Przybelski, Scott A.
    Machulda, Mary
    Knopman, David S.
    Mielke, Michelle M.
    Roberts, Rosebud O.
    Geda, Yonas E.
    Rocca, Walter A.
    Petersen, Ronald C.
    Jack, Clifford R., Jr.
    JAMA NEUROLOGY, 2014, 71 (08) : 1017 - 1024
  • [43] Selenium status in elderly: Relation to cognitive decline
    Cardoso, Barbara Rita
    Bandeira, Veronica Silva
    Jacob-Filho, Wilson
    Franciscato Cozzolino, Silvia Maria
    JOURNAL OF TRACE ELEMENTS IN MEDICINE AND BIOLOGY, 2014, 28 (04) : 422 - 426
  • [44] Plasma amyloid-beta oligomer is related to subjective cognitive decline and brain amyloid status
    Kim, Keun You
    Park, Jaesub
    Jeong, Yong Hyu
    Kim, Hyun Jeong
    Lee, Eun
    Park, Jin Young
    Kim, Eosu
    Kim, Woo Jung
    ALZHEIMERS RESEARCH & THERAPY, 2022, 14 (01)
  • [45] Androgen deprivation therapy and cognitive decline—associations with brain connectomes, endocrine status, and risk genotypes
    Cecilie R. Buskbjerg
    Ali Amidi
    Simon Buus
    Claus H. Gravholt
    S. M. Hadi Hosseini
    Robert Zachariae
    Prostate Cancer and Prostatic Diseases, 2022, 25 : 208 - 218
  • [46] The influence of APOE status on rate of cognitive decline
    Morrison, Cassandra
    Oliver, Michael D.
    Berry, Virginia
    Kamal, Farooq
    Dadar, Mahsa
    GEROSCIENCE, 2024, 46 (03) : 3263 - 3274
  • [47] Brain reserve and cognitive reserve in MS patients. Lifetime maximal brain size and early life cognitive leisure independently protect against disease-related cognitive decline
    Sumowski, J. F.
    Rocca, M. A.
    Leavitt, V. M.
    Riccitelli, G.
    Comi, G.
    DeLuca, J.
    Filippi, M.
    MULTIPLE SCLEROSIS JOURNAL, 2012, 18 : 212 - 213
  • [48] Plasma amyloid-beta oligomer is related to subjective cognitive decline and brain amyloid status
    Keun You Kim
    Jaesub Park
    Yong Hyu Jeong
    Hyun Jeong Kim
    Eun Lee
    Jin Young Park
    Eosu Kim
    Woo Jung Kim
    Alzheimer's Research & Therapy, 14
  • [49] The influence of APOE status on rate of cognitive decline
    Cassandra Morrison
    Michael D. Oliver
    Virginia Berry
    Farooq Kamal
    Mahsa Dadar
    GeroScience, 2024, 46 : 3263 - 3274