Late onset bipolar disorder and frontotemporal dementia with mutation in progranulin gene: a case report

Amyotroph Lateral Scler Frontotemporal Degener. 2017 Nov;18(7-8):624-626. doi: 10.1080/21678421.2017.1339716. Epub 2017 Jun 30.

Abstract

Bipolar disorder is a chronic psychiatric illness characterised by fluctuation in mood state, with a relapsing and remitting course. Frontotemporal dementia (FTD) is a clinically and genetically heterogeneous syndrome, with the most frequent phenotype being behavioural variant frontotemporal dementia (bvFTD). Here, we report the case of an Italian male presenting with late-onset bipolar disorder that developed into bvFTD over time, carrying a mutation in the GRN gene. Interestingly, the patient carried the c.1639 C > T variant in the GRN gene, resulting in a R547C substitution. Our case report further corroborates the notion that, in addition to FTD, progranulin may be involved in the neurobiology of bipolar disorder type 1, and suggests to screen patients with late-onset bipolar disorder for GRN mutations.

Keywords: Bipolar disorder type 1; frontotemporal dementia; progranulin gene.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Bipolar Disorder / diagnosis*
  • Bipolar Disorder / etiology
  • Bipolar Disorder / genetics*
  • Diagnosis, Differential
  • Frontotemporal Dementia / complications
  • Frontotemporal Dementia / diagnosis*
  • Frontotemporal Dementia / genetics*
  • Genetic Predisposition to Disease / genetics*
  • Humans
  • Intercellular Signaling Peptides and Proteins / genetics*
  • Late Onset Disorders
  • Male
  • Mutation / genetics
  • Polymorphism, Single Nucleotide / genetics*
  • Progranulins

Substances

  • GRN protein, human
  • Intercellular Signaling Peptides and Proteins
  • Progranulins