TY - JOUR
T1 - Early indicators of primary brain tumours
T2 - a population-based study with 10 years’ follow-up
AU - Marku, Mirketa
AU - Rasmussen, Birthe Krogh
AU - Dalton, Susanne Oksbjerg
AU - Johansen, Christoffer
AU - Hamerlik, Petra
AU - Andersen, Klaus Kaae
AU - Meier, Sandra Melanie
AU - Bidstrup, Pernille Envold
N1 - © 2020 European Academy of Neurology.
PY - 2021/1
Y1 - 2021/1
N2 - Background and purpose: To improve diagnoses of primary brain tumours, knowledge about early indicators is needed. Nationwide Danish health registries were used to conduct a population-based case–control study including all persons diagnosed with a primary brain tumour between 2005 and 2014 in Denmark. Methods: All 5135 adults diagnosed with a primary brain tumour in the Danish Cancer Registry were matched to 19 572 general population comparisons from the Danish Civil Registration System. Conditional logistic regression analyses were applied to estimate age- and multivariable-adjusted odds ratios (ORs) for the occurrence of a primary brain tumour up to 10 years after hospital diagnoses or prescription of medications related to nervous system diseases and mental and behavioural disorders. Results: Increased odds for primary brain tumour after nervous system diseases and mental and behavioural disorders manifested up to 10 years before tumour diagnosis were found. Increased odds were seen especially for hospital contacts for inflammatory nervous system diseases [OR 11.3; 95% confidence interval (CI) 6.5–19.7], epilepsy (OR 9.0; 95% CI 7.6–10.7) and antiepileptic medications (OR 3.6; 95% CI 3.2–4.0), whilst antidementia medications provided a strong, protective association for primary brain tumours (OR 0.5; 95% CI 0.3–0.8). Conclusions: Sub-groups of patients diagnosed with or being prescribed certain medications targeting nervous system diseases and mental and behavioural disorders may be at increased risk of being diagnosed with a primary brain tumour. Further studies should disentangle the potential underlying common pathogenetic pathways. The results are important for the development of systematic clinical approaches to ensure early diagnosis of primary brain tumours.
AB - Background and purpose: To improve diagnoses of primary brain tumours, knowledge about early indicators is needed. Nationwide Danish health registries were used to conduct a population-based case–control study including all persons diagnosed with a primary brain tumour between 2005 and 2014 in Denmark. Methods: All 5135 adults diagnosed with a primary brain tumour in the Danish Cancer Registry were matched to 19 572 general population comparisons from the Danish Civil Registration System. Conditional logistic regression analyses were applied to estimate age- and multivariable-adjusted odds ratios (ORs) for the occurrence of a primary brain tumour up to 10 years after hospital diagnoses or prescription of medications related to nervous system diseases and mental and behavioural disorders. Results: Increased odds for primary brain tumour after nervous system diseases and mental and behavioural disorders manifested up to 10 years before tumour diagnosis were found. Increased odds were seen especially for hospital contacts for inflammatory nervous system diseases [OR 11.3; 95% confidence interval (CI) 6.5–19.7], epilepsy (OR 9.0; 95% CI 7.6–10.7) and antiepileptic medications (OR 3.6; 95% CI 3.2–4.0), whilst antidementia medications provided a strong, protective association for primary brain tumours (OR 0.5; 95% CI 0.3–0.8). Conclusions: Sub-groups of patients diagnosed with or being prescribed certain medications targeting nervous system diseases and mental and behavioural disorders may be at increased risk of being diagnosed with a primary brain tumour. Further studies should disentangle the potential underlying common pathogenetic pathways. The results are important for the development of systematic clinical approaches to ensure early diagnosis of primary brain tumours.
KW - adult
KW - case–control study
KW - oncology
KW - primary brain tumour
KW - risk factors
UR - http://www.scopus.com/inward/record.url?scp=85092500007&partnerID=8YFLogxK
U2 - 10.1111/ene.14527
DO - 10.1111/ene.14527
M3 - Journal article
C2 - 32916012
SN - 1351-5101
VL - 28
SP - 278
EP - 285
JO - European Journal of Neurology
JF - European Journal of Neurology
IS - 1
ER -