4.3 Article

Evaluation of cardiovascular risk factors in long-term survivors of adult- and childhood-onset brain tumours: a pilot study

Journal

ENDOCRINE CONNECTIONS
Volume 12, Issue 8, Pages -

Publisher

BIOSCIENTIFICA LTD
DOI: 10.1530/EC-22-0491

Keywords

brain tumour; vascular risk; body composition; lipids; insulin resistance

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Survivors of childhood brain tumors and teenage and young adult cancer survivors have an adverse cardiovascular risk profile, including elevated total cholesterol, LDL-C, insulin, and increased insulin resistance. They also show adverse body composition, with increased total and truncal fat mass. Both childhood-onset and adult-onset brain tumor survivors exhibit an adverse metabolic profile and increased body fat, potentially increasing their risk of vascular morbidity and mortality.
Background: Survivors of childhood brain tumours (SCBT) and teenage and young adult cancer survivors have an adverse cardiovascular risk profile, which translates into an increased vascular mortality. Data on cardiovascular risk profiles in SCBT are limited, and furthermore, there are no data in adult-onset (AO) brain tumours. Patients and methods: Fasting lipids, glucose, insulin, 24-h blood pressure (BP), and body composition were measured in 36 brain tumour survivors (20 AO; 16 childhood-onset (CO)) and 36 age- and gender-matched controls. Results: Compared with controls, patients had elevated total cholesterol (5.3 +/- 1.1 vs 4.6 +/- 1.0 mmol/L, P = 0.007), LDL-C (3.1 +/- 0.8 vs 2.7 +/- 0.9 mmol/L, P = 0.011), insulin (13.4 +/- 13.1 vs 7.6 +/- 3.3 miu/L, P = 0.014), and increased insulin resistance (homeostatic model assessment for insulin resistance (HOMA-IR) 2.90 +/- 2.84 vs 1.66 +/- 0.73, P = 0.016). Patients showed adverse body composition, with increased total body fat mass (FM) (24.0 +/- 12.2 vs 15.7 +/- 6.6 kg, P < 0.001) and truncal FM (13.0 +/- 6.7 vs 8.2 +/- 3.7 kg, P < 0.001). After stratification by timing of onset, CO survivors showed significantly increased LDL-C, insulin, and HOMA-IR compared with controls. Body composition was characterized by the increased total body and truncal FM. Truncal fat mass was increased by 84.1% compared with controls. AO survivors showed similar adverse cardiovascular risk profiles, with increased total cholesterol and HOMA-IR. Truncal FM was increased by 41.0% compared with matched controls (P = 0.029). No difference in mean 24-h BP was noted between patients and controls irrespective of the timing of cancer diagnosis. Conclusion: The phenotype of both CO and AO brain tumour survivors is characterized by an adverse metabolic profile and body composition, putatively placing long-term survivors at increased risk of vascular morbidity and mortality.

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