Abnormal default-mode network in angiotensin converting enzyme D allele carriers with remitted geriatric depression

被引:33
作者
Wang, Zan [1 ,2 ]
Yuan, Yonggui [1 ,2 ]
Bai, Feng [1 ,2 ]
You, Jiayong [3 ]
Li, Lingjiang [4 ]
Zhang, Zhijun [1 ,2 ]
机构
[1] Southeast Univ, Affiliated ZhongDa Hosp, Dept Neuropsychiat, Nanjing 210009, Jiangsu, Peoples R China
[2] Southeast Univ, Inst Neuropsychiat, Nanjing 210009, Jiangsu, Peoples R China
[3] Nanjing Med Univ, Nanjing Brain Hosp, Dept Psychiat, Nanjing 210029, Jiangsu, Peoples R China
[4] Cent S Univ, Xiangya Hosp 2, Mental Hlth Inst, Changsha 410011, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
Remitted geriatric depression; Angiotensin-converting enzyme; Posterior cingulate cortex; Functional connectivity; Functional magnetic resonance imaging; Cognitive impairment; INSERTION DELETION POLYMORPHISM; POSTERIOR CINGULATE CORTEX; MILD COGNITIVE IMPAIRMENT; ALZHEIMERS-DISEASE; FUNCTIONAL CONNECTIVITY; I/D POLYMORPHISM; BRAIN-FUNCTION; STATE; GENE; SUSCEPTIBILITY;
D O I
10.1016/j.bbr.2012.02.011
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
010107 [宗教学]; 030301 [社会学]; 070906 [古生物学及地层学(含古人类学)];
摘要
Using a cross-sectional case-control study of remitted geriatric depression (RGD), we characterised the relationships among cognitive function, whole-brain functional connectivity of the posterior cingulate cortex (PCC), and the angiotensin-converting enzyme (ACE) insertion or deletion (I/D) polymorphism during resting state. A total of 26 RGD patients and 24 matched controls were recruited, and neuropsychological tests, functional magnetic resonance imaging (fMRI) and ACE I/D genotype were examined for each subject. A 2 x 2 factorial analysis of variance (ANOVA) model (presence/absence of depression and presence/absence of ACE-D)was used to detect the interaction effect. Subsequent analyses were restricted to the significant interaction regions. There were significant interactions between disease and genotype at two clusters: left superior temporal gyrus/middle temporal gyrus and left cerebellum. And the ACE I/D polymorphism has disease-specific effects on the left superior temporal gyrus/middle temporal gyrus and cerebellum crus I. Furthermore, there was a significant positive correlation between the functional connection of FCC-left cerebellum crus land the CFT-delayed recall test scores (r=0.668, P=0.003) in RGD group ACE-D allele carriers. These results suggest that the ACE I/D polymorphism can modulate the pathology of RGD, and the status of geriatric depression and the ACE-D allele may synergistically induce altered resting state network activity, which could influence the cognitive function and increase the mortality risk for cognitive impairment. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:325 / 332
页数:8
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[1]
Disruption of large-scale brain systems in advanced aging [J].
Andrews-Hanna, Jessica R. ;
Snyder, Abraham Z. ;
Vincent, Justin L. ;
Lustig, Cindy ;
Head, Denise ;
Raichle, Marcus E. ;
Buckner, Randy L. .
NEURON, 2007, 56 (05) :924-935
[2]
Altered self-referential network in resting-state amnestic type mild cognitive impairment [J].
Bai, Feng ;
Shi, Yongmei ;
Yuan, Yonggui ;
Wang, Yi ;
Yue, Chunxian ;
Teng, Yuhuan ;
Wu, Di ;
Zhang, Zhengsheng ;
Jia, Jianping ;
Zhang, Zhijun .
CORTEX, 2012, 48 (05) :604-613
[3]
Abnormal resting-state functional connectivity of posterior cingulate cortex in amnestic type mild cognitive impairment [J].
Bai, Feng ;
Watson, David R. ;
Yu, Hui ;
Shi, Yongmei ;
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Zhang, Zhijun .
BRAIN RESEARCH, 2009, 1302 :167-174
[4]
ANGIOTENSIN-II INHIBITS CORTICAL CHOLINERGIC FUNCTION - IMPLICATIONS FOR COGNITION [J].
BARNES, JM ;
BARNES, NM ;
COSTALL, B ;
HOROVITZ, ZP ;
IRONSIDE, JW ;
NAYLOR, RJ ;
WILLIAMS, TJ .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1990, 16 (02) :234-238
[5]
ANGIOTENSIN CONVERTING ENZYME DENSITY IS INCREASED IN TEMPORAL CORTEX FROM PATIENTS WITH ALZHEIMERS-DISEASE [J].
BARNES, NM ;
CHENG, CHK ;
COSTALL, B ;
NAYLOR, RJ ;
WILLIAMS, TJ ;
WISCHIK, CM .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1991, 200 (2-3) :289-292
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Persistence of neuropsychologic deficits in the remitted state of late-life depression [J].
Bhalla, RK ;
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Mulsant, BH ;
Begley, AE ;
Zmuda, MD ;
Schoderbek, B ;
Pollock, BG ;
Reynolds, CF ;
Becker, JT .
AMERICAN JOURNAL OF GERIATRIC PSYCHIATRY, 2006, 14 (05) :419-427
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Bluhm, Robyn ;
Williamson, Peter ;
Lanius, Ruth ;
Theberge, Jean ;
Densmore, Maria ;
Bartha, Robert ;
Neufeld, Richard ;
Osuch, Elizabeth .
PSYCHIATRY AND CLINICAL NEUROSCIENCES, 2009, 63 (06) :754-761
[8]
The nature and determinants of neuropsychological functioning in late-life depression [J].
Butters, MA ;
Whyte, EM ;
Nebes, RD ;
Begley, AE ;
Dew, MA ;
Mulsant, BH ;
Zmuda, MD ;
Bhalla, R ;
Meltzer, CC ;
Pollock, BG ;
Reynolds, CF ;
Becker, JT .
ARCHIVES OF GENERAL PSYCHIATRY, 2004, 61 (06) :587-595
[9]
Temporal dynamics of cerebro-cerebellar network recruitment during a cognitive task [J].
Chen, SHA ;
Desmond, JE .
NEUROPSYCHOLOGIA, 2005, 43 (09) :1227-1237
[10]
Study of the association between Alzheimer's disease and angiotensin-converting enzyme gene polymorphism using DNA from lymphocytes [J].
Cheng, CY ;
Hong, CJ ;
Liu, HC ;
Liu, TY ;
Tsai, SJ .
EUROPEAN NEUROLOGY, 2002, 47 (01) :26-29