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Copyright 2012 Aileen M. Echiverri-Cohen - University of Washington

Copyright 2012 Aileen M. Echiverri-Cohen - University of Washington

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and may not be regained. Indeed, older age is related to loss <strong>of</strong> inhibition function (Woodruff-<br />

Pak, 1997), and may be associated with general slowing <strong>of</strong> cognitive operations (Salthouse,<br />

1986), or may be related to education in attentional resources or working memory capacity<br />

(Salthouse, 1988). Inhibitory theories on aging posit that cognitive decline may be a direct<br />

consequence <strong>of</strong> deficits in inhibitory function (Hasher & Zacks, 1988; Posner & Snyder, 1975)<br />

with inhibitory processes declining with age. Indeed, older individuals fail to suppress irrelevant<br />

information on inhibitory measures including Stroop and negative priming (Swerdlow et al.,<br />

1993) and eye movement tasks (Butler & Zacks, 2006). Thus, improvement in inhibitory<br />

processes may be less likely in older individuals.<br />

The present findings point to a potential mechanism underlying treatment response<br />

particularly for PE, highlighting the role <strong>of</strong> temporal inhibitory attention processes. Future<br />

directions for treatment may involve the development <strong>of</strong> novel therapeutic applications that<br />

target attentional inhibitory processes. Attentional training, for instance, is associated with<br />

altering attentional mechanisms by improving performance on tasks involving executive control<br />

(Sturm, Willmes, Orgass & Hartje, 1997). It has also shown promise as a therapeutic approach in<br />

improving attention allocation and reducing clinical symptoms across anxiety disorders (Amir,<br />

Weber, Beard, Bomyea, & Taylor, 2008; Schmidt, Richey, Buckner, & Timpano, 2009).<br />

Pharmacological interventions, such as D-cycloserine, may similarly target inhibition by<br />

consolidating inhibitory learning in therapy, resulting in enhancing treatment response (H<strong>of</strong>fman<br />

et al., 2006; Ressler et al., 2004). In addition, the association between better PPI and treatment<br />

response points to the possibility <strong>of</strong> using a biomarker strategy in facilitating treatment response<br />

in PTSD. One clinical implication may be that biomarkers may reflect targets for<br />

pharmacotherapy or psychotherapy to strengthen treatment response in PTSD. In turn, using a<br />

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