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Changes in brain activities seen on functional magnetic resonance imaging (fMRI) during autobiographical tasks in patients with borderline personality disorder.

Differences in brain functioning with autobiographical task during fMRI between patients with borderline personality disorder and healthy controls.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12616000149460
Enrollment
45
Registered
2016-02-08
Start date
2015-10-01
Completion date
2018-02-28
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

The growing interest in the relationships between brain activity and psychopathology has recently produced an increasing number of neuroimaging studies aimed to register the changes of brain functioning in specific cerebral areas. The objective of the present study is to evaluate the relationships between identity disturbance in borderline personality disorder (BPD) and brain activity in specific areas involved in the mechanisms of self and identity. Cerebral regions of interest will be dorsolateral prefrontal cortex, insula, anterior cingulate cortex, and temporal parietal Junction. Patients with a diagnosis of BPD and a group of healthy subjects matched for age and gender will be enrolled and compared. All participants will be tested before fMRI with the following evaluation instruments: the Clinical Global Impression Scale (CGI-S); the Borderline Personality Disorder Severity Index (BPDSI); the Identity Disturbance Questionnaire (IDQ); the Hamilton for Anxiety and Depression (HAM-A and HAM-D); the Childhood Trauma Questionnaire (CTQ); the Social and Occupational Functioning Assessment Scale (SOFAS); and the Autobiographical Interview. Autobiographical Interview will allow to obtain 2 unresolved life events and 2 resolved life events. For each event subjects will provide 4 key-words that will be used to trigger active recall during fMRI. Study design will be a bloch design characterized by two conditions: life events/key-words (activation condition) and neutral events/key-words (resting state). Each bloch will be presented by fMRI glasses and will last 40 s. In response to each life-event and key-word, BPD patients and healthy controls will recall the event (resolved and unresolved). In response to the fixation cross, they will stop recall. Patients and controls will undergo neutral event and key-word as resting condition. Structural and functional images will be aquired and compared between patients and controls. Statistical analyses will be conducted with SPM-12 and ANOVA.

Interventions

The objective of the present study is to investigate with fMRI the differences in brain functioning between BPD patients and healthy controls during a task of autobiographical memory. In particular, we evaluated brain functioning in patients with identity diffusion, a core psychopathological factor of BPD that had not been assessed in previous investigations. Based on recent findings about neural correlates involved in patients with BPD during autobiographical memories we hypothesised that BPD p

The objective of the present study is to investigate with fMRI the differences in brain functioning between BPD patients and healthy controls during a task of autobiographical memory. In particular, we evaluated brain functioning in patients with identity diffusion, a core psychopathological factor of BPD that had not been assessed in previous investigations. Based on recent findings about neural correlates involved in patients with BPD during autobiographical memories we hypothesised that BPD patients with a deficit in identity integration may present a higher brain activation in dorsolateral prefrontal cortex, insula, anterior cingulate cortex, and temporal parietal junction during the recall of significant life events, both resolved and unresolved, in comparison with controls. Patients with a diagnosis of BPD and a group of healthy subjects will be enrolled. Assessment will be performed only on one occasion (baseline). Autobiographical Interview will be performed to all subjects a week before MRI by an expert clinician (psychiatrist). The duration of interview will be about 90 minutes. Autobiographical Interview will allow to obtain 2 unresolved life events and 2 resolved life events. For each event subjects will provide 4 key-words that will be used to trigger active recall during fMRI. All subjects will undergo a training session immediatly before fMRI. fMRI will be performed by a radiologist. During assessment, patients and controls will choose 4 neutral events from a pool of brief reports/events (24-26 words).Each report/event has 4 key-words. This pool of reports was previously administered to 100 subjects, who indicated what reports were neutral. Only reports that > 80% of subjects considered neutral will use in the task as resting condition. Study will be a bloch design characterized by the following conditions: - activation condition: presentation with eye-glasses a brief summary of life event (24-26 words for each event) for 10 seconds, fixation cross for 10 seconds, key-word event-related for 10 seconds, fixation cross for 10 seconds. - Resting condition: presentation of neutral report/event(24-26 words) for 10 seconds, fixation cross for 10 seconds, key-word report/event related for 10 seconds, fixation cross for 10 seconds. This cycle will be repeated for 32 times. Tasks will be projected from the computer to the specific MRI eye-glassess that patient will wear during fMRI. Activation condition will immediately follow resting condition. MRI registration will continue for all 32 cycle repeats. BPD patients and healthy controls will be undergone activation conditions and resting conditions. Each bloch will last 40 seconds. Functional images will be aquired and compared between patients and controls.

Sponsors

Centre for Personality Disorders, Psychiatric Clinic, Department of Neuroscience, Univerisity of Turin, Italy
Lead SponsorUniversity

Study design

Allocation
Non-randomised trial
Primary purpose
Diagnosis

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

Patients: diagnosis of borderline personality disorder. Controls: subjects mached for age and gender without psychiatric disorders and neurological diseases.

Exclusion criteria

Dementia, delirium, and other cognitive disorders; brain injuries; schizophrenia and other psychotic disorders; bipolar disorders; concurrent major depressive episode; substance abuse in the last two months; pharmacological treatments in the last three weeks; pregnant women.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026