Alterations in functional connectivity between the hippocampus and prefrontal cortex as a correlate of depressive symptoms in temporal lobe epilepsy

• Published in: Epilepsy & behavior 2013-12, Vol.29 (3), p.552-559
• Main Authors: Kemmotsu, Nobuko, Kucukboyaci, N. Erkut, Cheng, Christopher E, Girard, Holly M, Tecoma, Evelyn S, Iragui, Vicente J, McDonald, Carrie R
• Format: Article
• Language: English
• Subjects: Adult; Amygdala; Analysis of Variance; Asymmetry; Comorbidities; Depression; Depression - etiology; Depression - pathology; Epilepsy, Temporal Lobe - complications; Epilepsy, Temporal Lobe - pathology; Female; Functional connectivity; Functional Laterality; Hippocampus; Hippocampus - blood supply; Hippocampus - pathology; Hippocampus - physiopathology; Humans; Image Processing, Computer-Assisted; Magnetic Resonance Imaging; Male; Middle Aged; Neural Pathways - blood supply; Neural Pathways - physiology; Neurology; Oxygen - blood; Prefrontal Cortex - blood supply; Prefrontal Cortex - pathology; Prefrontal Cortex - physiopathology; Temporal lobe epilepsy
• ISSN: 1525-5050; 1525-5069
• DOI: 10.1016/j.yebeh.2013.09.039

Abstract Depression is a common comorbidity in temporal lobe epilepsy (TLE) that is thought to have a neurobiological basis. This study investigated the functional connectivity (FC) of medial temporal networks in depression symptomatology of TLE and the relative contribution of structural versus FC measures. Volumetric MRI and functional connectivity MRI (fcMRI) were performed on nineteen patients with TLE and 20 controls. The hippocampi and amygdalae were selected as seeds, and five prefrontal and five cingulate regions of interest (ROIs) were selected as targets. Low-frequency blood-oxygen-level-dependent signals were isolated from fcMRI data, and ROIs with synchronous signal fluctuations with the seeds were identified. Depressive symptoms were measured by the Beck Depression Inventory—II. The patients with TLE showed greater ipsilateral hippocampal atrophy (HA) and reduced FC between the ipsilateral hippocampus and the ventral posterior cingulate cortex (vPCC). Neither HA nor hippocampal–vPCC FC asymmetry was a robust contributor to depressive symptoms. Rather, hippocampal–anterior prefrontal FC was a stronger contributor to depressive symptoms in left TLE (LTLE). Conversely, right amygdala FC was correlated with depressive symptoms in both patient groups, with a positive and negative correlation in LTLE and right TLE (RTLE), respectively. Frontolimbic network dysfunction is a strong contributor to levels of depressive symptoms in TLE and a better contributor than HA in LTLE. In addition, the right amygdala may play a role in depression symptomatology regardless of the side of the epileptogenic focus. These findings may inform the treatment of depressive symptoms in TLE and inspire future research to help guide surgical planning.