Midlife Psychological Distress Associated With Late-Life Brain Atrophy and White Matter Lesions: A 32-Year Population Study of Women

被引:32
|
作者
Johansson, Lena [1 ]
Skoog, Ingmar [1 ]
Gustafson, Deborah R. [1 ,3 ]
Olesen, Pernille J. [1 ]
Waern, Margda [1 ]
Bengtsson, Calle [2 ]
Bjorkelund, Cecilia [2 ]
Pantoni, Leonardo [4 ]
Simoni, Michela [4 ]
Lissner, Lauren [2 ]
Guo, Xinxin [1 ]
机构
[1] Univ Gothenburg, Sahlgrenska Acad, Dept Psychiat & Neurochem, Neuropsychiat Epidemiol Unit, S-43141 Molndal, Sweden
[2] Univ Gothenburg, Sahlgrenska Acad, Dept Publ Hlth & Community Med, Gothenburg, Sweden
[3] SUNY Downstate Med Ctr Brooklyn, Dept Neurol & Med, New York, NY USA
[4] Univ Florence, Dept Neurol & Psychiat Sci, Florence, Italy
来源
PSYCHOSOMATIC MEDICINE | 2012年 / 74卷 / 02期
基金
美国国家卫生研究院; 英国医学研究理事会;
关键词
distress; white matter lesions; temporal lobe atrophy; computed tomography; epidemiology; population study; POSTTRAUMATIC-STRESS-DISORDER; ALZHEIMERS-DISEASE; COMPUTED-TOMOGRAPHY; HIPPOCAMPAL VOLUME; AMYLOID-BETA; RISK-FACTORS; DEMENTIA; 85-YEAR-OLDS; PREVALENCE; MRI;
D O I
10.1097/PSY.0b013e318246eb10
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective: Long-standing psychological distress increases the risk of dementia, especially Alzheimer's disease. The present study examines the relationship between midlife psychological distress and late-life brain atrophy and white matter lesions (WMLs), which are common findings on neuroimaging in elderly subjects. Methods: A population-based sample of 1462 women, aged 38 to 60 years, was examined in 1968, with subsequent examinations in 1974, 1980, 1992, and 2000. Computed tomography (CT) of the brain was done in 379 survivors in 2000, and of those, 344 had responded to a standardized question about psychological distress in 1968, 1974, and 1980. WMLs, cortical atrophy, and central atrophy (ventricular sizes) were measured at CT scans. Results: Compared with women reporting no distress, those reporting frequent or constant distress at one examination or more (in 1968, 1974, and 1980) more often had moderate-to-severe WMLs (multiadjusted odds ratio = 2.39, 95% confidence interval = 1.16-4.92) and moderate-to-severe temporal lobe atrophy (multiadjusted odds ratio = 2.51, 95% confidence interval = 1.04-6.05) on brain CT in 2000. Frequent/constant distress was also associated with central brain atrophy, that is, higher bicaudate ratio, higher cella media ratio, and larger third-ventricle width. Conclusions: Long-standing psychological distress in midlife increases risks. of cerebral atrophy and WMLs on CT in late life. More studies are needed to confirm these findings and to determine potential neurobiological mechanisms of these associations.
引用
收藏
页码:120 / 125
页数:6
相关论文
共 32 条
  • [21] White matter lesions and lacunar infarcts are differentially associated with brain atrophy: The smart-MR study
    Appelman, A. P.
    van der Graaf, Y.
    Tiehuis, A. M.
    Vincken, K. L.
    Witkamp, T. D.
    Mali, W. P.
    Geerlings, M. I.
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 2009, 283 (1-2) : 308 - 308
  • [22] Midlife Systemic Inflammatory Markers Are Associated With Late-Life Brain Volume The ARIC Study (vol 89, pg 2262, 2017)
    Walker, K. A.
    Hoogeveen, R. C.
    Folsom, A. R.
    NEUROLOGY, 2023, 101 (08) : 375 - 375
  • [23] White Matter Lesions and Lacunar Infarcts Are Independently and Differently Associated with Brain Atrophy: The SMART-MR Study
    Appelman, Auke P. A.
    Vincken, Koen L.
    van der Graaf, Yolanda
    Vlek, Anne L. M.
    Witkamp, Theo D.
    Mali, Willem P. T. M.
    Geerlings, Mirjam I.
    CEREBROVASCULAR DISEASES, 2010, 29 (01) : 28 - 35
  • [24] White matter and subcortical gray matter lesion volume changes and late-life depression outcome: a 4-year magnetic resonance imaging study
    Chen, Po See
    McQuoid, Douglas R.
    Payne, Martha E.
    Steffens, David C.
    INTERNATIONAL PSYCHOGERIATRICS, 2006, 18 (03) : 445 - 456
  • [25] Localized measures of callosal atrophy are associated with late-life hypertension in a population-based study: Age gene/environment susceptibility-Reykjavik study
    Harris, Peter
    Alcantara, Dan
    Amenta, Nina
    Lopez, Oscar
    Eiriksdottir, Gudny
    Sigurdsson, Sigurdur
    Thompson, Paul
    Launer, Lenore
    Gudnason, Vilmundur
    Carmichael, Owen
    NEUROLOGY, 2008, 70 (11) : A451 - A451
  • [26] A longitudinal observational population-based study of brain volume associated with changes in sleep timing from middle to late-life
    Kim, Regina E. Y.
    Kim, Hyeon Jin
    Kim, Soriul
    Abbott, Robert D.
    Thomas, Robert J.
    Yun, Chang-Ho
    Lee, Hyang Woon
    Shin, Chol
    SLEEP, 2021, 44 (04)
  • [27] Relationship between baseline white-matter changes and development of late-life depressive symptoms: 3-year results from the LADIS study
    Teodorczuk, A.
    Firbank, M. J.
    Pantoni, L.
    Poggesi, A.
    Erkinjuntti, T.
    Wallin, A.
    Wahlund, L. -O
    Scheltens, P.
    Waldemar, G.
    Schrotter, G.
    Ferro, J. M.
    Chabriat, H.
    Bazner, H.
    Visser, M.
    Inzitari, D.
    O'Brien, J. T.
    PSYCHOLOGICAL MEDICINE, 2010, 40 (04) : 603 - 610
  • [28] Heart failure is independently associated with white matter lesions: insights from the population-based LIFE-Adult Study
    Stegmann, Tina
    Chu, Mai L.
    Witte, Veronica A.
    Villringer, Arno
    Kumral, Denize
    Riedel-Heller, Steffi G.
    Roehr, Susanne
    Hagendorff, Andreas
    Laufs, Ulrich
    Loeffler, Markus
    Wachter, Rolf
    Zeynalova, Samira
    ESC HEART FAILURE, 2021, 8 (01): : 697 - 704
  • [29] Migraine Symptoms in Middle-Age Predict Brain Infarcts in Late-Life: A 25-Year Longitudinal Population-Based MRI Study
    Scher, Ann I.
    Ghambaryan, Anna
    Sigurdsson, Sigurdur
    Gudmundsson, Larus
    Eiriksdottir, Gudny
    Aspelund, Thor
    van Buchem, Mark A.
    Gudnason, Vilmundur
    Launer, Lenore J.
    NEUROLOGY, 2009, 72 (11) : A249 - A249
  • [30] Progression of brain white matter lesions in migraine? The 9-year follow-up population-based CAMERA-2 study
    Palm-Meinders, I. H.
    Koppen, H.
    Terwindt, G. M.
    Launer, L. J.
    van Buchem, M. A.
    Ferrari, M. D.
    Kruit, M. C.
    CEPHALALGIA, 2009, 29 (12) : 1351 - 1352