Abstract

Introduction: Older-age bipolar disorder (OABD) may involve neurocognitive decline and behavioral disturbances that could share features with the behavioral variant of frontotemporal dementia (bvFTD), making the differential diagnosis difficult in cases of suspected dementia.Objective: To compare the neuropsychological profile, brain morphometry, and structural connectivity patterns between patients diagnosed with bvFTD, patients classified as OABD with an early onset of the disease (EO-OABD), and healthy controls (HC).Methods: bvFTD patients (n = 25, age: 66 ± 7, female: 64%, disease duration: 6 ± 4 years), EO-OABD patients (n = 17, age: 65 ± 9, female: 71%, disease duration: 38 ± 8 years), and HC (n = 28, age: 62 ± 7, female: 64%) were evaluated through neuropsychological tests concerning attention, memory, executive function, praxis, and language. Brain morphometry was analyzed through surface-based morphometry (SBM), while structural brain connectivity was assessed through diffusion tensor imaging (DTI).Results: Both bvFTD and EO-OABD patients showed lower performance in neuropsychological tests of attention, verbal fluency, working memory, verbal memory, and praxis than HC. Comparisons between EO-OABD and bvFTD showed differences limited to cognitive flexibility delayed recall and intrusion errors in the memory test. SBM analysis demonstrated that several frontal, temporal, and parietal regions were altered in both bvFTD and EO-OABD compared to HC. In contrast, comparisons between bvFTD and EO-OABD evidenced differences exclusively in the right temporal pole and the left entorhinal cortex. DTI analysis showed alterations in association and projection fibers in both EO-OABD and bvFTD patients compared to HC. Commissural fibers were found to be particularly affected in EO-OABD. The middle cerebellar peduncle and the pontine crossing tract were exclusively altered in bvFTD. There were no significant differences in DTI analysis between EO-OABD and bvFTD.Discussion: EO-OABD and bvFTD may share an overlap in cognitive, brain morphometry, and structural connectivity profiles that could reflect common underlying mechanisms, even though the etiology of each disease can be different and multifactorial.

Highlights

  • Older-age bipolar disorder (OABD) may involve neurocognitive decline and behavioral disturbances that could share features with the behavioral variant of frontotemporal dementia, making the differential diagnosis difficult in cases of suspected dementia

  • Comparisons of the comorbidities and other clinical data between the group of patients showed significant differences regarding the familial history of psychiatric disease (p < 0.001), where early-onset older-age bipolar disorder (EO-OABD) patients showed a higher prevalence than behavioral variant of frontotemporal dementia (bvFTD) patients (94 vs. 32%, respectively)

  • Our results suggest that after a long evolution of a chronic psychiatric disease such as EO-OABD, structural features of gray matter and white matter (WM) may be affected in regions that may overlap with the areas involved in bvFTD, which may possibly explain similarities in the clinical features observed in both clinical conditions

Read more

Summary

Introduction

Older-age bipolar disorder (OABD) may involve neurocognitive decline and behavioral disturbances that could share features with the behavioral variant of frontotemporal dementia (bvFTD), making the differential diagnosis difficult in cases of suspected dementia. Bipolar disorder (BD) is a chronic psychiatric disease associated with excitotoxicity and neuroinflammation processes that may contribute, among other factors, to accelerate normal aging mechanisms [1, 2]; its progression as a neurodegenerative disorder has been explored [3, 4]. Patients with BD frequently suffer from cognitive deficits that may persist during periods of euthymia [5,6,7]. Other authors have suggested that elderly BD patients may progress to neurodegenerative disorders that could fall into syndromes belonging to the frontotemporal lobar degeneration (FTLD) spectrum [19, 20]

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call