Altered cerebral blood flow patterns associated with pathologic worry in the elderly.
Altered cerebral blood flow patterns associated with pathologic worry in the elderly.
复制标题
DOI:
10.1002/da.20799
复制
发表时间:
2011-03
影响因子:
7.4
通讯作者:
Aizenstein, Howard
中科院分区:
文献类型:
--
作者:
Andreescu, Carmen;Gross, James J.;Lenze, Eric;Edelman, Kathryn Dunfee;Snyder, Sara;Tanase, Costin;Aizenstein, Howard
Generalized Anxiety Disorder (GAD) is the most prevalent anxiety disorder among the elderly and has high functional and cognitive morbidity. However, late-life GAD is relatively understudied, and its functional neuroanatomy is uncharted. Several imaging studies have suggested abnormalities in the cognitive control systems of emotion regulation in anxiety disorders in young adults. The aim of this study was to examine the neural correlates of emotion regulation in late-life GAD. We compared seven elderly GAD subjects and ten elderly non-anxious comparison subjects using functional MRI. Regional cerebral blood flow (rCBF) was measured using Pulsed Arterial Spin Labeling (ASL) perfusion MRI at rest and during an emotion regulation paradigm. Relative to the rest condition, elderly non-anxious comparison subjects had increased rCBF during worry induction in the right insula, bilateral amygdala, and associative temporo-occipital areas. Elderly GAD subjects had increased rCBF during worry induction in the associative temporo-occipital areas, but not in the insula or the amygdala. During worry suppression, elderly non-anxious comparison subjects had increased rCBF in the prefrontal cortex (PFC) and dorsal ACC. Elderly GAD subjects had no changes in rCBF during worry suppression in the prefrontal cortex. When attempting to regulate their emotional responses, elderly anxious subjects failed to activate prefrontal regions involved in the down-regulation of negative emotions. These results, showing that elderly anxious subjects are not effectively engaging the PFC in suppressing worry, may be clinically relevant for developing personalized therapeutic strategies for the treatment of late-life GAD.
登录
查看更多内容
影响因子:
2.3
作者:
Hoehn-Saric, R;Schlund, MW;Wong, SHY
通讯作者:
Wong, SHY
影响因子:
7.2
作者:
Andreescu, Carmen;Belnap, Bea Herbeck;Lenze, Eric J.
通讯作者:
Lenze, Eric J.
DOI:
10.1176/appi.ajp.2009.09070931
发表时间:
2010-05
期刊:
The American journal of psychiatry
影响因子:
--
作者:
Etkin A;Prater KE;Hoeft F;Menon V;Schatzberg AF
通讯作者:
Schatzberg AF
影响因子:
5.7
作者:
Campbell-Sills, Laura;Simmons, Alan N.;Lovero, Kathryn L.;Rochlin, Alexis A.;Paulus, Martin P.;Stein, Murray B.
通讯作者:
Stein, Murray B.
影响因子:
6.9
作者:
de Beurs, E;Beekman, ATF;van Tilburg, W
通讯作者:
van Tilburg, W