6 research outputs found
Brain structure and function in primary adrenal insufficiency
Individuals with primary adrenal insufficiency (PAI), i.e., congenital adrenal hyperplasia (CAH) and
autoimmune Addison’s disease (AAD), suffer from impaired production of the adrenal gland hormones
cortisol and aldosterone, and in the case of AAD, also androgens. Replacement medication for these
hormones is sub-optimal due to the difficulties in replicating the natural rhythms of cortisol secretion.
The hormones are known to affect brain function via many mechanisms, and both pre- and postnatal
hormone dysregulation may affect cognitive functioning, brain structure and brain function. Therefore,
studying brain health in PAI is of interest and is needed to optimise treatment and patient wellbeing.
The present thesis investigated brain structure related to cognitive functioning in individuals with CAH,
and cognitive functioning, brain structure and resting-state functional connectivity in individuals with
AAD. We found that individuals with CAH have impairments in white matter microstructure, as well
as cortical thinning of the frontoparietal network that was related to weaker performance on a
visuospatial working memory task. On the other hand, individuals with AAD performed equally to
control subjects on most measures of cognitive functions assessed with standardized tests during the
lab-visit, but they self-reported executive function problems in daily life, which were related to
experienced mental fatigue. As opposed to individuals with CAH, those with AAD did not have
profound differences in the structure of the brain, apart from smaller total brain volumes. However, they
displayed increased resting-state functional connectivity, particularly in primary visual regions and the
orbitofrontal cortex. Our results suggest that the effects of adrenal hormone insufficiency affect
individuals with CAH and AAD differently. This difference may be related to the onset of the disease,
which is from conception for those with CAH and in adolescence or adulthood for those with AAD.
Long-term follow-up studies are needed to assess whether the observed differences contribute to
increased cognitive decline later in life and how to optimise replacement medication to sustain brain
health
First Trimester DEX Treatment Is Not Associated with Altered Brain Activity During Working Memory Performance in Adults
Young adult Swedish patients with autoimmune Addison's disease report difficulties with executive functions in daily life despite overall good cognitive performance
Objectives: Sub-optimal replacement of glucocorticoids (GC) in autoimmune Addison's disease (AAD) may affect cognitive functioning. The present study therefore sought to investigate cognitive performance and self-reported problems with executive functions in a cohort of young adult patients with AAD. Design and methods: 67 patients with AAD (39 females), mean age 32 yrs. (range 19–41), and 80 control participants (43 females), mean age 29 yrs. (range 19–43), completed neuropsychological tests estimating verbal and non-verbal intellectual ability, learning, memory and executive functioning, in addition to self-report scales assessing problems with executive functions, fatigue and symptoms of anxiety and depression. Results: Patients performed within the average range on all cognitive tests compared to population norms. However, female AAD patients reported more problems than controls with both hot (emotion regulation) and cold (cognitive regulation) executive functions in daily life. Moreover, experienced problems with executive functions in both male and female patients were associated with increased mental fatigue and lower GC replacement doses. Conclusions: Despite average performance in neuropsychological tests by both sexes, young adult female patients with AAD experience problems with executive functions in daily life. Coping with mental fatigue and optimization of pharmacotherapy may be important factors to be addressed in order to provide timely support for patients. Future research is needed to further determine other risk factors for experiencing executive function impairments in AAD