Associations of current and remitted major depressive disorder with brain atrophy: the AGES-Reykjavik Study

被引:30
|
作者
Geerlings, M. I. [1 ,2 ]
Sigurdsson, S. [3 ]
Eiriksdottir, G. [3 ]
Garcia, M. E. [1 ]
Harris, T. B. [1 ]
Sigurdsson, T. [4 ]
Gudnason, V. [3 ,5 ]
Launer, L. J. [1 ]
机构
[1] NIA, Lab Epidemiol Demog & Biometry, NIH, Bethesda, MD USA
[2] Univ Med Ctr Utrecht, Julius Ctr Hlth Sci & Primary Care, Utrecht, Netherlands
[3] Iceland Heart Assoc, Kopavogur, Iceland
[4] Landspitali Univ Hosp, Reykjavik, Iceland
[5] Univ Iceland, Reykjavik, Iceland
关键词
Brain; cohort; depression; elders; MRI; PITUITARY-ADRENAL AXIS; HIPPOCAMPAL VOLUME; GERIATRIC DEPRESSION; ALZHEIMER-DISEASE; MOOD DISORDERS; OLDER-ADULTS; SMART-MEDEA; DSM-IV; SYMPTOMS; RISK;
D O I
10.1017/S0033291712001110
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Background. To examine whether lifetime DSM-IV diagnosis of major depressive disorder (MDD), including age at onset and number of episodes, is associated with brain atrophy in older persons without dementia. Method. Within the population-based Age, Gene/Environment Susceptibility (AGES)-Reykjavik Study, 4354 persons (mean age 76 +/- 5 years, 58% women) without dementia had a 1.5-T brain magnetic resonance imaging (MRI) scan. Automated brain segmentation total and regional brain volumes were calculated. History of MDD, including age at onset and number of episodes, and MDD in the past 2 weeks was diagnosed according to DSM-IV criteria using the Mini-International Neuropsychiatric Interview (MINI). Results. Of the total sample, 4.5% reported a lifetime history of MDD; 1.5% had a current diagnosis of MDD (including 75% with a prior history of depression) and 3.0% had a past but no current diagnosis (remission). After adjusting for multiple covariates, compared to participants never depressed, those with current MDD (irrespective of past) had more global brain atrophy [B=-1.25%, 95% confidence interval (CI) -2.05 to -0.44], including more gray- and white-matter atrophy in most lobes, and also more atrophy of the hippocampus and thalamus. Participants with current, first-onset MDD also had more brain atrophy (B=-1.62%, 95% CI -3.30 to 0.05) whereas those remitted did not (B=0.06%, 95% CI -0.54 to 0.66). Conclusions. In older persons without dementia, current MDD, irrespective of prior history, but not remitted MDD was associated with widespread gray-and white-matter brain atrophy. Prospective studies should examine whether MDD is a consequence of, or contributes to, brain volume loss and development of dementia.
引用
收藏
页码:317 / 328
页数:12
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