Neuroanatomical correlates of apathy in late-life depression and antidepressant treatment response.

Neuroanatomical correlates of apathy in late-life depression and antidepressant treatment response.
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DOI:
10.1016/j.jad.2014.05.008
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发表时间:
2014-09
影响因子:
6.6
通讯作者:
Alexopoulos GS
Alexopoulos GS
中科院分区:
医学2区
文献类型:
--
作者:
Yuen GS;Gunning FM;Woods E;Klimstra SA;Hoptman MJ;Alexopoulos GS

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Apathy is a prominent feature of geriatric depression that predicts poor clinical outcomes and hinders depression treatment. Yet little is known about the neurobiology and treatment of apathy in late-life depression. This study examined apathy prevalence in a clinical sample of depressed elderly, response of apathy to selective serotonin reuptake inhibitor (SSRI) treatment, and neuroanatomical correlates that distinguished responders from nonresponders and healthy controls. Participants included 45 non-demented, elderly with major depression and 43 elderly comparison individuals. After a 2-week single-blind placebo period, depressed participants received escitalopram 10mg daily for 12 weeks. The Apathy Evaluation Scale (AES) and 24-item Hamilton Depression Rating Scale (HDRS) were administered at baseline and 12 weeks. MRI scans were acquired at baseline for concurrent structural and diffusion tensor imaging of anterior cingulate grey matter and associated white matter tracts. 35.5% of depressed patients suffered from apathy. This declined to 15.6% (p<0.1) following treatment, but 43% of initial sufferers continued to report significant apathy. Improvement of apathy with SSRI was independent of change in depression but correlated with larger left posterior subgenual cingulate volumes and greater fractional anisotropy of left uncinate fasciculi. modest sample size, no placebo control, post-hoc secondary analysis, use of 1.5T MRI scanner While prevalent in geriatric depression, apathy is separable from depression with regards to medication response. Structural abnormalities of the posterior subgenual cingulate and uncinate fasciculus may perpetuate apathetic states by interfering with prefrontal cortical recruitment of limbic activity essential to motivated behavior.
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