Abstract

Patients with active untreated acromegaly show mild to moderate neurocognitive disorders that are associated to chronic exposure to growth hormone (GH) and insulin-like growth factor (IGF-I) hypersecretion. However, it is unknown whether these disorders improve after controlling GH/IGF-I hypersecretion. The aim of this study was to compare neurocognitive functions of patients who successfully underwent GH-secreting adenoma transsphenoidal surgery (cured patients) with patients with naive acromegaly. In addition, we wanted to determine the impact of different clinical and biochemical variables on neurocognitive status in patients with active disease and after long-term cure. A battery of six standardized neuropsychological tests assessed attention, memory and executive functioning. In addition, a quantitative electroencephalography with Low-Resolution Electromagnetic Tomography (LORETA) solution was performed to obtain information about the neurophysiological state of the patients. Neurocognitive data was compared to that of a healthy control group. Multiple linear regression analysis was also conducted using clinical and hormonal parameters to obtain a set of independent predictors of neurocognitive state before and after cure. Both groups of patients scored significantly poorer than the healthy controls on memory tests, especially those assessing visual and verbal recall. Patients with cured acromegaly did not obtain better cognitive measures than naïve patients. Furthermore memory deficits were associated with decreased beta activity in left medial temporal cortex in both groups of patients. Regression analysis showed longer duration of untreated acromegaly was associated with more severe neurocognitive complications, regardless of the diagnostic group, whereas GH levels at the time of assessment was related to neurocognitive outcome only in naïve patients. Longer duration of post-operative biochemical remission of acromegaly was associated with better neurocognitive state. Overall, this data suggests that the effects of chronic exposure to GH/IGF-I hypersecretion could have long-term effects on brain functions.

Highlights

  • Is a rare but severe hormonal disorder resulting from aberrant growth hormone (GH) secretion and consequent increase of IGF-I, most commonly produced by pituitary adenomas

  • We should note that the hormonal analysis showed higher mean PRL serum levels in naıve patients (F = 4.79, p = 0.038), but this was due to the inclusion of patients with mixed GH/PRL secreting adenoma

  • Our results showed a lower prevalence of cognitive deficits in acromegaly patients, but it is important to note that the Sievers study included a heterogeneous sample group comprised of patients with a history of radiotherapy (25%) or uncontrolled disease (40%), which may explain the discrepancy between these results

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Summary

Introduction

Is a rare but severe hormonal disorder resulting from aberrant GH (growth hormone) secretion and consequent increase of IGF-I (insulin-like growth factor 1), most commonly produced by pituitary adenomas The development of this disease is insidious, with a mean duration of 5–10 years from symptom onset to diagnosis. Neurophysiological alterations have been described in active untreated (naıve) patients These patients display decreased amplitude of the cognitive potential P300 under the auditory oddball paradigm [3] as well as decreased alpha and beta activity in specific cortical regions such as prefrontal cortex (PFC) and medial temporal cortex (MTC) [4]. These observations strongly suggest that prolonged GH/IGF-I excess may have a negative effect on neural and cognitive function

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