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Hyperostosis frontalis interna, acromegaly and hyperprolactinaemia
J D Fulton1, J Shand, D Ritchie
1Department of Geriatric Medicine, Stobhill General Hospital, Glasgow, UK.
Insights
Hyperostosis frontalis interna (HFI) is more common in acromegaly patients, especially those with hyperprolactinaemia. This association warrants further investigation in acromegaly management.
Area of Science:
- Endocrinology
- Radiology
- Medical Imaging
Background:
- Hyperostosis frontalis interna (HFI) is a condition characterized by thickening of the inner table of the frontal bone.
- Acromegaly is a hormonal disorder caused by excessive growth hormone production.
- Hyperprolactinaemia is a condition of elevated prolactin levels in the blood.
Purpose of the Study:
- To investigate the association between hyperostosis frontalis interna (HFI) and acromegaly.
- To determine if hyperprolactinaemia influences the prevalence of HFI in acromegalic patients.
Main Methods:
- Skull X-rays of 36 acromegalic patients (19 with hyperprolactinaemia) were compared to 36 age-sex matched controls.
- Intra- and interobserver variability for HFI assessment was evaluated.
- Subgroup analyses were performed comparing acromegalics and acromegalics with hyperprolactinaemia to controls.
Main Results:
- HFI was significantly more prevalent in the acromegalic cohort compared to controls (P = 0.0002).
- This association was observed in both male and female acromegalic patients.
- Acromegalic patients with hyperprolactinaemia showed a higher HFI prevalence than controls (P = 0.0001).
- HFI severity correlated with age in both sexes and with disease duration in females.
Conclusions:
- A strong association exists between HFI and acromegaly, particularly when hyperprolactinaemia is present.
- The findings suggest HFI may have symptomatic significance in acromegaly.
- Confirmation or refutation of HFI is recommended for all acromegaly patients.
Abstract:
The association between hyperostosis frontalis interna (HFI), acromegaly and hyperprolactinaemia was investigated. Thirty six acromegalic patients, of whom 19 had hyperprolactinaemia, were compared with 36 randomly-selected, age-sex matched controls. There was a higher prevalence of HFI in the skull X-rays of the acromegalic cohort (P = 0.0002) when compared to the control group. This difference was apparent in both men (P = 0.01) and women (P = 0.01). Acromegalic patients with hyperprolactinaemia also expressed HFI in a higher proportion of individuals than the control group (P = 0.0001). Intra- and interobserver variability was assessed and concordance with 100% and 97% in the moderate and severe HFI sub-groups. The following sub-group analysis was undertaken: acromegalics and those acromegalics with hyperprolactinaemia were compared with the controls and a highly significant distinction was confirmed (P = 0.0007 and P = 0.00001 respectively). A relationship between HFI severity and the patient's age was noted in both male and female acromegalics. Also, the severity of HFI appeared related to disease duration in female acromegalics. The cause of HFI remains unknown but appears to be strongly associated with acromegaly, particularly in the presence of co-existent hyperprolactinaemia. The association may have symptomatic significance and the presence of HFI should be confirmed or refuted in all patients with acromegaly.
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