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  • Poster presentation
  • Open Access

MRI findings in bipolar I patients: preliminary data

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  • 1,
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  • 2,
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Annals of General Psychiatry20065 (Suppl 1) :S328

  • Published:


  • White Matter
  • Parietal Lobe
  • White Matter Lesion
  • Vascular Risk Factor
  • White Matter Hyperintense


Increased rates of white matter hyperintense lesions and temporal cortical atrophy have been reported in bipolar patients. However, the potential effects of age, vascular risk factors and illness severity on reported findings are not fully established. The current preliminary paper reports the MRI findings from 11 bipolar I patients and its possible relationship with vascular risk factors.

Materials and methods

11 bipolar I patients (5 males and 6 females) diagnosed according to DSM-IV criteria took part in the study. Their age was 53 ± 13.06 years (range 35–78). The diagnosis was achieved with the SCAN v.2.0. Apart from a full clinical and laboratory examination, they were especially investigated for the presence of diabetes mellitus (DM) and hypertension (HT). All underwent brain MRI. Their MRI was qualitatively rated (0: absent to 3: pronounced) for the presence of ventricular enlargement, cortical atrophy and white matter lesions visible in the T2 sequence.


Two patients had both DM and HT and one had HT alone. There was no patient with no abnormal MRI findings. Seven patients (63.63%) had bilateral ventricular enlargement, and another 7 had cortical atrophy to one or more brain regions. 10 patients (90.90%) had non specific white matter lesions spread throughout the brain. Age correlated significantly with all MRI ratings (R = 0.53–0.79). Patients with DM had more pronounced white matter pathology in the left parietal lobe (2.50 ± 0.70 vs. 0.88 ± 0.92), while patients with HT had more pronounced white matter pathology in both parietal lobes (2.33 ± 0.57 vs. 0.87 ± 0.83 and 2.34 ± 0.58 vs. 0.75 ± 0.88). Example MRIs are shown in the figures.


Brain lesions detectable with MRI may be present in the majority of bipolar I patients. Age and vascular risk factors may have an adverse effect on this brain pathology. The relation of these findings with the response to treatment and the course of the illness needs further research and clarification.

Authors’ Affiliations

3rd Department of Psychiatry, Aristotle University of Thessaloniki, Greece
3rd Department of Neurology, Aristotle University of Thessaloniki, Greece


© The Author(s) 2006